WO2000057787A2 - Method for localization of blood clots - Google Patents
Method for localization of blood clots Download PDFInfo
- Publication number
- WO2000057787A2 WO2000057787A2 PCT/US2000/007891 US0007891W WO0057787A2 WO 2000057787 A2 WO2000057787 A2 WO 2000057787A2 US 0007891 W US0007891 W US 0007891W WO 0057787 A2 WO0057787 A2 WO 0057787A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- substituted
- independently
- thrombus
- independently selected
- Prior art date
Links
- 208000007536 Thrombosis Diseases 0.000 title claims abstract description 49
- 238000000034 method Methods 0.000 title claims abstract description 38
- 230000004807 localization Effects 0.000 title claims description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 32
- 239000011159 matrix material Substances 0.000 claims abstract description 25
- 230000000704 physical effect Effects 0.000 claims abstract description 7
- 239000003446 ligand Substances 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 229910052757 nitrogen Inorganic materials 0.000 claims description 24
- 229910052717 sulfur Inorganic materials 0.000 claims description 22
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 21
- 125000005842 heteroatom Chemical group 0.000 claims description 20
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 19
- 125000000623 heterocyclic group Chemical group 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- -1 phenoxy, benzyloxy Chemical group 0.000 claims description 15
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 238000002603 single-photon emission computed tomography Methods 0.000 claims description 13
- 150000001413 amino acids Chemical class 0.000 claims description 12
- 230000027455 binding Effects 0.000 claims description 12
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- 208000010378 Pulmonary Embolism Diseases 0.000 claims description 11
- 229910006069 SO3H Inorganic materials 0.000 claims description 11
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- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 8
- 125000006242 amine protecting group Chemical group 0.000 claims description 8
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical group NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 claims description 8
- 125000004981 cycloalkylmethyl group Chemical group 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 7
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- 238000003491 array Methods 0.000 claims description 7
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- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 6
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- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 5
- 239000002738 chelating agent Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 4
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- 125000003545 alkoxy group Chemical group 0.000 claims description 4
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
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- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 3
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 claims description 3
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- 229910007161 Si(CH3)3 Inorganic materials 0.000 claims description 2
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Classifications
-
- 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
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/088—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins conjugates with carriers being peptides, polyamino acids or proteins
-
- 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
- A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
- A61K51/082—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins the peptide being a RGD-containing peptide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B6/00—Apparatus or devices for radiation diagnosis; Apparatus or devices for radiation diagnosis combined with radiation therapy equipment
- A61B6/02—Arrangements for diagnosis sequentially in different planes; Stereoscopic radiation diagnosis
- A61B6/03—Computed tomography [CT]
- A61B6/037—Emission tomography
Definitions
- the present invention relates to a medical diagnostic method and, in particular, to an in vivo diagnostic method for detecting a blood clot, such as a pulmonary embolism or a thrombus, employing a radiopharmaceutical contrast agent and volume rendering of single photon emission computed tomography (SPECT) images.
- SPECT single photon emission computed tomography
- Pulmonary embolism is a condition of the lung that emerges when a portion of a blood clot (i.e., thrombus) growing pathologically within a patient breaks off (i.e., embolizes) and travels to the lung.
- a portion of a blood clot i.e., thrombus
- embolizes i.e., embolizes
- the condition itself is immediately life-threatening.
- a patient presenting with symptoms characteristic of pulmonary embolism must be properly diagnosed to assure that the symptoms do not represent other diseases. Accordingly, detection and localization of pulmonary embolism are critical to insure that the patient receives the appropriate care.
- the technique involves localizing a contrast agent at the tumor and obtaining a series of image slices of the tumor using single photon emission computed tomography (SPECT) .
- SPECT single photon emission computed tomography
- the image slices are then individually inspected by a physician. As a result, the process is time consuming and expensive.
- a volume rendering technique for displaying SPECT data derived from a complete set of image slices through the tumor.
- a three-dimensional matrix of data is assembled from the image slices.
- the three- dimensional matrix of data is then scanned along an array of parallel lines at a given angle with respect to the tumor. For each parallel line, the value of the most intense pixel along the parallel line is determined and assigned to a pixel in a two-dimensional array whose position corresponds to the position of the corresponding parallel line in the array of parallel lines.
- the process is repeated for a series of angles over 360° to produce a series of two-dimensional images.
- the present invention should provide a significant qualitative improvement in the ability of a naive physician to identify and localize a thrombus .
- the shortcomings associated with the known methods for localization of blood clots are overcome to a large degree by a method in accordance with the present invention.
- the method according to the present invention comprises the step of localizing a radiolabelled compound at a thrombus by administering a radiopharmaceutical compound to the patient.
- Two-dimensional images representing a physical property associated with the radiolabelled thrombus such as single photon emission computed tomography (SPECT) images, are then acquired and assembled into a three-dimensional matrix of data.
- the three-dimensional matrix of data is then scanned along an array of parallel lines to determine a maximum value along each line.
- SPECT single photon emission computed tomography
- the maximum value along each line is then assigned to a pixel in a two-dimensional array, where the relative position of the pixel in the two-dimensional array corresponds to the relative position of the line in the array of parallel lines.
- the three-dimensional matrix of data is optionally scanned along additional arrays of parallel lines to produce a series of images of the thrombus as viewed from different angles.
- the series of images can be displayed sequentially to produce a rotating view of the thrombus.
- Fig. 1 is a flow chart depicting the steps of a method for imaging a thrombus in accordance with the present invention.
- the present invention relates to a method for imaging a thrombus, the steps of which are depicted in Fig. 1.
- the patient is administered a radiolabelled compound that preferentially binds to the thrombus.
- the radiolabelled compound may be administered by injecting approximately 20 mCi (740 Mbq) of the radiolabelled compound into the venous circulation system of the patient.
- the radiolabelled compound comprises a radiopharmaceutical of the type described in U.S. Patent No. 5,744,120 issued April 28, 1998 to Edwards et al . , U.S. Patent No. 5,879,657 issued March 9, 1999 to DeGrado et al . , U.S.
- d 1 is preferably between about 1 and 20, x is independently 1-2; y is independently 1-2; and z is independently 0-4.
- Q is a glycoprotein Ilb/IIIA binding compound selected from the group including the cyclic lib/IIla receptor antagonist compounds described in co-pending U.S. Serial No.08/415,908,861 (equivalent to WO 94/22494); the RGD containing peptides described in U.S. Patent Nos. 4,578,079 and 4,792,525, the patent applications PCT US88/04403, PCT
- Patent Nos. 4,427,646 and 5,270,030 the hirudin-based peptides described in U.S. Patent No. 5,279,812; the fibrin binding proteins described in U.S. Patent No. 5,217,705; the guanine derivatives that bind to the Ilb/IIIa receptor described in U.S. Patent No. 5,086,069; the tyrosine derivatives described in European Patent Application No. 0478328A1, and Hartman et . al . , J. Med. Chem. , 1992, 35, 4640; or an oxidized low density lipoprotein (LDL) .
- Q is of the formula (II) :
- R 31 is a C 6 -Ci 4 saturated, partially saturated, or aromatic carbocyclic ring system substituted with 0-4 R 10 or R 10a ;
- Z is S or O
- n" and n' are independently 0-2; R 1 and R 22 are independently selected from the following groups :
- heterocyclic ring system containing 1-4 heteroatoms independently selected from N, S, and O, said heterocyclic ring being substituted with 0-2 R 12 ;
- R 1 and R 21 can alternatively join to form a 3-7 membered carbocyclic ring substituted with 0-2 R 12 ;
- R 1 or R 21 can alternatively be taken together with R 1 or R 21 on an adjacent carbon atom to form a direct bond, thereby to form a double or triple bond between said carbon atoms;
- R 22 and R 23 can alternatively join to form a 3-7 membered carbocyclic ring substituted with 0-2 R 12 ;
- R 22 or R 23 can alternatively be taken together with R 22 or R 23 on an adjacent carbon atom to form a direct bond, thereby to form a double or triple bond between the adj acent carbon atoms ;
- R 1 and R 2 where R 21 is H, can alternatively join to form a 5-8 membered carbocyclic ring substituted with 0-2 R 12 ;
- R 11 is selected from one or more of the following:
- heterocyclic ring system containing 1-4 heteroatoms independently selected from N, S, and 0, said heterocyclic ring being substituted with 0-2 R 12 ;
- R 12 is selected from one or more of the following:
- R 13 is selected independently from: H, C1-C10 alkyl,
- R 13a i s C1-C10 alkyl, C3-C10 cycloalkyl, C4-C12 alkylcycloalkyl, aryl, - (C1-C10 alkyl) aryl, or C3-C10 alkoxyalkyl ;
- R 13 groups when two R 13 groups are bonded to a single N, said R 13 groups may alternatively be taken together to form - ( CH 2 ) 2-5- or - (CH 2 ) O ( CH2) - ;
- R 14 is OH, H, C1-C4 alkyl, or benzyl
- R 21 and R 23 are independently selected from:
- C1-C4 alkyl optionally substituted with 1-6 halogen; benzyl ;
- R 2 is H or C ⁇ -C8 alkyl; R 10 and R 10a are selected independently from one or more of the following:
- R 3 is H or C1-C8 alkyl
- R 4 is H or C1-C3 alkyl
- R 5 is selected from: hydrogen; i-C ⁇ alkyl substituted with 0-2 R 11 ; 2-C8 alkenyl substituted with 0-2 R 11 ;
- aryl substituted with 0-2 R 12 a 5-10-membered heterocyclic ring system containing 1-4 heteroatoms independently selected from N, S, or 0, said heterocyclic ring being substituted with 0-2 R 12 ;
- R 16 is selected from: an amine protecting group; 1-2 amino acids;
- R 6 is H or Ci-C ⁇ alkyl
- R 7 is selected from:
- q is independently 0-2 and substitution on the cyclohexyl is at the 3 or 4 position;
- X is selected from:
- R 6 and R 7 can alternatively be taken together to form (CH 2 ) n X
- n 0 or 1 and X is -NH2 or
- M is a D-isomer or L-isomer amino acid of structure
- q'. is 0-2; R is H, C1-C3 alkyl;
- R 8 is selected from:
- R 34 and R 35 are independently selected from: -OH,
- R 34 and R 35 can alternatively be taken together form: a cyclic boron ester where said chain or ring contains from 2 to 20 carbon atoms and, optionally, 1-4 heteroatoms independently selected from N, S, or O;
- a divalent cyclic boron amide where said chain or ring contains from 2 to 20 carbon atoms and, optionally, 1-4 heteroatoms independently selected from N, S, or O;
- a cyclic boron amide-ester where said chain or ring contains from 2 to 20 carbon atoms and, optionally, 1-4 heteroatoms independently selected from N, S, or 0.
- Q is of the formula (III) :
- the shown phenyl ring may be further substituted with 0-3 RlO.
- R 10 is selected independently from: H, Ci-Cs alkyl, phenyl, halogen, or C1-C4 alkoxy;
- R 1 is H, C 1 -C4 alkyl, phenyl, benzyl, or phenyl- (Ci- C4) alkyl ;
- R 2 is H or methyl
- R 13 is selected independently from: H, C1-C10 alkyl, C 3 -C 10 cycloalkyl, C4-C 1 2 alkylcycloalkyl, aryl, - (C1-C10 alkyl) aryl, or C3-C10 alkoxyalkyl;
- R 13a is C1-C 1 0 alkyl, C3-C10 cycloalkyl, C4-C12 alkylcycloalkyl, aryl, - (C1-C10 alkyDaryl, or C3-C10 alkoxyalkyl ; when two R 13 groups are bonded to a single N, said R 13 groups may alternatively be taken together to form -(CH 2 ) 2-5- or -(CH 2 )0(CH 2 )-;
- R 14 is OH, H, C1-C4 alkyl, or benzyl
- R 3 is H or CH3
- R 4 is H or C1-C3 alkyl
- R 16 is selected from: an amine protecting group; 1-2 amino acids; or
- R 3 and R 5 can alternatively be taken together to form -CH2CH2CH2-;
- R 6 is H or C1-C8 alkyl
- R 7 is:
- M is a D-isomer or L-isomer amino acid of structure
- q' is 0-2;
- R 17 is H, C1-C3 alkyl;
- R 8 is selected from:
- C h . is a radionuclide metal chelator or bonding unit bound to the biologically active compound Q, either directly or through the optional linking group L n .
- R40 i independently selected at each occurrence from the group consisting of: a bond to Ln, C1-C10 alkyl substituted with 0-3 R 52 , aryl substituted with 0-3 R 52 , cycloaklyl substituted with 0-3 R 52 , heterocycle substituted with 0-3 R 52 ' heterocycloalkyl substituted with 0-3 R 52 , aralkyl substituted with 0-3 R 52 and alkaryl substituted with 0-3 R 52 ;
- R 41 is independently selected from the group consisting of: hydrogen, aryl substituted with 0-3 R 52 , C1-C10 alkyl substituted with 0-3 R 52 , and a heterocycle substituted with 0-3 R 52 ;
- R 53 , R 53a , and R 54 are each independently selected at each occurrence from the group consisting of: hydrogen, C1-C6 alkyl, and a bond to L n -
- at least one other atom of the group located on R 40 must also be bound to the radionuclide.
- the atoms bound to the metal are termed donor atoms .
- the optional linking group L n is given by the formula:
- M 1 is -[(CH2)gZ 1 ]g'-(CR 55 R 56 )g"-;
- M 2 is - (CR 55 R 56 )g»- [Z 1 (CH2)g3g'-;
- g is independently 0-10;
- g' is independently 0-1;
- g" is independently 0-10;
- f is independently 0-10;
- f is independently 0-10;
- f" is independently 0-1;
- Z 1 is independently selected at each occurrence from a C6-C14 saturated, partially saturated, or aromatic carbocyclic ring system, substituted with 0-4 R 57 ; and a heterocyclic ring system, substituted with 0-4 R 57 ;
- R 55 and R 56 are independently selected at each occurrence from the group consisting of: hydrogen; C1-C10 alkyl substituted with 0-5 R 57 ; and alkaryl wherein the aryl is substituted with 0-5 R 57 ;
- R 58 is independently selected at each occurrence from the group: hydrogen; C ⁇ -C6 alkyl; benzyl, and phenyl.
- radiolabelled it is meant that the compound contains a radioisotope which is suitable for administration to a mammalian patient.
- Suitable radioisotopes are known to those skilled in the art and include, for example, isotopes of halogens (such as chlorine, fluorine, bromine and iodine) , technetium and indium.
- Preferable radioisotopes include 123 I, 125 I, 131 I, 99m Tc, and 1: ⁇ l In, more preferably li:L In, 123 I and 99m Tc, and most preferably 99 Tc.
- Radiolabelled compounds of the invention may be prepared using standard radiolabelling procedures well known to those skilled in the art.
- the glycoprotein Ilb/IIIa binding compound, Q is radiolabelled indirectly (that is, by incorporating the radiolabel into the compound through the chelating agent C h , ) .
- Such radiolabelling should also be reasonably stable, both chemically and metabolically, applying recognized standards in the art.
- the radiolabelled compound may be labeled in a variety of fashions with a variety of different radioisotopes, as those skilled in the art will recognize, such radiolabelling should be carried out in a manner such that the high binding affinity and specificity of the unlabeled glycoprotein Ilb/IIIa binding compound to the glycoprotein Ilb/IIIa receptor is not significantly affected.
- M ⁇ is a transition metal radionuclide which is attached to the biologically active compound Q via the chelator C h .
- Preferred radiolabelled compounds of the invention are radiolabelled compounds wherein the radiolabel is located on the carbocyclic ring system of R 31 of formula (II) .
- Even more preferred radiolabelled compounds of the invention are those of formula (III) , wherein the radiolabel is located at position R 10 or R 10a substituted on the benzene ring.
- the coordination sphere of the radionuclide includes all the ligands or groups bound to the radionuclide.
- Mt transition metal radionuclide
- Mt to be stable it typically has a coordination number comprised of an integer greater than or equal to 5 and less than or equal to 7; that is there are 5 to 7 atoms bound to the metal and it is said to have a complete coordination sphere.
- the coordination sphere is completed by donor atoms from other ligands, termed ancillary or co-ligands, which can be either terminal or chelating.
- a large number of ligands can serve as ancillary or co-ligands, the choice of which is determined by a variety of considerations such as the ease of synthesis of the radiopharmaceutical, the chemical and physical properties of the ancillary ligand, the rate of formation, the yield, the number of isomeric forms of the resulting radiopharmaceuticals, the ability to administer said ancillary or co-ligand to a patient without adverse physiological consequences to said patient, and the compatibility of the ligand in a lyophilized kit formulation.
- the charge and lipophilicity of the ancillary ligand will effect the charge and lipophilicity of the radiopharmaceuticals.
- the radiopharmaceuticals prepared from the reagents of the present invention can be comprised of one or two ancillary or co-ligands, designated A I, in a binary ligand system.
- the one or two ancillary or co-ligands, ALI, comprising the radiopharmaceuticals can be independently selected from the group consisting of: dioxygen ligands, functionalized aminocarboxylates and halides; provided that the coordination sphere of the radionuclide is complete.
- Ancillary dioxygen ligands include ligands that coordinate to the metal ion through at least two oxygen donor atoms. Examples include but are not limited to: glucoheptonate, gluconate, 2-hydroxyisobutyrate, lactate, tartrate, mannitol, glucarate, altol, Kojic acid, 2, 2-bis (hydroxymethyl)propionic acid, 4, 5-dihydroxy-l, 3 -benzene disulfonate, or substituted or unsubstituted 1,2 or 3,4 hydroxypyridinones, or pharmaceutically acceptable salts thereof .
- Functionalized aminocarboxylates include ligands that have a combination of nitrogen and oxygen donor atoms. Examples include but are not limited to: iminodiacetic acid, 2,3 diaminopropionic acid, nitrilotriacetic acid, N,N' -ethylenediamine diacetic acid, N,N,N' -ethylenediamine triacetic acid, hydroxyethylethylenediamine triacetic acid, N,N" -ethylenediamine bis-hydroxyphenylglycine, or the ligands described in Eur. Pat. Appl. No. 93302712.0, or pharmaceutically acceptable salts thereof.
- Halides which are suitable for use as the ancillary ligand A L1 can be chloride, bromide, fluoride, iodide, or pharmaceutically acceptable salts thereof.
- radiopharmaceuticals prepared from the reagents of the present invention comprised of two different types of ancillary or co-ligands, one or two ligands designated the first ancillary or co-ligand or ligands, ALI, and independently selected from the group: dioxygen ligands, functionalized aminocarboxylates and halides; and one to four ligands designated the second ancillary or co-ligand or ligands, A 2, selected from the group: trisubstituted phosphines, trisubstituted arsines, tetrasubstit ted diphosphines and tetrasubstituted diarsines, in a ternary ligand system.
- Radiopharmaceuticals comprised of one or more ancillary or co-ligands AL2 ⁇ e more stable compared to said radiopharmaceuticals that are not comprised of one or more ancillary ligands, AL2,' that is, they have a minimal number of isomeric forms, the relative ratios of which do not change significantly with time, and remain substantially intact upon dilution.
- the radiopharmaceutical compr ses a compoun o t e ormu a IV the radiopharmaceutical compr ses a compoun o t e ormu a IV :
- the radiopharmaceutical comprises a compound of the formula (V) :
- a series of image slices of the thrombus are acquired at step 12 of Fig. 1.
- the image slices reflect the concentration of radioactivity within the thrombus.
- Each image slice is composed of a two-dimensional array of pixels, wherein each pixel comprises an intensity value representative of the concentration of radioactivity at the particular position within the thrombus which corresponds to the pixel .
- the image slices are obtained using a gamma camera to record single photon emission computed tomography (SPECT) images .
- SPECT single photon emission computed tomography
- data should be acquired using parameters that enhance the sensitivity of the technique for small lesions.
- the parameters should include a 3 mm or smaller digital sampling (i.e., pixel size), and a minimum of 90 views over a 360 degree rotation or 45 views over a 180 degree rotation.
- very high-resolution collimators and multiple heads should be used to increase the resolution and sensitivity, respectively.
- the acquired data should be reconstructed using a spatial filter with a relatively high frequency cutoff (i.e., approximately 3.00 or higher) to minimize resolution loss due to smoothing.
- a minimum of thirty angles ensures a visually smooth effect when the views are intended to be displayed sequentially to produce a rotating view of the thrombus, as described below.
- the image slices are reconstructed and assembled into a three-dimensional matrix of data.
- the three-dimensional matrix of data is assembled by stacking the individual image slices in sequential order.
- the three-dimensional matrix of data is organized as a series of transaxial image slices.
- the matrix of data is scanned along an array of parallel lines (usually perpendicular to the vertical axis of the body), at step 16, to determine the maximum intensity value along each of the parallel lines.
- the maximum intensity value along a parallel line is equivalent to the most intense pixel within the matrix of data encountered along that parallel line.
- the most intense pixel is defined as the pixel corresponding to the position within the lesion where the radioactivity is most intense.
- the maximum value along each parallel line is assigned to a pixel in a two-dimensional image array.
- the relative position of the pixel in the two-dimensional image array corresponds to the relative position of the line in the array of parallel lines.
- the resulting two-dimensional image array therefore represents an image of the most intense pixels as viewed by an observer viewing the thrombus along the array of parallel lines.
- the three-dimensional matrix of data can be scanned along additional arrays of parallel lines in order to produce image arrays of the thrombus from different angles.
- the lesion is scanned along a minimum of 90 views over a series of angles over 360° or a minimum of 45 views over a series of angles over 180°.
- results are displayed at step 22.
- the results can be displayed as individual views of the thrombus by displaying one or more of the individual two-dimensional image arrays.
- the individual two-dimensional image arrays can be displayed sequentially by angle to produce a rotating view of the most intense pixels.
- the present invention is not intended to be so limited. Instead, the present invention is intended to relate to any medical condition capable of diagnosis using a clot-binding radiopharmaceutical contrast agent and SPECT. For example, it is recognized that the present invention is equally applicable to localization of thrombii in general and arterial coronary thrombii in particular.
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Abstract
Description
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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IL14513000A IL145130A0 (en) | 1999-03-26 | 2000-03-24 | Method for localization of blood clots |
CA002364753A CA2364753A1 (en) | 1999-03-26 | 2000-03-24 | Method for localization of blood clots |
AU40278/00A AU4027800A (en) | 1999-03-26 | 2000-03-24 | Method for localization of blood clots |
BR0010517-1A BR0010517A (en) | 1999-03-26 | 2000-03-24 | Imaging methods of a thrombus, pulmonary embolus, arterial thrombus and coronary thrombus |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US12635999P | 1999-03-26 | 1999-03-26 | |
US60/126,359 | 1999-03-26 |
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WO2000057787A2 true WO2000057787A2 (en) | 2000-10-05 |
WO2000057787A3 WO2000057787A3 (en) | 2001-02-22 |
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PCT/US2000/007891 WO2000057787A2 (en) | 1999-03-26 | 2000-03-24 | Method for localization of blood clots |
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AU (1) | AU4027800A (en) |
BR (1) | BR0010517A (en) |
CA (1) | CA2364753A1 (en) |
IL (1) | IL145130A0 (en) |
WO (1) | WO2000057787A2 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994022494A1 (en) * | 1993-03-30 | 1994-10-13 | The Du Pont Merck Pharmaceutical Company | RADIOLABELED PLATELET GPIIb/IIIa RECEPTOR ANTAGONISTS AS IMAGING AGENTS FOR THE DIAGNOSIS OF THROMBOEMBOLIC DISORDERS |
WO1996031243A1 (en) * | 1995-04-03 | 1996-10-10 | The Du Pont Merck Pharmaceutical Company | Ternary radiopharmaceutical complexes |
WO1996040637A1 (en) * | 1995-06-07 | 1996-12-19 | The Du Pont Merck Pharmaceutical Company | Stable reagents for the preparation of radiopharmaceuticals |
-
2000
- 2000-03-24 AU AU40278/00A patent/AU4027800A/en not_active Abandoned
- 2000-03-24 IL IL14513000A patent/IL145130A0/en unknown
- 2000-03-24 BR BR0010517-1A patent/BR0010517A/en not_active Application Discontinuation
- 2000-03-24 WO PCT/US2000/007891 patent/WO2000057787A2/en active Application Filing
- 2000-03-24 CA CA002364753A patent/CA2364753A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994022494A1 (en) * | 1993-03-30 | 1994-10-13 | The Du Pont Merck Pharmaceutical Company | RADIOLABELED PLATELET GPIIb/IIIa RECEPTOR ANTAGONISTS AS IMAGING AGENTS FOR THE DIAGNOSIS OF THROMBOEMBOLIC DISORDERS |
WO1996031243A1 (en) * | 1995-04-03 | 1996-10-10 | The Du Pont Merck Pharmaceutical Company | Ternary radiopharmaceutical complexes |
WO1996040637A1 (en) * | 1995-06-07 | 1996-12-19 | The Du Pont Merck Pharmaceutical Company | Stable reagents for the preparation of radiopharmaceuticals |
Non-Patent Citations (6)
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BR0010517A (en) | 2002-01-08 |
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IL145130A0 (en) | 2002-06-30 |
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