WO2011097649A2 - Methods and apparatus for synthesizing imaging agents, and intermediates thereof - Google Patents

Methods and apparatus for synthesizing imaging agents, and intermediates thereof Download PDF

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Publication number
WO2011097649A2
WO2011097649A2 PCT/US2011/024109 US2011024109W WO2011097649A2 WO 2011097649 A2 WO2011097649 A2 WO 2011097649A2 US 2011024109 W US2011024109 W US 2011024109W WO 2011097649 A2 WO2011097649 A2 WO 2011097649A2
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WIPO (PCT)
Prior art keywords
optionally substituted
imaging agent
imaging
alkyl
formula
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PCT/US2011/024109
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French (fr)
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WO2011097649A3 (en
Inventor
Richard R. Cesati
Edward H. Cheesman
Joel Lazewatsky
Heike S. Radeke
James F. Castner
Enrico Mongeau
Dianne D. Zdankiewicz
Robert Wilburn Siegler
Marybeth Devine
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Lantheus Medical Imaging, Inc.
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Priority to SG2012057279A priority Critical patent/SG183134A1/en
Priority to KR1020187013968A priority patent/KR20180055933A/en
Priority to KR1020177004163A priority patent/KR20170033873A/en
Priority to NO11740546A priority patent/NO2534136T3/no
Priority to BR112012019789A priority patent/BR112012019789A2/en
Priority to EP21216335.6A priority patent/EP4046990A1/en
Priority to NZ602291A priority patent/NZ602291A/en
Priority to MX2012009174A priority patent/MX348958B/en
Priority to EP11740546.4A priority patent/EP2534136B1/en
Priority to EP17189439.7A priority patent/EP3323810B1/en
Priority to ES11740546.4T priority patent/ES2651466T3/en
Priority to CA2789044A priority patent/CA2789044C/en
Priority to DK11740546.4T priority patent/DK2534136T3/en
Priority to RU2012138262A priority patent/RU2631500C2/en
Application filed by Lantheus Medical Imaging, Inc. filed Critical Lantheus Medical Imaging, Inc.
Priority to KR1020197015985A priority patent/KR20190067255A/en
Priority to US13/577,674 priority patent/US8936777B2/en
Priority to AU2011213568A priority patent/AU2011213568B2/en
Priority to JP2012552155A priority patent/JP6092628B2/en
Priority to CN201180016758.9A priority patent/CN102858752B/en
Priority to KR1020127023380A priority patent/KR101709372B1/en
Priority to KR1020217035027A priority patent/KR102438133B1/en
Publication of WO2011097649A2 publication Critical patent/WO2011097649A2/en
Publication of WO2011097649A3 publication Critical patent/WO2011097649A3/en
Priority to IL221253A priority patent/IL221253B/en
Priority to US14/561,594 priority patent/US9603951B2/en
Priority to US15/433,387 priority patent/US10022462B2/en
Priority to US15/901,286 priority patent/US10842892B2/en
Priority to IL263543A priority patent/IL263543B/en
Priority to US17/062,757 priority patent/US20210187131A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K49/00—Preparations for testing in vivo
    • A61K49/04—X-ray contrast preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K49/00—Preparations for testing in vivo
    • A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
    • A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
    • A61K49/10—Organic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04—Organic compounds
    • A61K51/041—Heterocyclic compounds
    • A61K51/044—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
    • A61K51/0459—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having six-membered rings with two nitrogen atoms as the only ring hetero atoms, e.g. piperazine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14—Oxygen atoms
    • C07D237/16—Two oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • compositions, Methods, and Systems for Imaging each of which is incorporated herein by reference.
  • the present invention relates to systems, compositions, methods, and apparatuses for synthesizing imaging agents, and precursors thereof.
  • Mitochondria are membrane-enclosed organelles distributed through the cytosol of most eukaryotic cells. Mitochondria are especially concentrated in myocardial tissue.
  • MC-1 is a membrane-bound protein complex of 46 dissimilar subunits. This enzyme complex is one of three energy-transducing complexes that constitute the respiratory chain in mammalian mitochondria. This NADH-ubiquinone oxidoreductase is the point of entry for the majority of electrons that traverse the respiratory chain, eventually resulting in the reduction of oxygen to water (Q. Rev. Biophys. 1992, 25, 253-324).
  • inhibitors of MC-1 include deguelin, piericidin A, ubicidin-3, rolliniastatin-1, rolliniastatin-2 (bullatacin), capsaicin, pyridaben, fenpyroximate, amytal, MPP+, quinolines, and quinolones (BBA 1998, 1364, 222-235). Studies have shown that interrupting the normal function of mitochondria could advantageously concentrate certain compounds in the mitochondria, and hence in the mitochondria-rich myocardial tissue. Compounds that include an imaging moiety
  • ⁇ e.g., F can be useful in determining such a build-up of compounds, thereby providing valuable diagnostic markers for myocardial perfusion imaging.
  • such compounds may find application for the diagnosis of coronary artery disease (CAD).
  • CAD coronary artery disease
  • CAD is a major cause of death in modern industrialized countries and it has been found previously that assessments of regional myocardial perfusion at rest and during stress (exercise or pharmacologic coronary vasodilation) are valuable for noninvasive diagnosis of CAD. While myocardial perfusion imaging (MPI) with Positron Emission Tomography (PET) has been shown to be superior in some embodiments as compared to single photon emission computed tomography (SPECT), widespread clinical use of PET MPI has been limited by the previously available PET myocardial perfusion tracers.
  • MPI myocardial perfusion imaging
  • PET Positron Emission Tomography
  • SPECT single photon emission computed tomography
  • PET blood flow tracers such as rubidium-82 ( 82 Rb) chloride, nitrogen- 13 ( 13 N) ammonia, and oxygen- 15 ( 15 0) water, have been developed and validated for assessment of myocardial perfusion. 13 N and 15 0 are cyclotron-produced isotopes with short half-lives. Therefore, their use is limited to facilities with an on-site cyclotron.
  • the invention provides, in a broad sense, methods for synthesizing imaging agents and their precursors, compounds that are imaging agents precursors, and methods of use thereof.
  • in invention provides a method of synthesizing an imaging agent comprising formula:
  • W is alkyl or heteroalkyl, optionally substituted;
  • R is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 3 can be the same or different and is alkyl optionally substituted with an imaging moiety or heteroalkyl optionally substituted with an imaging moiety; and
  • n is 1, 2, 3, 4, or 5; the method comprising steps of:
  • n 1, 2, 3, 4, or 5;
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • R 3 can be the same or different and are alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted,
  • R 5 is hydroxyl or halide;
  • R 6 is alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted, wherein, when R 5 is hydroxyl, at least one of R 6 and R 3 comprises a leaving group; or wherein R 5 is halide, at least one of R 6 or R 3 comprises a hydroxyl, to produce a compound comprising formula:
  • W is alkyl or heteroalkyl, optionally substituted;
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 3 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; wherein at least one R 3 comprises hydroxyl; and n is 1, 2, 3, 4, or 5;
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • R 3 can be the same or different and are alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted;
  • W is alkyl or heteroalkyl, optionally substituted;
  • R is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 3 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; wherein at least one R 3 comprises hydroxyl; and n is 1, 2, 3, 4, or 5; with a sulfonate- containing species to produce a sulfonate-containing compound comprising formula:
  • W is alkyl or heteroalkyl, optionally substituted;
  • R is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 3 can be the same or different and is alkyl optionally substituted with a sulfonate-containing group or heteroalkyl optionally substituted with a sulfonate-containing group; wherein at least one R 3 comprises a sulfonate-containing group; and n is 1, 2, 3, 4, or 5; replacing the sulfonate-containing group of the sulfonate-containing compound with an imaging moiety to yield a compound comprising formula:
  • W is alkyl or heteroalkyl, optionally substituted;
  • R is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 3 can be the same or different and is alkyl optionally substituted with an imaging moiety or heteroalkyl optionally substituted with an imaging moiety;
  • n is 1, 2, 3, 4, or 5; provided that at least one fluorine species is present in the compound.
  • the invention provides a method for F-labeling a compound comprising formula:
  • R 1 is alkyl
  • R 2 is hydrogen or halogen
  • R 3 is alkyl substituted with a sulfonate-containing group, alkoxy substituted with a sulfonate-containing group, or alkoxyalkyl substituted with a sulfonate-containing group.
  • the method comprises reacting the compound with an 18 F species in the presence of an ammonium salt or a bicarbonate salt to form a product comprising the 18 F species.
  • R 3 is alkoxyalkyl substituted with a sulfonate-containing group.
  • the sulfonate-containing group is mesylate, tosylate, triflate, or 1,2-cyclic sulfate.
  • R 2 is a halogen.
  • R 2 is chloride.
  • R 1 is a methyl, ethyl, propyl, n- butyl, 5-butyl, or i-butyl.
  • R 1 is i-butyl.
  • the product comprises formu
  • the invention provides a method for synthesizing a precursor to (or of) an imaging agent, comprising reacting a compound comprising formula (III) with a nucleophile, wherein formula (III) comprises the structure:
  • W is alkyl or heteroalkyl, optionally substituted;
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 3 can be the same or different and is an alkyl optionally substituted with a leaving group or heteroalkyl optionally substituted with a leaving group, provided R 3 comprises at least one leaving group; and n is 1, 2, 3, 4, or 5, provided at least one R 3 is substituted with a leaving group; with a nucleophile wherein the nucleophile replaces the at least one leaving group to produce a product (or precursor).
  • the nucleophile is ethylene glycol.
  • reacting the compound with the nucleophile occurs in the presence of a base.
  • the base may be but is not limited to a metal or a metal salt.
  • the base may be sodium metal, sodium hydride, potassium i-butoxide, potassium carbonate, or potassium hydroxide.
  • the base is potassium t-butoxide or potassium hydroxide.
  • the base is potassium t-butoxide.
  • reacting the compound with the nucleophile occurs in the presence of a catalyst.
  • the catalyst may be a tetraalkylammonium iodide including but not limited to a tetraethylammonium iodide.
  • the leaving group is a halide including but not limited to bromide.
  • W is -0( ⁇ 3 ⁇ 4)-; R 1 is i-butyl; R 2 is chloride; and R 3 is alkyl substituted with a leaving group.
  • the compound comprising formula (III) comprises the structure:
  • the compound comprising formula (III) comprises the structure:
  • the product (or precursor) comprises formula:
  • the product (or precursor) comprises formula:
  • the method further comprises reacting a compound comprising formula (IV) with a reactant comprising a leaving group to produce the compound comprising formula (III), wherein formula (IV) comprises the structure:
  • W is alkyl or heteroalkyl, optionally substituted;
  • R is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • each R 4 can be the same or different and is an alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; provided R 4 comprises at least one hydroxyl group; and n is 1, 2, 3, 4, or 5; and wherein the at least one hydroxyl is replaced with the leaving group.
  • reacting the compound comprising formula (IV) is performed in the presence of a halogenation reagent.
  • the halogenation reagent is a brominating reagent.
  • the brominating reagent may be phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine, although it is not so limited.
  • W is -0(CH 2 )-; R 1 is i-butyl; R 2 is chloride; and R 4 is alkyl substituted with hydroxyl.
  • the compound comprising formula (IV) comprises the structure:
  • the compound comprising formula (IV) comprises the structure:
  • the product comprises formula:
  • the compound comprising formula (IV) is formed by etherification of precursor compounds comprising formulae (IVa) and (IVb):
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • R 5 is hydroxyl or halide
  • R 6 and R 7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, each of which may be optionally and independently substituted, wherein when R 5 is hydroxyl at least one of R 6 and R 7 comprises a leaving group or a group that can be replaced by a leaving group, or when
  • R 5 is halide, at least one of R 6 and R 7 comprise a hydroxyl.
  • the compound comprising formula (IV) is formed by etherification of the compounds comprising formulae:
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • R 5 is hydroxyl or halide
  • R 6 and R 7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, any of which may be substituted, wherein when R 5 is hydroxyl at least one of R 6 and R 7 comprises a leaving group or a group that can be replaced by a leaving group, or when R 5 is halide, at least one of R 6 and R 7 comprises a hydroxyl.
  • the compound comprising formula (IV) is formed by etherification of precursor compounds comprising formulae (IVa) and (IVd):
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • R 5 is hydroxyl or halide; and
  • R 6 and R 7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, each of which may be optionally and independently substituted, wherein when R 5 is hydroxyl at least one of R 6 and R 7 comprises a leaving group, or when R 5 is halide, at least one of R 6 and R 7 comprises a hydroxyl.
  • the compound comprising formula (IV) is formed by etherification of compounds comprising formulae:
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide;
  • R 5 is hydroxyl or halide;
  • R 6 and R 7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, any of which may be substituted, wherein when R 5 is hydroxyl at least one of R 6 and R 7 comprises a leaving group, or when R 5 is halide, at least one of R 6 and R 7 comprises a hydroxyl, or when R 5 is halide, at least one of R 6 and R 7 comprises a hydroxyl..
  • the etherification comprises reacting the precursor compounds in the presence of a base.
  • the base comprises a carbonate ion.
  • R 5 is halide; and R 6 and R 7 is each substituted alkyl. In some embodiments, R 5 is chloride; and R 6 and R 7 is each alkyl substituted with a hydroxyl.
  • the compound comprising formula (IV) is synthesized by etherification of precursor compounds comprising formulae:
  • R 1 is alkyl, optionally substituted;
  • R 2 is hydrogen or halide; to form a product comprising formula:
  • the compound comprising formula (IV) is synthesized by etherification of compounds comprising formulae:
  • R 5 is hydroxyl; and R 6 is a carbonyl-containing group and R 7 is a substituted alkyl. In some embodiments, R 5 is hydroxyl; and R 6 is an ester and R 7 i iss a allkkvyll s suubbssttiittuutteedd w wiitthh a a l lee.aavviinngp g PTrOoUuTpV.
  • the compound comprising formula (IV) is synthesized by etherification of the compounds comprising formulae:
  • the method further comprises exposing the product to a reducing agent to convert the ester group to an alcohol.
  • the reducing agent may be lithium aluminum hydride, lithium borohydride, or diisobutylaluminum hydride
  • the invention provides a method for synthesizing an imaging agent comprising contacting an imaging agent precursor with a fluoride species and an ammonium salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species wherein the molar ratio of ammonium salt to imaging agent precursor is less than 1.5:1, including about 1:1 or less.
  • the molar ratio of ammonium salt to imaging agent precursor is about 1: 1 or less, or about 0.75:1 or less, or about 0.5:1 or less, or about 0.25:1 or less, or about 0.05: 1 or less. In some embodiments, the molar ratio of ammonium salt to imaging agent precursor is from about 1:1 to about 0.5:1. In some embodiments, the molar ratio of ammonium salt to imaging agent precursor ranges from about 1.4:1 to about 0.05: 1.
  • the ammonium salt is ammonium bicarbonate, ammonium hydroxide, ammonium acetate, ammonium lactate, ammonium trifluoroacetate, ammonium methanesulfonate, ammonium p-toluenesulfonate, ammonium nitrate, ammonium iodide, or ammonium bisulfate.
  • the ammonium salt is a tetraalkylammonium salt.
  • the ammonium salt may be R 4 NHCO 3 , wherein R is alkyl.
  • the ammonium salt may be Et 4 NHC0 3 .
  • the invention provides a method for synthesizing an imaging agent, comprising contacting an imaging agent precursor with a fluoride species and a bicarbonate salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species, wherein the molar ratio of bicarbonate salt to imaging agent precursor is less than 1.5:1, including about 1:1 or less.
  • the molar ratio of bicarbonate salt to imaging agent precursor is about 1:1 or less, or about 0.75:1 or less, or about 0.5: 1 or less, or about 0.25:1 or less, or about 0.05 : 1. In some embodiments, the molar ratio of bicarbonate salt to imaging agent precursor is from about 1: 1 to about 0.5:1. In some embodiments, the molar ratio of bicarbonate salt to imaging agent precursor ranges from about 1.4:1 to about 0.05:1. In some embodiments, wherein the molar ratio of bicarbonate salt to imaging agent precursor is from about 0.5: 1 to about 1:1.
  • the bicarbonate salt is a metal bicarbonate.
  • the bicarbonate salt may be sodium bicarbonate, calcium bicarbonate, potassium
  • bicarbonate or magnesium bicarbonate, although it is not so limited.
  • the bicarbonate salt is ammonium bicarbonate. In some embodiments, the bicarbonate salt is an tetraalkylammonium bicarbonate.
  • the bicarbonate salt comprises the formula R 4 NHCO 3 , wherein R is alkyl.
  • the bicarbonate salt may be Et 4 NHC0 3 .
  • the imaging agent precursor is further exposed to a cryptand, such as but not limited to 4,7,13,16,21,24-Hexaoxa-l,10-diazabicyclo[8.8.8]- hexacosane.
  • a cryptand such as but not limited to 4,7,13,16,21,24-Hexaoxa-l,10-diazabicyclo[8.8.8]- hexacosane.
  • contacting is performed in the absence of a carbonate salt such as but not limited to potassium carbonate.
  • the contacting is performed in the absence of a cryptand, such as but not limited to 4,7,13,16,21,24-Hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane.
  • a cryptand such as but not limited to 4,7,13,16,21,24-Hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane.
  • the invention provides a method for synthesizing an imaging agent, comprising contacting an imaging agent precursor with a fluoride species under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species, wherein the contacting is performed at a pH below 7. In some embodiments, the contacting is performed at a pH below 6, or at a pH below 5, or at a pH between 5 and 6.
  • the leaving group is a sulfonate-containing group.
  • the leaving group may be a mesylate, tosylate, triflate, or 1,2,-cyclic sulfate group.
  • the leaving group is a tosylate group.
  • the fluoride species is an 18 F ion.
  • the imaging agent precursor comprises formula (I):
  • K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
  • L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
  • M is selected from the group consisting of hydrogen, alkoxy
  • the imaging agent comprises formula (II):
  • K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C 6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
  • L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C 6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
  • M is selected from the group consisting of hydrogen, alkoxy
  • J is O.
  • R is methyl, ethyl, n- propyl, i-propyl, n-butyl, i-butyl, or t-butyl, each optionally substituted with a leaving group.
  • R 29 is t-butyl.
  • Q is chloro.
  • each of R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , and R 27 is hydrogen.
  • Y is carbon
  • K and L are hydrogen
  • M is selected from the group consisting of alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group.
  • Y is carbon, K and L is each hydrogen, and M is alkyloxy optionally substituted with a leaving group.
  • the imaging agent precursor comprises formula:
  • L is a leaving group
  • the imaging agent comprises formula:
  • Im is an imaging moiety
  • the imaging agent precursor comprises: wherein L is a leaving
  • Im is an imaging moiety
  • the imaging agent precursor comprises formula:
  • the imaging agent comprising the fluoride species comprises formula:
  • the method further comprises purifying the imaging agent using at least one purification technique.
  • the purification technique is chromatography such as but not limited to HPLC.
  • the purification technique is filtration such as but not limited to filtration through a C-18 resin.
  • the method further comprises combining the imaging agent with a stabilizing agent.
  • the stabilizing agent is ascorbic acid, or a salt thereof
  • the invention provides a method for manufacturing an imaging agent comprising formula:
  • step (b) comprises heating the mixture to a temperature between 50°C and 250°C. In some embodiments, step (b) comprises heating the mixture for less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes.
  • the method further comprises (g) contacting the diluted eluent of (f) with a C18 resin; (h) washing the contacted C18 resin with a solution of ascorbic acid or a salt thereof; (i) eluting
  • the method further comprises (k) aseptically filtering the diluted eluent of (j), and (1) optionally, determining the presence of
  • the invention provides imaging agents made by any of the preceding methods.
  • the invention provides an imaging agent comprising formula:
  • imaging agent is manufactured by (a) contacting a tosylate precursor comprising formula:
  • step (b) comprises heating the mixture to a temperature between 50°C and 250°C. In some embodiments, step (b) comprises heating the mixture less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes.
  • the manufacturing further comprises (g) contacting the diluted eluent of (f) with a C18 resin; (h) washing the contacted CI 8 resin with a solution of ascorbic acid or a salt thereof; (i) eluting
  • the manufacturing further comprises: (k) aseptically filtering the diluted eluent of (j), and (1) optionally, determining the presence of
  • the invention provides a method for synthesizing a fluorinated compound, comprising reacting, in the presence of a carbonate or bicarbonate, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl group substituted with a halide or a sulfonate-containing group, with (ii) a salt comprising a fluoride species and weakly coordinating cation.
  • the alkoxyalkyl group is substituted with a sulfonate- containing group.
  • the sulfonate-containing group is mesylate, tosylate, triflate or 1,2-cyclic sulfate.
  • the sulfonate-containing group is tosylate.
  • the weakly coordinating cation is a tetraalkylammonium cation.
  • the fluoride species is enriched for 18 F isotope.
  • the invention provides a method for synthesizing a fluorinated compound comprising reacting, in the presence of a carbonate or bicarbonate, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl substituted with a halide or a sulfonate-containing group, with (ii) an 18 F isotope.
  • the invention provides a method for synthesizing a fluorinated compound, comprising reacting (i) a precursor of the fluorinated compound comprising an alkoxyalkyl substituted with a halide or a sulfonate-containing group, with (ii) an 18 F isotope, in the presence of a tetraalkylammonium bicarbonate or tetraalkylammonium carbonate.
  • the reaction is carried out in the presence of a tetraalkylammonium bicarbonate.
  • the tetraalkylammonium bicarbonate is tetraethylammonium bicarbonate, tetrabutylammonium bicarbonate, or tetrahexylammonium bicarbonate.
  • the invention provides a method for 18 F-labeling comprising formula:
  • R is -lower alkyl-sulfonate
  • R 1 is an Ci-Cio alkyl
  • R 2 is H or a halogen, comprising reacting the compound with F in the presence of a tetraalkylammonium bicarbonate or tetraalkylammonium carbonate.
  • R is - (CH 2 )0(CH 2 )n-sulfonate-containing group, wherein n is an integer from 1 to 5.
  • the sulfonate-containing group is mesylate, tosylate, triflate, or 1,2-cyclic sulfate.
  • R 2 is a halogen.
  • R 2 is chloride.
  • R 1 is methyl, ethyl, propyl or butyl. In some embodiments, R 1 is i-butyl. In some embodiments, R is -CH 2 -0-CH 2 -CH 2 -tosylate, R 1 is i-butyl and R 2 is chloride.
  • the invention provides a method for synthesizing a precursor to an imaging agent, comprising reacting a compound comprising formula (V):
  • W is alkyl or heteroalkyl, optionally substituted;
  • R is alkyl, optionally substituted; and
  • R 2 is hydrogen or halide; with a nucleophile or a radical species to produce a compound comprising formula (VI):
  • the nucleophile is a hydride ion.
  • the hydride ion is generated from diisobutylaluminum hydride (DIBAL-H).
  • the radical species is ⁇ .
  • the compound comprising formula (V) wherein W is - OCH 2 - is synthesized by etherification of precursor compounds comprising formulae (Va) and (Vb):
  • R 1 is i-butyl and R 2 is CI.
  • etherification comprises reacting the precursor compounds in the presence of a base.
  • the base comprises a carbonate ion.
  • the base comprises a hydroxide ion.
  • the base is sodium hydroxide or tetramethyl ammonium hydroxide.
  • the etherification reaction comprises exposure to sodium hydroxide and benzyl
  • the compound comprising formula (Vb) is produced by exposing the compound comprising formula:
  • the reducing agent is lithium aluminum hydride or lithium borohydride. In some embodiments, the reducing agent is lithium aluminum hydride.
  • the invention provides a method for forming a sulfonate- containing precursor of an imaging agent, comprising reacting a compound comprising formula:
  • the sulfonate-containing group is mesylate, tosylate, or triflate. In some embodiments, the sulfonate-containing group is tosylate. In some embodiments, the sulfonate-containing precursor of an imaging agent comprising the formula:
  • the sulfonate-containing precursor is reacted with an imaging moiety to form an imaging agent.
  • the imaging moiety is a radioisotope. In some embodiments, the imaging moiety is n C, 13 N, 18 F, 123 1, 125 1, 99m Tc, 95 Tc, m In, 62 Cu, 64 Cu, 67 Ga, or 68 Ga. In some embodiments, the imaging moiety is 18 F.
  • the invention provides a method for synthesizing an imaging agent, comprising reac lae:
  • the method further comprises reacting the sulfonate-containing precursor of an imaging agent with an imaging moiety to form the imaging agent.
  • the invention provides a compound having the structure:
  • the invention provides a compound comprising formula:
  • the invention provides a compound comprising formula:
  • the invention provides a compound comprising formula:
  • the invention provides a compound comprising formula:
  • the invention provides a method of imaging a subject, comprising administering to a subject a first dose of imaging agent comprising the formula:
  • the second dose of the imaging agent is administered within less than about 48 hours, 24 hours, 18 hours, 12 hours, 6 hours, 5 hours, 4 hours, 3 hours, 2 hours, 1 hour, 30 minutes, or 15 minutes after acquiring the at least one first image.
  • the second dose of the imaging agent is at least 2.0 times greater than the first dose of the imaging agent.
  • the first image is obtained during an image acquisition period between 1 and 20 minutes.
  • the second image is obtained during an image acquisition period between 1 and 20 minutes.
  • the portion of the subject is at least a portion of the cardiovascular system.
  • the portion of the cardiovascular system is at least a portion of the heart.
  • the acquiring employs positron emission tomography.
  • the method further comprises determining the presence or absence of a cardiovascular disease or condition in the subject.
  • the cardiovascular disease is coronary artery disease or myocardial ischemia.
  • the imaging agent is administered as a formulation comprising water, less than about 5% ethanol, and less than about 50 mg/mL sodium ascorbate.
  • the formulation comprising the imaging agent is administered via an intravenous bolus injection.
  • the stress is induced by exercising the subject.
  • the second dose of the imaging agent is administered during the exercise.
  • the first dose of the imaging agent is between about 1.0 mCi to about 2.5 mCi. In some embodiments, the first dose of the imaging agent is between about 1.7 mCi to about 2.0 mCi. In some embodiments, the first dose of the imaging agent is between about 2.5 to about 3.0 mCi.
  • the wait time between acquiring at least one first image of a portion of the subject and administering to the subject a second dose of the imaging agent is 60 minutes.
  • the second dose of the imaging agent is administered in an amount that is at least 2.5, or at least 3.0 times greater than the first dose of the imaging agent.
  • the second dose of the imaging agent is administered in an amount between 2.5 and about 5.0, or 2.5 and 4.0, or 3.0 and 4.0 time greater, or between 3.0 and 5.0 times greater than the first dose of the imaging agent.
  • the second dose of the imaging agent is between about 8.6 mCi and about 9.0 mCi, or between about 8.6 mCi and about 9.5 mCi, or between about 9.0 to about 9.5 mCi.
  • the stress is pharmacological stress.
  • the pharmacological stress is induced by administering a pharmacological stress agent to the subject.
  • the pharmacological stress agent is a vasodilator.
  • the vasodilator is adenosine.
  • the second dose of the imaging agent is administered after the subject has been administered the pharmacological stress agent.
  • the second dose of the imaging agent is administered when the subject is at peak vasodilation from the pharmacological stress agent.
  • the first dose of the imaging agent is between about 2.0 mCi to about 3.5 mCi.
  • the first dose of the imaging agent is between about 2.4 mCi to about 3.0 mCi or between about 2.4 mCi to about 2.9 mCi. In some embodiments, the first dose of the imaging agent is between about 2.5 mCi to about 3.0 mCi or between about 2.5 mCi and about 3.5 mCi.
  • the wait time between acquiring at least one first image of a portion of the subject and administering to the subject a second dose of the imaging agent is 30 minutes.
  • the second dose of the imaging agent is administered in an amount at least 2.0 times greater than the first dose of the imaging agent.
  • the second dose of the imaging agent is administered in an amount that is between 2 to 3 times greater than the first dose of the imaging agent, including 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, or 2.9 times greater.
  • the second dose of the imaging agent is between about 5.7 mCi and about 6.2 mCi. In some embodiments, the second dose of the imaging agent is between about 6.0 mCi and about 6.5 mCi or between about 5.7 mCi and about 6.5 mCi. In some embodiments, the total of the first and second dose of the imaging agent does not exceed about 14 mCi.
  • the invention provides a syringe comprising a composition comprising the imaging agent comprises the formula:
  • the syringe adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13,% 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of the imaging agent. In some cases, the syringe adsorbs between about 1% and about 20%, or between about 5% and about 15%, or between about 1% and about 15%, or between 2% and about 10%, or between about 5% and about 20%.
  • the syringe comprises a plunger that adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13,% 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of the imaging agent.
  • the syringe comprises a plunger that is not rubber-tipped.
  • the syringe is a latex-free syringe.
  • the syringe comprises no rubber, and no silicon lubricants.
  • the syringe is a non-reactive syringe. In some cases, the syringe adsorbs between about 1% and about 20%, or between about 5% and about 15%, or between about 1% and about 15%, or between 2% and about 10%, or between about 5% and about 20%.
  • the syringe further comprises sodium ascorbate, ethanol, and water.
  • the imaging agent is in a solution comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water.
  • the imaging agent is present in the syringe in a dose between about 1.5 and about 14 mCi.
  • the invention provides a method of imaging a subject, comprising subjecting a subject to stress; administering to the subject a first dose of an imaging agent comprising the formula:
  • the amount of the second dose is more than 1.5 times the amount of the first dose.
  • the invention provides a method of imaging a subject, comprising subjecting a subject to stress; administering to the subject a dose of an imaging agent comprising formula:
  • the amount of the dose is less than 14 mCi. In some embodiments, the amount of the dose is between 1 mCi and 4 mCi.
  • the invention provides a cassette for the preparation of an imaging agent comprising formula:
  • the invention provides an automated reaction system, comprising:
  • the invention provides an apparatus for synthesizing an imaging agent comprising a linear arrangement of a plurality of stopcock manifolds connected one or more of the components selected from the group consisting of a [ 18 0]H 2 0 recovery system, gas inlet, reservoir with solution of imaging agent precursor, vial, anion exchange cartridge, C-18 cartridge, syringe, solvent reservoir, reaction vessel, HPLC system, collection vessel, reservoir for solution of ascorbic acid or salt thereof, and exhaust outlet.
  • the apparatus further comprising tubing. In some embodiment, the apparatus further comprising an imaging agent synthesis module, wherein the apparatus is fluidically connected to the apparatus. In some embodiments, the apparatus is capable of carrying out the method as described herein. In some embodiments, the apparatus is capable of preparing an imaging agent comprising formula:
  • the invention provides an apparatus comprising the components arranged as shown in Figure 8.
  • the components are arranged in the order: (1) gas inlet; (2) [ 18 0]H 2 0 recovery system; (3) anion exchange cartridge; (4) MeCN reservoir; (5) syringe; (6) reservoir with solution of imaging agent precursor; (7) reaction vessel; (8) HPLC system; (9) reservoir with solution of ascorbic acid or a salt thereof; (10) collection vessel; (11) ethanol reservoir; (12) vial with final product; (13) Sep-pack cartridge; (14) reservoir with solution of ascorbic acid or a salt thereof; (15) reaction vessel; and (16) exhaust outlet.
  • Figure 1 shows an example of a nucleophilic [ 18 F]-fluorination reaction using an imaging agent precursor and a fluoride source to form an imaging agent.
  • Figure 2 shows various reaction pathways of an imaging agent precursor during a nucleophilic fluorination reaction.
  • Figure 3 shows an exemplary synthesis of an intermediate compound.
  • Figure 4 shows an alternative synthesis of an intermediate compound.
  • Figure 5 shows another alternative synthesis of an intermediate compound.
  • Figure 6 shows a flow chart describing a method for synthesizing an imaging agent.
  • Figure 7 is a schematic representation of a system for synthesizing an imaging agent using a modified Explora GN synthesis module.
  • Figure 8 is a schematic representation of a cassette, with associated columns and reagents for synthesizing an imaging agent using a modified GE-Tracerlab-MX synthesis module.
  • Figure 9 includes (a) a graph illustrating the changes in product distribution as a function of molar concentration of bicarbonate salt, (b) a graph illustrating the product distribution as a function of reaction time, and (c) a graph illustrating the changes in product distribution as a function of molar concentration of imaging agent precursor.
  • Figure 10 illustrates non-limiting examples of imaging agents which may be prepared using the fluorination methods as described herein, in some embodiments.
  • Figure 11 shows whole body coronal sections at the level of the myocardium from a representative human subject at different time points after administration of imaging agent 1.
  • Figure 12 shows representative cardiac images of imaging agent 1 in control and chronic myocardial infarct (MI) rabbits.
  • Figure 13 shows a plot of reader's scores versus percentage decreases from the maximum value for rest image data of a study following administration of imaging agent 1 injection to subjects, according to a non-limiting embodiment.
  • the present invention generally relates to systems, compositions, cassettes, methods, and apparatuses for the synthesis of imaging agents and precursors thereof.
  • the invention relates to imaging agents synthesized using methods described herein.
  • the present invention relates to methods for synthesizing an imaging agent, for example, by reacting an imaging agent precursor with a source of an imaging moiety.
  • the method involves the use of one or more additives (e.g. , salts) that may facilitate a chemical reaction.
  • the methods may exhibit improved yields and may allow for the widespread synthesis of imaging agents, including imaging agents comprising a radioisotope (e.g. , 18 F).
  • the imaging agents may be useful as sensors, diagnostic tools, and the like.
  • Synthetic methods for preparing an imaging agent have also been designed to use an automated synthesis system to prepare and purify imaging agents that comprise a radioisotope.
  • the invention allows radiolabeled imaging agents to be made using a nucleophilic reaction system, including, but not limited to, the Explora GN or RN synthesis system (Siemens Medical Solutions USA, Inc.), GE-Tracerlab-MX synthesis system (GE Healthcare), Eckert & Zeigler Modular- Lab Synthesis system, etc. , which are commonly available at PET manufacturing facilities (PMF).
  • a nucleophilic reaction system including, but not limited to, the Explora GN or RN synthesis system (Siemens Medical Solutions USA, Inc.), GE-Tracerlab-MX synthesis system (GE Healthcare), Eckert & Zeigler Modular- Lab Synthesis system, etc. , which are commonly available at PET manufacturing facilities (PMF).
  • the present invention provides methods for synthesizing an imaging agent precursor, wherein the imaging agent precursor is reacted with a source of an imaging moiety to form the imaging agent.
  • the imaging agent precursor is reacted with a source of an imaging moiety to form the imaging agent.
  • the present invention provides methods of imaging, including methods of imaging in a subject that includes administering a composition or formulation ⁇ e.g. , that comprises imaging agent 1, as described herein) to the subject by injection, infusion, or any method of administration, and imaging a region of the subject that is of interest. Regions of interest may include, but are not limited to, the heart, cardiovascular system, cardiac vessels, blood vessels ⁇ e.g. , arteries, veins), brain, and other organs.
  • a parameter of interest such as blood flow, cardiac wall motion, or perfusion, can be imaged and detected using methods and/or systems of the invention.
  • methods for evaluating perfusion including myocardial perfusion, are provided.
  • imaging agent refers to any species that includes at least one atom, or group of atoms, that may generate a detectable signal itself, or upon exposure to an external source of energy ⁇ e.g., electromagnetic radiation, ultrasound, etc.).
  • the imaging agent may be administered to a subject in order to provide information relating to at least a portion of the subject ⁇ e.g. , human).
  • an imaging agent may be used to highlight a specific area of a subject, rendering organs, blood vessels, tissues, and/or other portions more detectable and more clearly imaged. By increasing the detectability and/or image quality of the object being studied, the presence and extent of disease and/or injury can be determined.
  • the imaging agent may include a radioisotope for nuclear medicine imaging.
  • a non-liming example of an imaging agent, also referred herein as imaging agent 1 comprises the formula:
  • an "imaging moiety” refers to an atom or group of atoms that is capable of producing a detectable signal itself or upon exposure to an external source of energy (e.g. , imaging agents comprising imaging moieties may allow for the detection, imaging, and/or monitoring of the presence and/or progression of a condition), pathological disorder, and/or disease.
  • Nuclear medicine imaging agents can include n C, 13 N, 18 F, 123 I, 125 1, 99m Tc, 95 Tc, m In, 62 Cu, 64 Cu, 67 Ga, and 68 Ga as the imaging moiety.
  • the imaging moiety is 18 F. Imaging agents based on 18 F have been used for imaging hypoxia and cancer (Drugs of the Future 2002, 27, 655-667).
  • a compound e.g. , an imaging agent, a fluoride species
  • a fluoride species may be isotopically-enriched with fluorine- 18.
  • “Isotopically-enriched” refers to a composition containing isotopes of an element such that the resultant isotopic composition is other than the natural isotopic composition of that element.
  • 18 F when a particular atomic position is designated as 18 F, it is to be understood that the abundance of 18 F at that position is substantially greater than the natural abundance of 18 F, which is essentially zero.
  • a fluorine designated as 18 F may have a minimum isotopic enrichment factor of about 0.01%, about 0.05%, about 0.1%, about 0.2%, about 0.3%, about 0.4%, about 0.5%, about 0.75%, about 1%, about 2%, about 3%, about 4%, about 5%, about 10%, about 15%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, or greater.
  • the isotopic enrichment of the compounds provided herein can be determined using conventional analytical methods known to one of ordinary skill in the art, including mass spectrometry and HPLC.
  • the imaging agent is formed by reacting an imaging agent precursor with an imaging moiety.
  • a method involves reacting between an imaging agent precursor comprising a leaving group with a source of an imaging moiety (e.g., a fluoride species).
  • a source of an imaging moiety e.g., a fluoride species.
  • the imaging moiety replaces the leaving group via a substitution reaction, such as an S N 2 or S N I reaction. That is, during the reaction an imaging moiety replaces the leaving group, thereby producing the imaging agent.
  • the methods described herein may be used for the synthesis of a wide variety of imaging agents from an imaging agent precursor.
  • the imaging agent precursor may include at least one leaving group that may be displaced by an imaging moiety, such as an 18 F species.
  • Imaging agent precursors may be synthesized using methods known to those of ordinary skill in the art and as described below.
  • the imaging agent precursor comprises formula (I):
  • K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
  • L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
  • M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group; or
  • L and M together with the atom to which they are attached, may form a three-, four-, five-, or six-membered carbocyclic ring;
  • Q is halo or haloalkyl
  • n 0, 1, 2, or 3;
  • R 21 , R 22 , R 27 , and R 28 are independently selected from hydrogen, Ci-C 6 alkyl optionally substituted with a leaving group, and a leaving group;
  • R 23 , R 24 , R 25 , and R 26 are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C 6 alkyl optionally substituted with a leaving group, and a leaving group;
  • R 29 is Ci-C 6 alkyl optionally substituted with a leaving group
  • Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with a leaving group and heteroaryl optionally substituted with a leaving group; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, and heteroaryl optionally substituted with a leaving group;
  • a method of the present invention comprises preparing an imaging agent comprising formula (II):
  • K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C 6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
  • L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C 6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
  • M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C 6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety; or
  • L and M together with the atom to which they are attached, may form a three-, four-, five-, or six-membered carbocyclic ring;
  • Q is halo or haloalkyl
  • n 0, 1, 2, or 3;
  • R , R , R , and R are independently selected from hydrogen, Ci-C 6 alkyl optionally substituted with an imaging moiety, and an imaging moiety;
  • R , R , R , and R are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C 6 alkyl optionally substituted with an imaging moiety, and an imaging moiety;
  • R 29 is Ci-C 6 alkyl optionally substituted with an imaging moiety
  • Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with an imaging moiety and heteroaryl optionally substituted with an imaging moiety; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C 6 alkyl optionally substituted with an imaging moiety, and heteroaryl optionally substituted with an imaging moiety;
  • the imaging agent comprising formula (II) is formed from an imaging agent precursor comprising formula (I), wherein a leaving group of the imaging agent precursor comprising formula (I) is replaced by an imaging moiety.
  • the imaging moiety is 18 F.
  • K is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy, aryl, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl, and a leaving group.
  • L is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy, aryl, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl, and a leaving group.
  • M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy, aryl, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl, and a leaving group.
  • L and M together with the atom to which they are attached, form a three- or four-membered carbocyclic ring.
  • Q is halo or haloalkyl.
  • n is 0, 1, 2, or 3.
  • R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , and R 27 are independently selected from hydrogen, Ci-C 6 alkyl optionally substituted with a leaving group, and a leaving group.
  • R 29 is Ci-C 6 alkyl optionally substituted with a leaving group.
  • Y is selected from a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent and M is selected from aryl and heteroaryl; and provided that when Y is oxygen, K and L are absent and M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, aryl, Ci-C 6 alkyl optionally substituted with a leaving group, and heteroaryl.
  • J is O.
  • R 29 is methyl, ethyl, H-propyl, z ' -propyl, n- butyl, z ' -butyl, or i-butyl, each may be optionally substituted with a leaving group.
  • R 29 is i-butyl.
  • Q is chloro. In some cases, all of R 21 ,
  • R , R , R , R , R , and R are hydrogen.
  • Y is carbon, K and L are hydrogen, and M is alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C 6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, or a leaving group.
  • Y is carbon, K and L are hydrogen, and M is alkyloxy optionally substituted with a leaving group.
  • the imaging agent precursor comprises the formula:
  • R , R , R , Q, J, and n are as described herein, and L is a leaving group.
  • the imaging agent comprises the formula:
  • R , R , R , Q, J, and n are as described herein, and I m is an imaging moiety.
  • the imaging agent precursor comprises the formula: wherein R and Q are as described herein, and L is a leaving group.
  • the imaging agent comprises the formula: wherein R 29 and Q are as described herein, and Im is an imaging moiety.
  • the imaging agent precursor comprises the formula: herein referred to as imaging agent precursor 1 (see Figure 1).
  • the imaging agent comprises the formula:
  • imaging agent 1 herein referred to as imaging agent 1 (see Figure 1).
  • imaging agents that may be prepared using a fluorination methods of the present invention are shown in Figure 10.
  • the imaging agent precursor is not a salt.
  • an imaging agent precursor of the formula (I) including an etherification reaction (e.g. , Mitsonobu reaction) between two alcohols, or between a phenol and an alcohol.
  • a leaving group may be installed by conversion of a hydroxyl group into a tosylate group or other leaving group, for example, by reaction with p-toluenesulfonate chloride in the presence of a base (e.g., DMAP).
  • a base e.g., DMAP
  • a method for synthesizing an imaging agent comprises contacting an imaging agent precursor (e.g. , a compound comprising formula (I)) with a fluoride species and an ammonium salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent (e.g. , a compound comprising formula (II)) comprising the fluorine species wherein the molar ratio of ammonium salt to imaging agent precursor is less than about 1.5 : 1, or about 1 : 1 or less (or any ratio described herein).
  • an imaging agent precursor e.g. , a compound comprising formula (I)
  • a method for synthesizing an imaging agent comprises contacting an imaging agent precursor (e.g. , a compound comprising formula (I)) with a fluoride species and a bicarbonate salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent (e.g. , a compound comprising formula (II)) comprising the fluorine species, wherein the molar ratio of bicarbonate salt to imaging agent precursor is less than about 1.5: 1, or is about 1 : 1 or less (or any ratio described herein).
  • an imaging agent precursor e.g. , a compound comprising formula (I)
  • a method for synthesizing an imaging agent comprises contacting an imaging agent precursor (e.g. , a compound comprising formula (I)) with a fluoride species under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent (e.g. , a compound comprising formula (II)) comprising the fluorine species, wherein the contacting is performed at a pH below 7.
  • an imaging agent precursor e.g. , a compound comprising formula (I)
  • an imaging agent e.g. , a compound comprising formula (II)
  • a method for 18 F-labeling a compound comprising the formula:
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halogen
  • R 3 is alkyl substituted with a sulfonate-containing group, alkoxy substituted with a sulfonate-containing group, or alkoxyalkyl substituted with a sulfonate-containing group, comprises reacting the compound with an 18 F species in the presence of an
  • ammonium salt or a bicarbonate salt to form a product comprising the F species.
  • a method for manufacturing an imaging agent comprising the formula:
  • step (b) comprises heating the mixture to a temperature between 50 °C and 250 °C. In some cases, the heating step (b) comprises heating the mixture for less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes. In some cases, the method further comprises:
  • the method further comprises
  • an imaging agent comprising the formula:
  • step (b) comprises heating the mixture to a temperature between 50 °C and 250 °C. In some cases, the heating step (b) comprises heating the mixture less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes. In some cases, the manufacturing further comprises:
  • the manufacturing further comprises:
  • a method for synthesizing a fluorinated compound comprises reacting, in the presences of a carbonate or bicarbonate ion, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl group substituted with a halide or a sulfonate-containing group, with (ii) a salt comprising a fluoride species and weakly coordinating cation.
  • the term "leaving group” is given its ordinary meaning in the art of synthetic organic chemistry and refers to an atom or a group capable of being displaced by a nucleophile.
  • suitable leaving groups include, but are not limited to, halides (such as chloride, bromide, or iodide), alkoxycarbonyloxy, aryloxycarbonyloxy, alkanesulfonyloxy, arenesulfonyloxy, alkyl-carbonyloxy (e.g. , acetoxy), arylcarbonyloxy, aryloxy, methoxy, ⁇ , ⁇ -dimethylhydroxylamino, pixyl, haloformates, and the like.
  • the leaving group is a sulfonic acid ester, such as toluenesulfonate (tosylate, TsO), methanesulfonate (mesylate, MsO), or
  • the leaving group may be a brosylate, such as p-bromobenzenesulfonyl. In some cases, the leaving group may be a nosylate, such as 2-nitrobenzenesulfonyl.
  • the leaving group may also be a
  • phosphineoxide e.g. , formed during a Mitsunobu reaction
  • an internal leaving group such as an epoxide or cyclic sulfate.
  • the leaving group is a sulfonate-containing group.
  • the leaving group is a tosylate group.
  • the invention provides methods of synthesizing an imaging agent comprising a halogen.
  • the method may involve a halogenation reaction.
  • methods for synthesizing an imaging agent comprising a fluoride e.g. , enriched with 18 F
  • the method comprises contacting an imaging agent precursor with a source of a fluoride under conditions that result in the fluoride replacing a leaving group of the precursor to produce an imaging agent comprising a fluoride species.
  • the method involves a nucleophilic fluorination reaction.
  • an imaging agent precursor comprising a leaving group is reacted in the presence of a fluoride species, whereby SN2 or SNI displacement of the leaving group by the fluoride species produces the imaging agent.
  • the fluoride species is enriched with 18 F.
  • Figure 1 shows an illustrative example, where imaging agent precursor 1 is treated with
  • one or more additives may be incorporated into the reaction mixture of the imaging agent precursor and the fluoride species.
  • the additive may, in some cases, facilitate reaction between the imaging agent precursor and the fluoride species and/or may aid in stabilizing the imaging agent.
  • the fluoride species may have relatively low reactivity (e.g. , nucleophilicity), and addition of an additive may enhance the reactivity of the fluoride species.
  • a fluorine species may be a negatively charged fluoride ion (e.g. , an
  • an additive may be used to bind to any positively charged counterions present within the reaction mixture, thereby enhancing the reactivity of the fluoride ion.
  • the additives may decrease the rate of undesired side reactions, as described below.
  • the additive may be combined with the fluoride species prior to contact with the imaging agent precursor.
  • a solution comprising the fluoride species and the additive is prepared, and the solution is added to the imaging agent precursor.
  • a solid comprising the fluoride species and the additive is prepared, and the solid is contacted with the imaging agent precursor.
  • the fluoride species is adsorbed onto a solid support (e.g. , an anion exchange column), and a solution comprising the additive is used to elute the fluoride species from the solid support. The eluted solution is then contacted with the imaging agent precursor, or is concentrated to produce a solid, which is then contacted with the imaging agent precursor.
  • the additive is a bicarbonate salt.
  • a carbonate salt such as KHCO 3
  • substitution of a carbonate salt with a bicarbonate salt results in considerable improvement of both fluorination efficiency and starting material integrity.
  • bicarbonate salt refers to a salt comprising a bicarbonate or hydrogen carbonate ion (HCO 3 " ion).
  • the bicarbonate salt may be a metal bicarbonate, such as sodium bicarbonate, calcium bicarbonate, potassium bicarbonate, magnesium bicarbonate, and the like.
  • the bicarbonate salt is potassium bicarbonate (KHCO 3 ).
  • the bicarbonate salt comprises a non-metal counterion, such as ammonium bicarbonate.
  • the bicarbonate salt may be a tetraalkylammonium bicarbonate salt having the formula, R 4 NHCO 3 , wherein R is alkyl.
  • R may be a lower alkyl, such as methyl, ethyl, propyl, butyl, pentyl, hexyl, or the like.
  • the ammonium salt is Et 4 NHC0 3 .
  • the salt is Me 4 NHC0 3 , i- Pr 4 NHC0 3 , «-Pr 4 NHC0 3 , «-Bu 4 NHC0 3 , z ' -Bu 4 NHC0 3 , or i-Bu 4 NHC0 3 .
  • a comprehensive screen of ammonium salts identified a dramatic enhancement of fluorination efficiency in the presence of bicarbonate anion (e.g. , see Table 1); only modest dependency on size of the alkyl substituent was observed within the series methyl -> ethyl -> butyl (e.g. , Example 14).
  • the additive is a salt comprising a cation that forms a weakly coordinating salt with a fluoride species.
  • a "cation that forms a weakly coordinating salt with a fluoride species” refers to a cation that renders a fluoride species reactive within a fluorination reaction.
  • the cation may not strongly bind to the fluoride species, allowing the fluoride species to act as a nucleophile during a nucleophilic fluorination reaction, Those of ordinary skill the art would be able to select an appropriate cation that would be suitable as a weakly coordinating counterion for a fluoride species.
  • the cation may be have a relatively large atomic radius and/or may be a weak Lewis base. In some cases, the cation may be selected to be lipophilic. In some cases, the cation may comprise one or more alkyl groups.
  • weakly coordinating cations include cesium ions, ammonium ions, and the like.
  • weakly coordinating cations include weakly coordinating salts of hexamethylpiperidindium, S(NMe 2 )3, P(NMe 2 )4, tetraaalkylphosphonium salts, tetraarylphosphonium salts, (e.g. tetraphenylphosphonium),
  • the additive is an ammonium salt, i.e., a salt comprising a substituted or unsubstituted ammonium ion.
  • the ammonium ion is a weakly coordinating cation.
  • the ammonium salt has the formula, R 4 NX, where each R can be the same or different and is alkyl, heteroalkyl, aryl, heteroaryl, or heterocyclic, each optionally substituted, and X is a negatively charged counterion.
  • R is alkyl, heteroalkyl, aryl, heteroaryl, or heterocyclic, each optionally substituted.
  • the ammonium salt may include a wide range of negatively charged counterions, including halides, carbonates, bicarbonates, and the like.
  • ammonium salts include, but are not limited to, ammonium bicarbonate salts, ammonium hydroxide salts, ammonium acetate salts, ammonium lactate salts, ammonium trifluoroacetate salts, ammonium methanesulfonate salts, ammonium p-toluenesulfonate salts, ammonium nitrate salts, ammonium halide salts (e.g. , ammonium iodide salts), ammonium bisulfate salts, and the like.
  • ammonium bicarbonate salts include, but are not limited to, ammonium bicarbonate salts, ammonium hydroxide salts, ammonium acetate salts, ammonium lactate salts, ammonium trifluoroacetate salts, ammonium methanesulfonate
  • the ammonium salt is a tetraalkylammonium salt, such as a tetraalkylammonium bicarbonate salt.
  • the ammonium salt may have the formula, R 4 NHCO 3 , wherein each R is independently alkyl. In some cases, R is optionally substituted.
  • the alkyl group is a lower Ci-C 6 alkyl group.
  • the tetraalkylammonium salt is a basic
  • the salt additive e.g., bicarbonate salt and/or ammonium salt
  • the salt additive may be utilized in the reaction such that the molar ratio of the salt additive to the imaging agent precursor is less than about 1.5:1. In some cases, the molar ratio is about 1.5:1 or less, about 1.4:1 or less, about 1.3:1 or less, about 1.25:1 or less, about 1.2:1 or less, about 1.1:1 or less, about 1:1 or less, about 0.75:1 or less, about 0.5:1 or less, about 0.25:1 or less, about 0.1:1 or less, or about 0.05:1 or less.
  • the ratio is greater than about 0.05:1, greater than about 0.01:1, or greater than about 0.25:1.
  • the molar ratio of salt additive to imaging agent precursor is about 0.5:1 to about 1:1, or about 0.25:1 to about 1:1, or about 0.25:1 to about 0.75:1, about 1.49:1 to about 0.05:1, or between about 1.4:1 to about 0.25:1, or between about 0.25:1 and about 1.4:1, or between about 0.25:1 and about 1.25:1.
  • bicarbonate and ammonium salts may aid in decreasing the rate of competing reactions such as hydrolysis during nucleophilic fluorination of an imaging agent precursor.
  • the additive may be used in combination with a species capable of enhancing the reactivity of the fluoride species or otherwise facilitating conversion of the imaging agent precursor to the imaging agent.
  • the species may be a compound capable of chelating one or more ions (e.g., metal ions) that may be present within the reaction mixture.
  • the species may be used to chelate a counterion to a fluoride species, such as a potassium ion, thereby increasing the reactivity (e.g., nucleophilicity) of the fluoride species.
  • the additive is used in combination with a multidentate ligand, such as a crown ether or a cryptand that is capable of chelating a metal ion.
  • a multidentate ligand such as a crown ether or a cryptand that is capable of chelating a metal ion.
  • the multidentate ligand e.g., cryptand
  • the multidentate ligand may be selected based on the metal ion to be chelated.
  • the multidentate ligand may be, for example, 4,7,13,16,21,24-hexaoxa-l,10- diazabicyclo[8.8.8]-hexacosane (e.g., Kryptofix ® 222).
  • Other cryptands will be known to those of ordinary skill in the art.
  • Some embodiments may involve the use of a bicarbonate salt in combination with 4,7,13,16,21,24-hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane.
  • potassium bicarbonate may be used in combination with 4,7,13,16,21,24- hexaoxa- 1 , 10-diazabicyclo [8.8.8] -hexacosane.
  • cryptand is given its ordinary meaning in the art and refers to a bi- or a polycyclic multidentate ligand for a cation.
  • the method may be carried out using an ammonium salt, in the absence of a cryptand (e.g., such as 4,7,13,16,21,24-hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane).
  • the method is performed in the absence of a carbonate salt.
  • the use of a salt additive in the reaction increases the yield by about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 100%, about 200%, about 300%, about 400%, about 500%, or greater, relative to conducting the reaction under essentially the same conditions but in the absence of a salt additive.
  • the imaging agent may be further processed using one or more purification techniques, and may optionally be combined with additional components, such as a stabilizing agent.
  • fluoride species refers to a fluoride atom or group of atoms comprising at least one fluoride atom, wherein the fluoride atom is capable of reacting with another compound (e.g. , an imaging agent precursor).
  • an isotopically-enriched 18 F species may be produced by the nuclear reaction 18 0(p,n) 18 F from proton bombardment of
  • the method may involve treating a solution of the F species to remove any impurities, such as unreacted [ 18 0]]3 ⁇ 40.
  • a solution of the 18 F species may be filtered through an anion exchange column, where the 18 F species is
  • the F species is then removed by washing the anion exchange column with various mixtures of solvents and optional additives (e.g. , salt additives), forming an 18 F-containing solution.
  • the anion exchange column is washed with an aqueous solution of a salt, such as KHC0 3 or Et 4 NHC0 3 .
  • the 18 F-containing solution is combined with additional components prior to reaction with an imaging agent precursor.
  • one or more solvents may be added to dilute the 18 F-containing solution to a selected concentration.
  • the F-containing solution is diluted with acetonitrile.
  • the 18 F-containing solution may be concentrated to dryness by exposure to elevated temperature and/or reduced pressure to form an anhydrous 18 F- containing solid.
  • the 18 F-containing solid may further comprise one or more additives ⁇ e.g. , salt additives).
  • the chemical composition of the 18 F- containing solid may depend on the number and kind of additives used in preparation of the 18 F-containing solution.
  • a solution of potassium bicarbonate may be used to elute the 18 F species from the anion exchange column, thereby resulting in an 18 F-containing solid comprising [ 18 F]KF.
  • a solution of ammonium bicarbonate is used to elute the 18 F species from the anion exchange column, thereby resulting in an 18 F-containing solid comprising [ 18 F]Et 4 NF.
  • the solution comprising the 18 F species is heated to a temperature ranging from room temperature to about 200 °C. In some embodiments, the solution is heated to a temperature ranging from 90-120 °C. In some cases, the solution is heated to about 75 °C, about 85 °C, about 95 °C, about 105 °C, about 115 °C, about 125 °C, or greater.
  • the solution is placed under a reduced pressure of about 100 mm Hg, about 125 mm Hg, about 150 mm Hg, about 175 mm Hg, about 200 mm Hg, about 225 mm Hg, about 250 mm Hg, about 275 mm Hg, about 300 mm Hg, about 325 mm Hg, about 350 mm Hg, about 375 mm Hg, about 400 mm Hg, or greater.
  • the solution is placed under a reduced pressure of about 100 mbar, about 125 mbar, about 150 mbar, about 175 mbar, about 200 mbar, about 225 mbar, about 250 mbar, about 275 mbar, about 280 mbar, about 300 mbar, about 325 mbar, about 350 mbar, about 375 mbar, about 400 mbar, about 450 mbar, about 500 mbar, or greater.
  • the solution is concentrated to dryness at about 150 mm Hg and about 115 °C.
  • the solution is concentrated to dryness at about 375 mm Hg and about 115 °C. In some embodiments, the solution is concentrated to dryness at about 400 mbar and about 110-150 °C. In some embodiments, the solution is concentrated to dryness at about 280 mbar and about 95-115 °C.
  • the fluoride species and/or the additive, if present, is then contacted with the imaging agent precursor under conditions that result in conversion of the imaging agent precursor to the imaging agent product via nucleophilic fluorination.
  • the ratio of fluoride species to imaging agent precursor may be selected to be about 1: 10,000 or more, about 1:5000 or more, about 1:3000 or more, about 1:2000 or more, 1: 1000 or more, 1:500 or more, 1: 100 or more, 1 :50 or more, 1 : 10 or more, 1 :5 or more, or, in some cases, 1 : 1 or more.
  • the fluoride species may be present at about 10 mol %, or about 5 mol , or about 3 mol , or about 2 mol , or about 1 mol or about 0.5 mol , or about 0.1 mol , or about 0.05 mol , or about 0.01 mol relative to the amount of imaging agent precursor. In some embodiments, at least of the fluoride species provided is enriched in 18 F.
  • the ratio of 18 F species to imaging agent precursor may be selected to be about 1: 1,000,000 or more, or about 1:500,000 or more, or about 1:250,000 or more, or about 1: 100,000 or more, or about 1:50,000 or more, or about 1 :25,000 or more, or about 1: 10,000 or more, about 1 :5000 or more, about 1:3000 or more, about 1 :2000 or more, 1: 1000 or more, 1:500 or more, 1: 100 or more, 1 :50 or more, 1: 10 or more, 1 :5 or more, or, in some cases, 1: 1 or more.
  • the nucleophilic fluorination reaction is carried out in the presence of one or more solvents, for example, an organic solvents, a non-organic solvent (e.g. , an aqueous solvent), or a combination thereof.
  • the solvent is a polar solvent or a non-polar solvent.
  • the solvent is an aqueous solution, such as water.
  • the solvent comprises at least about 0.001% water, at least about 0.01% water, at least about 0.1% water, at least about 1% water, at least about 5%, at least about 10%, at least about 20% water, at least about 30% water, at least about 40% water, at least about 50% water, or greater.
  • the solvent may comprise between about 0.1% and 100% water, about 1% to about 90%, about 1% to about 70%, about 1% to about 50%, or about 10% to about 50%. In some cases, the solvent comprises no more than 10% water, 5% water, 4% water, 3% water, 2% water, 1% water, or 0.5% water. In some cases, the solvent comprises between about 0.01% water and about 5% water, or between about 0.01% water and about 2% water, or between about 0.1% water and about 0.2% water.
  • solvents useful in the inventive methods include, but are not limited to, non-halogenated hydrocarbon solvents (e.g., pentane, hexane, heptane, cyclohexane, etc.), halogenated hydrocarbon solvents (e.g. , dichloromethane, chloroform, fluorobenzene, trifluoromethylbenzene, etc.), aromatic hydrocarbon solvents (e.g., toluene, benzene, xylene, etc.), ester solvents (e.g., ethyl acetate, etc.), ether solvents (e.g.
  • non-halogenated hydrocarbon solvents e.g., pentane, hexane, heptane, cyclohexane, etc.
  • halogenated hydrocarbon solvents e.g. , dichloromethane, chloroform, fluorobenzene, trifluoromethylbenzene, etc.
  • solvents e.g. , ethanol, methanol, propanol, isopropanol, etc.
  • solvents include acetone, acetic acid, formic acid, dimethyl sulfoxide, dimethyl formamide, acetonitrile, and pyridine.
  • the reaction is carried out in a polar solvent, such as acetonitrile.
  • an anhydrous 18 F-containing solid may be contacted with a solution of an imaging agent precursor (e.g. , a tosylate precursor), and the resulting solution is heated to an elevated temperature for a select period of time.
  • an imaging agent precursor e.g. , a tosylate precursor
  • the solution may be, for example, an acetonitrile solution.
  • a solution of the 18 F species and additive, if present, is contacted with a solid imaging agent precursor or a solution of the imaging agent precursor.
  • Some embodiments involve contacting the imaging agent precursor with the fluoride species in a solution having a pH below about 7, below about 6, or, below about 5.
  • the solution has a pH between about 5 and about 6, or between about 5 and, about 7 or between about 4 and about 7.
  • the solution comprising the 18 F species, imaging agent precursor, and, optionally, additive is heated at an elevated temperature for a period of time.
  • the solution may be heated to about 50 °C, about 60 °C, about 70 °C, about 80 °C, about 90 °C, about 100 °C, about 110 °C, about 120 °C, 150 °C, about 170 °C, about 200 °C, about 225 °C, about 250 °C or greater, for a period of 5 minutes or less, 10 minutes or less, 20 minutes or less, 30 minutes or less. It should be understood that other temperatures and reaction times may be used.
  • the reaction mixture is then cooled (e.g., to room temperature) and optionally diluted with a solvent, such as water.
  • the resulting imaging agent Upon completion of the fluorination reaction, the resulting imaging agent is optionally subjected to one or more purification steps.
  • the synthesis, purification, and/or formulation of an imaging agent may be prepared using an automated reaction system comprising a cassette, wherein the cassette may comprise a synthesis module, a purification module, and/or a formulation module. Automated reaction systems and cassettes are described herein.
  • Purification and isolation may be performed using methods known to those skilled in the art, including separation techniques like chromatography, or combinations of various separation techniques known in the art, for example, extractions, distillation, and crystallization.
  • HPLC high performance liquid chromatography
  • the eluent includes a mixture of water and acetonitrile, such as a 45 :55 watenacetonitrile mixture.
  • the content of water in the eluent may vary from, for example, about 1 % to about 50 .
  • HPLC may be performed using a C18 column.
  • the product may be further processed using additional purification techniques, such as filtration.
  • the imaging agent may be purified using HPLC, to produce a solution of HPLC mobile phase and the imaging agent.
  • the HPLC mobile phase may be subsequently exchanged for a solution of ascorbic acid or a salt thereof, and ethanol solution, by filtration through a C-18 resin (e.g. , CI 8 Sep-Pak ® cartridge).
  • the solution of the HPLC mobile phase and the imaging agent is filtered through a C- 18 resin, where the imaging agent remains on the resin and the other components, such as acetonitrile and/or other solvents or components, are removed via elution.
  • the C- 18 resin may be further washed with a solution of ascorbic acid or a salt thereof, and the filtrate discarded.
  • the C- 18 resin is washed with a solvent, such as ethanol, and the resulting solution is optionally further diluted with an ascorbic acid solution or a salt thereof, as described herein.
  • the recovered product is combined with one or more stabilizing agents, such as ascorbic acid or a salt thereof.
  • a solution comprising the purified imaging agent may be further diluted with a solution of ascorbic acid or a salt thereof.
  • a formulation may be prepared via an automated reaction system comprising a cassette.
  • a solution comprising the imaging agent product may be sterile filtered (e.g. , using a 13 mm diameter, Millipore, Millex PVDF 0.22 ⁇ sterilizing filter) into a sterile product vial.
  • the sterile product vial may be a commercially available, pre- sterilized unit that is not opened during the production process, as any imaging agents (or other components) may be aseptically inserted through the septum prior to use.
  • suitable vials and production components including commercially available, pre-sterilized units comprising a 0.22 ⁇ pore size membrane venting filter and quality control sampling syringes.
  • individual doses may be filled in syringes, labeled, and shipped to a clinical site.
  • Dosing administration techniques, kits, cassettes, method and systems (e.g., automated reaction systems) for synthesis of the imaging agent, and testing procedures are described herein.
  • the product is dispensed into a 3 or 5 mL syringe and labeled for distribution.
  • Labels may be prepared at a radiopharmacy and applied to a syringe shield and shipping container. Additional labels may be provided in the shipping container for inclusion in clinical site records.
  • the imaging agents may be used in a method of imaging, including methods of imaging a patient comprising administering the imaging agent to the patient by injection, infusion, or any other method, and imaging an area of the patient, as described herein. In some embodiments, a portion of a heart of the patient is imaged.
  • Imaging agent precursors and intermediates thereof.
  • the methods for synthesizing an imaging agent precursor ⁇ e.g. , a compound comprising formula (I)) exhibits improved yields and/or may allow for the large-scale synthesis of the imaging agent precursors and/or intermediates thereof.
  • Some embodiments provide the ability to synthesize a desired product without need for purification, such as chromatography, which can be time- consuming and/or expensive with the loss of product.
  • Figure 1 shows an illustrative example of an imaging agent precursor which has been utilized in the synthesis of an imaging agent for imaging myocardial perfusion.
  • the leaving group ⁇ i.e., tosylate group
  • an imaging moiety for example, 18 F, as described herein, thereby forming an imaging agent.
  • an imaging agent precursor is formed via a reaction in which a bond between a heteroatom and an alkyl, heteroalkyl, aryl, or heteroaryl group is formed.
  • the reaction may be an alkylation reaction, such as an
  • the reaction involves a hydroxyl- containing nucleophilic species reacting with an electrophilic species to form an ether linkage.
  • ether or “ether linkage” is given its ordinary meaning in the art and refers to the group, R a -0-R b , where R a and R b can be the same or different and are alkyl, heteroalkyl, aryl, or heteroaryl, any of which may be substituted.
  • the reaction may involve nucleophilic addition of the oxygen atom of the hydroxyl-containing species to an electrophilic species.
  • the reaction may involve coupling between two alcohols via, for example, a Mitsunobu reaction.
  • the etherification reaction includes formation of a bond between an oxygen atom and an alkyl, aryl, heteroalkyl, heteroaryl, carbocyclic, or heterocyclic group.
  • Figure 3 shows an illustrative embodiment of an etherification reaction between benzenedimethanol 12 and dichloropyridazinone 11 to form the benzyl alcohol 13.
  • Figure 4 shows an etherification reaction between benzenedimethanol 12 and dichloropyridazinone 11 to form the benzyl alcohol 13.
  • the inventive method involves reacting a compound comprising formula (III):
  • W is alkyl or heteroalkyl, optionally substituted
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • each R 3 can be the same or different and is alkyl optionally substituted with a leaving group, or heteroalkyl optionally substituted with a leaving group;
  • n 1, 2, 3, 4, or 5;
  • the nucleophile may be ethylene glycol, and an etherification reaction may be carried out as described herein.
  • the reaction is performed in the presence of a base, such as potassium i-butoxide or potassium hydroxide.
  • R 3 is alkyl substituted with a leaving group and/or n is 1.
  • the compound comprising formula (III) comprises the structure:
  • R 1 and R 2 are as defined herein.
  • a compound comprising formula (III) comprises the structure:
  • the compound comprising formula (III) may act as a nucleophile and may be reacted with an electrophile, to produce a product.
  • R 3 may be -CH 2 OH
  • the electrophile may be ethylene oxide.
  • the method comprises reacting a compound comprising formula (IV):
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • W is alkyl or heteroalkyl, optionally substituted
  • each R 4 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl;
  • n 1, 2, 3, 4, or 5; with a reactant, wherein the hydroxyl group is replaced with a portion of the reactant to form a leaving group associated with the compound.
  • R 4 is alkyl substituted with hydroxyl and/or n is 1.
  • reacting the compound comprising formula IV involves exposure to a halogenation reagent, such as phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine.
  • the halogenation reagent is phosphorus tribromide.
  • W is -0( ⁇ 3 ⁇ 4)-; R 1 is i-butyl; R 2 is chloride; and R 4 is alkyl substituted with hydroxyl. In some cases, n is 1.
  • the compound comprising formula (IV) comprises the structure:
  • the compound comprising formula (IV) comprises the structure:
  • a method for synthesizing a compound comprising formula (IV) comprises synthesizing the compound comprising formula (IV) via an etherification reaction between compounds comprising formulae (IVa) an
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • n 1, 2, 3, 4, or 5 or greater
  • R 5 is hydroxyl or halide
  • each R 6 and R 7 can be the same or different and are alkyl, heteroalkyl, or a acyl group, each optionally substituted,
  • R 5 when R 5 is hydroxyl, at least one of R 6 and R 7 comprises a leaving group or a moiety that can be replace by a leaving group (e.g., hydroxyl), or when R 5 is halide, at least one of R 6 and R 7 comprises a hydroxyl.
  • a compound comprising formula (IVa) comprises the structure:
  • R 5 is as described herein.
  • the compound comprising formula II is synthesized etherification reaction between compounds comprising formulae (IVa) and (IVd)
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • R 5 is hydroxyl or halide
  • R 6 and R 7 can be the same or different and are alkyl, heteroalkyl, or a carbonyl group, each optionally substituted,
  • R 5 when R 5 is hydroxyl, at least one of R 6 and R 7 comprises a leaving group, or when R 5 is halide, at least one of R 6 and R 7 comprises a hydroxyl.
  • R 5 is hydroxyl
  • R 6 is a carbonyl group
  • R 7 is a substituted alkyl.
  • R 5 is hydroxyl
  • R 6 is an ester
  • R 7 is alkyl substituted with a leaving group.
  • a compound comprising formula (IVa) comprises the structure:
  • R 5 is as defined herein.
  • the etherification reaction may be carried out as described herein, and may comprise exposure of the precursor compounds to a base, such as potassium carbonate.
  • R 5 is halide; and R 6 and R 7 are each alkyl, optionally substituted. In some embodiments, R 5 is chloride; and R 6 and R 7 are each alkyl substituted with hydroxyl. In one embodiment, an etherification reaction between compounds comprising formulae (IVe) and (IVf):
  • the product may be reduced with a reducing agent, such as lithium aluminum hydride, lithium borohydride, or diisobutylaluminum hydride (DIBAL-H), thereby converting the ester group into an alcohol.
  • a reducing agent such as lithium aluminum hydride, lithium borohydride, or diisobutylaluminum hydride (DIBAL-H)
  • benzenedimethanol 12 and dichloropyridazinone 11 may be reacted via an etherification reaction in the presence of potassium carbonate in DMF to form benzyl alcohol 13.
  • a disubstituted impurity is also formed wherein benzenedimethanol 12 becomes alkylated at both hydroxyl groups, which may later be removed via chromatographic purification.
  • Conversion of benzyl alcohol 13 to benzyl bromide 14 may be carried out with a variety of brominating agents, such as phosphorous tribromide in dichloromethane.
  • Subsequent conversion of benzyl bromide 14 to alcohol 15 may be completed by reaction with ethylene glycol in the presence of potassium i-butoxide in tetrahydrofuran, in some cases at elevated temperature. Alcohol 15 may then be purified by column chromatography to remove any impurities, including disubstituted impurities formed during the synthesis of benzyl alcohol 13. Alcohol 15 may then be further reacted with p-toluenesulfonyl chloride in the presence of DMAP, triethylamine, and dichloromethane to form imaging agent precursor 1 , which may be purified via recrystallization. Using the method shown in Figure 5, the overall yield for synthesizing alcohol 15 starting from compound 11 (e.g.
  • 2-(i-butyl)-4,5-dichloropyridazin-3(2H)-one) and compound 12 may be at least 10%, at least 20%, at least 30%, or at least 40%, using chromatography as the purification method. In some cases, the overall yield for synthesizing alcohol 15 starting from compound 11 and compound 12 is approximately 43%, using chromatography as the purification method.
  • Figure 4 shows an alternate approach to the synthesis of alcohol 13 involving reaction of dichloropyridazinone 11 with potassium hydroxide in ethylene glycol to afford chlorohydroxypyridazinone 17, which may then be reacted with methyl 4- bromomethylbenzoate in the presence of potassium carbonate in DMF to afford pyridazinone ester 18.
  • reduction of pyridazinone ester 18, for example, using either DIBAL-H or lithium aluminum hydride may produce benzyl alcohol 13, which may then be converted to alcohol 15 and imaging agent precursor 1 , as described herein.
  • One advantageous feature of the synthetic scheme shown in Figure 4 is the reduction or elimination of disubstituted impurities that may be formed in the synthetic scheme shown in Figure 3.
  • the overall yield for synthesizing alcohol 15 starting from compound 17 e.g. , 2-(?-butyl)-4-chloro-5- hydroxypyridazin-3(2H)-one
  • methyl 4-bromomethylbenzoate may be at least 10%, at least 20%, at least 30%, or at least 40%, without the use of chromatography for purification.
  • the overall yield for synthesizing alcohol 15 starting from compound 17 and methyl 4-bromomethylbenzoate is 48%, without the use of chromatography as a purification method.
  • an etherification reaction (e.g., see Figure 3, etherification reaction to form benzyl alcohol 13) is performed in the presence of a base.
  • the base may be, for example, a metal or a metal salt, such as a carbonate, a metal alkoxide, or the like.
  • the base may be an organic moiety, such as an amine. Examples of bases include, but are not limited to, metals (e.g.
  • alkoxides such as sodium f-butoxide or potassium i-butoxide
  • alkali metal amide such as sodium amide, lithium diisopropylamide or an alkali metal bis(trialkylsilyl)amides such as lithium bis(trimethylsilyl)amide or sodium bis(trimethylsilyl) amide
  • amines e.g.
  • alkali and alkaline earth carbonates alkali and alkaline earth bicarbonates, alkali and alkaline earth hydroxides (e.g. , sodium hydroxide, potassium hydroxide), and alkali and alkaline earth hydrides, (e.g. , NaH, LiH, KH, K 2 C0 3 , Na 2 C0 3 , TI2CO 3 , Cs 2 C0 3 , K(Oi-Bu), Li(Oi-Bu), Na(Oi-Bu) K(OPh), Na(OPh)).
  • alkali and alkaline earth carbonates alkali and alkaline earth bicarbonates
  • alkali and alkaline earth hydroxides e.g. , sodium hydroxide, potassium hydroxide
  • alkali and alkaline earth hydrides e.g. , NaH, LiH, KH, K 2 C0 3 , Na 2 C0 3 , TI2CO 3 , Cs 2 C0 3 , K(Oi
  • the base is sodium metal, sodium hydride, potassium f-butoxide, sodium methoxide, potassium carbonate, sodium carbonate, cesium carbonate, or potassium hydroxide. In some embodiments, the base is cesium carbonate. In some embodiments, the base is potassium hydroxide. In some embodiments, the base is sodium hydroxide. In some embodiments, the base is potassium i-butoxide. In some embodiments, the base is tetramethyl ammonium hydroxide. It should be understood that an etherification reaction may also be conducted in the absence of a base.
  • One or more additives may be incorporated into the etherification reaction mixture to facilitate the reaction.
  • the etherification reaction may be performed in the presence of a catalyst.
  • the catalyst may be a salt, such as an ammonium salt.
  • the catalyst may be a tetraalkylammonium halide, such as, but not limited to, tetraethylammonium iodide.
  • the catalyst may be a phase transfer catalyst.
  • phase transfer catalyst refers to any species capable of facilitating the migration of a compound from a first phase into a second, different phase, for example, during the course of a chemical reaction.
  • the phase transfer catalyst enhances migration of a compound from one phase into a different phase, wherein a chemical reaction takes place.
  • phase transfer catalysts include, but are not limited to, benzyl triethylammonium chloride, tetrabutylammonium chloride, tetraethyl ammonium chloride, tetrabutylammonium sulfate, tetraoctylammonium sulfate, and tetramethyl ammonium hydroxide.
  • the phase transfer catalyst may be used in combination with, for example, a base or other chemical reagent.
  • the reaction involves exposure to sodium hydroxide and a phase transfer catalyst, such as benzyl
  • An etherification reaction may optionally be carried out in the presence of one or more solvents.
  • the solvent may be, for example, an organic solvent (e.g. , toluene), an aqueous solvent, or a combination thereof.
  • the solvent may be a polar solvent (e.g. , polar protic solvents, polar aprotic solvents).
  • polar solvents include, but are not limited to, acetone, ethyl acetate, dimethylformamide (DMF), dimethyl sulfoxide (DMSO), acetonitrile, alcohols, or combinations thereof.
  • the etherification reaction is performed in the presence of DMF.
  • the etherification reaction is performed in the presence of THF. In some cases, the etherification reaction may be performed in the presence of an ionic liquid. In some embodiments, the etherification reaction is performed in the absence of solvent. For example, the compound may be reacted in neat ethylene glycol.
  • the components of an etherification reaction is heated or cooled to any temperature from about 0 °C to about 200 °C, for a period of time.
  • the solution is heated to a temperature from about 20 °C to about 100 °C, or from about 40 °C to about 70 °C In some cases, the solution may be heated to about 20 °C, about 30 °C, about 40 °C, about 50 °C, about 60 °C, about 70 °C, about 80 °C, or greater.
  • the etherification reaction mixture is maintained at about 20 °C. In some embodiments, the etherification reaction mixture is maintained at room temperature. In some embodiments, the etherification reaction mixture is heated to about 60 °C.
  • the etherification reaction mixture is heated to about 65 °C.
  • the reaction may be heated/cooled/maintained at a particular temperature for a period of time, such as up to about 1 hour, about 2 hours, about 3 hours, about 4 hours, about 5 hours, about 10 hours, about 15 hours, about 20 hours, about 25 hours, about 30 hours, or more.
  • the reaction mixture is heated at about 65 °C for about 4 hours.
  • the reaction mixture is maintained at about 20 °C for about 18 hours. It should be understood that other temperatures and reaction times may also be used.
  • the method involves a reduction reaction (e.g., see Figure 4, reduction of pyridazinone ester 18).
  • reduction reaction is given its ordinary meaning in the art and refers to a chemical reaction in which the oxidation state of at least one atom is reduced.
  • the reduction reaction may involve reduction of an ester or a ketone to an alcohol.
  • the reduction reaction may be carried out using reducing reagents known to those of ordinary skill in the art, including lithium aluminum hydride, lithium borohydride (with or without methanol additive), and diisobutylaluminum hydride (DIBAL-H) in a variety of solvents including lithium aluminum hydride, lithium borohydride (with or without methanol additive), and diisobutylaluminum hydride (DIBAL-H) in a variety of solvents including
  • the reduction reagent may be a 25% w/w solution of DIBAL-H in toluene, using 2-methyltetrahydrofuran as a cosolvent.
  • the invention provides methods for the synthesis of a compound (e.g. , intermediate compound) comprising a leaving group. Leaving groups are described herein. In some embodiments, the leaving group is a halide, such as a bromide.
  • the compound includes a moiety (e.g., hydroxyl) which may be readily converted into a leaving group.
  • the compound may include a hydroxyl group which is converted into a tosylate group upon reaction with p- toluenesulfonyl chloride.
  • a compound may include a hydroxyl group which may be treated with a phosphine (e.g. , triphenylphosphine, TPP) and diethylazodicarboxylate (DEAD) using Mitsunobu chemistry to form a leaving group.
  • a phosphine e.g. , triphenylphosphine, TPP
  • DEAD diethylazodicarboxylate
  • the method involves converting a hydroxyl group to a leaving group.
  • the method may involve replacing the hydroxyl group with a leaving group such as a halide (e.g. , bromide).
  • a leaving group such as a halide (e.g. , bromide).
  • the compound substituted with a hydroxyl group is exposed to a halogenation reagent.
  • the halogenation reagent is a brominating reagent, such as phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine.
  • the brominating reagent is phosphorus tribromide.
  • a halogenation reaction may be performed in the presence of one or more solvents.
  • the solvent is an organic solvent, such as
  • dichloromethane chloroform, benzene, or toluene.
  • the solvent used is dichloromethane.
  • the halogenation reaction mixture is heated or cooled to any temperature ranging from 0 °C to about 200 °C, for a period of time.
  • the solution is heated to a temperature ranging from about 20 °C to about 100 °C.
  • the solution is heated to about 20 °C, about 30 °C, about 40 °C, about 50 °C, or greater, including temperatures in between.
  • the halogenation reaction mixture is maintained at 20 °C.
  • the reaction may be
  • reaction mixture is maintained at 20 °C for 30 minutes. It should be understood that other temperatures and reaction times may also be used.
  • the synthesis of an imaging agent precursor may include other reactions, including ring-opening reactions, reduction reactions, protection/deprotection reactions, and the like.
  • the compounds (e.g. , intermediates, products) described herein may be subjected to one or more purification steps. Purification and isolation may be performed using methods known to those skilled in the art, including separation techniques like chromatography, or combinations of various separation techniques as are known the art. In some embodiments, column chromatography is used with silica or alumina as the stationary phase and a solvent, or mixture of solvents, as the eluent, to recover the product.
  • the eluent may include a mixture of a non-polar solvent and a polar solvent. For example, the eluent may include a mixture of heptane and ethyl acetate.
  • the synthesis or a particular reaction may be conducted without need for purification.
  • a compound or intermediate may be purified using recrystallization, a process which may be repeated until the desired level of purity of the product is obtained.
  • the compound or intermediate is recrystallized at least once, two times, three times, or four or more times to achieve the desired level of purity.
  • the compound or intermediate may be obtained at a purity of greater than or equal to 50%, 80%, 85%, 90%, 95%, 97%, 98%, 98.5%, or 99.8%.
  • Recrystallization may be achieved using a single solvent, or a combination of solvents.
  • recrystallization is achieved by dissolving the compound or intermediate in a solvent such as hexane at elevated temperatures, and then cooling the solution to produce a precipitate.
  • the compound is recrystallized from hexane.
  • a ring-opening reaction may be performed upon exposure of a compound comprising a ring to a nucleophile, optionally in the presence of a catalyst.
  • the nucleophile may be a hydride (e.g. , H " ).
  • the ring-opening reaction may be performed in the presence of a metal-containing catalyst, such as zirconium chloride.
  • the method involves reacting a compound comprising formula (V):
  • W is alkyl or heteroalkyl, optionally substituted
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • Some embodiments involve exposure of the compound comprising formula (V) to a nucleophile.
  • the nucleophile is a hydride ion (e.g. , H " ).
  • reacting the compound involves contacting the compound with
  • DIBAL-H diisobutylaluminum hydride
  • the ring-opening reaction may also occur via a radical reaction.
  • the compound comprising formula (V) may be exposed to a radical species, such as a hydrogen radical (e.g. , ⁇ ), in order to produce the compound comprising formula (VI).
  • a radical species such as a hydrogen radical (e.g. , ⁇ )
  • the radical species may be generated by a catalyst, such as Sml2.
  • methods are provided for synthesizing a compound comprising formula (VI). For example, an etherification reaction is performed between compounds comprising formulae (Va) and (Vb):
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide.
  • This etherification reaction may be performed as described herein and may involve exposure to a base (e.g. , cesium carbonate, sodium hydroxide, tetramethyl ammonium hydroxide), optionally in the presence of a phase transfer catalyst.
  • a base e.g. , cesium carbonate, sodium hydroxide, tetramethyl ammonium hydroxide
  • the etherification reaction involves exposure to sodium hydroxide and benzyl triethylammonium chloride.
  • the etherification reaction is performed in the presence of a phase transfer catalyst and an ionic liquid.
  • R is alkyl, optionally substituted
  • R 2 is hydrogen or halide.
  • Some embodiments may further involve the synthesis of a compound comprising formula (VII):
  • R a may be hydrogen, hydroxyl, halide (e.g. , chloride), O-alkyl, O-heteroalkyl, O-aryl, O-heteroaryl, S-alkyl, S-heteroalkyl, S-aryl, S-heteroaryl, alkyl, heteroalkyl, aryl, or heteroaryl, any of which may be optionally substituted.
  • R a is O-alkyl such as O-methyl, O-ethyl, O-propyl, and the like. In some embodiments, R a is O- methyl.
  • the method may involve the reaction of methyl 4-formyl benzoate with ethylene glycol in the presence of an acid to produce a compound comprising formula (VII).
  • the compound comprising formula (VII) may be further reacted, for example, to install a leaving group on the compound.
  • the leaving group is a hydroxyl group.
  • R a is methyl
  • the carboxy group is treated with a reducing agent such as lithium aluminum hydride, sodium bis(2- methoxyethoxy)aluminum hydride or lithium borohydride to produce a benzylic alcohol.
  • Figure 5 shows an illustrative embodiment for synthesizing alcohol 15 using a ring-opening reaction.
  • the first step involves the conversion of ether methyl 4-formyl benzoate or 4-formylbenzoic acid to the corresponding acetal through the reaction with ethylene glycol in the presence of an acid.
  • methyl 4-formyl benzoate and ethylene glycol are reacted in the presence of toluenesulfonic acid and toluene.
  • the solvent may be heated at reflux, using azeotropic distillation to remove any water that is produced in order to drive the reaction to completion.
  • the derived acid or ester 19 may then be reduced to benzyl alcohol 20 with lithium aluminum hydride, sodium bis(2-methoxyethoxy)aluminum hydride, lithium borohydride (e.g. , for an ester), or borane (e.g. , for an acid).
  • lithium aluminum hydride or sodium bis(2- methoxyethoxy) aluminum hydride may be used as the reducing agent.
  • Benzyl alcohol 20 may then be reacted with dichloropyridazinone 11 via an etherification reaction as described herein to afford compound 21.
  • the etherification reaction may be carried out with cesium carbonate, potassium carbonate, or sodium hydroxide in the presence of a variety of phase transfer catalysis reagents, such as, but not limited to, benzyl triethylammonium chloride.
  • the etherification reaction involves the use of cesium carbonate in dimethylformamide.
  • the etherification reaction involves the use of sodium hydroxide with 1- 10% benzyl triethylammonium chloride in toluene.
  • the acetal ring of compound 21 may then be opened to the corresponding alcohol 15 using diisobutylaluminum hydride (DIBAL-H).
  • DIBAL-H diisobutylaluminum hydride
  • the ring-opening reaction may be carried out in the presence of a catalyst, such as a metal-containing catalyst (e.g. , zirconium chloride) or an organic catalyst (e.g. , 9-borabicyclononane (9- BBN) dimer).
  • a catalyst such as a metal-containing catalyst (e.g. , zirconium chloride) or an organic catalyst (e.g. , 9-borabicyclononane (9- BBN) dimer).
  • the components of the ring-opening reaction is heated or cooled to any temperature from about -78 °C to about 200 °C, for a period of time.
  • the reaction mixture may be maintained at any temperature from about -78 °C to about room temperature.
  • the reaction mixture may be maintained at about -60 °C, about -50 °C, about -40 °C, about -30 °C, about -20 °C, about - 10 °C, about 0 °C, including all temperatures in between, or greater.
  • the ring- opening reaction mixture may be maintained at -40 °C. In some embodiments, the ring- opening reaction mixture may be maintained at room temperature.
  • the reaction may be heated/cooled/maintained at a particular temperature for a period of time, such as about 10 minutes, about 30 minutes, about 1 hour, about 2 hours, about 3 hours, about 4 hours, about 5 hours, about 10 hours, or any amount of time in between, or more.
  • the reaction mixture may be maintained at about -40 °C for about 1 hour. It should be understood that other temperatures and reaction times may also be used.
  • Purification of compound 16 may be performed by successive recrystallizations from cumene and/or isobutyl acetate. For example, see Example 37E.
  • the overall yield for synthesizing alcohol 15 starting from methyl 4-formylbenzoate may be at least 10%, at least 20%, at least 30%, at least 40%, or at least 50%, without or with the use of chromatography for purification. In some cases, the overall yield for synthesizing alcohol 15 starting from methyl 4- formylbenzoate is approximately 50%, without the use of chromatography for purification.
  • Any of the methods for synthesizing an imaging agent precursor described herein may further comprise the act of exposing the compound comprising formula (VIII):
  • W is alkyl or heteroalkyl, optionally substituted
  • R 1 is alkyl, optionally substituted
  • R 2 is hydrogen or halide
  • L is a leaving group
  • the reagent is a sulfonate-containing species and the leaving group is a sulfonate-containing group (e.g. , a sulfonate-containing precursor of an imaging agent).
  • the sulfonate-containing group is mesylate, tosylate, or triflate. In one set of embodiments, the sulfonate-containing group is tosylate. Additional examples of leaving groups are described herein.
  • R 1 , R 2 , and L are as described herein.
  • an imaging agent precursor described herein provides novel compounds (e.g. , intermediates).
  • the compound comprises the structure:
  • the present invention relates to methods of imaging, including methods of imaging in a subject that includes administering a composition or formulation that includes imaging agent 1 to the subject by injection, infusion, or any other known method, and imaging a region of the subject that is of interest.
  • a composition or formulation that includes imaging agent 1 to the subject by injection, infusion, or any other known method, and imaging a region of the subject that is of interest.
  • imaging agent 1 As described herein, (2-i-butyl-4-chloro-5-[4-(2-( 18 F)fluoroethoxymethyl)-benzyloxy]-2H-pyridazin- 3-1, or imaging agent 1,
  • Imaging agent 1 binds to the mitochondrial complex I of the electron transport chain with high affinity. Imaging agent 1 shows selective uptake to the heart due to the high density of mitochondria in the myocardium. Regions of interest may include, but are not limited to, the heart, cardiovascular system, cardiac vessels, blood vessels (e.g. , arteries, veins) brain, and other organs. A parameter of interest, such as blood flow, cardiac wall motion, etc., can be imaged and detected using methods and/or systems of the invention. In some aspects of the invention, methods for evaluating perfusion, including myocardial perfusion, are provided.
  • methods of the present invention include (a) administering to a subject a composition that includes imaging agent 1, and (b) acquiring at least one image of at least a portion of the subject.
  • acquiring employs positron emission tomography (PET) for visualizing the distribution of imaging agent 1 within at least a portion of the subject.
  • PET positron emission tomography
  • imaging using methods of the invention may include full body imaging of a subject, or imaging of a specific body region or tissue of the subject that is of interest. For example, if a subject is known to have, or is suspected of having myocardial ischemia, methods of the invention may be used to image the heart of the subject. In some embodiments, imaging may be limited to the heart, or may include the heart and its associated vascular system.
  • a cardiovascular disease can be any disease of the heart or other organ or tissue nourished by the vascular system.
  • the vascular system includes coronary arteries, and all peripheral arteries supplying nourishment to the peripheral vascular system and the brain, as well as veins, arterioles, venules, and capillaries.
  • cardiovascular diseases include diseases of the heart, such as coronary artery disease, myocardial infarction, myocardial ischemia, angina pectoris, congestive heart failure, cardiomyopathy (congenital or acquired), arrhythmia, or valvular heart disease.
  • the methods disclosed herein are useful for monitoring and measuring coronary artery disease and/or myocardial perfusion.
  • a method described herein can determine the presence or absence of coronary artery disease and/or the presence or absence of myocardial infarct.
  • Conditions of the heart may include damage, not brought on by disease but resulting from injury - e.g. , traumatic injury, surgical injury.
  • methods of the invention may include determining a parameter of, or the presence or absence of, myocardial ischemia, rest (R) and/or stress (S) myocardial blood flows (MBFs), coronary flow reserve (CFR), coronary artery disease (CAD), left ventricular ejection fraction (LVEF), end-systolic volume (ESV), end-diastolic volume (EDV), and the like.
  • MVFs myocardial blood flows
  • CFR coronary flow reserve
  • CAD coronary artery disease
  • LVEF left ventricular ejection fraction
  • ESV end-systolic volume
  • EDV end-diastolic volume
  • a subject to whom a method of the invention is applied may have signs or symptoms suggestive of myocardial ischemia or myocardial infarction.
  • methods of the invention can be used to identify early or pre-disease conditions that indicate that a subject is at increased risk of a disease.
  • methods of the invention can be used to determine a subject's risk of future cardiac events such as myocardial infarction or cardiac death.
  • Imaging methods of the invention can be used to detect myocardial ischemia in subjects already diagnosed as having a myocardial ischemia disorder or condition, or in subjects that have no history or diagnosis of such a condition.
  • methods of the invention can be used to obtain measurements that provide a diagnosis or aid in providing a diagnosis of a myocardial ischemia disorder or condition.
  • a subject may be already be undergoing drug therapy for a myocardial ischemia disorder or condition, while in other instances a subject may not be undergoing therapy for myocardial ischemia.
  • methods of the invention can be used to assess efficacy of a treatment for a disease or condition.
  • the heart can be visualized using imaging agents of the invention before, during, and/or after treatment of a condition affecting the heart of a subject. Such visualization may be used to assess a disease or condition, and aid in selection of a treatment regimen, e.g. therapy, surgery, medications, for the subject.
  • a PET imaging agent may have a high first-pass extraction fraction and can track regional myocardial blood flow over a wide range. These features may permit detection of milder decreases in coronary flow reserve and accurate estimation of absolute myocardial blood flow (MBF). PET imaging agents of the invention provide these and other features and are also available as a unit dose from regional PET radiopharmacies, obviating the need for on-site cyclotrons or costly Rb-82 generators.
  • imaging agent 1 is used as an imaging agent in combination with positron emission tomography (PET) or with other imaging methods including, but not limited to SPECT imaging.
  • imaging agent 1 is administered to a subject and imaged in the subject using PET.
  • PET is a non-invasive technique that allows serial images and measurements to be obtained in a single subject over a time period.
  • PET imaging used in methods of the invention may be carried out using known systems, methods, and/or devices.
  • PET imaging is conducted using a cardiac imaging system.
  • a cardiac imaging system may include PET imaging functionality and a control unit configured to drive the imaging functionality to perform a PET imaging procedure on a portion of the subject before, during, and/or after administration of imaging agent 1 to the subject.
  • the control unit is configured to drive the imaging functionality to perform a PET imaging procedure.
  • the control unit may comprise a computer system and/or software.
  • the computer system may be programmed or configured to execute the required methods for acquiring and/or analyzing the images.
  • the system may include a data storage device that is readable by a machine, embodying a set of instructions executable by the machine to perform the required methods of acquiring and/or analyzing the images.
  • the useful dosage of the imaging agent to be administered and the particular mode of administration will vary depending upon such factors as age, weight, and particular region to be imaged, as well as the particular imaging agent used, the diagnostic use contemplated, and the form of the formulation, for example, suspension, emulsion, microsphere, liposome, or the like, as described herein, and as will be readily apparent to those skilled in the art.
  • an imaging agent is administered at a low dosage and the dosage increased until the desirable diagnostic effect is achieved.
  • the above-described imaging agents may be administered by intravenous injection, usually in saline solution, at a dose of about 0.1 to about 100 mCi per 70 kg body weight (and all combinations and subcombinations of dosage ranges and specific dosages therein), or between about 0.5 and about 50 mCi, or between about 0.1 mCi and about 30 mCi, or between 0.5 mCi and about 20 mCi.
  • the imaging agents, dosages, administered by intravenous injection may range from about 0.1 pmol/kg to about 1000 pmol/kg (and all combinations and
  • Imaging systems and components thereof will be known to those of ordinary skill in the art. Many imaging systems and components (e.g. , cameras, software for analyzing the images, etc.) are known and commercially available, for example, a Siemens Biograph-64 scanner. Any technique, software, or equipment that reduces or eliminates motion in static perfusion images may be used in methods of the invention, because spatial blurring and artifacts can be caused by patient motion during image acquisition.
  • images may be acquired in list mode, and may be static, dynamic, or gated images. An appropriate period of time for acquiring images can be determined by one of ordinary skill in the art, and may vary depending on the cardiac imaging system, the imaging agent (e.g. , amount administered, composition of the imaging agent, subject parameters, area of interest).
  • a "period of acquiring images” or an “image acquisition period” may be a period of obtaining a single continuous image, or may be a period during which one or more individual discrete images are obtained.
  • a period of image acquisition can be a period during which one or more images of one or more regions of a subject are acquired.
  • a period of image acquisition after administration of an imaging agent of the invention to a subject may be between about 30 seconds and about 60 minutes, between about 1 minute and about 30 minutes, between about 5 minutes and about 20 minutes, or at least about 1 minute, about 3 minutes, about 5 minutes, about 6 minutes, about 7 minutes, about 8 minutes, about 9 minutes, about 10 minutes, about 15 minutes, about 20 minutes, about 30 minutes, 4 about 5 minutes, about 60 minutes, or greater.
  • imaging may be continuous over the imaging period of time, or images may be acquired at intervals such as in periodic or gated imaging.
  • gated acquisition is used to acquire images from a subject to whom an imaging agent prepared by methods of such as imaging agent 1 has been administered.
  • Gated imaging can be used in various aspects of the invention, and for example, may provide images of a beating heart of a subject and may be used to attain a functional evaluation of how well a heart is beating.
  • Gated imaging can be performed by acquiring separate images from the subject at specific intervals during a period of image acquisition.
  • a non-limiting example of gated imaging is a case when a period of image acquisition is about 10 minutes long, and images are acquired at repeated intervals during the 10 minute period.
  • the frequency of acquisition of images during the period can be set by the operator, for example, the frequency can be at least every about 1 msec, about 5 msec, about 10 msec, about 20 msec, about 50 msec, about 100 msec, about 125 msec, about 250 msec, or more.
  • the length of the interval is set by the operator to be triggered by an event, such as a cardiac R wave, with the length of the interval is defined by the number of time bins desired per R wave to R wave interval.
  • Image acquisition in gated imaging can be triggered at specific intervals, for example, image acquisition can be triggered using an EKG of the heart.
  • an R wave-gated scanner may trigger acquisition of an image and the mean length of time between one R wave of a heart and the next can be stored. The number of images to collect can then be determined. For example, a first image can be acquired at 125 msec, a second image can be acquired at 250 msec, a third image can be acquired at 375 msec, etc. - thus images in that R interval may be acquired at 125 msec intervals.
  • Use of gated imaging may provide data with which to judge perfusion of the heart, such as ejection fraction, and to visualize and identify reduced, absent, paradoxical or asynchronous wall motion. Use of gated imaging may also provide data with which to improve assessment of myocardial perfusion, judge cardiac function and to visualize and identify asynchronous wall motion.
  • PET imaging may be used to assess myocardial viability via the ability of this technique to demonstrate metabolic consequences of myocardial ischemia. Using PET imaging, myocardial segments that are likely to improve after
  • PET imaging may be used in the detection of coronary artery disease and can also serve as an alternative test for subjects who cannot undergo treadmill exercise stress testing.
  • a stress test method e.g. , pharmacological stress, exercise stress
  • pharmacological stress exercise stress
  • methods of the invention to qualitatively or quantitatively assess one or more parameters of cardiac function during infusion of the imaging agent.
  • Agents for, and methods of, inducing stress for example, using exercise or pharmacological stress are well known in the art. Suitable induction of stress can be carried out using established, known agents and methods.
  • Functions usefully measured using methods of the invention include, but are not limited to, in various embodiments, imaging of myocardial perfusion, imaging, or measurement of ventricular function, and measuring coronary blood flow velocity.
  • methods for imaging the heart of a subject may include administering a first dose of imaging agent 1 to the subject while the subject is at rest, acquiring at least one first image of the heart, followed by subjecting the subject to stress (e.g. , exercise stress or pharmacological stress) and administering a second dose of imaging agent 1 to the subject during the period of stress, and acquiring at least one other image of the heart.
  • stress e.g. , exercise stress or pharmacological stress
  • the dose of imaging agent 1 to be used during exercise- induced stress in a rest/stress protocol is greater than that necessary for
  • the dose of imaging agent 1 administered for imaging during the pharmacological stress is a minimum of two times the dose of imaging agent 1 administered for imaging at rest.
  • the dose of imaging agent 1 administered for imaging during the exercise-induced stress is a minimum of three times the dose of imaging agent 1 administered for imaging at rest. In some embodiments of the invention, for imaging first at rest followed by imaging with stress, the dose of imaging agent 1 administered at rest will be lower than the dose of imaging agent 1 administered at stress.
  • imaging methods of the invention may be completed in a single day (e.g. , less than about 24 hours, less than about 12 hours, less than about 6 hours, less than about 4 hours, less than about 2 hours, less than about 1 hour), as described herein. In other cases, methods may be completed in longer periods of time, e.g. over more than about 24 hours, about 36 hours, or about 48 hours.
  • Imaging agent 1 may be provided in any suitable form, for example, in a pharmaceutically acceptable form. In some cases, imaging agent 1 is included in a pharmaceutically acceptable composition. In some embodiments, imaging agent 1 is provided as a composition comprising ethanol, sodium ascorbate, and water. In some cases, the composition comprises less than 20 weight ethanol, less than 15 weight ethanol, less than 10 weight ethanol, less than 8 weight ethanol, less than 6 weight ethanol, less than 5 weight ethanol, less than 4 weight ethanol, less than 3 weight ethanol, or less ethanol.
  • the composition comprises less than 100 mg/mL, less than 75 mg/mL, less than 60 mg/mL, less than 50 mg/mL, less than 40 mg/mL, less than 30 mg/mL, or less sodium ascorbate in water.
  • imaging agent 1 is provided as a solution in water comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water.
  • Imaging agent 1 composition for injection may be prepared in an injection syringe.
  • Imaging agent 1 may be prepared by a radiopharmacy (e.g. , using the methods described herein) and/or a PET manufacturing center and provided to a health-care professional for administration.
  • imaging agent 1 is provided, for example, in a syringe or other container, with ⁇ 50 mg/mL sodium ascorbate in water, ⁇ 4 wt ethanol, and about 1 to 14 mCi of imaging agent 1.
  • the amount of imaging agent 1 may vary depending on whether a rest or stress dose is being administered.
  • a higher amount of imaging agent 1 may be provided in a syringe or container for use in a stress dose administration than provided in a syringe for use in a rest administration.
  • a dose of imaging agent 1 may be diluted with saline (e.g. , as described herein), if needed to obtain a practical dose volume.
  • the solution can be diluted, e.g. , with sterile saline, so the syringe contains 0.5 ml to 4 or more ml of an imaging agent 1 solution for
  • an injection volume for imaging agent 1 is between 0.5 and 5 ml, 1 and 4 ml, 2 and 3 ml, at least 0.5 ml, 1 ml, 2 ml, 3 ml, 4 ml, 5 ml, 6 ml, 7 ml, 8 ml, 9 ml, 10 ml, or more.
  • imaging agent 1 is provided in a container such as a vial, bottle, or syringe, and may be transferred, as necessary, into a suitable container, such as a syringe for administration.
  • Syringes that include an adsorbent plunger tip may result in 10 to 25% of imaging agent 1 activity remaining in the syringe after injection.
  • Syringes lacking an adsorbent plunger tip may be used, such as a 3 or 5 mL NORM-JECT (Henke Sass Wolf, Dudley, MA) or other equivalent syringe lacking an adsorbent plunger tip. Reduction of adsorption in the syringe can increase the amount of imaging agent 1 that is transferred from the syringe and administered to the subject in methods of the invention.
  • a syringe used in methods of the invention may comprise imaging agent 1 , and be a non-adsorbing, or reduced adsorbent syringe.
  • a non-adsorbent or reduced- adsorbent syringe is a syringe that has been coated or treated to reduce imaging agent 1 adsorption.
  • a non-adsorbent or reduced-adsorbent syringe is a syringe that lacks an adsorbent plunger tip.
  • a syringe used in conjunction with the invention adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11 %, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1 %, or 0.5% of imaging agent 1 it contains.
  • a syringe that contains imaging agent 1 does not include a rubber or latex tip on the plunger.
  • a syringe used in methods of the invention includes a plunger that adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11 %, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of imaging agent 1 that the syringe contains.
  • a syringe of the invention may also comprise sodium ascorbate, ethanol, and water, and certain embodiments of the invention include a syringe containing imaging agent 1 in a solution comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water.
  • a syringe of the invention may be a syringe that is latex free, rubber free, and/or lubricant free.
  • a syringe of the invention may contain imaging agent 1 in an amount between about 1.5 and about 14 mCi.
  • a syringe of the invention may contain about 20 mCi or less of imaging agent 1.
  • Components of a composition comprising imaging agent 1 may be selected depending on the mode of administration to the subject. Various modes of
  • the imaging agent is administered intravenously (e.g. , intravenous bolus injection) using methods known to those of ordinary skill in the art.
  • a dose that is "administered to a subject” means an amount of the imaging agent, e.g. imaging agent 1, that enters the body of the subject.
  • the amount of an imaging agent such as imaging agent 1 that is measured or determined to be in the a syringe or other equipment prepared for administration may be more than the amount in the dose that is administered to the subject.
  • an injection of an imaging agent is followed by a flushing injection of normal saline, into the subject, using the same tubing, needle, port, etc. , used for administration of imaging agent 1.
  • Flushing may be performed immediately following administration of imaging agent 1, or up to 1 min, 2 min, 3 min, 5 min, or more, after the administration.
  • the volume of saline or other agent for flushing may be up to 5 ml, 6 ml, 7 ml, 8 ml, 9 ml, 10 ml, 15 ml, 20 ml, or more.
  • the true amount of imaging agent 1 administered to the subject may be corrected for any imaging agent 1 that remains in the container.
  • the amount of radioactivity remaining in the container, and tubing and needle or delivery instrument that carried the imaging agent from the container and into the subject can be determined after the imaging agent has been administered to the subject and the difference between the starting amount of radioactivity and the amount remaining after administration indicates the amount that was delivered into the subject.
  • the container or injection device e.g. , catheter, syringe
  • a solution e.g. , saline solution
  • the total amount of imaging agent 1 administered to a subject over a given period of time is less than or equal to about 50 mCi, less than or equal to 40 mCi, less than or equal to 30 mCi, less than or equal to 20 mCi, less than or equal to 18 mCi, less than or equal to 16 mCi, less than or equal to 15 mCi, less than or equal to 14 mCi, less than or equal to 13 mCi, less than or equal to 12 mCi, less than or equal to 10 mCi, less than or equal to 8 mCi, less than or equal to 6 mCi, less than or equal to 4 mCi, less than or equal to 2 mCi, less than or equal to 1 mCi, less than or equal to 0.5 mCi.
  • the total amount administered may be determined based on a single dose or multiple doses administered to a subject within a given
  • the desirable maximum dose administered to a subject may be based on determining the amount of imaging agent 1 which limits the radiation dose to about 5 rem to the critical organ and/or about 1 rem effective dose (ED) or lower, as will be understood by those of ordinary skill in the art.
  • the desirable maximum dose or total amount of imaging agent 1 administered is less than or equal to about 25 mCi, or less than or equal to about 14 mCi over a period of time of up to 30 min, 1 hour, 2 hours, 6 hours, 12 hours, 24 hours, 48 hours, or more.
  • the maximum dose of imaging agent 1 administered to a subject may be less than 3.5 ⁇ g per 50 kg of body weight per day. That is, in some embodiments of the invention, the maximum dose of imaging agent 1 administered to a subject may be less than about 0.07 ⁇ g of imaging agent 1 per kg of body weight per day.
  • methods of the invention include administering to a subject a first dose (e.g. , rest dose) of imaging agent 1 while the subject is at rest, and performing a first PET imaging procedure (e.g. , a PET rest imaging procedure) and acquiring at least a first image of a portion of a subject.
  • a first dose e.g. , rest dose
  • a first PET imaging procedure e.g. , a PET rest imaging procedure
  • the subject may be subjected to stress and during the stress a second dose (e.g. , stress dose) of an imaging agent such as imaging agent 1 is administered to the subject, and a second PET imaging procedure (e.g. , a PET stress imaging procedure) is performed on the subject and at least one other image of a portion of the subject may be acquired.
  • a second dose e.g. , stress dose
  • a second PET imaging procedure e.g. , a PET stress imaging procedure
  • the wait time between the completion of the first PET imaging procedure and administration of the second imaging agent dose is referred to as the wait time.
  • a rest-stress test may be completed in a period of time of less than 48 hours, less than 36 hours, less than 24 hours, less than 12 hours, less than 6 hours, less than 5 hours, less than 4 hours, less than 3 hours, less than 2 hours, less than 1 hour, less than 30 minutes, or less.
  • the amount of imaging agent 1 administered in a first dose to a subject at rest is between about 1 mCi and about 5 mCi, between about 2 mCi and about 4 mCi, between about 2.5 mCi and about 3.5 mCi, or about 3 mCi.
  • a PET imaging procedure may be performed and at least one first image may be acquired of at least a portion of the subject.
  • the amount of imaging agent 1 administered to a subject during stress may be based on the amount of imaging agent 1 administered to the subject at rest. That is, the dosing during stress may be based, at least in part, on a dosing ratio (DR) (e.g. , ratio of stress-dose to rest-dose).
  • DR dosing ratio
  • the DR may depend on numerous factors as will be known to those of ordinary skill in the art, and in some cases, may depend on the method of inducing stress in the subject.
  • the DR is between 1 and 5, between 1 and 4, between 1 and 3, between 2 and 5, or between 2 and 4.
  • the DR is at least 1, at least 1.5, at least 2, at least 3, at least 4, or at least 5.
  • the DR is between 2.5 and 5.0, or 2.5 and 4.0, or 3.0 and 4.0, or 3.0 and 5.0 times greater than the first dose of the imaging agent.
  • the DR required for a subject subjected to exercise stress is more than the DR and/or time interval used for a subject subjected to pharmacological stress. This may be due, in part, to a lower net myocardial uptake of radioactivity with exercise.
  • the DR employed for a subject subjected to exercise stress is between 2 and 4, between 2.5 and 3.5, or at least 3.0, at least 3.5, at least 4.0, or more, in embodiments wherein the wait time is at least 15 minutes 30 minutes, 1 hour, 1.5 hours, 2 hours, or the like.
  • the DR employed for a subject subjected to pharmacological stress is between 1 and 3, or between 1.5 and 2.5, or at least 2.0, at least 2.2, or at least 2.5, or more, in embodiments wherein the wait time is at least 15 minutes, 30 minutes, 1 hour, 1.5 hours, 2 hours, or the like.
  • a DR of at least 2.2 for a wait time of at least 15 minutes or at least 30 minutes is employed, and/or for a subject subjected to exercise stress, a DR of at least 3.0 for a wait time of at least 30 minutes or at least 1 hour is employed.
  • the imaging agent is between about 2.0 mCi and about 3.5 mCi, or
  • a dose of about 2.9 mCi to about 3.4 mCi rest is provided during rest, and a dose of about 2.0 to about 2.4 times the rest dose is provided during stress, with a wait time of at least about 15 minutes or at least about 30 minutes.
  • the second dose of the imaging agent is between about 5.7 mCi and about 6.2 mCi, or between about 6.0 mCi and about 6.5 mCi, and about 5.7 mCi and about 6.5 mCi.
  • a dose of about 1.7 mCi to about 2.0 mCi is provided during rest, and a dose of about 3.0 to about 3.6 times the rest dose is provided during stress, with a wait time of at least about 30 minute or at least about 60 minutes.
  • the second dose of the imaging agent is between about 8.6 mCi and about 9.0 mCi, or between about 9.0 and about 9.5 mCi, or between about 8.6 mCi and about 9.5 mCi.
  • a dose of between about 2.4 mCi and about 2.9 mCi is administered during rest, and a dose between about 5.7 mCi and about 6.2 mCi is administered during stress (e.g. , DR of at least about 2), wherein the wait time is at least about 15 minutes or at least about 30 minutes.
  • a dose of between about 1.7 mCi and about 2.0 mCi is administered during rest, and a dose of between about 8.6 mCi and about 9.0 mCi is administered during stress (e.g. , DR at least about 3), wherein the wait time is at least 30 minutes or at least 60 minutes.
  • a dose of about 2.9 mCi to about 3.3 mCi rest is provided during rest, and a dose of 2.0 to 2.4 times the rest dose is provided during stress, with a wait time of at least 15 minutes or at least 30 minutes.
  • a dose of about 2.9 mCi to about 3.3 mCi is provided during rest, and a dose of 3.0 to 3.6 times the rest dose is provided during stress, with a wait time of at least 30 minute or at least 60 minutes.
  • a dose of about 2.5 mCi to about 3.0 mCi rest is provided during rest and a dose about 6 mCi to about 6.5 mCi is provided during stress.
  • a dose of about 2.5 mCi to about 3.0 mCi rest is provided during rest and a dose about 9 mCi to about 9.5 mCi is provided during stress.
  • administering during the stress includes beginning administering the second dose within a period of time after completing the rest imaging procedure (e.g. , the wait period).
  • the second dose may be administered at a period of time of at least 5 minutes, 10 minutes, 15 minutes, 20 minutes, 30 minutes, 40 minutes, 45 minutes, 50 minutes, 60 minutes, 70 minutes, 80 minutes, 90 minutes, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours, or greater, after completing the rest imaging procedure.
  • the second dose is administered at a time period of between 5 minutes and 30 days, between 5 minutes and 20 days, between 5 minutes and 10 days, between 5 minutes and 5 days, between 5 minutes and 4 days, between 5 minutes and 3 days, between 5 minutes and 48 hours, between 5 minutes and 24 hours, between 5 minutes and 12 hours, between 5 minutes and 2 hours, between 5 minutes and 90 minutes, between 10 minutes and 60 minutes after completing the rest imaging procedure.
  • a subject may be subjected to stress using procedures known to those of ordinary skill in the art. In some cases, the subject may be subjected to stress using procedures including exercise stress and/or
  • Pharmacological stress may be induced by administering to the subject a pharmacological agent such as a vasodilator. Examples of useful
  • pharmacological stress agents include, but are not limited to adenosine, dobutamine, dipyridamole, regadenoson, binodeneson, apadeneson, and other adenosine A2a receptor agonists.
  • Dosing and administration of pharmacological stress inducing agents are well known in the art and can be determined for use in conjunction with methods and systems of the invention.
  • Exercise stress may be induced using a treadmill, exercise bicycle, hand crank, or other equipment suitable to increase a subject's heart rate through increased exertion.
  • a rest/stress method is followed.
  • a period of rest and imaging is followed by a period of stress and imaging, with the order being rest first, followed by stress.
  • a stress/rest method may be used.
  • a period of stress and imaging is followed by a period of rest and imaging, with the order being stress first, followed by rest.
  • imaging agent 1 can be used in a "stress only” method, in which stress is induced in a subject for imaging with imaging agent 1 with no rest imaging during the subject session.
  • imaging agent 1 can be used in a "rest only” method, in which a subject does not undergo stress induction, but is only imaged with imaging agent 1 at rest in that session.
  • an imaging agent e.g., imaging agent 1
  • an imaging agent may be prepared using an automated reaction system comprising a disposable or single use cassette.
  • the cassette may comprise all the non-radioactive reagents, solvents, tubing, valves, reaction vessels, and other apparatus and/or components necessary to carry out the preparation of a given batch of imaging agent.
  • the cassette allows the reaction system to have the flexibility to make a variety of different imaging agents with minimal risk of cross-contamination, by simply changing the cassette.
  • a cassette is meant a piece of apparatus designed to fit removably and interchangeably onto automated reaction systems, in such a way that mechanical movement of moving parts of the automated reaction system controls the operation of the cassette from outside the cassette, ie., externally.
  • a cassette comprises a linear arrangement of valves, each linked to a port where various reagents, cartridges, syringes, and/or vials can be attached, by either needle puncture of a septum-sealed vial, or by gas- tight, marrying joints.
  • Each valve may have a male-female joint which interfaces with a corresponding moving arm of the automated synthesizer.
  • An automated reaction system may further include a controller and one or more controllable valves in electrical communication with the controller.
  • An automated reaction system may also include additional vessels, valves, sensors, heaters, pressurizing elements, etc. , in electrical communication with the controller.
  • An automated reaction system may be operated by a controller using suitable software for control of valve openings and closings, heating, cooling, pressure levels, fluid movement, flow rate, etc.
  • the automated reaction system may optionally include a computer operating system, software, controls, etc., or other component.
  • the automated reaction system may comprise a mount for the cassette.
  • automated reaction systems include, but are not limited to, the Explora GN or RN synthesis system (Siemens Medical Solutions USA, Inc.), GE-Tracerlab-MX synthesis system (GE Healthcare), Eckert & Zeigler Modular- Lab Synthesis system, etc. , which are commonly available at PET manufacturing facilities.
  • the automated reaction systems may carry-out numerous steps, as outlined in Figure 6, including, but not limited to, preparation of the 18 F fluoride species, providing an imaging agent precursor, optionally in a solution (e.g. , as described herein, for example, imaging agent precursor 1 in acetonitrile), a radiolabeling reaction (e.g.
  • reaction of the 18 F species and the imaging agent precursor to form the imaging agent optionally in a synthesis module, purification (e.g. , by preparative HPLC), solvent exchange (e.g. , by SepPak), aseptic filtration, and release into a container.
  • purification e.g. , by preparative HPLC
  • solvent exchange e.g. , by SepPak
  • aseptic filtration e.g. , by SepPak
  • the automated reaction system may make use of a cassette comprising a reaction module in fluid connection with a purification module and/or a formulation module.
  • Figures 7 and 8 show schematic representations of cassettes in connection with exemplary reaction systems for synthesizing an imaging agent comprising a reaction module, a purification module, and/or a formulation module.
  • the reaction module may include a reaction chamber in which conversion of the imaging agent precursor to the imaging agent is performed.
  • the reaction module may include a source of a fluoride species (e.g. , 18 F), a source of the imaging agent precursor, a source of an additive (e.g. , salt additive), and other sources of additional components such as solvents, each of which may optionally be fluidly connected to the reaction chamber.
  • the reaction module may also comprise an anion exchange column for purification of the fluoride species, prior to introduction into the reaction chamber.
  • the purification module may include, for example, a column (e.g. , an HPLC column) fluidly connected to one or more sources of solvents to be used as eluents.
  • the purification module may further comprise a source of a stabilizing agent (e.g. , ascorbic acid or a salt thereof), which may be added to the imaging agent upon purification (e.g. , by HPLC).
  • the purified imaging agent is then transferred to the formulation module, where further purification and formulation may be performed.
  • the formulation module may include a filter for aseptic filtration and/or a C- 18 column for solvent exchange.
  • a cassette comprises a reaction module and a formulation module.
  • a reaction module of the invention may include a source of 18 F, a filter to remove unreacted [ 0]H 2 0, a source of an ammonium salt, a source for a diluent for the 18 F, a source for an imaging agent precursor, ⁇ e.g. , imaging agent precursor 1 shown in Figure 1, or other imaging agent precursor), a source for an 3 ⁇ 40 diluent for the imaging agent precursor, a reaction vessel for reacting the 18 F and the imaging agent precursor, a solid phase extraction column (e.g., a CI 8 column, or other suitable column) in fluid communication with the reaction vessel.
  • a solid phase extraction column e.g., a CI 8 column, or other suitable column
  • the solid phase extraction column includes a solid sorbent to adsorb the radiolabeled imaging agent product on the sorbent. At least a portion of the residual reaction impurities pass through solid phase extraction column without adsorbing on the sorbent.
  • the reaction module also includes a source of wash solutions in fluid communication with the solid phase extraction column for providing wash solutions to elute the remaining impurities on the sorbent, and includes a source of an eluent ⁇ e.g. , as H20/MeCN, or other suitable eluent) in fluid communication with the solid phase extraction column for eluting the radiolabeled imaging agent product off the sorbent.
  • the reaction module may also include a source of a diluent for the eluted radiolabeled imaging agent.
  • a formulation module of an apparatus of the invention may be in fluid communication with a reaction module and may include a solid phase extraction cartridge that includes a solid sorbent ⁇ e.g. , C-18, or other suitable sorbent) to adsorb the diluted radiolabeled imaging agent, a source of wash solutions ⁇ e.g. , comprising ascorbic acid, a salt thereof, or other suitable wash solution) in fluid communication with the solid phase extraction cartridge for providing wash solutions to wash off any remaining impurities on the sorbent, and a source of eluting fluid ⁇ e.g. , ethanol, or other suitable eluting fluid) in fluid communication with the solid phase extraction cartridge for eluting the radiolabeled imaging agent product off the sorbent.
  • a solid phase extraction cartridge that includes a solid sorbent ⁇ e.g. , C-18, or other suitable sorbent) to adsorb the diluted radiolabeled imaging agent, a source of wash solutions ⁇ e.g. , comprising ascorbic
  • the formulation module may also include a source of a diluent ⁇ e.g. , comprising ascorbic acid, a salt thereof, or other suitable diluent), for diluting the eluted radiolabeled imaging agent.
  • a source of a diluent e.g. , comprising ascorbic acid, a salt thereof, or other suitable diluent
  • the formulation module may also be in fluid communication with a sterilizing filter ⁇ e.g. , a Millipore Millex GV PVDF sterilizing filter, or other suitable sterilizing filter).
  • a cassette is provided for use with an automated synthesis module, for example, a GE TRACERlab MX synthesis module.
  • a cassette comprises a disposable sterilized assembly of molded stopcock manifolds specifically designed for use with the automated synthesis module ⁇ e.g. , GE TRACERlab MX synthesis module). Individual manifolds are connected in a linear or non-linear fashion to form a directional array that dictates the flow path of reagents used in the preparation of an imaging agent (e.g., imaging agent 1) injection.
  • an imaging agent e.g., imaging agent 1
  • the main body of the cassette contains at least one manifold comprising a plurality of manifold positions (e.g., stockcocks).
  • the main body may comprise at least one, two, three, four or more, manifolds.
  • the cassette may comprise between 1 to 20 manifold positions, between 1 to 15 manifold positions, between 5 and 20 manifold positions, between 5 and 15 manifold positions.
  • Each of the manifolds may or may not be symmetrical.
  • the main body of the cassette contains three plastic manifolds each fitted with five standard molded stopcocks, thereby having a total of 15 total manifold positions.
  • the cassette comprises a linear arrangement of a plurality of stopcock manifolds connected one or more of the components selected from the group consisting of a gas inlet, anion exchange cartridge, C-18 cartridge, syringe, solvent reservoir, reaction vessel, HPLC system, collection vessel, reservoir for solution of ascorbic acid or salt thereof, and exhaust outlet.
  • the cassette further comprises tubing. In some cases, the cassette further comprising an imaging agent synthesis module, wherein the apparatus is fluidically connected to the cassette. In some cases, the apparatus is capable carrying out the method of synthesizing an imaging agent as described herein (e.g., a method of synthesizing imaging agent 1).
  • the cassette configuration required for the preparation of imaging 1 injection is depicted in Figure 8.
  • the following provides a description of the attachments to each of the 15 manifold positions: 1) luer connection (2) - gas inlet and [ 18 0]H 2 0 recovery; 2) anion exchange cartridge - QMA Light; 3) spike connection - MeCN; 4) syringe - empty; 5) spike connection - imaging agent precursor 1; 6) luer connection - reaction vessel; 7) HPLC inlet; 8) spike connection - ascorbic acid; 9) luer connection - collection vessel; 10) syringe - EtOH; 11) luer connection - final product vial; 12) spike connection - SWFI; 13) spike connection - ascorbic acid; 14) syringe - empty; 15) luer connection (2) - reaction vessel and exhaust.
  • Manifold one (stopcocks 1-5) is joined to manifold two (stopcocks 6-10) using two male luer connections fitted with a short length of silicon tubing.
  • Manifold two is connected to manifold three (stopcocks 11-15) using a C-18 Sep- Pak® and the appropriate luer adapters. Individual manifold connections, luer fittings and all silicon tubing are readily available from commercial suppliers.
  • the present invention provides a cassette for the preparation of an imaging agent comprising the formula:
  • an imaging agent or an imaging agent precursor may be combined with one or more pharmaceutically acceptable excipients to form a pharmaceutical composition that is suitable for administering to a subject, including a human.
  • the excipients may be chosen, for example, based on the route of administration as described below, the agent being delivered, time course of delivery of the agent, and/or the health/condition of the subject.
  • compositions of the present invention and for use in accordance with the present invention may include a pharmaceutically acceptable excipient or carrier.
  • pharmaceutically acceptable excipient or carrier.
  • “pharmaceutically acceptable carrier” means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type.
  • materials which can serve as pharmaceutically acceptable carriers are sugars such as lactose, glucose, and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose, and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols such as propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; detergents such as Tween 80; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid;
  • pyrogen- free water isotonic saline; Ringer's solution; ethyl alcohol; and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.
  • compositions of this invention can be administered to humans and/or to animals, parenterally, intranasally, intraperitoneally, or via a nasal spray.
  • the mode of administration will vary depending on the intended use, as is well known in the art.
  • formulations of the present invention may be administered parenterally as injections (intravenous, intramuscular, or subcutaneous). These formulations may be prepared by conventional means, and, if desired, the subject compositions may be mixed with any conventional additive.
  • sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution, suspension, or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.
  • acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S. P. and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil can be employed including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid are used in the preparation of injectables.
  • the injectable formulations can be sterilized, for example, by filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use.
  • kits for the preparation of an imaging agent are provided for detecting, imaging, and/or monitoring myocardial perfusion.
  • kits for the administration of an imaging agent are provided.
  • Kits of the invention may include, for example, a container comprising an imaging agent, or an imaging agent precursor, and instructions for use. Kits may include a sterile, non-pyrogenic, formulation comprising a predetermined amount of an imaging agent (e.g., imaging agent 1), and optionally other components.
  • a kit may include one or more syringes that contain an imaging agent (e.g.
  • imaging agent 1 to be prepared for administration to a subject.
  • a container that may be used in conjunction with an imaging agent e.g. , imaging agent 1) (e.g. to deliver and/or administer an imaging agent (e.g., imaging agent 1) to a subject) may be a syringe, bottle, vial, tubes, etc.
  • Exemplary syringes that may be included in a kit of the invention are syringes lacking an adsorbent plunger tip, such as a 3 or 5 mL NORM-JECT (Henke Sass Wolf, Dudley, MA), or other equivalent syringe lacking an adsorbent plunger tip.
  • An imaging agent e.g.
  • imaging agent 1) may be provided in a kit and additional preparations before use may optionally include diluting the imaging agent to a usable concentration.
  • Instructions in a kit of the invention may relate to methods for, methods of diluting the imaging agent, methods of administering the imaging agent to a subject for diagnostic imaging, or other instructions for use.
  • a kit can also include one or more vials containing a diluent for preparing an imaging agent (e.g. , imaging agent 1) composition for administration to a subject (e.g. , human).
  • a diluent vial may contain a diluent such as physiological saline, water, buffered solution, etc. for diluting an imaging agent (e.g. , imaging agent 1).
  • the imaging agent e.g. , imaging agent l
  • the imaging agent may be packaged in a kit in a ready- to-inject formulation, or may require some reconstitution or dilution whereby a final composition/formulation for injection or infusion is prepared.
  • Instructions in a kit of the invention may also include instructions for administering the imaging agent (e.g. , imaging agent 1) to a subject and may include information on dosing, timing, stress induction, etc.
  • a kit may include an imaging agent described herein, along with instructions describing the intended application and the proper administration of the agent.
  • "instructions" can define a component of instruction and/or promotion, and typically involve written instructions on or associated with packaging of the invention. Instructions also can include any oral or electronic instructions provided in any manner such that a user will clearly recognize that the instructions are to be associated with the kit, for example, audiovisual (e.g. , videotape, DVD, etc.), Internet, and/or web-based communications, etc.
  • the written instructions may be in a form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which instructions can also reflects approval by the agency of manufacture, use or sale for human administration.
  • the instructions can include instructions for mixing a particular amount of the diluent with a particular amount of a concentrated solution of the imaging agent or a solid preparation of the imaging agent, whereby a final formulation for injection or infusion is prepared for example, such that the resulting solution is at a suitable concentration for administration to a subject (e.g. , at a concentration as described herein).
  • a kit may include a whole treatment regimen of the inventive compound (e.g. , a rest dose and a stress dose).
  • the kit may contain any one or more of the components described herein in one or more containers.
  • the kit may include instructions for mixing one or more components of the kit and/or isolating and mixing a sample and applying to a subject.
  • the kit may include a container housing an agent described herein.
  • the agent may be in the form of a liquid, gel or solid (powder).
  • the agent may be prepared sterilely, packaged in syringe and shipped refrigerated. Alternatively it may be housed in a vial or other container for storage. A second container may have other agents prepared sterilely.
  • the kit may include an active agent premixed and shipped in a syringe, vial, tube, or other container.
  • the kit may have one or more or all of the components required to administer the agents to a patient, such as a syringe, topical application devices, or iv needle tubing and bag.
  • kits containing the components of a kit of the invention can include additional indicia such as conventional markings that change color when the preparation has been autoclaved or otherwise sterilized.
  • a kit of the invention may further include other components, such as syringes, labels, vials, tubing, catheters, needles, ports, and the like.
  • a kit may include a single syringe containing the imaging agent (e.g.
  • imaging agent 1) sufficient for administration and in some aspects of the invention a kit may include two separate syringes, one comprising imaging agent 1 to be administered to a subject for rest imaging, and a second syringe comprising imaging agent 1 for administration to a subject for stress imaging.
  • Buffers useful in the preparation of imaging agents and kits include, for example, phosphate, citrate, subsalicylate, and acetate buffers. A more complete list can be found in the United States Pharmacopoeia. Lyophilization aids useful in the preparation of imaging agents and kits include, for example, mannitol, lactose, sorbitol, dextran, FICOLL ® polymer, and polyvinylpyrrolidine (PVP). Stabilization aids useful in the preparation of imaging agents and kits include, for example, ascorbic acid, cysteine, monothioglycerol, sodium bisulfite, sodium metabisulfite, gentisic acid, and inositol.
  • Solubilization aids useful in the preparation of imaging agents and kits include, for example, ethanol, glycerin, polyethylene glycol, propylene glycol, polyoxyethylene sorbitan monooleate, sorbitan monoloeate, polysorbates, poly(oxyethylene)- poly(oxypropylene)-poly(oxyethylene) block copolymers ("Pluronics") and lecithin.
  • the solubilizing aids are polyethylene glycol, cyclodextrins, and Pluronics.
  • Bacteriostats useful in the preparation of imaging agents and kits include, for example, benzyl alcohol, benzalkonium chloride, chlorbutanol, and methyl, propyl, or butyl paraben.
  • Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms.
  • the present invention contemplates all such compounds, including cis- and fraws-isomers, R- and S-enantiomers, diastereomers, (D)-isomers, (L)- isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention.
  • Additional asymmetric carbon atoms may be present in a substituent such as an alkyl group. All such isomers, as well as mixtures thereof, are intended to be included in this invention.
  • Isomeric mixtures containing any of a variety of isomer ratios may be utilized in accordance with the present invention. For example, where only two isomers are combined, mixtures containing 50:50, 60:40, 70:30, 80:20, 90: 10, 95:5, 96:4, 97:3, 98:2, 99: 1, or 100:0 isomer ratios are all contemplated by the present invention. Those of ordinary skill in the art will readily appreciate that analogous ratios are contemplated for more complex isomer mixtures.
  • a particular enantiomer of a compound of the present invention may be prepared by asymmetric synthesis, or by derivation with a chiral auxiliary, where the resulting diastereomeric mixture is separated and the auxiliary group cleaved to provide the pure desired enantiomers.
  • the molecule contains a basic functional group, such as amino, or an acidic functional group, such as carboxyl, diastereomeric salts are formed with an appropriate optically-active acid or base, followed by resolution of the diastereomers thus formed by fractional
  • alkyl is given its ordinary meaning in the art and refers to the radical of saturated aliphatic groups, including straight-chain alkyl groups, branched-chain alkyl groups, cycloalkyl (alicyclic) groups, alkyl substituted cycloalkyl groups, and cycloalkyl substituted alkyl groups.
  • the alkyl group may be a lower alkyl group, i.e. , an alkyl group having 1 to 10 carbon atoms (e.g.
  • a straight chain or branched chain alkyl may have 30 or fewer carbon atoms in its backbone, and, in some cases, 20 or fewer.
  • a straight chain or branched chain alkyl may have 12 or fewer carbon atoms in its backbone (e.g., Ci-Ci 2 for straight chain, C3-C 12 for branched chain), 6 or fewer, or 4 or fewer.
  • cycloalkyls may have from 3-10 carbon atoms in their ring structure, or 5, 6 or 7 carbons in the ring structure.
  • alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, isobutyl, i-butyl, cyclobutyl, hexyl, cyclochexyl, and the like.
  • alkenyl and “alkynyl” are given their ordinary meaning in the art and refer to unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but that contain at least one double or triple bond respectively.
  • the alkyl, alkenyl and alkynyl groups employed in the invention contain 1-20 aliphatic carbon atoms. In certain other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-4 carbon atoms.
  • Illustrative aliphatic groups thus include, but are not limited to, for example, methyl, ethyl, n-propyl, isopropyl, allyl, n-butyl, sec-butyl, isobutyl, i-butyl, n-pentyl, sec-pentyl, isopentyl, i-pentyl, n-hexyl, sec-hexyl, moieties and the like, which again, may bear one or more substituents.
  • Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, l-methyl-2-buten-l-yl, and the like.
  • Representative alkynyl groups include, but are not limited to, ethynyl, 2- propynyl (propargyl), 1-propynyl and the like.
  • cycloalkyl refers specifically to groups having three to ten, preferably three to seven carbon atoms. Suitable cycloalkyls include, but are not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like, which, as in the case of other aliphatic, heteroaliphatic, or hetercyclic moieties, may optionally be substituted with substituents including, but not limited to aliphatic;
  • heteroaliphatic aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy;
  • heteroarylalkyl wherein any of the aliphatic, heteroaliphatic, arylalkyl, or
  • heteroarylalkyl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl or heteroaryl substituents described above and herein may be substituted or unsubstituted. Additional examples of generally applicable substitutents are illustrated by the specific embodiments shown in the Examples that are described herein.
  • heteroalkyl is given its ordinary meaning in the art and refers to an alkyl group as described herein in which one or more carbon atoms is replaced by a heteroatom. Suitable heteroatoms include oxygen, sulfur, nitrogen, phosphorus, and the like. Examples of heteroalkyl groups include, but are not limited to, alkoxy, amino, thioester, poly(ethylene glycol), alkyl-substituted amino, tetrahydrofuranyl, piperidinyl, morpholinyl, etc.
  • heteroalkenyl and “heteroalkynyl” are given their ordinary meaning in the art and refer to unsaturated aliphatic groups analogous in length and possible substitution to the heteroalkyls described above, but that contain at least one double or triple bond respectively.
  • substituents of the above-described aliphatic (and other) moieties of compounds of the invention include, but are not limited to aliphatic;
  • heteroaliphatic aryl; heteroaryl; alkylaryl; alkylheteroaryl; alkoxy; aryloxy;
  • aliphatic, alycyclic, heteroaliphatic, heterocyclic, aryl, heteroaryl, alkylaryl, or alkylheteroaryl independently includes, but is not limited to, aliphatic, alycyclic, heteroaliphatic, heterocyclic, aryl, heteroaryl, alkylaryl, or alkylheteroaryl, wherein any of the aliphatic, heteroaliphatic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl or heteroaryl substituents described above and herein may be substituted or unsubstituted. Additional examples of generally applicable substituents are illustrated by the specific embodiments shown in the Examples that are described herein.
  • aryl is given its ordinary meaning in the art and refers to aromatic carbocyclic groups, optionally substituted, having a single ring (e.g. , phenyl), multiple rings (e.g., biphenyl), or multiple fused rings in which at least one is aromatic (e.g., 1,2,3,4-tetrahydronaphthyl, naphthyl, anthryl, or phenanthryl). That is, at least one ring may have a conjugated pi electron system, while other, adjoining rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls and/or heterocyclyls.
  • the aryl group may be optionally substituted, as described herein.
  • Substituents include, but are not limited to, any of the previously mentioned substitutents, i.e. , the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound.
  • an aryl group is a stable mono- or polycyclic unsaturated moieties having preferably 3-14 carbon atoms, each of which may be substituted or unsubstituted.
  • Carbocyclic aryl groups refer to aryl groups wherein the ring atoms on the aromatic ring are carbon atoms. Carbocyclic aryl groups include monocyclic carbocyclic aryl groups and polycyclic or fused compounds (e.g. , two or more adjacent ring atoms are common to two adjoining rings) such as naphthyl groups.
  • heteroaryl is given its ordinary meaning in the art and refers to aryl groups comprising at least one heteroatom as a ring atom.
  • a “heteroaryl” is a stable heterocyclic or polyheterocyclic unsaturated moieties having preferably 3-14 carbon atoms, each of which may be substituted or unsubstituted. Substituents include, but are not limited to, any of the previously mentioned substitutents, i.e. , the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound.
  • a heteroaryl is a cyclic aromatic radical having from five to ten ring atoms of which one ring atom is selected from S, O, and N; zero, one, or two ring atoms are additional heteroatoms independently selected from S, O, and N; and the remaining ring atoms are carbon, the radical being joined to the rest of the molecule via any of the ring atoms, such as, for example, pyridyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl,oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, and the like.
  • aryl and heteroaryl moieties may be attached via an alkyl or heteroalkyl moiety and thus also include -(alkyl)aryl, -(heteroalkyl)aryl, -(heteroalkyl)heteroaryl, and -(heteroalkyl)heteroaryl moieties.
  • aryl or heteroaryl moieties and “aryl, heteroaryl, - (alkyl)aryl, -(heteroalkyl)aryl, -(heteroalkyl)heteroaryl, and -(heteroalkyl)heteroaryl" are interchangeable.
  • Substituents include, but are not limited to, any of the previously mentioned substituents, i.e. , the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound.
  • aryl and heteroaryl groups can be unsubstituted or substituted, wherein substitution includes replacement of one or more of the hydrogen atoms thereon independently with any one or more of the following moieties including, but not limited to: aliphatic; alicyclic; heteroaliphatic; heterocyclic; aromatic; heteroaromatic; aryl; heteroaryl; alkylaryl; heteroalkylaryl; alkylheteroaryl; heteroalkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI ; Br; I; -OH; -N0 2 ; -CN; -CF 3 ; - CH 2 F; -CHF 2 ; -CH 2 CF 3 ; -CHC1 2 ; -CH 2 OH; -CH 2 CH 2 OH
  • any two adjacent groups taken together may represent a 4, 5, 6, or 7- membered substituted or unsubstituted alicyclic or heterocyclic moiety. Additional examples of generally applicable substituents are illustrated by the specific embodiments described herein.
  • heterocycle is given its ordinary meaning in the art and refers to refer to cyclic groups containing at least one heteroatom as a ring atom, in some cases, 1 to 3 heteroatoms as ring atoms, with the remainder of the ring atoms being carbon atoms. Suitable heteroatoms include oxygen, sulfur, nitrogen, phosphorus, and the like. In some cases, the heterocycle may be 3- to 10-membered ring structures or 3- to 7-membered rings, whose ring structures include one to four heteroatoms.
  • heterocycle may include heteroaryl groups, saturated heterocycles (e.g. , cycloheteroalkyl) groups, or combinations thereof.
  • the heterocycle may be a saturated molecule, or may comprise one or more double bonds.
  • the heterocycle is a nitrogen heterocycle, wherein at least one ring comprises at least one nitrogen ring atom.
  • the heterocycles may be fused to other rings to form a polycylic heterocycle.
  • the heterocycle may also be fused to a spirocyclic group.
  • the heterocycle may be attached to a compound via a nitrogen or a carbon atom in the ring.
  • Heterocycles include, for example, thiophene, benzothiophene, thianthrene, furan, tetrahydrofuran, pyran, isobenzofuran, chromene, xanthene, phenoxathiin, pyrrole, dihydropyrrole, pyrrolidine, imidazole, pyrazole, pyrazine, isothiazole, isoxazole, pyridine, pyrazine, pyrimidine, pyridazine, indolizine, isoindole, indole, indazole, purine, quinolizine, isoquinoline, quinoline, phthalazine, naphthyridine, quinoxaline, quinazoline, cinnoline, pteridine, carbazole, carboline, triazole, tetrazole, oxazole, isoxazole, thiazole, isothiazole
  • heterocyclic ring can be optionally substituted at one or more positions with such substituents as described herein.
  • the heterocycle may be bonded to a compound via a heteroatom ring atom (e.g. , nitrogen).
  • the heterocycle may be bonded to a compound via a carbon ring atom.
  • the heterocycle is pyridine, imidazole, pyrazine, pyrimidine, pyridazine, acridine, acridin-9-amine, bipyridine, naphthyridine, quinoline, benzoquinoline, benzoisoquinoline, phenanthridine- 1,9-diamine, or the like.
  • haloalkyl denotes an alkyl group, as defined above, having one, two, or three halogen atoms attached thereto and is exemplified by such groups as
  • amino refers to a primary (-NH 2 ), secondary (-NHR X ), tertiary (-NR x R y ), or quaternary (-N + R x R y R z ) amine, where R x , R y and R z are
  • amino groups include, but are not limited to, methylamino, dimethylamino, ethylamino, diethylamino, diethylaminocarbonyl, methylethylamino, iso-propylamino, piperidino, trimethylamino, and propylamino.
  • alkyne is given its ordinary meaning in the art and refers to branched or unbranched unsaturated hydrocarbon groups containing at least one triple bond.
  • Non- limiting examples of alkynes include acetylene, propyne, 1-butyne, 2-butyne, and the like.
  • the alkyne group may be substituted and/or have one or more hydrogen atoms replaced with a functional group, such as a hydroxyl, halogen, alkoxy, and/or aryl group.
  • alkoxy refers to an alkyl group, as previously defined, attached to the parent molecular moiety through an oxygen atom or through a sulfur atom.
  • the alkyl group contains 1-20 aliphatic carbon atoms.
  • the alkyl group contains 1-10 aliphatic carbon atoms.
  • the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms.
  • the alkyl group contains 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl group contains 1-4 aliphatic carbon atoms.
  • alkoxy include but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, t- butoxy, neopentoxy and n-hexoxy.
  • thioalkyl include, but are not limited to, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, and the like.
  • aryloxy refers to the group, -O-aryl.
  • acyloxy refers to the group, -O-acyl.
  • alkoxyalkyl refers to an alkyl group substituted with at least one alkoxy group (e.g. , one, two, three, or more, alkoxy groups).
  • an alkoxyalkyl group may be -(Ci_6-alkyl)-0-(Ci_6-alkyl), optionally substituted.
  • the alkoxyalkyl group may be optionally substituted with another alkyoxyalkyl group (e.g., -(Ci-6-alkyl)-0-(Ci-6-alkyl)-0-(Ci_6-alkyl) , optionally substituted.
  • any of the above groups may be optionally substituted.
  • substituted is contemplated to include all permissible substituents of organic compounds, "permissible” being in the context of the chemical rules of valence known to those of ordinary skill in the art.
  • substituted whether preceded by the term “optionally” or not, and substituents contained in formulas of this invention, refer to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent.
  • substituent When more than one position in any given structure may be substituted with more than one substituent selected from a specified group, the substituent may be either the same or different at every position. It will be understood that “substituted” also includes that the substitution results in a stable compound, e.g., which does not spontaneously undergo transformation such as by rearrangement, cyclization, elimination, etc. In some cases, “substituted” may generally refer to replacement of a hydrogen with a substituent as described herein. However,
  • substituted does not encompass replacement and/or alteration of a key functional group by which a molecule is identified, e.g., such that the "substituted” functional group becomes, through substitution, a different functional group.
  • a "substituted phenyl group” must still comprise the phenyl moiety and can not be modified by substitution, in this definition, to become, e.g. , a. pyridine ring.
  • the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and nonaromatic substituents of organic compounds.
  • Illustrative substituents include, for example, those described herein.
  • the permissible substituents can be one or more and the same or different for appropriate organic compounds.
  • the heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valencies of the heteroatoms.
  • this invention is not intended to be limited in any manner by the permissible substituents of organic compounds. Combinations of substituents and variables envisioned by this invention are preferably those that result in the formation of stable compounds useful for the formation of an imaging agent or an imaging agent precursor.
  • stable as used herein, preferably refers to compounds which possess stability sufficient to allow manufacture and which maintain the integrity of the compound for a sufficient period of time to be detected and preferably for a sufficient period of time to be useful for the purposes detailed herein.
  • substituents include, but are not limited to, halogen, azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, hydroxyl, alkoxyl, amino, nitro, sulfhydryl, imino, amido, phosphonate, phosphinate, carbonyl, carboxyl, silyl, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester, heterocyclyl, aromatic or heteroaromatic moieties, -CF 3 , -CN, aryl, aryloxy, perhaloalkoxy, aralkoxy, heteroaryl, heteroaryloxy, heteroarylalkyl, heteroaralkoxy, azido, amino, halide, alkylthio, oxo, acylalkyl, carboxy esters, -carboxamido, acyloxy, amino
  • determining generally refers to the analysis of a species or signal, for example, quantitatively or qualitatively, and/or the detection of the presence or absence of the species or signals. “Determining” may also refer to the analysis of an interaction between two or more species or signals, for example, quantitatively or qualitatively, and/or by detecting the presence or absence of the interaction.
  • acquiring an image means obtaining an image.
  • diagnostic imaging refers to a procedure used to detect an imaging agent.
  • a “diagnostic kit” or “kit” comprises a collection of components, termed the formulation, in one or more vials, which are used in a clinical or pharmacy setting to synthesize diagnostic radiopharmaceuticals.
  • the kit may be used by the practicing end user in a clinical or pharmacy setting to synthesize and/or use diagnostic radiopharmaceuticals.
  • the kit may provide all the requisite components to synthesize and/or use the diagnostic pharmaceutical except those that are commonly available to the practicing end user, such as water or saline for injection, a solution of the radionuclide, equipment for processing the kit during the synthesis and manipulation of the radiopharmaceutical, if required, equipment necessary for administering the radiopharmaceutical to the subject such as syringes, shielding, imaging equipment, and the like.
  • imaging agents may be provided to the end user in their final form in a formulation contained typically in one vial or syringe, as either a lyophilized solid or an aqueous solution.
  • a "portion of a subject” refers to a particular region of a subject, location of the subject.
  • a portion of a subject may be the brain, heart, vasculature, cardiac vessels, of a subject.
  • a "session" of testing may be a single testing protocol that a subject undergoes.
  • a session may include rest/stress imaging protocol; stress/rest imaging protocol; rest only imaging protocol; or a stress only imaging protocol.
  • a session of testing can take place in less than 24 hours or less than 48 hour.
  • the term "subject” refers to a human or non-human mammal or animal.
  • Non-human mammals include livestock animals, companion animals, laboratory animals, and non-human primates.
  • Non-human subjects also specifically include, without limitation, horses, cows, pigs, goats, dogs, cats, mice, rats, guinea pigs, gerbils, hamsters, mink, and rabbits.
  • a subject is referred to as a "patient.”
  • a patient or subject may be under the care of a physician or other health care worker, including, but not limited to, someone who has consulted with, received advice from or received a prescription or other recommendation from a physician or other health care worker.
  • Any of the compounds described herein may be in a variety of forms, such as, but not limited to, salts, solvates, hydrates, tautomers, and isomers.
  • the imaging agent is a pharmaceutically acceptable salt of the imaging agent.
  • pharmaceutically acceptable salt refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio.
  • Pharmaceutically acceptable salts are well known in the art. For example, Berge et ah, describe pharmaceutically acceptable salts in detail in /. Pharmaceutical Sciences, 1977, 66, 1-19, incorporated herein by reference.
  • Pharmaceutically acceptable salts of the compounds of this invention include those derived from suitable inorganic and organic acids and bases.
  • Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange.
  • inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid
  • organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange.
  • salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate,
  • Salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N + (Ci ⁇ alkyl)4 salts.
  • Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like.
  • Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, loweralkyl sulfonate and aryl sulfonate.
  • the compound is in the form of a hydrate or solvate.
  • hydrate refers to a compound non-covalently associated with one or more molecules of water.
  • solvate refers to a compound non- covalently associated with one or more molecules of an organic solvent.
  • the compound described herein may exist in various tautomeric forms.
  • tautomer as used herein includes two or more
  • interconvertable compounds resulting from at least one formal migration of a hydrogen atom and at least one change in valency e.g., a single bond to a double bond, a triple bond to a single bond, or vice versa.
  • the exact ratio of the tautomers depends on several factors, including temperature, solvent, and pH.
  • Tautomerizations i.e., the reaction providing a tautomeric pair
  • Exemplary tautomerizations include keto-to-enol; amide-to-imide; lactam-to-lactim; enamine-to- imine; and enamine-to-(a different) enamine tautomerizations.
  • the compounds described herein may exist in various isomeric forms.
  • the term "isomer” as used herein includes any and all geometric isomers and stereoisomers (e.g., enantiomers, diasteromers, etc.).
  • “isomer” include cis- and fraws-isomers, E- and Z- isomers, R- and ⁇ -enantiomers,
  • an isomer/enantiomer may, in some embodiments, be provided substantially free of the corresponding enantiomer, and may also be referred to as "optically enriched.”
  • “Optically-enriched,” as used herein, means that the compound is made up of a significantly greater proportion of one enantiomer.
  • the compound of the present invention is made up of at least about 90% by weight of a preferred enantiomer. In other embodiments the compound is made up of at least about 95%, 98%, or 99% by weight of a preferred enantiomer.
  • Preferred enantiomers may be isolated from racemic mixtures by any method known to those skilled in the art, including chiral high pressure liquid chromatography (HPLC) and the formation and crystallization of chiral salts or prepared by asymmetric syntheses.
  • HPLC high pressure liquid chromatography
  • Jacques, et al Enantiomers, Racemates and Resolutions (Wiley Interscience, New York, 1981); Wilen, S.H., et al, Tetrahedron 33:2725 (1977); Eliel, E.L. Stereochemistry of Carbon Compounds (McGraw-Hill, NY, 1962); Wilen, S.H. Tables of Resolving Agents and Optical Resolutions p. 268 (E.L. Eliel, Ed., Univ. of Notre Dame Press, Notre Dame, IN 1972).
  • the chemical form of the 18 O is 3 ⁇ 418 O.
  • the chemical form of the resulting 18 F is fluoride ion.
  • Imaging agent precursor 1 Acetontrile Concentrate Imaging agent precursor 1 (20.4 g, 39.2 mmol), as shown in Figure 1, was dissolved in anhydrous MeCN (3400 mL) then transferred through an Opticap XL2 Durapore filter (0.2 ⁇ ) into 5 mL glass vials; 2.0 mL fill volume. The vials were then fitted with rubber septa, sealed with an aluminum crimp and stored at ambient temperature prior to use.
  • the following example describes a general procedure for synthesizing imaging agent 1, as shown in Figure 1.
  • Aqueous [ 18 F]fluoride, as prepared in Example 7, was transferred from the cyclotron to a synthesis module, then filtered through an anion exchange column to remove unreacted [ 1 l 8 o 0]H 2 0; [ 1 1 8 0 F]fluoride was retained within the cationic resin matrix.
  • the column was then washed with aqueous Et 4 NHC0 3 with transfer to the reaction vessel.
  • the resulting solution was diluted with MeCN then concentrated to dryness using elevated temperature and reduced pressure.
  • [ 18 F] fluoride was retained within the cationic resin matrix.
  • the column was then washed with Et 4 NHC0 3 (5.75 ⁇ ; 0.500 mL of a 11.5 mM solution in H 2 0) with transfer to the reaction vessel.
  • the resulting solution was diluted with MeCN (0.500 mL) then concentrated to dryness; 150 mm Hg at 115 °C for 4 min.
  • the mixture of anhydrous [ 18 F]Et 4 NF and Et 4 NHC0 3 thus obtained was treated with the product of Example 8 (11.5 ⁇ ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 90 °C and maintained 20 min.
  • the solution was diluted with H 2 0 (1.00 mL) then directly purified by HPLC on a Waters Xterra MS CI 8 column (10 ⁇ ; 10 x 250 mm) using a 45:55 H 2 0/MeCN eluent at a flow rate of 5 mL/min.
  • the main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in H 2 0; pH 2) then transferred to the formulation module; 58% decay corrected radiochemical yield.
  • Et 4 NHC0 3 was 11.5 ⁇ (0.500 mL of a 23.0 mM solution in H 2 0); the solution was concentrated to dryness at 280 mbar, 95-115 °C, 4 min; the mixture of anhydrous
  • Example 7 The product of Example 7 was transferred from cyclotron to the synthesis module then filtered through an anion exchange column to remove unreacted [ 18 0]H 2 0;
  • [ 18 F] fluoride was retained within the cationic resin matrix.
  • the column was then washed with Et 4 NHC0 3 (11.5 ⁇ ; 0.500 mL of a 23.0 mM solution in H 2 0) with transfer to the reaction vessel.
  • the resulting solution was diluted with MeCN (0.500 mL) then concentrated to dryness; 375 mm Hg at 115 °C for 10 min.
  • the mixture of anhydrous [ 18 F]Et 4 NF and Et 4 NHC0 3 thus obtained was treated with the product of Example 8 (11.5 ⁇ ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 110 °C and maintained 10 min.
  • the solution was diluted with 3 ⁇ 40 (1.00 mL) then directly purified by HPLC on a Waters Xterra MS C18 column (10 ⁇ ; 10 x 250 mm) using a 45:55 H 2 0/MeCN eluent at a flow rate of 5 mL/min.
  • the main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in 3 ⁇ 40; pH 2) then transferred to the formulation module; 68% decay corrected radiochemical yield.
  • [ 18 F] fluoride was retained within the cationic resin matrix.
  • the column was then washed with Et 4 NHC0 3 (11.5 ⁇ ; 1.00 mL of a 11.5 mM solution in H 2 0) with transfer to the reaction vessel.
  • the resulting solution was diluted with MeCN (1.00 mL) then concentrated to dryness; 110-115 °C. Additional MeCN (1.50 mL) was then added and the solution concentrated to dryness once again.
  • the mixture of anhydrous [ ⁇ FJEt t NF and Et 4 NHC0 3 thus obtained was treated with the product of Example 8 (11.5 ⁇ ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 120 °C and maintained 10 min.
  • the solution was diluted with H 2 0/MeCN (3.00 mL; 2:1 v/v) then directly purified by HPLC on a Waters Xterra MS CI 8 column (10 ⁇ ; 10 x 250 mm) using a 45:55 H 2 0/MeCN eluent at a flow rate of 5 mL/min.
  • the main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in 3 ⁇ 40; pH 2) then transferred to the formulation module; 68% decay corrected radiochemical yield.
  • ascorbic acid 10 mL of a 0.28 M solution in 3 ⁇ 40; pH 2
  • [ 18 F] fluoride was retained within the cationic resin matrix.
  • the column was then washed with Et 4 NHC0 3 (23.0 ⁇ ; 0.500 mL of a 46.0 mM solution in 1:1 H 2 0/MeCN) with transfer to the reaction vessel.
  • the resulting solution was diluted with MeCN then concentrated to dryness; 150 mbar, 105 °C, 8 min. Additional MeCN was then added and the drying process repeated; the process of MeCN addition followed by evaporation was repeated three times.
  • Example 10 or 11 was transferred from purification to the formulation module then filtered through a CI 8 Sep-Pak® cartridge to remove MeCN; Imaging agent 1 was retained within the CI 8 resin matrix and the filtrate discarded.
  • the cartridge was successively washed with ascorbic acid (10 mL of a 0.28 M solution in H 2 0; pH 2), the filtrate discarded, then absolute EtOH (0.50 mL), and the filtrate collected.
  • the ethanol concentrate of imaging agent 1 thus obtained was further diluted with ascorbic acid (10.0 mL of a 0.28 M solution in H 2 0) in preparation for final aseptic filtration.
  • the final product vial assembly was constructed from the following pre- sterilized components: one 30 mL product vial, one Millipore Millex GV4 venting filter (0.22 ⁇ x 4 mm), one tuberculin syringe (1 mL) and one insulin syringe (0.5 mL).
  • the product of Example 12 was then transferred from formulation to the final product vial assembly through a Millipore Millex GV PVDF sterilizing filter (0.22 ⁇ x 13 mm). Quality control samples are then removed, using the syringe assemblies, to complete all product release requirements.
  • Figure 2 shows various possible reaction pathways, which traces unproductive consumption of starting material to a series of base-mediated hydrolysis reactions and dimerization events.
  • Variable time and temperature experiments confirmed the comparable rates of hydrolysis and fluorination in the nucleophilic fluorination reaction shown in Figure 1 , using the K 2 C0 3 /Kryptofix ® 222 in the presence of K 2 C0 3 .
  • reaction conditions which activate larger differential rates of fluorination are desired in order to advance a more efficient and chemoselective process; that is, a decreased rate of hydrolysis and/or increased rate of fluorination.
  • K2CO 3 did little to enhance fluorination over baseline levels and served primarily a detrimental role in the reaction.
  • added KHCO 3 produced a marked increase in fluorination over the same dynamic range, while decomposition pathways remained poorly differentiated.
  • a series of different bases was used in the nucleophilic fluorination of a tosylate precursor using TBAF as a source of fluoride (shown above), according to the following procedure.
  • a 2 mL glass vial was charged with both Bu 4 NF (1.15 ⁇ ; 13.4 ⁇ ⁇ of a 85.9 mM solution in H 2 0) and Bu 4 NHC0 3 (10.4 ⁇ ; 138 ⁇ . of a 75.0 mM solution in 3 ⁇ 40), then warmed to 95 °C and maintained 10 min under a stream of dry nitrogen.
  • the resulting solid mixture was treated with the product of Example 8 (11.5 ⁇ ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 90 °C and maintained 10 min.
  • the resulting solution was diluted with 3 ⁇ 40 then directly analyzed by HPLC on a Zorbax SB-C18 column (4.6 x 50 mm) using a H 2 0/MeCN gradient containing 0.1 % HCO2H with a flow rate of 1.00 mL/min.
  • the reaction yield was then calculated through comparison of the integrated peak area for the product in the crude reaction mixture to that of the authentic standard product (Table 1); results obtained through substitution of several alternate salt forms are also provided for comparison.
  • Figure 9 shows (A) a graph illustrating the changes in product distribution as a function of molar concentration of bicarbonate salt and (B) a graph illustrating the product distribution as a function of reaction time.
  • Figure 9C illustrates a threshold of >3 mg/ml.
  • tetraalkylammonium bicarbonate allows the reaction to be conducted at a lower absolute pH (e.g. , a pH of about 5-6).
  • imaging agent 1 and 82 Rb PET versus SPECT for detection of myocardial ischemia.
  • myocardial uptake of imaging agent 1 exhibits a stronger relationship with myocardial blood flow across the range of achievable flow than 201 T1, 99m Tc sestamibi and 82 Rb.
  • the following experiments were conducted to determine if the improved extraction and retention of imaging agent 1 would result in a greater difference between PET and SPECT ischemia
  • SDS summed stress score
  • SRS summed rest scores
  • Imaging agent 1 PET showed an increase in the amount of ischemia detected relative to 99m Tc sestamibi SPECT that was not seen when comparing 82 Rb PET to SPECT in a comparable patient group. These results suggest that imaging agent 1 show greater improvement in detection of myocardial ischemia when PET is compared to
  • Imaging agent 1 is a new myocardial perfusion PET tracer that targets mitochondrial complex 1.
  • R rest
  • S stress
  • CFR coronary flow reserve
  • imaging agent 1 myocardial perfusion PET imaging.
  • the following describes an iterative technique for optimizing injected tracer dosage and acquisition time for 18 F-labeled myocardial perfusion tracer imaging agent 1.
  • Public and staff concerns about radiation exposure necessitate optimization of the dosage acquisition time product (DATP) to obtain the optimal tradeoff between dose, acquisition time, and image noise.
  • DATP dosage acquisition time product
  • An iterative algorithm was developed for determining optimal dosage and acquisition time based on a task-limited noise level.
  • SD standard deviation
  • ROI region of interest
  • MSD mean/SD
  • Using SD and a surrogate for "noise” has its limitations: 1) intrinsic count variability due to partial volume, and tracer uptake and, 2) non-Poisson nature of reconstructed and post filtered data.
  • the iterative algorithm was used to fit a model to the limiting MSD. From this, an optimal acquisition time was determined for a target MSD to detect a 5% perfusion defect.
  • Phantom data simulating patient distributions and a 40% septal defect were acquired on a Biograph 64 slice PET/CT scanner using a 30 minute listmode acquisition. The technique was also tested in 18 subjects. Patients received a 2 mCi at rest and ⁇ 2 mCi stress on the following day. A dynamic series for 10, 20, 40, 80, 160, and 320 seconds was acquired 10 minutes post injection. The myocardial ROI was taken from a separate 600 second acquisition using >70% of the maximum myocardial voxel limit.
  • LVEF left ventricular ejection fraction
  • ESV end-systolic volume
  • EDV end-diastolic volume
  • Data acquisition from 23 patients from two study centers. Data for this study was acquired using a same day, rest stress study. Patients received ⁇ 2 mCi at rest and also received a ⁇ 6 mCi "same day" stress (8 EX, 13 AD) dosage. Functional values from shorter rebinning times were compared with the longest acquisition time dataset.
  • a one-day rest-stress protocol for myocardial perfusion imaging needs minimization of wait time between injections (WT) as shorter times require greater stress/rest dosing ratios (DR) and minimum rest dose is dictated by image statistics.
  • WT wait time between injections
  • DR stress/rest dosing ratios
  • a method for determining the dependence of DR on WT and to identify a WT for acceptable total dose was developed.
  • Two-day rest-stress imaging agent 1 PET image data of the heart (5 adenosine (AD) and 5 exercise (EX) stress) from 20 patients with known reversible defects on Tc-99m MPI were combined to create artificial blended images by adding 16%, 23%, 48% or 100% of rest image to the stress image. These were paired with rest images, 2-day stress images and read by 3 blinded readers. Results were recorded by segment as reader response (RR) (0 to 4) and as quantitative defect severity (QDS) in % decrease.
  • RR reader response
  • QDS quantitative defect severity
  • RR was found to be linearly related to the QDS. In general, decreases greater than 80% of maximum were read as 0, 70% to 80% as 1, 60% to 70% as "2,” 50% to 60% as “3” and below 50% as "4.” Analysis of RR indicated that greater than 1 unit change from the 2-day data were observed in reader response in general only for the 48% and 100% blended image sets. Therefore 23% was deemed the maximum tolerable rest-to-stress contamination. Using the relationship between rest-stress contamination and dosing, it was found that, for AD a minimum DR of 2.2 was required with a 0.5 hour WT, and for EX a minimum DR of 3.0 was needed with a 1-hour WT.
  • the minimum rest dose for a given imaging acquisition time in which the count- related signal-to-noise did not meaningfully contribute to reader error was determined. This was done by simulating increasing doses using multiple rebinnings of patient rest study with increasingly greater amounts of data. This method uses the increasing number of coincidence events in sequential rebinnings to create images that model increasing dose and/or acquisition duration. This method is valid for relatively low concentrations of radioactivity, such as are used here.
  • the rest dose for Cohort 2 was calculated. After considering the dosing required for a range of acquisition times from two minutes up to a practical maximum of 10 minutes, five minutes was selected. This permitted an initial dose of 2.9 mCi for the rest acquisition.
  • the dosing ratio was determined. To do this, first, the maximum tolerable contribution of the rest dose to the- stress image was determined. This was assessed by creating simulated stress images with a range of rest dose contributions using combinations of data from the Study Day 1 rest and Study Day 2 stress studies.
  • the final step of the method is the need to maintain the total dose below a limit of 14 mCi, with some additional margin, to limit the radiation dose to 5 rem to the critical organ and 1 rem effective dose (ED) or lower.
  • a dosing interval of 60 minutes was chosen which corresponded to a dose ratio of 3.0.
  • the rest acquisition time was increased to 7 minutes and the rest dose reduced to 1.7 mCi to allow for the greater required stress/rest dose ratio while still maintaining the total comfortably within the 14 mCi limit.
  • the dose and dose ratio values above were set as the lower limits of 15% to 20% ranges for each variable and the acquisition times increased to a minimum of 15 minutes for all acquisitions to account for the possibility of lower sensitivity of the 2D PET scanners.
  • the data acquisition was broken into sections so that images derived from shorter acquisition times may be obtained from the same data as necessary. This resulted in the final specified dosing of 2.9 mCi to 3.4 mCi rest with a stress dose of 2.0 to 2.4 times the rest dose for adenosine stress.
  • the final doses were set at 1.7 mCi to 2.0 mCi for rest with a stress dose 3.0 to 3.6 times the rest dose. These doses are intended to reflect the actual net injected radioactivity so that additional radioactivity is required in the syringe prior to injection to compensate for losses due to adsorption and the dead volume of the syringe.
  • 18 F-labeled imaging agent 1 myocardial perfusion PET tracer.
  • 18 F-labeled imaging agent 1 is a novel myocardial perfusion imaging PET tracer that targets mitochondrial complex 1. Studies of human safety, dosimetry, biodistribution, and myocardial imaging characteristics of this tracer were evaluated.
  • mCi of imaging agent 1 injected in the body of the subject assessing parameters such as mCi of imaging agent 1 injected in the body of the subject; mCi of imaging agent 1 injected from the syringe; acquisition time of images after injection; delay between rest and stress studies, etc. Parameters varied for rest and stress, for example, the injected dose (in the body) for exercise stress was at least three times the injected dose (in the body) at rest. In addition, the injected dose (in the body) for pharmacological stress was at least two times the injected does (in the body) at rest. Results are shown in Table 7.
  • Imaging agent 1 doses, acquisition times and dosing delay for exercise and pharmacologic stress.
  • Effective Dose Developed by the ICRP for occupational radiation protection, the ED enables the comparison of radiation detriment from a uniform external dose and a non-uniform internal dose.
  • the risk for a 1 rem ED determined for an non-uniform internal dose is equal to the risk from a 1 rem uniform external exposure (total body dose).
  • total body dose As defined in ICRP publication 60 [ICRP-60 1991].
  • EDE Effective Dose Equivalent
  • MIRD Methodology The methodology developed by the Medical Internal Radiation Dose Committee for the determination of radiation absorbed dose. This methodology included the use of radiation transport factors (S-values), and bio-kinetic parameters (residence times). As defined in the MIRD Primer, Society of Nuclear Medicine, 1991.
  • %CV is Coefficient of variation (Ratio of the standard deviation to the mean times 100).
  • Percent Injected Dose vs. Time from Whole Body Images Percent injected activity as a function of time was determined for brain, heart wall, kidneys, liver, lungs, red marrow (lumbar region), salivary glands, spleen, stomach wall, thyroid, and urinary bladder. On average, the organ that showed the largest peak uptake was the liver with approximately 19.1% of the injected activity (data not shown). The next largest peak uptake occurred in the kidneys with approximately 9.4% of the injected activity (data not shown).
  • Study design This was a non-randomized, open-label, single-dose study.
  • a total of 13 healthy adult subjects were enrolled and administered a single dose of imaging agent 1 at a single study center in the United States.
  • Subjects were screened within 14 days prior to enrollment to confirm subject eligibility, and began baseline assessments at the study center the day before study drug administration. Subjects remained at the study center until completion of the Study Day 2 safety assessments (24 ⁇ 8 hours post- dose).
  • a telephone call was made to study subjects 48 ⁇ 8 hours post-dose for adverse event (AE) monitoring. All subjects returned to the study center approximately one week (5-7 days) post-dose for a follow-up safety visit, and were contacted by telephone approximately 14-17 days post-dose for final serious AE monitoring.
  • AE adverse event
  • the 8 mCi target dose was selected to provide adequate count statistics and was projected to be well below the maximum acceptable radiation exposure based on preclinical data.
  • the maximum dose of imaging agent 1 that may be administered to a human without exceeding 50 mSv (5 rem) to the target was 742 MBq (20.0 mCi) and the injected dose that yielded an effective dose (ED) of ⁇ 10 mSv (1 rem) was 666 MBq (18.0 mCi) (Stabin, M G, Sparks, RB, et al, OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine.” J Nucl Med 2005 46(6): 1023-7).
  • each subject received a 1-3 mL intravenous bolus injection of imaging agent 1 in a sterile solution of ⁇ 5 ethanol containing ⁇ 50 mg/mL sodium ascorbate in water, calculated to deliver approximately the target dose of imaging agent 1 at the time of injection.
  • the dose was administered in less than 10 seconds, followed immediately by a 3-5 mL saline flush.
  • the net injected dose was calculated by subtracting the decay-corrected radioactivity in the syringe and injection tubing after injection from the assayed and decay-corrected radioactivity in the syringe prior to injection.
  • PET imaging protocol Whole -body PET imaging from head to mid thigh was performed at protocol-specified time-windows.
  • Dosimetry analyses Estimates of radiation dosimetry for the standard organs of the adult male and female models and for the, salivary glands as well as the effective dose equivalent (EDE) (International Commission on Radiological Protection (ICRP), Recommendations of the International Commission on Radiological Protection, Publication 26. Ann ICRP. 1977; 1(3)) and the effective dose (ED) (International Commission on Radiological Protection (ICRP), 1990 Recommendations of the International Commission on Radiological Protection, 60. Ann ICRP.
  • EEE Effective dose equivalent
  • ICRP International Commission on Radiological Protection
  • ICRP International Commission on Radiological Protection
  • ICRP International Commission on Radiological Protection
  • the attenuation corrected transverse image data slice planes were combined into a single three-dimensional image matrix for each subject and each time point using custom software. These images were then divided into 6 image sets ("anterior”, “posterior”, “salivary”, “thyroid”, “source”, and “full") of combined coronal plane image data for each subject at each time point, grouping organs with similar anterior to posterior depths. This was done to optimize the ROI creation, and minimize background contribution to the organs contained in each combined coronal plane image.
  • the "anterior” images contained stomach wall, heart wall, and urinary bladder.
  • the "posterior” images contained kidneys, lumbar spine, and spleen (when visible).
  • the “salivary” images contained the salivary glands (parotid and submandibular).
  • the “thyroid” images contained the thyroid.
  • the “full” images combined all of the coronal image planes that contained subject image data and was used for quantification of the brain and liver.
  • the “source” images contained the calibration source.
  • Regions of interest were drawn around all organs that showed uptake above background using custom software developed and validated for this purpose. Absolute radioactivity was determined by normalizing ROI sums by a calibration factor derived from the calibration source. Region counts were also adjusted for activity containing underlying and overlying tissue that was not part of the organ or tissue being quantified by utilization of background regions of interest. Total body region counts were also corrected for off body background counts. Appropriate normalization of region sizes for organ and adjacent regions were made. Unobstructed regions of organs with significant overlap from other activity containing organs were also employed where necessary. In order to estimate the activity in the lower legs (which were not imaged), a region of interest on the upper thigh was utilized. Activities were also normalized where necessary to account for 100% of the injected activity, and to insure conservative (slight over-estimates) determination of absorbed dose. Where urinary excretion data were available beyond the end of the imaging regimen, these data were used to determine whole body retention.
  • Equation 1 Kinetic data for brain, heart wall, kidneys, liver, red marrow (lumbar spine regions were utilized), salivary glands, spleen, stomach wall, thyroid, and urinary bladder for the subjects in the study were determined using image quantification methodology. Absolute activity was converted to fractional dose by dividing by the total activity administered. Organ and tissue data were fit using non-linear least-squares regression with sums of exponentials of the form shown in Equation 1, where f and ⁇ are the model parameters that are determined in the fitting process, Fy(t) is the fraction of the total injected activity, t is the time post injection, i is the i th ROI, j is the j th subject, and k is the k th exponential term. Between one and four exponential terms were employed, as appropriate. Equation 1.
  • the regression was performed using custom software that determines initial parameter values based on the temporal variation of the kinetic data, and the use of pre- tabulated estimates for various time activity scenarios as selected by the user. Once these data were fit, residence times were determined by integration of these empirically determined functions (sums of exponentials) from time equal zero to infinity, taking into account physical decay. Remainder of Body residence times were determined by subtraction of appropriate organ residence times from whole body residence times. Urinary bladder residence times were determined using the parameters determined by fitting the whole body activity data with a urinary bladder model as implemented in the OLINDA/EXM software with 3.5 hour bladder voiding interval. Red marrow residence time was determined based on a region of interest drawn on a portion of the lumbar spine. The lumbar spine was assumed to contain 16.1% (International Commission on Radiological Protection (ICRP) Publication 23, Report of the Task Group on Reference Man. Pergamon Press. 1975, page 125) of the total red marrow.
  • ICRP International Commission on Radiological Protection
  • Organ/Tissue Dosimetry Estimates. Absorbed dose estimates for all target organs were determined using the OLINDA/EXM software using the adult "male" model. The resulting absorbed dose estimates were scaled based on the total body mass of the individual subjects relative to that of the radiation transport phantom. Salivary gland dosimetry was determined by using a conservative estimate of the S-value for salivary glands based on the reference man total mass of the parotid and submaxilary salivary glands (International Commission on Radiological Protection (ICRP) Publication 23, Report of the Task Group on Reference Man. Pergamon Press. 1975, page 125) and assuming a spherical shape.
  • ICRP International Commission on Radiological Protection
  • S-Values for spheres were produced by the OLINDA/EXM software, and were linearly scaled based on the relative total body mass of reference man to that of subject. These S-values were then multiplied by the residence times to produce final salivary gland dose estimates.
  • Results Patient demography. Of the 26 subjects who were screened, 13 subjects (12 males and one female) were administered imaging agent 1, and completed all safety evaluations. The mean age was 23.4 years (range: 19-34 years) and the mean BMI was 23.4 (range: 20-26). One patient was not included in the analyses of dosimetry, biodistribution and radiokinetics, due to the inability to confirm the dose calibrator assay data for the standards preparation. Radiation dosimetry. The intravenous bolus injection was calculated to deliver no more than 8 mCi of 18 F at the time of injection.
  • the mean (SD) final decay-corrected dose was 6 (0.6) mCi of 18 F, with a range of 4.6 to 6.6 mCi (170 to 244 MBq).
  • the difference between the target dose and the final dose was due to the retention of imaging agent 1 in the syringe.
  • the absorbed dose summary statistics are presented in Table 9 (mSv/MBq).
  • the organ receiving the largest mean absorbed dose was the kidneys at 0.066 mSv/MBq (0.24 rem/mCi), followed by the heart wall at 0.048 mSv/MBq (0.18 rem/mCi).
  • the mean ED was 0.019 mSv/MBq (0.072 rem/mCi).

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Abstract

The present invention generally relates to methods and system for the synthesis of imaging agents, and precursors thereof. The methods may exhibit improved yields and may allow for the large-scale synthesis of imaging agents, including imaging agents comprising a radioisotope (e.g., 18F). Various embodiments of the invention may be useful as sensors, diagnostic tools, and the like. In some cases, methods for evaluating perfusion, including myocardial perfusion, are provided. Synthetic methods of the invention have also been incorporated into an automated synthesis unit to prepare and purify imaging agents that comprise a radioisotope. In some embodiments, the present invention provides a novel methods and systems comprising imaging agent 1, including methods of imaging in a subject comprising administering a composition comprising imaging agent 1 to a subject by injection, infusion, or any other known method, and imaging the area of the subject wherein the event of interest is located.

Description

METHODS AND APPARATUS FOR SYNTHESIZING IMAGING AGENTS, AND INTERMEDIATES THEREOF
Related Applications
The present application claims priority under 35 U.S.C. § 119(e) to U.S.
provisional application, U.S. S.N. 61/302,477, filed February 8, 2010, entitled "Methods and Apparatus for Synthesizing Contrast Agents, Including Radiolabeled Contrast Agents;" U.S. provisional application, U.S.S.N. 61/315,376, filed March 18, 2010, entitled "Methods for Synthesizing Contrast Agents and Precursors Thereof;" and U.S. provisional application, U.S.S.N. 61/333,693, filed May 11, 2010, entitled
"Compositions, Methods, and Systems for Imaging," each of which is incorporated herein by reference.
Field of the Invention
The present invention relates to systems, compositions, methods, and apparatuses for synthesizing imaging agents, and precursors thereof.
Background of the Invention
Mitochondria are membrane-enclosed organelles distributed through the cytosol of most eukaryotic cells. Mitochondria are especially concentrated in myocardial tissue.
Complex 1 ("MC-1") is a membrane-bound protein complex of 46 dissimilar subunits. This enzyme complex is one of three energy-transducing complexes that constitute the respiratory chain in mammalian mitochondria. This NADH-ubiquinone oxidoreductase is the point of entry for the majority of electrons that traverse the respiratory chain, eventually resulting in the reduction of oxygen to water (Q. Rev. Biophys. 1992, 25, 253-324). Examples of inhibitors of MC-1 include deguelin, piericidin A, ubicidin-3, rolliniastatin-1, rolliniastatin-2 (bullatacin), capsaicin, pyridaben, fenpyroximate, amytal, MPP+, quinolines, and quinolones (BBA 1998, 1364, 222-235). Studies have shown that interrupting the normal function of mitochondria could advantageously concentrate certain compounds in the mitochondria, and hence in the mitochondria-rich myocardial tissue. Compounds that include an imaging moiety
18
{e.g., F) can be useful in determining such a build-up of compounds, thereby providing valuable diagnostic markers for myocardial perfusion imaging. In addition, such compounds may find application for the diagnosis of coronary artery disease (CAD).
CAD is a major cause of death in modern industrialized countries and it has been found previously that assessments of regional myocardial perfusion at rest and during stress (exercise or pharmacologic coronary vasodilation) are valuable for noninvasive diagnosis of CAD. While myocardial perfusion imaging (MPI) with Positron Emission Tomography (PET) has been shown to be superior in some embodiments as compared to single photon emission computed tomography (SPECT), widespread clinical use of PET MPI has been limited by the previously available PET myocardial perfusion tracers.
Several PET blood flow tracers, such as rubidium-82 ( 82 Rb) chloride, nitrogen- 13 (13N) ammonia, and oxygen- 15 (150) water, have been developed and validated for assessment of myocardial perfusion. 13N and 150 are cyclotron-produced isotopes with short half-lives. Therefore, their use is limited to facilities with an on-site cyclotron.
Although 82 Rb is a generator-produced tracer, its short half-life, the high cost of the generator, and the inability to perform studies in conjunction with treadmill exercise have made this tracer impractical for widespread use. Tracers that comprise 18F have, however, found potential application as imaging agents.
While current methods for preparing compounds comprising an imaging moiety include [ 18 F] -fluorination chemistry, many methods focus on nucleophilic [ 18 F]- fluorination chemistry using potassium fluoride (KF). Characteristically, these methods generate the elemental fluoride source through anion exchange between, for example, potassium carbonate (K2CO3) and a cyclotron-produced [18F] -containing species, and often require addition of the aza-crown ether Kryptofix® 222 (4,7, 13, 16,21, 24-hexaoxa- l,10-diazabicyclo[8.8.8]-hexacosane) to enhance reactivity. While suitable for production of clinical quantities, the moderate efficiency, demanding purification and complex implementation of such method may not be suitable for widespread commercial application.
Accordingly, improved methods, systems, and apparatuses are needed for the synthesis of imaging agents. Summary of the Invention
The invention provides, in a broad sense, methods for synthesizing imaging agents and their precursors, compounds that are imaging agents precursors, and methods of use thereof.
In one aspect, in invention provides a method of synthesizing an imaging agent comprising formula:
Figure imgf000004_0001
wherein W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted; R2 is hydrogen or halide; each R3 can be the same or different and is alkyl optionally substituted with an imaging moiety or heteroalkyl optionally substituted with an imaging moiety; and n is 1, 2, 3, 4, or 5; the method comprising steps of:
etherification of precursor compounds comprising formulae:
Figure imgf000004_0002
wherein n is 1, 2, 3, 4, or 5; R1 is alkyl, optionally substituted; R2 is hydrogen or halide; R3 can be the same or different and are alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted, R5 is hydroxyl or halide; and R6 is alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted, wherein, when R5 is hydroxyl, at least one of R6 and R3 comprises a leaving group; or wherein R5 is halide, at least one of R6 or R3 comprises a hydroxyl, to produce a compound comprising formula:
Figure imgf000004_0003
wherein W is alkyl or heteroalkyl, optionally substituted; R1 is alkyl, optionally substituted; R2 is hydrogen or halide; each R3 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; wherein at least one R3 comprises hydroxyl; and n is 1, 2, 3, 4, or 5; R1 is alkyl, optionally substituted; R2 is hydrogen or halide; R3 can be the same or different and are alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted;
reacting a compound comprising formula:
Figure imgf000005_0001
wherein W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted; R2 is hydrogen or halide; each R3 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; wherein at least one R3 comprises hydroxyl; and n is 1, 2, 3, 4, or 5; with a sulfonate- containing species to produce a sulfonate-containing compound comprising formula:
Figure imgf000005_0002
wherein W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted; R2 is hydrogen or halide; each R3 can be the same or different and is alkyl optionally substituted with a sulfonate-containing group or heteroalkyl optionally substituted with a sulfonate-containing group; wherein at least one R3 comprises a sulfonate-containing group; and n is 1, 2, 3, 4, or 5; replacing the sulfonate-containing group of the sulfonate-containing compound with an imaging moiety to yield a compound comprising formula:
Figure imgf000005_0003
wherein W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted; R2 is hydrogen or halide; each R3 can be the same or different and is alkyl optionally substituted with an imaging moiety or heteroalkyl optionally substituted with an imaging moiety; and n is 1, 2, 3, 4, or 5; provided that at least one fluorine species is present in the compound. In one aspect, the invention provides a method for F-labeling a compound comprising formula:
Figure imgf000006_0001
wherein R1 is alkyl; R2 is hydrogen or halogen; and R3 is alkyl substituted with a sulfonate-containing group, alkoxy substituted with a sulfonate-containing group, or alkoxyalkyl substituted with a sulfonate-containing group. The method comprises reacting the compound with an 18F species in the presence of an ammonium salt or a bicarbonate salt to form a product comprising the 18F species.
In some embodiments, R3 is alkoxyalkyl substituted with a sulfonate-containing group. In some embodiments, the sulfonate-containing group is mesylate, tosylate, triflate, or 1,2-cyclic sulfate. In some embodiments, R2 is a halogen. In one
embodiment, R2 is chloride. In some embodiments, R1 is a methyl, ethyl, propyl, n- butyl, 5-butyl, or i-butyl. In some embodiments, R1 is i-butyl. In some embodiments, the product comprises formu
Figure imgf000006_0002
In another aspect, the invention provides a method for synthesizing a precursor to (or of) an imaging agent, comprising reacting a compound comprising formula (III) with a nucleophile, wherein formula (III) comprises the structure:
Figure imgf000006_0003
wherein W is alkyl or heteroalkyl, optionally substituted; R1 is alkyl, optionally substituted; R2 is hydrogen or halide; each R3 can be the same or different and is an alkyl optionally substituted with a leaving group or heteroalkyl optionally substituted with a leaving group, provided R3 comprises at least one leaving group; and n is 1, 2, 3, 4, or 5, provided at least one R3 is substituted with a leaving group; with a nucleophile wherein the nucleophile replaces the at least one leaving group to produce a product (or precursor).
In some embodiments, the nucleophile is ethylene glycol. In some embodiments, reacting the compound with the nucleophile occurs in the presence of a base. The base may be but is not limited to a metal or a metal salt. The base may be sodium metal, sodium hydride, potassium i-butoxide, potassium carbonate, or potassium hydroxide. In some embodiments, the base is potassium t-butoxide or potassium hydroxide. In some embodiments, the base is potassium t-butoxide.
In some embodiments, reacting the compound with the nucleophile occurs in the presence of a catalyst. The catalyst may be a tetraalkylammonium iodide including but not limited to a tetraethylammonium iodide.
In some embodiments, the leaving group is a halide including but not limited to bromide.
In some embodiments, W is -0(Ο¾)-; R1 is i-butyl; R2 is chloride; and R3 is alkyl substituted with a leaving group.
In some embodiments, the compound comprising formula (III) comprises the structure:
Figure imgf000007_0001
In some embodiments, the compound comprising formula (III) comprises the structure:
Figure imgf000007_0002
In some embodiments, the product (or precursor) comprises formula:
Figure imgf000007_0003
In some embodiments, the product (or precursor) comprises formula:
Figure imgf000008_0001
In some embodiments, the method further comprises reacting a compound comprising formula (IV) with a reactant comprising a leaving group to produce the compound comprising formula (III), wherein formula (IV) comprises the structure:
Figure imgf000008_0002
wherein W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted; R2 is hydrogen or halide; each R4 can be the same or different and is an alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; provided R4 comprises at least one hydroxyl group; and n is 1, 2, 3, 4, or 5; and wherein the at least one hydroxyl is replaced with the leaving group.
In some embodiments, reacting the compound comprising formula (IV) is performed in the presence of a halogenation reagent. In some embodiments, the halogenation reagent is a brominating reagent. The brominating reagent may be phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine, although it is not so limited.
In some embodiments, W is -0(CH2)-; R1 is i-butyl; R2 is chloride; and R4 is alkyl substituted with hydroxyl.
In some embodiments, the compound comprising formula (IV) comprises the structure:
Figure imgf000008_0003
In some embodiments, the compound comprising formula (IV) comprises the structure:
Figure imgf000009_0001
In some embodiments, the product comprises formula:
In some embodime a:
Figure imgf000009_0002
In some embodiments, the compound comprising formula (IV) is formed by etherification of precursor compounds comprising formulae (IVa) and (IVb):
Figure imgf000009_0003
wherein m is 1, 2, 3, 4, or 5 or greater; R1 is alkyl, optionally substituted; R2 is hydrogen or halide; R5 is hydroxyl or halide; and R6 and R7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, each of which may be optionally and independently substituted, wherein when R5 is hydroxyl at least one of R6 and R7 comprises a leaving group or a group that can be replaced by a leaving group, or when
R5 is halide, at least one of R6 and R7 comprise a hydroxyl.
In some embodiments, the compound comprising formula (IV) is formed by etherification of the compounds comprising formulae:
Figure imgf000009_0004
wherein m is 1 or greater; R1 is alkyl, optionally substituted; R2 is hydrogen or halide; R5 is hydroxyl or halide; and R6 and R7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, any of which may be substituted, wherein when R5 is hydroxyl at least one of R6 and R7 comprises a leaving group or a group that can be replaced by a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl.
In some embodiment, the compound comprising formula (IV) is formed by etherification of precursor compounds comprising formulae (IVa) and (IVd):
Figure imgf000010_0001
wherein R1 is alkyl, optionally substituted; R2 is hydrogen or halide; R5 is hydroxyl or halide; and R6 and R7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, each of which may be optionally and independently substituted, wherein when R5 is hydroxyl at least one of R6 and R7 comprises a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl.
In some embodiments, the compound comprising formula (IV) is formed by etherification of compounds comprising formulae:
Figure imgf000010_0002
wherein R1 is alkyl, optionally substituted; R2 is hydrogen or halide; R5 is hydroxyl or halide; and R6 and R7 can be the same or different and each is alkyl, heteroalkyl, or a carbonyl-containing group, any of which may be substituted, wherein when R5 is hydroxyl at least one of R6 and R7 comprises a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl..
In some embodiments, the etherification comprises reacting the precursor compounds in the presence of a base. In some embodiments, the base comprises a carbonate ion.
In some embodiments, R5 is halide; and R6 and R7 is each substituted alkyl. In some embodiments, R5 is chloride; and R6 and R7 is each alkyl substituted with a hydroxyl.
In some embodiments, the compound comprising formula (IV) is synthesized by etherification of precursor compounds comprising formulae:
Figure imgf000011_0001
wherein R1 is alkyl, optionally substituted; R2 is hydrogen or halide; to form a product comprising formula:
Figure imgf000011_0002
In some embodiments, the compound comprising formula (IV) is synthesized by etherification of compounds comprising formulae:
to form a product com
Figure imgf000011_0003
In some embodiments, R5 is hydroxyl; and R6 is a carbonyl-containing group and R7 is a substituted alkyl. In some embodiments, R5 is hydroxyl; and R6 is an ester and R7 i iss a allkkvyll s suubbssttiittuutteedd w wiitthh a a l lee.aavviinngp g PTrOoUuTpV.
In some embodiments, the compound comprising formula (IV) is synthesized by etherification of the compounds comprising formulae:
Figure imgf000011_0004
to form a product comprising formula:
Figure imgf000011_0005
In some embodiments, the method further comprises exposing the product to a reducing agent to convert the ester group to an alcohol. The reducing agent may be lithium aluminum hydride, lithium borohydride, or diisobutylaluminum hydride
(DIBAL-H), although it is not so limited.
In another aspect, the invention provides a method for synthesizing an imaging agent comprising contacting an imaging agent precursor with a fluoride species and an ammonium salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species wherein the molar ratio of ammonium salt to imaging agent precursor is less than 1.5:1, including about 1:1 or less.
In some embodiments, the molar ratio of ammonium salt to imaging agent precursor is about 1: 1 or less, or about 0.75:1 or less, or about 0.5:1 or less, or about 0.25:1 or less, or about 0.05: 1 or less. In some embodiments, the molar ratio of ammonium salt to imaging agent precursor is from about 1:1 to about 0.5:1. In some embodiments, the molar ratio of ammonium salt to imaging agent precursor ranges from about 1.4:1 to about 0.05: 1.
In some embodiments, the ammonium salt is ammonium bicarbonate, ammonium hydroxide, ammonium acetate, ammonium lactate, ammonium trifluoroacetate, ammonium methanesulfonate, ammonium p-toluenesulfonate, ammonium nitrate, ammonium iodide, or ammonium bisulfate. In some embodiments, the ammonium salt is a tetraalkylammonium salt. The ammonium salt may be R4NHCO3, wherein R is alkyl. The ammonium salt may be Et4NHC03.
In another aspect, the invention provides a method for synthesizing an imaging agent, comprising contacting an imaging agent precursor with a fluoride species and a bicarbonate salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species, wherein the molar ratio of bicarbonate salt to imaging agent precursor is less than 1.5:1, including about 1:1 or less.
In some embodiments, the molar ratio of bicarbonate salt to imaging agent precursor is about 1:1 or less, or about 0.75:1 or less, or about 0.5: 1 or less, or about 0.25:1 or less, or about 0.05 : 1. In some embodiments, the molar ratio of bicarbonate salt to imaging agent precursor is from about 1: 1 to about 0.5:1. In some embodiments, the molar ratio of bicarbonate salt to imaging agent precursor ranges from about 1.4:1 to about 0.05:1. In some embodiments, wherein the molar ratio of bicarbonate salt to imaging agent precursor is from about 0.5: 1 to about 1:1.
In some embodiments, the bicarbonate salt is a metal bicarbonate. The bicarbonate salt may be sodium bicarbonate, calcium bicarbonate, potassium
bicarbonate, or magnesium bicarbonate, although it is not so limited.
In some embodiments, the bicarbonate salt is ammonium bicarbonate. In some embodiments, the bicarbonate salt is an tetraalkylammonium bicarbonate. The bicarbonate salt comprises the formula R4NHCO3, wherein R is alkyl. The bicarbonate salt may be Et4NHC03.
In some embodiments, the imaging agent precursor is further exposed to a cryptand, such as but not limited to 4,7,13,16,21,24-Hexaoxa-l,10-diazabicyclo[8.8.8]- hexacosane.
In some embodiments, contacting is performed in the absence of a carbonate salt such as but not limited to potassium carbonate.
In some embodiments, the contacting is performed in the absence of a cryptand, such as but not limited to 4,7,13,16,21,24-Hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane.
In another aspect, the invention provides a method for synthesizing an imaging agent, comprising contacting an imaging agent precursor with a fluoride species under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species, wherein the contacting is performed at a pH below 7. In some embodiments, the contacting is performed at a pH below 6, or at a pH below 5, or at a pH between 5 and 6.
In some embodiments, the leaving group is a sulfonate-containing group. The leaving group may be a mesylate, tosylate, triflate, or 1,2,-cyclic sulfate group. In some embodiments, the leaving group is a tosylate group. In some embodiments, the fluoride species is an 18F ion.
In some embodiments, the imaging agent precursor comprises formula (I):
Figure imgf000014_0001
wherein J is selected from the group consisting of N(R ), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, and C(=0)N(R27); when present, K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group; when present, L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group; M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group; or L and M, together with the atom to which they are attached, may form a three-, four-, five-, or six- membered carbocyclic ring; Q is halo or haloalkyl; n is 0, 1, 2, or 3; R 21 , R 22 , R 27 , and R28 are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group; R , R , R , and R are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group; R29 is Ci-C6 alkyl optionally substituted with a leaving group; and Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with a leaving group and heteroaryl optionally substituted with a leaving group; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, and heteroaryl optionally substituted with a leaving group; provided that at least one leaving group is present in formula (I).
In some embodiments, the imaging agent comprises formula (II):
Figure imgf000015_0001
wherein J is selected from the group consisting of N(R ), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, and C(=0)N(R27); when present, K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety; when present, L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety; M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety; or L and M, together with the atom to which they are attached, may form a three- or four-membered carbocyclic ring; Q is halo or haloalkyl; n is 0, 1, 2, or 3; R 21 , R 22 , R 27 , and R 28 are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with an imaging moiety, and an imaging moiety; R , R , R , and R are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C6 alkyl optionally substituted with an imaging moiety, and an imaging moiety; R29 is Ci-C6 alkyl optionally substituted with an imaging moiety; and Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with an imaging moiety and heteroaryl optionally substituted with an imaging moiety; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, and heteroaryl optionally substituted with an imaging moiety; provided that at least one imaging moiety is present in formula (II), wherein the imaging moiety is
18-
'F.
In some embodiments, J is O. In some embodiments, R is methyl, ethyl, n- propyl, i-propyl, n-butyl, i-butyl, or t-butyl, each optionally substituted with a leaving group. In some embodiments, R29 is t-butyl. In some embodiments, Q is chloro. In some embodiments, each of R21, R22, R23, R24, R25, R26, and R27 is hydrogen.
In some embodiments, Y is carbon, K and L are hydrogen, and M is selected from the group consisting of alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group.
In some embodiments, Y is carbon, K and L is each hydrogen, and M is alkyloxy optionally substituted with a leaving group.
In some embodiments, the imaging agent precursor comprises formula:
Figure imgf000016_0001
wherein L is a leaving group.
In some embodiments, the imaging agent comprises formula:
Figure imgf000016_0002
wherein Im is an imaging moiety.
In some embodiments, the imaging agent precursor comprises: wherein L is a leaving
In some embodi a:
Figure imgf000017_0001
wherein Im is an imaging moiety.
In some embodiments, the imaging agent precursor comprises formula:
Figure imgf000017_0002
In some embodiments, the imaging agent comprising the fluoride species comprises formula:
Figure imgf000017_0003
In some embodiments, the method further comprises purifying the imaging agent using at least one purification technique. In some embodiments, the purification technique is chromatography such as but not limited to HPLC. In some embodiments, the purification technique is filtration such as but not limited to filtration through a C-18 resin.
In some embodiments, the method further comprises combining the imaging agent with a stabilizing agent. In some embodiments, the stabilizing agent is ascorbic acid, or a salt thereof
In another aspect, the invention provides a method for manufacturing an imaging agent comprising formula:
Figure imgf000018_0001
the method comprising, (a) contacting a tosylate precursor comprising formula:
Figure imgf000018_0002
with an anhydrous fluoride species associated with an ammonium salt; (b) heating the mixture of (a); (c) cooling the heated mixture; (d) adding ¾0 to the cooled mixture; (e) purifying the mixture from the hydrated mixture of (d) using HPLC with an H20/MeCN eluent; and (f) diluting the eluent with a solution of ascorbic acid or a salt thereof.
In some embodiments, step (b) comprises heating the mixture to a temperature between 50°C and 250°C. In some embodiments, step (b) comprises heating the mixture for less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes.
In some embodiments, the method further comprises (g) contacting the diluted eluent of (f) with a C18 resin; (h) washing the contacted C18 resin with a solution of ascorbic acid or a salt thereof; (i) eluting
Figure imgf000018_0003
from the CI 8 resin with absolute ETOH; and (j) diluting the eluent of (i) with a solution or ascorbic acid or a salt thereof.
In some embodiments, the method further comprises (k) aseptically filtering the diluted eluent of (j), and (1) optionally, determining the presence of
Figure imgf000018_0004
in a sample of the aseptic filtrate of (k). In other aspects, the invention provides imaging agents made by any of the preceding methods.
Thus, in one aspect, the invention provides an imaging agent comprising formula:
Figure imgf000019_0001
wherein the imaging agent is manufactured by (a) contacting a tosylate precursor comprising formula:
Figure imgf000019_0002
with an anhydrous fluoride species associated with an ammonium salt; (b) heating the mixture of (a); (c) cooling the heated mixture; (d) adding ¾0 to the cooled mixture; (e) purifying the mixture from the hydrated mixture of (d) using HPLC with an H20/MeCN eluent; and (f) diluting the eluent with a solution of ascorbic acid or a salt thereof.
In some embodiments, step (b) comprises heating the mixture to a temperature between 50°C and 250°C. In some embodiments, step (b) comprises heating the mixture less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes.
In some embodiments, the manufacturing further comprises (g) contacting the diluted eluent of (f) with a C18 resin; (h) washing the contacted CI 8 resin with a solution of ascorbic acid or a salt thereof; (i) eluting
Figure imgf000019_0003
from the CI 8 resin with absolute ETOH; and (j) diluting the eluent of (i) with a solution of ascorbic acid or a salt thereof.
In some embodiments, the manufacturing further comprises: (k) aseptically filtering the diluted eluent of (j), and (1) optionally, determining the presence of
Figure imgf000020_0001
in a sample of the aseptic filtrate of (k).
In another aspect, the invention provides a method for synthesizing a fluorinated compound, comprising reacting, in the presence of a carbonate or bicarbonate, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl group substituted with a halide or a sulfonate-containing group, with (ii) a salt comprising a fluoride species and weakly coordinating cation.
In some embodiments, the alkoxyalkyl group is substituted with a sulfonate- containing group. In some embodiments, the sulfonate-containing group is mesylate, tosylate, triflate or 1,2-cyclic sulfate. In some embodiments, the sulfonate-containing group is tosylate. In some embodiments, the weakly coordinating cation is a tetraalkylammonium cation. In some embodiments, the fluoride species is enriched for 18F isotope.
In another aspect, the invention provides a method for synthesizing a fluorinated compound comprising reacting, in the presence of a carbonate or bicarbonate, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl substituted with a halide or a sulfonate-containing group, with (ii) an 18F isotope.
In another aspect, the invention provides a method for synthesizing a fluorinated compound, comprising reacting (i) a precursor of the fluorinated compound comprising an alkoxyalkyl substituted with a halide or a sulfonate-containing group, with (ii) an 18F isotope, in the presence of a tetraalkylammonium bicarbonate or tetraalkylammonium carbonate. In some embodiments, the reaction is carried out in the presence of a tetraalkylammonium bicarbonate.
In some embodiments, the tetraalkylammonium bicarbonate is tetraethylammonium bicarbonate, tetrabutylammonium bicarbonate, or tetrahexylammonium bicarbonate.
In another aspect, the invention provides a method for 18F-labeling comprising formula:
Figure imgf000021_0001
wherein R is -lower alkyl-sulfonate, R1 is an Ci-Cio alkyl, and R2 is H or a halogen, comprising reacting the compound with F in the presence of a tetraalkylammonium bicarbonate or tetraalkylammonium carbonate. In some embodiments, R is - (CH2)0(CH2)n-sulfonate-containing group, wherein n is an integer from 1 to 5. In some embodiments, the sulfonate-containing group is mesylate, tosylate, triflate, or 1,2-cyclic sulfate. In some embodiments, R2 is a halogen. In some embodiments, R2 is chloride. In some embodiments, R1 is methyl, ethyl, propyl or butyl. In some embodiments, R1 is i-butyl. In some embodiments, R is -CH2-0-CH2-CH2-tosylate, R1 is i-butyl and R2 is chloride.
In another aspect, the invention provides a method for synthesizing a precursor to an imaging agent, comprising reacting a compound comprising formula (V):
Figure imgf000021_0002
wherein W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted; and R2 is hydrogen or halide; with a nucleophile or a radical species to produce a compound comprising formula (VI):
Figure imgf000021_0003
In some embodiments, the nucleophile is a hydride ion. In some embodiments, the hydride ion is generated from diisobutylaluminum hydride (DIBAL-H). In some embodiments, the radical species is Η·.
In some embodiments, the compound comprising formula (V) wherein W is - OCH2- is synthesized by etherification of precursor compounds comprising formulae (Va) and (Vb):
Figure imgf000022_0001
to form a product comprising formula:
Figure imgf000022_0002
In some embodiments, R1 is i-butyl and R2 is CI.
In some embodiments, etherification comprises reacting the precursor compounds in the presence of a base. In some embodiments, the base comprises a carbonate ion. In some embodiments, the base comprises a hydroxide ion. In some embodiments, the base is sodium hydroxide or tetramethyl ammonium hydroxide. In some embodiments, the etherification reaction comprises exposure to sodium hydroxide and benzyl
triethylammonium chloride.
In some embodiments, the compound comprising formula (Vb) is produced by exposing the compound comprising formula:
Figure imgf000022_0003
to a reducing agent. In some embodiments, the reducing agent is lithium aluminum hydride or lithium borohydride. In some embodiments, the reducing agent is lithium aluminum hydride.
In some embodiments, the compound comprising formula:
Figure imgf000022_0004
is produced by reacting methyl 4-formyl benzoate with ethylene glycol in the presence of an acid. In another aspect, the invention provides a method for forming a sulfonate- containing precursor of an imaging agent, comprising reacting a compound comprising formula:
Figure imgf000023_0001
with a sulfonate-containing species to form a product comprising a sulfonate-containing precursor of an imaging agent.
In some embodiments, the sulfonate-containing group is mesylate, tosylate, or triflate. In some embodiments, the sulfonate-containing group is tosylate. In some embodiments, the sulfonate-containing precursor of an imaging agent comprising the formula:
Figure imgf000023_0002
In some cases, the sulfonate-containing precursor is reacted with an imaging moiety to form an imaging agent.
In some embodiments, the imaging moiety is a radioisotope. In some embodiments, the imaging moiety is nC, 13N, 18F, 1231, 1251, 99mTc, 95Tc, mIn, 62Cu, 64Cu, 67 Ga, or 68Ga. In some embodiments, the imaging moiety is 18F.
In some embodime :
Figure imgf000023_0003
In another aspect, the invention provides a method for synthesizing an imaging agent, comprising reac lae:
Figure imgf000023_0004
via an etherification reaction to form a first compound comprising the formula:
Figure imgf000024_0001
exposing the first compound to a reducing agent to form a second compound comprising a benzylic alcohol; treating the second compound with phosphorus tribromide to form a third compound comprising a benzylic bromide; reacting the third compound with ethylene glycol to produce a fourth compound comprising the formula:
Figure imgf000024_0002
reacting the fourth compound with a sulfonate-containing species to form a product comprising a sulfonate-containing precursor of an imaging agent. In some cases, the method further comprises reacting the sulfonate-containing precursor of an imaging agent with an imaging moiety to form the imaging agent.
In another aspect, the invention provides a compound having the structure:
Figure imgf000024_0003
wherein the compound is synthesized using any of the preceding methods.
In another aspect, the invention provides a compound comprising formula:
Figure imgf000024_0004
In another aspect, the invention provides a compound comprising formula:
Figure imgf000024_0005
In another aspect, the invention provides a compound comprising formula:
Figure imgf000025_0001
In another aspect, the invention provides a compound comprising formula:
Figure imgf000025_0002
In another aspect, the invention provides a method of imaging a subject, comprising administering to a subject a first dose of imaging agent comprising the formula:
Figure imgf000025_0003
in an amount between about 1 mCi and about 4 mCi; acquiring at least one first image of a portion of the subject; subjecting the subject to stress; administering to the subject undergoing stress a second dose of the imaging agent in an amount greater than the first dose of the imaging agent by at least about 1.5 times the first dose of the imaging agent; and acquiring at least one second image of the portion of the subject.
In some embodiments, the second dose of the imaging agent is administered within less than about 48 hours, 24 hours, 18 hours, 12 hours, 6 hours, 5 hours, 4 hours, 3 hours, 2 hours, 1 hour, 30 minutes, or 15 minutes after acquiring the at least one first image. In some embodiments, the second dose of the imaging agent is at least 2.0 times greater than the first dose of the imaging agent. In some embodiments, the first image is obtained during an image acquisition period between 1 and 20 minutes. In some embodiments, the second image is obtained during an image acquisition period between 1 and 20 minutes. In some embodiments, the portion of the subject is at least a portion of the cardiovascular system. In some embodiments, the portion of the cardiovascular system is at least a portion of the heart. In some embodiments, the acquiring employs positron emission tomography.
In some embodiments, the method further comprises determining the presence or absence of a cardiovascular disease or condition in the subject. In some embodiments, the cardiovascular disease is coronary artery disease or myocardial ischemia.
In some embodiments, the imaging agent is administered as a formulation comprising water, less than about 5% ethanol, and less than about 50 mg/mL sodium ascorbate. In some embodiments, the formulation comprising the imaging agent is administered via an intravenous bolus injection. In some embodiments, the stress is induced by exercising the subject. In some embodiments, the second dose of the imaging agent is administered during the exercise.
In some embodiments, the first dose of the imaging agent is between about 1.0 mCi to about 2.5 mCi. In some embodiments, the first dose of the imaging agent is between about 1.7 mCi to about 2.0 mCi. In some embodiments, the first dose of the imaging agent is between about 2.5 to about 3.0 mCi.
In some embodiments, the wait time between acquiring at least one first image of a portion of the subject and administering to the subject a second dose of the imaging agent is 60 minutes. In some embodiments, the second dose of the imaging agent is administered in an amount that is at least 2.5, or at least 3.0 times greater than the first dose of the imaging agent. In some embodiments, the second dose of the imaging agent is administered in an amount between 2.5 and about 5.0, or 2.5 and 4.0, or 3.0 and 4.0 time greater, or between 3.0 and 5.0 times greater than the first dose of the imaging agent. In some embodiments, the second dose of the imaging agent is between about 8.6 mCi and about 9.0 mCi, or between about 8.6 mCi and about 9.5 mCi, or between about 9.0 to about 9.5 mCi.
In some embodiments, the stress is pharmacological stress. In some
embodiments, the pharmacological stress is induced by administering a pharmacological stress agent to the subject. In some embodiments, the pharmacological stress agent is a vasodilator. In some embodiments, the vasodilator is adenosine. In some embodiments, the second dose of the imaging agent is administered after the subject has been administered the pharmacological stress agent. In some embodiments, the second dose of the imaging agent is administered when the subject is at peak vasodilation from the pharmacological stress agent. In some embodiments, the first dose of the imaging agent is between about 2.0 mCi to about 3.5 mCi. In some embodiments, the first dose of the imaging agent is between about 2.4 mCi to about 3.0 mCi or between about 2.4 mCi to about 2.9 mCi. In some embodiments, the first dose of the imaging agent is between about 2.5 mCi to about 3.0 mCi or between about 2.5 mCi and about 3.5 mCi.
In some embodiments, the wait time between acquiring at least one first image of a portion of the subject and administering to the subject a second dose of the imaging agent is 30 minutes. In some embodiments, the second dose of the imaging agent is administered in an amount at least 2.0 times greater than the first dose of the imaging agent. In some embodiments, the second dose of the imaging agent is administered in an amount that is between 2 to 3 times greater than the first dose of the imaging agent, including 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, or 2.9 times greater.
In some embodiments, the second dose of the imaging agent is between about 5.7 mCi and about 6.2 mCi. In some embodiments, the second dose of the imaging agent is between about 6.0 mCi and about 6.5 mCi or between about 5.7 mCi and about 6.5 mCi. In some embodiments, the total of the first and second dose of the imaging agent does not exceed about 14 mCi.
In another aspect, the invention provides a syringe comprising a composition comprising the imaging agent comprises the formula:
Figure imgf000027_0001
wherein the syringe adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13,% 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of the imaging agent. In some cases, the syringe adsorbs between about 1% and about 20%, or between about 5% and about 15%, or between about 1% and about 15%, or between 2% and about 10%, or between about 5% and about 20%.
In some embodiments, the syringe comprises a plunger that adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13,% 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of the imaging agent. In some embodiments, the syringe comprises a plunger that is not rubber-tipped. In some embodiments, the syringe is a latex-free syringe. In some embodiments, the syringe comprises no rubber, and no silicon lubricants. In some embodiments, the syringe is a non-reactive syringe. In some cases, the syringe adsorbs between about 1% and about 20%, or between about 5% and about 15%, or between about 1% and about 15%, or between 2% and about 10%, or between about 5% and about 20%.
In some embodiments, the syringe further comprises sodium ascorbate, ethanol, and water. In some embodiments, the imaging agent is in a solution comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water.
In some embodiments, the imaging agent is present in the syringe in a dose between about 1.5 and about 14 mCi.
In another aspect, the invention provides a method of imaging a subject, comprising subjecting a subject to stress; administering to the subject a first dose of an imaging agent comprising the formula:
Figure imgf000028_0001
in an amount between aboutl mCi and about 4 mCi; acquiring at least one first image of a portion of the subject; administering to the subject a second dose of the imaging agent in an amount greater than the first dose of the imaging agent; and acquiring at least one second image of the portion of the subject.
In some embodiments, the amount of the second dose is more than 1.5 times the amount of the first dose.
In another aspect, the invention provides a method of imaging a subject, comprising subjecting a subject to stress; administering to the subject a dose of an imaging agent comprising formula:
Figure imgf000028_0002
in an amount less 20 mCi; and acquiring at least one first image of a portion of the subject.
In some embodiments, the amount of the dose is less than 14 mCi. In some embodiments, the amount of the dose is between 1 mCi and 4 mCi. In another aspect, the invention provides a cassette for the preparation of an imaging agent comprising formula:
Figure imgf000029_0001
comprising: (i) a vessel containing an imaging agent precursor comprising formula:
Figure imgf000029_0002
and (ii) a conduit for adding a source of F.
In another aspect, the invention provides an automated reaction system, comprising:
the foregoing cassette. In another aspect, the invention provides an apparatus for synthesizing an imaging agent comprising a linear arrangement of a plurality of stopcock manifolds connected one or more of the components selected from the group consisting of a [180]H20 recovery system, gas inlet, reservoir with solution of imaging agent precursor, vial, anion exchange cartridge, C-18 cartridge, syringe, solvent reservoir, reaction vessel, HPLC system, collection vessel, reservoir for solution of ascorbic acid or salt thereof, and exhaust outlet..
In some embodiments, the apparatus further comprising tubing. In some embodiment, the apparatus further comprising an imaging agent synthesis module, wherein the apparatus is fluidically connected to the apparatus. In some embodiments, the apparatus is capable of carrying out the method as described herein. In some embodiments, the apparatus is capable of preparing an imaging agent comprising formula:
Figure imgf000029_0003
In some embodiments, the invention provides an apparatus comprising the components arranged as shown in Figure 8. In some cases, the components are arranged in the order: (1) gas inlet; (2) [180]H20 recovery system; (3) anion exchange cartridge; (4) MeCN reservoir; (5) syringe; (6) reservoir with solution of imaging agent precursor; (7) reaction vessel; (8) HPLC system; (9) reservoir with solution of ascorbic acid or a salt thereof; (10) collection vessel; (11) ethanol reservoir; (12) vial with final product; (13) Sep-pack cartridge; (14) reservoir with solution of ascorbic acid or a salt thereof; (15) reaction vessel; and (16) exhaust outlet.
Brief Description of the Drawings
Figure 1 shows an example of a nucleophilic [18F]-fluorination reaction using an imaging agent precursor and a fluoride source to form an imaging agent.
Figure 2 shows various reaction pathways of an imaging agent precursor during a nucleophilic fluorination reaction.
Figure 3 shows an exemplary synthesis of an intermediate compound.
Figure 4 shows an alternative synthesis of an intermediate compound.
Figure 5 shows another alternative synthesis of an intermediate compound.
Figure 6 shows a flow chart describing a method for synthesizing an imaging agent.
Figure 7 is a schematic representation of a system for synthesizing an imaging agent using a modified Explora GN synthesis module.
Figure 8 is a schematic representation of a cassette, with associated columns and reagents for synthesizing an imaging agent using a modified GE-Tracerlab-MX synthesis module.
Figure 9 includes (a) a graph illustrating the changes in product distribution as a function of molar concentration of bicarbonate salt, (b) a graph illustrating the product distribution as a function of reaction time, and (c) a graph illustrating the changes in product distribution as a function of molar concentration of imaging agent precursor.
Figure 10 illustrates non-limiting examples of imaging agents which may be prepared using the fluorination methods as described herein, in some embodiments.
Figure 11 shows whole body coronal sections at the level of the myocardium from a representative human subject at different time points after administration of imaging agent 1. Figure 12 shows representative cardiac images of imaging agent 1 in control and chronic myocardial infarct (MI) rabbits.
Figure 13 shows a plot of reader's scores versus percentage decreases from the maximum value for rest image data of a study following administration of imaging agent 1 injection to subjects, according to a non-limiting embodiment.
Other aspects, embodiments, and features of the invention will become apparent from the following detailed description when considered in conjunction with the accompanying drawings. The accompanying figures are schematic and are not intended to be drawn to scale. For purposes of clarity, not every component is labeled in every figure, nor is every component of each embodiment of the invention shown where illustration is not necessary to allow those of ordinary skill in the art to understand the invention. All patent applications and patents incorporated herein by reference are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control.
Detailed Description of Certain Embodiments of the Invention
The present invention generally relates to systems, compositions, cassettes, methods, and apparatuses for the synthesis of imaging agents and precursors thereof. In some aspects the invention relates to imaging agents synthesized using methods described herein.
In some embodiments, the present invention relates to methods for synthesizing an imaging agent, for example, by reacting an imaging agent precursor with a source of an imaging moiety. As described herein, in some cases, the method involves the use of one or more additives (e.g. , salts) that may facilitate a chemical reaction. The methods may exhibit improved yields and may allow for the widespread synthesis of imaging agents, including imaging agents comprising a radioisotope (e.g. , 18F). The imaging agents may be useful as sensors, diagnostic tools, and the like. Synthetic methods for preparing an imaging agent have also been designed to use an automated synthesis system to prepare and purify imaging agents that comprise a radioisotope. In some aspects, the invention allows radiolabeled imaging agents to be made using a nucleophilic reaction system, including, but not limited to, the Explora GN or RN synthesis system (Siemens Medical Solutions USA, Inc.), GE-Tracerlab-MX synthesis system (GE Healthcare), Eckert & Zeigler Modular- Lab Synthesis system, etc. , which are commonly available at PET manufacturing facilities (PMF).
In some embodiments, the present invention provides methods for synthesizing an imaging agent precursor, wherein the imaging agent precursor is reacted with a source of an imaging moiety to form the imaging agent. As will be understood by those of ordinary skill in the art, it is advantageous to utilize methods which involve high- yielding reactions and a relatively low number of synthetic and/or purification steps. Accordingly, many of the methods provided herein for synthesizing an imaging agent precursor provide the imaging agent precursor in fewer steps than previously reported, with greater ease of synthesis and/or at a higher yield.
In some embodiments, the present invention provides methods of imaging, including methods of imaging in a subject that includes administering a composition or formulation {e.g. , that comprises imaging agent 1, as described herein) to the subject by injection, infusion, or any method of administration, and imaging a region of the subject that is of interest. Regions of interest may include, but are not limited to, the heart, cardiovascular system, cardiac vessels, blood vessels {e.g. , arteries, veins), brain, and other organs. A parameter of interest, such as blood flow, cardiac wall motion, or perfusion, can be imaged and detected using methods and/or systems of the invention. In some cases, methods for evaluating perfusion, including myocardial perfusion, are provided.
As used herein, the term "imaging agent" refers to any species that includes at least one atom, or group of atoms, that may generate a detectable signal itself, or upon exposure to an external source of energy {e.g., electromagnetic radiation, ultrasound, etc.). Typically, the imaging agent may be administered to a subject in order to provide information relating to at least a portion of the subject {e.g. , human). In some cases, an imaging agent may be used to highlight a specific area of a subject, rendering organs, blood vessels, tissues, and/or other portions more detectable and more clearly imaged. By increasing the detectability and/or image quality of the object being studied, the presence and extent of disease and/or injury can be determined. The imaging agent may include a radioisotope for nuclear medicine imaging. A non-liming example of an imaging agent, also referred herein as imaging agent 1 , comprises the formula:
Figure imgf000033_0001
As used herein, an "imaging moiety" refers to an atom or group of atoms that is capable of producing a detectable signal itself or upon exposure to an external source of energy (e.g. , imaging agents comprising imaging moieties may allow for the detection, imaging, and/or monitoring of the presence and/or progression of a condition), pathological disorder, and/or disease. Nuclear medicine imaging agents can include nC, 13N, 18F, 123I, 1251, 99mTc, 95Tc, mIn, 62Cu, 64Cu, 67Ga, and 68Ga as the imaging moiety. In some embodiments, the imaging moiety is 18F. Imaging agents based on 18F have been used for imaging hypoxia and cancer (Drugs of the Future 2002, 27, 655-667).
In some embodiments, a compound (e.g. , an imaging agent, a fluoride species) may be isotopically-enriched with fluorine- 18. "Isotopically-enriched" refers to a composition containing isotopes of an element such that the resultant isotopic composition is other than the natural isotopic composition of that element. With regard to the compounds provided herein, when a particular atomic position is designated as 18F, it is to be understood that the abundance of 18F at that position is substantially greater than the natural abundance of 18F, which is essentially zero. In some embodiments, a fluorine designated as 18F may have a minimum isotopic enrichment factor of about 0.01%, about 0.05%, about 0.1%, about 0.2%, about 0.3%, about 0.4%, about 0.5%, about 0.75%, about 1%, about 2%, about 3%, about 4%, about 5%, about 10%, about 15%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, or greater. The isotopic enrichment of the compounds provided herein can be determined using conventional analytical methods known to one of ordinary skill in the art, including mass spectrometry and HPLC.
Exemplary Methods for Synthesizing Imaging Agents
The present invention provides methods for synthesizing imaging agents. In some cases, the imaging agent is formed by reacting an imaging agent precursor with an imaging moiety. In certain embodiments, a method involves reacting between an imaging agent precursor comprising a leaving group with a source of an imaging moiety (e.g., a fluoride species). For example, the imaging moiety replaces the leaving group via a substitution reaction, such as an SN2 or SNI reaction. That is, during the reaction an imaging moiety replaces the leaving group, thereby producing the imaging agent.
The methods described herein may be used for the synthesis of a wide variety of imaging agents from an imaging agent precursor. Generally, the imaging agent precursor may include at least one leaving group that may be displaced by an imaging moiety, such as an 18 F species. Imaging agent precursors may be synthesized using methods known to those of ordinary skill in the art and as described below.
In some embodiments, the imaging agent precursor comprises formula (I):
Figure imgf000034_0001
wherein:
J is selected from the group consisting of N(R28), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, and C(=0)N(R27);
when present, K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
when present, L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group; or
L and M, together with the atom to which they are attached, may form a three-, four-, five-, or six-membered carbocyclic ring;
Q is halo or haloalkyl;
n is 0, 1, 2, or 3;
R21, R22, R27, and R28 are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group;
R 23 , R 24 , R 25 , and R 26 are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group;
R29 is Ci-C6 alkyl optionally substituted with a leaving group; and
Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with a leaving group and heteroaryl optionally substituted with a leaving group; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, and heteroaryl optionally substituted with a leaving group;
provided that at least one leaving group is present in formula (I).
In some embodiments, a method of the present invention comprises preparing an imaging agent comprising formula (II):
Figure imgf000035_0001
wherein:
J is selected from the group consisting of N(R28), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, and C(=0)N(R27);
when present, K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
when present, L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety; or
L and M, together with the atom to which they are attached, may form a three-, four-, five-, or six-membered carbocyclic ring;
Q is halo or haloalkyl;
n is 0, 1, 2, or 3;
21 22 27 28
R , R , R , and R are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with an imaging moiety, and an imaging moiety;
R , R , R , and R are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C6 alkyl optionally substituted with an imaging moiety, and an imaging moiety;
R29 is Ci-C6 alkyl optionally substituted with an imaging moiety; and
Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with an imaging moiety and heteroaryl optionally substituted with an imaging moiety; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, and heteroaryl optionally substituted with an imaging moiety;
provided that at least one imaging moiety is present in formula (II). That is, the imaging agent comprising formula (II) is formed from an imaging agent precursor comprising formula (I), wherein a leaving group of the imaging agent precursor comprising formula (I) is replaced by an imaging moiety. In some embodiments, the imaging moiety is 18F.
In some cases, J is selected from N(R27), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, or C(=0)N(R27). In some cases when present, K is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy, aryl, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl, and a leaving group. In some cases, when present, L is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy, aryl, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl, and a leaving group. In some case, M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy, aryl, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl, and a leaving group. In some cases, L and M, together with the atom to which they are attached, form a three- or four-membered carbocyclic ring. In some cases Q is halo or haloalkyl. In some cases, n is 0, 1, 2, or 3. In some cases, R21, R22, R23, R24, R25, R26, and R27 are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group. In some cases R29 is Ci-C6 alkyl optionally substituted with a leaving group. In some cases, Y is selected from a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent and M is selected from aryl and heteroaryl; and provided that when Y is oxygen, K and L are absent and M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, aryl, Ci-C6 alkyl optionally substituted with a leaving group, and heteroaryl.
In some cases, J is O. In some cases R29 is methyl, ethyl, H-propyl, z'-propyl, n- butyl, z'-butyl, or i-butyl, each may be optionally substituted with a leaving group. In certain embodiment, R29 is i-butyl. In some cases, Q is chloro. In some cases, all of R21,
22 23 24 25 26 27
R , R , R , R , R , and R are hydrogen. In some cases, Y is carbon, K and L are hydrogen, and M is alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, or a leaving group. In some cases, Y is carbon, K and L are hydrogen, and M is alkyloxy optionally substituted with a leaving group.
In some embodiments, the imaging agent precursor comprises the formula:
Figure imgf000038_0001
wherein R , R , R , Q, J, and n are as described herein, and L is a leaving group.
In some embodiments, the imaging agent comprises the formula:
Figure imgf000038_0002
wherein R , R , R , Q, J, and n are as described herein, and Im is an imaging moiety.
In some embodiments, the imaging agent precursor comprises the formula:
Figure imgf000038_0003
wherein R and Q are as described herein, and L is a leaving group.
In some embodiments, the imaging agent comprises the formula:
Figure imgf000038_0004
wherein R29 and Q are as described herein, and Im is an imaging moiety.
In one set of embodiments, the imaging agent precursor comprises the formula:
Figure imgf000038_0005
herein referred to as imaging agent precursor 1 (see Figure 1).
In some cases, the imaging agent comprises the formula:
Figure imgf000039_0001
herein referred to as imaging agent 1 (see Figure 1).
Other non-limiting examples of imaging agents that may be prepared using a fluorination methods of the present invention are shown in Figure 10. In some cases, the imaging agent precursor is not a salt.
Various methods may be used to synthesize an imaging agent precursor of the formula (I), including an etherification reaction (e.g. , Mitsonobu reaction) between two alcohols, or between a phenol and an alcohol. In some cases, a leaving group may be installed by conversion of a hydroxyl group into a tosylate group or other leaving group, for example, by reaction with p-toluenesulfonate chloride in the presence of a base (e.g., DMAP). Additional methods for the synthesis of an imaging agent having the structure comprising formula (II) or an imaging agent precursor having the structure comprising formula (I) are described in International Publication No. WO2005/079391 , the contents of which are incorporated herein by reference.
In some embodiments, a method for synthesizing an imaging agent comprises contacting an imaging agent precursor (e.g. , a compound comprising formula (I)) with a fluoride species and an ammonium salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent (e.g. , a compound comprising formula (II)) comprising the fluorine species wherein the molar ratio of ammonium salt to imaging agent precursor is less than about 1.5 : 1, or about 1 : 1 or less (or any ratio described herein).
In some embodiments, a method for synthesizing an imaging agent comprises contacting an imaging agent precursor (e.g. , a compound comprising formula (I)) with a fluoride species and a bicarbonate salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent (e.g. , a compound comprising formula (II)) comprising the fluorine species, wherein the molar ratio of bicarbonate salt to imaging agent precursor is less than about 1.5: 1, or is about 1 : 1 or less (or any ratio described herein).
In some embodiments, a method for synthesizing an imaging agent comprises contacting an imaging agent precursor (e.g. , a compound comprising formula (I)) with a fluoride species under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent (e.g. , a compound comprising formula (II)) comprising the fluorine species, wherein the contacting is performed at a pH below 7.
In some embodiments, a method for 18F-labeling a compound comprising the formula:
Figure imgf000040_0001
wherein:
R1 is alkyl, optionally substituted;
R2 is hydrogen or halogen; and
R3 is alkyl substituted with a sulfonate-containing group, alkoxy substituted with a sulfonate-containing group, or alkoxyalkyl substituted with a sulfonate-containing group, comprises reacting the compound with an 18F species in the presence of an
18
ammonium salt or a bicarbonate salt to form a product comprising the F species.
In some embodiments, a method for manufacturing an imaging agent comprising the formula:
Figure imgf000040_0002
comprises
(a) contacting a tosylate precursor comprising the formula:
Figure imgf000040_0003
a fluoride species associated with an ammonium
(b) heating the mixture of (a);
(c) cooling the heated mixture;
(d) adding ¾0 to the cooled mixture; (e) purifying the mixture from the hydrated mixture of (d) using HPLC with an H20/MeCN eluent; and
(f) diluting the eluent with a solution of ascorbic acid or a salt thereof.
In some cases, step (b) comprises heating the mixture to a temperature between 50 °C and 250 °C. In some cases, the heating step (b) comprises heating the mixture for less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes. In some cases, the method further comprises:
(g) contacting the diluted eluent of (f) with a C18 resin;
(h) washing the contacted C18 resin with a solution of ascorbic acid or a salt thereof;
(i) eluting
Figure imgf000041_0001
from the CI 8 resin with absolute ethanol; and
(j) diluting the eluent of (i) with a solution of ascorbic acid or a salt thereof (e.g., sodium salt).
In some cases, the method further comprises
(k) aseptically filtering the diluted eluent of (j), and
(1) optionally, determining the presence of
Figure imgf000041_0002
in a sample of the aseptic filtrate of (k).
In some embodiments, an imaging agent comprising the formula:
Figure imgf000041_0003
is manufactured by:
(a) contacting a tosylate precursor comprising the formula:
Figure imgf000042_0001
with an anhydrous fluoride species associated with an ammonium salt;
(b) heating the mixture of (a);
(c) cooling the heated mixture;
(d) adding ¾0 to the cooled mixture;
(e) purifying the mixture from the hydrated mixture of (d) using HPLC with an H20/MeCN eluent; and
(f) diluting the eluent with a solution of ascorbic acid or a salt thereof.
In some cases, step (b) comprises heating the mixture to a temperature between 50 °C and 250 °C. In some cases, the heating step (b) comprises heating the mixture less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes. In some cases, the manufacturing further comprises:
(g) contacting the diluted eluent of (f) with a C18 resin;
(h) washing the contacted CI 8 resin with a solution of ascorbic acid or a salt thereof;
(i) eluting
Figure imgf000042_0002
from the CI 8 resin with absolute ethanol; and
(j) diluting the eluent of (i) with a solution of ascorbic acid or a salt thereof. In some cases, the manufacturing further comprises:
(k) aseptically filtering the diluted eluent of (j), and
(1) optionally, determining the presence of
Figure imgf000042_0003
in a sample of the aseptic filtrate of (k). In some embodiments, a method for synthesizing a fluorinated compound comprises reacting, in the presences of a carbonate or bicarbonate ion, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl group substituted with a halide or a sulfonate-containing group, with (ii) a salt comprising a fluoride species and weakly coordinating cation.
As used herein, the term "leaving group" is given its ordinary meaning in the art of synthetic organic chemistry and refers to an atom or a group capable of being displaced by a nucleophile. Examples of suitable leaving groups include, but are not limited to, halides (such as chloride, bromide, or iodide), alkoxycarbonyloxy, aryloxycarbonyloxy, alkanesulfonyloxy, arenesulfonyloxy, alkyl-carbonyloxy (e.g. , acetoxy), arylcarbonyloxy, aryloxy, methoxy, Ν,Ο-dimethylhydroxylamino, pixyl, haloformates, and the like. In some cases, the leaving group is a sulfonic acid ester, such as toluenesulfonate (tosylate, TsO), methanesulfonate (mesylate, MsO), or
trifluoromethanesulfonate (triflate, TfO). In some cases, the leaving group may be a brosylate, such as p-bromobenzenesulfonyl. In some cases, the leaving group may be a nosylate, such as 2-nitrobenzenesulfonyl. The leaving group may also be a
phosphineoxide (e.g. , formed during a Mitsunobu reaction) or an internal leaving group such as an epoxide or cyclic sulfate. In some embodiments, the leaving group is a sulfonate-containing group. In some embodiments, the leaving group is a tosylate group.
In certain embodiments, the invention provides methods of synthesizing an imaging agent comprising a halogen. For example, the method may involve a halogenation reaction. In some embodiments, methods for synthesizing an imaging agent comprising a fluoride (e.g. , enriched with 18F) are provided. The method comprises contacting an imaging agent precursor with a source of a fluoride under conditions that result in the fluoride replacing a leaving group of the precursor to produce an imaging agent comprising a fluoride species. In certain embodiments, the method involves a nucleophilic fluorination reaction. That is, an imaging agent precursor comprising a leaving group is reacted in the presence of a fluoride species, whereby SN2 or SNI displacement of the leaving group by the fluoride species produces the imaging agent. In some embodiments, the fluoride species is enriched with 18F. Figure 1 shows an illustrative example, where imaging agent precursor 1 is treated with
18
an F species to produce imaging agent 1 via a substitution reaction. In some embodiments, one or more additives may be incorporated into the reaction mixture of the imaging agent precursor and the fluoride species. The additive may, in some cases, facilitate reaction between the imaging agent precursor and the fluoride species and/or may aid in stabilizing the imaging agent. For example, the fluoride species may have relatively low reactivity (e.g. , nucleophilicity), and addition of an additive may enhance the reactivity of the fluoride species. As an illustrative embodiment, a fluorine species may be a negatively charged fluoride ion (e.g. , an
18
isotopically-enriched F ion), and an additive may be used to bind to any positively charged counterions present within the reaction mixture, thereby enhancing the reactivity of the fluoride ion. In some embodiments, the additives may decrease the rate of undesired side reactions, as described below.
In some cases, the additive may be combined with the fluoride species prior to contact with the imaging agent precursor. For example, in certain embodiments a solution comprising the fluoride species and the additive is prepared, and the solution is added to the imaging agent precursor. In other embodiments, a solid comprising the fluoride species and the additive is prepared, and the solid is contacted with the imaging agent precursor. In certain embodiments, the fluoride species is adsorbed onto a solid support (e.g. , an anion exchange column), and a solution comprising the additive is used to elute the fluoride species from the solid support. The eluted solution is then contacted with the imaging agent precursor, or is concentrated to produce a solid, which is then contacted with the imaging agent precursor.
In some embodiments, the additive is a bicarbonate salt. In certain embodiments, it has been discovered that substitution of a carbonate salt with a bicarbonate salt (such as KHCO3) results in considerable improvement of both fluorination efficiency and starting material integrity. As used herein, the term "bicarbonate salt" refers to a salt comprising a bicarbonate or hydrogen carbonate ion (HCO3 " ion). The bicarbonate salt may be a metal bicarbonate, such as sodium bicarbonate, calcium bicarbonate, potassium bicarbonate, magnesium bicarbonate, and the like. In certain embodiments, the bicarbonate salt is potassium bicarbonate (KHCO3). In some embodiments, the bicarbonate salt comprises a non-metal counterion, such as ammonium bicarbonate. For example, the bicarbonate salt may be a tetraalkylammonium bicarbonate salt having the formula, R4NHCO3, wherein R is alkyl. In some embodiments, R may be a lower alkyl, such as methyl, ethyl, propyl, butyl, pentyl, hexyl, or the like. In certain embodiments, the ammonium salt is Et4NHC03. In other embodiments, the salt is Me4NHC03, i- Pr4NHC03, «-Pr4NHC03, «-Bu4NHC03, z'-Bu4NHC03, or i-Bu4NHC03.
As described further in Example 14, it is thought that reaction conditions which activate larger differential rates of fluorination would result in a more efficient and chemoselective process; that is, a decreased rate of hydrolysis or increased rate of fluorination would result. The studies outlined herein revealed that although required for anion exchange, Ι¾003 did little to enhance fluorination over baseline levels and served primarily a detrimental role in the fluorination reaction. However, in contrast, addition of KHC03 produced a marked increase in fluorination over the same concentration range, while decomposition pathways remained poorly differentiated. These facts, coupled with the observation that [18F]NaF exchange with tetraalkylammonium cations can directly produce a highly active nucleophilic fluoride source, led to investigation of a series of salts in an effort to identify related counterion affects that increase the rate of fluorination.
A comprehensive screen of ammonium salts identified a dramatic enhancement of fluorination efficiency in the presence of bicarbonate anion (e.g. , see Table 1); only modest dependency on size of the alkyl substituent was observed within the series methyl -> ethyl -> butyl (e.g. , Example 14).
Subsequent optimization of salt stoichiometry revealed that at levels as low as 25 mol of the tetraalkylammonium bicarbonate to an imaging agent precursor (e.g. , 0.25 : 1) resulted in near complete conversion of the imaging agent precursor to the imaging agent; once again, unproductive consumption of starting material occurred with increasing base concentration revealing an optimum stoichiometry range for the modified reaction conditions. Related studies directed toward determination of the optimal precursor concentration revealed a concentration threshold.
This reagent combination also demonstrated rapid conversion and significantly improved chemoselectivity toward fluorination over the K2C03/Kryptofix® 222 method. In fact, a more detailed evaluation of crude reaction mixtures revealed a dramatic reduction in overall decomposition rates as evidenced by the absence of hydrolytic impurities (e.g. , as described in Example 14); a result which may be attributed to a lower solution pH in the absence of Kryptofix® 222 (5-6 vs. 9-10).
In some embodiments, the additive is a salt comprising a cation that forms a weakly coordinating salt with a fluoride species. As used herein, a "cation that forms a weakly coordinating salt with a fluoride species" refers to a cation that renders a fluoride species reactive within a fluorination reaction. For example, the cation may not strongly bind to the fluoride species, allowing the fluoride species to act as a nucleophile during a nucleophilic fluorination reaction, Those of ordinary skill the art would be able to select an appropriate cation that would be suitable as a weakly coordinating counterion for a fluoride species. For example, the cation may be have a relatively large atomic radius and/or may be a weak Lewis base. In some cases, the cation may be selected to be lipophilic. In some cases, the cation may comprise one or more alkyl groups. Examples of weakly coordinating cations include cesium ions, ammonium ions, and the like. Examples of weakly coordinating cations include weakly coordinating salts of hexamethylpiperidindium, S(NMe2)3, P(NMe2)4, tetraaalkylphosphonium salts, tetraarylphosphonium salts, (e.g. tetraphenylphosphonium),
hexakis(dimethylamino)diphosphazenium, tris(dimethylamino)sulfonium, etc.
In some embodiments, the additive is an ammonium salt, i.e., a salt comprising a substituted or unsubstituted ammonium ion. In some cases, the ammonium ion is a weakly coordinating cation. In some cases, the ammonium salt has the formula, R4NX, where each R can be the same or different and is alkyl, heteroalkyl, aryl, heteroaryl, or heterocyclic, each optionally substituted, and X is a negatively charged counterion. In some cases, R is alkyl, heteroalkyl, aryl, heteroaryl, or heterocyclic, each optionally substituted. The ammonium salt may include a wide range of negatively charged counterions, including halides, carbonates, bicarbonates, and the like. Examples of ammonium salts include, but are not limited to, ammonium bicarbonate salts, ammonium hydroxide salts, ammonium acetate salts, ammonium lactate salts, ammonium trifluoroacetate salts, ammonium methanesulfonate salts, ammonium p-toluenesulfonate salts, ammonium nitrate salts, ammonium halide salts (e.g. , ammonium iodide salts), ammonium bisulfate salts, and the like.
In one set of embodiments, the ammonium salt is a tetraalkylammonium salt, such as a tetraalkylammonium bicarbonate salt. For example, the ammonium salt may have the formula, R4NHCO3, wherein each R is independently alkyl. In some cases, R is optionally substituted. In some embodiments, the alkyl group is a lower Ci-C6 alkyl group. In some embodiments, the tetraalkylammonium salt is a basic
tetraalkylammonium salt. The salt additive (e.g., bicarbonate salt and/or ammonium salt) may be utilized in the reaction such that the molar ratio of the salt additive to the imaging agent precursor is less than about 1.5:1. In some cases, the molar ratio is about 1.5:1 or less, about 1.4:1 or less, about 1.3:1 or less, about 1.25:1 or less, about 1.2:1 or less, about 1.1:1 or less, about 1:1 or less, about 0.75:1 or less, about 0.5:1 or less, about 0.25:1 or less, about 0.1:1 or less, or about 0.05:1 or less. In some cases, the ratio is greater than about 0.05:1, greater than about 0.01:1, or greater than about 0.25:1. In some embodiments, the molar ratio of salt additive to imaging agent precursor is about 0.5:1 to about 1:1, or about 0.25:1 to about 1:1, or about 0.25:1 to about 0.75:1, about 1.49:1 to about 0.05:1, or between about 1.4:1 to about 0.25:1, or between about 0.25:1 and about 1.4:1, or between about 0.25:1 and about 1.25:1.
Without wishing to be bound by theory, the use of bicarbonate and ammonium salts may aid in decreasing the rate of competing reactions such as hydrolysis during nucleophilic fluorination of an imaging agent precursor.
In some embodiments, the additive may be used in combination with a species capable of enhancing the reactivity of the fluoride species or otherwise facilitating conversion of the imaging agent precursor to the imaging agent. For example, the species may be a compound capable of chelating one or more ions (e.g., metal ions) that may be present within the reaction mixture. Without wishing to be bound by theory, the species may be used to chelate a counterion to a fluoride species, such as a potassium ion, thereby increasing the reactivity (e.g., nucleophilicity) of the fluoride species. In certain embodiments, the additive is used in combination with a multidentate ligand, such as a crown ether or a cryptand that is capable of chelating a metal ion. The multidentate ligand (e.g., cryptand) may be selected based on the metal ion to be chelated. The multidentate ligand may be, for example, 4,7,13,16,21,24-hexaoxa-l,10- diazabicyclo[8.8.8]-hexacosane (e.g., Kryptofix® 222). Other cryptands will be known to those of ordinary skill in the art.
Some embodiments may involve the use of a bicarbonate salt in combination with 4,7,13,16,21,24-hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane. In a specific embodiment, potassium bicarbonate may be used in combination with 4,7,13,16,21,24- hexaoxa- 1 , 10-diazabicyclo [8.8.8] -hexacosane.
In another set of embodiments, it may be advantageous to utilize the methods described herein in the absence of a cryptand. The term "cryptand" is given its ordinary meaning in the art and refers to a bi- or a polycyclic multidentate ligand for a cation. For example, the method may be carried out using an ammonium salt, in the absence of a cryptand (e.g., such as 4,7,13,16,21,24-hexaoxa-l,10-diazabicyclo[8.8.8]-hexacosane).
In another set of embodiments, the method is performed in the absence of a carbonate salt.
In some embodiments, the use of a salt additive in the reaction increases the yield by about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 100%, about 200%, about 300%, about 400%, about 500%, or greater, relative to conducting the reaction under essentially the same conditions but in the absence of a salt additive.
Those of ordinary skill in the art will be able to select and/or determine the appropriate set of reaction conditions (e.g. , concentration, temperature, pressure, reaction time, solvents, etc.) suitable for use in a particular application. The imaging agent may be further processed using one or more purification techniques, and may optionally be combined with additional components, such as a stabilizing agent.
Those of ordinary skill in the art would be able to select a source of a fluoride species suitable for use in the methods described herein. The term "fluoride species" as used herein refers to a fluoride atom or group of atoms comprising at least one fluoride atom, wherein the fluoride atom is capable of reacting with another compound (e.g. , an imaging agent precursor). In some embodiments, an isotopically-enriched 18F species may be produced by the nuclear reaction 180(p,n)18F from proton bombardment of
18 18
[ 0]]¾0 in a cyclotron. The method may involve treating a solution of the F species to remove any impurities, such as unreacted [180]]¾0. For example, a solution of the 18F species may be filtered through an anion exchange column, where the 18F species is
18 18
retained on the cationic resin matrix while the [ 0]]¾0 is eluted. The F species is then removed by washing the anion exchange column with various mixtures of solvents and optional additives (e.g. , salt additives), forming an 18F-containing solution. In some cases, the anion exchange column is washed with an aqueous solution of a salt, such as KHC03 or Et4NHC03.
In some cases, the 18F-containing solution is combined with additional components prior to reaction with an imaging agent precursor. For example, one or more solvents may be added to dilute the 18F-containing solution to a selected concentration. In one set of embodiments, the F-containing solution is diluted with acetonitrile.
In some cases, the 18 F-containing solution may be concentrated to dryness by exposure to elevated temperature and/or reduced pressure to form an anhydrous 18F- containing solid. In some embodiments, the 18F-containing solid may further comprise one or more additives {e.g. , salt additives). The chemical composition of the 18F- containing solid may depend on the number and kind of additives used in preparation of the 18 F-containing solution. For example, a solution of potassium bicarbonate may be used to elute the 18F species from the anion exchange column, thereby resulting in an 18F-containing solid comprising [18F]KF. In another example, a solution of ammonium bicarbonate is used to elute the 18 F species from the anion exchange column, thereby resulting in an 18 F-containing solid comprising [ 18 F]Et4NF.
In some cases, the solution comprising the 18 F species is heated to a temperature ranging from room temperature to about 200 °C. In some embodiments, the solution is heated to a temperature ranging from 90-120 °C. In some cases, the solution is heated to about 75 °C, about 85 °C, about 95 °C, about 105 °C, about 115 °C, about 125 °C, or greater. In some cases, the solution is placed under a reduced pressure of about 100 mm Hg, about 125 mm Hg, about 150 mm Hg, about 175 mm Hg, about 200 mm Hg, about 225 mm Hg, about 250 mm Hg, about 275 mm Hg, about 300 mm Hg, about 325 mm Hg, about 350 mm Hg, about 375 mm Hg, about 400 mm Hg, or greater. In some cases, the solution is placed under a reduced pressure of about 100 mbar, about 125 mbar, about 150 mbar, about 175 mbar, about 200 mbar, about 225 mbar, about 250 mbar, about 275 mbar, about 280 mbar, about 300 mbar, about 325 mbar, about 350 mbar, about 375 mbar, about 400 mbar, about 450 mbar, about 500 mbar, or greater. Those of ordinary skill in the art would be able to select and/or determine conditions suitable for a particular reaction. In some embodiments, the solution is concentrated to dryness at about 150 mm Hg and about 115 °C. In some embodiments, the solution is concentrated to dryness at about 375 mm Hg and about 115 °C. In some embodiments, the solution is concentrated to dryness at about 400 mbar and about 110-150 °C. In some embodiments, the solution is concentrated to dryness at about 280 mbar and about 95-115 °C.
The fluoride species and/or the additive, if present, is then contacted with the imaging agent precursor under conditions that result in conversion of the imaging agent precursor to the imaging agent product via nucleophilic fluorination. Those of ordinary skill in the art would be able to select conditions suitable for use in a particular reaction. For example, the ratio of fluoride species to imaging agent precursor may be selected to be about 1: 10,000 or more, about 1:5000 or more, about 1:3000 or more, about 1:2000 or more, 1: 1000 or more, 1:500 or more, 1: 100 or more, 1 :50 or more, 1 : 10 or more, 1 :5 or more, or, in some cases, 1 : 1 or more. In some embodiments, the fluoride species may be present at about 10 mol %, or about 5 mol , or about 3 mol , or about 2 mol , or about 1 mol or about 0.5 mol , or about 0.1 mol , or about 0.05 mol , or about 0.01 mol relative to the amount of imaging agent precursor. In some embodiments, at least of the fluoride species provided is enriched in 18F. For example, the ratio of 18F species to imaging agent precursor may be selected to be about 1: 1,000,000 or more, or about 1:500,000 or more, or about 1:250,000 or more, or about 1: 100,000 or more, or about 1:50,000 or more, or about 1 :25,000 or more, or about 1: 10,000 or more, about 1 :5000 or more, about 1:3000 or more, about 1 :2000 or more, 1: 1000 or more, 1:500 or more, 1: 100 or more, 1 :50 or more, 1: 10 or more, 1 :5 or more, or, in some cases, 1: 1 or more.
In some embodiments, the nucleophilic fluorination reaction is carried out in the presence of one or more solvents, for example, an organic solvents, a non-organic solvent (e.g. , an aqueous solvent), or a combination thereof. In some cases, the solvent is a polar solvent or a non-polar solvent. In some embodiments, the solvent is an aqueous solution, such as water. The solvent comprises at least about 0.001% water, at least about 0.01% water, at least about 0.1% water, at least about 1% water, at least about 5%, at least about 10%, at least about 20% water, at least about 30% water, at least about 40% water, at least about 50% water, or greater. In some cases, the solvent may comprise between about 0.1% and 100% water, about 1% to about 90%, about 1% to about 70%, about 1% to about 50%, or about 10% to about 50%. In some cases, the solvent comprises no more than 10% water, 5% water, 4% water, 3% water, 2% water, 1% water, or 0.5% water. In some cases, the solvent comprises between about 0.01% water and about 5% water, or between about 0.01% water and about 2% water, or between about 0.1% water and about 0.2% water.
Other non-limiting examples of solvents useful in the inventive methods include, but are not limited to, non-halogenated hydrocarbon solvents (e.g., pentane, hexane, heptane, cyclohexane, etc.), halogenated hydrocarbon solvents (e.g. , dichloromethane, chloroform, fluorobenzene, trifluoromethylbenzene, etc.), aromatic hydrocarbon solvents (e.g., toluene, benzene, xylene, etc.), ester solvents (e.g., ethyl acetate, etc.), ether solvents (e.g. , tetrahydrofuran, dioxane, diethyl ether, dimethoxyethane, etc.), and alcohol solvents (e.g. , ethanol, methanol, propanol, isopropanol, etc.). Other non- limiting examples of solvents include acetone, acetic acid, formic acid, dimethyl sulfoxide, dimethyl formamide, acetonitrile, and pyridine. In some embodiments, the reaction is carried out in a polar solvent, such as acetonitrile.
In one set of embodiments, an anhydrous 18F-containing solid, optionally comprising an additive, may be contacted with a solution of an imaging agent precursor (e.g. , a tosylate precursor), and the resulting solution is heated to an elevated temperature for a select period of time. The solution may be, for example, an acetonitrile solution. In other embodiments, a solution of the 18F species and additive, if present, is contacted with a solid imaging agent precursor or a solution of the imaging agent precursor.
Some embodiments involve contacting the imaging agent precursor with the fluoride species in a solution having a pH below about 7, below about 6, or, below about 5. In some cases, the solution has a pH between about 5 and about 6, or between about 5 and, about 7 or between about 4 and about 7.
In some cases, the solution comprising the 18F species, imaging agent precursor, and, optionally, additive, is heated at an elevated temperature for a period of time. For example, the solution may be heated to about 50 °C, about 60 °C, about 70 °C, about 80 °C, about 90 °C, about 100 °C, about 110 °C, about 120 °C, 150 °C, about 170 °C, about 200 °C, about 225 °C, about 250 °C or greater, for a period of 5 minutes or less, 10 minutes or less, 20 minutes or less, 30 minutes or less. It should be understood that other temperatures and reaction times may be used. Upon completion of the reaction, the reaction mixture is then cooled (e.g., to room temperature) and optionally diluted with a solvent, such as water.
Upon completion of the fluorination reaction, the resulting imaging agent is optionally subjected to one or more purification steps. In some cases, the synthesis, purification, and/or formulation of an imaging agent (e.g., a compound comprising formula (II)) may be prepared using an automated reaction system comprising a cassette, wherein the cassette may comprise a synthesis module, a purification module, and/or a formulation module. Automated reaction systems and cassettes are described herein.
Purification and isolation may be performed using methods known to those skilled in the art, including separation techniques like chromatography, or combinations of various separation techniques known in the art, for example, extractions, distillation, and crystallization. In one embodiment, high performance liquid chromatography (HPLC) is used with a solvent, or mixture of solvents, as the eluent, to recover the product. In some cases, the eluent includes a mixture of water and acetonitrile, such as a 45 :55 watenacetonitrile mixture. The content of water in the eluent may vary from, for example, about 1 % to about 50 . In some cases, HPLC may be performed using a C18 column.
The product may be further processed using additional purification techniques, such as filtration. In some cases, the imaging agent may be purified using HPLC, to produce a solution of HPLC mobile phase and the imaging agent. The HPLC mobile phase may be subsequently exchanged for a solution of ascorbic acid or a salt thereof, and ethanol solution, by filtration through a C-18 resin (e.g. , CI 8 Sep-Pak® cartridge). In some embodiments, the solution of the HPLC mobile phase and the imaging agent is filtered through a C- 18 resin, where the imaging agent remains on the resin and the other components, such as acetonitrile and/or other solvents or components, are removed via elution. The C- 18 resin may be further washed with a solution of ascorbic acid or a salt thereof, and the filtrate discarded. To recover the purified imaging agent, the C- 18 resin is washed with a solvent, such as ethanol, and the resulting solution is optionally further diluted with an ascorbic acid solution or a salt thereof, as described herein.
Optionally, the recovered product is combined with one or more stabilizing agents, such as ascorbic acid or a salt thereof. For example, a solution comprising the purified imaging agent may be further diluted with a solution of ascorbic acid or a salt thereof. As described herein, a formulation may be prepared via an automated reaction system comprising a cassette.
In some cases, a solution comprising the imaging agent product may be sterile filtered (e.g. , using a 13 mm diameter, Millipore, Millex PVDF 0.22 μιη sterilizing filter) into a sterile product vial. The sterile product vial may be a commercially available, pre- sterilized unit that is not opened during the production process, as any imaging agents (or other components) may be aseptically inserted through the septum prior to use. Those of ordinary skill in the art would be able to select suitable vials and production components, including commercially available, pre-sterilized units comprising a 0.22 μιη pore size membrane venting filter and quality control sampling syringes.
Following aseptic filtration, individual doses may be filled in syringes, labeled, and shipped to a clinical site. Dosing administration techniques, kits, cassettes, method and systems (e.g., automated reaction systems) for synthesis of the imaging agent, and testing procedures are described herein. In some embodiments, the product is dispensed into a 3 or 5 mL syringe and labeled for distribution. Labels may be prepared at a radiopharmacy and applied to a syringe shield and shipping container. Additional labels may be provided in the shipping container for inclusion in clinical site records.
The imaging agents may be used in a method of imaging, including methods of imaging a patient comprising administering the imaging agent to the patient by injection, infusion, or any other method, and imaging an area of the patient, as described herein. In some embodiments, a portion of a heart of the patient is imaged.
Exemplary Methods for the Synthesis of Imaging agent Precursors
Methods are also provided for synthesizing imaging agent precursors, and intermediates thereof. In some cases, the methods for synthesizing an imaging agent precursor {e.g. , a compound comprising formula (I)) exhibits improved yields and/or may allow for the large-scale synthesis of the imaging agent precursors and/or intermediates thereof. Some embodiments provide the ability to synthesize a desired product without need for purification, such as chromatography, which can be time- consuming and/or expensive with the loss of product. As noted above, Figure 1 shows an illustrative example of an imaging agent precursor which has been utilized in the synthesis of an imaging agent for imaging myocardial perfusion. The leaving group {i.e., tosylate group) is replaced with an imaging moiety, for example, 18F, as described herein, thereby forming an imaging agent.
In some embodiments, an imaging agent precursor is formed via a reaction in which a bond between a heteroatom and an alkyl, heteroalkyl, aryl, or heteroaryl group is formed. For example, the reaction may be an alkylation reaction, such as an
etherification reaction. In some embodiments, the reaction involves a hydroxyl- containing nucleophilic species reacting with an electrophilic species to form an ether linkage. As used herein, the term "ether" or "ether linkage" is given its ordinary meaning in the art and refers to the group, Ra-0-Rb, where Ra and Rb can be the same or different and are alkyl, heteroalkyl, aryl, or heteroaryl, any of which may be substituted. For example, the reaction may involve nucleophilic addition of the oxygen atom of the hydroxyl-containing species to an electrophilic species. In some embodiments, the reaction may involve coupling between two alcohols via, for example, a Mitsunobu reaction.
In some cases, the etherification reaction includes formation of a bond between an oxygen atom and an alkyl, aryl, heteroalkyl, heteroaryl, carbocyclic, or heterocyclic group. Figure 3 shows an illustrative embodiment of an etherification reaction between benzenedimethanol 12 and dichloropyridazinone 11 to form the benzyl alcohol 13. In another embodiment, Figure 4 shows an etherification reaction between
hydroxychloropyridazinone 17 and methyl 4-bromomethylbenzoate to afford pyridazinone ester 18.
In some embodiments, the inventive method involves reacting a compound comprising formula (III):
Figure imgf000054_0001
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with a leaving group, or heteroalkyl optionally substituted with a leaving group; and
n is 1, 2, 3, 4, or 5;
with a nucleophile, wherein the nucleophile replaces the leaving group to produce a product. For example, the nucleophile may be ethylene glycol, and an etherification reaction may be carried out as described herein. In some embodiments, the reaction is performed in the presence of a base, such as potassium i-butoxide or potassium hydroxide. In some cases, R3 is alkyl substituted with a leaving group and/or n is 1. In some embodiments, the compound comprising formula (III) comprises the structure:
Figure imgf000054_0002
wherein the leaving group is Br, and the product of the reaction comprises formula:
Figure imgf000055_0001
wherein R1 and R2 are as defined herein.
In some cases, a compound comprising formula (III) comprises the structure:
Figure imgf000055_0002
and the product of the etherification reaction comprises the formula:
Figure imgf000055_0003
In some cases, the compound comprising formula (III) may act as a nucleophile and may be reacted with an electrophile, to produce a product. For example, R3 may be -CH2OH, and the electrophile may be ethylene oxide.
In some embodiments, the method comprises reacting a compound comprising formula (IV):
Figure imgf000055_0004
wherein:
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
W is alkyl or heteroalkyl, optionally substituted;
each R4 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; and
n is 1, 2, 3, 4, or 5; with a reactant, wherein the hydroxyl group is replaced with a portion of the reactant to form a leaving group associated with the compound. In some cases, R4 is alkyl substituted with hydroxyl and/or n is 1. In some embodiments, reacting the compound comprising formula IV involves exposure to a halogenation reagent, such as phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine. In some embodiments, the halogenation reagent is phosphorus tribromide.
In some embodiments, W is -0(Ο¾)-; R1 is i-butyl; R2 is chloride; and R4 is alkyl substituted with hydroxyl. In some cases, n is 1.
In some embodiments, the compound comprising formula (IV) comprises the structure:
and the product comprises the structure:
Figure imgf000056_0002
In some embodiments, the compound comprising formula (IV) comprises the structure:
Figure imgf000056_0003
and the product comprises the structure:
Figure imgf000056_0004
In some cases, a method is provided for synthesizing a compound comprising formula (IV). In some cases, the method comprises synthesizing the compound comprising formula (IV) via an etherification reaction between compounds comprising formulae (IVa) an
Figure imgf000057_0001
wherein:
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
m is 1, 2, 3, 4, or 5 or greater;
R5 is hydroxyl or halide; and
each R6 and R7 can be the same or different and are alkyl, heteroalkyl, or a acyl group, each optionally substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R7 comprises a leaving group or a moiety that can be replace by a leaving group (e.g., hydroxyl), or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl.
In some cases, a compound comprising formula (IVa) comprises the structure:
Figure imgf000057_0002
wherein R5 is as described herein.
In one set of embodiments, the compound comprising formula II is synthesized etherification reaction between compounds comprising formulae (IVa) and (IVd)
Figure imgf000057_0003
wherein:
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
R5 is hydroxyl or halide; and
R6 and R7 can be the same or different and are alkyl, heteroalkyl, or a carbonyl group, each optionally substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R7 comprises a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl. In one set of embodiments, R5 is hydroxyl, R6 is a carbonyl group, and R7 is a substituted alkyl. In some cases, R5 is hydroxyl, R6 is an ester, and R7 is alkyl substituted with a leaving group.
In some cases, a compound comprising formula (IVa) comprises the structure:
Figure imgf000058_0001
wherein R5 is as defined herein.
The etherification reaction may be carried out as described herein, and may comprise exposure of the precursor compounds to a base, such as potassium carbonate.
In some embodiments, R5 is halide; and R6 and R7 are each alkyl, optionally substituted. In some embodiments, R5 is chloride; and R6 and R7 are each alkyl substituted with hydroxyl. In one embodiment, an etherification reaction between compounds comprising formulae (IVe) and (IVf):
Figure imgf000058_0002
forms a product comprising the formula:
Figure imgf000058_0003
In one embodiment, an etherification reaction between compounds comprising formulae:
Figure imgf000058_0004
forms a product comprising formula:
Figure imgf000058_0005
In one embodiment, an etherification reaction between compounds comprising formulae:
Figure imgf000059_0001
forms a product comprising formula:
Figure imgf000059_0002
The product may be reduced with a reducing agent, such as lithium aluminum hydride, lithium borohydride, or diisobutylaluminum hydride (DIBAL-H), thereby converting the ester group into an alcohol.
As shown by the illustrative embodiment in Figure 3, benzenedimethanol 12 and dichloropyridazinone 11 may be reacted via an etherification reaction in the presence of potassium carbonate in DMF to form benzyl alcohol 13. In some embodiments, a disubstituted impurity is also formed wherein benzenedimethanol 12 becomes alkylated at both hydroxyl groups, which may later be removed via chromatographic purification. Conversion of benzyl alcohol 13 to benzyl bromide 14 may be carried out with a variety of brominating agents, such as phosphorous tribromide in dichloromethane. Subsequent conversion of benzyl bromide 14 to alcohol 15 may be completed by reaction with ethylene glycol in the presence of potassium i-butoxide in tetrahydrofuran, in some cases at elevated temperature. Alcohol 15 may then be purified by column chromatography to remove any impurities, including disubstituted impurities formed during the synthesis of benzyl alcohol 13. Alcohol 15 may then be further reacted with p-toluenesulfonyl chloride in the presence of DMAP, triethylamine, and dichloromethane to form imaging agent precursor 1 , which may be purified via recrystallization. Using the method shown in Figure 5, the overall yield for synthesizing alcohol 15 starting from compound 11 (e.g. , 2-(i-butyl)-4,5-dichloropyridazin-3(2H)-one) and compound 12 (e.g. , 1 ,4- benzenedimethanol) may be at least 10%, at least 20%, at least 30%, or at least 40%, using chromatography as the purification method. In some cases, the overall yield for synthesizing alcohol 15 starting from compound 11 and compound 12 is approximately 43%, using chromatography as the purification method.
Figure 4 shows an alternate approach to the synthesis of alcohol 13 involving reaction of dichloropyridazinone 11 with potassium hydroxide in ethylene glycol to afford chlorohydroxypyridazinone 17, which may then be reacted with methyl 4- bromomethylbenzoate in the presence of potassium carbonate in DMF to afford pyridazinone ester 18. Next, reduction of pyridazinone ester 18, for example, using either DIBAL-H or lithium aluminum hydride, may produce benzyl alcohol 13, which may then be converted to alcohol 15 and imaging agent precursor 1 , as described herein. One advantageous feature of the synthetic scheme shown in Figure 4 is the reduction or elimination of disubstituted impurities that may be formed in the synthetic scheme shown in Figure 3. This provides the ability to purify benzyl alcohol 13 without the use of chromatography. In some cases, recrystallization methods alone may be used to afford an intermediate compound of very high purity. For example, benzyl alcohol 13 may be purified by recrystallization from isopropyl acetate. Additionally, the synthetic scheme shown in Figure 4 may provide a more simplified process, which may be performed with high-yield reactions and without the need for additional
protection/deprotection steps. Using the method shown in Figure 4, the overall yield for synthesizing alcohol 15 starting from compound 17 (e.g. , 2-(?-butyl)-4-chloro-5- hydroxypyridazin-3(2H)-one) and methyl 4-bromomethylbenzoate may be at least 10%, at least 20%, at least 30%, or at least 40%, without the use of chromatography for purification. In some cases, the overall yield for synthesizing alcohol 15 starting from compound 17 and methyl 4-bromomethylbenzoate is 48%, without the use of chromatography as a purification method.
In some embodiments, an etherification reaction (e.g., see Figure 3, etherification reaction to form benzyl alcohol 13) is performed in the presence of a base. The base may be, for example, a metal or a metal salt, such as a carbonate, a metal alkoxide, or the like. In some embodiments, the base may be an organic moiety, such as an amine. Examples of bases include, but are not limited to, metals (e.g. , sodium metal), alkoxides such as sodium f-butoxide or potassium i-butoxide, an alkali metal amide such as sodium amide, lithium diisopropylamide or an alkali metal bis(trialkylsilyl)amides such as lithium bis(trimethylsilyl)amide or sodium bis(trimethylsilyl) amide, amines (e.g. , triethylamine, trimethylamine, Et(z'-Pr)2N, Cy2MeN, 4-(dimethylamino)pyridine (DMAP), 2,6-lutadine, N-methylpyrrolidine (NMP), quinuclidine), l ,5-diazabicycl[4.3.0]non-5-ene (DBN), 1 ,5- diazabicyclo[5.4.0]undec-5-ene (DBU), ammonium salts (e.g. , ammonium hydroxide, tetramethyl ammonium hydroxide), alkali and alkaline earth carbonates, alkali and alkaline earth bicarbonates, alkali and alkaline earth hydroxides (e.g. , sodium hydroxide, potassium hydroxide), and alkali and alkaline earth hydrides, (e.g. , NaH, LiH, KH, K2C03, Na2C03, TI2CO3, Cs2C03, K(Oi-Bu), Li(Oi-Bu), Na(Oi-Bu) K(OPh), Na(OPh)). In some embodiments, the base is sodium metal, sodium hydride, potassium f-butoxide, sodium methoxide, potassium carbonate, sodium carbonate, cesium carbonate, or potassium hydroxide. In some embodiments, the base is cesium carbonate. In some embodiments, the base is potassium hydroxide. In some embodiments, the base is sodium hydroxide. In some embodiments, the base is potassium i-butoxide. In some embodiments, the base is tetramethyl ammonium hydroxide. It should be understood that an etherification reaction may also be conducted in the absence of a base.
One or more additives may be incorporated into the etherification reaction mixture to facilitate the reaction. In some cases, the etherification reaction may be performed in the presence of a catalyst. For example, the catalyst may be a salt, such as an ammonium salt. In some embodiments, the catalyst may be a tetraalkylammonium halide, such as, but not limited to, tetraethylammonium iodide. In some embodiments, the catalyst may be a phase transfer catalyst. As used herein, the term "phase transfer catalyst" refers to any species capable of facilitating the migration of a compound from a first phase into a second, different phase, for example, during the course of a chemical reaction. In some embodiments, the phase transfer catalyst enhances migration of a compound from one phase into a different phase, wherein a chemical reaction takes place. Some examples of phase transfer catalysts include, but are not limited to, benzyl triethylammonium chloride, tetrabutylammonium chloride, tetraethyl ammonium chloride, tetrabutylammonium sulfate, tetraoctylammonium sulfate, and tetramethyl ammonium hydroxide. The phase transfer catalyst may be used in combination with, for example, a base or other chemical reagent. In some embodiments, the reaction involves exposure to sodium hydroxide and a phase transfer catalyst, such as benzyl
triethylammonium chloride.
An etherification reaction may optionally be carried out in the presence of one or more solvents. The solvent may be, for example, an organic solvent (e.g. , toluene), an aqueous solvent, or a combination thereof. In some cases, the solvent may be a polar solvent (e.g. , polar protic solvents, polar aprotic solvents). Examples of polar solvents include, but are not limited to, acetone, ethyl acetate, dimethylformamide (DMF), dimethyl sulfoxide (DMSO), acetonitrile, alcohols, or combinations thereof. In one set of embodiments, the etherification reaction is performed in the presence of DMF. In one set of embodiments, the etherification reaction is performed in the presence of THF. In some cases, the etherification reaction may be performed in the presence of an ionic liquid. In some embodiments, the etherification reaction is performed in the absence of solvent. For example, the compound may be reacted in neat ethylene glycol.
In some cases, the components of an etherification reaction is heated or cooled to any temperature from about 0 °C to about 200 °C, for a period of time. In some embodiments, the solution is heated to a temperature from about 20 °C to about 100 °C, or from about 40 °C to about 70 °C In some cases, the solution may be heated to about 20 °C, about 30 °C, about 40 °C, about 50 °C, about 60 °C, about 70 °C, about 80 °C, or greater. In some embodiments, the etherification reaction mixture is maintained at about 20 °C. In some embodiments, the etherification reaction mixture is maintained at room temperature. In some embodiments, the etherification reaction mixture is heated to about 60 °C. In some embodiments, the etherification reaction mixture is heated to about 65 °C. The reaction may be heated/cooled/maintained at a particular temperature for a period of time, such as up to about 1 hour, about 2 hours, about 3 hours, about 4 hours, about 5 hours, about 10 hours, about 15 hours, about 20 hours, about 25 hours, about 30 hours, or more. In one set of embodiments, the reaction mixture is heated at about 65 °C for about 4 hours. In another set of embodiments, the reaction mixture is maintained at about 20 °C for about 18 hours. It should be understood that other temperatures and reaction times may also be used.
In some embodiments, the method involves a reduction reaction (e.g., see Figure 4, reduction of pyridazinone ester 18). The term "reduction reaction" is given its ordinary meaning in the art and refers to a chemical reaction in which the oxidation state of at least one atom is reduced. For example, the reduction reaction may involve reduction of an ester or a ketone to an alcohol. The reduction reaction may be carried out using reducing reagents known to those of ordinary skill in the art, including lithium aluminum hydride, lithium borohydride (with or without methanol additive), and diisobutylaluminum hydride (DIBAL-H) in a variety of solvents including
tetrahydrofuran, methyltetrahydrofuran, and dichloromethane. In one set of embodiments, the reduction reagent may be a 25% w/w solution of DIBAL-H in toluene, using 2-methyltetrahydrofuran as a cosolvent.
In some embodiments, the invention provides methods for the synthesis of a compound (e.g. , intermediate compound) comprising a leaving group. Leaving groups are described herein. In some embodiments, the leaving group is a halide, such as a bromide.
In some cases, the compound includes a moiety (e.g., hydroxyl) which may be readily converted into a leaving group. For example, the compound may include a hydroxyl group which is converted into a tosylate group upon reaction with p- toluenesulfonyl chloride. In other embodiments, a compound may include a hydroxyl group which may be treated with a phosphine (e.g. , triphenylphosphine, TPP) and diethylazodicarboxylate (DEAD) using Mitsunobu chemistry to form a leaving group.
In one set of embodiments, the method involves converting a hydroxyl group to a leaving group. For example, the method may involve replacing the hydroxyl group with a leaving group such as a halide (e.g. , bromide). In some embodiments, the compound substituted with a hydroxyl group is exposed to a halogenation reagent. In some cases, the halogenation reagent is a brominating reagent, such as phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine. In one set of embodiments, the brominating reagent is phosphorus tribromide.
A halogenation reaction may be performed in the presence of one or more solvents. In some embodiments, the solvent is an organic solvent, such as
dichloromethane, chloroform, benzene, or toluene. In one set of embodiments, the solvent used is dichloromethane.
In some cases, the halogenation reaction mixture is heated or cooled to any temperature ranging from 0 °C to about 200 °C, for a period of time. In some embodiments, the solution is heated to a temperature ranging from about 20 °C to about 100 °C. In some cases, the solution is heated to about 20 °C, about 30 °C, about 40 °C, about 50 °C, or greater, including temperatures in between. In some embodiments, the halogenation reaction mixture is maintained at 20 °C. The reaction may be
heated/cooled/maintained at a particular temperature for a period of time, such as up to 10 minutes, 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 10 hours, or more. In another set of embodiments, the reaction mixture is maintained at 20 °C for 30 minutes. It should be understood that other temperatures and reaction times may also be used. The synthesis of an imaging agent precursor may include other reactions, including ring-opening reactions, reduction reactions, protection/deprotection reactions, and the like.
After any reaction, the compounds (e.g. , intermediates, products) described herein may be subjected to one or more purification steps. Purification and isolation may be performed using methods known to those skilled in the art, including separation techniques like chromatography, or combinations of various separation techniques as are known the art. In some embodiments, column chromatography is used with silica or alumina as the stationary phase and a solvent, or mixture of solvents, as the eluent, to recover the product. In some cases, the eluent may include a mixture of a non-polar solvent and a polar solvent. For example, the eluent may include a mixture of heptane and ethyl acetate.
In some cases, the synthesis or a particular reaction may be conducted without need for purification. In some embodiments, a compound or intermediate may be purified using recrystallization, a process which may be repeated until the desired level of purity of the product is obtained. In one embodiment, the compound or intermediate is recrystallized at least once, two times, three times, or four or more times to achieve the desired level of purity. For example, the compound or intermediate may be obtained at a purity of greater than or equal to 50%, 80%, 85%, 90%, 95%, 97%, 98%, 98.5%, or 99.8%. Recrystallization may be achieved using a single solvent, or a combination of solvents. In some cases, recrystallization is achieved by dissolving the compound or intermediate in a solvent such as hexane at elevated temperatures, and then cooling the solution to produce a precipitate. In certain embodiments the compound is recrystallized from hexane.
Some embodiments may involve a ring-opening reaction. For example, a ring- opening reaction may be performed upon exposure of a compound comprising a ring to a nucleophile, optionally in the presence of a catalyst. In some embodiments, the nucleophile may be a hydride (e.g. , H"). In some embodiments, the ring-opening reaction may be performed in the presence of a metal-containing catalyst, such as zirconium chloride.
In some embodiments, the method involves reacting a compound comprising formula (V):
Figure imgf000065_0001
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted; and
R2 is hydrogen or halide,
with a nucleophile or a radical species to produce a compound comprising formula (VI),
Figure imgf000065_0002
Some embodiments involve exposure of the compound comprising formula (V) to a nucleophile. In some embodiments, the nucleophile is a hydride ion (e.g. , H"). In some cases, reacting the compound involves contacting the compound with
diisobutylaluminum hydride (DIBAL-H).
The ring-opening reaction may also occur via a radical reaction. For example, the compound comprising formula (V) may be exposed to a radical species, such as a hydrogen radical (e.g. , Η·), in order to produce the compound comprising formula (VI). In some embodiments, the radical species may be generated by a catalyst, such as Sml2.
In some embodiments, methods are provided for synthesizing a compound comprising formula (VI). For example, an etherification reaction is performed between compounds comprising formulae (Va) and (Vb):
Figure imgf000065_0003
to form a product comprising the formula:
Figure imgf000066_0001
wherein:
R1 is alkyl, optionally substituted; and
R2 is hydrogen or halide.
For example, an etherification reaction between compounds comprising the formulae:
Figure imgf000066_0002
forms a product comprising the formula:
Figure imgf000066_0003
This etherification reaction may be performed as described herein and may involve exposure to a base (e.g. , cesium carbonate, sodium hydroxide, tetramethyl ammonium hydroxide), optionally in the presence of a phase transfer catalyst. In some embodiments, the etherification reaction involves exposure to sodium hydroxide and benzyl triethylammonium chloride. In some cases, the etherification reaction is performed in the presence of a phase transfer catalyst and an ionic liquid.
In one set of embodiments, an etherification reaction between compounds comprising formu (Vb):
Figure imgf000066_0004
under Mitsunobu conditions (e.g. , PPI13 and DEAD) forms a product comprising the formula:
Figure imgf000067_0001
wherein R is alkyl, optionally substituted; and
R2 is hydrogen or halide.
For example, an etherification reaction between compounds comprising formulae:
Figure imgf000067_0002
under Mitsunobu conditions (e.g. , PPI13 and DEAD) forms a product comprising the formula:
Figure imgf000067_0003
Some embodiments may further involve the synthesis of a compound comprising formula (VII):
Figure imgf000067_0004
wherein Ra may be hydrogen, hydroxyl, halide (e.g. , chloride), O-alkyl, O-heteroalkyl, O-aryl, O-heteroaryl, S-alkyl, S-heteroalkyl, S-aryl, S-heteroaryl, alkyl, heteroalkyl, aryl, or heteroaryl, any of which may be optionally substituted. In some cases, Ra is O-alkyl such as O-methyl, O-ethyl, O-propyl, and the like. In some embodiments, Ra is O- methyl. For example, the method may involve the reaction of methyl 4-formyl benzoate with ethylene glycol in the presence of an acid to produce a compound comprising formula (VII). The compound comprising formula (VII) may be further reacted, for example, to install a leaving group on the compound. In some cases, the leaving group is a hydroxyl group. In one set of embodiments, Ra is methyl, and the carboxy group is treated with a reducing agent such as lithium aluminum hydride, sodium bis(2- methoxyethoxy)aluminum hydride or lithium borohydride to produce a benzylic alcohol.
Figure 5 shows an illustrative embodiment for synthesizing alcohol 15 using a ring-opening reaction. The first step involves the conversion of ether methyl 4-formyl benzoate or 4-formylbenzoic acid to the corresponding acetal through the reaction with ethylene glycol in the presence of an acid. In some embodiments, methyl 4-formyl benzoate and ethylene glycol are reacted in the presence of toluenesulfonic acid and toluene. The solvent may be heated at reflux, using azeotropic distillation to remove any water that is produced in order to drive the reaction to completion. The derived acid or ester 19 may then be reduced to benzyl alcohol 20 with lithium aluminum hydride, sodium bis(2-methoxyethoxy)aluminum hydride, lithium borohydride (e.g. , for an ester), or borane (e.g. , for an acid). In some cases, lithium aluminum hydride or sodium bis(2- methoxyethoxy) aluminum hydride may be used as the reducing agent. Benzyl alcohol 20 may then be reacted with dichloropyridazinone 11 via an etherification reaction as described herein to afford compound 21. For example, the etherification reaction may be carried out with cesium carbonate, potassium carbonate, or sodium hydroxide in the presence of a variety of phase transfer catalysis reagents, such as, but not limited to, benzyl triethylammonium chloride. In one set of embodiments, the etherification reaction involves the use of cesium carbonate in dimethylformamide. In another set of embodiments, the etherification reaction involves the use of sodium hydroxide with 1- 10% benzyl triethylammonium chloride in toluene.
The acetal ring of compound 21 may then be opened to the corresponding alcohol 15 using diisobutylaluminum hydride (DIBAL-H). In some cases, the ring-opening reaction may be carried out in the presence of a catalyst, such as a metal-containing catalyst (e.g. , zirconium chloride) or an organic catalyst (e.g. , 9-borabicyclononane (9- BBN) dimer).
In some cases, the components of the ring-opening reaction is heated or cooled to any temperature from about -78 °C to about 200 °C, for a period of time. In some embodiments, the reaction mixture may be maintained at any temperature from about -78 °C to about room temperature. In some cases, the reaction mixture may be maintained at about -60 °C, about -50 °C, about -40 °C, about -30 °C, about -20 °C, about - 10 °C, about 0 °C, including all temperatures in between, or greater. In some embodiments, the ring- opening reaction mixture may be maintained at -40 °C. In some embodiments, the ring- opening reaction mixture may be maintained at room temperature. The reaction may be heated/cooled/maintained at a particular temperature for a period of time, such as about 10 minutes, about 30 minutes, about 1 hour, about 2 hours, about 3 hours, about 4 hours, about 5 hours, about 10 hours, or any amount of time in between, or more. In another set of embodiments, the reaction mixture may be maintained at about -40 °C for about 1 hour. It should be understood that other temperatures and reaction times may also be used.
Purification of compound 16 may be performed by successive recrystallizations from cumene and/or isobutyl acetate. For example, see Example 37E.
Using the method shown in Figure 6, the overall yield for synthesizing alcohol 15 starting from methyl 4-formylbenzoate may be at least 10%, at least 20%, at least 30%, at least 40%, or at least 50%, without or with the use of chromatography for purification. In some cases, the overall yield for synthesizing alcohol 15 starting from methyl 4- formylbenzoate is approximately 50%, without the use of chromatography for purification.
Any of the methods for synthesizing an imaging agent precursor described herein may further comprise the act of exposing the compound comprising formula (VIII):
Figure imgf000069_0001
with a reagent comprising a leaving group to form a compound comprising formula (IX):
Figure imgf000069_0002
wherein W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide; and
L is a leaving group.
In some cases, the reagent is a sulfonate-containing species and the leaving group is a sulfonate-containing group (e.g. , a sulfonate-containing precursor of an imaging agent). In some embodiments, the sulfonate-containing group is mesylate, tosylate, or triflate. In one set of embodiments, the sulfonate-containing group is tosylate. Additional examples of leaving groups are described herein.
For example, the act of exposing the compound comprising the formula:
Figure imgf000070_0001
to a reactant comprising a leaving group forms a product comprising the formula:
Figure imgf000070_0002
wherein R1, R2, and L are as described herein.
In one embodiment, exposure of a compound comprising the formula:
Figure imgf000070_0003
to a reactant comprising a tosylate group forms the product comprising the formula:
Figure imgf000070_0004
Some embodiments for synthesizing an imaging agent precursor described herein provide novel compounds (e.g. , intermediates). In some embodiments, the compound comprises the structure:
Figure imgf000071_0001
Exemplary Methods and Applications of Imaging agents
In some embodiments, the present invention relates to methods of imaging, including methods of imaging in a subject that includes administering a composition or formulation that includes imaging agent 1 to the subject by injection, infusion, or any other known method, and imaging a region of the subject that is of interest. As described herein, (2-i-butyl-4-chloro-5-[4-(2-(18F)fluoroethoxymethyl)-benzyloxy]-2H-pyridazin- 3-1, or imaging agent 1,
Figure imgf000071_0002
Imaging agent 1 binds to the mitochondrial complex I of the electron transport chain with high affinity. Imaging agent 1 shows selective uptake to the heart due to the high density of mitochondria in the myocardium. Regions of interest may include, but are not limited to, the heart, cardiovascular system, cardiac vessels, blood vessels (e.g. , arteries, veins) brain, and other organs. A parameter of interest, such as blood flow, cardiac wall motion, etc., can be imaged and detected using methods and/or systems of the invention. In some aspects of the invention, methods for evaluating perfusion, including myocardial perfusion, are provided.
In some embodiments, methods of the present invention include (a) administering to a subject a composition that includes imaging agent 1, and (b) acquiring at least one image of at least a portion of the subject. In some cases, acquiring employs positron emission tomography (PET) for visualizing the distribution of imaging agent 1 within at least a portion of the subject. As will be understood by those of ordinary skill in the art, imaging using methods of the invention may include full body imaging of a subject, or imaging of a specific body region or tissue of the subject that is of interest. For example, if a subject is known to have, or is suspected of having myocardial ischemia, methods of the invention may be used to image the heart of the subject. In some embodiments, imaging may be limited to the heart, or may include the heart and its associated vascular system.
In some embodiments of the invention, methods of diagnosing or assisting in diagnosing a disease or condition, assessing efficacy of treatment of a disease or condition, or imaging in a subject with a known or suspected cardiovascular disease or condition are provided. A cardiovascular disease can be any disease of the heart or other organ or tissue nourished by the vascular system. The vascular system includes coronary arteries, and all peripheral arteries supplying nourishment to the peripheral vascular system and the brain, as well as veins, arterioles, venules, and capillaries. Examples of cardiovascular diseases include diseases of the heart, such as coronary artery disease, myocardial infarction, myocardial ischemia, angina pectoris, congestive heart failure, cardiomyopathy (congenital or acquired), arrhythmia, or valvular heart disease. In some embodiments, the methods disclosed herein are useful for monitoring and measuring coronary artery disease and/or myocardial perfusion. For example, a method described herein can determine the presence or absence of coronary artery disease and/or the presence or absence of myocardial infarct. Conditions of the heart may include damage, not brought on by disease but resulting from injury - e.g. , traumatic injury, surgical injury. In some cases, methods of the invention may include determining a parameter of, or the presence or absence of, myocardial ischemia, rest (R) and/or stress (S) myocardial blood flows (MBFs), coronary flow reserve (CFR), coronary artery disease (CAD), left ventricular ejection fraction (LVEF), end-systolic volume (ESV), end-diastolic volume (EDV), and the like.
In some cases, a subject to whom a method of the invention is applied, may have signs or symptoms suggestive of myocardial ischemia or myocardial infarction. In some cases methods of the invention can be used to identify early or pre-disease conditions that indicate that a subject is at increased risk of a disease. In some instances, methods of the invention can be used to determine a subject's risk of future cardiac events such as myocardial infarction or cardiac death. Imaging methods of the invention can be used to detect myocardial ischemia in subjects already diagnosed as having a myocardial ischemia disorder or condition, or in subjects that have no history or diagnosis of such a condition. In other instances, methods of the invention can be used to obtain measurements that provide a diagnosis or aid in providing a diagnosis of a myocardial ischemia disorder or condition. In some instances, a subject may be already be undergoing drug therapy for a myocardial ischemia disorder or condition, while in other instances a subject may not be undergoing therapy for myocardial ischemia. In some embodiments, methods of the invention can be used to assess efficacy of a treatment for a disease or condition. For example, the heart can be visualized using imaging agents of the invention before, during, and/or after treatment of a condition affecting the heart of a subject. Such visualization may be used to assess a disease or condition, and aid in selection of a treatment regimen, e.g. therapy, surgery, medications, for the subject.
A PET imaging agent may have a high first-pass extraction fraction and can track regional myocardial blood flow over a wide range. These features may permit detection of milder decreases in coronary flow reserve and accurate estimation of absolute myocardial blood flow (MBF). PET imaging agents of the invention provide these and other features and are also available as a unit dose from regional PET radiopharmacies, obviating the need for on-site cyclotrons or costly Rb-82 generators.
In some embodiments of the invention, imaging agent 1 is used as an imaging agent in combination with positron emission tomography (PET) or with other imaging methods including, but not limited to SPECT imaging. In some embodiments of the invention, imaging agent 1 is administered to a subject and imaged in the subject using PET. As will be known to those of ordinary skill in the art, PET is a non-invasive technique that allows serial images and measurements to be obtained in a single subject over a time period. PET imaging used in methods of the invention may be carried out using known systems, methods, and/or devices. In some embodiments of the invention, PET imaging is conducted using a cardiac imaging system. A cardiac imaging system may include PET imaging functionality and a control unit configured to drive the imaging functionality to perform a PET imaging procedure on a portion of the subject before, during, and/or after administration of imaging agent 1 to the subject. In some cases, the control unit is configured to drive the imaging functionality to perform a PET imaging procedure. The control unit may comprise a computer system and/or software. In such a case, the computer system may be programmed or configured to execute the required methods for acquiring and/or analyzing the images. Further, the system may include a data storage device that is readable by a machine, embodying a set of instructions executable by the machine to perform the required methods of acquiring and/or analyzing the images.
The useful dosage of the imaging agent to be administered and the particular mode of administration will vary depending upon such factors as age, weight, and particular region to be imaged, as well as the particular imaging agent used, the diagnostic use contemplated, and the form of the formulation, for example, suspension, emulsion, microsphere, liposome, or the like, as described herein, and as will be readily apparent to those skilled in the art.
In some embodiments, an imaging agent is administered at a low dosage and the dosage increased until the desirable diagnostic effect is achieved. In one embodiment, the above-described imaging agents may be administered by intravenous injection, usually in saline solution, at a dose of about 0.1 to about 100 mCi per 70 kg body weight (and all combinations and subcombinations of dosage ranges and specific dosages therein), or between about 0.5 and about 50 mCi, or between about 0.1 mCi and about 30 mCi, or between 0.5 mCi and about 20 mCi. For use as nuclear medicine imaging agents, the imaging agents, dosages, administered by intravenous injection, may range from about 0.1 pmol/kg to about 1000 pmol/kg (and all combinations and
subcombinations of dosage ranges and specific dosages therein), and in some embodiments, less than 150 pmol/kg.
Imaging systems and components thereof will be known to those of ordinary skill in the art. Many imaging systems and components (e.g. , cameras, software for analyzing the images, etc.) are known and commercially available, for example, a Siemens Biograph-64 scanner. Any technique, software, or equipment that reduces or eliminates motion in static perfusion images may be used in methods of the invention, because spatial blurring and artifacts can be caused by patient motion during image acquisition. In some embodiments of the invention, images may be acquired in list mode, and may be static, dynamic, or gated images. An appropriate period of time for acquiring images can be determined by one of ordinary skill in the art, and may vary depending on the cardiac imaging system, the imaging agent (e.g. , amount administered, composition of the imaging agent, subject parameters, area of interest). As used herein a "period of acquiring images" or an "image acquisition period" may be a period of obtaining a single continuous image, or may be a period during which one or more individual discrete images are obtained. Thus, a period of image acquisition can be a period during which one or more images of one or more regions of a subject are acquired.
In some embodiments of the invention, a period of image acquisition after administration of an imaging agent of the invention to a subject may be between about 30 seconds and about 60 minutes, between about 1 minute and about 30 minutes, between about 5 minutes and about 20 minutes, or at least about 1 minute, about 3 minutes, about 5 minutes, about 6 minutes, about 7 minutes, about 8 minutes, about 9 minutes, about 10 minutes, about 15 minutes, about 20 minutes, about 30 minutes, 4 about 5 minutes, about 60 minutes, or greater. For example, in a rest/stress imaging protocol there would be at least two periods of image acquisition with at least one corresponding to the rest segment and least one corresponding to the stress segment. In some embodiments, imaging may be continuous over the imaging period of time, or images may be acquired at intervals such as in periodic or gated imaging.
In some aspects of the invention, gated acquisition is used to acquire images from a subject to whom an imaging agent prepared by methods of such as imaging agent 1 has been administered. Gated imaging can be used in various aspects of the invention, and for example, may provide images of a beating heart of a subject and may be used to attain a functional evaluation of how well a heart is beating. Gated imaging can be performed by acquiring separate images from the subject at specific intervals during a period of image acquisition. A non-limiting example of gated imaging is a case when a period of image acquisition is about 10 minutes long, and images are acquired at repeated intervals during the 10 minute period. The frequency of acquisition of images during the period can be set by the operator, for example, the frequency can be at least every about 1 msec, about 5 msec, about 10 msec, about 20 msec, about 50 msec, about 100 msec, about 125 msec, about 250 msec, or more. The length of the interval is set by the operator to be triggered by an event, such as a cardiac R wave, with the length of the interval is defined by the number of time bins desired per R wave to R wave interval. Those of skill in the art will be familiar with the concept and methods of gated image acquisition and can use known methods to obtain gated images using imaging agent 1 as an imaging agent.
Image acquisition in gated imaging can be triggered at specific intervals, for example, image acquisition can be triggered using an EKG of the heart. In a non- limiting example, an R wave-gated scanner may trigger acquisition of an image and the mean length of time between one R wave of a heart and the next can be stored. The number of images to collect can then be determined. For example, a first image can be acquired at 125 msec, a second image can be acquired at 250 msec, a third image can be acquired at 375 msec, etc. - thus images in that R interval may be acquired at 125 msec intervals. When the next R interval begins, the collection of images resets and image data is then acquired into the "first" image at 125 msec from that R interval start time, and then into the "second" image collected 250 msec from that R interval start time, etc. Thus, within each R interval image acquisition is added into the initial image of the series and incremented into successive images in the series so that a sequence of images can be collected at a desired frequency with the zero time being reset at the start of each R interval. Acquired gated images can be used to provide an image of heart motion and can provide information on heart wall thickness, whether or not one or more sections of the heart are not moving or beating (e.g. a wall motion defect). Use of gated imaging may provide data with which to judge perfusion of the heart, such as ejection fraction, and to visualize and identify reduced, absent, paradoxical or asynchronous wall motion. Use of gated imaging may also provide data with which to improve assessment of myocardial perfusion, judge cardiac function and to visualize and identify asynchronous wall motion.
In some cases, PET imaging may be used to assess myocardial viability via the ability of this technique to demonstrate metabolic consequences of myocardial ischemia. Using PET imaging, myocardial segments that are likely to improve after
revascularization can be identified. In some cases, PET imaging may be used in the detection of coronary artery disease and can also serve as an alternative test for subjects who cannot undergo treadmill exercise stress testing. In some embodiments, a stress test method (e.g. , pharmacological stress, exercise stress) may be employed with PET using methods of the invention to qualitatively or quantitatively assess one or more parameters of cardiac function during infusion of the imaging agent. Agents for, and methods of, inducing stress, for example, using exercise or pharmacological stress are well known in the art. Suitable induction of stress can be carried out using established, known agents and methods. Functions usefully measured using methods of the invention include, but are not limited to, in various embodiments, imaging of myocardial perfusion, imaging, or measurement of ventricular function, and measuring coronary blood flow velocity.
In some cases, methods for imaging the heart of a subject may include administering a first dose of imaging agent 1 to the subject while the subject is at rest, acquiring at least one first image of the heart, followed by subjecting the subject to stress (e.g. , exercise stress or pharmacological stress) and administering a second dose of imaging agent 1 to the subject during the period of stress, and acquiring at least one other image of the heart.
In some embodiments, the dose of imaging agent 1 to be used during exercise- induced stress in a rest/stress protocol is greater than that necessary for
pharmacologically-induced stress with the ratio of exercise-induced stress dose to pharmacologically-induced stress dose being greater then or equal to about 1.2, about 1.3, about 1.4, about 1.5, about 1.6, about 1.7, about 1.8, about 1.9, or greater. With respect to pharmacological stress, in some embodiments of the invention that involve rest/stress imaging methods, the dose of imaging agent 1 administered for imaging during the pharmacological stress is a minimum of two times the dose of imaging agent 1 administered for imaging at rest. With respect to exercise stress, in some embodiments of the invention that involve rest/stress imaging methods, the dose of imaging agent 1 administered for imaging during the exercise-induced stress is a minimum of three times the dose of imaging agent 1 administered for imaging at rest. In some embodiments of the invention, for imaging first at rest followed by imaging with stress, the dose of imaging agent 1 administered at rest will be lower than the dose of imaging agent 1 administered at stress.
In some cases, imaging methods of the invention may be completed in a single day (e.g. , less than about 24 hours, less than about 12 hours, less than about 6 hours, less than about 4 hours, less than about 2 hours, less than about 1 hour), as described herein. In other cases, methods may be completed in longer periods of time, e.g. over more than about 24 hours, about 36 hours, or about 48 hours.
Imaging agent 1 may be provided in any suitable form, for example, in a pharmaceutically acceptable form. In some cases, imaging agent 1 is included in a pharmaceutically acceptable composition. In some embodiments, imaging agent 1 is provided as a composition comprising ethanol, sodium ascorbate, and water. In some cases, the composition comprises less than 20 weight ethanol, less than 15 weight ethanol, less than 10 weight ethanol, less than 8 weight ethanol, less than 6 weight ethanol, less than 5 weight ethanol, less than 4 weight ethanol, less than 3 weight ethanol, or less ethanol. In some cases, the composition comprises less than 100 mg/mL, less than 75 mg/mL, less than 60 mg/mL, less than 50 mg/mL, less than 40 mg/mL, less than 30 mg/mL, or less sodium ascorbate in water. In a particular non-limiting embodiment, imaging agent 1 is provided as a solution in water comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water.
An imaging agent 1 composition for injection may be prepared in an injection syringe. Imaging agent 1 may be prepared by a radiopharmacy (e.g. , using the methods described herein) and/or a PET manufacturing center and provided to a health-care professional for administration. In some aspects of the invention, imaging agent 1 is provided, for example, in a syringe or other container, with < 50 mg/mL sodium ascorbate in water, < 4 wt ethanol, and about 1 to 14 mCi of imaging agent 1. The amount of imaging agent 1 may vary depending on whether a rest or stress dose is being administered. For example, a higher amount of imaging agent 1 may be provided in a syringe or container for use in a stress dose administration than provided in a syringe for use in a rest administration. A dose of imaging agent 1 may be diluted with saline (e.g. , as described herein), if needed to obtain a practical dose volume. For example, if the activity concentration of imaging agent 1 is so high that only 0.1 mL is need for an appropriate dose for a subject, the solution can be diluted, e.g. , with sterile saline, so the syringe contains 0.5 ml to 4 or more ml of an imaging agent 1 solution for
administration. In some embodiments of the invention, an injection volume for imaging agent 1 is between 0.5 and 5 ml, 1 and 4 ml, 2 and 3 ml, at least 0.5 ml, 1 ml, 2 ml, 3 ml, 4 ml, 5 ml, 6 ml, 7 ml, 8 ml, 9 ml, 10 ml, or more. Those of skill in the art will recognize how to dilute imaging agent 1 to produce a sufficient dose volume for administration. In some aspects of the invention, imaging agent 1 is provided in a container such as a vial, bottle, or syringe, and may be transferred, as necessary, into a suitable container, such as a syringe for administration.
Syringes that include an adsorbent plunger tip may result in 10 to 25% of imaging agent 1 activity remaining in the syringe after injection. Syringes lacking an adsorbent plunger tip may be used, such as a 3 or 5 mL NORM-JECT (Henke Sass Wolf, Dudley, MA) or other equivalent syringe lacking an adsorbent plunger tip. Reduction of adsorption in the syringe can increase the amount of imaging agent 1 that is transferred from the syringe and administered to the subject in methods of the invention. A syringe used in methods of the invention may comprise imaging agent 1 , and be a non-adsorbing, or reduced adsorbent syringe. In some embodiments a non-adsorbent or reduced- adsorbent syringe is a syringe that has been coated or treated to reduce imaging agent 1 adsorption. In some embodiments, a non-adsorbent or reduced-adsorbent syringe is a syringe that lacks an adsorbent plunger tip. In some embodiments, a syringe used in conjunction with the invention adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11 %, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1 %, or 0.5% of imaging agent 1 it contains. In certain aspects of the invention, a syringe that contains imaging agent 1 does not include a rubber or latex tip on the plunger. In some cases a syringe used in methods of the invention, includes a plunger that adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11 %, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of imaging agent 1 that the syringe contains. A syringe of the invention may also comprise sodium ascorbate, ethanol, and water, and certain embodiments of the invention include a syringe containing imaging agent 1 in a solution comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water. A syringe of the invention may be a syringe that is latex free, rubber free, and/or lubricant free. A syringe of the invention may contain imaging agent 1 in an amount between about 1.5 and about 14 mCi. A syringe of the invention may contain about 20 mCi or less of imaging agent 1.
Components of a composition comprising imaging agent 1 may be selected depending on the mode of administration to the subject. Various modes of
administration that effectively deliver imaging agents of the invention to a desired tissue, cell, organ, or bodily fluid will be known to one of ordinary skill in the art. In some embodiments, the imaging agent is administered intravenously (e.g. , intravenous bolus injection) using methods known to those of ordinary skill in the art. As used herein, a dose that is "administered to a subject" means an amount of the imaging agent, e.g. imaging agent 1, that enters the body of the subject. In some embodiments, due to factors such as partial retention of imaging agent such as imaging agent 1 in a syringe, tubing, needles, catheter, or other equipment used to administer the imaging agent to a subject, the amount of an imaging agent such as imaging agent 1 that is measured or determined to be in the a syringe or other equipment prepared for administration may be more than the amount in the dose that is administered to the subject. In some
embodiments, an injection of an imaging agent is followed by a flushing injection of normal saline, into the subject, using the same tubing, needle, port, etc. , used for administration of imaging agent 1. Flushing may be performed immediately following administration of imaging agent 1, or up to 1 min, 2 min, 3 min, 5 min, or more, after the administration. The volume of saline or other agent for flushing may be up to 5 ml, 6 ml, 7 ml, 8 ml, 9 ml, 10 ml, 15 ml, 20 ml, or more. As will be understood by those of ordinary skill in the art, in embodiments where imaging agent 1 is administered using a syringe or other container, the true amount of imaging agent 1 administered to the subject may be corrected for any imaging agent 1 that remains in the container. For example, the amount of radioactivity remaining in the container, and tubing and needle or delivery instrument that carried the imaging agent from the container and into the subject can be determined after the imaging agent has been administered to the subject and the difference between the starting amount of radioactivity and the amount remaining after administration indicates the amount that was delivered into the subject. In some cases, the container or injection device (e.g. , catheter, syringe) may be rinsed with a solution (e.g. , saline solution) following administration of imaging agent 1.
In some embodiments of the invention, the total amount of imaging agent 1 administered to a subject over a given period of time, e.g., in one session, is less than or equal to about 50 mCi, less than or equal to 40 mCi, less than or equal to 30 mCi, less than or equal to 20 mCi, less than or equal to 18 mCi, less than or equal to 16 mCi, less than or equal to 15 mCi, less than or equal to 14 mCi, less than or equal to 13 mCi, less than or equal to 12 mCi, less than or equal to 10 mCi, less than or equal to 8 mCi, less than or equal to 6 mCi, less than or equal to 4 mCi, less than or equal to 2 mCi, less than or equal to 1 mCi, less than or equal to 0.5 mCi. The total amount administered may be determined based on a single dose or multiple doses administered to a subject within a given time period of up to 1 minute, 10 minutes, 30 minutes, 1 hour, 2 hours, 6 hours, 12 hours, 24 hours, 48 hours, or more.
Based on radiation dose studies, the desirable maximum dose administered to a subject may be based on determining the amount of imaging agent 1 which limits the radiation dose to about 5 rem to the critical organ and/or about 1 rem effective dose (ED) or lower, as will be understood by those of ordinary skill in the art. In a particular embodiment, the desirable maximum dose or total amount of imaging agent 1 administered is less than or equal to about 25 mCi, or less than or equal to about 14 mCi over a period of time of up to 30 min, 1 hour, 2 hours, 6 hours, 12 hours, 24 hours, 48 hours, or more. In some embodiments, the maximum dose of imaging agent 1 administered to a subject may be less than 3.5 μg per 50 kg of body weight per day. That is, in some embodiments of the invention, the maximum dose of imaging agent 1 administered to a subject may be less than about 0.07 μg of imaging agent 1 per kg of body weight per day.
In some embodiments, methods of the invention include administering to a subject a first dose (e.g. , rest dose) of imaging agent 1 while the subject is at rest, and performing a first PET imaging procedure (e.g. , a PET rest imaging procedure) and acquiring at least a first image of a portion of a subject. In some cases, after
administering an imaging agent such as imaging agent 1 while the subject is at rest, the subject may be subjected to stress and during the stress a second dose (e.g. , stress dose) of an imaging agent such as imaging agent 1 is administered to the subject, and a second PET imaging procedure (e.g. , a PET stress imaging procedure) is performed on the subject and at least one other image of a portion of the subject may be acquired. The above is an example of a method that may be referred to as a rest-stress test. The time between the completion of the first PET imaging procedure and administration of the second imaging agent dose is referred to as the wait time. In some cases, a rest-stress test may be completed in a period of time of less than 48 hours, less than 36 hours, less than 24 hours, less than 12 hours, less than 6 hours, less than 5 hours, less than 4 hours, less than 3 hours, less than 2 hours, less than 1 hour, less than 30 minutes, or less.
In some embodiments, the amount of imaging agent 1 administered in a first dose to a subject at rest (e.g. , rest dose in a rest-stress test) is between about 1 mCi and about 5 mCi, between about 2 mCi and about 4 mCi, between about 2.5 mCi and about 3.5 mCi, or about 3 mCi. Following administration of the first dose of imaging agent 1 , a PET imaging procedure may be performed and at least one first image may be acquired of at least a portion of the subject.
In some cases, the amount of imaging agent 1 administered to a subject during stress may be based on the amount of imaging agent 1 administered to the subject at rest. That is, the dosing during stress may be based, at least in part, on a dosing ratio (DR) (e.g. , ratio of stress-dose to rest-dose). The DR may depend on numerous factors as will be known to those of ordinary skill in the art, and in some cases, may depend on the method of inducing stress in the subject. In some cases, the DR is between 1 and 5, between 1 and 4, between 1 and 3, between 2 and 5, or between 2 and 4. In some cases, the DR is at least 1, at least 1.5, at least 2, at least 3, at least 4, or at least 5. In some cases, the DR is between 2.5 and 5.0, or 2.5 and 4.0, or 3.0 and 4.0, or 3.0 and 5.0 times greater than the first dose of the imaging agent. In some cases, the DR required for a subject subjected to exercise stress is more than the DR and/or time interval used for a subject subjected to pharmacological stress. This may be due, in part, to a lower net myocardial uptake of radioactivity with exercise. In some cases, the DR employed for a subject subjected to exercise stress is between 2 and 4, between 2.5 and 3.5, or at least 3.0, at least 3.5, at least 4.0, or more, in embodiments wherein the wait time is at least 15 minutes 30 minutes, 1 hour, 1.5 hours, 2 hours, or the like. In some cases, the DR employed for a subject subjected to pharmacological stress is between 1 and 3, or between 1.5 and 2.5, or at least 2.0, at least 2.2, or at least 2.5, or more, in embodiments wherein the wait time is at least 15 minutes, 30 minutes, 1 hour, 1.5 hours, 2 hours, or the like. In a particular embodiment, for a subject subjected to pharmacological stress, a DR of at least 2.2 for a wait time of at least 15 minutes or at least 30 minutes is employed, and/or for a subject subjected to exercise stress, a DR of at least 3.0 for a wait time of at least 30 minutes or at least 1 hour is employed.
In some cases, the imaging agent is between about 2.0 mCi and about 3.5 mCi, or
2.4 mCi to about 2.9 mCi, or between about 2.5 mCi to about 3.0 mCi, or between about
2.5 mCi and about 3.5 mCi.
In a particular embodiment, for pharmacological stress (e.g. , vasodilator stress induced by administration of adenosine or regadenoson), a dose of about 2.9 mCi to about 3.4 mCi rest is provided during rest, and a dose of about 2.0 to about 2.4 times the rest dose is provided during stress, with a wait time of at least about 15 minutes or at least about 30 minutes. In some cases, the second dose of the imaging agent is between about 5.7 mCi and about 6.2 mCi, or between about 6.0 mCi and about 6.5 mCi, and about 5.7 mCi and about 6.5 mCi.
In another embodiment, for exercise stress, a dose of about 1.7 mCi to about 2.0 mCi is provided during rest, and a dose of about 3.0 to about 3.6 times the rest dose is provided during stress, with a wait time of at least about 30 minute or at least about 60 minutes. In some cases, the second dose of the imaging agent is between about 8.6 mCi and about 9.0 mCi, or between about 9.0 and about 9.5 mCi, or between about 8.6 mCi and about 9.5 mCi.
In another embodiment, for pharmacological stress, a dose of between about 2.4 mCi and about 2.9 mCi is administered during rest, and a dose between about 5.7 mCi and about 6.2 mCi is administered during stress (e.g. , DR of at least about 2), wherein the wait time is at least about 15 minutes or at least about 30 minutes. In another embodiment, for exercise stress, a dose of between about 1.7 mCi and about 2.0 mCi is administered during rest, and a dose of between about 8.6 mCi and about 9.0 mCi is administered during stress (e.g. , DR at least about 3), wherein the wait time is at least 30 minutes or at least 60 minutes.
In a particular embodiment, for pharmacological stress, a dose of about 2.9 mCi to about 3.3 mCi rest is provided during rest, and a dose of 2.0 to 2.4 times the rest dose is provided during stress, with a wait time of at least 15 minutes or at least 30 minutes. In another embodiment, for exercise stress, a dose of about 2.9 mCi to about 3.3 mCi is provided during rest, and a dose of 3.0 to 3.6 times the rest dose is provided during stress, with a wait time of at least 30 minute or at least 60 minutes.
In yet another embodiment, for pharmacological stress, a dose of about 2.5 mCi to about 3.0 mCi rest is provided during rest and a dose about 6 mCi to about 6.5 mCi is provided during stress. In still yet another embodiment, for exercise stress, a dose of about 2.5 mCi to about 3.0 mCi rest is provided during rest and a dose about 9 mCi to about 9.5 mCi is provided during stress.
In some embodiments, administering during the stress includes beginning administering the second dose within a period of time after completing the rest imaging procedure (e.g. , the wait period). In some cases, the second dose may be administered at a period of time of at least 5 minutes, 10 minutes, 15 minutes, 20 minutes, 30 minutes, 40 minutes, 45 minutes, 50 minutes, 60 minutes, 70 minutes, 80 minutes, 90 minutes, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours, or greater, after completing the rest imaging procedure. In some cases, the second dose is administered at a time period of between 5 minutes and 30 days, between 5 minutes and 20 days, between 5 minutes and 10 days, between 5 minutes and 5 days, between 5 minutes and 4 days, between 5 minutes and 3 days, between 5 minutes and 48 hours, between 5 minutes and 24 hours, between 5 minutes and 12 hours, between 5 minutes and 2 hours, between 5 minutes and 90 minutes, between 10 minutes and 60 minutes after completing the rest imaging procedure.
For stress testing in methods of the invention, a subject may be subjected to stress using procedures known to those of ordinary skill in the art. In some cases, the subject may be subjected to stress using procedures including exercise stress and/or
pharmacological stress. Pharmacological stress may be induced by administering to the subject a pharmacological agent such as a vasodilator. Examples of useful
pharmacological stress agents, include, but are not limited to adenosine, dobutamine, dipyridamole, regadenoson, binodeneson, apadeneson, and other adenosine A2a receptor agonists. Dosing and administration of pharmacological stress inducing agents, such as vasodilators, are well known in the art and can be determined for use in conjunction with methods and systems of the invention. Exercise stress may be induced using a treadmill, exercise bicycle, hand crank, or other equipment suitable to increase a subject's heart rate through increased exertion.
In some embodiments of the invention a rest/stress method is followed. In a rest/stress method a period of rest and imaging is followed by a period of stress and imaging, with the order being rest first, followed by stress. In certain embodiments of the invention, a stress/rest method may be used. In a stress/rest method, a period of stress and imaging is followed by a period of rest and imaging, with the order being stress first, followed by rest. In some aspects of the invention, imaging agent 1 can be used in a "stress only" method, in which stress is induced in a subject for imaging with imaging agent 1 with no rest imaging during the subject session. In some embodiments of the invention, imaging agent 1 can be used in a "rest only" method, in which a subject does not undergo stress induction, but is only imaged with imaging agent 1 at rest in that session.
Exemplary Cassettes and Reaction Systems In some embodiments, systems, methods, kits, and cassettes are provided for the synthesis of an imaging agent (e.g., imaging agent 1). In some embodiments, an imaging agent may be prepared using an automated reaction system comprising a disposable or single use cassette. The cassette may comprise all the non-radioactive reagents, solvents, tubing, valves, reaction vessels, and other apparatus and/or components necessary to carry out the preparation of a given batch of imaging agent. The cassette allows the reaction system to have the flexibility to make a variety of different imaging agents with minimal risk of cross-contamination, by simply changing the cassette. By the term "cassette" is meant a piece of apparatus designed to fit removably and interchangeably onto automated reaction systems, in such a way that mechanical movement of moving parts of the automated reaction system controls the operation of the cassette from outside the cassette, ie., externally. In certain embodiments, a cassette comprises a linear arrangement of valves, each linked to a port where various reagents, cartridges, syringes, and/or vials can be attached, by either needle puncture of a septum-sealed vial, or by gas- tight, marrying joints. Each valve may have a male-female joint which interfaces with a corresponding moving arm of the automated synthesizer. External rotation of the arm can control the opening or closing of the valve when the cassette is attached to the automated reaction system. Additional moving parts of the automated reaction system are designed to clip onto syringe plunger tips, and thus raise or depress syringe barrels. An automated reaction system may further include a controller and one or more controllable valves in electrical communication with the controller. An automated reaction system may also include additional vessels, valves, sensors, heaters, pressurizing elements, etc. , in electrical communication with the controller. An automated reaction system may be operated by a controller using suitable software for control of valve openings and closings, heating, cooling, pressure levels, fluid movement, flow rate, etc. The automated reaction system may optionally include a computer operating system, software, controls, etc., or other component. In addition, the automated reaction system may comprise a mount for the cassette.
Examples of automated reaction systems (e.g. , a nucleophilic reaction system), include, but are not limited to, the Explora GN or RN synthesis system (Siemens Medical Solutions USA, Inc.), GE-Tracerlab-MX synthesis system (GE Healthcare), Eckert & Zeigler Modular- Lab Synthesis system, etc. , which are commonly available at PET manufacturing facilities. The automated reaction systems may carry-out numerous steps, as outlined in Figure 6, including, but not limited to, preparation of the 18F fluoride species, providing an imaging agent precursor, optionally in a solution (e.g. , as described herein, for example, imaging agent precursor 1 in acetonitrile), a radiolabeling reaction (e.g. , reaction of the 18F species and the imaging agent precursor to form the imaging agent) optionally in a synthesis module, purification (e.g. , by preparative HPLC), solvent exchange (e.g. , by SepPak), aseptic filtration, and release into a container. For example, see Examples 9, 10, and 11.
In some embodiments, the automated reaction system may make use of a cassette comprising a reaction module in fluid connection with a purification module and/or a formulation module. Figures 7 and 8 show schematic representations of cassettes in connection with exemplary reaction systems for synthesizing an imaging agent comprising a reaction module, a purification module, and/or a formulation module.
For example, the reaction module may include a reaction chamber in which conversion of the imaging agent precursor to the imaging agent is performed. The reaction module may include a source of a fluoride species (e.g. , 18F), a source of the imaging agent precursor, a source of an additive (e.g. , salt additive), and other sources of additional components such as solvents, each of which may optionally be fluidly connected to the reaction chamber. The reaction module may also comprise an anion exchange column for purification of the fluoride species, prior to introduction into the reaction chamber.
Upon reaction, the resulting imaging agent product is transferred from the reaction module to the purification module for further processing, treatment, and/or purification. The purification module may include, for example, a column (e.g. , an HPLC column) fluidly connected to one or more sources of solvents to be used as eluents. The purification module may further comprise a source of a stabilizing agent (e.g. , ascorbic acid or a salt thereof), which may be added to the imaging agent upon purification (e.g. , by HPLC). The purified imaging agent is then transferred to the formulation module, where further purification and formulation may be performed. The formulation module may include a filter for aseptic filtration and/or a C- 18 column for solvent exchange.
In another embodiment, a cassette comprises a reaction module and a formulation module. A reaction module of the invention may include a source of 18F, a filter to remove unreacted [ 0]H20, a source of an ammonium salt, a source for a diluent for the 18F, a source for an imaging agent precursor, {e.g. , imaging agent precursor 1 shown in Figure 1, or other imaging agent precursor), a source for an ¾0 diluent for the imaging agent precursor, a reaction vessel for reacting the 18 F and the imaging agent precursor, a solid phase extraction column (e.g., a CI 8 column, or other suitable column) in fluid communication with the reaction vessel. The solid phase extraction column includes a solid sorbent to adsorb the radiolabeled imaging agent product on the sorbent. At least a portion of the residual reaction impurities pass through solid phase extraction column without adsorbing on the sorbent. The reaction module also includes a source of wash solutions in fluid communication with the solid phase extraction column for providing wash solutions to elute the remaining impurities on the sorbent, and includes a source of an eluent {e.g. , as H20/MeCN, or other suitable eluent) in fluid communication with the solid phase extraction column for eluting the radiolabeled imaging agent product off the sorbent. The reaction module may also include a source of a diluent for the eluted radiolabeled imaging agent.
A formulation module of an apparatus of the invention may be in fluid communication with a reaction module and may include a solid phase extraction cartridge that includes a solid sorbent {e.g. , C-18, or other suitable sorbent) to adsorb the diluted radiolabeled imaging agent, a source of wash solutions {e.g. , comprising ascorbic acid, a salt thereof, or other suitable wash solution) in fluid communication with the solid phase extraction cartridge for providing wash solutions to wash off any remaining impurities on the sorbent, and a source of eluting fluid {e.g. , ethanol, or other suitable eluting fluid) in fluid communication with the solid phase extraction cartridge for eluting the radiolabeled imaging agent product off the sorbent. The formulation module may also include a source of a diluent {e.g. , comprising ascorbic acid, a salt thereof, or other suitable diluent), for diluting the eluted radiolabeled imaging agent. The formulation module may also be in fluid communication with a sterilizing filter {e.g. , a Millipore Millex GV PVDF sterilizing filter, or other suitable sterilizing filter).
In a particular embodiment, a cassette is provided for use with an automated synthesis module, for example, a GE TRACERlab MX synthesis module. In one embodiment, a cassette comprises a disposable sterilized assembly of molded stopcock manifolds specifically designed for use with the automated synthesis module {e.g. , GE TRACERlab MX synthesis module). Individual manifolds are connected in a linear or non-linear fashion to form a directional array that dictates the flow path of reagents used in the preparation of an imaging agent (e.g., imaging agent 1) injection. In some
embodiments, the main body of the cassette contains at least one manifold comprising a plurality of manifold positions (e.g., stockcocks). For example, the main body may comprise at least one, two, three, four or more, manifolds. The cassette may comprise between 1 to 20 manifold positions, between 1 to 15 manifold positions, between 5 and 20 manifold positions, between 5 and 15 manifold positions. Each of the manifolds may or may not be symmetrical. In one embodiment, the main body of the cassette contains three plastic manifolds each fitted with five standard molded stopcocks, thereby having a total of 15 total manifold positions. Individual stopcocks are adapted with luer fittings to accommodate solvents, reagents, syringes, tubing required for gas and liquid handling, etc. The stopcocks are adapted for solvents and reagents and may be fitted with plastic spikes upon which inverted punch vials are located, while those featuring tubing and syringes are fitted with male luer connections according to function. In some embodiments, the cassette comprises a linear arrangement of a plurality of stopcock manifolds connected one or more of the components selected from the group consisting of a gas inlet, anion exchange cartridge, C-18 cartridge, syringe, solvent reservoir, reaction vessel, HPLC system, collection vessel, reservoir for solution of ascorbic acid or salt thereof, and exhaust outlet. In some cases, the cassette further comprises tubing. In some cases, the cassette further comprising an imaging agent synthesis module, wherein the apparatus is fluidically connected to the cassette. In some cases, the apparatus is capable carrying out the method of synthesizing an imaging agent as described herein (e.g., a method of synthesizing imaging agent 1).
The cassette configuration required for the preparation of imaging 1 injection is depicted in Figure 8. The following provides a description of the attachments to each of the 15 manifold positions: 1) luer connection (2) - gas inlet and [180]H20 recovery; 2) anion exchange cartridge - QMA Light; 3) spike connection - MeCN; 4) syringe - empty; 5) spike connection - imaging agent precursor 1; 6) luer connection - reaction vessel; 7) HPLC inlet; 8) spike connection - ascorbic acid; 9) luer connection - collection vessel; 10) syringe - EtOH; 11) luer connection - final product vial; 12) spike connection - SWFI; 13) spike connection - ascorbic acid; 14) syringe - empty; 15) luer connection (2) - reaction vessel and exhaust. Manifold one (stopcocks 1-5) is joined to manifold two (stopcocks 6-10) using two male luer connections fitted with a short length of silicon tubing. Manifold two is connected to manifold three (stopcocks 11-15) using a C-18 Sep- Pak® and the appropriate luer adapters. Individual manifold connections, luer fittings and all silicon tubing are readily available from commercial suppliers.
In some embodiments, the present invention provides a cassette for the preparation of an imaging agent comprising the formula:
Figure imgf000089_0001
comprising: (i) a vessel containing an imaging agent precursor comprising the formula:
Figure imgf000089_0002
and (ii) a conduit for adding a source of F.
Pharmaceutical Compositions
Once an imaging agent or an imaging agent precursor has been prepared or obtained, it may be combined with one or more pharmaceutically acceptable excipients to form a pharmaceutical composition that is suitable for administering to a subject, including a human. As would be appreciated by one of skill in this art, the excipients may be chosen, for example, based on the route of administration as described below, the agent being delivered, time course of delivery of the agent, and/or the health/condition of the subject.
Pharmaceutical compositions of the present invention and for use in accordance with the present invention may include a pharmaceutically acceptable excipient or carrier. As used herein, the term "pharmaceutically acceptable excipient" or
"pharmaceutically acceptable carrier" means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials which can serve as pharmaceutically acceptable carriers are sugars such as lactose, glucose, and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose, and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols such as propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; detergents such as Tween 80; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid;
pyrogen- free water; isotonic saline; Ringer's solution; ethyl alcohol; and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.
The pharmaceutical compositions of this invention can be administered to humans and/or to animals, parenterally, intranasally, intraperitoneally, or via a nasal spray. The mode of administration will vary depending on the intended use, as is well known in the art. Alternatively, formulations of the present invention may be administered parenterally as injections (intravenous, intramuscular, or subcutaneous). These formulations may be prepared by conventional means, and, if desired, the subject compositions may be mixed with any conventional additive.
Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension, or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S. P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables.
The injectable formulations can be sterilized, for example, by filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use.
Exemplary Kits
In some embodiments, systems, methods, kits, and cassettes kits for the preparation of an imaging agent (e.g. , imaging agent 1) are provided for detecting, imaging, and/or monitoring myocardial perfusion. In some embodiments, kits for the administration of an imaging agent (e.g. , imaging agent 1) are provided. Kits of the invention may include, for example, a container comprising an imaging agent, or an imaging agent precursor, and instructions for use. Kits may include a sterile, non-pyrogenic, formulation comprising a predetermined amount of an imaging agent (e.g., imaging agent 1), and optionally other components. In some aspects of the invention, a kit may include one or more syringes that contain an imaging agent (e.g. , imaging agent 1) to be prepared for administration to a subject. A container that may be used in conjunction with an imaging agent (e.g. , imaging agent 1) (e.g. to deliver and/or administer an imaging agent (e.g., imaging agent 1) to a subject) may be a syringe, bottle, vial, tubes, etc. Exemplary syringes that may be included in a kit of the invention are syringes lacking an adsorbent plunger tip, such as a 3 or 5 mL NORM-JECT (Henke Sass Wolf, Dudley, MA), or other equivalent syringe lacking an adsorbent plunger tip. An imaging agent (e.g. , imaging agent 1) may be provided in a kit and additional preparations before use may optionally include diluting the imaging agent to a usable concentration. Instructions in a kit of the invention may relate to methods for, methods of diluting the imaging agent, methods of administering the imaging agent to a subject for diagnostic imaging, or other instructions for use.
In some cases, a kit can also include one or more vials containing a diluent for preparing an imaging agent (e.g. , imaging agent 1) composition for administration to a subject (e.g. , human). A diluent vial may contain a diluent such as physiological saline, water, buffered solution, etc. for diluting an imaging agent (e.g. , imaging agent 1). For example, the imaging agent (e.g. , imaging agent l)may be packaged in a kit in a ready- to-inject formulation, or may require some reconstitution or dilution whereby a final composition/formulation for injection or infusion is prepared.
Instructions in a kit of the invention may also include instructions for administering the imaging agent (e.g. , imaging agent 1) to a subject and may include information on dosing, timing, stress induction, etc. For example, a kit may include an imaging agent described herein, along with instructions describing the intended application and the proper administration of the agent. As used herein, "instructions" can define a component of instruction and/or promotion, and typically involve written instructions on or associated with packaging of the invention. Instructions also can include any oral or electronic instructions provided in any manner such that a user will clearly recognize that the instructions are to be associated with the kit, for example, audiovisual ( e.g. , videotape, DVD, etc.), Internet, and/or web-based communications, etc. The written instructions may be in a form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which instructions can also reflects approval by the agency of manufacture, use or sale for human administration. In some cases, the instructions can include instructions for mixing a particular amount of the diluent with a particular amount of a concentrated solution of the imaging agent or a solid preparation of the imaging agent, whereby a final formulation for injection or infusion is prepared for example, such that the resulting solution is at a suitable concentration for administration to a subject (e.g. , at a concentration as described herein). A kit may include a whole treatment regimen of the inventive compound (e.g. , a rest dose and a stress dose).
The kit may contain any one or more of the components described herein in one or more containers. As an example, in one embodiment, the kit may include instructions for mixing one or more components of the kit and/or isolating and mixing a sample and applying to a subject. The kit may include a container housing an agent described herein. The agent may be in the form of a liquid, gel or solid (powder). The agent may be prepared sterilely, packaged in syringe and shipped refrigerated. Alternatively it may be housed in a vial or other container for storage. A second container may have other agents prepared sterilely. Alternatively the kit may include an active agent premixed and shipped in a syringe, vial, tube, or other container. The kit may have one or more or all of the components required to administer the agents to a patient, such as a syringe, topical application devices, or iv needle tubing and bag.
It also will be understood that containers containing the components of a kit of the invention, whether the container is a bottle, a vial (e.g., with a septum), an ampoule, an infusion bag, or the like, can include additional indicia such as conventional markings that change color when the preparation has been autoclaved or otherwise sterilized. A kit of the invention may further include other components, such as syringes, labels, vials, tubing, catheters, needles, ports, and the like. In some aspect of the invention, a kit may include a single syringe containing the imaging agent (e.g. , imaging agent 1) sufficient for administration and in some aspects of the invention a kit may include two separate syringes, one comprising imaging agent 1 to be administered to a subject for rest imaging, and a second syringe comprising imaging agent 1 for administration to a subject for stress imaging.
Buffers useful in the preparation of imaging agents and kits include, for example, phosphate, citrate, subsalicylate, and acetate buffers. A more complete list can be found in the United States Pharmacopoeia. Lyophilization aids useful in the preparation of imaging agents and kits include, for example, mannitol, lactose, sorbitol, dextran, FICOLL® polymer, and polyvinylpyrrolidine (PVP). Stabilization aids useful in the preparation of imaging agents and kits include, for example, ascorbic acid, cysteine, monothioglycerol, sodium bisulfite, sodium metabisulfite, gentisic acid, and inositol. Solubilization aids useful in the preparation of imaging agents and kits include, for example, ethanol, glycerin, polyethylene glycol, propylene glycol, polyoxyethylene sorbitan monooleate, sorbitan monoloeate, polysorbates, poly(oxyethylene)- poly(oxypropylene)-poly(oxyethylene) block copolymers ("Pluronics") and lecithin. In certain embodiments, the solubilizing aids are polyethylene glycol, cyclodextrins, and Pluronics. Bacteriostats useful in the preparation of imaging agents and kits include, for example, benzyl alcohol, benzalkonium chloride, chlorbutanol, and methyl, propyl, or butyl paraben.
Definitions
For convenience, certain terms employed in the specification, examples, and appended claims are listed here.
Definitions of specific functional groups and chemical terms are described in more detail below. For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75th Ed., inside cover, and specific functional groups are generally defined as described therein. Additionally, general principles of organic chemistry, as well as specific functional moieties and reactivity, are described in "Organic Chemistry," Thomas Sorrell, University Science Books, Sausalito: 1999, the entire contents of which are incorporated herein by reference.
Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms. The present invention contemplates all such compounds, including cis- and fraws-isomers, R- and S-enantiomers, diastereomers, (D)-isomers, (L)- isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention. Additional asymmetric carbon atoms may be present in a substituent such as an alkyl group. All such isomers, as well as mixtures thereof, are intended to be included in this invention.
Isomeric mixtures containing any of a variety of isomer ratios may be utilized in accordance with the present invention. For example, where only two isomers are combined, mixtures containing 50:50, 60:40, 70:30, 80:20, 90: 10, 95:5, 96:4, 97:3, 98:2, 99: 1, or 100:0 isomer ratios are all contemplated by the present invention. Those of ordinary skill in the art will readily appreciate that analogous ratios are contemplated for more complex isomer mixtures.
If, for instance, a particular enantiomer of a compound of the present invention is desired, it may be prepared by asymmetric synthesis, or by derivation with a chiral auxiliary, where the resulting diastereomeric mixture is separated and the auxiliary group cleaved to provide the pure desired enantiomers. Alternatively, where the molecule contains a basic functional group, such as amino, or an acidic functional group, such as carboxyl, diastereomeric salts are formed with an appropriate optically-active acid or base, followed by resolution of the diastereomers thus formed by fractional
crystallization or chromatographic means well known in the art, and subsequent recovery of the pure enantiomers.
As used herein, the term "alkyl" is given its ordinary meaning in the art and refers to the radical of saturated aliphatic groups, including straight-chain alkyl groups, branched-chain alkyl groups, cycloalkyl (alicyclic) groups, alkyl substituted cycloalkyl groups, and cycloalkyl substituted alkyl groups. In some cases, the alkyl group may be a lower alkyl group, i.e. , an alkyl group having 1 to 10 carbon atoms (e.g. , methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, or decyl, etc.). In some embodiments, a straight chain or branched chain alkyl may have 30 or fewer carbon atoms in its backbone, and, in some cases, 20 or fewer. In some embodiments, a straight chain or branched chain alkyl may have 12 or fewer carbon atoms in its backbone (e.g., Ci-Ci2 for straight chain, C3-C12 for branched chain), 6 or fewer, or 4 or fewer. Likewise, cycloalkyls may have from 3-10 carbon atoms in their ring structure, or 5, 6 or 7 carbons in the ring structure. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, isobutyl, i-butyl, cyclobutyl, hexyl, cyclochexyl, and the like. The terms "alkenyl" and "alkynyl" are given their ordinary meaning in the art and refer to unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but that contain at least one double or triple bond respectively.
In certain embodiments, the alkyl, alkenyl and alkynyl groups employed in the invention contain 1-20 aliphatic carbon atoms. In certain other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-4 carbon atoms. Illustrative aliphatic groups thus include, but are not limited to, for example, methyl, ethyl, n-propyl, isopropyl, allyl, n-butyl, sec-butyl, isobutyl, i-butyl, n-pentyl, sec-pentyl, isopentyl, i-pentyl, n-hexyl, sec-hexyl, moieties and the like, which again, may bear one or more substituents. Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, l-methyl-2-buten-l-yl, and the like. Representative alkynyl groups include, but are not limited to, ethynyl, 2- propynyl (propargyl), 1-propynyl and the like.
The term "cycloalkyl," as used herein, refers specifically to groups having three to ten, preferably three to seven carbon atoms. Suitable cycloalkyls include, but are not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like, which, as in the case of other aliphatic, heteroaliphatic, or hetercyclic moieties, may optionally be substituted with substituents including, but not limited to aliphatic;
heteroaliphatic; aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy;
heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroaryl thio; -F; -CI; -Br; -I; -OH; -N02; -CN; -CF3; -CH2CF3; -CHC12; -CH2OH; -CH2CH2OH; -CH2NH2; - CH2S02CH3; -C(0)Rx; -C02(Rx); -CON(Rx)2; -OC(0)Rx; -OC02Rx; -OCON(Rx)2; - N(RX)2; -S(0)2Rx; -NRx(CO)Rx, wherein each occurrence of Rx independently includes, but is not limited to, aliphatic, heteroaliphatic, aryl, heteroaryl, arylalkyl, or
heteroarylalkyl, wherein any of the aliphatic, heteroaliphatic, arylalkyl, or
heteroarylalkyl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl or heteroaryl substituents described above and herein may be substituted or unsubstituted. Additional examples of generally applicable substitutents are illustrated by the specific embodiments shown in the Examples that are described herein.
The term "heteroalkyl" is given its ordinary meaning in the art and refers to an alkyl group as described herein in which one or more carbon atoms is replaced by a heteroatom. Suitable heteroatoms include oxygen, sulfur, nitrogen, phosphorus, and the like. Examples of heteroalkyl groups include, but are not limited to, alkoxy, amino, thioester, poly(ethylene glycol), alkyl-substituted amino, tetrahydrofuranyl, piperidinyl, morpholinyl, etc.
The terms "heteroalkenyl" and "heteroalkynyl" are given their ordinary meaning in the art and refer to unsaturated aliphatic groups analogous in length and possible substitution to the heteroalkyls described above, but that contain at least one double or triple bond respectively.
Some examples of substituents of the above-described aliphatic (and other) moieties of compounds of the invention include, but are not limited to aliphatic;
heteroaliphatic; aryl; heteroaryl; alkylaryl; alkylheteroaryl; alkoxy; aryloxy;
heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI ; Br; I; -OH; -N02; -CN; -CF3; -CHF2; -CH2F; -CH2CF3; -CHC12; -CH2OH; -CH2CH2OH; -CH2NH2; -CH2S02CH3; -C(0)Rx; -C02(Rx); -CON(Rx)2; -OC(0)Rx; -OC02Rx; - OCON(Rx)2; -N(RX)2; -S(0)2Rx; -NRx(CO)Rx wherein each occurrence of Rx
independently includes, but is not limited to, aliphatic, alycyclic, heteroaliphatic, heterocyclic, aryl, heteroaryl, alkylaryl, or alkylheteroaryl, wherein any of the aliphatic, heteroaliphatic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl or heteroaryl substituents described above and herein may be substituted or unsubstituted. Additional examples of generally applicable substituents are illustrated by the specific embodiments shown in the Examples that are described herein.
The term "aryl" is given its ordinary meaning in the art and refers to aromatic carbocyclic groups, optionally substituted, having a single ring (e.g. , phenyl), multiple rings (e.g., biphenyl), or multiple fused rings in which at least one is aromatic (e.g., 1,2,3,4-tetrahydronaphthyl, naphthyl, anthryl, or phenanthryl). That is, at least one ring may have a conjugated pi electron system, while other, adjoining rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls and/or heterocyclyls. The aryl group may be optionally substituted, as described herein. Substituents include, but are not limited to, any of the previously mentioned substitutents, i.e. , the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound. In some cases, an aryl group is a stable mono- or polycyclic unsaturated moieties having preferably 3-14 carbon atoms, each of which may be substituted or unsubstituted. "Carbocyclic aryl groups" refer to aryl groups wherein the ring atoms on the aromatic ring are carbon atoms. Carbocyclic aryl groups include monocyclic carbocyclic aryl groups and polycyclic or fused compounds (e.g. , two or more adjacent ring atoms are common to two adjoining rings) such as naphthyl groups.
The terms "heteroaryl" is given its ordinary meaning in the art and refers to aryl groups comprising at least one heteroatom as a ring atom. A "heteroaryl" is a stable heterocyclic or polyheterocyclic unsaturated moieties having preferably 3-14 carbon atoms, each of which may be substituted or unsubstituted. Substituents include, but are not limited to, any of the previously mentioned substitutents, i.e. , the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound. In some cases, a heteroaryl is a cyclic aromatic radical having from five to ten ring atoms of which one ring atom is selected from S, O, and N; zero, one, or two ring atoms are additional heteroatoms independently selected from S, O, and N; and the remaining ring atoms are carbon, the radical being joined to the rest of the molecule via any of the ring atoms, such as, for example, pyridyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl,oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, and the like.
It will also be appreciated that aryl and heteroaryl moieties, as defined herein may be attached via an alkyl or heteroalkyl moiety and thus also include -(alkyl)aryl, -(heteroalkyl)aryl, -(heteroalkyl)heteroaryl, and -(heteroalkyl)heteroaryl moieties. Thus, as used herein, the phrases "aryl or heteroaryl moieties" and "aryl, heteroaryl, - (alkyl)aryl, -(heteroalkyl)aryl, -(heteroalkyl)heteroaryl, and -(heteroalkyl)heteroaryl" are interchangeable. Substituents include, but are not limited to, any of the previously mentioned substituents, i.e. , the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound.
It will be appreciated that aryl and heteroaryl groups (including bicyclic aryl groups) can be unsubstituted or substituted, wherein substitution includes replacement of one or more of the hydrogen atoms thereon independently with any one or more of the following moieties including, but not limited to: aliphatic; alicyclic; heteroaliphatic; heterocyclic; aromatic; heteroaromatic; aryl; heteroaryl; alkylaryl; heteroalkylaryl; alkylheteroaryl; heteroalkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI ; Br; I; -OH; -N02; -CN; -CF3; - CH2F; -CHF2; -CH2CF3; -CHC12; -CH2OH; -CH2CH2OH; -CH2NH2; -CH2S02CH3; - C(0)Rx; -C02(Rx); -CON(Rx)2; -OC(0)Rx; -OC02Rx; -OCON(Rx)2; -N(RX)2; -S(0)Rx; - S(0)2Rx; -NRx(CO)Rx wherein each occurrence of Rx independently includes, but is not limited to, aliphatic, alicyclic, heteroaliphatic, heterocyclic, aromatic, heteroaromatic, aryl, heteroaryl, alkylaryl, alkylheteroaryl, heteroalkylaryl or heteroalkylheteroaryl, wherein any of the aliphatic, alicyclic, heteroaliphatic, heterocyclic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, saturated or unsaturated, and wherein any of the aromatic, heteroaromatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl substituents described above and herein may be substituted or unsubstituted. Additionally, it will be appreciated, that any two adjacent groups taken together may represent a 4, 5, 6, or 7- membered substituted or unsubstituted alicyclic or heterocyclic moiety. Additional examples of generally applicable substituents are illustrated by the specific embodiments described herein.
The term "heterocycle" is given its ordinary meaning in the art and refers to refer to cyclic groups containing at least one heteroatom as a ring atom, in some cases, 1 to 3 heteroatoms as ring atoms, with the remainder of the ring atoms being carbon atoms. Suitable heteroatoms include oxygen, sulfur, nitrogen, phosphorus, and the like. In some cases, the heterocycle may be 3- to 10-membered ring structures or 3- to 7-membered rings, whose ring structures include one to four heteroatoms.
The term "heterocycle" may include heteroaryl groups, saturated heterocycles (e.g. , cycloheteroalkyl) groups, or combinations thereof. The heterocycle may be a saturated molecule, or may comprise one or more double bonds. In some cases, the heterocycle is a nitrogen heterocycle, wherein at least one ring comprises at least one nitrogen ring atom. The heterocycles may be fused to other rings to form a polycylic heterocycle. The heterocycle may also be fused to a spirocyclic group. In some cases, the heterocycle may be attached to a compound via a nitrogen or a carbon atom in the ring. Heterocycles include, for example, thiophene, benzothiophene, thianthrene, furan, tetrahydrofuran, pyran, isobenzofuran, chromene, xanthene, phenoxathiin, pyrrole, dihydropyrrole, pyrrolidine, imidazole, pyrazole, pyrazine, isothiazole, isoxazole, pyridine, pyrazine, pyrimidine, pyridazine, indolizine, isoindole, indole, indazole, purine, quinolizine, isoquinoline, quinoline, phthalazine, naphthyridine, quinoxaline, quinazoline, cinnoline, pteridine, carbazole, carboline, triazole, tetrazole, oxazole, isoxazole, thiazole, isothiazole, phenanthridine, acridine, pyrimidine, phenanthroline, phenazine, phenarsazine, phenothiazine, furazan, phenoxazine, pyrrolidine, oxolane, thiolane, oxazole, oxazine, piperidine, homopiperidine (hexamnethyleneimine), piperazine (e.g. , N-methyl piperazine), morpholine, lactones, lactams such as azetidinones and pyrrolidinones, sultams, sultones, other saturated and/or unsaturated derivatives thereof, and the like. The heterocyclic ring can be optionally substituted at one or more positions with such substituents as described herein. In some cases, the heterocycle may be bonded to a compound via a heteroatom ring atom (e.g. , nitrogen). In some cases, the heterocycle may be bonded to a compound via a carbon ring atom. In some cases, the heterocycle is pyridine, imidazole, pyrazine, pyrimidine, pyridazine, acridine, acridin-9-amine, bipyridine, naphthyridine, quinoline, benzoquinoline, benzoisoquinoline, phenanthridine- 1,9-diamine, or the like.
The terms "halo" and "halogen" as used herein refer to an atom selected from fluorine, chlorine, bromine, and iodine.
The term "haloalkyl" denotes an alkyl group, as defined above, having one, two, or three halogen atoms attached thereto and is exemplified by such groups as
chloromethyl, bromoethyl, trifluoromethyl, and the like.
The term "amino," as used herein, refers to a primary (-NH2), secondary (-NHRX), tertiary (-NRxRy), or quaternary (-N+RxRyRz) amine, where Rx, Ry and Rz are
independently an aliphatic, alicyclic, heteroaliphatic, heterocyclic, aryl, or heteroaryl moiety, as defined herein. Examples of amino groups include, but are not limited to, methylamino, dimethylamino, ethylamino, diethylamino, diethylaminocarbonyl, methylethylamino, iso-propylamino, piperidino, trimethylamino, and propylamino.
The term "alkyne" is given its ordinary meaning in the art and refers to branched or unbranched unsaturated hydrocarbon groups containing at least one triple bond. Non- limiting examples of alkynes include acetylene, propyne, 1-butyne, 2-butyne, and the like. The alkyne group may be substituted and/or have one or more hydrogen atoms replaced with a functional group, such as a hydroxyl, halogen, alkoxy, and/or aryl group.
The term "alkoxy" (or "alkyloxy"), or "thioalkyl" as used herein refers to an alkyl group, as previously defined, attached to the parent molecular moiety through an oxygen atom or through a sulfur atom. In certain embodiments, the alkyl group contains 1-20 aliphatic carbon atoms. In certain other embodiments, the alkyl group contains 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other
embodiments, the alkyl group contains 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl group contains 1-4 aliphatic carbon atoms. Examples of alkoxy, include but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, t- butoxy, neopentoxy and n-hexoxy. Examples of thioalkyl include, but are not limited to, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, and the like.
The term "aryloxy" refers to the group, -O-aryl. The term "acyloxy" refers to the group, -O-acyl.
The term "alkoxyalkyl" refers to an alkyl group substituted with at least one alkoxy group (e.g. , one, two, three, or more, alkoxy groups). For example, an alkoxyalkyl group may be -(Ci_6-alkyl)-0-(Ci_6-alkyl), optionally substituted. In some cases, the alkoxyalkyl group may be optionally substituted with another alkyoxyalkyl group (e.g., -(Ci-6-alkyl)-0-(Ci-6-alkyl)-0-(Ci_6-alkyl) , optionally substituted.
It will be appreciated that the above groups and/or compounds, as described herein, may be optionally substituted with any number of substituents or functional moieties. That is, any of the above groups may be optionally substituted. As used herein, the term "substituted" is contemplated to include all permissible substituents of organic compounds, "permissible" being in the context of the chemical rules of valence known to those of ordinary skill in the art. In general, the term "substituted" whether preceded by the term "optionally" or not, and substituents contained in formulas of this invention, refer to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent. When more than one position in any given structure may be substituted with more than one substituent selected from a specified group, the substituent may be either the same or different at every position. It will be understood that "substituted" also includes that the substitution results in a stable compound, e.g., which does not spontaneously undergo transformation such as by rearrangement, cyclization, elimination, etc. In some cases, "substituted" may generally refer to replacement of a hydrogen with a substituent as described herein. However,
"substituted," as used herein, does not encompass replacement and/or alteration of a key functional group by which a molecule is identified, e.g., such that the "substituted" functional group becomes, through substitution, a different functional group. For example, a "substituted phenyl group" must still comprise the phenyl moiety and can not be modified by substitution, in this definition, to become, e.g. , a. pyridine ring. In a broad aspect, the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and nonaromatic substituents of organic compounds. Illustrative substituents include, for example, those described herein. The permissible substituents can be one or more and the same or different for appropriate organic compounds. For purposes of this invention, the heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valencies of the heteroatoms.
Furthermore, this invention is not intended to be limited in any manner by the permissible substituents of organic compounds. Combinations of substituents and variables envisioned by this invention are preferably those that result in the formation of stable compounds useful for the formation of an imaging agent or an imaging agent precursor. The term "stable," as used herein, preferably refers to compounds which possess stability sufficient to allow manufacture and which maintain the integrity of the compound for a sufficient period of time to be detected and preferably for a sufficient period of time to be useful for the purposes detailed herein.
Examples of substituents include, but are not limited to, halogen, azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, hydroxyl, alkoxyl, amino, nitro, sulfhydryl, imino, amido, phosphonate, phosphinate, carbonyl, carboxyl, silyl, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester, heterocyclyl, aromatic or heteroaromatic moieties, -CF3, -CN, aryl, aryloxy, perhaloalkoxy, aralkoxy, heteroaryl, heteroaryloxy, heteroarylalkyl, heteroaralkoxy, azido, amino, halide, alkylthio, oxo, acylalkyl, carboxy esters, -carboxamido, acyloxy, aminoalkyl, alkylaminoaryl, alkylaryl, alkylaminoalkyl, alkoxyaryl, arylamino, aralkylamino, alkylsulfonyl, -carboxamidoalkylaryl,
-carboxamidoaryl, hydroxyalkyl, haloalkyl, alkylaminoalkylcarboxy-,
aminocarboxamidoalkyl-, cyano, alkoxyalkyl, perhaloalkyl, arylalkyloxyalkyl, and the like. As used herein, the term "determining" generally refers to the analysis of a species or signal, for example, quantitatively or qualitatively, and/or the detection of the presence or absence of the species or signals. "Determining" may also refer to the analysis of an interaction between two or more species or signals, for example, quantitatively or qualitatively, and/or by detecting the presence or absence of the interaction.
As used herein the term "acquiring" an image means obtaining an image.
The term "diagnostic imaging," as used herein, refers to a procedure used to detect an imaging agent.
A "diagnostic kit" or "kit" comprises a collection of components, termed the formulation, in one or more vials, which are used in a clinical or pharmacy setting to synthesize diagnostic radiopharmaceuticals. For example, the kit may be used by the practicing end user in a clinical or pharmacy setting to synthesize and/or use diagnostic radiopharmaceuticals. In some embodiments, the kit may provide all the requisite components to synthesize and/or use the diagnostic pharmaceutical except those that are commonly available to the practicing end user, such as water or saline for injection, a solution of the radionuclide, equipment for processing the kit during the synthesis and manipulation of the radiopharmaceutical, if required, equipment necessary for administering the radiopharmaceutical to the subject such as syringes, shielding, imaging equipment, and the like. In some embodiments, imaging agents may be provided to the end user in their final form in a formulation contained typically in one vial or syringe, as either a lyophilized solid or an aqueous solution.
As used herein, a "portion of a subject" refers to a particular region of a subject, location of the subject. For example, a portion of a subject may be the brain, heart, vasculature, cardiac vessels, of a subject.
As used herein a "session" of testing may be a single testing protocol that a subject undergoes. In some cases a session may include rest/stress imaging protocol; stress/rest imaging protocol; rest only imaging protocol; or a stress only imaging protocol. A session of testing can take place in less than 24 hours or less than 48 hour.
As used herein, the term "subject" refers to a human or non-human mammal or animal. Non-human mammals include livestock animals, companion animals, laboratory animals, and non-human primates. Non-human subjects also specifically include, without limitation, horses, cows, pigs, goats, dogs, cats, mice, rats, guinea pigs, gerbils, hamsters, mink, and rabbits. In some embodiments of the invention, a subject is referred to as a "patient." In some embodiments, a patient or subject may be under the care of a physician or other health care worker, including, but not limited to, someone who has consulted with, received advice from or received a prescription or other recommendation from a physician or other health care worker.
Any of the compounds described herein may be in a variety of forms, such as, but not limited to, salts, solvates, hydrates, tautomers, and isomers.
In certain embodiments, the imaging agent is a pharmaceutically acceptable salt of the imaging agent. The term "pharmaceutically acceptable salt" as used herein refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, Berge et ah, describe pharmaceutically acceptable salts in detail in /. Pharmaceutical Sciences, 1977, 66, 1-19, incorporated herein by reference. Pharmaceutically acceptable salts of the compounds of this invention include those derived from suitable inorganic and organic acids and bases. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3- phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate, undecanoate, valerate salts, and the like. Salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N+(Ci^alkyl)4 salts. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, loweralkyl sulfonate and aryl sulfonate.
In certain embodiments, the compound is in the form of a hydrate or solvate. The term "hydrate" as used herein refers to a compound non-covalently associated with one or more molecules of water. Likewise, the term "solvate" refers to a compound non- covalently associated with one or more molecules of an organic solvent.
In certain embodiments, the compound described herein may exist in various tautomeric forms. The term "tautomer" as used herein includes two or more
interconvertable compounds resulting from at least one formal migration of a hydrogen atom and at least one change in valency (e.g., a single bond to a double bond, a triple bond to a single bond, or vice versa). The exact ratio of the tautomers depends on several factors, including temperature, solvent, and pH. Tautomerizations (i.e., the reaction providing a tautomeric pair) may catalyzed by acid or base. Exemplary tautomerizations include keto-to-enol; amide-to-imide; lactam-to-lactim; enamine-to- imine; and enamine-to-(a different) enamine tautomerizations.
In certain embodiments, the compounds described herein may exist in various isomeric forms. The term "isomer" as used herein includes any and all geometric isomers and stereoisomers (e.g., enantiomers, diasteromers, etc.). For example, "isomer" include cis- and fraws-isomers, E- and Z- isomers, R- and ^-enantiomers,
diastereomers, (D)-isomers, (L)-isomers, racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention. For instance, an isomer/enantiomer may, in some embodiments, be provided substantially free of the corresponding enantiomer, and may also be referred to as "optically enriched." "Optically-enriched," as used herein, means that the compound is made up of a significantly greater proportion of one enantiomer. In certain embodiments the compound of the present invention is made up of at least about 90% by weight of a preferred enantiomer. In other embodiments the compound is made up of at least about 95%, 98%, or 99% by weight of a preferred enantiomer. Preferred enantiomers may be isolated from racemic mixtures by any method known to those skilled in the art, including chiral high pressure liquid chromatography (HPLC) and the formation and crystallization of chiral salts or prepared by asymmetric syntheses. See, for example, Jacques, et al , Enantiomers, Racemates and Resolutions (Wiley Interscience, New York, 1981); Wilen, S.H., et al, Tetrahedron 33:2725 (1977); Eliel, E.L. Stereochemistry of Carbon Compounds (McGraw-Hill, NY, 1962); Wilen, S.H. Tables of Resolving Agents and Optical Resolutions p. 268 (E.L. Eliel, Ed., Univ. of Notre Dame Press, Notre Dame, IN 1972).
These and other aspects of the present invention will be further appreciated upon consideration of the following Examples, which are intended to illustrate certain particular embodiments of the invention but are not intended to limit its scope, as defined by the claims.
Examples
Example 1
Synthesi -(2-hydroxyethoxymethyl)benzoic acid methyl ester
Figure imgf000105_0001
To a two-neck round bottom flask, which was equipped with a Dewar condenser, a solution of 4-hydroxymethylbenzoic acid methyl ester (2.50 g, 0.015 mol) in anhydrous dichloromethane (30 mL) was cooled to -10 °C in a salt/ice bath. Ethylene oxide (1.10 mL) was added to the cooled stirring solution dropwise followed by the addition of boron trifluoride etherate (0.51 ml). The reaction mixture was stirred for 45 minutes and then warmed to room temperature for 30 minutes to boil off any excess of ethylene oxide from the reaction mixture. The reaction mixture was then diluted with brine. The aqueous layer was extracted with dichloromethane (3 times). All of the organic layers were combined, dried over Na2S04, filtered, and concentrated to provide an oil. The crude material was purified using silica gel chromatography (4: 1 pentane: ethyl acetate) to provide the desired product (537 mg, 2.56 mmol) in 17% yield. Ή (CDC138.36, 600 MHz): δ (2H, d, 7=8.4 Hz), 7.41 (2H, d, 7=8.5 Hz), 4.62 (3H, s), 3.92 (2H, s), 3.78 (m, 2H), 3.63 (2H, m); 13C (CDC13167.1, 143.5, 130.0, 129.8, 127.5, 72.9, 72.0, 150 MHz): δ
62.1, 52.3.
Example 2
Synthesis of 4-[2-(i-butyldimethylsilanyloxy)ethoxymethyl]benzoic acid methyl ester
Figure imgf000106_0001
To a solution of the product of Example 1 (544.5 mg, 2.59 mmol) in anhydrous DMF (26 mL) was added imidazole (264 mg, 3.89 mmol) and TBDMS-Cl (586 mg, 3.89 mmol). The reaction mixture stirred at room temperature overnight and was quenched with water. The aqueous layer was extracted with ethyl acetate (3x). All combined organic layers were dried over Na2S04, filtered, and concentrated. The crude material was purified using silica gel chromatography (4:1 pentane:ethyl acetate) to provide the desired product (677.5 mg, 2.19 mmol) in 84% yield. JH (CDC13 8.01, 600 MHz): δ (2H, d, 7=8.3 Hz), 7.42 (2H, d, 7=8.4 Hz), 4.63 (2H, s), 3.91 (2H, s), 3.82 (2H, t, 7=5.0), 3.58 (2H, t, 7=5.1 Hz), 0.91 (9H, s), 0.07 (6H, s); 13C (CDC13166.5, 143.5, 129.2, 128.8, 126.5, 72.1, 71.6, 150 MHz): δ 62.3, 51.5, 25.4, 17.9, -5.8.
Example 3
Synthesi -[2-(i-butyldimethylsilanyloxy)ethoxymethyl]phenyl}methanol
Figure imgf000106_0002
To a solution of the product of Example 2 (670 mg, 2.18 mmol) dissolved in anhydrous THF (22 mL) was added a solution of LAH (1.0 M solution in THF, 2.18 mL, 2.18 mmol) dropwise. After completion of addition the reaction mixture was stirred at room temperature for 3 hours. The reaction mixture was diluted with water. The aqueous layer was extracted with ethyl acetate (3x). All combined organic layers were dried over Na2S04, filtered, and concentrated to provide an oil (587 mg, 1.98 mmol), which was used in the next step without any further purification (91% yield). JH (CDCI3 7.34 (4H, s), 4.68 (2H, s), 4.57 (2H, s), 3.80, 600 MHz): δ (2H, t, 7=5.2 Hz), 3.56 (2H, t, 7=5.3 Hz), 1.69 (1H, br s), 0.90 (9H, s), 0.07 (6H, s); 13C (CDC13 140.4, 138.3, 128.0, 127.2, 73.2, 71.9, 65.4, 150 MHz): δ 63.0, 26.2, 18.6, -5.0. Example 4
Synthesis of 2-i-butyl-5- {4-[2-(i-butyldimethylsilanyloxy)ethoxymethyl]benzyloxy }-4- -2H-pyridazin-3 -one
Figure imgf000107_0001
To solution of the product of Example 3 (437 mg, 1.48 mmol) and 2-?-butyl-4- chloro-5-hydroxy-2H-pyridazin-3-one (250 mg, 1.23 mmol) dissolved in anhydrous THF (12 mL) was added solid PPI13 (485 mg, 1.85 mmol) and diisopropyl azodicarboxylate (DIAD, 0.358 mL, 1.85 mmol). After completion of addition the reaction mixture continued to stir at room temperature. After 20 hours, the reaction mixture was diluted with water. The aqueous layer was separated and extracted with ethyl acetate (3x). All combined organic layers were dried over Na2S04, filtered, and concentrated to provide an oil. The crude material was purified using silica gel chromatography (4: 1 pentane: ethyl acetate) to provide the desired product 528 mg, 1.10 mmol) in 89% yield. JH (CDCI3 7.70 (1H, s), 7.38 (4H, m), 5.30 (2H, s), 4.58, 600 MHz): δ (2H, s), 3.80 (2H, t, /= 5.4 Hz), 3.57 (2H, t, 7=5.4 Hz), 1.63 (9H, br s), 0.90 (9H, s), 0.07 (6H, s); 13C (CDC13159.0, 153.7, 138.8, 134.4, 128.3, 127.3, 150 MHz): δ 125.1, 118.5, 72.8, 71.7, 71.6, 66.4, 61.9, 29.7, 27.9, 25.6, -5.1. ; HRMS calcd for C24H37ClN204Si: 481.228389, found 481.2282.
Example 5
Synthesis of 2- i-butyl-4-chloro-5-[4-(2-hydroxyethoxymethyl)benzyloxy]-2H-pyridazin- -one
Figure imgf000107_0002
To a solution of the product of Example 4 (528 mg, 1.09 mmol) dissolved in anhydrous THF (11 mL) was added a solution of TBAF (1.0 M solution in THF, 1.65 mL, 1.65 mmol) dropwise. After completion of addition the reaction was stirred at room temperature for 1 hour and then quenched with water. The aqueous layer was separated and extracted with ethyl acetate (3x). All combined organic layers were dried over Na2S04, filtered, and concentrated to provide an oil. The crude material was purified using silica gel chromatography (4:1 hexanes: ethyl acetate) to provide the desired product (311 mg, 0.850 mmol) in 78% yield. JH (CDC13, 600 MHz): δ 7.70 (1H, s), 7.38 (4H, m), 5.30 (2H, s), 4.56 (2H, s), 3.76 (2H, t, 7=4.9 Hz), 3.60 (2H, t, 7=4.8 Hz), 2.00 (1H, br s), 1.61 (9H, br s); 13C (CDC13159.0, 153.6, 150 MHz): δ 138.8, 134.4, 128.2, 127.2, 125.1, 118.3, 72.8, 71.6, 71.6, 66.4, 61.9, 27.8; HRMS calcd for Ci8H23ClN204: 367.141911, found 367.1419.
Example 6
Synthesis of toluene-4-sulfonic acid 2-[4-(l-i-butyl-5-chloro-6-oxo-l,6-dihydro- -4-yloxymethyl)-benzyloxy]-ethyl ester
Figure imgf000108_0001
To a solution of the product of Example 5 (200 mg, 0.546 mmol) dissolved in anhydrous dichloromethane (5.50 mL) was added TsCI (125 mg, 0.656 mmol), DMAP (100 mg, 0.819 mmol) and triethylamine (0.091 mL, 0.656 mmol). The reaction mixture continued stirring at room temperature. After 22 hours the reaction mixture was diluted with water. The aqueous layer was separated and extracted with ethyl acetate (3x). All combined organic layers were dried over Na2S04, filtered, and concentrated to provide an oil. The crude material was purified using silica gel chromatography (3:2
pentane:ethyl acetate) to provide the desired product (232 mg, 0.447 mmol) in 82% yield. Ή (CDC 7.79, 600 MHz): δ (2H, d, 7=8.3 Hz), 7.71 (1H, s), 7.38 (2H, d, 7=8.2 Hz), 7.32 (4H, m), 5.30 (2H, s), 4.50 (2H, s), 4.21 (2H, m), 3.69 (2H, m), 2.43 (3H, s), 1.63 (9H, br s); 13C (CDC13 159.0, 153.7, 144.8, 138.8, 150 MHz): δ 134.4, 133.1, 129.8, 128.1, 128.0, 127.2, 125.1, 118.4, 72.8, 71.7, 69.2, 67.8, 66.4, 27.9, 21.6; HRMS calcd for C25H29CIN2O6: 521.150762, found 521.1503.
Example 7
Preparation of [18F] fluoride [ FJFluoride was produced by proton bombardment of [ 0]H20 in a cyclotron; the nuclear chemical transformation is shown below and may be summarized as
18 0(p,n)18 F. For purposes of the bombardment, the chemical form of the 18 O is ¾18 O. The chemical form of the resulting 18F is fluoride ion.
180 + proton→ 18F + neutron
According to established industry procedures, [180]¾0 (2-3 mL) housed within a tantalum target body using Havar® foil, was bombarded with 11 MeV protons (nominal energy); where the proton threshold energy for the reaction is 2.57 MeV and the energy of maximum cross section is 5 MeV. Target volume, bombardment time and proton energy each may be adjusted to manage the quantity of [18F]fluoride produced.
Example 8
Preparation of Imaging Agent Precursor 1 Acetontrile Concentrate Imaging agent precursor 1 (20.4 g, 39.2 mmol), as shown in Figure 1, was dissolved in anhydrous MeCN (3400 mL) then transferred through an Opticap XL2 Durapore filter (0.2 μιη) into 5 mL glass vials; 2.0 mL fill volume. The vials were then fitted with rubber septa, sealed with an aluminum crimp and stored at ambient temperature prior to use.
Example 9
General Preparation of Imaging agent 1
The following example describes a general procedure for synthesizing imaging agent 1, as shown in Figure 1. Aqueous [18F]fluoride, as prepared in Example 7, was transferred from the cyclotron to a synthesis module, then filtered through an anion exchange column to remove unreacted [ 1l8o0]H20; [ 1180F]fluoride was retained within the cationic resin matrix. The column was then washed with aqueous Et4NHC03 with transfer to the reaction vessel. The resulting solution was diluted with MeCN then concentrated to dryness using elevated temperature and reduced pressure. The mixture of anhydrous [18F]Et4NF and and Et4NHC03 thus obtained was treated with the acetonitrile solution of imaging agent precursor 1, as prepared in Example 8, then warmed to 90-100 °C and maintained 10-20 min. After cooling, the solution was diluted with ¾0 then directly purified by HPLC on a Waters Xterra MS CI 8 column using a H20/MeCN eluent. The main product peak was collected, diluted with ascorbic acid then transferred to the formulation module. In another case, similar steps and conditions were employed as above except the solution was warmed to 85-120 °C and maintained 5- 20 min, followed by cooling and diluting with 1 : 1 H20/MeCN.
Example 10
Preparation of imaging agent 1 using the Explora RN Synthesis Module The product of Example 7 was transferred from cyclotron to the synthesis module then filtered through an anion exchange column to remove unreacted [180]H20;
[18F] fluoride was retained within the cationic resin matrix. The column was then washed with Et4NHC03 (5.75 μιηοΐ; 0.500 mL of a 11.5 mM solution in H20) with transfer to the reaction vessel. The resulting solution was diluted with MeCN (0.500 mL) then concentrated to dryness; 150 mm Hg at 115 °C for 4 min. The mixture of anhydrous [18F]Et4NF and Et4NHC03 thus obtained was treated with the product of Example 8 (11.5 μιηοΐ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 90 °C and maintained 20 min. After cooling to 35 °C, the solution was diluted with H20 (1.00 mL) then directly purified by HPLC on a Waters Xterra MS CI 8 column (10 μιη; 10 x 250 mm) using a 45:55 H20/MeCN eluent at a flow rate of 5 mL/min. The main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in H20; pH 2) then transferred to the formulation module; 58% decay corrected radiochemical yield.
In another case, similar steps and conditions were employed as above except the Et4NHC03 was 11.5 μιηοΐ (0.500 mL of a 23.0 mM solution in H20); the solution was concentrated to dryness at 280 mbar, 95-115 °C, 4 min; the mixture of anhydrous
[18F]Et4NF and Et4NHC03 treated with the product of Example 8 was warmed to 90 °C and maintained 10 min; and the product had 61% decay corrected radiochemical yield.
Example 11a
Preparation of Imaging agent 1 using the Eckhert & Ziegler Modular- Lab Synthesis
Module
The product of Example 7 was transferred from cyclotron to the synthesis module then filtered through an anion exchange column to remove unreacted [180]H20;
[18F] fluoride was retained within the cationic resin matrix. The column was then washed with Et4NHC03 (11.5 μιηοΐ; 0.500 mL of a 23.0 mM solution in H20) with transfer to the reaction vessel. The resulting solution was diluted with MeCN (0.500 mL) then concentrated to dryness; 375 mm Hg at 115 °C for 10 min. The mixture of anhydrous [18F]Et4NF and Et4NHC03 thus obtained was treated with the product of Example 8 (11.5 μιηοΐ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 110 °C and maintained 10 min. After cooling to 20 °C, the solution was diluted with ¾0 (1.00 mL) then directly purified by HPLC on a Waters Xterra MS C18 column (10 μιη; 10 x 250 mm) using a 45:55 H20/MeCN eluent at a flow rate of 5 mL/min. The main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in ¾0; pH 2) then transferred to the formulation module; 68% decay corrected radiochemical yield.
In another case, similar steps and conditions were employed as above except the ersulting solution was concentrated to dryness a 400 mbar, 110-150 °C, 10 min; the mixture of anhydrous [18F]Et4NF and Et4NHC(¾ treated with the product of Example 8 was warmed to 120 °C and maintained 10 min; and the cooling was conducted at 35 °C.
Example l ib
Preparation of Imaging Agent 1 using the Explora GN Synthesis Module The product of Example 7 was transferred from cyclotron to the synthesis module then filtered through an anion exchange column to remove unreacted [180]H20;
[18F] fluoride was retained within the cationic resin matrix. The column was then washed with Et4NHC03 (11.5 μιηοΐ; 1.00 mL of a 11.5 mM solution in H20) with transfer to the reaction vessel. The resulting solution was diluted with MeCN (1.00 mL) then concentrated to dryness; 110-115 °C. Additional MeCN (1.50 mL) was then added and the solution concentrated to dryness once again. The mixture of anhydrous [^FJEttNF and Et4NHC03 thus obtained was treated with the product of Example 8 (11.5 μιηοΐ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 120 °C and maintained 10 min. After cooling to 60 °C, the solution was diluted with H20/MeCN (3.00 mL; 2:1 v/v) then directly purified by HPLC on a Waters Xterra MS CI 8 column (10 μιη; 10 x 250 mm) using a 45:55 H20/MeCN eluent at a flow rate of 5 mL/min. The main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in ¾0; pH 2) then transferred to the formulation module; 68% decay corrected radiochemical yield. - I ll -
Example 11c
Preparation of Imaging Agent 1 using the GE TRACERLab MX Synthesis Module The product of Example 7 was transferred from cyclotron to the synthesis module then filtered through an anion exchange column to remove unreacted [180]H20;
[18F] fluoride was retained within the cationic resin matrix. The column was then washed with Et4NHC03 (23.0 μιηοΐ; 0.500 mL of a 46.0 mM solution in 1:1 H20/MeCN) with transfer to the reaction vessel. The resulting solution was diluted with MeCN then concentrated to dryness; 150 mbar, 105 °C, 8 min. Additional MeCN was then added and the drying process repeated; the process of MeCN addition followed by evaporation was repeated three times. The mixture of anhydrous [ 18 F]Et4NF and Et4NHC03 thus obtained was treated with the product of Example 8 (23.0 μιηοΐ; 2.00 mL of a 11.5 mM solution in MeCN) then warmed to 85 °C and maintained 10 min. The resulting solution was then diluted with H20 (2.00 mL) and directly purified by HPLC on a Waters Xterra MS C18 column (10 μιη; 10 x 250 mm) using a 45:55 H20/MeCN eluent at a flow rate of 5 mL/min. The main product peak eluting at 11 min was collected, diluted with ascorbic acid (10 mL of a 0.28 M solution in H20; pH 2) then transferred to the formulation module; 63% decay corrected radiochemical yield.
Example 12
Solvent Exchange Process
The product of Example 10 or 11 was transferred from purification to the formulation module then filtered through a CI 8 Sep-Pak® cartridge to remove MeCN; Imaging agent 1 was retained within the CI 8 resin matrix and the filtrate discarded. The cartridge was successively washed with ascorbic acid (10 mL of a 0.28 M solution in H20; pH 2), the filtrate discarded, then absolute EtOH (0.50 mL), and the filtrate collected. The ethanol concentrate of imaging agent 1 thus obtained was further diluted with ascorbic acid (10.0 mL of a 0.28 M solution in H20) in preparation for final aseptic filtration.
Example 13
Aseptic Filtration Process
The final product vial assembly was constructed from the following pre- sterilized components: one 30 mL product vial, one Millipore Millex GV4 venting filter (0.22 μιη x 4 mm), one tuberculin syringe (1 mL) and one insulin syringe (0.5 mL). The product of Example 12 was then transferred from formulation to the final product vial assembly through a Millipore Millex GV PVDF sterilizing filter (0.22 μιη x 13 mm). Quality control samples are then removed, using the syringe assemblies, to complete all product release requirements.
Example 14
Upon evaluation of several experimental parameters in the nucleophilic fluorination of imaging agent precursor 1 (Figure 1) using K2C03/Kryptofix® 222 overall reaction complexity was shown to increase with added K2CO3; comparable fluorination efficiency was observed regardless of reagent stoichiometry. Elevated base (e.g. , carbonate) levels were simply correlated to unproductive consumption of starting material (e.g. , imaging agent precursor). Substitution of K2CO3 with KHCO3 resulted in considerable improvement of both fluorination efficiency and starting material integrity. The solution pH remained uniform regardless of base identity and reagent stoichiometry; the presence or absence of Kryptofix® 222 determines global solution pH. The fluorination efficiency remained stable regardless of reagent stoichiometry, indicating a more complex role of added base within the reaction coordinate.
Figure 2 shows various possible reaction pathways, which traces unproductive consumption of starting material to a series of base-mediated hydrolysis reactions and dimerization events. Variable time and temperature experiments confirmed the comparable rates of hydrolysis and fluorination in the nucleophilic fluorination reaction shown in Figure 1 , using the K2C03/Kryptofix® 222 in the presence of K2C03. Thus, reaction conditions which activate larger differential rates of fluorination are desired in order to advance a more efficient and chemoselective process; that is, a decreased rate of hydrolysis and/or increased rate of fluorination.
As noted above, K2CO3 did little to enhance fluorination over baseline levels and served primarily a detrimental role in the reaction. In contrast, added KHCO3 produced a marked increase in fluorination over the same dynamic range, while decomposition pathways remained poorly differentiated. These facts, coupled with the knowledge that [18F]NaF exchange with tetraalkylammonium cations is known to directly produce a highly active nucleophilic fluoride source, led to the investigation of a series of commercially available salts in an effort to identify related counterion affects that amplify the rate of fluorination (e.g. , see Figure 1).
A series of different bases was used in the nucleophilic fluorination of a tosylate precursor using TBAF as a source of fluoride (shown above), according to the following procedure. A 2 mL glass vial was charged with both Bu4NF (1.15 μιηοΐ; 13.4 μΐ^ of a 85.9 mM solution in H20) and Bu4NHC03 (10.4 μιηοΐ; 138 μΐ. of a 75.0 mM solution in ¾0), then warmed to 95 °C and maintained 10 min under a stream of dry nitrogen. The resulting solid mixture was treated with the product of Example 8 (11.5 μιηοΐ; 1.00 mL of a 11.5 mM solution in MeCN) then warmed to 90 °C and maintained 10 min. After cooling to 22 °C, the resulting solution was diluted with ¾0 then directly analyzed by HPLC on a Zorbax SB-C18 column (4.6 x 50 mm) using a H20/MeCN gradient containing 0.1 % HCO2H with a flow rate of 1.00 mL/min. The reaction yield was then calculated through comparison of the integrated peak area for the product in the crude reaction mixture to that of the authentic standard product (Table 1); results obtained through substitution of several alternate salt forms are also provided for comparison.
An enhancement of fluorination efficiency was observed in the presence of bicarbonate anion. Additionally, a modest dependence on size of the alkyl substituent was observed when R = methyl -> ethyl -> butyl (data not shown).
A - 1.5 -fold improvement in yield was observed using the KF-Kryptofix® 222 method when changing from no added salt, to one equivalent potassium carbonate, to one equivalent potassium bicarbonate.
Table 1. Comparison of salt form identity and fluorination yield.
salt form % yield
bicarbonate 81.4
hydroxide 35.5
acetate 2.8
lactate 38.7
trifluoroacetate 3.7
methanesulfonate 39.6
p-toluenesulfonate 15.0
nitrate 45.1
iodide 44.6
bisulfate <2
none 44.1 Additionally, the amount of salt additive was varied, relative to the amount of starting material (e.g. , imaging agent precursor), in order to investigate the effect of salt additive concentration on the reaction. Figure 9 shows (A) a graph illustrating the changes in product distribution as a function of molar concentration of bicarbonate salt and (B) a graph illustrating the product distribution as a function of reaction time.
Investigation of the salt stoichiometry revealed that 25 mol % (or 0.25 equivalents, relative to the imaging agent precursor) of tetraalkylammonium bicarbonate was needed for complete conversion and unproductive consumption of starting material occurred with increasing base concentration revealing an optimum stoichiometry range for the modified reaction conditions. Related studies directed toward determination of the optimal precursor concentration revealed a rather distinct concentration threshold.
Figure 9C illustrates a threshold of >3 mg/ml.
The use of tetraalkylammonium bicarbonate as an additive in the absence of Kryptofix® 222 during nucleophilic fluorination resulted in rapid conversion to the desired product and significantly improved chemoselectivity toward fluorination, relative to the use of K^CCVKryptofix® 222 method. A detailed evaluation of crude reaction mixtures revealed a dramatic reduction in overall decomposition rates when
tetraalkylammonium bicarbonate was used, as evidenced by the absence of four hydrolytic impurities present when K^COs/Kryptofix® 222 was used. Without wishing to be bound by theory, this may be attributed to the fact that the use of a
tetraalkylammonium bicarbonate allows the reaction to be conducted at a lower absolute pH (e.g. , a pH of about 5-6).
Example 15
Figure imgf000115_0001
Imaaina Aaent Precursor 1
Imaging Agent 1
The following example investigates the effect of the presence of potassium carbonate in a nucleophilic fluorination reaction. A yield of 36% is obtained in the presence of potassium carbonate, while a yield of 35% is obtained in the absence of potassium carbonate. Example 16
Figure imgf000116_0001
. . . _ ., Imaqinq Aqent 1
Imaging Agent Precursor 1
The following example describes the effect that different salt additives may have on nucleophilic fluorination. A yield of 35% is obtained in the presence of potassium carbonate, while a yield of 71% is obtained in the presence of potassium bicarbonate.
Example 17
Figure imgf000116_0002
Imaqinq Aqent 1
The following example describes the results obtained using different fluoride sources in a nucleophilic fluorination reaction. A yield of 71% is obtained in the presence of KF/Kryptofix® 222, while a yield of 83% is obtained in the presence of tetrabutylammonium fluoride.
Example 18
Figure imgf000116_0003
Imaging Agent Precursor 1 Imaqinq Aqent 1
The following example describes the results obtained using different bases in a nucleophilic fluorination reaction utilizing tetrabutylammonium fluoride as the fluoride salt. A yield of 83% is obtained in the presence of the bicarbonate base, while a yield of 36% is obtained in the presence of the hydroxide base. Example 19
The following describes a comparison of imaging agent 1 and 82Rb PET versus SPECT for detection of myocardial ischemia. In preclinical studies, myocardial uptake of imaging agent 1 exhibits a stronger relationship with myocardial blood flow across the range of achievable flow than 201T1, 99mTc sestamibi and 82Rb. The following experiments were conducted to determine if the improved extraction and retention of imaging agent 1 would result in a greater difference between PET and SPECT ischemia
82
detection by imaging agent 1 versus Rb.
Methods: Twenty-six patients (20 men) who underwent 99mTc sestamibi SPECT and imaging agent 1 PET within 6 months at a single center in a phase II clinical trial were compared to 23 patients (matched by summed difference score (SDS) on SPECT) who underwent 99mTc sestamibi SPECT and 82Rb PET (25-50mCi) within 6 months without change in clinical state. PET was performed with imaging agent 1 at rest (2.3- 3.9 mCi) followed 60 min or 24 h later with exercise or adenosine stress (7.3-8.6 mCi). Perfusion defects on SPECT and PET were assessed by computer-assisted visual interpretation, using the standard 17 segment, 5 point-scoring model (0=normal;
4=absent uptake). The extent and severity of ischemia (SDS) was derived from the difference between summed stress score (SSS) and summed rest scores (SRS).
Results: In 14 patients with abnormal SPECT (SSS >4), mean SDS was greater with imaging agent 1 than with SPECT (9.6 + 1.8 versus 5.4 + 0.7, p=0.02). In a
82 matched group of 13 patients with abnormal SPECT, mean SDS was similar with Rb PET and SPECT (4.9 + 1.4 versus 4.6+ 1.3, p=0.8). In patients with normal SPECT (SSS <4), no differences in SDS were observed with either imaging agent 1 (n=12) or 82Rb (n=10) PET when compared to SPECT.
Imaging agent 1 PET showed an increase in the amount of ischemia detected relative to 99mTc sestamibi SPECT that was not seen when comparing 82Rb PET to SPECT in a comparable patient group. These results suggest that imaging agent 1 show greater improvement in detection of myocardial ischemia when PET is compared to
82
SPECT than is associated with the use of "Rb.
Example 20
The following describes multicenter development of normal perfusion and function limits for stress and rest cardiac PET. The study included development of normal perfusion distribution limits and characterization of normal cardiac function measured by a cardiac perfusion 18F based agent (imaging agent 1).
Methods: Normal limits were established from 15 low likelihood patients (7F/8M) average age 54.7 y, average weight 74.2 kg with treadmill exercise stress/rest datasets (30 datasets in total), recruited in a clinical trial (phase 2) for the 18F imaging agent 1 perfusion agent, acquired on a Siemens Biograph-64 PET/CT scanner in list mode. Standard reconstruction (2D Attenuation Weighted Ordered Subsets Expectation Maximization) with voxel size of 2.6 x 2.6 x 2.0 (mm) 8-bin gating was used for the gated reconstruction. 5 -minute reconstructions were considered obtained approximately 5 min after isotope injection for stress and rest. The Cedars-Sinai QPET PET function and perfusion analysis software was used for all the processing and for the normal perfusion database creation. 2 out of 30 scans (6.7%) for gated studies and 1 out of 30 for ungated studies (3.3%) required manual intervention in the definition of the left ventricle (LV) all other processing was fully automatic.
Results: Left ventricular counts were 33.33+6.44 million counts, range (22.76- 44.29) for stress and 7.56+1.86 million counts, range (5.12 -11.77) for rest. The stress/rest count ratio was 4.53+0.88 (2.88-6.16). Average trans-ischemic dilation (TID) was 0.974+0.124 with upper normal limit of 1.22. QPET relative perfusion normal limits were created for stress and rest scans. There was evidence of apical thinning on stress and rest with apical counts at 80/79% respectively. The variation of counts in the normal database was between 5-9% in all 17 AHA segments. The functional parameters are given in Table 2:
Table 2. Functional Parameters from Stress and Rest Scans
Figure imgf000118_0001
Example 21
The following describes results of absolute quantification of rest and stress myocardial blood flow with imaging agent 1 PET in normal and coronary artery disease patients. Imaging agent 1 is a new myocardial perfusion PET tracer that targets mitochondrial complex 1. In this study, the quantification of rest (R) and stress (S) myocardial blood flows (MBFs) and coronary flow reserve (CFR) was explored with this tracer in normal and coronary artery disease (CAD) patients.
Methods: Eleven patients (8 with a low likelihood of CAD and 3 with CAD and presence of reversible defects) received IV injection of imaging agent 1 at rest and at peak adenosine pharmacological vasodilation. Dynamic PET images were obtained for 10 minutes, beginning with the administration of the tracer. On reoriented short axis images, regions of interest were placed on the normal and defect regions of the myocardium and the left ventricular blood pool, from which time activity curves (TACs) were generated. Patlak analysis was applied to myocardial TAC (-0.4-1.5 min) using the blood pool TAC as the input function to give the uptake constant (K) in the myocardium. Partial volume and spillover corrections were applied to blood pool and myocardial TACs to ensure the intercept of the regression line on the Patlak plot was close to zero. The first pass extraction fraction for imaging agent 1 in humans was assumed to be 0.94 (i.e. , MBF=K/0.94), equivalent to that observed in prior studies (e.g. , see Huisman et al. , JNucl Med 2008;49:630-6).
Results: S MBF was similar (p=NS) in LL patients and in the myocardial regions which were supplied by normal coronary arteries in CAD patients (NCA). R MBF, however, was higher (p<0.05) in NCA versus LL, resulting in a lower (p<0.05) CFR in NCA patients. In contrast, S MBF and CFR were significantly lower in CAD regions (see Table 3). These findings are in agreement with the published literature using N-13 ammonia PET.
Table 3.
Figure imgf000119_0001
humans using imaging agent 1 myocardial perfusion PET imaging.
Example 22
The following describes an iterative technique for optimizing injected tracer dosage and acquisition time for 18F-labeled myocardial perfusion tracer imaging agent 1. Public and staff concerns about radiation exposure necessitate optimization of the dosage acquisition time product (DATP) to obtain the optimal tradeoff between dose, acquisition time, and image noise. An iterative algorithm was developed for determining optimal dosage and acquisition time based on a task-limited noise level.
Methods: The mean and standard deviation (SD) were determined from a region of interest (ROI) of the myocardium to define a ratio: mean/SD (MSD). Using SD and a surrogate for "noise" has its limitations: 1) intrinsic count variability due to partial volume, and tracer uptake and, 2) non-Poisson nature of reconstructed and post filtered data. The iterative algorithm was used to fit a model to the limiting MSD. From this, an optimal acquisition time was determined for a target MSD to detect a 5% perfusion defect.
Data Acquisitions: Phantom data simulating patient distributions and a 40% septal defect were acquired on a Biograph 64 slice PET/CT scanner using a 30 minute listmode acquisition. The technique was also tested in 18 subjects. Patients received a 2 mCi at rest and ~2 mCi stress on the following day. A dynamic series for 10, 20, 40, 80, 160, and 320 seconds was acquired 10 minutes post injection. The myocardial ROI was taken from a separate 600 second acquisition using >70% of the maximum myocardial voxel limit.
Data analysis: The phantom data converged to theoretical DATP of 9.5 mCi (simulated) *min. In patients, the iterative algorithm converged to a solution in 18 Rest , 9 Ad and 8 Ex. The results are summarized in Table 4:
Table 4. DATP for detection of 5% defect. 95% time is the limit in which 95% of patients would have detection of the 5% defect.
Figure imgf000120_0001
The iterative technique for solving for optimal dosage acquisition time product converged for phantom and patient studies. Using this result, an optimal acquisition times for rest, adenosine and exercise stress was determined. Furthermore, it was determined that the algorithm can be used to test alternative filtering, and detection limit and used to extrapolate to the performance of lower sensitivity scanners. Example 23
The following describes the independence of myocardial functional parameters (LVEF, EDV and ESV) across a large range of acquisition times as measured from radiotracer, imaging agent 1. The accurate measurement of functional parameters using myocardial perfusion PET requires adequate count density. The correlation of functional parameters [left ventricular ejection fraction (LVEF), end-systolic volume (ESV), and end-diastolic volume (EDV)] were examined with acquisition time.
Methods: To analyze the robustness of functional measurements to variations in count density, a series of low count [1, 3, 5 minute adenosine (AD), 3, 5 minute rest, 5, 10 minute exercise (EX)] to high count (15 minute AD, 10 minute rest, 15 minute EX) ECG gated (16 time bin) PET data sets from "listmode" data were produced. LVEF, ESV and EDV were measured using the QPET analysis program.
Data acquisition: from 23 patients from two study centers. Data for this study was acquired using a same day, rest stress study. Patients received ~2 mCi at rest and also received a ~6 mCi "same day" stress (8 EX, 13 AD) dosage. Functional values from shorter rebinning times were compared with the longest acquisition time dataset.
Correlations were determined using linear regression analysis.
Results: For all acquisition times examined, regression slopes were within 10% of unity (with the exception of the 1 minute adenosine, 20%). Correlation coefficients are in Table 5.
Table 5. Correlation coefficient between list rebinning and longest acquisition.
Figure imgf000121_0001
The high count density present in cardiac imaging agent 1 myocardial perfusion PET images showed robust functional measurements across a wide range of count densities is possible. Modest variations in parameters affecting count density, such as BMI and variations in dosage, are unlikely to alter functional measurements. Example 24
The following describes the development of a method for the determination of minimum inter-injection interval for a one-day rest-stress protocol with imaging agent 1 PET myocardial perfusion. A one-day rest-stress protocol for myocardial perfusion imaging (MPI) needs minimization of wait time between injections (WT) as shorter times require greater stress/rest dosing ratios (DR) and minimum rest dose is dictated by image statistics. A method for determining the dependence of DR on WT and to identify a WT for acceptable total dose was developed.
Methods: Two-day rest-stress imaging agent 1 PET image data of the heart (5 adenosine (AD) and 5 exercise (EX) stress) from 20 patients with known reversible defects on Tc-99m MPI were combined to create artificial blended images by adding 16%, 23%, 48% or 100% of rest image to the stress image. These were paired with rest images, 2-day stress images and read by 3 blinded readers. Results were recorded by segment as reader response (RR) (0 to 4) and as quantitative defect severity (QDS) in % decrease.
Results: RR was found to be linearly related to the QDS. In general, decreases greater than 80% of maximum were read as 0, 70% to 80% as 1, 60% to 70% as "2," 50% to 60% as "3" and below 50% as "4." Analysis of RR indicated that greater than 1 unit change from the 2-day data were observed in reader response in general only for the 48% and 100% blended image sets. Therefore 23% was deemed the maximum tolerable rest-to-stress contamination. Using the relationship between rest-stress contamination and dosing, it was found that, for AD a minimum DR of 2.2 was required with a 0.5 hour WT, and for EX a minimum DR of 3.0 was needed with a 1-hour WT.
Maximum tolerated rest-to-stress contamination levels were determined from modeled images. The uptake properties of imaging agent 1 with elevated coronary flow made it possible to tolerate a relatively low DR and short WT for AD studies while a longer WT and higher DR is needed for EX studies.
Example 25
The following describes the design of a 1-day rest-stress PET MPI protocol that requires selection of doses and imaging times for both rest and stress phases as well as the interval between rest and stress doses. These parameters were determined using three properties of imaging agent 1 in myocardial perfusion imaging: 1) the injected dose at rest that yields a diagnostic quality image for a given acquisition time, 2) the maximum acceptable contribution of the rest dose to the stress image and 3) the maximum total injected dose that may be
administered based on radiation dose considerations.
The minimum rest dose for a given imaging acquisition time in which the count- related signal-to-noise did not meaningfully contribute to reader error was determined. This was done by simulating increasing doses using multiple rebinnings of patient rest study with increasingly greater amounts of data. This method uses the increasing number of coincidence events in sequential rebinnings to create images that model increasing dose and/or acquisition duration. This method is valid for relatively low concentrations of radioactivity, such as are used here.
When the relationship between the dose and acquisition time are known, the rest dose for Cohort 2 was calculated. After considering the dosing required for a range of acquisition times from two minutes up to a practical maximum of 10 minutes, five minutes was selected. This permitted an initial dose of 2.9 mCi for the rest acquisition.
To determine the stress dose for a given rest dose, the dosing ratio was determined. To do this, first, the maximum tolerable contribution of the rest dose to the- stress image was determined. This was assessed by creating simulated stress images with a range of rest dose contributions using combinations of data from the Study Day 1 rest and Study Day 2 stress studies.
The final step of the method is the need to maintain the total dose below a limit of 14 mCi, with some additional margin, to limit the radiation dose to 5 rem to the critical organ and 1 rem effective dose (ED) or lower.
Using the maximum rest contribution to the stress image from the analysis, a range of dosing intervals was considered from a minimum of 15 minutes (essentially immediately) to a maximum practical limit of 2 hours. Based on this it was possible to select a 30 minute interval for adenosine stress that yielded a corresponding ratio of the stress dose to the rest dose of 2.0.
For exercise stress, a combination of a longer dosing interval and greater dose ratio was needed due to the lower net myocardial uptake of radioactivity with exercise. Thus, a dosing interval of 60 minutes was chosen which corresponded to a dose ratio of 3.0. The rest acquisition time was increased to 7 minutes and the rest dose reduced to 1.7 mCi to allow for the greater required stress/rest dose ratio while still maintaining the total comfortably within the 14 mCi limit.
In order to allow some range of dosing and to avoid variations in dosing that might jeopardize the integrity of the study, the dose and dose ratio values above were set as the lower limits of 15% to 20% ranges for each variable and the acquisition times increased to a minimum of 15 minutes for all acquisitions to account for the possibility of lower sensitivity of the 2D PET scanners. The data acquisition was broken into sections so that images derived from shorter acquisition times may be obtained from the same data as necessary. This resulted in the final specified dosing of 2.9 mCi to 3.4 mCi rest with a stress dose of 2.0 to 2.4 times the rest dose for adenosine stress. For exercise stress, the final doses were set at 1.7 mCi to 2.0 mCi for rest with a stress dose 3.0 to 3.6 times the rest dose. These doses are intended to reflect the actual net injected radioactivity so that additional radioactivity is required in the syringe prior to injection to compensate for losses due to adsorption and the dead volume of the syringe.
Example 26
The following describes human safety, dosimetry, biodistribution, and rest-stress myocardial imaging characteristics of 18F-labeled imaging agent 1 myocardial perfusion PET tracer. 18F-labeled imaging agent 1 is a novel myocardial perfusion imaging PET tracer that targets mitochondrial complex 1. Studies of human safety, dosimetry, biodistribution, and myocardial imaging characteristics of this tracer were evaluated.
Methods: 25 normal subjects were enrolled in 2 studies: 13 received 222 MBq I.V. At rest (R) only and 12 more subjects received 94 MBq at R and, on a second day, 124 MBq at peak adenosine stress (Adeno, n=6) or at peak treadmill exercise (Ex, n=6). Physical exam, laboratory, vital signs, ECG, and EEG were monitored pre- and post- injection. Myocardial (Myo), liver, blood pool and lung Standardized Uptake Values (SUV) were determined from sequential PET images over time. Mean dose for various organs and mean effective dose (ED in mSv/MBq) were estimated.
Results: There were no adverse events related to the tracer. The top highest-dose organs were kidneys at R and heart with Adeno and Ex . ED was 0.019 at R and with Adeno and 0.015 with Ex. Myo SUV's remained high during imaging. Ex myo SUV was lower with Ex due to higher skeletal muscle uptake. Ex myo SUV was lower with Ex due to higher skeletal muscle uptake. Myo/liver was highest with Ex, followed by Adeno and R (see Table 6). Myo/blood and Myo/lung were high and rapidly improved with time.
Table 6.
Figure imgf000125_0001
Example 27
Studies were performed in subjects to determine dosing protocols for imaging agent 1 under various conditions. Determining dosing protocols included assessing parameters such as mCi of imaging agent 1 injected in the body of the subject; mCi of imaging agent 1 injected from the syringe; acquisition time of images after injection; delay between rest and stress studies, etc. Parameters varied for rest and stress, for example, the injected dose (in the body) for exercise stress was at least three times the injected dose (in the body) at rest. In addition, the injected dose (in the body) for pharmacological stress was at least two times the injected does (in the body) at rest. Results are shown in Table 7.
Table 7. Imaging agent 1 doses, acquisition times and dosing delay for exercise and pharmacologic stress.
Delay
Injected Injected Dose between
Dose in the in the Syringe Acquisition Studies
Stress Test Study Body (mCi) (mCi) Time (min) (min)
Rest 1.7 - 2.0 2.5-3.0 10 60
Exercise
Stress 8.6 to 9.0 9.0-9.5
Minimum
Rest to
x3 injected
Stress ratio
Rest dose
Pharmacologic Rest 2.4 - 2.9 2.5 - 3.0 10 30
Stress 5.7 - 6.2 6.0 - 6.5
Rest to Minimum
Stress ratio x2 injected I I Rest dose | | |
Various parameters have been determined for dosing imaging agent 1 in human subjects, including injected does, delay between studies, ration of rest to stress dosing, and the amount in the syringe compared to the amount injected from the syringe.
Example 28
The following provides results obtained from a study regarding a single-dose dosimetry, biodistribution, and safety trial of imaging agent 1 in healthy subjects. Whole body PET image data for the 12 healthy volunteers were obtained using imaging agent 1 at approximately 10 minutes, 30 minutes, 50 minutes, 2 hours, 2.5 hours, 3.83 hours, and 4.5 hours post injection. Image data were attenuation corrected at the imaging site, and were quantified based on the Medical Internal Radiation Dose (MIRD) 16 methodology by Dosimetry Analysis Laboratory, CDE Dosimetry Services (CDE) to determine kinetic data in all organs showing significant uptake of activity. Dosimetry estimates were created via kinetic modeling of the quantified image data to determine residence times, and the standard MIRD methodology. These estimates were determined using 3 assumptions regarding urinary bladder voiding intervals (2.0, 3.5, and 4.8 hr). Kinetic data, residence times, and the dosimetry estimates are reported for individuals, and as summary statistics.
Terminology. Effective Dose (ED): Developed by the ICRP for occupational radiation protection, the ED enables the comparison of radiation detriment from a uniform external dose and a non-uniform internal dose. The risk for a 1 rem ED determined for an non-uniform internal dose is equal to the risk from a 1 rem uniform external exposure (total body dose). As defined in ICRP publication 60 [ICRP-60 1991].
Effective Dose Equivalent (EDE): Developed by the ICRP for occupational radiation protection, the EDE enables the comparison of radiation detriment from a uniform external dose and a non-uniform internal dose. The risk for a 1 rem EDE determined for an non-uniform internal dose is equal to the risk from a 1 rem uniform external exposure (total body dose). As defined in ICRP publication 30 [ICRP-30 1981].
MIRD Methodology: The methodology developed by the Medical Internal Radiation Dose Committee for the determination of radiation absorbed dose. This methodology included the use of radiation transport factors (S-values), and bio-kinetic parameters (residence times). As defined in the MIRD Primer, Society of Nuclear Medicine, 1991.
%CV is Coefficient of variation (Ratio of the standard deviation to the mean times 100).
Percent Injected Dose vs. Time from Whole Body Images. Percent injected activity as a function of time was determined for brain, heart wall, kidneys, liver, lungs, red marrow (lumbar region), salivary glands, spleen, stomach wall, thyroid, and urinary bladder. On average, the organ that showed the largest peak uptake was the liver with approximately 19.1% of the injected activity (data not shown). The next largest peak uptake occurred in the kidneys with approximately 9.4% of the injected activity (data not shown).
Dosimetry Estimates. On average, for the urinary bladder voiding interval of 3.5 hours the organ receiving the largest absorbed dose was the kidneys at 0.24 rem/mCi (0.066 mSv/MBq) and the heart wall at 0.18 rem/mCi (0.048 mSv/MBq). The mean ED (effective dose) was 0.071 rem/mCi (0.019 mSv/MBq). Table 8 shows the absorbed dose estimates (rem/mCi). The mean adsorbed dose for the listed organs is found in column one of Table 8.
Table 8.
Mean CV Min Max
Adrenals 5.8E-02 7% 4.9E-02 6.4E-02
Brain 9.4E-02 25% 5.7E-02 1.3E-01
Breasts 3.2E-02 8% 2.8E-02 3.5E-02
Gallbladder Wall 6.4E-02 8% 5.4E-02 7.1E-02
LLI Wall 4.3E-02 8% 3.7E-02 4.8E-02
Small Intestine 4.7E-02 8% 4.0E-02 5.2E-02
Stomach Wall 1.5E-01 26% 9.0E-02 2.3E-01
ULI Wall 4.7E-02 7% 4.1E-02 5.2E-02
Heart Wall 1.8E-01 17% 1.2E-01 2.4E-01
Kidneys 2.4E-01 22% 1.6E-01 3.5E-01
Liver 1.5E-01 19% l.OE-01 1.9E-01
Lungs 4.2E-02 7% 3.6E-02 4.6E-02
Muscle 3.8E-02 8% 3.2E-02 4.1E-02
Ovaries 4.5E-02 8% 3.9E-02 5.0E-02
Pancreas 5.9E-02 8% 4.8E-02 6.7E-02
Red Marrow 6.0E-02 11% 4.7E-02 6.9E-02
Osteogenic Cells 6.9E-02 8% 5.7E-02 7.8E-02
Salivary 1.3E-01 38% 8.6E-02 2.5E-01
Skin 2.9E-02 8% 2.5E-02 3.2E-02
Spleen 6.0E-02 21% 4.0E-02 7.6E-02
Testes 3.4E-02 9% 3.0E-02 3.8E-02
Thymus 4.1E-02 8% 3.5E-02 4.5E-02
Thyroid 1.2E-01 30% 7.1E-02 1.8E-01
Urinary Bladder
Wall 8.4E-02 18% 6.5E-02 l.lE-01
Uterus 4.6E-02 8% 4.0E-02 5.1E-02
Total Body 4.5E-02 7% 3.7E-02 4.9E-02
EDE 8.0E-02 11% 6.3E-02 9.1E-02
ED 7.1E-02 12% 5.5E-02 8.9E-02
Example 29
Results related to a human study of imaging agent 1, a novel 18F-labeled tracer for myocardial perfusion PET imaging; dosimetry, biodistribution, safety, and imaging characteristics after a single injection at rest are described.
Methods: Study population. Healthy adults (as determined by medical history, physical examination, vital signs, ECG, EEG, neurological examination, and clinical laboratory testing), ages 18-40 years, participated in the study. In order to be enrolled, subjects had to meet all protocol-specified inclusion criteria and none of the exclusion criteria.
Study design. This was a non-randomized, open-label, single-dose study. A total of 13 healthy adult subjects were enrolled and administered a single dose of imaging agent 1 at a single study center in the United States. Subjects were screened within 14 days prior to enrollment to confirm subject eligibility, and began baseline assessments at the study center the day before study drug administration. Subjects remained at the study center until completion of the Study Day 2 safety assessments (24 ±8 hours post- dose). A telephone call was made to study subjects 48 ±8 hours post-dose for adverse event (AE) monitoring. All subjects returned to the study center approximately one week (5-7 days) post-dose for a follow-up safety visit, and were contacted by telephone approximately 14-17 days post-dose for final serious AE monitoring.
Determination of dose and method of administration. The 8 mCi target dose was selected to provide adequate count statistics and was projected to be well below the maximum acceptable radiation exposure based on preclinical data. These data demonstrated that the maximum dose of imaging agent 1 that may be administered to a human without exceeding 50 mSv (5 rem) to the target was 742 MBq (20.0 mCi) and the injected dose that yielded an effective dose (ED) of < 10 mSv (1 rem) was 666 MBq (18.0 mCi) (Stabin, M G, Sparks, RB, et al, OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine." J Nucl Med 2005 46(6): 1023-7).
On day 1, each subject received a 1-3 mL intravenous bolus injection of imaging agent 1 in a sterile solution of <5 ethanol containing <50 mg/mL sodium ascorbate in water, calculated to deliver approximately the target dose of imaging agent 1 at the time of injection. The dose was administered in less than 10 seconds, followed immediately by a 3-5 mL saline flush.
The net injected dose was calculated by subtracting the decay-corrected radioactivity in the syringe and injection tubing after injection from the assayed and decay-corrected radioactivity in the syringe prior to injection.
PET imaging protocol. Whole -body PET imaging from head to mid thigh was performed at protocol-specified time-windows.
Dosimetry analyses. Estimates of radiation dosimetry for the standard organs of the adult male and female models and for the, salivary glands as well as the effective dose equivalent (EDE) (International Commission on Radiological Protection (ICRP), Recommendations of the International Commission on Radiological Protection, Publication 26. Ann ICRP. 1977; 1(3)) and the effective dose (ED) (International Commission on Radiological Protection (ICRP), 1990 Recommendations of the International Commission on Radiological Protection, 60. Ann ICRP. 1990; 21(1-3)) were determined using the OLINDA/EXM software (Stabin, M G, Sparks, RB, et al, OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine." J Nucl Med 2005 46(6): 1023-7) Assessment of radiation dosimetry was based on the MIRD method, with data derived from imaging studies, using methods consistent with MIRD Pamphlet no.16 (Siegel JA, Thomas SR, Stubbs JB, et al. MIRD pamphlet no. 16: Techniques for quantitative
radiopharmaceutical biodistribution data acquisition and analysis for use in human radiation dose estimates. J Nucl Med. 1999 Feb;40(2):37S-61S).
The attenuation corrected transverse image data slice planes were combined into a single three-dimensional image matrix for each subject and each time point using custom software. These images were then divided into 6 image sets ("anterior", "posterior", "salivary", "thyroid", "source", and "full") of combined coronal plane image data for each subject at each time point, grouping organs with similar anterior to posterior depths. This was done to optimize the ROI creation, and minimize background contribution to the organs contained in each combined coronal plane image. The "anterior" images contained stomach wall, heart wall, and urinary bladder. The
"posterior" images contained kidneys, lumbar spine, and spleen (when visible). The "salivary" images contained the salivary glands (parotid and submandibular). The "thyroid" images contained the thyroid. The "full" images combined all of the coronal image planes that contained subject image data and was used for quantification of the brain and liver. The "source" images contained the calibration source.
Regions of interest were drawn around all organs that showed uptake above background using custom software developed and validated for this purpose. Absolute radioactivity was determined by normalizing ROI sums by a calibration factor derived from the calibration source. Region counts were also adjusted for activity containing underlying and overlying tissue that was not part of the organ or tissue being quantified by utilization of background regions of interest. Total body region counts were also corrected for off body background counts. Appropriate normalization of region sizes for organ and adjacent regions were made. Unobstructed regions of organs with significant overlap from other activity containing organs were also employed where necessary. In order to estimate the activity in the lower legs (which were not imaged), a region of interest on the upper thigh was utilized. Activities were also normalized where necessary to account for 100% of the injected activity, and to insure conservative (slight over-estimates) determination of absorbed dose. Where urinary excretion data were available beyond the end of the imaging regimen, these data were used to determine whole body retention.
Kinetic data for brain, heart wall, kidneys, liver, red marrow (lumbar spine regions were utilized), salivary glands, spleen, stomach wall, thyroid, and urinary bladder for the subjects in the study were determined using image quantification methodology. Absolute activity was converted to fractional dose by dividing by the total activity administered. Organ and tissue data were fit using non-linear least-squares regression with sums of exponentials of the form shown in Equation 1, where f and λ are the model parameters that are determined in the fitting process, Fy(t) is the fraction of the total injected activity, t is the time post injection, i is the ith ROI, j is the jth subject, and k is the kth exponential term. Between one and four exponential terms were employed, as appropriate.
Figure imgf000131_0001
Equation 1.
k
The regression was performed using custom software that determines initial parameter values based on the temporal variation of the kinetic data, and the use of pre- tabulated estimates for various time activity scenarios as selected by the user. Once these data were fit, residence times were determined by integration of these empirically determined functions (sums of exponentials) from time equal zero to infinity, taking into account physical decay. Remainder of Body residence times were determined by subtraction of appropriate organ residence times from whole body residence times. Urinary bladder residence times were determined using the parameters determined by fitting the whole body activity data with a urinary bladder model as implemented in the OLINDA/EXM software with 3.5 hour bladder voiding interval. Red marrow residence time was determined based on a region of interest drawn on a portion of the lumbar spine. The lumbar spine was assumed to contain 16.1% (International Commission on Radiological Protection (ICRP) Publication 23, Report of the Task Group on Reference Man. Pergamon Press. 1975, page 125) of the total red marrow.
Organ/Tissue Dosimetry Estimates. Absorbed dose estimates for all target organs were determined using the OLINDA/EXM software using the adult "male" model. The resulting absorbed dose estimates were scaled based on the total body mass of the individual subjects relative to that of the radiation transport phantom. Salivary gland dosimetry was determined by using a conservative estimate of the S-value for salivary glands based on the reference man total mass of the parotid and submaxilary salivary glands (International Commission on Radiological Protection (ICRP) Publication 23, Report of the Task Group on Reference Man. Pergamon Press. 1975, page 125) and assuming a spherical shape. S-Values for spheres were produced by the OLINDA/EXM software, and were linearly scaled based on the relative total body mass of reference man to that of subject. These S-values were then multiplied by the residence times to produce final salivary gland dose estimates.
Statistical Analyses. All statistical analyses and all summary tables and listings were prepared using SAS® release 9.1.3 (SAS Institute, Inc., Cary, NC). Standard descriptive summaries included the N, mean, median, standard deviation (SD) and/or coefficient of variation (%CV), minimum and maximum for continuous variables, and the number and percent for categorical variables.
Results: Patient demography. Of the 26 subjects who were screened, 13 subjects (12 males and one female) were administered imaging agent 1, and completed all safety evaluations. The mean age was 23.4 years (range: 19-34 years) and the mean BMI was 23.4 (range: 20-26). One patient was not included in the analyses of dosimetry, biodistribution and radiokinetics, due to the inability to confirm the dose calibrator assay data for the standards preparation. Radiation dosimetry. The intravenous bolus injection was calculated to deliver no more than 8 mCi of 18F at the time of injection. The mean (SD) final decay-corrected dose was 6 (0.6) mCi of 18F, with a range of 4.6 to 6.6 mCi (170 to 244 MBq). The difference between the target dose and the final dose was due to the retention of imaging agent 1 in the syringe.
The absorbed dose summary statistics are presented in Table 9 (mSv/MBq). The organ receiving the largest mean absorbed dose was the kidneys at 0.066 mSv/MBq (0.24 rem/mCi), followed by the heart wall at 0.048 mSv/MBq (0.18 rem/mCi). The mean ED was 0.019 mSv/MBq (0.072 rem/mCi).
Table 9. Absorbed Dose Estimates (mSv/MBq), N= 12, Void Interval = 3.5 hours.
Mean CV Min Max
Adrenals 1.6E a -02 7% 1.3E-02 1.7E-02
Brain 2.5E-02 25% 1.5E-02 3.6E-02
Breasts 8.8E-03 8% 7.5E-03 9.6E-03
Gallbladder Wall 1.7E-02 8% 1.5E-02 1.9E-02
LLI Wall 1.2E-02 8% 1.0E-02 1.3E-02
Small Intestine 1.3E-02 8% 1.1E-02 1.4E-02
Stomach Wall 4.0E-02 26% 2.4E-02 6.2E-02
ULI Wall 1.3E-02 7% 1.1E-02 1.4E-02
Heart Wall 4.8E-02 17% 3.4E-02 6.4E-02
Kidneys 6.6E-02 22% 4.4.E-02 9.5E-02
Liver 3.9E-02 19% 2.7E-02 5.2E-02
Lungs 1.1E-02 7% 9.7E-03 1.2E-02
Muscle 1.0E-02 8% 8.7E-03 1.3E-02
Ovaries 1.2E-02 8% 1.1E-02 1.3E-02
Pancreas 1.6E-02 8% 1.3E-02 1.8E-02
Red Marrow 1.6E-02 11% 1.3E-02 1.9E-02
Osteogenic Cells 1.9E-02 8% 1.6E-02 2.1E-02
Salivary 3.5E-02 38% 2.3E-02 6.8E-02
Skin 7.9E-03 8% 6.8E-03 8.7E-03
Spleen 1.6E-02 21% 1.1E-02 2.1E-02
Testes 9.2E-03 9% 8.1E-03 1.0E-02
Thymus 1.1E-02 8% 9.6E-03 1.2E-02
Thyroid 3.2E-02 30% 1.9E-02 4.9E-02
Urinary Bladder Wall 2.3E-02 18% 1.7E-02 3.0E-02
Uterus 1.2E-02 8% 1.1E-02 1.4E-02
Total Body 1.2E-02 7% 1.0E-02 1.3E-02
EDE 2.2E-02 11% 1.7E-02 2.5E-02
ED 1.9E-02 12% 1.5E-02 2.4E-02 a "E" followed by a "-" is the exponent multiple of 3 convention for decimal presentation.
Whole-organ biodistribution. The biodistribution of imaging agent 1 , calculated as the whole-organ percent injected radioactivity as a function of time, was determined for brain, heart wall, kidneys, liver, lungs, red marrow (lumbar region), salivary glands, spleen, stomach wall, thyroid, and urinary bladder (Table 10 and Figure 11). Figure 11 shows whole body coronal images through the body at the level of the myocardium from a representative subject at different time points after administration of imaging agent 1. Images have been corrected for 18F decay. It can be seen that the heart exhibits high and sustained retention of 18F from the earliest images through approximately 5 hours after injection. The liver also appears, generally exhibiting an intensity similar to that of the heart, peaking between 10 and 30 minutes after injection and clearing by approximately 2 hours. The organ that showed the largest mean peak uptake was the liver with approximately 19.1% of the injected activity. The next largest mean peak uptake occurred in the kidneys with approximately 9.4% of the injected activity, followed by the brain with approximately 8.3% of the injected activity. Data from subjects in the study were used to determine the urinary excretion rate for each subject and the residence time for radioactivity in the bladder using a standard model, with a theoretical fixed voiding interval of 3.5 hours post-dose. The largest mean residence times were for remainder tissues (1.8 hours), liver (0.28 hours), and brain (0.14 hours). Summary residence time statistics are presented in Table 11.
Table 10. Mean Percent (%) Administered Dose versus Time (Hours Post-dose) N=12,
18F, Decay Corrected.
Figure imgf000135_0001
a Nominal times in hours post-dose (beginning of time window)
NA=not available
Table 11. Residence Times (Hours) Summary Statistics (N=12, Void Interval=3.5
Hours).
Figure imgf000135_0002
"E" followed by a "-" is the exponent multiple of 3 convention for decimal presentation
18
Early elimination of F in urine. Urine collected pre-dose (Baseline), and all voids up to 8 hours post-dose were collected and assayed for 18F. However, as in blood collection, the urine collection terminated near the 7-hour minimum specified in the protocol. Mean urinary excretion over the approximate 7-hour void interval was 4.83 %ID with a %CV of 64.7 and a range of 0.64 %ID to 12.41 %ID. This finding is in reasonable agreement with cumulative urine excretion of 5% as measured with PET imaging.
Discussion: The critical organ for imaging agent 1 was the kidneys, with a mean estimated dose of 0.066 mSv/MBq (0.24 rem/mCi) The maximum injected dose of the compound that may be administered without exceeding 50 mSv to the critical organ is therefore 770 MBq. This is somewhat higher than the 185 MBq to 370 mBq recommended in the widely-used guidance by the Center for Drug Evaluation and Research (CDER) that describes recommended package insert wording for facilities applying to manufacture [18F]-FDG) (PET Drug Applications - Content and Format for NDAs and AND As: Fludeoxy glucose F 18 Injection, Ammonia N 13 Injection, Sodium Fluoride F 18 Injection, Attachment II, Sample Formats; Labeling for Ammonia N 13 Injection, Fludeoxyglucose F 18 Injection and Sodium Fluoride F 18 Injection,
Attachment II (CDER 2000)). This behavior is a result of the very rapid urinary
18
excretion of a large fraction of [ FJ-FDG shortly after administration, resulting in a substantially higher exposure to the urinary bladder for that compound compared with that of imaging agent 1. The ED due to imaging agent 1 (0.019 mSv/MBq), is the same
18
as the ED of [ FJ-FDG (International Commission on Radiological Protection (ICRP), Radiation Dose to Patients from Radiopharmaceuticals, Addendum 2 to ICRP
Publication 53, Publication 80, Ann ICRP. 1999; 28(3)). It can therefore be concluded that the radiation dose from imaging agent 1 is comparable to or less than that due to [18F]-FDG.
Since the mean estimated effective dose (ED) for imaging agent 1 is 0.019 mSv/MBq (0.072 rem/mCi), the maximum injected dose that may be administered without exceeding 10 mSv ED is therefore 521 MBq.
The radiation dose estimates from this study are consistent with those derived from non-human primates (Lazewatsky J, Azure M, Guaraldi M et al. Dosimetry of BMS747158, a novel 18F labeled tracer for myocardial perfusion imaging, in nonhuman primates at rest. J Nucl Med. 2009;49(Supplement l): 15p.) and the high and sustained retention of imaging agent 1 in the heart is consistent with data in both non-human primates and in other species (Yu M, Guaraldi MT, Mistry M, Kagan M, McDonald JL, Drew K, Radeke H, Purohit A, Azure M, Casebier DS, Robinson SP. BMS-747158-02: a Novel PET Myocardial Perfusion Imaging Agent. Journal Nuclear Cardiology 2007 Nov-Dec; 14(6):789-98). Although the critical organ in the primate-derived estimates was seen to be the heart wall, the estimated human radiation dose for the heart wall in that study was 0.067 mSv/MBq, which is very similar to the critical organ value of 0.066 mSv/MBq seen for the kidneys in this study. The doses to both organs were among the highest in both the non-human primates -derived results and in the current study and are within two standard deviations of one another.
Imaging agent 1 was well-tolerated and no clinically significant safety concerns were raised. Changes from baseline in vital signs, laboratory values (hematology, coagulation, clinical chemistry and urinalysis), ECGs, and EEGs were not clinically significant. Potential cardiotoxicity (signaled through coagulation studies and changes in Troponin-T levels) were not exhibited. Physical and neurological examinations did not reveal any pre-dose or post-dose abnormalities. The DMC did not raise safety concerns following periodic reviews of the safety data.
The results obtained in this study demonstrated that imaging agent 1 appeared to be safe and was well tolerated and exhibited a substantial and sustained retention in myocardium. The critical organ after resting injection of imaging agent 1 was determined to be the kidneys with 0.066 mSv/MBq. Based on the observed mean ED, the maximum injected dose that may be administered without exceeding 1 rem ED is 14 mCi (521 MBq). The ED from imaging agent lis the same as that of [18F]-FDG, while the critical organ (kidney) dose of imaging agent 1 is significantly less than the critical organ (urinary bladder) dose of [18F]-FDG.
Example 30
The following example describes studies relating to cardiac imaging and safety evaluation of imaging agent 1, a novel PET myocardial perfusion imaging agent, in chronic myocardial compromised rabbits.
Imaging agent 1 is an 18F labeled imaging agent for myocardial perfusion imaging (MPI) with positron emission tomography (PET) (Yu M, Guaraldi MT, Mistry M, Kagan M, McDonald JL, Drew K et al. : a novel PET myocardial perfusion imaging agent. J Nucl Cardiol 2007;14:789-98). Cardiac imaging with this agent shows clear myocardium and identification of acute myocardial ischemia and tissue necrosis in animal models of acute coronary ligation and ischemia reperfusion injury (Yu M, Guaraldi MT, Mistry M, Kagan M, McDonald JL, Drew K et al: a novel PET myocardial perfusion imaging agent. J Nucl Cardiol 2007;14:789-98; Nekolla SG, Reder S, Higuchi T, Dzewas G, Poethko T, Preissl A et al. Assessment of Imaging Properties of a New F-18 Labelled Flow Tracer in a Pig Model. J Am Coll Cardiol 2008;51:A170; and Maddahi J, Schiepers C, Czernin J, Huang H, Schelbert H, Wijatyk A et al. First human study of BMS747158, a novel F-18 labeled tracer for myocardial perfusion imaging. J Nucl Med 2008;49:70P). In model systems imaging agent 1 has demonstrated superior characteristics over the currently available MPI agents. In comparison with single photon emission computer tomography (SPECT) based agents (99mTc-Sestamibi
201
and Thalium), Imaging agent 1 has the advantage of PET technology with accurate attenuation correction and quantification of myocardial perfusion in absolute terms. Furthermore, imaging agent 1 heart uptake correlates better with myocardial perfusion at a large range of flow rates invitrol and at rest and stress conditions in-vivo (Nekolla SG, Reder S, Saraste A, Higuchi T, Dzewas G, Preissel A et al. Evaluation of the novel myocardial perfusion positron-emission tomography tracer 18F-BMS-747158-02:
comparison to 13N-ammonia and validation with microspheres in a pig model.
Circulation 2009; 119:2333-42). In comparison with current PET agents, like 13N- Ammonia and 82Rubidium, the long half-life (110 minutes) of 18F enables imaging agent 1 to be radio- synthesized and supplied centrally. It also provides the opportunity f or imaging under excise stress, in addition to pharmacological stress.
Safety and radio-dosimetry studies in multiple normal species show imaging agent 1 has acceptable safety margin for clinical development (Mistry M, Onthank D, Green J, Cicio S, Casebier D, Robinson S et al. Toxicological Evaluation of BMS- 747158, a PET Myocardial Perfusion Imaging Agent. The Toxicologist 2008;102:476; and Lazewatsky J, Azure M, Guaraldi M, Kagan M, MacDonald J, Yu M et al.
Dosimetry of BMS747158, a novel 18F labeled tracer for myocardial perfusion imaging, in nonhuman primates at rest. J Nucl Med 2009;49: 15p). The critical organ for radiation is the heart and the radiation doses were comparable with the commercial available agent 18F-fluorodeoxy glucose (Lazewatsky J, Azure M, Guaraldi M, Kagan M, MacDonald J, Yu M et al. Dosimetry of BMS747158, a novel 18F labeled tracer for myocardial perfusion imaging, in nonhuman primates at rest. J Nucl Med 2009;49: 15p).
Methods: Rabbit Model of Myocardial Infarction. Male New Zealand rabbits (body weight 2.5-3.5 kg) were purchased from Harlan (Oakwood, MI) and maintained in the A AALAC- accredited Animal Care Facility at Lantheus Medical Imaging. The study protocol was approved by the Institutional Animal Care and Use Committee. The procedure of developing a rabbit model of myocardial infarction (MI) was similar to the method described previously (Fujita M, Morimoto Y, Ishihara M, Shimizu M, Takase B, Maehara T et al. A new rabbit model of myocardial infarction without endotracheal intubation. J Surg Res 2004;116: 124-8). Briefly, the rabbit was anesthetized with ketamine (40 mg/Kg, im) and xylazine (9 mg/Kg, im) and placed in a supine position. The surgery was performed under aseptic conditions. A mid-sternotomy was performed carefully to avoid injury of parietal pleura. The pericardial sac was exposed and incised. The left ventricular anterior and lateral wall was revealed and a major branch of the left coronary artery was ligated. Success of the ligation was verified by the color change to pale in the affected area of the left ventricular wall. The chest was then closed and the animal allowed to recover. Four weeks after the surgery, the rabbit was used for the imaging and cardiovascular evaluation study.
Imaging and Cardiovascular Evaluation. PET images and cardiovascular parameters were evaluated in both normal and MI rabbits. Prior to imaging, the rabbit was anesthetized with ketamine (25 mg/Kg, im) and xylazine (5 mg/Kg, im) and the marginal ear vein was catheterized for imaging agent 1 injection. The right femoral artery was isolated and canulated with a Millar catheter (SPC340, Millar Instruments, Houston, TX) for arterial pressure measurement. Then the animal was positioned in a microPET camera (Focus220, CTI Molecular Imaging, Inc. Knoxville, TN) for cardiac imaging. The Millar catheter was connected to a computer driven data acquisition system (MP35, BIOPAC Systems, Goleta, CA) for recording of mean arterial pressure (MAP), and systolic and diastolic arterial pressure (SAP and DAP). In addition, electrocardiogram (ECG) was also recorded with 3 non-invasive limb leads in lead II configuration using the BIOPAC system. Heart rate (HR) and QT interval were derived from ECG recording. After a stabilization period, cardiovascular parameters: MAP, SBP, DBP and ECG, were recorded 5 minutes before imaging agent 1 intravenous injection (-1.5 mCi) and the recording continued for additional 20 minutes post- injection. The rabbit was imaged for 30 minutes.
Image Reconstruction and Analysis. After the acquisition, images were reconstructed in a matrix of 256 x 256 pixels with 95 transverse slices using the
OSEM2D algorithm and decay corrected (microPET Manager and ASIPro, CTI Molecular Imaging, Inc. Knoxville, TN). The pixel size was 0.47 mm and the slice thickness was 0.80 mm. The images were reoriented regarding cardiac axis and serial tomographic cardiac image frames were then generated for a 10-minute period from 20 to 30 minutes. Polar map images were then generated from reconstructed cardiac short- axis image using QPS 2008 software (Cedars-Sinai Medical
Center, Los Angles, CA).
Radiopharmaceutical Agent. The chemical structure and radiosynthesis of imaging agent 1 have been described previously (Yu M, Guaraldi MT, Mistry M, Kagan M, McDonald JL, Drew K et al. : a novel PET myocardial perfusion imaging agent. J Nucl Cardiol 2007;14:789-98; and Purohit A, Radeke H, Azure M, Hanson K, Benetti R, Su F et al. Synthesis and biological evaluation of pyridazinone analogues as potential cardiac positron emission tomography tracers. J Med Chem 2008;51:2954-70). The radiochemical purity used in this study was 99.1- 99.9%, and the specific activity was 3265-7016 Ci/mmol. The agent was prepared in 5% ethanol (v/v) and 50 mg/ml ascorbic acid in water following the clinical protocol.
Data Analysis. Data are expressed as mean + SD and unpaired student t-test (assuming unequal variances) was used for comparison of baseline values between control and MI rabbits. p<0.05 was considered statistically significant. At each timepoint (before and 1-, 5-, 10- and 20-minute after imaging agent 1 injection), MAP, SAP and DAP measured intraarterially averaged every 10-second, and HR and QTc interval derived from ECG recording averaged every 12 heart beats. The QT interval was manually defined by one investigator and QTc was generated from QT corrected by RR interval using Fridericia method (QTc=QT/RRl/3).9
Results: The body weight of control and MI rabbits at the time of study was similar (3.35+0.19 versus 3.06+0.28 kg).
Cardiac Images Representative cardiac short-, long-axis and polar map images of control and MI rabbits are shown in Figure 12. Figure 12 shows representative cardiac images of imaging agent 1 in control and chronic myocardial infarct (MI) rabbits. These images were acquired at 20-30 min after imaging agent 1 injection and presented in cardiac short- and long-axis views, and polar maps. Defect areas were clearly identified in the MI rabbit. In the control rabbit, the myocardium was clearly visible with uniform distribution of radioactivity and minimal background interference. In the MI rabbit, a perfusion defect area in the left ventricular wall was clearly detected in the cardiac short- and long-axis, and polar map views. ECG Evaluation. As shown in Table 12, baseline ECG tracing (before imaging agent 1 injection) recorded in lead II configuration showed a normal waveform with positive QRS complexes and T waves in the control rabbit. In contrast, the QRS complex and T wave were negative with enlarged Q wave in the MI rabbit. The study obtained ECG tracing before, 1-min and 5-min after imaging agent 1 injection in control and myocardial infarct (MI) rabbits. Table 12 shows baseline values of QTc interval (corrected by Fridericia method) and averaged changes from the baseline at 1, 5, 10 and 20 min after imaging agent 1 injection in control and MI rabbits. Similar to control, no changes in ECG wave form and QTc interval were observed after injection in MI rabbits.
Table 12.
Figure imgf000141_0001
However, the baseline values of QTc and HR (Table 12 and Table 13) were comparable in these two groups. Intravenous administration of imaging agent 1 did not alter the ECG waveform, cardiac rhythm, HR and QTc interval from the baseline values at 1-, 5-, 10- and 20-minute post injection in either control or MI rabbits. The study, in part, showed averaged heart rate (HR) tracings of control and myocardial infarct (MI) rabbits 5-min before and 20-min after imaging agent 1 administration. Table 13 shows baseline values of HR and averaged changes from the baseline at 1, 5, 10 and 20 min after the injection in control and MI rabbits. Similar to control, no changes in HR were observed after injection in MI rabbits.
Table 13.
Figure imgf000141_0002
Arterial Pressure Measurement. In contrast to HR and QTc, the baseline values of MAP, SAP and DAP (Table 14 and Table 15) were significantly lower in MI rabbits than in control rabbits. In control rabbits, injection of imaging agent 1 did not induce changes in MAP (Table 14), SAP and DAP (Table 15). In agreement with the control animal, no alterations of these parameters were observed in the MI rabbits during and after administration of imaging agent 1. The study, in part, demonstrated averaged mean arterial pressure (AP) tracings of control and myocardial infarct (MI) rabbits 5-min before and 20-min after imaging agent 1 administration. Table 14 shows baseline values of mean AP and averaged changes from the baseline at 1, 5, 10 and 20 min after the injection in control and MI rabbits. Similar to control, no changes in mean AP were observed after injection in MI rabbits. * indicates p<0.05 vs. control. The study, in part, demonstrated averaged systolic and diastolic arterial pressure (AP) tracings of control and myocardial infarct (MI) rabbits 5-min before and 20-min after imaging agent 1 administration. Table 15 shows baseline values of systolic and diastolic AP and averaged changes from the baseline at 1, 5, 10, and 20 min after the injection in control and MI rabbits. Similar to control, no changes in mean AP were observed after injection in MI rabbits. * indicates p<0.05 vs. control.
Table 14.
Figure imgf000142_0001
Table 15.
Figure imgf000142_0002
Discussion: The study was designed to study imaging agent 1 as a PET imaging agent for evaluation of myocardial perfusion in diagnosis and prognosis of coronary heart disease. It was evaluated for safety in normal animals and imaged in animal models of acute myocardial ischemia and MI induced by ischemia-reperfusion injury (Yu M, Guaraldi MT, Mistry M, Kagan M, McDonald JL, Drew K et al. : a novel PET myocardial perfusion imaging agent. J Nucl Cardiol 2007;14:789-98; Nekolla SG, Reder S, Higuchi T, Dzewas G, Poethko T, Preissl A et al. Assessment of Imaging Properties of a New F-18 Labelled Flow Tracer in a Pig Model. J Am Coll Cardiol 2008;51:A170; and Mistry M, Onthank D, Green J, Cicio S, Casebier D, Robinson S et al. Toxicological Evaluation of BMS-747158, a PET Myocardial Perfusion Imaging Agent. The
Toxicologist 2008; 102:476). This study was designed to further assess this agent in a chronic cardiac compromised animal model. The model was created by chronic ligation of coronary artery in rabbits. This rabbit model was chosen based on several characteristics: 1) Similar to humans and compared to other species, rabbits have poor collateral circulation in the heart and develop MI readily after sudden coronary artery occlusion (Bell DR. Special Circulations. In: Rhoades R, Bell DR, editors. Medical Physiology: Principles for Clinical Medicine . 3rd ed. 2008. p. 290-304; and Maxwell MP, Hearse DJ, Yellon DM. Species variation in the coronary collateral circulation during regional myocardial ischaemia: a critical determinant of the rate of evolution and extent of myocardial infarction. Cardiovasc Res 1987;21:737-46). 2) Cardiac fibroblasts and regulation of collagen biosynthesis, which are critical in wound healing after myocardial injury, in rabbits are similar to that observed in humans with regard to angiotensin system (Gallagher AM, Bahnson TD, Yu H, Kim NN, Printz MP. Species variability in angiotensin receptor expression by cultured cardiac fibroblasts and the infarcted heart. Am J Physiol 1998;274:H801-H809). 3) After coronary ligation, plasma and myocardial norepinephrine levels increase (Makino T, Hattori Y, Matsuda N, Onozuka H, Sakuma I, Kitabatake A. Effects of angiotensin-converting enzyme inhibition and angiotensin II type 1 receptor blockade on beta-adrenoceptor signaling in heart failure produced by myocardial Infarction in rabbits: reversal of altered expression of beta-adrenoceptor kinase and G i alpha. J Pharmacol Exp Ther 2003;304:370-9; and Fujii T, Yamazaki T, Akiyama T, Sano S, Mori H. Extraneuronal enzymatic degradation of myocardial interstitial norepinephrine in the ischemic region. Cardiovasc Res 2004;64: 125-31). Norepinephrine clearance in the heart of rabbit is mainly via neuronal norepinephrine transporter (Gao DW, Stillson CA, O'Connell JW. Absence of MIBG uptake in the denervated rabbit heart. J Nucl Med 1996;37: 106p), similar to in humans (Eisenhofer G, Friberg P, Rundqvist B, Quyyumi AA, Lambert G, Kaye DM et al. Cardiac sympathetic nerve function in congestive heart failure. Circulation
1996;93: 1667-76). 5) Species size is appropriate for high quality PET imaging in a microPET camera while allowing concurrent ECG monitoring. In contrast to ECG waveform in the control rabbit, a negative QRS complex with an enlarged Q wave and inverted T wave were observed in lead II configuration in the MI rabbit, indicating an abnormal ventricular depolarization and repolarization. Following complete obstruction of a coronary artery branch (coronary ligation), oxygen carried to the region is reduced or ceased depending on collateral circulation, leading to cell death and tissue necrosis. A rapid tissue repair process is then started, including initial inflammation followed by angiogenesis, increased fibroblast proliferation and collagen production and deposition. These changes ultimately result in formation of scar tissue to 10 rebuild the necrotic region in the heart (Abbate A, Biondi-Zoccai GG, Van Tassell BW, Baldi A. Cellular preservation therapy in acute myocardial infarction. Am J Physiol Heart Circ Physiol 2009;296:H563-H565; and Sun Y, Weber KT. Infarct scar: a dynamic tissue. Cardiovasc Res 2000;46:250-6). Histological examination has indicated that increased fibroblast proliferation and scar formation initiate at about 2 and 18 days respectively post coronary ligation in rabbits (Morales C, Gonzalez GE, Rodriguez M, Bertolasi CA, Gelpi RJ. Histopathologic time course of myocardial infarct in rabbit hearts. Cardiovasc Pathol 2002; 11 :339- 45). In present study, the formation of scar tissue in the left ventricle of our rabbits 4-week post coronary ligation is consistent with the findings of enlarged Q wave in ECG 20 and in other similar studies (Gonzalez GE, Palleiro J, Monroy S, Perez S, Rodriguez M, Masucci A et al. Effects of the early administration of losartan on the functional and morphological aspects of postmyocardial infarction ventricular remodeling in rabbits. Cardiovasc Pathol 2005;14:88-95; and Connelly CM, Vogel WM, Wiegner AW, Osmers EL, Bing OH, Kloner RA et al. Effects of reperfusion after coronary artery occlusion on post-infarction scar tissue. Circ Res 1985;57:562-77). Previously, imaging agent 1 has been demonstrated to be capable of detecting regions of acute myocardial ischemia and necrosis induced by coronary ligation and ischemia- reperfusion injury in rats, rabbits and pigs (Yu M, Guaraldi MT, Mistry M, Kagan M, McDonald JL, Drew K et al. : a novel PET myocardial perfusion imaging agent. J Nucl Cardiol 2007;14:789-981; Nekolla SG, Reder S, Saraste A, Higuchi T, Dzewas G, Preissel A et al. Evaluation of the novel myocardial perfusion positron-emission tomography tracer 18F-BMS-747158-02: comparison to 13N-ammonia and validation with microspheres in a pig model. Circulation 2009; 119:2333-42; and Higuchi T, Nekolla SG, Huisman MM, Reder S, Poethko T, Yu M et al. A new 18F-labeled myocardial PET tracer: myocardial uptake after permanent and transient coronary occlusion in rats. J Nucl Med 2008;49: 1715-22). Imaging in this study in a rabbit model of chronic MI clearly demonstrated that imaging agent 1 imaging can detect chronic MI, possibly scar tissue suggested by ECG and other studies, imaging agent 1 has high affinity to mitochondrial complex I and, at very high concentrations (>200 μg/kg), induces transit clinical signs, such as rapid and labored breathing, decreased activity, hunched posture, urination, in normal rats and dogs (Mistry M, Onthank D, Green J, Cicio S, Casebier D, Robinson S et al. Toxicological Evaluation of BMS-747158, a PET Myocardial Perfusion Imaging Agent. The Toxicologist 2008; 102:476). However, these signs were not observed when the dose was equal or below 100 μg/kg. In anesthetized naive dogs, no cardiovascular changes (MAP, HR, left ventricular contractility etc) were observed during and after intravenously injection of imaging agent 1 at doses of equal or less than 10 μg/kg (unpublished data). This represents a large safety margin over the maximal clinical imaging agent 1 dose of 0.07 μg/kg.
In the present study, baseline values of MAP, SAP and DAP were lower in the MI rabbits than in control rabbits, indicating the chronic MI had compromised the cardiovascular system in these rabbits. The dose of imaging agent 1 used for rabbit imaging was in the clinical formulation and approximately 0.5 mCi/kg (-1.5 mCi in a 3- kg rabbit) which is also approximately 3-fold higher than the clinical dose (total rest and stress 11 doses: -10 mCi in a 60 kg individual). With this dose and in a cardiac compromised condition, no change in arterial pressure, heart rates and ECG waveform were produced. These findings indicate that imaging with imaging agent 1 is safe even in a cardiac compromised condition.
The results show that cardiac PET imaging with imaging agent 1 detects chronic myocardial infarction (fibrosis and scar formation) in addition to myocardial ischemia and necrosis under an acute condition. At imaging dose levels, imaging agent 1 is safe to be used even in cardiac compromised condition, at least in rabbits.
Example 31
The following example describes brain imaging of imaging agent 1 and evaluation of the blood brain barrier permeability in rats. PET imaging in animals and humans indicate this compound crosses the normal blood brain barrier (BBB) and can image CNS disease. Studies to date have not assessed how effectively imaging agent 1 crosses the BBB. The present studies compared brain uptake in rats in the presence and absence of BBB disruption.
Methods: Male Sprague-Dawley rats were anesthetized with sodium
pentobarbital and the left external carotid artery was cannulated close to the internal and external carotid bifurcation. Using saline as control and 25% D-mannitol as hypertonic solution, each were perfused retrogradely in six animals (0.3 mL/kg/sec) for 30 seconds. Two minutes later, ~ 1 mCi imaging agent 1 was injected via tail vein and the brain was imaged with a microPET camera for 30 minutes. Evans blue (2%, 5 mL/kg) was also injected intravenously and only animals demonstrating clear BBB disruption by Evans blue staining were included in the study. Following completion of imaging, the brain was harvested, photographed and dissected into left and right hemispheres and cerebellum. The tissue content of imaging agent 1 radioactivity was measured by gamma counter and Evans blue levels were determined by fluorescence method for calculation of the % injected dose/gram tissue and μg Evan blue/gram tissue, respectively.
Results: See Table 16. Infusion of 25% D-mannitol resulted in a marked increase in Evans blue uptake in the left hemisphere (633%) and some increased uptake in the right hemisphere (216%) and cerebellum (186%) compared to saline control. In normal rats and saline infused control rats a high level of imaging agent 1 accumulated in the brain shortly after administration. PET imaging showed this high uptake of imaging agent 1 in saline control rats was only minimally increased in brain region following BBB disruption.
Imaging agent 1 has a high BBB permeability that is only minimally increased following disruption and may be used for brain imaging.
Table 16.
Brain right hemisphere left hemisphere cerebellum uptake control BBBD control BBBD control BBBD
Evan blue
19+2 60+8 21+2 154+13 29+4 83+12 imaging
agent 1 0.72+0.0 0.81+0.0 0.72+0.0 0.93+0.0 0.78+0.0 0.95+0.0
(%ID/g) 3 4 3 6 3 5 - 146-
Example 32
The following example is related to 18F labeled imaging agent 1 PET myocardial perfusion imaging detecting more severe and extensive stress induced myocardial ischemia than Tc-99m Sestamibi SPECT. In this study, rest-stress Tc-99m Sestamibi SPECT and imaging agent 1 PET MPI were compared for evaluation of stress induced myocardial perfusion abnormalities.
Methods: Thirteen patients, from a single center, underwent rest-stress Tc-99m Sestamibi SPECT MPI, rest-stress imaging agent IPET MPI and coronary angiography. In each patient, 17 myocardial segments were visually scored for rest and stress images by independent observers who were blinded to all other results. For each patient, summed stress scores (SSS), summed rest scores (SRS), and summed difference scores (SDS) were determined from segmental scores. Percent narrowing in each coronary artery was evaluated blindly and 70% luminal diameter narrowing was considered significant.
Results: There were 15 diseased coronary arteries; 7 left anterior descending, 5 left circumflex and 3 right coronary arteries. In myocardial segments that were supplied by diseased coronary arteries, SSS and SDS were significantly higher by PET than SPECT (Table 17).
These data showed that as compared to Sestamibi SPECT, rest-stress 18F labeled imaging agent 1 PET MPI demonstrated more severe and extensive stress induced perfusion abnormalities in myocardial regions that are supplied by diseased coronary arteries.
Table 17.
Figure imgf000148_0001
Example 33
The following example describes a comparison of myocardial stress perfusion defect assessment using 99mTc sestamibi SPECT versus imaging agent 1 PET.
Myocardial uptake of imaging agent 1 exhibits a stronger relationship with myocardial blood flow across the range of achievable flow than 99mTc sestamibi. The assessment of myocardial perfusion defects by imaging agent 1 PET and 99mTc sestamibi SPECT were compared.
Methods and Results: Twenty six patients (20 men) underwent SPECT and PET within 6- months. PET was performed with imaging agent 1 at rest (2.3-3.9 mCi) followed 60 min (n=18) or 24 h (n=8) later with exercise (n=16) or adenosine (n=10) stress (7.3-8.6 mCi). Image quality of SPECT and PET was consensually assessed by 2 independent blinded readers and graded as excellent, good, or fair. Stress and rest perfusion defects on SPECT and PET were assessed by the same readers by computer- assisted visual interpretation, using the standard 17 segment, 5 point-scoring model (0=normal; 4=absent uptake). The extent and severity of ischemia (summed difference score (SDS)) was derived from the difference between summed stress (SSS) and summed rest scores (SRS). Image quality with PET was excellent in 24 and good in 2 patients. In contrast, there were 7 excellent, 18 good, and 1 fair quality study, p < 0.001 by SPECT. In 14 patients with abnormal SPECT (SSS > 4), mean SDS was greater with PET than with SPECT (9.6 + 1.8 vs. 5.4 + 0.7, p=0.02). In all 12 patients with normal SPECT (SSS < 4), SDS was zero by PET and SPECT.
Compared to 99mTc sestamibi SPECT, imaging agent 1 PET provides better image quality and results in a significant increase in the SDS in patients with abnormal SPECT. These results showed that PET imaging with imaging agent 1 provided better assessment of the magnitude of myocardial ischemia than SPECT.
Example 34
The following describes cardiac phantom simulation of dose injection parameters for one-day rest/stress myocardial perfusion (MP1) PET imaging with imaging agent 1 tracer. A 1-day rest/stress (RS) protocol for MPI with imaging agent 1 can create cross contamination (CC) in the stress image. A phantom simulation was conducted to assess the impact of CC on image characteristics for a range of conditions.
Methods: A F18 phantom with myocardium (M)=0.21 uCi/ml and liver (L)=0.22, simulating normal rest, was scanned on a Siemens Biograph-64 PET/CT for 30 min. It was washed and refilled with L=0.42, torso=0.09 and M=0.9 with a 40% defect in septal wall, then scanned for another 30 min. SUV from 12 patients in a Phase II trial was used to assure realistic simulation. Registered RS images were blended to simulate CC for combinations of dose ratio (DR=l-5) and wait time (WT=30-120 min) between RS injections using blending coefficients determined by M-SUV, DR, rest dose decay and WT. Each blended image set was measured for defect contrast (DC) using (SUVn- SUVdVSUVn, defect volume (DV) using pixel values >(SUVn+SUVd)/2 in defect, and wall uniformity (WU) using (SD/mean) in normal wall. Degradation <10% for DC, DV and WU was applied to determine the minimal WT for DR.
Results: WU (<7.6 ) and DV (<2 ) for any type of stress were not significantly affected by any combination. DC degradation was reduced to the acceptable range by increasing DR, WT or both.
Example 35
The following describes high definition cardiac perfusion PET using a new 18F imaging agent, imaging agent 1. HD'PET technology improves spatial resolution and signal-to-noise on reconstructed PET images (IEEE TMI 2006:25:7:907-921) but the
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thermal path of the positron emitted by rubidium limits its benefits in Rb perfusion images. To evaluate its full potential for high-resolution cardiac imaging, HD'PET with myocardial perfusion images obtained with a new 18F based agent (imaging agent 1) was evaluated.
Methods: Images of 15 subjects in a study of imaging agent 1 perfusion agent were acquired on a 4-ring Siemens Biograph-64. Static and 8-bin ECG-gated images were generated using standard reconstruction (SR - 2D Attenuation Weighted Ordered Subsets Expectation Maximization) and HD'PET. The wall/cavity contrast and contrast-to-noise ratio (CNR), and maximum to defect contrast were computed. Wall thickness at three different levels of heart (basal, mid, apical), wall motion, wall thickening and ejection fraction (EF) were also estimated with automatic
quantification.
Results: HD'PET showed significant contrast change compared to SR
(+32.3+17.9%, p<0.05). CNR also was improved with HD'PET (+26.7+22.3% vs. SR, p<0.05). The average contrast between the maximum in the myocardium and the 22 defects in the 15 patients was increased with HD'PET (4.0+1.7) compared to SR (3.2+1.2, p<0.05). The average wall thickness was 16:3+2.9mm, 16.7+2.9min and 15.6+2.2min (basal, mid, apical) with SR compared with 14.7+2.8mm, 14.1+3,0min and 13.0+1.7mm with HD'PET (p<0.05). EF, wall motion and wall thickening did not show any Significant differences with HD'PET.
Conclusion: Perfusion studies with imaging agent 1 show significantly improved image resolution, contrast and contrast-to-noise with HD'PET reconstruction as compared with the standard reconstruction technique.
Example 36
Using tracer kinetic modeling with imaging agent 1 PET, absolute quantification of myocardial blood flow (MBF) was shown to be feasible even at high flow rates. The study examined whether retention and SUV calculations were also suitable for the assessment of coronary flow reserve (CFR) in a pig model.
Methods: Nine pigs were subjected to dynamic PET imaging of 100-200MBq imaging agent 1 at rest and stress. MBF was evaluated using both imaging agent 1 PET 3-compartmental modeling and the co-injected microspheres. Retention was calculated as uptake between 5-10 and 10-20min divided by the integral under the input function. Standard SUV calculation for the same time points was also used.
Results: MBF ranged from 0.5-2.8 mL/min/g. Both retention and SUV showed good correlation with both imaging agent 1 and microsphere MBF (5-10min: r=0.69, p<0.05 and 0.69, p<0.05 for retention, r=0.86, p<0.001 and 0.88, p<0.001 for SUV). Linear regression analysis revealed good results only for the earlier interval
(y=8.27x+1.45 and 7.11x+3.63 for retention, 1.11x40.01 and 0.99x+0.26 for SUV), but at later interval an underestimation was found. Calculation of stress/rest ratio for retention and SUV allows assessment of CFR. The agreement between retention and SUV derived CFR and both imaging agent 1 and microspheres CFR, yielded modest mean differences in the early interval (0.1 and -0.05, for retention, 0.05 and -0.09 for SUV) and larger deviations in the late interval (-0.47 and -0.62 for retention, -0.4 and - 0.54 for SUV).
Using imaging agent 1 , a simplified kinetic analysis model for the assessment of MBF index and CFR was feasible. Furthermore, SUV derived values were suitable for tracer injection outside the imaging device and allowed for a physical stress test. These results provided a basis for a simplified quantitative approach in the routine clinical setting.
Example 37
The following example describes the synthesis of imaging agent precursor 1, according to the scheme shown in Figure 3. Example 37 A
Synthesis of 2-(i-butyl)-4,5-dichloropyridazin-3(2H)-one (Compound 11) Solid i-butyl hydrazine hydrochloride (1 equiv) was added to a stirred solution of sodium hydroxide (0.95 equiv) dissolved in 10% water/toluene mixture (6 vol) at ambient temperature. The resulting white suspension was cooled slightly while mucochloric acid (1 equiv) was slowly added. After completion of the addition, the reaction mixture was stirred at ambient temperature for 20-30 minutes followed by dropwise addition of acetic acid (0.95 equiv). The reaction mixture was heated to 45 - 50 °C and stirred for 18 h, until starting material was consumed, as measured by HPLC. The reaction solution was allowed to cool to ambient temperature and then was diluted with water (~7 vol) and the organic layer separated. The organic layer was cooled to 0 °C and washed with 30% NaOH (3.6 vol), followed by 35% HC1 (3.6 vol) and water (2 x 3.6 vol). The organic solution was concentrated under vacuum and restripped with methanol (1.5 vol) to yield compound 11 as a brown solid that was dried under vacuum at 35 °C (65-75% yield, 100% purity by HPLC).
Example 37B
Synthesis of 2-(i-butyl)-4-chloro-5-((4-(hydroxymethyl)benzyl)oxy)pyridazin-3(2H)-one
(Compound 13)
A solution of compound 11 (222 g) in dry dimethylformamide (780 mL) was slowly added to a stirred mixture of 1,4-phenylenedimethanol (compound 2, 690 g) and cesium carbonate (1.3 kg) in dry dimethylformamide (2.22L) heated to 65 °C. The resultant mixture was stirred at 65 °C for an additional 4 h, when the reaction was cooled and filtered. The filtrate was diluted with 5% brine and extracted with toluene. The combined toluene extracts were washed twice with 5% brine and the organics concentrated under reduced pressure. The resulting crude was crystallized from hot methanol/water mixture, filtered, washed with methanol/water and dried under vacuum at 40-45 °C to afford compound 3 (224 g) as an off-white powder in 69% yield, contaminated with 6% of the product of dialkylation of compound 12 with compound 11. Example 37C
Synthesis of 5-((4-(bromomethyl)benzyl)oxy)-2-(i-butyl)-4-chloropyridazin-3(2H)-one
(Compound 14)
A dry vessel was charged with anhydrous dichloromethane (670 mL) and compound 13 (224 g). A 1.0M solution of phosphorous tribromide in dichloromethane (345 mL) was added to the mixture over 30 min at 25 °C and the solution stirred for another 30 min. The reaction was diluted with dichloromethane (450 mL) and water (670 mL), the layers separated, and the aqueous phase extracted with dichloromethane (670 mL). The combined organic layers were washed twice with 5% brine, concentrated under vacuum, and dried for 34 h under vacuum at 40 °C to yield compound 14 as an off-white solid (258 g, 96% yield).
Example 37D
Synthesis of 2-(i-butyl)-4-chloro-5-((4-((2-hydroxyethoxy)methyl)benzyl)oxy) pyridazin-3(2H)-one (Compound 15)
Ethylene glycol (2.9 L) was charged into a dry vessel and treated with solid potassium i-butoxide (74 g). The suspension was heated to 60 °C to form a solution and then cooled to 20-25 °C. A solution of compound 14 (290 g) in dry THF (1.45 L) was added in one portion to the stirring ethylene glycoxide solution. The resultant mixture was heated to 60 °C and stirred at this temperature for 16.5 h when it was then cooled to 25 °C and diluted with water (2.9L) and toluene (4.35L). The organic layer was separated, washed three times with water and concentrated under vacuum. Another charge of toluene (4.35 L) was added and concentrated under vacuum again to afford crude compound 15 as a brown viscous oil (260 g, 95% yield)
Crude compound 15 (690 g) was dissolved in dichloromethane (0.5 kg/L) and purified by chromatography (silica column, 1 : 1 heptane/ethyl acetate, flow rate = 6 L/min, 10L fractions). The combined fractions were combined and concentrated under vacuum to afford compound 15 as a clear, viscous oil (520 g, 70% yield).
Example 37D- 1
The following example describes the synthesis of compound 15, using an alternate synthetic method relative to Example 37D. Into a clean, dry reactor equipped with overhead stirrer and temperature probe was charged anhydrous ethylene glycol (2900 mL), followed by potassium i-butoxide (42.2 g) at ambient temperature. The solution was heated to 55 to 60 °C to form a clear solution of the ethylene glycoxide and then cooled to 20 °C to 30 °C under an inert atmosphere. This solution was assayed for total base content. A separate vessel was charged with anhydrous tetrahydrofuran (725 mL) and compound 14 (145 g) with stirring to form a solution at ambient temperature. This solution was added in a single portion directly to the ethylene glycoxide solution at 20 to 30 °C. The mixture was heated to 60 °C and stirred at this temperature. When the reaction was complete, it was cooled to 20 °C and toluene (2200 mL) and water (2200 mL) were added with stirring to form two layers when allowed to settle. The layers were separated and the organic layer washed with 2200 mL each of sodium bicarbonate solution and water (twice). The organic layer was concentrated at <50 °C under vacuum to give compound 15 as a viscous oil (133.4 g, 91% when corrected for residual toluene).
Example 37E
Synthesis of Constrast Agent Precursor 1
A dry reactor was charged sequentially with dichloromethane (6.6 L), compound 15 (510 g) dissolved in dichloromethane (1.1L), triethylamine (0.25 L), p- toluenesulfonyl chloride (305 g), and dimethylaminopyridine (7 g). The solution was stirred at ambient temperature for 28 h when it was washed with 1.0 M HC1 (2x 10 L), water (10 L), 5% sodium bicarbonate (2 x 10 L), and water (10 L). The organic solution was filtered and dichloromethane removed under reduced pressure to afford imaging agent precursor 1 as a thick oil.
Crude imaging agent precursor 1 (21.5 g) was added to cumene (125 mL) and heated to 60 °C to dissolve the solids. It was cooled to 40 °C and 1% w/w imaging agent precursor 1 crystals added to seed the crystallization. The solution was held for 3 h at 35 °C to allow crystallization, and then cooled to ambient temperature and stirred for 6 h to complete crystallization. The solids were filtered, dried briefly under vacuum, and then added to isobutyl acetate (125 mL). After heating to 70 °C, the solids dissolved, and the solution was then cooled to 40-50 °C and seeded with 1% w/w imaging agent precursor 1. After holding at 40-50 °C for five hours, the slurry was cooled to ambient temperature over 2 hours and held for 12 h. The resulting solids were filtered, rinsed with cold isobutyl acetate, and dried under vacuum to afford 12.8 g of imaging agent precursor 1 (60% from compound 15). In some cases, the triethylamine stoichiometry was increased from about 1.15 to about 1.40 equiv. In some cases, the p-toluenesulfonyl chloride stoichiometry was increased from about 1.15 to about 1.20 equiv. In some cases, the
dimethylaminopyridine stoichiometry was increased from about 0.04 to about 0.10 equiv.
In some embodiments, the cumene crystallization wass completed under the following conditions: Dilution: 10.0 volumes; Seeding temperature: 45 °C;
Crystallization hold time at seeding temperature: 3 h; Cooling rate: 5 °C/h; Granulation temperature: 20 °C; Granulation time: >3 h; Filtration temperature: 20 °C.
In other embodiments, the cumene crystallization was completed under the following conditions: Dilution: 6.5 volumes; Seeding temperature: 50 °C; Crystallization hold time at seeding temperature: 6 h; Cooling rate: 10 °C/h; Granulation temperature: 10 °C; Granulation time: >8 h; Filtration temperature: 10 °C.
In a certain embodiment, compound 16 (20.0 g) was suspended in cumene (6.5 volumes) then warmed to 68 °C. The resulting solution was cooled to 50 °C then seeded with compound 16; slow formation of a precipitate was observed. The resulting suspension was held at 50 °C for 6 h then cooled at 10 °C/h to 10 °C, maintained 12 h, filtered and washed. Following in vacuo drying at 60 °C, 16.4 g of compound 6 was obtained (82% recovery; 96% solvent and purity adjusted).
In some embodiments, the isobutyl actetate crystallization was conducted under the following conditions: Dilution: 8 volumes; Seeding temperature: 50 °C;
Crystallization hold time at seeding temperature: 3 h; Cooling rate: 5 °C per hour;
Granulation temperature: 20 °C; Granulation time: >10 h; Filtration temperature: 20 °C.
In other embodiments, the isobutyl actetate crystallization was conducted under the following conditions: Dilution: 5 volumes; Seeding temperature: 48 °C;
Crystallization hold time at seeding temperature: 10 h; Cooling rate: 2.5°C/h;
Granulation time: 0 h; Filtration temperature: 10 °C.
In a certain embodiment, cumene crystallized compound 16 (15.40 g) was suspended in isobutyl acetate (5 volumes) then warmed to 68 °C. The resulting solution was cooled to 48 °C then seeded with BMS-747155-01 (0.1% w/w); immediate formation of a precipitate was observed. The resulting suspension was held at 48 °C for 10 h then cooled at 2.5°C/h to 10°C, filtered and washed. Following in vacuo drying at 60 °C, 13.10 g of compound 16 was obtained (85% recovery) which passed all specifications.
Example 38
The following example describes an alternate route to synthesizing 2-(?-butyl)-4- chloro-5-((4-(hydroxymethyl)benzyl)oxy) pyridazin-3(2H)-one (compound 13), as shown in Figure 4.
Example 38 A
Synthesis of 2-(i-butyl)-4-chloro-5-hydroxypyridazin-3(2H)-one (Compound 17) A dry vessel was sequentially charged while stirring with compound 11 (lOOg), potassium hydroxide (76.1 g), and ethylene glycol (1 L). The resulting suspension was heated to 115 °C and stirred at this temperature for 5 hrs. The brown solution was cooled to 0 °C and 1 M hydrochloric acid solution (1 L) added slowly with stirring over 60 minutes, keeping the temperature below 25 °C during the addition, resulting in precipitation of a light brown solid. The slurry was stirred for 2 hrs and filtered, washing the cake with cold water (4 x 500 mL) and ethanol (100 mL). The Crude compound 17 thus obtained was then recrystallized from hot ethanol (1 L), filtered, and dried under vacuum for 34 h at 45 °C to yield pure compound 17 (68.3 g, 75% yield).
Example 38B
Synthesis of methyl 4-(((l-(i-butyl)-5-chloro-6-oxo-l ,6-dihydropyridazin-4- yl)oxy)methyl)benzoate (Compound 18)
A dry vessel under nitrogen atmosphere was charged sequentially with compound 17 (66 g), dimethylformamide (660 mL) and potassium carbonate (45 g). To this was added methyl 4-(bromomethyl)benzoate (78 g) and the resulting suspension stirred for 18 h at 20 °C. Water (700 mL) was added over 30 minutes to precipitate the product and dissolve remaining salts. The slurry was stirred for 1.5 h and the resulting solids filtered, washed with water (4 x 300 mL) and cyclohexane (2 x 150 mL) and dried under vacuum at 45 °C to afford compound 18 (112.8 g, 99%) as a white powder.
Example 38C
Alternate synthesis of 2-(i-butyl)-4-chloro-5-((4-(hydroxymethyl)benzyl)oxy) pyridazin-
3(2H)-one (Compound 13) A dry vessel with overhead agitation under an atmosphere of dry nitrogen was charged sequentially with 2-methyltetrahydrofuran (500 mL) and compound 18 (50 g) at ambient temperature. The resulting suspension was cooled to -7 °C and a solution of diisobutylaluminum hydride in toluene (1.5M, 119 mL) added drop-wise over 1 h keeping the temperature below 3 °C. After stirring for 1.5 h at -5 °C - 0 °C, the reaction was quenched by addition of propan-2-ol (50 mL) at a rate to keep the temperature below 4 °C. The quenched reaction mixture was then added dropwise to a solution of hydrochloric acid (2M, 500 mL) over 75 min, keeping the temperature below 7 °C. The biphasic solution was warmed to 22 °C and the layers separated. The organic layer was then washed with 500 mL each of 2M hydrochloric acid, saturated sodium bicarbonate solution and water and then concentrated under reduced pressure to afford crude compound 13 as an off-white solid (42.4 g). This was recrystallized from hot isopropyl acetate (200 mL), seeding the solution at 65 °C and holding at this temperature for one h, followed by cooling to 0 °C over 4 h. The resulting white solid was filtered and dried under vacuum at 45 °C to afford compound 13 (35 g, 76% yield).
In some cases, the above experiment was performed with both lithium aluminum hydride and sodium bis(2-methoxyethyoxy)aluminum hydride (Red Al) as well as diisobutylaluminum hydride (DIBAL-H). In some cases, solutions of DIBAL-H in dichloromethane, toluene, and hexane were employed. In some cases, selection of 2- MeTHF (vs. THF) as co-solvent was performed due to its reduced aqueous solubility. In some cases, stress studies revealed the DIBAL reduction performed well, in particular, at temperatures between -15 to +10 °C. In some cases, the DIBAL-H was charged in two portions; 2.20 equiv followed by additional reagent if incomplete reaction was observed. In some cases, residual water was found to have hydrolyzed DIBAL-H and the impurity profile remained unchanged.
In some embodiments, the reaction was conducted under the following conditions: -15 to +10 °C; up to -2.35 equiv DIBAL-H; up to 5% H20 (w/w) in precursor; <0.75% precursor remaining at full conversion.
Example 39
The following example described an alternate synthetic route to 2-(?-butyl)-4- chloro-5-((4-((2-hydroxyethoxy)methyl) benzyl)oxy) pyridazin-3(2H)-one (Compound 15), as shown in Figure 5. Example 39A
Preparation of methyl 4-(l,3-dioxolan-2-yl)benzoate (compound 19)
Methyl 4-formylbenzoate (3.28 g, 20.0 mmol) was suspended in ethylene glycol (4.46 mL, 80.0 mmol), then successively treated with triethyl orthoformate (3.66 mL, 22.0 mmol) and Me3NPhBr3 (376 mg, 1.00 mmol) at 22 °C; within 5 min, all solids dissolved. The resulting orange solution was stirred 0.5 h, then diluted with saturated aqueous NaHCC>3 (50 mL), transferred to separatory funnel and washed with EtOAc (3 x 50 mL). The combined EtOAc washes were dried over MgS04, filtered and
concentrated in vacuo to a colorless oil (Rf 0.4 in 4: 1 pentane/EtOAc, KMn04). This material was used without further purification in the subsequent reduction step.
Example 39B
Preparation of (4-(l,3-dioxolan-2-yl)phenyl)methanol (Compound 20) The crude acetal (20.0 mmol theoretical) was dissolved in dry THF (100.0 mL), cooled to 0 °C and treated with LiAlH4 (20.00 mmol; 20.00 mL of a 1.0 M solution in THF) at a rate of 1.0 mL/min using a syringe pump. Upon completion of the addition, excess LiAlH4 was consumed by the careful addition of ¾0 (800 \lL). CAUTION: vigorous gas evolution! The resulting white suspension was successively treated with 15% aqueous NaOH (800 iL) and H20 (2.40 mL), then stirred 0.5 h to a fine white slurry. The solids were removed by filtration through a pad of Celite then exhaustively washed with Et20. The combined filtrates were concentrated in vacuo to a colorless oil and purified by chromatography on silica (50 x 175 mm) using 1 : 1 pentane/EtOAc. The main product peak eluting 470-790 mL was collected, pooled and concentrated in vacuo to a colorless oil, which solidified in the freezer (2.46 g, 13.7 mmol; 68.3% over two steps).
Example 39C
Synthesis of (4-(l,3-dioxolan-2-yl)phenyl)methanol (Compound 20) Methyl 4-formylbenzoate (4.92 g, 30.0 mmol) was dissolved in dry toluene (50.0 mL), successively treated with ethylene glycol (1.84 mL, 33.0 mmol) and /?-TsOH H20 (57.1 mg, 0.30 mmol), then heated to reflux under Dean-Stark conditions; acetal formation was complete within 1 h. The solution was then cooled to 22 °C and treated with sodium bis(2-methoxyethoxy)aluminum hydride (45.0 mmol; 12.7 mL of a 70.3 wt. % solution in toluene) at a rate of 0.5 mL/min using a syringe pump. CAUTION:
vigorous gas evolution! Upon completion of the addition, the resulting solution was further cooled to 0 °C, carefully treated with a saturated aqueous solution of K,Na- tartrate (100 ml), then vigorously stirred 1 h; steady formation of a clear solution was observed. The resulting biphase was then diluted with EtOAc (50 mL), with transfer to a conical funnel, and the layers separated. The aqueous layer was then washed with EtOAc (3 x 50 mL) and the combined EtOAc and toluene solutions dried over MgS04, filtered and concentrated in vacuo to a colorless oil. The crude product was then purified by chromatography on silica (50 x 135 mm) using 1 : 1 pentane/EtOAc. The main product peak eluting 425-725 mL was collected, pooled and concentrated in vacuo to a colorless oil, which solidified in the freezer (4.50 g, 83.2% over two steps).
Example 39D
Synthesis of 2-(i-butyl)-4-chloro-5-[(4-(l,3-dioxolan-2-yl)phenyl)methoxy]-2- hydropyridazin-3-one (Compound 21)
A solution of 2-(i-butyl)-4,5-dichloro-2-hydropyridazin-3-one (829 mg, 3.75 mmol) and the compound 10 (451 mg, 2.50 mmol) in dry DMF (12.5 mL) was treated with CS2CO3 (1.63 g, 5.00 mmol) in one portion at 22 °C. The resulting suspension was then immersed in a pre-heated oil bath (65 °C) and maintained 6 h with vigorous stirring. After cooling to ambient temperature, the suspension was partitioned between EtOAc and H2O (50 mL each), with transfer to a conical funnel, and the layers separated. The remaining aqueous layer was washed with additional EtOAc (3 x 50 mL) then discarded. The combined EtOAc solutions were further washed with saturated aqueous NaCl (5 x 50 mL), then dried over MgS04, filtered and concentrated in vacuo to an off-white solid. In some cases, trituration with several small volumes of pentane was performed to generate the solid. The crude product was then recrystallized from hot EtOAc/hexanes to afford colorless needles that were collected on a scintered glass funnel of medium porosity, exhaustively washed with pentane and dried in vacuo (573 mg, 62.8%).
Example 39E
Synthesis of 2-(i-butyl)-4-chloro-5-[(4-(l,3-dioxolan-2-yl)phenyl)methoxy]-2- hydropyridazin-3-one (Compound 21) To a vessel charged with (4-(l,3-dioxolan-2-yl)phenyl)methanol (20 g, 110 mmol), benzyltriethylammonium chloride (2.27 g, 10 mmol), toluene (100 mL) and sodium hydroxide (50% in water, 22 mL, 420 mmol) was added a solution of 2-(?-butyl)- 4,5-dichloro-2-hydropyridazin-3-one (22.1 g, 100 mmol) in toluene (100 mL) over 5 min. A gradual and accelerating exotherm occurred with the final internal temperature reaching 39 °C. After 2.5 h stirring was halted and MTBE (50 mL) and water (100 mL) added. The phases were split and the organic layer was washed with water (100 mL) and brine (100 mL). The organic extracts were dried (MgS04), filtered, and concentrated under vacuum to afford a tan solid (39 g). The solids were slurried in toluene/heptane (430 mL, 1 : 1) at 40 °C for 2 h, cooled to ambient temperature, filtered and dried under vacuum at 40 °C for 24 h (29.7 g, 69%).
Example 39F
Synthesis of 2-(i-butyl)-4-chloro-5-({4-[(2-hydroxyethoxy)methyl]phenyl}methoxy)-2- hydropyridazin-3-one (Compound 15)
A solution of compound 21 (365 mg, 1.00 mmol) in dry CH2CI2 (10.0 mL) was cooled to -40 °C using a dry ice/MeCN bath, then treated with DIBAL-H (4.00 mmol; 4.00 mL of a 1.0 M solution in CH2CI2) at a rate of 0.25 mL/min using a syringe pump. The solution was maintained 1 h with periodic addition of dry ice to the cooling bath, then carefully treated with wet MeOH (1 mL) and warmed to 22 °C. The resulting solution was diluted with EtOAc (20 mL), treated with an equal volume of saturated aqueous K,Na-tartrate, then vigorously stirred 1 h; steady formation of a clear solution should be observed. The resulting biphase was further diluted with ¾0 (50 mL), with transfer to a conical funnel, and the layers separated. The aqueous layer was then washed with EtOAc (3 x 50 mL) and discarded. The combined EtOAc washes were dried over MgS04, filtered and concentrated in vacuo to a colorless oil (Rf 0.2 in 1: 1 pentane/EtOAc, KMn04). The crude product was purified by chromatography on silica (30 x 190 mm) using a step gradient from 1 : 1 pentane/EtOAc (250 mL) to 3:2 pentane/EtOAc (500 mL). The main product eluting between 415-580 mL was collected, pooled and concentrated in vacuo to a colorless oil (286 mg, 0.780 mmol; 78.0%). Example 40
Synthesis of 2-((4-(((l-(i-butyl)-5-chloro-6-oxo-l,6-dihydropyridazin-4- yl)oxy)methyl)benzyl)oxy)ethyl 4-methylbenzenesulfonate (imaging agent precursor 1) A dry reactor was charged sequentially with dichloromethane (6.6 L), compound 15 (510 g) dissolved in dichloromethane (1.1L), triethylamine (0.25 L), p- toluenesulfonyl chloride (305 g), and dimethylaminopyridine (7 g). The solution was stirred at ambient temperature for 28 h when it was washed with 1.0M HC1 (2x 10 L), water (10 L), 5% sodium bicarbonate (2 x 10 L), and water (10 L). The organic solution was filtered and dichloromethane exchanged for ethyl acetate. The product was crystallized from hot 1 : 1 heptane/ethyl acetate (-11 L). by slowly cooling to 0-5 °C. The resulting solids were filtered, washed with cold ethyl acetate/heptane and dried under vacuum at 40 °C for 42 h to yield imaging agent precursor 1(555 g, 77% yield).
Example 41
The following describes remote camera qualification (RCQ) of PET and PET/CT scanners for imaging agent 1 myocardial perfusion using a standardized phantom procedure.
As will be known to those of ordinary skill in the art, in a medical imaging clinical trial, camera qualification is a critical step in assessing whether individual clinical site (CS) possesses the capability to execute the protocol. In some cases, a challenge lies in how to standardize a task-specific phantom and the associated qualification procedure that can effectively determine if specific site scanners meet the study requirement to join the trial.
Methods. Using various cameras, the RCQ procedure with an imaging manual customized for each scanner model utilized step-by-step instruction for CS to follow. A low-cost, standardized phantom using a 2 liter soda bottle with an acrylic rod
(L=21cm, D=2cm) sealed inside the cap was provided to each CS (see Example 42 for more details). CS injected 3-4 mCi F18 solution to the water-filled phantom to acquire image data and to test existing cardiac misregistration (MR) correction software in each system. The RCQ procedure was performed by the CS with telephone support as necessary. All image data was sent to the imaging core laboratory to analyze in terms of quantitative imaging parameters. Minimum performance criteria were established to identify cameras whose performance was inconsistent with accepted norms. The results are shown in Table 18.
Table 18.
Figure imgf000162_0001
Conclusions. Remote camera qualification when integrated with a standardized phantom, comprehensive imaging manuals, full technical support and centralized data analysis can be a cost-effective and efficient method to assess the performance of PET and PET/CT scanners in a large clinical trial.
Example 42
The following example describes a low cost refillable phantom for
standardization of PET Scanners
Standardization and harmonization of imaging methodology and scanner performance is critical to the success of clinical studies using PET (e.g., as described in Example 41). Generally, this may be accomplished with a test object called a phantom that is loaded with an appropriate quantity of radioactive material and imaged in the same way with each scanner. Phantoms may be constructed either of solid materials with long-lived positron-emitters embedded or they may be filled with water and shortlived radioactivity added as needed. Differences in observed imaging performance allow adjustment of methods or repair of equipment as necessary to assure uniformity of image quality among all systems used. Conventional phantoms, both solid and refillable are sufficiently expensive that the cost of simultaneous assessment at a large number of sites is prohibitive. The device described in this example is a simple task- specific phantom for cardiac PET using readily available materials that can be constructed for
approximately 1% the price of a conventional refillable phantom. When combined with routine quality control, it allows the simultaneous characterization of a large number of PET and PET-CT systems for standardization in PET cardiac clinical trials.
Materials and Methods. The phantom was constructed from a standard 2-liter soda bottle. A rod of acrylic plastic 8¼ inches long and ¾ inches in diameter was centered and fixed to the inside of the cap of the bottle using an external screw. The surface between the end of the rod and the inside of the cap and under the screw head was sealed with glue appropriate to the materials prior to final tightening of the screw and the phantom tested for leakage.
The phantom was filled in the following way:
1. The phantom was placed on an absorbent surface or, preferably, in a sink and filled the phantom with tap water to the top. Bubbles were minimized using a slow rate of water flow into the bottle.
2. The acrylic rod (attached to the cap) was inserted into the soda bottle fully and the cap screwed in place. The entire overflow was allowed to be removed from the phantom. It was important not to squeeze the phantom while doing this. The cap was unscrewed and the rod slowly removed to allow any water clinging to it to drain back into the phantom.
3. A clean syringe was used to draw 2 ml of water from the phantom.
Approximately 10 drops of liquid soap was added into the phantom to prevent FDG or other F18 compounds from sticking to the inner surface of bottle or the rod. The phantom was shaken by tilting it up and down vertically for at least 30 sec to ensure uniform distribution of liquid soap.
4. 18F activity (3-4 mCi) and the volume (several ml) in a syringe was measured and then recorded, including volume and assay time.
5. 18F was injected into the phantom slowly and the syringe drawn back and forth to flush the remaining activity from the syringe vigorously three times.
6. The same syringe was used to carefully draw out a volume of liquid from the phantom equal to the volume plus 1 ml of the 18F solution injected into it. This ensured the solution will not overflow when the rod is replaced and will include a small bubble to facilitate mixing. 7. The Factivity in the syringe was measured and the radioactivity and assay time was recorded.
8. The rod was reinserted into the phantom and the cap was hand-tightened in place and ensured that it was secure and leak-free.
9. The surface of the phantom was wiped with a paper towel which was checked for radioactive contamination prior to discarding.
10. Image data was then acquired using any PET scanner that was to be evaluated, under any conditions or acquisition settings that are to be evaluated.
The resulting image data were assessed using conventional tools. A large region of interest covering the central 60% of several slices that do not include the acrylic rod may be used to determine the degree of uniformity and correctness of calibration factors. Region-of-interest analysis with one or more slices containing the acrylic rod may also be used to determine the contrast between the radioactivity- filled volume and the area within the acrylic rod from which radioactivity is excluded. Integration of a line profile including the edge between the rod and the liquid may be used to assess resolution. A variety of other factors may also be assessed, including calibration linearity and the capacity and accuracy of PET-CT mismatch correction using appropriate data acquisition.
Example 43
The following example describes a comparison of imaging agent 1 and 18F fluorodeoxyglucose (FDG) for assessment of left ventricular viability following myocardial infarction in rats.
18F fluorodeoxyglucose (FDG) imaging of the heart is used to assess myocardial viability. This example describes a comparision of the volume of viable tissue in the left ventricle of normal and myocardial infarcted (MI) rats determined by imaging agent 1 imaging with that detected by FDG imaging.
Methods. MI was induced in rats by 30 minutes of\ coronary occlusion followed reperfusion. Imaging agent 1 (1 mCi) and FDG (1 mCi) cardiac imaging in 2 days apart was performed in rats of before, two days (early MI) and four weeks (late MI) post surgery. A regimen of glucose and insulin was injected before FDG imaging to ensure high cardiac uptake. Viable left ventricle was quantified in images as the volume with >50% of maximum activity. Results. In control rats, cardiac imaging with both imaging agent 1 and FDG showed well-defined left ventricular wall and the left ventricular volume was measured as 1.17+0.04 and 1.11+0.07 cm3 respectively before surgery. In early and late stage MI rats, the myocardial defect area was clearly identified by imaging with both agents. The viable left ventricular tissue volume measured with imaging agent 1 was slightly larger than the viable tissue area measured with FDG (0.94+0.01 vs. 0.75+0.04 and 1.18+0.04 vs. 0.99+0.09 cm3 at early and late stage MI). In addition, imaging agent 1 imaging showed similar detectable left ventricular areas at 20 and 80 minutes post injection (no refill-in) in both early and late stage MI. This example shows that imaging agent 1 has the potential to be used to assess myocardial viability, like FDG, however without the need for insulin pre-treatment.
Example 44
The following demonstrates that a quantitative and perceived defect severity are proportional with imaging agent 1 PET myocardial perfusion imaging.
In order to identify the minimum rest dose of imaging agent 1, a comparison was made between the count-related variation in normal myocardium and the minimum change in defect severity that would result in 50% probability of a reader's changing a segmental score by 1. In order to determine this limiting change in defect severity, a comparison was made between reader scores from a blinded read and the corresponding quantitative defect severity.
Method. Patients selected for one or more at least partially reversible defects on SPECT studies were evaluated as part the first cohort in the Phase 2 study of imaging agent 1. Rest and stress images were read by a panel of three blinded readers. Reader' scores using a 17-segment model from the rest image data only derived from the first 20 patients were compared with the percentage decreases from the maximum value in each image as calculated by standard cardiac MPI analysis software (Cedars QPS). The values were plotted and a linear regression calculated for the data from each reader (see Figure 13).
Results. Although there was significant range in quantitative severity values at each reader score value (%SD -20% of image maximum), the data was well modeled with the simple linear regression resulting in R2 values of 1.00, 0.978 and 0.984 for readers 1, 2 and 3 respectively. The intercept values were 84.18%, 82.33% and 84.96% respectively while the slopes were -13.8, -9.86 and -8.53 respectively.
Discussion. These results suggest that, at least with imaging agent 1, it may be possible to estimate reader responses using a simple linear relationship and the quantitative fraction of the maximum value without the need for a normal database. Based on a mean slope of -10.7, it was estimated that a 50% probability of a change of 1 in reader score corresponded to a change in quantitative severity by 5.4%
Example 45
The following examples describes a comparison of imaging agent 1 and Tc-99m labeled SPECT myocardial perfusion imaging for identifying severity and extent of stress induced myocardial ischemia in Phase 2 clinical trials
In this multi-center Phase 2 study, imaging agent 1 and Tc-99m labeled SPECT rest-stress MPI were compared for evaluation of stress induced myocardial perfusion abnormalities in patients (Pts) with coronary artery disease (CAD).
Methods: 84 Pts from 21 centers, presenting with an intermediate to high CAD pre-test likelihood, underwent rest-stress Tc-99m labeled SPECT MPI, imaging agent 1 PET MPI and coronary angiography. Their mean age was 64.5 years (range: 36-85) and 68 were males. In each patient, 17 myocardial segments were visually scored on rest and stress images by 3 independent, blinded readers. For each pt, summed difference scores (SDS) were determined from segmental scores. Percent narrowing in each coronary artery was quantitatively and blindly determined and >50% luminal diameter narrowing was considered significant. Of the 84 Pts, 52 had CAD and 32 had insignificant CAD/normal coronary arteries.
Results. There were 105 diseased coronary arteries in 52 patients; 40 left anterior descending, 30 left circumflex and 35 right coronary arteries. In patients with at least one diseased artery, the mean (SD) PET SDS score ranged among the three readers from 6.8 (5.75) to 9.4 (7.51) and the mean (SD) SPECT SDS score ranged from 4.1 (4.75) to 5.7 (6.51). The differences in SDS scores between PET and SPECT were statistically significant in all readers (p<0.01). In 52 patients with multivessel disease and multi- readers, the adjusted mean PET SDS score was significantly higher than that of SPECT SDS score (p<0.001).
Conclusions. These data suggest that as compared to Tc-99m SPECT, rest-stress imaging agent 1 PET MPI demonstrates more severe and extensive stress induced perfusion abnormalities in myocardial regions that are supplied by diseased coronary arteries.
Example 46
The following example describes a Phase 2 clinical comparison of imaging agent 1 injection PET and Tc-99m labeled SPECT myocardial perfusion imaging for diagnosis of coronary artery disease.
In the Phase 2 study, the clinical safety of imaging agent 1 injection was evaluated and its diagnostic performance for detection of coronary artery disease (CAD) was compared to rest-stress Tc-99m labeled SPECT MPI.
Methods. 143 patients (Pts) from 21 centers, presenting with a broad spectrum of CAD pre-test likelihoods, underwent rest-stress Tc-99m labeled SPECT MPI and imaging agent 1 PET MPI. 84/143 who had an intermediate to high CAD likelihood underwent coronary angiography. Their mean age was 64.5 (range: 36-85) years and 68 were males. % narrowing in each coronary artery was quantified blindly. 52/84 Pts had significant CAD (>50% luminal diameter narrowing) and 32/84 had insignificant CAD/normal coronary arteries. In each patient, 17 myocardial segments were visually scored on rest and stress images by 3 independent, blinded readers and majority rule interpretation was determined in each patient for both PET and SPECT studies.
Diagnostic performance of PET was compared to that of SPECT using ROC analysis.
Results. A significantly higher % of images were rated as either excellent or good on PET vs SPECT stress images (99.2% vs. 88.8%, p<0.01) and rest images (96.8% vs. 64.8%, p<0.01). Diagnostic certainty of interpretation (% of cases with definitely abnormal/normal interpretation) was significantly higher for PET vs. SPECT (92.0% vs. 76.8%, P<0.01). The area under the ROC curve for overall diagnosis of CAD was significantly higher for PET vs. SPECT (0.79±0.05 vs. 0.67±0.05, p<0.05). 61/143 patients reported 100 treatment emergent adverse events (AEs). Of these, 7 AEs reported in 2 patients were judged to be related to the study drag, but none were serious. No clinical laboratory changes from baseline were reported as TEAEs or considered as clinically significant. The ECG data at rest revealed no evidence of any clinically relevant effect on heart rate, atrio-ventricular conduction (PR interval), depolarization (QRS duration) or repolarization (QTcF duration).
Conclusions. Within this Phase 2 clinical trial imaging agent 1 appeared to be safe and superior to Tc-99m labeled SPECT with respect to image quality, certainty of image interpretation and overall diagnosis of CAD.
Example 47
The following described a streamlined quantification of absolute myocardial blood flow at rest and stress with imaging agent 1 injection PET in normal subjects and patients with coronary artery disease.
Objectives. The feasibility of streamlined quantification of rest (R) and stress (S) myocardial blood flows (MBFs) and coronary flow reserve (CFR) with imaging agent 1 for clinical use in normal subjects and coronary artery disease (CAD) patients (Pts) was evaluated.
Methods. Ten Pts [6 with a low likelihood of CAD and 4 with CAD (>50 stenosis) and reversible defects] received imaging agent 1 injection at Rand at peak adenosine S followed by 10-min dynamic acquisition. The R-S imaging protocol was same-day in 5 Pts and separate-day in 5 Pts. Rand S polar maps were automatically generated from summed dynamic scans ( 0.5-2 min post injection) and the 3 coronary territories (LAD, RCA, LCX) and the left ventricular blood pool (LV) were defined automatically. Reversible defects were manually assigned on the polar maps, from which time activity curves (TACs) were generated. A single-compartment model that included an irreversible uptake constant (K) and a spillover from blood pool activity was used to fit the tissue TACs at early times (0-2 min). LV TAC was used as the input function. Recovery coefficient due to partial volume effect of myocardium was estimated as (1-spf), with spf denoting the blood spillover fraction determined from model fitting. The first pass extraction fraction for imaging agent 1 in humans was assumed to be 0.94 equivalent to that observed in pre-clinical studies. CFR was calculated as S/R MBF.
Results. MBF and CFR were compared between 18 normal territories ( in 6 low likelihood Pts) and 5 reversible defect territories which were supplied by CAD coronaries (Table 19 , *=p<0.05). The results are in agreement with the published literature using N-13 ammonia PET. Table 19.
Conclusions. Quantification of MBF using imaging agent 1 injection PET myocardial perfusion imaging can be streamlined in clinical applications to give robust MBF results.
Example 48
Synthesis of 5-((4-((2-bromoethoxy)methyl)benzyl)oxy)-2-(i-butyl)-4-chloropyridazin-
3(2H)-one
A solution of imaging agent precursor 1 (0.521 g, 1.00 mmol) in dry acetone (10.0 mL) was treated with LiBr (0.261 g, 3.00 mmol) in one portion at 22 °C then warmed to 56 °C and maintained 2.5 h. The now heterogeneous reaction mixture was cooled to ambient temperature and all volatiles removed in vacuo. The crude product was then purified by chromatography on silica (30 x 190 mm) using 3: 1 pentane/EtOAc. The main product peak eluting 180-360 mL was collected, pooled and concentrated in vacuo to a colorless oil. Final purification through recrystallization from warm EtOAc and pentane afforded a white crystalline solid (0.369 g, 0.859 mmol; 85.9%).
Example 48
Syringe Adsorption of Imaging Agent 1
Three two-component syringes (Henke Sass Wolf) as well as three three- component syringes (Becton and Dickinson) were each filled with a 1 mL solution of imaging agent 1 (<5 volume % EtOH in ¾0 containing <50 mg/mL ascorbic acid); total initial radioactivity in each syringe was comparable. The two sets of filled syringes were maintained at ambient temperature and humidity for a period of three hours, at which time the contents were injected into a clean 5 cc glass vial; a consistent volume of imaging agent 1 (0.1 mL) remained in the hub of each syringe. The total radioactivity content of both the vial and syringe were measured, decay corrected and the percent retention calculated. The values of percent radioactivity retained in each syringe are summarized in Table 20. The difference in percent retained activity is statistically significant at the 95% confidence level (i.e. Prob >ltl 0.0005).
Table 20: Compiled Data for imaging agent 1 Retained in Syringes
Figure imgf000170_0001
Example 49
Syringe Component Adsorption of imaging agent 1 To further identify the contact surface material that contributed to syringe retention of imaging agent 1, three additional B&D syringes were each filled with a 1 mL solution of imaging agent 1 then maintained at ambient temperature and humidity for a period of three hours. Following transfer of the individual doses as described in Example 1 , the syringe barrel and butyl rubber tip plunger were then separated, measured for retained radioactivity and decay corrected. The values of percent retained radioactivity for each syringe component are summarized in Table 21. The difference in percent retained activity is statistically significant at the 95% confidence level (i.e. Prob >ltl 0.0017). Table 21: Percent imaging agent 1 Retained in B&D Syringe Components Post-Injection
Figure imgf000171_0001
It will be evident to one skilled in the art that the present disclosure is not limited to the foregoing illustrative examples, and that it can be embodied in other specific forms without departing from the essential attributes thereof. It is therefore desired that the examples be considered in all respects as illustrative and not restrictive, reference being made to the appended claims, rather than to the foregoing examples, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
While several embodiments of the present invention have been described and illustrated herein, those of ordinary skill in the art will readily envision a variety of other means and/or structures for performing the functions and/or obtaining the results and/or one or more of the advantages described herein, and each of such variations and/or modifications is deemed to be within the scope of the present invention. More generally, those skilled in the art will readily appreciate that all parameters, dimensions, materials, and configurations described herein are meant to be exemplary and that the actual parameters, dimensions, materials, and/or configurations will depend upon the specific application or applications for which the teachings of the present invention is/are used. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, the invention may be practiced otherwise than as specifically described and claimed. The present invention is directed to each individual feature, system, article, material, kit, and/or method described herein. In addition, any combination of two or more such features, systems, articles, materials, kits, and/or methods, if such features, systems, articles, materials, kits, and/or methods are not mutually inconsistent, is included within the scope of the present invention.
The indefinite articles "a" and "an," as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to mean "at least one."
The phrase "and/or," as used herein in the specification and in the claims, should be understood to mean "either or both" of the elements so conjoined, i.e., elements that are conjunctively present in some cases and disjunctively present in other cases. Other elements may optionally be present other than the elements specifically identified by the "and/or" clause, whether related or unrelated to those elements specifically identified unless clearly indicated to the contrary. Thus, as a non-limiting example, a reference to "A and/or B," when used in conjunction with open-ended language such as "comprising" can refer, in one embodiment, to A without B (optionally including elements other than B); in another embodiment, to B without A (optionally including elements other than A); in yet another embodiment, to both A and B (optionally including other elements); etc.
As used herein in the specification and in the claims, "or" should be understood to have the same meaning as "and/or" as defined above. For example, when separating items in a list, "or" or "and/or" shall be interpreted as being inclusive, i.e. , the inclusion of at least one, but also including more than one, of a number or list of elements, and, optionally, additional unlisted items. Only terms clearly indicated to the contrary, such as "only one of or "exactly one of," or, when used in the claims, "consisting of," will refer to the inclusion of exactly one element or a list of elements. In general, the term "or" as used herein shall only be interpreted as indicating exclusive alternatives (i.e. "one or the other but not both") when preceded by terms of exclusivity, such as "either," "one of," "only one of," or "exactly one of." "Consisting essentially of," when used in the claims, shall have its ordinary meaning as used in the field of patent law.
As used herein in the specification and in the claims, the phrase "at least one," in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements. This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase "at least one" refers, whether related or unrelated to those elements specifically identified. Thus, as a non-limiting example, "at least one of A and B" (or, equivalently, "at least one of A or B," or, equivalently "at least one of A and/or B") can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.
In the claims, as well as in the specification above, all transitional phrases such as "comprising," "including," "carrying," "having," "containing," "involving," "holding," and the like are to be understood to be open-ended, i.e., to mean including but not limited to. Only the transitional phrases "consisting of and "consisting essentially of shall be closed or semi-closed transitional phrases, respectively, as set forth in the United States Patent Office Manual of Patent Examining Procedures, Section 2111.03.

Claims

Claims
What is claimed:
1. A method of synthesizing an imaging agent comprising formula:
Figure imgf000174_0001
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with an imaging moiety or heteroalkyl optionally substituted with an imaging moiety; and n is 1, 2, 3, 4, or 5; the method comprising steps of:
etherification of precursor compounds comprising formulae:
Figure imgf000174_0002
wherein:
n is 1, 2, 3, 4, or 5;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
R3 can be the same or different and are alkyl, heteroalkyl, or a carbonyl- containing group, each optionally substituted,
R5 is hydroxyl or halide; and
R6 is alkyl, heteroalkyl, or a carbonyl-containing group, each optionally substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R3 comprises a leaving group; or wherein R5 is halide, at least one of R6 or R3 comprises a hydroxyl, to produce a compound comprising formula:
Figure imgf000175_0001
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; wherein at least one R3 comprises hydroxyl; and
n is 1, 2, 3, 4, or 5;
reacting a compound comprising formula:
Figure imgf000175_0002
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; wherein at least one R3 comprises hydroxyl; and
n is 1, 2, 3, 4, or 5; with a sulfonate-containing species to produce a sulfonate-containing compound comprising formula:
Figure imgf000175_0003
wherein:
W is alkyl or heteroalkyl, optionally substituted; R is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with a sulfonate-containing group or heteroalkyl optionally substituted with a sulfonate-containing group; wherein at least one R3 comprises a sulfonate- containing group; and
n is 1, 2, 3, 4, or 5;
replacing the sulfonate-containing group of the sulfonate-containing compound with an imaging moiety to yield a compound comprising formula:
Figure imgf000176_0001
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with an imaging moiety or heteroalkyl optionally substituted with an imaging moiety; and
n is 1, 2, 3, 4, or 5; provided that at least one fluorine species is present the compound.
A method for 18 F-labeling a compound comprising formula:
Figure imgf000176_0002
wherein:
R is alkyl;
R2 is hydrogen or halogen; and R3 is alkyl substituted with a sulfonate-containing group, alkoxy substituted with a sulfonate-containing group, or alkoxyalkyl substituted with a sulfonate-containing group, comprising:
reacting the compound with an 18F species in the presence of an ammonium salt or a bicarbonate salt to form a product comprising the 18F species.
3. The method of claim 2, wherein the sulfonate-containing group is mesylate, tosylate, triflate, or 1,2-cyclic sulfate.
4. The method of claim 2, wherein R1 is a methyl, ethyl, propyl, H-butyl, s-butyl, or i-butyl.
5. The method of claim 2, wherein the product comprising formula:
Figure imgf000177_0001
6. A method for synthesizing a precursor to an imaging agent comprising:
reacting a compound comprising formula (III):
Figure imgf000177_0002
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
each R3 can be the same or different and is alkyl optionally substituted with a leaving group or heteroalkyl optionally substituted with a leaving group; and
n is 1, 2, 3, 4, or 5;
provided at least one R3 is substituted with a leaving group; with a nucleophile, wherein the nucleophile replaces the at least one leaving group to produce the precursor.
A method of claim 6, wherein reacting the compound with the nucleophile occurs the presence of a base.
8. A method of claim 7, wherein the base is a metal or metal salt.
9. A method of claim 6 or 7, wherein reacting the compound with the nucleophile occurs in the presence of a catalyst.
A method of claim 9, wherein the catalyst is a tetraalkylammonium iodide.
11. A method of claim 6, wherein:
W is -0(CH2 ;
R1 is i-butyl;
R2 is chloride; and
R3 is alkyl substituted with a leaving group.
12. A method of claim 6, wherein the compound comprising formula (III) comprises the structure:
Figure imgf000178_0001
A method of claim 6, wherein the precursor comprises the structure:
Figure imgf000178_0002
14. A method of claim 12 or 13, wherein R1 is i-butyl; and R2 is CI.
15. A method of claim 6, further comprising:
reacting a compound comprising formula (IV):
Figure imgf000179_0001
wherein:
R is alkyl, optionally substituted;
R2 is hydrogen or halide;
W is alkyl or heteroalkyl, optionally substituted;
each R4 can be the same or different and is alkyl optionally substituted with hydroxyl or heteroalkyl optionally substituted with hydroxyl; and
n is 1, 2, 3, 4, or 5;
provided at least one R4 is substituted with hydroxyl;
with a reactant comprising a leaving group to produce a compound comprising formula (III), wherein the at least one hydroxyl is replaced with the leaving group.
16. A method of claim 15, wherein reacting the compound comprising formula (IV) is performed in the presence of a halogenation reagent.
17. A method of claim 16, wherein the halogenation reagent is a brominating reagent.
18. A method of claim 17, wherein the brominating reagent is phosphorus tribromide, pyridinium dibromide, or a combination of carbon tetrabromide and triphenylphospine.
19. A method of claim 15, wherein:
W is -0(CH2 ;
R1 is i-butyl;
R2 is chloride; and
R4 is alkyl substituted with hydroxyl. A method of claim 15, wherein the compound comprising formula (IV)
Figure imgf000180_0001
A method of claim 15, wherein the product comprises the structure
Figure imgf000180_0002
22. A method of claim 20 or 21, wherein R1 is i-butyl and R2 is CI.
23. A method of claim 15, wherein the compound comprising formula (IV) is formed by etherification of precursor compounds comprising formulae (IVa) and (IVb):
Figure imgf000180_0003
wherein:
m is 1, 2, 3, 4, or 5 or greater;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
R5 is hydroxyl or halide; and
R6 and R7 can be the same or different and are alkyl, heteroalkyl, or a carbonyl- containing group, each optionally substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R7 comprises a leaving group or a group that can be replaced by a leaving group or when R5 is halide, at least one of R6 and R7 comprise a hydroxyl.
24. A method of claim 15, wherein the compound comprising formula (IV) is formed by etherification of the compounds comprising formulae:
Figure imgf000181_0001
wherein:
m is 1 or greater;
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
R5 is hydroxyl or halide; and
R6 and R7 can be the same or different and are alkyl, heteroalkyl, or a carbonyl- containing group, any of which may be substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R7 comprises a leaving group or a group that can be replaced by a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl.
25. A method of claim 15, wherein the compound comprising formula (IV) is formed by etherification o s comprising formulae (IVa) and (IVd):
Figure imgf000181_0002
and \=/ (IVd), wherein:
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
R5 is hydroxyl or halide; and
R6 and R7 can be the same or different and are alkyl, heteroalkyl, or a carbonyl- containing group, each optionally substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R7 comprises a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl.
26. A method of claim 15, wherein the compound comprising formula (IV) is formed by etherification of compounds comprising formulae:
Figure imgf000182_0001
wherein:
R1 is alkyl, optionally substituted;
R2 is hydrogen or halide;
R5 is hydroxyl or halide; and
R6 and R7 can be the same or different and are alkyl, heteroalkyl, or a carbonyl- containing group, any of which may be substituted,
wherein, when R5 is hydroxyl, at least one of R6 and R7 comprises a leaving group, or when R5 is halide, at least one of R6 and R7 comprises a hydroxyl.
27. A method of claim 26, wherein etherification comprises reacting the precursor compounds in the presence of a base.
28. A method of claim 27, wherein the base comprises a carbonate ion.
A method of any one of claims 25-28, wherein:
R5 is halide; and
R6 and R7 are each substituted alkyl.
30. A method of claim 15, wherein the compound comprising formula (IV) is synthesized by etherification of precursor compounds comprising formulae:
Figure imgf000182_0002
to form a product comprising formula:
Figure imgf000182_0003
wherein R1 is alkyl, optionally substituted; and
R2 is hydrogen or halide.
31. A method of claim 15, wherein the compound comprising formula (IV) is synthesized by etherification of compounds comprising formulae:
Figure imgf000183_0001
to form a product comprising formula:
Figure imgf000183_0002
A method of claim 24 or 25, wherein:
R5 is hydroxyl;
R6 is a carbonyl-containing group; and
R7 is a substituted alkyl.
A method of claim 24 or 25, wherein:
R5 is hydroxyl;
R6 is an ester; and
R7 is alkyl substituted with a leaving g
34. A method of claim 15, wherein the compound comprising formula (IV) is synthesized by etherification of the compounds comprising formulae:
Figure imgf000183_0003
to form a product comprising the formula:
Figure imgf000183_0004
35. A method of claim 34, further comprising the act of exposing the product to a reducing agent to convert the ester group to an alcohol.
36. A method for synthesizing an imaging agent, comprising:
contacting an imaging agent precursor with a fluoride species and an ammonium salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species wherein the molar ratio of ammonium salt to imaging agent precursor is less than about 1.5:1.
37. A method of claim 36, wherein the molar ratio of ammonium salt to imaging agent precursor is about 1 : 1 or less, or about 0.75: 1 or less, or about 0.5: 1 or less, or about 0.25:1 or less, or about 0.05:1 or less.
38. A method of claim 36, wherein the molar ratio of ammonium salt to imaging agent precursor is from about 0.5:1 to about 1:1.
39. A method of claim 36, wherein the ammonium salt is an ammonium bicarbonate salt, ammonium hydroxide salt, ammonium acetate salt, ammonium lactate salt, ammonium trifluoroacetate salt, ammonium methanesulfonate salt, ammonium p- toluenesulfonate salt, ammonium nitrate salt, ammonium iodide salt, or ammonium bisulfate salt.
40. A method of claim 36, wherein the ammonium salt is a tetraalkylammonium salt.
41. A method for synthesizing an imaging agent, comprising:
contacting an imaging agent precursor with a fluoride species and a bicarbonate salt under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species,
wherein the molar ratio of bicarbonate salt to imaging agent precursor is less than about 1:5:1.
42. A method of claim 41, wherein the molar ratio of bicarbonate salt to imaging agent precursor is about 1: 1 or less, or about 0.75:1 or less, or about 0.5:1 or less, or about 0.25:1 or less, or about 0.05:1 or less.
43. A method of claim 41, wherein the molar ratio of bicarbonate salt to imaging agent precursor is from about 0.5:1 to about 1:1.
44. A method of claim 41, wherein the bicarbonate salt is a metal bicarbonate.
45. A method of claim 41, wherein the bicarbonate salt is sodium bicarbonate, calcium bicarbonate, potassium bicarbonate, or magnesium bicarbonate.
46. A method of claim 41, wherein the bicarbonate salt is an ammonium bicarbonate.
47. A method of claim 41, wherein the bicarbonate salt is an tetraalkylammonium bicarbonate.
48. A method of claim 36 or 41, wherein the ammonium salt or the bicarbonate salt comprising the formula:
Figure imgf000185_0001
wherein R is alkyl.
49. A method of claim 36 or 41, wherein the ammonium salt or the bicarbonate salt is Et4NHC03.
50. A method of claim 41, wherein the imaging agent precursor is further exposed to a cryptand.
51. A method of claim 41, wherein the contacting is performed in the absence of a carbonate salt.
52. A method of claim 41, wherein the contacting is performed in the absence of a cryptand.
53. A method for synthesizing an imaging agent, comprising:
contacting an imaging agent precursor with a fluoride species under conditions that result in the fluoride species replacing the leaving group to produce an imaging agent comprising the fluoride species,
wherein the contacting is performed at a pH below 7, or at a pH below 6, or at a pH below 5.
54. A method of claim 53, wherein the contacting is performed at a pH between 5 and 6.
55. A method of claim 53, wherein the leaving group is a sulfonate-containing group.
56. A method of claim 53, wherein the leaving group is a mesylate, tosylate, triflate, or 1,2,-cyclic sulfate group.
57. A method of claim 53, wherein the fluoride species is an 18F ion.
58. A method of claim 53, wherein the imaging agent precursor comprising formula
Figure imgf000186_0001
J is selected from the group consisting of N(R ), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, and C(=0)N(R27);
when present, K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
when present, L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group;
M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group; or
L and M, together with the atom to which they are attached, may form a three-, four-, five-, or six-membered carbocyclic ring;
Q is halo or haloalkyl;
n is 0, 1, 2, or 3;
21 22 27 28
R , R , R , and R are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group;
R , R , R , and R are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C6 alkyl optionally substituted with a leaving group, and a leaving group;
R29 is Ci-C6 alkyl optionally substituted with a leaving group;
Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with a leaving group and heteroaryl optionally substituted with a leaving group; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, and heteroaryl optionally substituted with a leaving group;
provided that at least one leaving group is present in formula (I).
59. A method of claim 58, wherein the imaging agent comprising formula (II):
Figure imgf000188_0001
wherein:
J is selected from the group consisting of N(R28), S, O, C(=0), C(=0)0, NHCH2CH20, a bond, and C(=0)N(R27);
when present, K is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
when present, L is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety;
M is selected from the group consisting of hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, alkyloxy optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, heteroaryl optionally substituted with an imaging moiety, and an imaging moiety; or
L and M, together with the atom to which they are attached, may form a three-, four-, five-, or six-membered carbocyclic ring;
Q is halo or haloalkyl;
n is 0, 1, 2, or 3;
R 21 , R 22 , R 27 , and R 28 are independently selected from hydrogen, Ci-C6 alkyl optionally substituted with an imaging moiety, and an imaging moiety;
R 23 , R 24 , R 25 , and R 26 are independently selected from hydrogen, halogen, hydroxyl, alkyloxy, Ci-C6 alkyl optionally substituted with an imaging moiety, and an imaging moiety;
R29 is Ci-C6 alkyl optionally substituted with an imaging moiety; and
Y is selected from the group consisting of a bond, carbon, and oxygen; provided that when Y is a bond, K and L are absent, and M is selected from the group consisting of aryl optionally substituted with an imaging moiety and heteroaryl optionally substituted with an imaging moiety; and provided that when Y is oxygen, K and L are absent, and M is selected from hydrogen, alkoxyalkyl optionally substituted with an imaging moiety, aryl optionally substituted with an imaging moiety, Ci-C6 alkyl optionally substituted with an imaging moiety, and heteroaryl optionally substituted with an imaging moiety;
provided that at least one imaging moiety is present in formula (II).
60. A method of claim 58, wherein J is O.
61. A method of claim 58, wherein R29 is methyl, ethyl, H-propyl, z'-propyl, H-butyl, i- butyl, or i-butyl, each optionally substituted with a leaving group.
62. A method of claim 58, wherein Q is chloro.
63. A method of claim 58, wherein each of R21, R22, R23, R24, R25, R26, and R27 are hydrogen.
64. A method of claim 58, wherein Y is carbon, K and L are hydrogen, and M is selected from the group consisting of alkoxyalkyl optionally substituted with a leaving group, alkyloxy optionally substituted with a leaving group, aryl optionally substituted with a leaving group, Ci-C6 alkyl optionally substituted with a leaving group, heteroaryl optionally substituted with a leaving group, and a leaving group.
65. A method of claim 58, wherein the imaging agent precursor comprises the formula:
Figure imgf000190_0001
wherein L is a leaving group.
A method of clai ses the formula:
Figure imgf000190_0002
wherein Im is an imaging moiety.
67. A method of claim 65, wherein J is O, and R and R is each H.
68. A method of claim 66, wherein J is O, and R and R is each H.
69. A method of claim 66, wherein the imaging agent precursor comprises the formula:
Figure imgf000190_0003
A method of claim 66, wherein the imaging agent comprises the formula:
Figure imgf000190_0004
71. A method of claim 66, further comprising:
purifying the imaging agent using at least one purification technique.
72. A method of claim 66, further comprising:
combining the imaging agent with a stabilizing agent.
73. A method of claim 72, wherein the stabilizing agent is ascorbic acid or a salt thereof.
74. A method for manufacturing an imaging agent comprises the formula:
Figure imgf000191_0001
the method comprising,
(a) contacting a tosylate precursor comprising the structure:
Figure imgf000191_0002
with an anhydrous fluoride species associated with an ammonium salt;
(b) heating the mixture of (a);
(c) cooling the heated mixture;
(d) adding ¾0 to the cooled mixture;
(e) purifying the mixture from the hydrated mixture of (d) using HPLC with an H20/MeCN eluent; and
(f) diluting the eluent with a solution of ascorbic acid or a salt thereof.
75. The method of claim 74, wherein step (b) comprises heating the mixture to a temperature between 50 °C and 250 °C.
76. The method of claim 74 or 75, wherein heating step (b) comprises heating the mixture for less than 5 minutes, less than 10 minutes, less than 20, minutes, or less than 30 minutes.
77. The method any one of claims 74-76, further comprising:
(g) contacting the diluted eluent of (f) with a CI 8 resin;
(h) washing the contacted C18 resin with a solution of ascorbic acid
thereof;
(i) eluting
Figure imgf000192_0001
from the CI 8 resin with absolute ethanol; and
(j) diluting the eluent of (i) with a solution of ascorbic acid or a salt thereof.
The method of claim 77, further comprising:
(k) aseptically filtering the diluted eluent of (j), and
(1) optionally, determining the presence of
Figure imgf000192_0002
in a sample of the aseptic filtrate of (k).
79. An imaging agent made by a method of claim 74.
80. A method for synthesizing a fluorinated compound, comprising:
reacting, in the presence of a carbonate or bicarbonate, (i) a precursor of the fluorinated compound comprising an alkoxyalkyl group substituted with a halide or a sulfonate-containing group, with (ii) a salt comprising a fluoride species and weakly coordinating cation.
81. The method of claim 80, wherein the alkoxyalkyl group is substituted with a sulfonate-containing group.
82. The method of claim 80, wherein the weakly coordinating cation is a
tetraalkylammonium cation.
83. The method of claim 80, wherein the fluoride is enriched with F isotope. 84. A method for 18 F-labeling a compound comprising the formula:
Figure imgf000193_0001
wherein R is -(lower alkyl)-sulfonate, R is an d-do alkyl, and R2 is H or a halogen, comprising reacting the compound with 18F in the presence of a tetraalkylammonium bicarbonate or tetraalkylammonium carbonate.
85. The method of claim 84, wherein R is -(CH2)0(CH2)n-sulfonate-containing group, wherein n is an integer from 1 to 5.
86. The method of claim 84, wherein the sulfonate-containing group is mesylate, tosylate, triflate, or 1,2-cyclic sulfate.
87. The method of any of claims 84-86, wherein R2 is a halogen. 88. The method of any of claims 84-87, wherein R1 is methyl, ethyl, propyl or butyl. 89. A method for synthesizing a precursor to an imaging agent, comprising:
reacting a compound comprising formula (V):
Figure imgf000193_0002
wherein:
W is alkyl or heteroalkyl, optionally substituted;
R1 is alkyl, optionally substituted; and R2 is hydrogen or halide,
with a nucleophile or a radical species to produce a compound comprising formula (VI):
Figure imgf000194_0001
90. A method of claim 89, wherein the nucleophile is a hydride ion.
91. A method of claim 90, wherein the hydride is generated from
diisobutylaluminum hydride.
92. A method of claim 89, wherein the radical species is Η·.
93. A method of claim 89, wherein the compound comprising formula (V) wherein W is -0(CH2)- is synthesized by etherification of precursor compounds comprising formulae (Va) and (Vb):
Figure imgf000194_0002
to form a product comprising formula:
Figure imgf000194_0003
wherein R is alkyl, optionally substituted; and
R2 is hydrogen or halide,.
94. A method of claim 93 or 94, wherein R1 is i-butyl and R2 is CI.
95. A method of claim 93 or 94, wherein etherification comprises reacting the precursor compounds in the presence of a base.
96. A method of claim 95, wherein the base comprises a carbonate ion.
97. A method of claim 95, wherein the base comprises a hydroxide ion.
98. A method of claim 97, wherein the base is sodium hydroxide or tetramethyl ammonium hydroxide.
99. A method of claim 93 or 94, wherein the etherification reaction comprises exposure to sodium hydroxide and benzyl triethylammonium chloride.
100. A method of claim 93, wherein the compound comprising formula (Vb) is produced by exposing the compound comprising formula:
Figure imgf000195_0001
to a reducing agent.
101. A method of claim 100, wherein the reducing agent is lithium aluminum hydride or lithium borohydride.
102. A method of claim 100, wherein the compound comprises formula:
Figure imgf000195_0002
is produced by reacting methyl 4-formyl benzoate with ethylene glycol in the presence of an acid.
103. A method for forming a sulfonate-containing precursor of an imaging agent, comprising reacting a compound comprising formula:
Figure imgf000196_0001
with a sulfonate-containing species to form a product comprising a sulfonate-containing precursor of an imaging agent.
104. A method of claim 103, wherein the sulfonate-containing group is mesylate, tosylate, or triflate.
105. A method of claim 103, wherein the sulfonate-containing precursor of an imaging agent comprises formula:
Figure imgf000196_0002
106. A method of claims 103, 104, or 105, further comprising reacting the sulfonate- containing precursor with an imaging moiety to form an imaging agent.
107. A method of claim 106, wherein the imaging moiety is a radioisotope.
108. A method of claim 107, wherein the imaging moiety is 11 C, 13 N, 18 F, 123 I, 125 I, 99mTc, 95Tc, mIn, 62Cu, 64Cu, 67Ga, or 68Ga.
109. A method of claim 106, wherein the imaging agent comprises formula:
Figure imgf000196_0003
110. A method for synthesizing an imaging agent, comprising:
reacting precursor compounds comprising formulae:
Figure imgf000197_0001
via an etherification reaction to form a first compound comprising the formula:
Figure imgf000197_0002
exposing the first compound to a reducing agent to form a second compound comprising a benzylic alcohol;
treating the second compound with phosphorus tribromide to form a third compound comprising a benzylic bromide;
reacting the third compound with ethylene glycol to produce a fourth compound comprising the formula:
Figure imgf000197_0003
reacting the fourth compound with a sulfonate-containing species to form a product comprising a sulfonate-containing precursor of an imaging agent.
111. The method of claim 110, further comprising reacting the sulfonate-containing precursor of an imaging agent with an imaging moiety to form the imaging agent.
112. A compound comprising formula:
Figure imgf000198_0001
113. A method of imaging a subject, comprising:
administering to a subject a first dose of imaging agent comprising the formula:
Figure imgf000198_0002
in an amount between about 1 mCi and about 4 mCi;
acquiring at least one first image of a portion of the subject;
subjecting the subject to stress;
administering to the subject undergoing stress a second dose of the imaging agent in an amount greater than the first dose of the imaging agent by at least about 1.5 times the first dose of the imaging agent; and
acquiring at least one second image of the portion of the subject.
114. The method of claim 113, wherein the second dose of the imaging agent is administered within less than about 48 hours, about 24 hours, about 18 hours, about 12 hours, about 6 hours, about 5 hours, about 4 hours, about 3 hours, about 2 hours, about 1 hour, about 30 minutes, or about 15 minutes after acquiring the at least one first image.
115. The method of claim 113, wherein the second dose of the imaging agent is at least about 2.0 times greater than the first dose of the imaging agent.
116. The method of claim 113, wherein the first image is obtained during an image acquisition period between about 1 and about 20 minutes.
117. The method of claim 113, wherein the second image is obtained during an image acquisition period between about 1 and about 20 minutes.
118. The method of claim 113, wherein the portion of the subject is at least a portion of the cardiovascular system.
119. The method of claim 118, wherein the portion of the cardiovascular system is at least a portion of the heart.
120. The method of claim 113, wherein the acquiring employs positron emission tomography.
121. The method of claim 113, further comprising determining the presence or absence of a cardiovascular disease or condition in the subject.
122. The method of claim 121, wherein the cardiovascular disease is coronary artery disease or myocardial ischemia.
123. The method of claim 113, wherein the imaging agent is administered as a formulation comprising water, less than about 5% ethanol, and less than about 50 mg/mL sodium ascorbate.
124. The method of claim 123, wherein the formulation comprising the imaging agent is administered via an intravenous bolus injection.
125. The method of claim 113, wherein the stress is induced by exercising the subject.
126. The method of claim 125, wherein the second dose of the imaging agent is administered during the exercise.
127. The method of claim 125, wherein the wait time between acquiring at least one first image of a portion of the subject and administering to the subject a second dose of the imaging agent is about 60 minutes.
128. The method of claim 113, wherein the second dose of the imaging agent is administered in an amount that is at least about 2.5, or at least about 3.0 times greater than the first dose of the imaging agent.
129. The method of claim 128, wherein the second dose of the imaging agent is administered in an amount between about 2.5 and about 5.0, or about 2.5 and about 4.0, or about 3.0 and about 4.0, or about 3.0 and about 5.0 times greater than the first dose of the imaging agent.
130. The method of claim 125, wherein the second dose of the imaging agent is between about 8.6 mCi and about 9.0 mCi, or between about 9.0 and about 9.5 mCi, or between about 8.6 mCi and about 9.5 mCi.
131. The method of claim 113, wherein the stress is pharmacological stress.
132. The method of claim 131, wherein the pharmacological stress is induced by administering a pharmacological stress agent to the subject.
133. The method of claim 132, wherein the pharmacological stress agent is a vasodilator.
134. The method of claim 133, wherein the vasodilator is adenosine, regadenoson, and apadeneson.
135. The method of claim 131, wherein the second dose of the imaging agent is administered after the subject has been administered the pharmacological stress agent.
136. The method of claim 131, wherein the second dose of the imaging agent is administered when the subject is at peak vasodilation from the pharmacological stress agent.
137. The method of claim 113, wherein the first dose of the imaging agent is between about 2.0 mCi to about 3.5 mCi.
138. The method of claim 137, wherein the first dose of the imaging agent is between about 2.4 mCi to about 2.9 mCi, or between about 2.5 mCi to about 3.0 mCi, or between about 2.5 mCi and about 3.5 mCi.
139. The method of claim 138, wherein the second dose of the imaging agent is between about 5.7 mCi and about 6.2 mCi, or between about 6.0 mCi and about 6.5 mCi, and about 5.7 mCi and about 6.5 mCi.
140. The method of claim 113, wherein the total of the first and second dose of the imaging agent does not exceed about 14 mCi.
141. A syringe comprising a composition comprising the imaging agent comprising the formula:
Figure imgf000201_0001
wherein the syringe adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13% 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of the imaging agent.
142. The syringe of claim 141, wherein the syringe comprises a plunger that adsorbs less than 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13% 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or 0.5% of the imaging agent.
143. The syringe of claim 141, wherein the syringe comprises a plunger that is not rubber-tipped.
144. The syringe of claim 141, wherein the syringe further comprises sodium ascorbate, ethanol, and water.
145. The syringe of claim 142, wherein the imaging agent is in a solution comprising less than 4% ethanol and less than 50 mg/mL sodium ascorbate in water.
146. The syringe of claim 141, wherein the imaging agent in the syringe is between about 1.5 and about 14 mCi.
147. The syringe of claim 141, wherein the syringe comprises no rubber, and no silicon lubricants.
148. The syringe of claim 141, wherein the syringe is a non-reactive syringe.
149. The syringe of claim 142, wherein the syringe adsorbs between about 1% and about 20%, or between about 5% and about 15%, or between about 1% and about 15%, or between 2% and about 10%, or between about 5% and about 20%.
150. A method of imaging a subject, comprising:
subjecting a subject to stress;
administering to the subject a first dose of an imaging agent comprising the formula:
Figure imgf000202_0001
in an amount between about 1 mCi and about 4 mCi;
acquiring at least one first image of a portion of the subject;
administering to the subject a second dose of the imaging agent in an amount greater than the first dose of the imaging agent; and
acquiring at least one second image of the portion of the subject.
151. The method of claim 150, wherein the amount of the second dose is more than about 1.5 times the amount of the first dose.
152. A method of imaging a subject, comprising:
subjecting a subject to stress;
administering to the subject a dose of an imaging agent comprising the formula:
Figure imgf000203_0001
in an amount less about 20 mCi; and
acquiring at least one first image of a portion of the subject.
153. The method of claim 152, wherein the amount of the dose is less than about 14 mCi.
154. The method of claim 152, wherein the amount of the dose is between about 1 mCi and about 4 mCi.
155. A cassette for the preparation of an imaging agent comprising the formula:
Figure imgf000203_0002
comprising: (i) a vessel containing an imaging agent precursor comprising the formula:,
Figure imgf000203_0003
and (ii) a conduit for adding a source
An automated reaction system, comprising:
the cassette of claim 155.
157. An apparatus for synthesizing an imaging agent comprising a linear arrangement of a plurality of stopcock manifolds connected to one or more of the components selected from the group consisting of a [180]¾0 recovery system, gas inlet, reservoir with solution of imaging agent precursor, vial, anion exchange cartridge, C-18 cartridge, syringe, solvent reservoir, reaction vessel, HPLC system, collection vessel, reservoir for solution of ascorbic acid or salt thereof, and exhaust outlet.
158. The apparatus of claim 157, further comprising tubing.
159. The apparatus of claim 158, further comprising an imaging agent synthesis module, wherein the apparatus is fluidically connected to the apparatus.
160. The apparatus of claim 159, wherein the apparatus is capable of carrying out the method of claim 74.
161. The apparatus of claim 157, wherein the apparatus is capable of preparing an imaging agent comprising the formula:
Figure imgf000204_0001
162. The apparatus of claim 157, with the components arranged as shown in Figure 8.
163. The apparatus of claim 157, comprising components arranged in the order: (1) gas inlet; (2) [180]¾0 recovery system; (3) anion exchange cartridge; (4) MeCN reservoir; (5) syringe; (6) reservoir with solution of imaging agent precursor; (7) reaction vessel; (8) HPLC system; (9) reservoir with solution of ascorbic acid or a salt thereof; (10) collection vessel; (11) ethanol reservoir; (12) vial with final product; (13) Sep-pack cartridge; (14) reservoir with solution of ascorbic acid or a salt thereof; (15) reaction vessel; and (16) exhaust outlet.
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Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8226929B2 (en) 2004-02-13 2012-07-24 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
US8263042B2 (en) 2004-04-28 2012-09-11 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
WO2013036869A2 (en) 2011-09-09 2013-03-14 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
WO2013070471A1 (en) 2011-11-11 2013-05-16 Lantheus Medical Imaging, Inc. Evaluation of presence of and vulnerability to atrial fibrillation and other indications using matrix metalloproteinase-based imaging
US8491868B2 (en) 2006-12-26 2013-07-23 Lantheus Medical Imaging, Inc. Ligands for imaging cardiac innervation
WO2013172979A1 (en) * 2012-05-14 2013-11-21 University Of Southern California Methods and compositions for positron emission tomography myocardial perfusion imaging
WO2013173004A2 (en) 2012-04-10 2013-11-21 Lantheus Medical Imaging, Inc. Radiopharmaceutical synthesis methods
WO2014026079A2 (en) 2012-08-10 2014-02-13 Lantheus Medical Imaging, Inc. Compositions, methods, and systems of the synthesis and use of imaging agents
US8936777B2 (en) 2010-02-08 2015-01-20 Lantheus Medical Imaging, Inc. Methods and apparatus for synthesizing imaging agents, and intermediates thereof
US9388125B2 (en) 2010-05-11 2016-07-12 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
US9408927B2 (en) 2008-02-29 2016-08-09 Lantheus Medical Imaging, Inc. Contrast agents for applications including perfusion imaging
US9687571B2 (en) 2009-04-15 2017-06-27 Lantheus Medical Imaging, Inc. Stabilization of radiopharmaceutical compositions using ascorbic acid
WO2019185933A1 (en) * 2018-03-29 2019-10-03 Ge Healthcare Limited Solid phase extraction
RU2721551C2 (en) * 2015-05-20 2020-05-20 Аут Энд Аут Кемистри С.П.Р.Л. Method for carrying out a plurality of synthesis processes for producing a radiopharmaceutical in series, a device and a cassette for realizing said method
WO2021078814A1 (en) 2019-10-21 2021-04-29 Ge Healthcare Limited Use of cyclodextrins as a radiostabilizer
GB202108608D0 (en) 2021-06-16 2021-07-28 Ge Healthcare Ltd Preparation of a ph-adjusted ascorbic acid solution
GB202108605D0 (en) 2021-06-16 2021-07-28 Ge Healthcare Uk Ltd Effect of water content
US11290885B2 (en) 2018-12-19 2022-03-29 Rohde & Schwarz Gmbh & Co. Kg Communication system and method

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10109385B2 (en) 2009-09-23 2018-10-23 Abt Molecular Imaging, Inc. Dose synthesis card for use with automated biomarker production system
US11129911B2 (en) 2011-05-05 2021-09-28 Cedars-Sinai Medical Center Assessment of coronary heart disease with carbon dioxide
CA2845308C (en) * 2011-05-05 2021-01-26 Cedars-Sinai Medical Center Assessment of coronary heart disease with carbon dioxide
CA2852395C (en) * 2011-10-21 2020-04-28 Lantheus Medical Imaging, Inc. Compositions comprising ascorbic acid and pyridaben and pyridaben analogs attached to an imaging moiety and related methods
CA2794281C (en) * 2012-04-30 2019-07-02 Elazar A. Bienenstock Single photon emission computed tomography imaging method
WO2015021078A1 (en) 2013-08-05 2015-02-12 Cedars-Sinai Medical Center Methods for reducing ischemia-reperfusion injury
JP6190240B2 (en) 2013-10-16 2017-08-30 浜松ホトニクス株式会社 Diagnostic agent for therapeutic effect on cancer
US9031300B1 (en) 2013-10-25 2015-05-12 General Electric Company System and method reconstructing a nuclear medicine image using deformed attenuation image
CN107530455A (en) * 2015-02-10 2018-01-02 Abt分子成像公司 With automatic biological label production system associated with dosage synthesize card
CN105553594B (en) * 2015-12-09 2018-02-16 沈阳东软医疗系统有限公司 A kind of PET clock synchronizing methods and device
US11109819B2 (en) 2016-04-11 2021-09-07 The General Hospital Corporation System and method for quantitatively mapping mitochondrial membrane potential
JP6060302B1 (en) * 2016-06-10 2017-01-11 日本メジフィジックス株式会社 Method and apparatus for analyzing myocardial nuclear medicine image data
TWI649067B (en) * 2017-03-01 2019-02-01 醫百科技股份有限公司 Positioning corrector
CN108129673B (en) * 2017-12-26 2020-10-13 武汉大学 Preparation and application of high-sensitivity water-soluble dendritic macromolecule F19 developer
CN108658868A (en) * 2018-05-07 2018-10-16 四川大学 A kind of bicarbonate ion liquid and preparation method thereof and a kind of recrystallization method of photoacoustic spectroscopy
CN109806822B (en) * 2019-01-30 2021-07-30 杭州吉蕊科技有限公司 Modularized and multifunctional PET probe automatic synthesis system
CN109896934A (en) * 2019-03-08 2019-06-18 山东省药学科学院 A kind of preparation method of high-purity 2- benzyloxy bromoethane
GB201919016D0 (en) * 2019-12-20 2020-02-05 Ge Healthcare Ltd Apparatus and method for solid phase extraction
CN111333638A (en) * 2020-03-17 2020-06-26 四川大学华西医院 18F-labeled isoquinolino pyridazinone compound and synthesis method and application thereof
JP7362561B2 (en) * 2020-07-30 2023-10-17 富士フイルム株式会社 Radiographic image processing device, method and program
WO2022261502A1 (en) * 2021-06-11 2022-12-15 Jubilant Draximage Inc. Non-invasive imaging methods of diagnosing peripheral arterial disease
CN114700006B (en) * 2022-06-07 2023-03-24 北京先通国际医药科技股份有限公司 Production equipment of liquid composition and preparation method and application thereof
CN114716415B (en) * 2022-06-09 2022-09-02 北京先通国际医药科技股份有限公司 Apparatus for producing liquid composition, method for producing the same and use thereof
CN114732918B (en) * 2022-06-10 2022-09-13 北京先通国际医药科技股份有限公司 Production equipment of liquid composition and preparation method and application thereof
CN114773179B (en) * 2022-06-23 2022-09-16 北京先通国际医药科技股份有限公司 Preparation method of compound I liquid composition and application of compound I liquid composition in myocardial metabolism PET imaging

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005079391A2 (en) 2004-02-13 2005-09-01 Bristol-Myers Squibb Pharma Company Contrast agents for myocardial perfusion imaging

Family Cites Families (125)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1073999A (en) 1965-01-29 1967-06-28 Ncr Co Process for forming stable images in photochromic material
US4510125A (en) 1982-12-08 1985-04-09 Mallinckrodt, Inc. Process for making lyophilized radiographic imaging kit
JPS604173A (en) 1983-06-23 1985-01-10 Nissan Chem Ind Ltd Pyridazinone derivative, its preparation and insecticidal, miticidal and fungicidal agent
DE3574870D1 (en) 1984-06-23 1990-01-25 Nissan Chemical Ind Ltd METHOD FOR PRODUCING 2-TERT.-BUTYL-4,5-DICHLORO-3 (2H) -PYRIDAZINONE.
JPH07116161B2 (en) 1984-07-04 1995-12-13 日産化学工業株式会社 Pyridazinone derivative
JPS61130275A (en) 1984-11-29 1986-06-18 Nissan Chem Ind Ltd Pyridazinone derivative, preparation thereof, and insecticidal, miticidal and fungicidal agent
DE3578304D1 (en) 1984-11-29 1990-07-26 Nissan Chemical Ind Ltd PYRIDAZINE DERIVATIVES, THEIR PRODUCTION AND INSECTICIDAL, ACARICIDIC, NEMATICIDIC, FUNGICIDIC COMPOSITIONS.
CA1265798A (en) 1984-12-10 1990-02-13 Motoo Mutsukado 3(2h)pyridazinone, process for its preparation and anti-allergic agent containing it
US5393512A (en) 1985-01-14 1995-02-28 Vanderheyden; Jean-Luc Stable therapeutic radionuclide compositions and methods for preparation thereof
JPH0641454B2 (en) 1985-02-27 1994-06-01 日産化学工業株式会社 Pyridazinone derivative
JPS61260018A (en) * 1985-05-14 1986-11-18 Nissan Chem Ind Ltd Anti-allergic agent
YU134686A (en) 1985-07-30 1988-02-29 Nissan Chemical Ind Ltd Process for preparing new derivatives 3-(2h)-pyridazinone
JPH0739397B2 (en) 1985-07-30 1995-05-01 日産化学工業株式会社 Pyridazinone derivatives and pest control agents
JPH07110815B2 (en) 1985-11-18 1995-11-29 ボ−ド・オブ・リ−ジェンツ、ザ・ユニバ−シティ−・オブ・テキサス・システム Polychelating agent for image and spectral enhancement (and spectral shift)
JPS6315974A (en) 1986-07-09 1988-01-23 小泉コンピユ−タ−株式会社 Balling game score table display apparatus
US5252317A (en) 1986-11-10 1993-10-12 The State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of The University Of Oregon Amplifier molecules for diagnosis and therapy derived from 3,5-bis[1-(3-amino-2,2-bis (aminomethyl)-propyl) oxymethyl] benzoic acid
US5567411A (en) 1986-11-10 1996-10-22 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of The University Of Oregon Dendritic amplifier molecules having multiple terminal active groups stemming from a benzyl core group
JPS63159372A (en) 1986-12-24 1988-07-02 Nissan Chem Ind Ltd Pyridazinone compound and insecticide, acaricide and nematocide
JPS63159374A (en) 1986-12-24 1988-07-02 Nissan Chem Ind Ltd Pyridazinone derivative and insecticide, acaricide and nematocide
JPS63159373A (en) 1986-12-24 1988-07-02 Nissan Chem Ind Ltd Pyridazinones and insecticide, acaricide and nematocide
DE3824210A1 (en) 1988-07-16 1990-01-18 Basf Ag 3 (2H) -PYRIDAZINONE DERIVATIVES FOR CONTROLLING SNAILS
IT1229684B (en) 1989-04-05 1991-09-06 Mini Ricerca Scient Tecnolog PYRIDAZINONE WITH INSECTICIDE AND ACARICIDE ACTIVITY
JPH02279676A (en) 1989-04-19 1990-11-15 Otsuka Chem Co Ltd Pyridazinone derivative
US5087440A (en) 1989-07-31 1992-02-11 Salutar, Inc. Heterocyclic derivatives of DTPA used for magnetic resonance imaging
GB8923843D0 (en) 1989-10-23 1989-12-13 Salutar Inc Compounds
US5377681A (en) 1989-11-13 1995-01-03 University Of Florida Method of diagnosing impaired blood flow
US5585112A (en) 1989-12-22 1996-12-17 Imarx Pharmaceutical Corp. Method of preparing gas and gaseous precursor-filled microspheres
US5228446A (en) 1989-12-22 1993-07-20 Unger Evan C Gas filled liposomes and their use as ultrasonic contrast agents
US5088499A (en) 1989-12-22 1992-02-18 Unger Evan C Liposomes as contrast agents for ultrasonic imaging and methods for preparing the same
US5679810A (en) 1990-01-19 1997-10-21 Salutar, Inc. Linear oligomeric polychelant compounds
JPH03220177A (en) 1990-01-25 1991-09-27 Nissan Chem Ind Ltd Insecticidal/miticidal agent composition
WO1992017215A1 (en) 1990-03-28 1992-10-15 Nycomed Salutar, Inc. Contrast media
GB9006977D0 (en) 1990-03-28 1990-05-23 Nycomed As Compositions
JPH04235975A (en) 1991-01-21 1992-08-25 Nissan Chem Ind Ltd Pyridazinone drivative and insect pest control agent
US5205290A (en) 1991-04-05 1993-04-27 Unger Evan C Low density microspheres and their use as contrast agents for computed tomography
US5093105A (en) 1991-04-09 1992-03-03 Merck Frosst Canada, Inc. Radiopharmaceutical bacteriostats
US5306482A (en) 1991-04-09 1994-04-26 Merck Frosst Canada, Inc. Radiopharmaceutical bacteriostats
ES2150916T3 (en) 1991-08-29 2000-12-16 Mallinckrodt Medical Inc USE OF GENISTIC ACID OR GENTISILIC ALCOHOL TO STABILIZE RADIO-MARKED PEPTIDES AND PROTEINS.
US5169942A (en) 1991-11-21 1992-12-08 General Electric Company Method for making 2-(18F)fluoro-2-deoxy-D-glucose
WO1994012479A1 (en) 1992-12-03 1994-06-09 Otsuka Kagaku Kabushiki Kaisha Pyridazinone derivative and insecticidal and miticidal agent
US5760191A (en) 1993-02-05 1998-06-02 Nycomed Imaging As Macrocyclic complexing agents and targeting immunoreagents useful in therapeutic and diagnostic compositions and methods
WO1994021653A1 (en) 1993-03-22 1994-09-29 General Electric Company Method for making 2-fluoro-2-deoxyglucose
CA2158249A1 (en) 1993-03-31 1994-10-13 James W. Brodack Radiopharmaceutical formulations having non-stannous reductants
US5417959A (en) 1993-10-04 1995-05-23 Mallinckrodt Medical, Inc. Functionalized aza-crytand ligands for diagnostic imaging applications
US5493026A (en) 1993-10-25 1996-02-20 Organix, Inc. Substituted 2-carboxyalkyl-3-(fluorophenyl)-8-(3-halopropen-2-yl) nortropanes and their use as imaging for agents for neurodegenerative disorders
JPH07252236A (en) 1994-01-28 1995-10-03 Takeda Chem Ind Ltd Anticancer agent
EP0665223A1 (en) 1994-01-28 1995-08-02 Takeda Chemical Industries, Ltd. Antitumor agent, novel 3(2H)-pyridazinone derivatives and their preparation
AU7312694A (en) 1994-06-03 1996-01-04 Mallinckrodt Medical, Inc. Rapidly clearing technetium-99m phosphonate skeletal imaging agents
US5520904A (en) 1995-01-27 1996-05-28 Mallinckrodt Medical, Inc. Calcium/oxyanion-containing particles with a polymerical alkoxy coating for use in medical diagnostic imaging
EP0727225A3 (en) 1995-02-14 1997-01-15 Sonus Pharma Inc Compositions and methods for directed ultrasound imaging
US5587491A (en) 1995-03-15 1996-12-24 Regents Of The University Of Minnesota Method for the synthesis of bis-tetrahydrofuranyl Annonaceous acetogenins
US5801228A (en) 1995-06-07 1998-09-01 Nycomed Imaging As Polymeric contrast agents for medical imaging
US5811073A (en) 1995-06-19 1998-09-22 President And Fellows Of Harvard College Method for radioisotopic detection and localization of inflammation in a host
US5827073A (en) 1995-07-05 1998-10-27 Ludwig Institute For Cancer Research Photoreactive peptide derivatives
US6066309A (en) 1996-02-02 2000-05-23 Rhomed Incorporated Post-labeling stabilization of radiolabeled proteins and peptides
US5804161A (en) 1996-05-14 1998-09-08 Nycomed Salutar Inc. Contrast agents
US5846517A (en) 1996-09-11 1998-12-08 Imarx Pharmaceutical Corp. Methods for diagnostic imaging using a renal contrast agent and a vasodilator
US6565889B2 (en) 1996-12-02 2003-05-20 The Regents Of The University Of California Bilayer structure which encapsulates multiple containment units and uses thereof
US5961955A (en) 1997-06-03 1999-10-05 Coulter Pharmaceutical, Inc. Radioprotectant for peptides labeled with radioisotope
AU5671699A (en) 1998-08-14 2000-03-06 Smithkline Beecham Corporation Grp receptor ligands
US6056939A (en) 1998-08-28 2000-05-02 Desreux; Jean F. Self-assembling heteropolymetallic chelates as imaging agents and radiopharmaceuticals
EP1119356B1 (en) 1998-09-29 2009-08-19 Merck & Co., Inc. Radiolabeled neurokinin-1 receptor antagonists
US6645508B1 (en) 1999-06-18 2003-11-11 Jivn-Ren Chen Stable L-ascorbic acid composition
WO2001087354A2 (en) 2000-05-17 2001-11-22 Bristol-Myers Squibb Pharma Company Use of small molecule radioligands for diagnostic imaging
GB0019357D0 (en) 2000-08-07 2000-09-27 Melacure Therapeutics Ab Novel phenyl guanidines
WO2002020008A1 (en) 2000-09-06 2002-03-14 The Scripps Research Institute Inhibitors of nadh:ubiquinone oxidoreductase
TWI247609B (en) 2001-01-23 2006-01-21 Nihon Mediphysics Co Ltd Agent for diagnosis of tissue proliferation activity or the treatment of proliferative disease
GB0115927D0 (en) 2001-06-29 2001-08-22 Nycomed Amersham Plc Solid-phase nucleophilic fluorination
US20030044354A1 (en) 2001-08-16 2003-03-06 Carpenter Alan P. Gas microsphere liposome composites for ultrasound imaging and ultrasound stimulated drug release
US20030082191A1 (en) 2001-08-29 2003-05-01 Poduslo Joseph F. Treatment for central nervous system disorders
US7186241B2 (en) * 2001-10-03 2007-03-06 Medical Instill Technologies, Inc. Syringe with needle penetrable and laser resealable stopper
JP2005529840A (en) 2001-10-16 2005-10-06 ヒプニオン， インコーポレイテッド Treatment of CNS disorders using CNS targeted modulators
JP4530665B2 (en) 2002-02-06 2010-08-25 ジョンズ ホプキンス ユニバーシティ Non-invasive imaging techniques for mitochondria by using radiolabeled lipophilic salts
EA009334B1 (en) 2002-03-29 2007-12-28 Янссен Фармацевтика Н.В. Radiolabelled quinoline and quinolinone derivatives and their use as metabotropic glutamate receptor ligands
AU2003224747A1 (en) 2002-04-08 2003-10-27 Biostream, Inc. Technetium-labeled rotenone derivatives, and methods of use thereof
GB0229683D0 (en) 2002-12-20 2003-01-29 Imaging Res Solutions Ltd Preparation of radiopharmaceuticals
CN1984660B (en) 2003-07-03 2010-12-15 美瑞德生物工程公司 4-arylamino-quinazolines as activators of aspartic acid specificity cysteine protease and inducers of apoptosis
WO2005007632A1 (en) 2003-07-18 2005-01-27 Pharmacia Corporation Substituted pyridazinones as inhibitors of p38
CA2783275A1 (en) 2003-07-24 2005-02-03 Bracco Imaging S.P.A. Stable radiopharmaceutical compositions and methods for their preparation
GB0317920D0 (en) 2003-07-31 2003-09-03 Amersham Plc Solid-phase synthesis
US7927616B2 (en) 2004-01-16 2011-04-19 Thomas T. Yamashita Pesticide compositions and methods for their use
AU2005216949B2 (en) * 2004-02-24 2011-09-22 The General Hospital Corporation Catalytic radiofluorination
WO2005085200A1 (en) 2004-03-05 2005-09-15 Banyu Pharmaceutical Co., Ltd. Pyridone derivative
AT500838B1 (en) 2004-04-20 2007-11-15 Veterinaermedizinische Uni Wie MULTIPLE HSE
US7485283B2 (en) 2004-04-28 2009-02-03 Lantheus Medical Imaging Contrast agents for myocardial perfusion imaging
US20060083681A1 (en) 2004-10-18 2006-04-20 Ajay Purohit Compounds for myocardial perfusion imaging
US7534418B2 (en) 2004-12-10 2009-05-19 The Regents Of The University Of Michigan Imaging agents
KR100789847B1 (en) 2004-12-15 2007-12-28 (주)퓨쳐켐 A Preparation Method of Organo Fluoro Compounds in Alcohol Solvents
EP1893244A4 (en) 2005-06-23 2009-06-24 Univ Emory Imaging agents
US7824659B2 (en) 2005-08-10 2010-11-02 Lantheus Medical Imaging, Inc. Methods of making radiolabeled tracers and precursors thereof
JP2007112725A (en) * 2005-10-18 2007-05-10 Inst Nuclear Energy Research Rocaec Method for producing amino acid o-(2-[18f] fluoroethyl)-l-tyrosine labeled with 18f of non-substrate
GB0524851D0 (en) * 2005-12-06 2006-01-11 Ge Healthcare Ltd Radiolabelling method using polymers
US7871623B2 (en) * 2005-12-21 2011-01-18 The Board Of Trustees Of The Leland Stanford Junior University Compositions and methods for imaging pain and stress in vivo
EP2023919A4 (en) 2006-05-08 2010-12-22 Molecular Neuroimaging Llc Compounds and amyloid probes thereof for therapeutic and imaging uses
US10328164B2 (en) 2006-06-21 2019-06-25 Ge Healthcare Limited Radiopharmaceutical products
WO2008022979A1 (en) 2006-08-25 2008-02-28 Boehringer Ingelheim International Gmbh New pyridone derivatives with mch antagonistic activity and medicaments comprising these compounds
WO2009110894A1 (en) * 2008-03-05 2009-09-11 Rhino Technologies Llc Tensionable spiral bolt with resin nut and related method
GB0625523D0 (en) 2006-12-21 2007-01-31 Ge Healthcare Ltd In vivo imaging agents
EP2474525B1 (en) 2006-12-26 2020-04-15 Lantheus Medical Imaging, Inc. Ligands for imaging cardiac innervation
JP5504563B2 (en) 2006-12-27 2014-05-28 住友化学株式会社 Composition and light-emitting device using the composition
CA2683433C (en) 2007-04-05 2016-10-11 Siemens Medical Solutions Usa, Inc. Nitro-imidazole hypoxia imaging agents
GB0718386D0 (en) 2007-09-21 2007-10-31 Ge Healthcare As Improved radiopharmaceutical formulation
CN101157649A (en) * 2007-10-23 2008-04-09 江苏省原子医学研究所 18F-Fallypride automatically synthesizing method
KR101068835B1 (en) * 2007-10-26 2011-09-30 한국과학기술연구원 Isoindolones with high binding affinity to ?-amyloid aggregates and fibrils, and preparation method thereof
CL2008003785A1 (en) 2007-12-21 2009-10-09 Du Pont Pyridazine derived compounds; herbicidal compositions comprising said compounds; and method of controlling the growth of unwanted vegetation.
WO2009103478A1 (en) 2008-02-19 2009-08-27 Boehringer Ingelheim International Gmbh Pyridone and pyridazinone derivatives as mch antagonists
WO2010011367A2 (en) 2008-02-22 2010-01-28 Illinois Institute Of Technology Bimodal ligands with macrocyclic and acyclic binding moieties, complexes and compositions thereof, and methods of using
PT2257315T (en) * 2008-02-29 2020-01-27 Lantheus Medical Imaging Inc Contrast agents for applications including perfusion imaging
US8258134B2 (en) 2008-04-16 2012-09-04 Hoffmann-La Roche Inc. Pyridazinone glucokinase activators
WO2009146388A1 (en) 2008-05-28 2009-12-03 The Trustees Of Columbia University In The City Of New York Voxel-based methods for assessing subjects using positron emission tomography
KR20110121632A (en) * 2009-02-25 2011-11-07 포컬 테크놀러지스 코퍼레이션 Low-loss collimators for use in fiber optic rotary joints
EP2406233B1 (en) 2009-03-09 2013-11-13 Bristol-Myers Squibb Company Aza pyridone analogs useful as melanin concentrating hormone receptor-1 antagonists
PT2419096T (en) 2009-04-15 2020-02-19 Lantheus Medical Imaging Inc Stabilization of radiopharmaceutical compositions using ascorbic acid
CN101555232B (en) 2009-05-21 2011-01-05 北京师范大学 Pyridazinone compound marked by fluorine-18, preparation method and applications
KR20120051641A (en) 2009-07-11 2012-05-22 바이엘 파마 악티엔게젤샤프트 Non-polar and polar leaving groups
PT2534136T (en) 2010-02-08 2017-12-15 Lantheus Medical Imaging Inc Methods for synthesizing imaging agents, and intermediates thereof
CA2798488C (en) 2010-05-11 2019-06-04 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
DE102010036356A1 (en) * 2010-07-12 2012-01-12 Abx Advanced Biochemical Compounds Gmbh Apparatus for the synthesis of radioactively labeled compounds
JP5842594B2 (en) 2010-12-27 2016-01-13 住友化学株式会社 Pyridazinone compounds, herbicides containing them, and harmful arthropod control agents
CN102336741B (en) 2011-07-06 2013-04-10 北京师范大学 Fluorine-18-marked myocardial perfusion developing agent and preparation method and application thereof
CN104159890B (en) 2011-09-09 2018-04-10 蓝瑟斯医学影像公司 Composition, method and system for synthesizing and using developer
CA2852395C (en) 2011-10-21 2020-04-28 Lantheus Medical Imaging, Inc. Compositions comprising ascorbic acid and pyridaben and pyridaben analogs attached to an imaging moiety and related methods
AU2013203000B9 (en) 2012-08-10 2017-02-02 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
US20150246143A1 (en) 2012-08-13 2015-09-03 Lantheus Medical Imaging, Inc. System and method for quantitative mapping of mitochondrial complex 1
WO2014047446A1 (en) 2012-09-21 2014-03-27 The General Hospital Corporation System and method for single-scan rest-stress cardiac pet

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005079391A2 (en) 2004-02-13 2005-09-01 Bristol-Myers Squibb Pharma Company Contrast agents for myocardial perfusion imaging

Non-Patent Citations (16)

* Cited by examiner, † Cited by third party
Title
BBA, vol. 1364, 1998, pages 222 - 235
ELIEL, E.L.: "Stereochemistry of Carbon Compounds", 1962, MCGRAW-HILL
HIGUCHI T; NEKOLLA SG; HUISMAN MM; REDER S; POETHKO T; YU M ET AL.: "A new 18F-labeled myocardial PET tracer: myocardial uptake after permanent and transient coronary occlusion in rats", J NUCL MED, vol. 49, 2008, pages 1715 - 22
HUISMAN ET AL., J NUCL MED, vol. 49, 2008, pages 630 - 6
IEEE TMI, vol. 25, no. 7, 2006, pages 907 - 921
J. PHARMACEUTICAL SCIENCES, vol. 66, 1977, pages 1 - 19
JACQUES ET AL.: "Enantiomers, Racemates and Resolutions", 1981, WILEY INTERSCIENCE, NEW YORK
MISTRY M; ONTHANK D; GREEN J; CICIO S; CASEBIER D; ROBINSON S ET AL.: "Toxicological Evaluation of BMS-747158, a PET Myocardial Perfusion Imaging Agent", THE TOXICOLOGIST, vol. 102, 2008, pages 476
NEKOLLA SG: "Reder with microspheres in a pig model", CIRCULATION, vol. 119, 2009, pages 2333 - 42
Q. REV. BIOPHYS., vol. 25, 1992, pages 253 - 324
See also references of EP2534136A4
STABIN, M G; SPARKS, RB ET AL.: "OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine", J NUCL MED, vol. 46, no. 6, 2005, pages 1023 - 7
THOMAS SORRELL: "Organic Chemistry", 1999, UNIVERSITY SCIENCE BOOKS, SAUSALITO
WILEN, S.H. ET AL., TETRAHEDRON, vol. 33, 1977, pages 2725
WILEN, S.H.: "Tables of Resolving Agents and Optical Resolutions", 1972, UNIV. OF NOTRE DAME PRESS, pages: 268
YU M; GUARALDI MT; MISTRY M; KAGAN M; MCDONALD JL; DREW K ET AL.: "a novel PET myocardial perfusion imaging agent", J NUCL CARDIOL, vol. 14, 2007, pages 789 - 98

Cited By (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9161997B2 (en) 2001-08-16 2015-10-20 David S. Casebier Contrast agents for myocardial perfusion imaging
US10125106B2 (en) 2004-02-13 2018-11-13 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
US9718786B2 (en) 2004-02-13 2017-08-01 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
US8226929B2 (en) 2004-02-13 2012-07-24 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
US10889550B2 (en) 2004-02-13 2021-01-12 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
US8263042B2 (en) 2004-04-28 2012-09-11 Lantheus Medical Imaging, Inc. Contrast agents for myocardial perfusion imaging
US8491868B2 (en) 2006-12-26 2013-07-23 Lantheus Medical Imaging, Inc. Ligands for imaging cardiac innervation
US10010631B2 (en) 2006-12-26 2018-07-03 Lantheus Medical Imaging, Inc. Ligands for imaging cardiac innervation
US11241509B2 (en) 2006-12-26 2022-02-08 Lantheus Medical Imaging, Inc. Ligands for imaging cardiac innervation
US10245332B2 (en) 2008-02-29 2019-04-02 Lantheus Medical Imaging, Inc. Contrast agents for applications including perfusion imaging
US9408927B2 (en) 2008-02-29 2016-08-09 Lantheus Medical Imaging, Inc. Contrast agents for applications including perfusion imaging
US9687571B2 (en) 2009-04-15 2017-06-27 Lantheus Medical Imaging, Inc. Stabilization of radiopharmaceutical compositions using ascorbic acid
US10842892B2 (en) 2010-02-08 2020-11-24 Lantheus Medical Imaging, Inc. Methods and apparatus for synthesizing imaging agents, and intermediates thereof
US9603951B2 (en) 2010-02-08 2017-03-28 Lantheus Medical Imaging, Inc. Methods and apparatus for synthesizing imaging agents, and intermediates thereof
US10022462B2 (en) 2010-02-08 2018-07-17 Lantheus Medical Imaging, Inc. Methods and apparatus for synthesizing imaging agents, and intermediates thereof
US8936777B2 (en) 2010-02-08 2015-01-20 Lantheus Medical Imaging, Inc. Methods and apparatus for synthesizing imaging agents, and intermediates thereof
US11174223B2 (en) 2010-05-11 2021-11-16 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
US9388125B2 (en) 2010-05-11 2016-07-12 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
US9682927B2 (en) 2010-05-11 2017-06-20 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
CN108484449A (en) * 2011-09-09 2018-09-04 蓝瑟斯医学影像公司 Composition, method and system for synthesizing and using developer
EP2753605A4 (en) * 2011-09-09 2015-07-22 Lantheus Medical Imaging Inc Compositions, methods, and systems for the synthesis and use of imaging agents
TWI568714B (en) * 2011-09-09 2017-02-01 藍瑟斯醫學影像公司 Compositions, methods, and systems for the synthesis and use of imaging agents
KR101946089B1 (en) * 2011-09-09 2019-02-08 랜티우스 메디컬 이메징, 인크. Compositions, methods, and systems for the synthesis and use of imaging agents
WO2013036869A2 (en) 2011-09-09 2013-03-14 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
CN104159890A (en) * 2011-09-09 2014-11-19 蓝瑟斯医学影像公司 Compositions, methods, and systems for the synthesis and use of imaging agents
JP2014531434A (en) * 2011-09-09 2014-11-27 ランセウス メディカル イメージング， インコーポレイテッド Compositions, methods and systems for the synthesis and use of contrast agents
EP3567029A1 (en) 2011-09-09 2019-11-13 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
US9550000B2 (en) 2011-09-09 2017-01-24 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
WO2013070471A1 (en) 2011-11-11 2013-05-16 Lantheus Medical Imaging, Inc. Evaluation of presence of and vulnerability to atrial fibrillation and other indications using matrix metalloproteinase-based imaging
US11865195B2 (en) 2011-11-11 2024-01-09 Lantheus Medical Imaging, Inc. Evaluation of presence of and vulnerability to atrial fibrillation and other indications using matrix metalloproteinase-based imaging
WO2013173004A2 (en) 2012-04-10 2013-11-21 Lantheus Medical Imaging, Inc. Radiopharmaceutical synthesis methods
US10568978B2 (en) 2012-04-10 2020-02-25 Lantheus Medical Imaging, Inc. Radiopharmaceutical synthesis methods
WO2013173004A3 (en) * 2012-04-10 2014-03-13 Lantheus Medical Imaging, Inc. Radiopharmaceutical synthesis methods
US9789211B2 (en) 2012-05-14 2017-10-17 University Of Southern California Methods and compositions for positron emission tomography myocardial perfusion imaging
WO2013172979A1 (en) * 2012-05-14 2013-11-21 University Of Southern California Methods and compositions for positron emission tomography myocardial perfusion imaging
EP3653621A1 (en) 2012-08-10 2020-05-20 Lantheus Medical Imaging, Inc. Apparatus for synthesizing the imaging agent 4-chloro-2-(1,1-dimethylethyl)-5-[[4-[[2-(fluoro-[18f])ethoxy]methyl]phenyl]methoxy]-3(2h)-pyridazinone (fluorpiridaz [18f])
IL267696B (en) * 2012-08-10 2022-09-01 Lantheus Medical Imaging Inc Compositions, methods, and systems for the synthesis and use of imaging agents
AU2013203000B2 (en) * 2012-08-10 2016-12-15 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
WO2014026079A2 (en) 2012-08-10 2014-02-13 Lantheus Medical Imaging, Inc. Compositions, methods, and systems of the synthesis and use of imaging agents
US10500293B2 (en) 2012-08-10 2019-12-10 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
JP2018123134A (en) * 2012-08-10 2018-08-09 ランセウス メディカル イメージング， インコーポレイテッド Compositions, methods, and systems for the synthesis and use of imaging agents
US11744906B2 (en) 2012-08-10 2023-09-05 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
KR20150040348A (en) * 2012-08-10 2015-04-14 랜티우스 메디컬 이메징, 인크. Compositions, methods, and systems for the synthesis and use of imaging agents
JP2020169175A (en) * 2012-08-10 2020-10-15 ランセウス メディカル イメージング， インコーポレイテッド Compositions, methods and systems for synthesis and use of imaging agents
US9919064B2 (en) 2012-08-10 2018-03-20 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
US9713651B2 (en) 2012-08-10 2017-07-25 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
KR102223883B1 (en) * 2012-08-10 2021-03-08 랜티우스 메디컬 이메징, 인크. Compositions, methods, and systems for the synthesis and use of imaging agents
KR20210027519A (en) * 2012-08-10 2021-03-10 랜티우스 메디컬 이메징, 인크. Compositions, methods, and systems for the synthesis and use of imaging agents
AU2019204121B2 (en) * 2012-08-10 2021-03-11 Lantheus Medical Imaging, Inc. Compositions, methods, and systems for the synthesis and use of imaging agents
KR102357235B1 (en) * 2012-08-10 2022-02-08 랜티우스 메디컬 이메징, 인크. Compositions, methods, and systems for the synthesis and use of imaging agents
EP2882719A4 (en) * 2012-08-10 2016-10-05 Lantheus Medical Imaging Inc Compositions, methods, and systems for the synthesis and use of imaging agents
JP6991273B2 (en) 2012-08-10 2022-01-12 ランセウス メディカル イメージング， インコーポレイテッド Compositions, Methods and Systems for the Synthesis and Use of Contrast Agents
JP2015531760A (en) * 2012-08-10 2015-11-05 ランセウス メディカル イメージング， インコーポレイテッド Compositions, methods and systems for the synthesis and use of contrast agents
US11820790B2 (en) 2015-05-20 2023-11-21 Out And Out Chemistry S.P.R.L. Device and cassette for performing a plurality of synthesis processes of preparing a radiopharmaceutical in series
RU2721551C2 (en) * 2015-05-20 2020-05-20 Аут Энд Аут Кемистри С.П.Р.Л. Method for carrying out a plurality of synthesis processes for producing a radiopharmaceutical in series, a device and a cassette for realizing said method
US11565257B2 (en) 2018-03-29 2023-01-31 Ge Healthcare Limited Stabilized radiolabelling reaction
WO2019185932A1 (en) * 2018-03-29 2019-10-03 Ge Healthcare Limited Stabilised radiolabelling reaction
WO2019185933A1 (en) * 2018-03-29 2019-10-03 Ge Healthcare Limited Solid phase extraction
IL277638B2 (en) * 2018-03-29 2023-09-01 Ge Healthcare Ltd Solid phase extraction
IL277638B1 (en) * 2018-03-29 2023-05-01 Ge Healthcare Ltd Solid phase extraction
US11290885B2 (en) 2018-12-19 2022-03-29 Rohde & Schwarz Gmbh & Co. Kg Communication system and method
WO2021078814A1 (en) 2019-10-21 2021-04-29 Ge Healthcare Limited Use of cyclodextrins as a radiostabilizer
WO2022263592A1 (en) 2021-06-16 2022-12-22 Ge Healthcare Limited Preparation of a ph-adjusted ascorbic acid solution
WO2022263594A1 (en) 2021-06-16 2022-12-22 Ge Healthcare Limited Method for preparing an [18f] radiolabelled compound with low water content during labelling step
GB202108605D0 (en) 2021-06-16 2021-07-28 Ge Healthcare Uk Ltd Effect of water content
GB202108608D0 (en) 2021-06-16 2021-07-28 Ge Healthcare Ltd Preparation of a ph-adjusted ascorbic acid solution

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