US20220111052A1 - Eluent solution - Google Patents
Eluent solution Download PDFInfo
- Publication number
- US20220111052A1 US20220111052A1 US17/557,755 US202117557755A US2022111052A1 US 20220111052 A1 US20220111052 A1 US 20220111052A1 US 202117557755 A US202117557755 A US 202117557755A US 2022111052 A1 US2022111052 A1 US 2022111052A1
- Authority
- US
- United States
- Prior art keywords
- composition
- radiotracer
- facbc
- citrate buffer
- concentration
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000003480 eluent Substances 0.000 title description 2
- 238000000034 method Methods 0.000 claims abstract description 40
- 238000006243 chemical reaction Methods 0.000 claims abstract description 34
- KRHYYFGTRYWZRS-BJUDXGSMSA-M fluorine-18(1-) Chemical compound [18F-] KRHYYFGTRYWZRS-BJUDXGSMSA-M 0.000 claims abstract description 21
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 19
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 18
- 239000000203 mixture Substances 0.000 claims description 61
- 229940027541 fluciclovine f-18 Drugs 0.000 claims description 42
- 239000000700 radioactive tracer Substances 0.000 claims description 37
- 239000011541 reaction mixture Substances 0.000 claims description 23
- 239000007979 citrate buffer Substances 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 18
- 238000002414 normal-phase solid-phase extraction Methods 0.000 claims description 17
- 229910052782 aluminium Inorganic materials 0.000 claims description 16
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 14
- 230000002285 radioactive effect Effects 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 11
- 239000002243 precursor Substances 0.000 claims description 10
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 8
- 125000006242 amine protecting group Chemical group 0.000 claims description 6
- YGECRYNXJYBQCL-UHFFFAOYSA-N 1-amino-3-chlorocyclobutane-1-carboxylic acid Chemical compound OC(=O)C1(N)CC(Cl)C1 YGECRYNXJYBQCL-UHFFFAOYSA-N 0.000 claims description 3
- OEQBVNDAVKXWBS-UHFFFAOYSA-N 1-amino-3-hydroxycyclobutane-1-carboxylic acid Chemical compound OC(=O)C1(N)CC(O)C1 OEQBVNDAVKXWBS-UHFFFAOYSA-N 0.000 claims description 3
- UNYNVICDCJHOPO-UHFFFAOYSA-N quabalactone III Natural products CC1OC(=O)C(O)=C1C UNYNVICDCJHOPO-UHFFFAOYSA-N 0.000 claims description 3
- 150000005846 sugar alcohols Chemical class 0.000 claims description 3
- 238000002600 positron emission tomography Methods 0.000 abstract description 18
- 238000002360 preparation method Methods 0.000 abstract description 5
- 239000008364 bulk solution Substances 0.000 abstract 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 38
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 23
- 229940126534 drug product Drugs 0.000 description 16
- 239000000825 pharmaceutical preparation Substances 0.000 description 16
- 239000007790 solid phase Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- -1 aluminum ions Chemical class 0.000 description 14
- 239000012535 impurity Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 239000012351 deprotecting agent Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000000746 purification Methods 0.000 description 9
- 125000001424 substituent group Chemical group 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 150000001412 amines Chemical group 0.000 description 7
- 239000000523 sample Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- NTEDWGYJNHZKQW-DGMDOPGDSA-N fluciclovine ((18)F) Chemical compound OC(=O)[C@]1(N)C[C@H]([18F])C1 NTEDWGYJNHZKQW-DGMDOPGDSA-N 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 238000004809 thin layer chromatography Methods 0.000 description 6
- NTEDWGYJNHZKQW-KWCOIAHCSA-N 1-amino-3-fluoranylcyclobutane-1-carboxylic acid Chemical group OC(=O)C1(N)CC([18F])C1 NTEDWGYJNHZKQW-KWCOIAHCSA-N 0.000 description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 125000006239 protecting group Chemical group 0.000 description 5
- 238000010926 purge Methods 0.000 description 5
- 238000003608 radiolysis reaction Methods 0.000 description 5
- 239000012217 radiopharmaceutical Substances 0.000 description 5
- 229940121896 radiopharmaceutical Drugs 0.000 description 5
- 230000002799 radiopharmaceutical effect Effects 0.000 description 5
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 5
- 239000012491 analyte Substances 0.000 description 4
- 238000010511 deprotection reaction Methods 0.000 description 4
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical group OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000002372 labelling Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000008194 pharmaceutical composition Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- 239000004713 Cyclic olefin copolymer Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 3
- STMJKHJZKJVYOE-WRXNHJIOSA-N [H][C@]1(C)C[C@](NC)(C(=O)OC)C1 Chemical compound [H][C@]1(C)C[C@](NC)(C(=O)OC)C1 STMJKHJZKJVYOE-WRXNHJIOSA-N 0.000 description 3
- BNIZQKROTKQKEM-CCVSRJTISA-N [H][C@]1([18F])C[C@@](NC)(C(=O)OC)C1 Chemical compound [H][C@]1([18F])C[C@@](NC)(C(=O)OC)C1 BNIZQKROTKQKEM-CCVSRJTISA-N 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229940098779 methanesulfonic acid Drugs 0.000 description 3
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000001509 sodium citrate Substances 0.000 description 3
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 3
- 229940038773 trisodium citrate Drugs 0.000 description 3
- NLMDJJTUQPXZFG-UHFFFAOYSA-N 1,4,10,13-tetraoxa-7,16-diazacyclooctadecane Chemical compound C1COCCOCCNCCOCCOCCN1 NLMDJJTUQPXZFG-UHFFFAOYSA-N 0.000 description 2
- HWTDMFJYBAURQR-UHFFFAOYSA-N 80-82-0 Chemical compound OS(=O)(=O)C1=CC=CC=C1[N+]([O-])=O HWTDMFJYBAURQR-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 238000012879 PET imaging Methods 0.000 description 2
- 239000004696 Poly ether ether ketone Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- JLXUJKGUYLVUMR-MGTUHJRNSA-N [H][C@]1([18F])C[C@@](NC)(C(=O)O)C1 Chemical compound [H][C@]1([18F])C[C@@](NC)(C(=O)O)C1 JLXUJKGUYLVUMR-MGTUHJRNSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- QYHYQHPUNPVNDV-UHFFFAOYSA-N aluminane Chemical compound C1CC[AlH]CC1 QYHYQHPUNPVNDV-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
- 229940092714 benzenesulfonic acid Drugs 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 125000003636 chemical group Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000007810 chemical reaction solvent Substances 0.000 description 2
- 238000012864 cross contamination Methods 0.000 description 2
- 239000002739 cryptand Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000003682 fluorination reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000011194 good manufacturing practice Methods 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 150000003949 imides Chemical group 0.000 description 2
- 238000002354 inductively-coupled plasma atomic emission spectroscopy Methods 0.000 description 2
- 238000001990 intravenous administration Methods 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- AFDMODCXODAXLC-UHFFFAOYSA-N phenylmethanimine Chemical compound N=CC1=CC=CC=C1 AFDMODCXODAXLC-UHFFFAOYSA-N 0.000 description 2
- 229920002530 polyetherether ketone Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 150000005621 tetraalkylammonium salts Chemical class 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000010977 unit operation Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- XLYOFNOQVPJJNP-NJFSPNSNSA-N ((18)O)water Chemical compound [18OH2] XLYOFNOQVPJJNP-NJFSPNSNSA-N 0.000 description 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- NTEDWGYJNHZKQW-UHFFFAOYSA-N 1-amino-3-fluorocyclobutane-1-carboxylic acid Chemical compound OC(=O)C1(N)CC(F)C1 NTEDWGYJNHZKQW-UHFFFAOYSA-N 0.000 description 1
- AUFVJZSDSXXFOI-UHFFFAOYSA-N 2.2.2-cryptand Chemical compound C1COCCOCCN2CCOCCOCCN1CCOCCOCC2 AUFVJZSDSXXFOI-UHFFFAOYSA-N 0.000 description 1
- 108050005273 Amino acid transporters Proteins 0.000 description 1
- 102000034263 Amino acid transporters Human genes 0.000 description 1
- 125000006847 BOC protecting group Chemical group 0.000 description 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical group NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- CCLJEDIDFUMTIF-BEVCDTGJSA-N CCOC(=O)C1(NC(=O)OC(C)(C)C)CC(C)C1.CCOC(=O)C1(NC(=O)OC(C)(C)C)CC([18F])C1.I.II Chemical compound CCOC(=O)C1(NC(=O)OC(C)(C)C)CC(C)C1.CCOC(=O)C1(NC(=O)OC(C)(C)C)CC([18F])C1.I.II CCLJEDIDFUMTIF-BEVCDTGJSA-N 0.000 description 1
- CGRIQSIRTILKAD-OPIGLTTDSA-N CCOC(=O)C1(NC(=O)OC(C)(C)C)CC([18F])C1.II.I[IH]I.NC1(C(=O)O)CC([18F])C1 Chemical compound CCOC(=O)C1(NC(=O)OC(C)(C)C)CC([18F])C1.II.I[IH]I.NC1(C(=O)O)CC([18F])C1 CGRIQSIRTILKAD-OPIGLTTDSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical group [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 206010060862 Prostate cancer Diseases 0.000 description 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 1
- 208000008385 Urogenital Neoplasms Diseases 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-IGMARMGPSA-N [16OH2] Chemical compound [16OH2] XLYOFNOQVPJJNP-IGMARMGPSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical group 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 238000005102 attenuated total reflection Methods 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical group NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000008499 blood brain barrier function Effects 0.000 description 1
- 210000001218 blood-brain barrier Anatomy 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000007257 deesterification reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000012537 formulation buffer Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 239000010857 liquid radioactive waste Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- BCVXHSPFUWZLGQ-UHFFFAOYSA-N mecn acetonitrile Chemical compound CC#N.CC#N BCVXHSPFUWZLGQ-UHFFFAOYSA-N 0.000 description 1
- COTNUBDHGSIOTA-UHFFFAOYSA-N meoh methanol Chemical compound OC.OC COTNUBDHGSIOTA-UHFFFAOYSA-N 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 238000000163 radioactive labelling Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000006833 reintegration Effects 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- 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
- A61K51/0404—Lipids, e.g. triglycerides; Polycationic carriers
- A61K51/0406—Amines, polyamines, e.g. spermine, spermidine, amino acids, (bis)guanidines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B59/00—Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
- C07B59/001—Acyclic or carbocyclic compounds
Definitions
- the present invention relates to a drug product composition and in particular to a composition comprising a positron emission tomography (PET) tracer.
- PET positron emission tomography
- the non-natural amino acid 18 F-1-amino-3-fluorocyclobutane-1-carboxylic acid 18 F-FACBC also known as 18 F-Fluciclovine is taken up specifically by amino acid transporters and shows promise for positron emission tomography (PET) imaging of prostate cancer (Nanni et al 2014 Clinical Genitourinary Cancer; 12(2): 106-110).
- PET positron emission tomography
- Production of 18 F-FACBC comprises labelling of a triflate precursor compound with 18 F-fluoride:
- a combination of solid phases is used: ion retardation to remove excess Na + and excess Cl ⁇ left over from the deprotection steps, alumina to remove 18 F-fluoride and a reversed phase to remove FACBC-related impurities such as 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid (hydroxyl-ACBC) and 1-amino-3-chloro-cyclo butane-1-carboxylic acid (chloro-ACBC).
- hydroxyl-ACBC 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid
- chloro-ACBC 1-amino-3-chloro-cyclo butane-1-carboxylic acid
- the synthesis is currently typically carried out by means of an automated radiosynthesis procedure employing a so-called “cassette” or “cartridge” designed to fit removably and interchangeably onto an automated synthesis apparatus such as those that are commercially available from GE Healthcare, CTI Inc, Ion Beam Applications S.A. (Chemin du Cyclotron 3, B-1348 Louvain-La-Neuve, Belgium); Raytest (Germany) and Bioscan (USA).
- the cassette comprises all the reagents, reaction vessels and apparatus necessary to carry out the preparation of 18 F-FACBC following introduction of suitably prepared 18 F-fluoride by methods well-known in the field of PET tracer production.
- a known cassette for the synthesis of 18 F-FACBC is a FASTlabTM cassette from GE Healthcare is shown in FIG. 1 .
- the present inventors have found that the quality of the final 18 F-FACBC drug product obtained using the above-described known FASTlabTM cassette and process can be somewhat variable. Residual acetonitrile levels have been found to range from about 100 ⁇ g/ml to about 600 ⁇ g/ml. While acceptable in terms of permitted daily exposure and in the context of the acceptance criteria for 18 F-FACBC drug product, the amount and observed variability is less than ideal.
- the present inventors have also found that residual aluminum have been found to range from about 7 ⁇ g/ml to nearly 20 ⁇ g/ml, which would mean a potential amount of 100 ⁇ g in a 5 ml 18 F-FACBC.
- the 18 F-FACBC drug product also comprises citrate buffer, complexes of aluminum and citrate are likely to be present, which is problematic as it is known that such complexes cross the blood-brain barrier (Rengel 2004 Biometals; 17: 669-689).
- the present invention provides a drug product composition comprising 18 F-FACBC that overcomes the problems seen with known such compositions.
- the composition of the present invention has an improved impurity profile, making it safer and more effective for imaging as compared with the prior art.
- Low and predictable levels of acetonitrile and/or aluminum in the final drug product mean that the composition of the invention more easily meets worldwide pharmacopeia requirements.
- removal of the alumina cartridge has the allied advantages that a shorter and simplified process is permitted and that no particles arising from this cartridge are present, which the present inventors have noted can block the sterile filter used prior to injection of the drug product.
- the advantages of the present invention are achieved with only minor changes to the known process and without impairing the desirable qualities of known 18 F-FACBC compositions.
- FIG. 1 shows a FASTlabTM cassette of prior art.
- FIG. 2 shows a cassette for producing a radiotracer according to an embodiment of the invention.
- the present invention relates to a positron emission tomography (PET) tracer composition
- PET positron emission tomography
- 18 F-FACBC anti-1-amino-3- 18 F-fluorocyclobutyl-1-carboxylic acid
- said composition comprises no more than 5.0 ⁇ g/mL dissolved aluminum (Al).
- the present invention relates to a PET tracer composition
- a PET tracer composition comprising (18F-FACBC) which comprises 50-100 mM citrate buffer and has a pH of 4.0-5.0.
- the composition has 60-90 mM citrate buffer, most preferably 75-85 mM citrate buffer.
- the composition has a pH of 4.0 or more, and more preferably 4.3-4.4.
- the present invention relates to a positron emission tomography (PET) tracer composition
- PET positron emission tomography
- 18 F-FACBC anti-1-amino-3- 18 F-fluorocyclobutyl-1-carboxylic acid
- said composition comprises no more than 5.0 ⁇ g/mL dissolved aluminum (Al) and no more than 50 ⁇ g/mL acetonitrile (MeCN).
- PET tracer composition refers to a composition comprising a PET tracer together with a biocompatible carrier in a form suitable for mammalian administration.
- the PET tracer composition of the invention is referred to hereunder also as the composition of the invention.
- a “PET tracer” is defined herein as a biologically active molecule comprising an atom which is a positron emitter suitable for intravenous administration to a mammalian subject followed by PET imaging to obtain one or more clinically-useful images of the location and/or distribution of the PET tracer.
- a “biocompatible carrier” as defined herein is a fluid, especially a liquid, in which a pharmaceutical is suspended or dissolved, such that the composition is physiologically tolerable, i.e. can be administered to the mammalian body without toxicity or undue discomfort.
- the biocompatible carrier is suitably an injectable carrier liquid such as sterile, pyrogen-free water for injection or an aqueous solution such as saline.
- the compound “ 18 F-FACBC” is represented by the following chemical structure:
- not more than should be understood to mean any amount less than and including the quoted quantity.
- zero ⁇ g/mL of an impurity is unlikely and at least a trace amount of each impurity remains in the composition.
- the term “not more than” acknowledges that a trace amount of one or more impurities is present in a PET tracer composition, and defines a concentration limit above which the composition would not be deemed acceptable for use.
- the composition of the invention comprises not more than not more than 3.0 ⁇ g/mL dissolved Al, and in another embodiment not more than 1.5 ⁇ g/mL dissolved Al.
- composition of the present invention comprises MeCN at a concentration not more than 20 ⁇ g/mL.
- the composition of the invention in one embodiment has an end of synthesis (EOS) radiochemical purity (RCP) of at least 95%, in another embodiment at least 98%, and in yet another embodiment at least 99%.
- the composition preferably also has a radioactive concentration (RAC) of at least 1000 MBq/mL, alternatively at least 1500 MBq/ml.
- end of synthesis refers to the point in time when the labelled compound is collected in the product collection vial.
- the pharmaceutical composition of the present invention has a favorable impurity profile, with the main non-radioactive impurities being 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid (hydroxyl-ACBC), 1-amino-3-fluoro-cyclobutane-1-carboxylic acid (FACBC) and 1-amino-3-chloro-cyclobutane-1-carboxylic acid (chloro-ACBC).
- hydroxyl-ACBC 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid
- FACBC 1-amino-3-fluoro-cyclobutane-1-carboxylic acid
- chloro-ACBC 1-amino-3-chloro-cyclobutane-1-carboxylic acid
- hydroxyl-ACBC there is not more than 150 ⁇ g/mL hydroxyl-ACBC, most preferably not more than 80 ⁇ g/mL hydroxyl-ACBC.
- FACBC there is not more than 0.15 ⁇ g/mL FACBC, most preferably not more than 0.10 ⁇ g/mL FACBC.
- chloro-ACBC there is not more than 2.0 ⁇ g/mL chloro-ACBC, most preferably not more than 1.0 ⁇ g/mL chloro-ACBC.
- aluminum breakthrough refers to aluminum ions present in the product resulting from partial breakdown of the alumina column.
- concentration of aluminum in the end-product higher than that found when an alumina column is not used.
- not more than should be understood to mean any amount less than the quoted quantity. Therefore, not more than 100 ⁇ g/mL means any amount between 0-100 ⁇ g/mL, and in an ideal embodiment of the composition of the present invention there would be zero ⁇ g/mL of each impurity present in the composition of the invention. However, in reality, zero ⁇ g/mL of an impurity might not be achievable and it is more likely that at least a trace amount of the impurity remains in the composition, i.e. in the case of hydroxyl-ACBC the term not more than 150 ⁇ g/mL covers e.g. 50-150 ⁇ g/mL, not more than 0.10 ⁇ g/mL for FACBC covers e.g. 0.05-0.10 ⁇ g/mL, and not more than 1.0 ⁇ g/mL chloro-ACBC covers e.g. 0.25-1.0 ⁇ g/mL.
- composition of the present invention is that the pH, stability and impurity profile can be kept within a very narrow range over a long shelf-life, at high activities, and when manipulated e.g. by autoclaving or by dilution with 0.9% saline.
- the pharmaceutical composition of the invention does not comprise a radiostabilizer. It is common for pharmaceutical compositions comprising radioactive pharmaceuticals to include a radiostabilizer.
- known pharmaceutical compositions of [ 18 F]FACBC include a sugar alcohol or a sugar lactone.
- EP 2080526 discloses that radiolysis can be inhibited by adding a sugar lactone such as ascorbic acid and glucono-o-lactone to [ 18 F]FACBC
- BP 2119458 discloses that a sugar alcohol such as erythritol xylitol, sorbitol or mannitol can be added as an additive to inhibit radiolysis and improve stability. No such radiostabilizer is required in the radiopharmaceutical composition of the present invention in order to maintain a shelf-life of up to around 10 hours.
- EP 2119458 (Al) teaches that a more stable formulation of 18 F-FACBC is achieved when the pH is maintained within the range 2.0-5.9.
- use of citrate buffer allows the pH to be maintained within an even narrower range, provides resistance to degradation and enables the formulation to be autoclaved.
- the composition of the present invention therefore comprises around 50-100 mM citrate buffer, in another embodiment around 60-90 mM citrate buffer and in yet another embodiment around 75-85 mM citrate buffer.
- the term “around” in this context incorporates the exact values of the ranges as well as a small variation around these values that would be expected by the skilled person to achieve the same stabilization effect.
- the present invention provides a method to prepare a PET tracer composition of the invention wherein said method comprises:
- the present invention provides a method to prepare a PET tracer composition of the invention wherein said method comprises:
- the “source of 18 F-fluoride” suitable for use in step (a) of the method of the invention is normally obtained as an aqueous solution from the nuclear reaction 18 O(p,n) 18 F.
- water is typically removed from 18F-fluoride prior to the reaction, and fluorination reactions are carried out using anhydrous reaction solvents (Aigbirhio et al 1995 J Fluor Chem; 70: 279-87).
- a further step that is used to improve the reactivity of 18 F-fluoride for radiofluorination reactions is to add a cationic counterion prior to the removal of water.
- the counterion should possess sufficient solubility within the anhydrous reaction solvent to maintain the solubility of the 18 F-fluoride. Therefore, counterions that are typically used include large but soft metal ions such as rubidium or cesium, potassium complexed with a cryptand such as KryptofixTM, or tetraalkylammonium salts, wherein potassium complexed with a cryptand such as KryptofixTM, or tetraalkylammonium salts are preferred.
- the “precursor compound” for step (a) of the method of the invention comprises a non-radioactive derivative of a radiolabeled compound, designed so that chemical reaction with a convenient chemical form of the detectable label occurs site-specifically, can be conducted in the minimum number of steps (ideally a single step), and without the need for significant purification (ideally no further purification), to give the desired radiolabeled compound.
- Such precursor compounds are synthetic and can conveniently be obtained in good chemical purity.
- a suitable “leaving group” in the context of the compound of Formula I in step (a) of the method of the present invention is a chemical group that can be displaced by nucleophilic displacement reaction with fluoride ion. These are well-known in the art of synthetic chemistry.
- the leaving group of the present invention is a linear or branched C 1-10 haloalkyl sulfonic acid substituent, a linear or branched C 1-10 alkyl sulfonic acid substituent, a fluorosulfonic acid substituent, or an aromatic sulfonic acid substituent.
- the leaving group is selected from methanesulfonic acid, toluenesulfonic acid, nitrobenzenesulfonic acid, benzenesulfonic acid, trifluoromethanesulfonic acid, fluorosulfonic acid, and perfluoroalkylsulfonic acid.
- the leaving group is either methanesulfonic acid, trifluoromethanesulfonic acid or toluenesulfonic acid and in another embodiment the leaving group is trifluoromethanesulfonic acid.
- protecting group refers to a group which inhibits or suppresses undesirable chemical reactions, but which is designed to be sufficiently reactive that it may be cleaved from the functional group in question to obtain the desired product under mild enough conditions that do not modify the rest of the molecule.
- Protecting groups are well known to those skilled in the art and are described in ‘Protective Groups in Organic Synthesis’, Theorodora W. Greene and Peter G. M. Wuts, (Fourth Edition, John Wiley & Sons, 2007).
- the PG1 “carboxy protecting group” herein is preferably linear or branched C 1-10 alkyl chain or an aryl substituent.
- alkyl used either alone or as part of another group is defined as any straight, branched or cyclic, saturated or unsaturated CnHzn+1 group.
- aryl refers to any C6-14 molecular fragment or group which is derived from a monocyclic or polycyclic aromatic hydrocarbon, or a monocyclic or polycyclic heteroaromatic hydrocarbon.
- PG1 is selected from methyl, ethyl, t-butyl and phenyl.
- PG1 is methyl or ethyl and in yet another embodiment PG1 is ethyl.
- the PG2 “amine protecting group” herein refers to a chemical group that suitably prevents reaction between 18F and the amino group in the process of providing the compound of Formula II.
- suitable amine protecting groups include various carbamate substituents, various amide substituents, various imide substituents, and various amine substituents.
- the amine protecting group is selected from the group consisting of linear or branched C 2-7 alkyloxycarbonyl substituents, linear or branched C 3-7 alkenyloxycarbonyl substituents, C 7-12 benzyloxycarbonyl substituents that may have a modifying group, C 2-7 alkyldithiooxycarbonyl substituents, linear or branched C 1-6 alkylamide substituents, linear or branched C 2-6 alkenylamide substituents, C 6-11 benzamide substituents that may have a modifying group, C 4-10 cyclic imide substituents, C 6-11 aromatic imine substituents that may have a substituent, linear or branched C 1-6 alkylamine substituents, linear or branched C 2-6 alkenylamine substituents, and C 6-11 benzylamine substituents that may have a modifying group.
- PG 2 is selected from t-butoxycarbonyl, allyloxycarbonyl, phthalimide, and N-benzylideneamine. In other embodiments PG 2 is selected from t-butoxycarbonyl or phthalimide. In one embodiment of the invention PG 2 is t-butoxycarbonyl.
- step (a) of the method of the invention refers to bringing two or more chemical substances (typically referred to in the art as “reactants” or “reagents”) together to result in a chemical change in one or both/all of the chemical substances.
- the “removal of PG1 in step (b) of the method of the invention is suitably carried out by contacting the compound of Formula II, comprised within the reaction mixture obtained in step (a), with a carboxy deprotecting agent.
- a suitable carboxy deprotecting agent may be either an acid or an alkaline solution, as is well-known to the skilled person (see Greene and Wuts, supra).
- the concentration of the carboxy deprotecting agent is suitably just sufficient to remove the carboxy protecting group.
- the carboxy deprotecting agent is an alkaline solution.
- the carboxy deprotecting agent is a sodium hydroxide or a potassium hydroxide solution and in a preferred embodiment is a sodium hydroxide solution, for example of 0.5-2.0M.
- the temperature and the duration used for deprotection may in some embodiments be tailored to permit removal of PG1.
- the reacting step is carried out at room temperature and for a duration of around 1-5 minutes.
- removal of PG1 is carried out by passing the reaction mixture comprising the compound of Formula II through a solid phase extraction (SPE) column where the compound of Formula II binds to the solid phase. Once the compound of Formula II is bound, the outlet of the SPE column is closed so that the carboxy deprotecting agent is retained therein for a defined amount of time.
- a suitable solid phase for use in this manner is a reversed phase solid phase, e.g. tC18.
- Step (c) comprises applying heat to the reaction vessel using methods well-known to those of skill in the art, e.g. using a dedicated heater into which the reaction vessel is placed for the duration of the radiosynthesis.
- the application of heat must be so that the reaction vessel can be used for the subsequent step (d), i.e. so that the reaction vessel is intact and undamaged, and also so that residual solvent is effectively removed.
- This step (c) is carried out at the same time as removal of PG1, i.e. after the reaction mixture comprising the compound of Formula II has been transferred out of said reaction vessel.
- a suitable temperature for this heating step should be no greater than the tolerance of the reaction vessel, e.g.
- the temperature used to heat the reaction vessel in step (c) may be selected to be as close as possible to the temperature used during the labelling step (a). Suitable temperatures for radiolabeling step (a) are in the range of about 80-140° C., in other embodiments 85-130° C.
- the “removal of PG2 in step (d) of the method of the invention is carried out by contacting the compound of Formula III with an amine deprotecting agent.
- a suitable amine deprotecting agent may be either an acid or an alkaline solution, as is well-known to the skilled person (see Greene and Wuts, supra).
- the concentration of the amine deprotecting agent is suitably just sufficient to remove PG2.
- Preferably the amine deprotecting agent is an acid solution.
- a suitable acid is an acid selected from inorganic acids such as hydrochloric acid (HCl), sulfuric acid (H2SO4) and nitric acid (HNO3), and organic acids such as perfluoroalkyl carboxylic acids, e.g.
- the amine deprotecting agent is HCl, e.g. at a concentration of 1.0-4.0M.
- Removal of PG2 is in one embodiment carried out with heat to allow the deprotection to proceed more rapidly. The time depends on the reaction temperature or other conditions. For example, in one embodiment removal of PG2 is carried out at 60° C., with a reaction time of 5 minutes.
- the aim of the “purifying” step (e) is to obtain substantially pure 18 F-FACBC.
- the term “substantially” refers to the complete or nearly complete extent or degree of an action, characteristic, property, state, structure, item, or result.
- the term “substantially pure” as used herein in the context of 18 F-FACBC encompasses completely pure 18F-FACBC or 18 F-FACBC that is sufficiently pure to be suitable for use as a PET tracer.
- suitable for use as a PET tracer means that the purified 18 F-FACBC product is suitable for intravenous administration to a mammalian subject followed by PET imaging to obtain one or more clinically-useful images of the location and/or distribution of 18 F-FACBC.
- a suitable purifying step comprises:
- HLB solid phase is a reversed phase solid phase having hydrophilic and lipophilic components suitable for a range of purposes.
- HLB solid phase is commercially available as SPE cartridges suitable for use in the method of the present invention, e.g. the Oasis HLB SPE cartridge.
- alumina solid phase is an aluminum oxide normal phase solid phase routinely used in 18F labelling methods as a means to remove free 18 F-fluoride and optimize the radiochemical purity of the final product.
- Alumina solid phase is commercially-available as SPE cartridges suitable for use in the method of the present invention, e.g. the Waters Alumina N Light.
- steps (a)-(c) or (a)-(e) are carried out in sequence.
- the substituent LG in the compound of Formula I is a linear or branched C 1-10 haloalkyl sulfonic acid substituent, a linear or branched C 1-10 alkyl sulfonic acid substituent, a fluorosulfonic acid substituent, or an aromatic sulfonic acid substituent.
- LG include methanesulfonic acid, toluenesulfonic acid, nitrobenzenesulfonic acid, benzenesulfonic acid, trifluoromethanesulfonic acid, fluorosulfonic acid, and perfluoroalkylsulfonic acid. In one embodiment LG is trifluoromethanesulfonic acid.
- the substituent PG1 in the compounds of Formula I and II is a linear or branched C 1-10 alkyl chain or an aryl substituent.
- PG1 can be methyl, ethyl, t-butyl or phenyl.
- PG1 is methyl or ethyl.
- PG1 is ethyl.
- the substituent PG2 in the compounds of Formulas I-III is a carbamate substituent, an amide substituent, an imide substituent or an amine substituent.
- Examples include t-butoxycarbonyl, allyloxycarbonyl, phthalimide, and N-benzylideneamine.
- PG2 is t-butoxycarbonyl.
- the method of the present invention may further comprise the step of formulating the purified reaction mixture obtained in step (e) with citrate buffer.
- this formulating step results in a concentration of 50-100 mM citrate buffer, in another embodiment 60-90 mM citrate buffer and in yet another embodiment 75-85 mM citrate buffer.
- the method of the invention is automated, e.g. carried out on an automated synthesis apparatus.
- 18 F-labelled PET tracers are often conveniently prepared on automated radiosynthesis apparatus.
- automated radiosynthesis apparatus is meant an automated module based on the principle of unit operations as described by Satyamurthy et al (1999 Clin Positr Imag; 2(5): 233-253).
- a known method for production of 18 F-FACBC drug product using this FASTlabTM cassette is described in Example 1 of WO 2013/093025.
- unit operations means that complex processes are reduced to a series of simple operations or reactions, which can be applied to a range of materials.
- Suitable automated synthesiser apparatus are commercially available from a range of suppliers including: GE Healthcare Ltd (Chalfont St Giles, UK); CTI Inc. (Knoxville, USA); Ion Beam Applications S.A. (Chemin du Cyclotron 3, B-1348 Louvain-La-Neuve, Belgium); Raytest (Straubenhardt, Germany) and Bioscan (Washington D.C., USA).
- Automated radiosynthesis apparatus also provide suitable containers for the liquid radioactive waste generated as a result of the radiopharmaceutical preparation.
- Automated radiosynthesis apparatus are not typically provided with radiation shielding, since they are designed to be employed in a suitably configured radioactive work cell.
- the radioactive work cell also termed a hot cell, provides suitable radiation shielding to protect the operator from potential radiation dose, as well as ventilation to remove chemical and/or radioactive vapours.
- the automated synthesis apparatus preferably comprises a cassette.
- cassette is meant a piece of apparatus designed to fit removably and interchangeably onto an automated synthesis apparatus, in such a way that mechanical movement of moving parts of the synthesizer controls the operation of the cassette from outside the cassette, i.e. externally.
- Suitable cassettes comprise a linear array of valves, each linked to a port where reagents or vials can be attached, by either needle puncture of an inverted septum-sealed vial, or by gas-tight, marrying joints. Each valve has a male-female joint which interfaces with a corresponding moving arm of the automated synthesis apparatus.
- the cassette is versatile, typically having several positions where reagents can be attached, and several suitable for attachment of syringe vials of reagents or chromatography cartridges (e.g. for SPE).
- the cassette always comprises a reaction vessel.
- Such reaction vessels are preferably 0.5 to 10 mL, more preferably 0.5 to 5 mL and most preferably 0.5 to 4 mL in volume and are configured such that 3 or more ports of the cassette are connected thereto, to permit transfer of reagents or solvents from various ports on the cassette.
- the cassette has 15 to 40 valves in a linear array, most preferably 20 to 30, with 25 being especially preferred.
- the valves of the cassette are preferably each identical, and most preferably are 3-way valves.
- the cassettes are designed to be suitable for radiopharmaceutical manufacture and are therefore manufactured from materials which are of pharmaceutical grade and ideally also are resistant to radiolysis.
- Preferred automated radiosynthesis apparatus of the present invention are those which interact with a disposable or single use “cassette” (also commonly referred to as a “cartridge”) which comprises all the reagents, reaction vessels and apparatus necessary to carry out the preparation of a given batch of radiopharmaceutical.
- cassettes also commonly referred to as a “cartridge”
- the automated radiosynthesis apparatus has the flexibility to be capable of making a variety of different radiopharmaceuticals with minimal risk of cross-contamination, by simply changing the cassette.
- the cassette approach also has the advantages of: simplified set-up and hence reduced risk of operator error; improved GMP (Good Manufacturing Practice) compliance; multi-tracer capability; rapid change between production runs; pre-run automated diagnostic checking of the cassette and reagents; automated barcode cross-check of chemical reagents vs the synthesis to be carried out; reagent traceability; single-use and hence no risk of cross-contamination, tamper and abuse resistance.
- GMP Good Manufacturing Practice
- the cassette has been simplified by removal of the alumina cartridge.
- the alumina cartridge was present in prior cassette configurations to remove residues of free 18F-fluoride from insufficient purification and/or from radiolysis.
- the present inventors have found that the rest activity on the alumina cartridge is very low (0.1-0.3%) indicating both a robust purification process and a low degree of radiolysis.
- These data suggest that the alumina cartridge is superfluous and can be removed. This has the additional benefit of there being no risk of any particles from the alumina cartridge being present in drug product, which pose a risk of blocking the sterile filter.
- the process has been improved by the addition of a concurrent step of removal of residual acetonitrile from the reactor while the deesterification step proceeds on the tC18 cartridge. This results in a final drug product having a lower and more predictable concentration of residual acetonitrile than that obtained using prior art methods.
- the cassette ( 100 ) is built around a one-piece-molded manifold with 25 three-way stopcocks (1-25), all made of polypropylene.
- the cassette includes a 5 ml reactor ( 106 ), which is made from cyclic olefin copolymer, one 1 ml syringe ( 103 ) and two 5 ml syringes ( 107 , 116 ), 14 cm tubing to the target recovery vessel ( 101 ), a fluoride inlet ( 105 ), spikes for connection with five prefilled vials 102 (Vial A), 108 (Vial D), 109 (Vial B), 110 (Vial C), 112 (Vial E), one 100 ml water bag ( 111 ) as well as various SPE cartridges: tC18 cartridge ( 113 ), alumina cartridge ( 114 ), and hydrophilic lipophilic balanced (HLB) cartridge ( 115 ) and filters.
- tC18 cartridge 113
- Vial C ( 110 ) contained the precursor (48.4 mg, 123.5 ⁇ mol) in its dry form (stored at ⁇ 20° C. until cassette assembly).
- Vial D ( 108 ) contained 4M HCl (2.0 ml).
- Vial E ( 112 ) contained 2 M NaOH (4.1 ml).
- the 30 ml product collection glass vial ( 117 ) was filled with 200 mM trisodium citrate buffer (10 ml).
- No-carrier-added 18 F-fluoride was produced via the 18O(p,n)18F nuclear reaction on a GE PETtrace 6 cyclotron (Norwegian Cyclotron Centre, Oslo). Irradiations were performed using a dual-beam, 30 ⁇ A current on two equal Ag targets with HAVAR foils using 16.5 MeV protons. Each target contained 1.6 ml of 2: 96% [ 18 O]water (Marshall Isotopes). Subsequent to irradiation and delivery to a hotcell, each target was washed with [ 16 O]water (Merck, water for GR analysis).
- Aqueous 18 F-fluoride (1-1.5 ml, 100-200 Mbq) was passed through the QMA cartridge ( 104 ) and into the 18 O—H2O recovery vial ( 101 ). The QMA cartridge ( 104 ) was then flushed with MeCN and sent to waste.
- the trapped 18 F-fluoride was eluted into the reactor ( 106 ) using 730 ⁇ l eluent from vial A ( 102 ) and then concentrated to dryness by azeotropic distillation with 80 ⁇ l acetonitrile from vial C ( 110 ). Approximately 1.7 ml of MeCN was mixed with precursor in vial C ( 110 ) from which 1.0 ml of the dissolved precursor (corresponds to 72.7 mmol precursor) was added to the reactor and heated for 3 min to 85° C.
- the reaction mixture was diluted with water and sent through the tC18 cartridge ( 113 ).
- the reactor ( 106 ) was washed with water and sent through the tC18 cartridge ( 113 ).
- the labelled intermediate, fixed on the tC18 cartridge ( 113 ) was washed with water, and then incubated with 2M NaOH (2.0 ml) for 5 minutes after which the 2M NaOH was sent to waste.
- the labelled intermediate (without the ester group) was then eluted off the tC18 cartridge ( 113 ) into the reactor ( 106 ) using water.
- the BOC group was hydrolyzed by adding 4M HCl (1.4 ml) and heating the reactor for 5 min at 60° C.
- the reactor ( 106 ) content with the crude 18 F-FACBC was sent through the HLB ( 115 ) and alumina cartridge ( 114 ) and into the 30 ml product vial.
- the HLB cartridge ( 115 ) and alumina cartridges ( 114 ) were washed with water (9.1 ml total) and collected in the product vial ( 117 ).
- Acetonitrile (MeCN) concentration was determined using a gas chromatographic system with FID, an automated liquid injector, a fused silica capillary column with USP stationary phase G43 (6% cyanopropylphenyl-94% dimethyl polysiloxane) and a reporting integrator or data system with reintegration capacity. 1000 ⁇ g/ml of MeCN was used as a standard. Blank was prepared by transferring 1 ml of purified water to a 2 ml GC crimp cap vial, which was capped immediately. 1 ml of the standard was transferred to a 2 ml GC crimp cap vials and capped immediately. 0.20 ml of the sample was transferred to a 2 ml GC crimp cap vial with low volume insert (0.25 ml) and capped immediately.
- the experimental conditions of the GC instrument were as follows:
- the column was conditioned at 250° C. for at least one hour prior to use.
- Cstd Concentration of the analyte in calibration standard ( ⁇ g/ml)
- Aluminum concentration was determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES).
- Radiochemical purity (RCP) and radioactive concentration (RAC) of 18 F-FACBC were measured.
- RCP was determined by thin layer chromatography (TLC).
- TLC strip was eluted using a mobile phase consisting of acetonitrile:methanol:water:acetic acid, 20:5:5:1 v/v.
- the RCP and any radiochemical impurities including 18 F-fluoride were reported as percentages of the net sum of all peaks.
- a modified FASTlabTM cassette was used, as illustrated in FIG. 2 .
- the cassette ( 200 ) is modified relative to that used in Example 1 by removing the alumina column ( 114 ) and capping the connectors in its place at positions 20 and 21.
- the cassette ( 200 ) is built around a one-piece-molded manifold with 25 three-way stopcocks (1-25).
- the cassette ( 200 ) includes a reactor ( 206 ), one 1 ml syringe ( 203 ), and two 5 ml syringes ( 207 , 216 ), 14 cm tubing to the target recovery vessel ( 201 ), a fluoride inlet ( 205 ), spikes for connection with five prefilled vials 202 (Vial A), 208 (Vial D), 209 (Vial B), 120 (Vial C), 212 (Vial E), one 200 ml water bag ( 211 ) as well as various SPE cartridges: tC18 cartridge ( 213 ) and hydrophilic lipophilic balanced (HLB) cartridge ( 215 ) and filters.
- a reactor 206
- one 1 ml syringe ( 203 ) and two 5 ml syringes ( 207 , 216 ), 14 cm tubing to the target recovery vessel ( 201 ), a fluoride inlet ( 205 ), spikes for connection
- Vial A ( 202 ) contained K222 (58.8 mg, 156 ⁇ mol), K 2 CO 3 (8.1 mg, 60.8 ⁇ mol) in 79.5% (v/v) MeCN(aq) (1105 ⁇ l).
- Vial B ( 209 ) contained MeCN (4.1 ml).
- Vial C ( 210 ) contained the precursor (48.4 mg, 123.5 ⁇ mol) in its dry form (stored at ⁇ 20° C. until cassette assembly).
- Vial D ( 208 ) contained 4M HCl (2.0 ml).
- Vial E ( 212 ) contained 2 M NaOH (4.1 ml).
- the 30 ml product collection glass vial ( 217 ) was filled with 200 mM trisodium citrate buffer (10 ml).
- the cassette includes three SPE cartridges: QMA ( 204 ), tC18 ( 213 ), and HLB ( 215 ).
- the alumina cartridge has been omitted.
- no other type of SPE is provided in its place.
- the crude product is passed to the product vial through only the HLB cartridge ( 215 ).
- the alumina cartridge in the cassette of FIG. 1 is used to remove residual unreactive radioactive fluoride ions, which if present in the end product contribute to low radiochemical purity.
- Vial A ( 202 ) contained K222 (58.8 mg, 156 ⁇ mol), K 2 CO 3 (8.1 mg, 60.8 ⁇ mol) in 79.5% (v/v) MeCN(aq) (1105 ⁇ l).
- Vial B ( 209 ) contained 4M HCl (2.0 ml).
- Vial C ( 210 ) contained MeCN (4.1 ml).
- Vial D ( 208 ) contained the precursor (48.4 mg, 123.5 ⁇ mol) in its dry form (stored at ⁇ 20° C. until cassette assembly).
- Vial E ( 212 ) contained 2 M NaOH (4.1 ml).
- the 30 ml product collection glass vial ( 217 ) was filled with 200 mM trisodium citrate buffer (10 ml).
- Example 1 The sequence described in Example 1 was used except that the sequence included the extra heating/purging of the reaction vessel.
- the hydrolysis step was replaced with two steps, the first step of which included hydrolysis and in parallel heating of the reactor at 85° C., nitrogen purging (600 mbar HF) of the reaction vessel and vacuum ( ⁇ 600 mbar).
- the second step also included hydrolysis, but heating of the reaction vessel was stopped. Nitrogen purging (600 mbar HF) and vacuum ( ⁇ 600 mbar) were used for cooling of the reaction vessel.
- the alumina SPE was removed and the sequence was changed to transfer the product directly to the formulation buffer vial after the HLB cartridge step.
- Example 2 The analysis methods as described in Example 1 were used for Example 2. Notably, the radiochemical purity in in Example 2 is similar to that found in Example 1. This is unexpected because the alumina column was thought necessary to trap residual radioactive fluoride ions, which contribute to lower radiochemical purity. This resulting product did not exhibit aluminum breakthrough since the process omitted an alumina column. In other words, the product contained only trace aluminum from the reactants used to manufacture the radiotracer. In addition, it omitted any other column such as an ion retardation column that could be used to remove residual fluoride components.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
The present invention provides a novel method for the preparation of 18F-fluoride (18F) for use in radiofluorination reactions. The method of the invention finds use especially in the preparation of 18F-labelled positron emission tomography (PET) tracers. The method of the invention is particularly advantageous where bulk solutions are prepared and stored in prefilled vials rather than being freshly prepared on the day of synthesis. Also provided by the present invention is a radiofluorination reaction which comprises the method of the invention, as well as a cassette for use in carrying out the method of the invention and/or the radiofluorination method of the invention on an automated radiosynthesis apparatus.
Description
- This application is a continuation-in-part of U.S. application Ser. No. 15/318,599 filed Dec. 13, 2016, which is a national stage of PCT/EP2015/064796 filed Jun. 30, 2015, which claims priority to UK Patent Application No. 1411569.5 filed Jun. 30, 2014; this application is a continuation-in-part of U.S. application Ser. No. 16/288,650 filed Feb. 28, 2019, which is a divisional of U.S. application Ser. No. 14/367,649 filed Jun. 20, 2014, which is a national stage of PCT/EP2012/076689 filed Dec. 21, 2012, which claims priority to PCT/EP2011/073670 filed Dec. 21, 2011. The disclosures of each of the above applications are incorporated herein in their entirety.
- The present invention relates to a drug product composition and in particular to a composition comprising a positron emission tomography (PET) tracer. The composition of the present invention and its method of synthesis have certain advantages over the prior art.
- The non-natural amino acid 18F-1-amino-3-fluorocyclobutane-1-carboxylic acid 18F-FACBC, also known as 18F-Fluciclovine is taken up specifically by amino acid transporters and shows promise for positron emission tomography (PET) imaging of prostate cancer (Nanni et al 2014 Clinical Genitourinary Cancer; 12(2): 106-110).
- Production of 18F-FACBC comprises labelling of a triflate precursor compound with 18F-fluoride:
- before removal of the two protecting groups:
- Following the deprotection steps purification is carried out to remove impurities. In the currently-practiced methods a combination of solid phases is used: ion retardation to remove excess Na+ and excess Cl− left over from the deprotection steps, alumina to remove 18F-fluoride and a reversed phase to remove FACBC-related impurities such as 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid (hydroxyl-ACBC) and 1-amino-3-chloro-cyclo butane-1-carboxylic acid (chloro-ACBC).
- The synthesis is currently typically carried out by means of an automated radiosynthesis procedure employing a so-called “cassette” or “cartridge” designed to fit removably and interchangeably onto an automated synthesis apparatus such as those that are commercially available from GE Healthcare, CTI Inc, Ion Beam Applications S.A. (Chemin du Cyclotron 3, B-1348 Louvain-La-Neuve, Belgium); Raytest (Germany) and Bioscan (USA). The cassette comprises all the reagents, reaction vessels and apparatus necessary to carry out the preparation of 18F-FACBC following introduction of suitably prepared 18F-fluoride by methods well-known in the field of PET tracer production. A known cassette for the synthesis of 18F-FACBC is a FASTlab™ cassette from GE Healthcare is shown in
FIG. 1 . - The present inventors have found that the quality of the final 18F-FACBC drug product obtained using the above-described known FASTlab™ cassette and process can be somewhat variable. Residual acetonitrile levels have been found to range from about 100 μg/ml to about 600 μg/ml. While acceptable in terms of permitted daily exposure and in the context of the acceptance criteria for 18F-FACBC drug product, the amount and observed variability is less than ideal.
- The present inventors have also found that residual aluminum have been found to range from about 7 μg/ml to nearly 20 μg/ml, which would mean a potential amount of 100 μg in a 5 ml 18F-FACBC. Where the 18F-FACBC drug product also comprises citrate buffer, complexes of aluminum and citrate are likely to be present, which is problematic as it is known that such complexes cross the blood-brain barrier (Rengel 2004 Biometals; 17: 669-689).
- There is therefore scope to for an improved 18F-FACBC drug product formulation.
- The present invention provides a drug product composition comprising 18F-FACBC that overcomes the problems seen with known such compositions. In particular, the composition of the present invention has an improved impurity profile, making it safer and more effective for imaging as compared with the prior art. Low and predictable levels of acetonitrile and/or aluminum in the final drug product mean that the composition of the invention more easily meets worldwide pharmacopeia requirements. In addition to a significant reduction in the concentration of aluminum in the final drug product, removal of the alumina cartridge has the allied advantages that a shorter and simplified process is permitted and that no particles arising from this cartridge are present, which the present inventors have noted can block the sterile filter used prior to injection of the drug product. Furthermore, the advantages of the present invention are achieved with only minor changes to the known process and without impairing the desirable qualities of known 18F-FACBC compositions.
-
FIG. 1 shows a FASTlab™ cassette of prior art. -
FIG. 2 shows a cassette for producing a radiotracer according to an embodiment of the invention. - To more clearly and concisely describe and point out the subject matter of the claimed invention, definitions are provided in the detailed description hereinbelow for specific terms used throughout the present specification and claims. Any exemplification of specific terms herein should be considered as non-limiting examples.
- In one aspect the present invention relates to a positron emission tomography (PET) tracer composition comprising anti-1-amino-3-18F-fluorocyclobutyl-1-carboxylic acid (18F-FACBC) characterized in that said composition comprises no more than 5.0 μg/mL dissolved aluminum (Al).
- In another aspect, the present invention relates to a PET tracer composition comprising (18F-FACBC) which comprises 50-100 mM citrate buffer and has a pH of 4.0-5.0. Preferably the composition has 60-90 mM citrate buffer, most preferably 75-85 mM citrate buffer. Preferably the composition has a pH of 4.0 or more, and more preferably 4.3-4.4.
- In one aspect the present invention relates to a positron emission tomography (PET) tracer composition comprising anti-1-amino-3-18F-fluorocyclobutyl-1-carboxylic acid (18F-FACBC) characterized in that said composition comprises no more than 5.0 μg/mL dissolved aluminum (Al) and no more than 50 μg/mL acetonitrile (MeCN).
- In the context of the present invention a “PET tracer composition” refers to a composition comprising a PET tracer together with a biocompatible carrier in a form suitable for mammalian administration. The PET tracer composition of the invention is referred to hereunder also as the composition of the invention. A “PET tracer” is defined herein as a biologically active molecule comprising an atom which is a positron emitter suitable for intravenous administration to a mammalian subject followed by PET imaging to obtain one or more clinically-useful images of the location and/or distribution of the PET tracer. A “biocompatible carrier” as defined herein is a fluid, especially a liquid, in which a pharmaceutical is suspended or dissolved, such that the composition is physiologically tolerable, i.e. can be administered to the mammalian body without toxicity or undue discomfort. The biocompatible carrier is suitably an injectable carrier liquid such as sterile, pyrogen-free water for injection or an aqueous solution such as saline.
- The compound “18F-FACBC” is represented by the following chemical structure:
- The term “not more than” as used herein should be understood to mean any amount less than and including the quoted quantity. In an idealized embodiment of the composition of the present invention. there would be zero μg/mL of each impurity present. However, in reality, zero μg/mL of an impurity is unlikely and at least a trace amount of each impurity remains in the composition. The term “not more than” acknowledges that a trace amount of one or more impurities is present in a PET tracer composition, and defines a concentration limit above which the composition would not be deemed acceptable for use.
- In one embodiment, the composition of the invention comprises not more than not more than 3.0 μg/mL dissolved Al, and in another embodiment not more than 1.5 μg/mL dissolved Al.
- In one embodiment the composition of the present invention comprises MeCN at a concentration not more than 20 μg/mL.
- The composition of the invention in one embodiment has an end of synthesis (EOS) radiochemical purity (RCP) of at least 95%, in another embodiment at least 98%, and in yet another embodiment at least 99%. The composition preferably also has a radioactive concentration (RAC) of at least 1000 MBq/mL, alternatively at least 1500 MBq/ml.
- The term “end of synthesis” refers to the point in time when the labelled compound is collected in the product collection vial.
- The pharmaceutical composition of the present invention has a favorable impurity profile, with the main non-radioactive impurities being 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid (hydroxyl-ACBC), 1-amino-3-fluoro-cyclobutane-1-carboxylic acid (FACBC) and 1-amino-3-chloro-cyclobutane-1-carboxylic acid (chloro-ACBC).
- It is preferred that there is not more than 150 μg/mL hydroxyl-ACBC, most preferably not more than 80 μg/mL hydroxyl-ACBC.
- It is preferred that there is not more than 0.15 μg/mL FACBC, most preferably not more than 0.10 μg/mL FACBC.
- It is preferred that there is not more than 2.0 μg/mL chloro-ACBC, most preferably not more than 1.0 μg/mL chloro-ACBC.
- The term “aluminum breakthrough” refers to aluminum ions present in the product resulting from partial breakdown of the alumina column. The term refers to a concentration of aluminum in the end-product higher than that found when an alumina column is not used.
- The term “not more than” should be understood to mean any amount less than the quoted quantity. Therefore, not more than 100 μg/mL means any amount between 0-100 μg/mL, and in an ideal embodiment of the composition of the present invention there would be zero μg/mL of each impurity present in the composition of the invention. However, in reality, zero μg/mL of an impurity might not be achievable and it is more likely that at least a trace amount of the impurity remains in the composition, i.e. in the case of hydroxyl-ACBC the term not more than 150 μg/mL covers e.g. 50-150 μg/mL, not more than 0.10 μg/mL for FACBC covers e.g. 0.05-0.10 μg/mL, and not more than 1.0 μg/mL chloro-ACBC covers e.g. 0.25-1.0 μg/mL.
- An advantage of the composition of the present invention is that the pH, stability and impurity profile can be kept within a very narrow range over a long shelf-life, at high activities, and when manipulated e.g. by autoclaving or by dilution with 0.9% saline.
- In a preferred embodiment, the pharmaceutical composition of the invention does not comprise a radiostabilizer. It is common for pharmaceutical compositions comprising radioactive pharmaceuticals to include a radiostabilizer. For example, known pharmaceutical compositions of [18F]FACBC include a sugar alcohol or a sugar lactone.
- EP 2080526 (Al) discloses that radiolysis can be inhibited by adding a sugar lactone such as ascorbic acid and glucono-o-lactone to [18F]FACBC, and BP 2119458 (Al) discloses that a sugar alcohol such as erythritol xylitol, sorbitol or mannitol can be added as an additive to inhibit radiolysis and improve stability. No such radiostabilizer is required in the radiopharmaceutical composition of the present invention in order to maintain a shelf-life of up to around 10 hours.
- EP 2119458 (Al) teaches that a more stable formulation of 18F-FACBC is achieved when the pH is maintained within the range 2.0-5.9. As discussed in WO 2013/093025, use of citrate buffer allows the pH to be maintained within an even narrower range, provides resistance to degradation and enables the formulation to be autoclaved. In one embodiment, the composition of the present invention therefore comprises around 50-100 mM citrate buffer, in another embodiment around 60-90 mM citrate buffer and in yet another embodiment around 75-85 mM citrate buffer. The term “around” in this context incorporates the exact values of the ranges as well as a small variation around these values that would be expected by the skilled person to achieve the same stabilization effect.
- In another aspect, the present invention provides a method to prepare a PET tracer composition of the invention wherein said method comprises:
-
- a) reacting in a reaction vessel a source of 18F-fluoride with a precursor compound of Formula I:
-
-
- wherein:
- LG is a leaving group;
- PG1 is a carboxy protecting group; and,
- PG2 is an amine protecting group;
- to obtain a reaction mixture comprising a compound of Formula II:
-
-
-
- wherein PG1 and PG2 are as defined for Formula I;
- b) carrying out removal of PG1 and PG2 to obtain a reaction mixture comprising 18F-FACBC; and
- c) purifying said reaction mixture comprising 18F-FACBC by passing it through a hydrophilic lipophilic balanced (HLB) solid phase, characterized in that said purifying does not comprise passing the reaction mixture comprising 18F-FACBC through an alumina solid phase.
-
- In another aspect, the present invention provides a method to prepare a PET tracer composition of the invention wherein said method comprises:
-
- a) reacting in a reaction vessel a source of 18F-fluoride with a precursor compound of Formula I:
-
-
- wherein
- LG is a leaving group;
- PG1 is a carboxy protecting group; and, PG2 is an amine protecting group;
- wherein said reacting step is carried out in acetonitrile;
- to obtain a reaction mixture comprising a compound of Formula II:
-
-
- wherein PG1 and PG2 are as defined for Formula I;
- b) transferring said reaction mixture comprising said compound of Formula II out of said reaction vessel and carrying out removal of PG1 to obtain a reaction mixture comprising a compound of Formula III:
-
- wherein PG2 is as defined for Formula I;
- c) applying heat to said reaction vessel at the same time as carrying out removal of PG1;
- d) transferring said reaction mixture comprising said compound of Formula III back into said reaction vessel and carrying out removal of PG2 to obtain a reaction mixture comprising 18F-FACBC;
- e) purifying said reaction mixture comprising 18F-FACBC by passing it through a hydrophilic lipophilic balanced (HLB) solid phase, characterized in that said purifying does not comprise passing the reaction mixture comprising 18F-FACBC through an alumina solid phase.
- The “source of 18F-fluoride” suitable for use in step (a) of the method of the invention is normally obtained as an aqueous solution from the nuclear reaction 18O(p,n)18F. In order to increase the reactivity of fluoride and to reduce or minimize hydroxylated by-products resulting from the presence of water, water is typically removed from 18F-fluoride prior to the reaction, and fluorination reactions are carried out using anhydrous reaction solvents (Aigbirhio et al 1995 J Fluor Chem; 70: 279-87). A further step that is used to improve the reactivity of 18F-fluoride for radiofluorination reactions is to add a cationic counterion prior to the removal of water. Suitably, the counterion should possess sufficient solubility within the anhydrous reaction solvent to maintain the solubility of the 18F-fluoride. Therefore, counterions that are typically used include large but soft metal ions such as rubidium or cesium, potassium complexed with a cryptand such as Kryptofix™, or tetraalkylammonium salts, wherein potassium complexed with a cryptand such as Kryptofix™, or tetraalkylammonium salts are preferred.
- The “precursor compound” for step (a) of the method of the invention comprises a non-radioactive derivative of a radiolabeled compound, designed so that chemical reaction with a convenient chemical form of the detectable label occurs site-specifically, can be conducted in the minimum number of steps (ideally a single step), and without the need for significant purification (ideally no further purification), to give the desired radiolabeled compound. Such precursor compounds are synthetic and can conveniently be obtained in good chemical purity.
- A suitable “leaving group” in the context of the compound of Formula I in step (a) of the method of the present invention is a chemical group that can be displaced by nucleophilic displacement reaction with fluoride ion. These are well-known in the art of synthetic chemistry. In some embodiments the leaving group of the present invention is a linear or branched C1-10 haloalkyl sulfonic acid substituent, a linear or branched C1-10 alkyl sulfonic acid substituent, a fluorosulfonic acid substituent, or an aromatic sulfonic acid substituent. In other embodiments of the invention the leaving group is selected from methanesulfonic acid, toluenesulfonic acid, nitrobenzenesulfonic acid, benzenesulfonic acid, trifluoromethanesulfonic acid, fluorosulfonic acid, and perfluoroalkylsulfonic acid. In some embodiments the leaving group is either methanesulfonic acid, trifluoromethanesulfonic acid or toluenesulfonic acid and in another embodiment the leaving group is trifluoromethanesulfonic acid.
- The term “protecting group” as used in connection with the substituents PG1 and PG2 refers to a group which inhibits or suppresses undesirable chemical reactions, but which is designed to be sufficiently reactive that it may be cleaved from the functional group in question to obtain the desired product under mild enough conditions that do not modify the rest of the molecule. Protecting groups are well known to those skilled in the art and are described in ‘Protective Groups in Organic Synthesis’, Theorodora W. Greene and Peter G. M. Wuts, (Fourth Edition, John Wiley & Sons, 2007).
- The PG1 “carboxy protecting group” herein is preferably linear or branched C 1-10 alkyl chain or an aryl substituent. The term “alkyl” used either alone or as part of another group is defined as any straight, branched or cyclic, saturated or unsaturated CnHzn+1 group. The term “aryl” refers to any C6-14 molecular fragment or group which is derived from a monocyclic or polycyclic aromatic hydrocarbon, or a monocyclic or polycyclic heteroaromatic hydrocarbon. In one embodiment of the method of the invention PG1 is selected from methyl, ethyl, t-butyl and phenyl. In another embodiment of the invention PG1 is methyl or ethyl and in yet another embodiment PG1 is ethyl.
- The PG2 “amine protecting group” herein refers to a chemical group that suitably prevents reaction between 18F and the amino group in the process of providing the compound of Formula II. Examples of suitable amine protecting groups include various carbamate substituents, various amide substituents, various imide substituents, and various amine substituents. Preferably, the amine protecting group is selected from the group consisting of linear or branched C2-7 alkyloxycarbonyl substituents, linear or branched C3-7 alkenyloxycarbonyl substituents, C7-12 benzyloxycarbonyl substituents that may have a modifying group, C2-7 alkyldithiooxycarbonyl substituents, linear or branched C1-6 alkylamide substituents, linear or branched C2-6 alkenylamide substituents, C6-11 benzamide substituents that may have a modifying group, C4-10 cyclic imide substituents, C6-11 aromatic imine substituents that may have a substituent, linear or branched C1-6 alkylamine substituents, linear or branched C2-6 alkenylamine substituents, and C6-11 benzylamine substituents that may have a modifying group. In some embodiments of the invention PG2 is selected from t-butoxycarbonyl, allyloxycarbonyl, phthalimide, and N-benzylideneamine. In other embodiments PG2 is selected from t-butoxycarbonyl or phthalimide. In one embodiment of the invention PG2 is t-butoxycarbonyl.
- The term “reacting” in step (a) of the method of the invention as is well known to those of skill in the art refers to bringing two or more chemical substances (typically referred to in the art as “reactants” or “reagents”) together to result in a chemical change in one or both/all of the chemical substances.
- The “removal of PG1 in step (b) of the method of the invention is suitably carried out by contacting the compound of Formula II, comprised within the reaction mixture obtained in step (a), with a carboxy deprotecting agent. A suitable carboxy deprotecting agent may be either an acid or an alkaline solution, as is well-known to the skilled person (see Greene and Wuts, supra). The concentration of the carboxy deprotecting agent is suitably just sufficient to remove the carboxy protecting group. Preferably the carboxy deprotecting agent is an alkaline solution. In certain embodiments the carboxy deprotecting agent is a sodium hydroxide or a potassium hydroxide solution and in a preferred embodiment is a sodium hydroxide solution, for example of 0.5-2.0M. The temperature and the duration used for deprotection may in some embodiments be tailored to permit removal of PG1. For example, in certain embodiments the reacting step is carried out at room temperature and for a duration of around 1-5 minutes. In one embodiment, removal of PG1 is carried out by passing the reaction mixture comprising the compound of Formula II through a solid phase extraction (SPE) column where the compound of Formula II binds to the solid phase. Once the compound of Formula II is bound, the outlet of the SPE column is closed so that the carboxy deprotecting agent is retained therein for a defined amount of time. A suitable solid phase for use in this manner is a reversed phase solid phase, e.g. tC18.
- Step (c) comprises applying heat to the reaction vessel using methods well-known to those of skill in the art, e.g. using a dedicated heater into which the reaction vessel is placed for the duration of the radiosynthesis. The application of heat must be so that the reaction vessel can be used for the subsequent step (d), i.e. so that the reaction vessel is intact and undamaged, and also so that residual solvent is effectively removed. This step (c) is carried out at the same time as removal of PG1, i.e. after the reaction mixture comprising the compound of Formula II has been transferred out of said reaction vessel. A suitable temperature for this heating step should be no greater than the tolerance of the reaction vessel, e.g. for a reaction vessel made from cyclic olefin copolymer (COC) a temperature of no greater than about 130° C. and for a reaction vessel made from polyetheretherketone (PEEK) a temperature of no greater than about 200° C. For convenience, the temperature used to heat the reaction vessel in step (c) may be selected to be as close as possible to the temperature used during the labelling step (a). Suitable temperatures for radiolabeling step (a) are in the range of about 80-140° C., in other embodiments 85-130° C.
- The “removal of PG2 in step (d) of the method of the invention is carried out by contacting the compound of Formula III with an amine deprotecting agent. A suitable amine deprotecting agent may be either an acid or an alkaline solution, as is well-known to the skilled person (see Greene and Wuts, supra). The concentration of the amine deprotecting agent is suitably just sufficient to remove PG2. Preferably the amine deprotecting agent is an acid solution. A suitable acid is an acid selected from inorganic acids such as hydrochloric acid (HCl), sulfuric acid (H2SO4) and nitric acid (HNO3), and organic acids such as perfluoroalkyl carboxylic acids, e.g. trifluoroacetic acid (CF3CO2H). In certain embodiments, the amine deprotecting agent is HCl, e.g. at a concentration of 1.0-4.0M. Removal of PG2 is in one embodiment carried out with heat to allow the deprotection to proceed more rapidly. The time depends on the reaction temperature or other conditions. For example, in one embodiment removal of PG2 is carried out at 60° C., with a reaction time of 5 minutes.
- The aim of the “purifying” step (e) is to obtain substantially pure 18F-FACBC. The term “substantially” refers to the complete or nearly complete extent or degree of an action, characteristic, property, state, structure, item, or result. The term “substantially pure” as used herein in the context of 18F-FACBC encompasses completely pure 18F-FACBC or 18F-FACBC that is sufficiently pure to be suitable for use as a PET tracer. The term “suitable for use as a PET tracer” means that the purified 18F-FACBC product is suitable for intravenous administration to a mammalian subject followed by PET imaging to obtain one or more clinically-useful images of the location and/or distribution of 18F-FACBC.
- A suitable purifying step comprises:
-
- i. carrying out a first purification step comprising passing said reaction mixture through a hydrophilic lipophilic balanced (HLB) solid phase; and,
- ii. optionally carrying out a second purification step comprising passing said reaction mixture through an alumina solid phase.
- A “HLB solid phase” is a reversed phase solid phase having hydrophilic and lipophilic components suitable for a range of purposes. HLB solid phase is commercially available as SPE cartridges suitable for use in the method of the present invention, e.g. the Oasis HLB SPE cartridge.
- An “alumina solid phase” is an aluminum oxide normal phase solid phase routinely used in 18F labelling methods as a means to remove free 18F-fluoride and optimize the radiochemical purity of the final product. Alumina solid phase is commercially-available as SPE cartridges suitable for use in the method of the present invention, e.g. the Waters Alumina N Light.
- In the method of the invention, steps (a)-(c) or (a)-(e) are carried out in sequence.
- In one embodiment of the method of the present invention, the substituent LG in the compound of Formula I is a linear or branched C1-10 haloalkyl sulfonic acid substituent, a linear or branched C1-10 alkyl sulfonic acid substituent, a fluorosulfonic acid substituent, or an aromatic sulfonic acid substituent. Examples of LG include methanesulfonic acid, toluenesulfonic acid, nitrobenzenesulfonic acid, benzenesulfonic acid, trifluoromethanesulfonic acid, fluorosulfonic acid, and perfluoroalkylsulfonic acid. In one embodiment LG is trifluoromethanesulfonic acid.
- In one embodiment of the method of the present invention the substituent PG1 in the compounds of Formula I and II is a linear or branched C1-10 alkyl chain or an aryl substituent. For example, PG1 can be methyl, ethyl, t-butyl or phenyl. In one embodiment PG1 is methyl or ethyl. In another embodiment, PG1 is ethyl.
- In one embodiment of the method of the present invention the substituent PG2 in the compounds of Formulas I-III is a carbamate substituent, an amide substituent, an imide substituent or an amine substituent. Examples include t-butoxycarbonyl, allyloxycarbonyl, phthalimide, and N-benzylideneamine. In one embodiment, PG2 is t-butoxycarbonyl.
- The method of the present invention may further comprise the step of formulating the purified reaction mixture obtained in step (e) with citrate buffer. In one embodiment, this formulating step results in a concentration of 50-100 mM citrate buffer, in another embodiment 60-90 mM citrate buffer and in yet another embodiment 75-85 mM citrate buffer.
- In one embodiment, the method of the invention is automated, e.g. carried out on an automated synthesis apparatus. 18F-labelled PET tracers are often conveniently prepared on automated radiosynthesis apparatus. By the term “automated radiosynthesis apparatus” is meant an automated module based on the principle of unit operations as described by Satyamurthy et al (1999 Clin Positr Imag; 2(5): 233-253). A known method for production of 18F-FACBC drug product using this FASTlab™ cassette is described in Example 1 of WO 2013/093025.
- The term “unit operations” means that complex processes are reduced to a series of simple operations or reactions, which can be applied to a range of materials. Suitable automated synthesiser apparatus are commercially available from a range of suppliers including: GE Healthcare Ltd (Chalfont St Giles, UK); CTI Inc. (Knoxville, USA); Ion Beam Applications S.A. (Chemin du Cyclotron 3, B-1348 Louvain-La-Neuve, Belgium); Raytest (Straubenhardt, Germany) and Bioscan (Washington D.C., USA).
- Commercial automated radiosynthesis apparatus also provide suitable containers for the liquid radioactive waste generated as a result of the radiopharmaceutical preparation. Automated radiosynthesis apparatus are not typically provided with radiation shielding, since they are designed to be employed in a suitably configured radioactive work cell. The radioactive work cell, also termed a hot cell, provides suitable radiation shielding to protect the operator from potential radiation dose, as well as ventilation to remove chemical and/or radioactive vapours.
- The automated synthesis apparatus preferably comprises a cassette. By the term “cassette” is meant a piece of apparatus designed to fit removably and interchangeably onto an automated synthesis apparatus, in such a way that mechanical movement of moving parts of the synthesizer controls the operation of the cassette from outside the cassette, i.e. externally. Suitable cassettes comprise a linear array of valves, each linked to a port where reagents or vials can be attached, by either needle puncture of an inverted septum-sealed vial, or by gas-tight, marrying joints. Each valve has a male-female joint which interfaces with a corresponding moving arm of the automated synthesis apparatus. External rotation of the arm thus controls the opening or closing of the valve when the cassette is attached to the automated synthesis apparatus. Additional moving parts of the automated. synthesis apparatus are designed to clip onto syringe plunger tips, and thus raise or depress syringe barrels.
- The cassette is versatile, typically having several positions where reagents can be attached, and several suitable for attachment of syringe vials of reagents or chromatography cartridges (e.g. for SPE). The cassette always comprises a reaction vessel. Such reaction vessels are preferably 0.5 to 10 mL, more preferably 0.5 to 5 mL and most preferably 0.5 to 4 mL in volume and are configured such that 3 or more ports of the cassette are connected thereto, to permit transfer of reagents or solvents from various ports on the cassette. Preferably the cassette has 15 to 40 valves in a linear array, most preferably 20 to 30, with 25 being especially preferred. The valves of the cassette are preferably each identical, and most preferably are 3-way valves. The cassettes are designed to be suitable for radiopharmaceutical manufacture and are therefore manufactured from materials which are of pharmaceutical grade and ideally also are resistant to radiolysis.
- Preferred automated radiosynthesis apparatus of the present invention are those which interact with a disposable or single use “cassette” (also commonly referred to as a “cartridge”) which comprises all the reagents, reaction vessels and apparatus necessary to carry out the preparation of a given batch of radiopharmaceutical. By use of such cassettes the automated radiosynthesis apparatus has the flexibility to be capable of making a variety of different radiopharmaceuticals with minimal risk of cross-contamination, by simply changing the cassette. The cassette approach also has the advantages of: simplified set-up and hence reduced risk of operator error; improved GMP (Good Manufacturing Practice) compliance; multi-tracer capability; rapid change between production runs; pre-run automated diagnostic checking of the cassette and reagents; automated barcode cross-check of chemical reagents vs the synthesis to be carried out; reagent traceability; single-use and hence no risk of cross-contamination, tamper and abuse resistance.
- The cassette has been simplified by removal of the alumina cartridge. The alumina cartridge was present in prior cassette configurations to remove residues of free 18F-fluoride from insufficient purification and/or from radiolysis. However, the present inventors have found that the rest activity on the alumina cartridge is very low (0.1-0.3%) indicating both a robust purification process and a low degree of radiolysis. These data suggest that the alumina cartridge is superfluous and can be removed. This has the additional benefit of there being no risk of any particles from the alumina cartridge being present in drug product, which pose a risk of blocking the sterile filter.
- The process has been improved by the addition of a concurrent step of removal of residual acetonitrile from the reactor while the deesterification step proceeds on the tC18 cartridge. This results in a final drug product having a lower and more predictable concentration of residual acetonitrile than that obtained using prior art methods.
- The following non-limiting examples serve to illustrate particular embodiments of the subject matter of the present invention.
-
-
- ATR attenuated total reflectance
- DTGS deuterated triglycine sulphate
- [18F]FACBC 1-amino-3-[18F]fluorocyclobutane-I-carboxylic acid
- FT-IR Fourier transform infrared
- K.222
- BOC tert-Butyloxycarbonyl
- DP drug product
- HLB hydrophobic-lipophilic balance
- K222 Kryptofix 222
- MeCN acetonitrile
- MeOH methanol
- QMA quaternary methyl ammonium
- RCY radiochemical yield
- RAC radioactive concentration
- RCP: radiochemical purity
- SPE solid-phase extraction
- TLC thin layer chromatography
- UV ultraviolet
- All reagents and solvents were purchased from Merck and used without further purification. The [18F]FACBC precursor, Syn-1-(N-(tert-butoxycarbonyl)amino)-3-[[(trifluoromethyl)sulfonyl]oxy]-cyclobutane-1-carboxylic acid ethyl ester was obtained from GE Healthcare. The Oasis HLB plus cartridge and the Sep-Pak cartridges: QMA light Plus (K.2C03 form), tC18 light, Alumina N light were purchased from Waters (Milford, Mass., USA). A Capintec Nal ion chamber was used for all radioactive measurements (model CRC15R). Radio-thin layer chromatography (radio-TLC) was performed on a Packard instant imager using pre-coated plates of silica gel (Merck 60F254).
- 1(i) FASTlab Cassette
- All radiochemistry was performed on a commercially-available GE FASTlab™ with single-use cassettes, as shown in
FIG. 1 . - The cassette (100) is built around a one-piece-molded manifold with 25 three-way stopcocks (1-25), all made of polypropylene. Briefly, the cassette includes a 5 ml reactor (106), which is made from cyclic olefin copolymer, one 1 ml syringe (103) and two 5 ml syringes (107, 116), 14 cm tubing to the target recovery vessel (101), a fluoride inlet (105), spikes for connection with five prefilled vials 102 (Vial A), 108 (Vial D), 109 (Vial B), 110 (Vial C), 112 (Vial E), one 100 ml water bag (111) as well as various SPE cartridges: tC18 cartridge (113), alumina cartridge (114), and hydrophilic lipophilic balanced (HLB) cartridge (115) and filters. 42 cm tubing (118) connects to the right-hand side of the reactor vessel. Fluid paths are controlled with nitrogen purging, vacuum and the three syringes. The fully automated system is designed for single-step fluorinations with cyclotron-produced 18F-fluoride. The FASTlab was programmed by the software package in a step-by-step time-dependent sequence of events such as moving the syringes, nitrogen purging, vacuum, and temperature regulation. Vial A (102) contained K222 (58.8 mg, 156 ρmol), K2CO3 (8.1 mg, 60.8 ρmol) in 79.5% (v/v) MeCN(aq) (1105 μl). Vial B (109) contained MeCN (4.1 ml). Vial C (110) contained the precursor (48.4 mg, 123.5 ρmol) in its dry form (stored at −20° C. until cassette assembly). Vial D (108) contained 4M HCl (2.0 ml). Vial E (112) contained 2 M NaOH (4.1 ml). The 30 ml product collection glass vial (117) was filled with 200 mM trisodium citrate buffer (10 ml).
- 1(ii) Production of 18F-Fluoride
- No-carrier-added 18F-fluoride was produced via the 18O(p,n)18F nuclear reaction on a GE PETtrace 6 cyclotron (Norwegian Cyclotron Centre, Oslo). Irradiations were performed using a dual-beam, 30 μA current on two equal Ag targets with HAVAR foils using 16.5 MeV protons. Each target contained 1.6 ml of 2: 96% [18O]water (Marshall Isotopes). Subsequent to irradiation and delivery to a hotcell, each target was washed with [16O]water (Merck, water for GR analysis). Aqueous 18F-fluoride (1-1.5 ml, 100-200 Mbq) was passed through the QMA cartridge (104) and into the 18O—H2O recovery vial (101). The QMA cartridge (104) was then flushed with MeCN and sent to waste.
- 1(iii)18F-Fluoride Labelling
- The trapped 18F-fluoride was eluted into the reactor (106) using 730 μl eluent from vial A (102) and then concentrated to dryness by azeotropic distillation with 80 μl acetonitrile from vial C (110). Approximately 1.7 ml of MeCN was mixed with precursor in vial C (110) from which 1.0 ml of the dissolved precursor (corresponds to 72.7 mmol precursor) was added to the reactor and heated for 3 min to 85° C.
- (iv) Removal of Ester Protecting Group
- The reaction mixture was diluted with water and sent through the tC18 cartridge (113). The reactor (106) was washed with water and sent through the tC18 cartridge (113). The labelled intermediate, fixed on the tC18 cartridge (113) was washed with water, and then incubated with 2M NaOH (2.0 ml) for 5 minutes after which the 2M NaOH was sent to waste.
- 1(v) Removal of BOC Protecting Group
- The labelled intermediate (without the ester group) was then eluted off the tC18 cartridge (113) into the reactor (106) using water. The BOC group was hydrolyzed by adding 4M HCl (1.4 ml) and heating the reactor for 5 min at 60° C.
- 1(vi) Purification
- The reactor (106) content with the crude 18F-FACBC was sent through the HLB (115) and alumina cartridge (114) and into the 30 ml product vial. The HLB cartridge (115) and alumina cartridges (114) were washed with water (9.1 ml total) and collected in the product vial (117).
- 1(vii) Formulation
- 2M NaOH and water was added to the product vial (117), giving a purified drug product (DP) with a total volume of 26 ml.
- 1(viii) Acetonitrile Concentration
- Acetonitrile (MeCN) concentration was determined using a gas chromatographic system with FID, an automated liquid injector, a fused silica capillary column with USP stationary phase G43 (6% cyanopropylphenyl-94% dimethyl polysiloxane) and a reporting integrator or data system with reintegration capacity. 1000 μg/ml of MeCN was used as a standard. Blank was prepared by transferring 1 ml of purified water to a 2 ml GC crimp cap vial, which was capped immediately. 1 ml of the standard was transferred to a 2 ml GC crimp cap vials and capped immediately. 0.20 ml of the sample was transferred to a 2 ml GC crimp cap vial with low volume insert (0.25 ml) and capped immediately. The experimental conditions of the GC instrument were as follows:
-
- Carrier gas flow, Helium: 2.0 ml/min
- Oven temperature program: 40° C. for 6 minutes then 20° C./min to 240° C. for 4 minutes
- Injector temperature: 225° C.
- Split ratio: 10:1 Detector: FID
- Detector temperature: 250° C.
- Hydrogen flow rate: 30 ml/min
- Air flow rate: 400 ml/min
- Make up gas flow rate (He): 25 ml/min
- The experimental conditions of the automatic liquid injector were as follows:
-
- Solvent pre-washes: 3
- Sample pumps: 3
- Solvent post washes: 3 Injection volume: 1 ml
- The column was conditioned at 250° C. for at least one hour prior to use.
- One injection of each standard and two replicate injections of the sample solution were performed in addition to blank injections in the following order:
-
- Blank
- Calibration standard
- Calibration standard
- Blank
- Sample, replicate 1
- Sample, replicate 2
- Blank
- The concentration of each analyte, Csample, was calculated in μg/ml using the following formula:
-
- where:
- Asample: Peak area of the analyte in sample
- Cstd: Concentration of the analyte in calibration standard (μg/ml)
- Astd: Peak area of the analyte in calibration standard, average of 2 injections
- 1(ix) Aluminum Concentration
- Aluminum concentration was determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES).
- 1(x) Radiochemical Parameters
- Radiochemical purity (RCP) and radioactive concentration (RAC) of 18F-FACBC were measured.
- RCP was determined by thin layer chromatography (TLC). The TLC strip was eluted using a mobile phase consisting of acetonitrile:methanol:water:acetic acid, 20:5:5:1 v/v. The RCP and any radiochemical impurities including 18F-fluoride were reported as percentages of the net sum of all peaks.
- 1(xi) Results
- The following results were obtained:
-
Production RAC MeCN Al # (MBq/ml) RCP(¾)TO (μg/ml) (μg/ml) 1 1915 t > 99 506 14 2 1804 r > 99 324 14 3 1950 t > 99 302 13 4 1698 t > 99 89 15 5 1570 r > 99 596 17 6 1815 t > 99 218 15 - A modified FASTlab™ cassette was used, as illustrated in
FIG. 2 . The cassette (200) is modified relative to that used in Example 1 by removing the alumina column (114) and capping the connectors in its place atpositions - As can be appreciated from
FIG. 2 , the cassette includes three SPE cartridges: QMA (204), tC18 (213), and HLB (215). Compared to the cassette ofFIG. 1 , the alumina cartridge has been omitted. Moreover, no other type of SPE is provided in its place. Thus, the crude product is passed to the product vial through only the HLB cartridge (215). The alumina cartridge in the cassette ofFIG. 1 is used to remove residual unreactive radioactive fluoride ions, which if present in the end product contribute to low radiochemical purity. - Vial A (202) contained K222 (58.8 mg, 156 ρmol), K2CO3 (8.1 mg, 60.8 ρmol) in 79.5% (v/v) MeCN(aq) (1105 μl). Vial B (209) contained 4M HCl (2.0 ml). Vial C (210) contained MeCN (4.1 ml). Vial D (208) contained the precursor (48.4 mg, 123.5 ρmol) in its dry form (stored at −20° C. until cassette assembly). Vial E (212) contained 2 M NaOH (4.1 ml). The 30 ml product collection glass vial (217) was filled with 200 mM trisodium citrate buffer (10 ml).
- 2(i) Modified Sequence
- The sequence described in Example 1 was used except that the sequence included the extra heating/purging of the reaction vessel. The hydrolysis step was replaced with two steps, the first step of which included hydrolysis and in parallel heating of the reactor at 85° C., nitrogen purging (600 mbar HF) of the reaction vessel and vacuum (−600 mbar). The second step also included hydrolysis, but heating of the reaction vessel was stopped. Nitrogen purging (600 mbar HF) and vacuum (−600 mbar) were used for cooling of the reaction vessel. Furthermore, the alumina SPE was removed and the sequence was changed to transfer the product directly to the formulation buffer vial after the HLB cartridge step.
- 2(ii) Analysis
- The analysis methods as described in Example 1 were used for Example 2. Notably, the radiochemical purity in in Example 2 is similar to that found in Example 1. This is unexpected because the alumina column was thought necessary to trap residual radioactive fluoride ions, which contribute to lower radiochemical purity. This resulting product did not exhibit aluminum breakthrough since the process omitted an alumina column. In other words, the product contained only trace aluminum from the reactants used to manufacture the radiotracer. In addition, it omitted any other column such as an ion retardation column that could be used to remove residual fluoride components.
-
Production RAC MeCN Al # (MBQ/ml) RCP(¾)TO (μg/ml) (μg/ml) 7 3112 99.1 20 0.7 8 3900 99.1 20 0.8 9 1631 99.1 21 1.3 10 731 99.9 22 0.8 11 1831 99.8 25 0.8 12 1654 99.9 24 1.3 13 1573 99.1 21 1.1 14 1750 99.4 23 1.1 15 788 99.0 19 1.1 16 1023 99.2 17 1.1 - Other embodiments and uses of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. All references cited herein, including all U.S. and foreign patents and patent applications, are specifically and entirely hereby incorporated herein by reference. It is intended that the specification and examples be considered exemplary only, with the true scope and spirit of the invention indicated by the following claims.
Claims (17)
1-26. (canceled)
27. A radiotracer composition comprising a purified reaction mixture of the 18F-FACBC made according to the process comprising:
(a) reacting in a reaction vessel of the cassette system a source of 18F-fluoride with a precursor compound of Formula I:
wherein:
LG is a leaving group;
PG1 is a carboxy protecting group;
and, PG2 is an amine protecting group;
to obtain a reaction mixture comprising a compound of Formula II:
wherein PG1 and PG2 are as defined for Formula I;
(b) removing PG1 to obtain a reaction mixture comprising a compound of Formula III:
wherein PG1 is as defined for Formula I;
(c) removing PG2 to obtain a reaction mixture comprising anti-1-amino-3-18F-fluorocyclobutyl-1-carboxylic acid (18F-FACBC); and
(d) purifying said reaction mixture comprising 18F-FACBC by passing it through only one solid phase extraction cartridge of the cassette system, wherein the solid phase extraction cartridge is a hydrophilic lipophilic balanced (HLB) solid phase extraction cartridge.
28. The radiotracer composition of claim 27 , further comprising a citrate buffer in a concentration range of 50-100 mM and a pH of 4.0-5.0.
29. The radiotracer composition of claim 27 , further comprising a citrate buffer in a concentration range of 60-90 mM and a pH of 4.0-5.0.
30. The radiotracer composition of claim 27 , further comprising a citrate buffer in a concentration range of 75-85 mM and a pH of 4.0-5.0.
31. The radiotracer composition of claim 27 , wherein the composition lacks breakthrough aluminum.
32. The radiotracer composition of claim 27 , with the proviso that said composition does not comprise a radiostabilizer.
33. The radiotracer composition of claim 27 , with the proviso that said composition does not comprise a sugar lactone or a sugar alcohol.
34. An aqueous pharmaceutical radiotracer composition comprising:
an 18F-FACBC radiotracer; and
a citrate buffer, the citrate buffer being present in said aqueous pharmaceutical radiotracer composition at a concentration of 50-100 mM, wherein the aqueous pharmaceutical radiotracer composition has a pH of 4.0-5.0 and lacks breakthrough aluminum.
35. The radiotracer composition of claim 34 , wherein the concentration of the citrate buffer is in a range of 60-90 mM.
36. The radiotracer composition of claim 34 , wherein the concentration of the citrate buffer is in a range of 75-85 mM.
37. The radiotracer composition of claim 34 that has an end of synthesis (EOS) radioactive concentration (RAC) of at least 1000 MBq/mL.
38. The radiotracer composition of claim 34 that has an end of synthesis (EOS) radioactive concentration (RAC) of at least 1500 MBq/ml.
39. The radiotracer composition of claim 34 which comprises not more than 150 μg/mL 1-amino-3-hydroxyl-cyclobutane-1-carboxylic acid (hydroxyl-ACBC).
40. The radiotracer composition of claim 34 , which comprises not more than 80 μg/mL hydroxyl-ACBC.
41. The radiotracer composition of claim 34 , which comprises not more than 2.0 μg/mL 1-amino-3-chloro-cyclobutane-1-carboxylic acid (chloro-ACBC).
42. The radiotracer composition of claim 34 , which comprises not more than 1.0 μg/mL chloro-ACBC.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17/557,755 US20220111052A1 (en) | 2011-12-21 | 2021-12-21 | Eluent solution |
Applications Claiming Priority (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2011/073670 WO2012089594A1 (en) | 2010-12-29 | 2011-12-21 | Eluent solution |
EPPCT/EP2011/073670 | 2011-12-21 | ||
PCT/EP2012/076689 WO2013093025A1 (en) | 2011-12-21 | 2012-12-21 | 18f - fluciclovine compositions in citrate buffers |
US201414367649A | 2014-06-20 | 2014-06-20 | |
GB1411569.5 | 2014-06-30 | ||
GBGB1411569.5A GB201411569D0 (en) | 2014-06-30 | 2014-06-30 | Novel formulation and method of synthesis |
PCT/EP2015/064796 WO2016001199A1 (en) | 2014-06-30 | 2015-06-30 | Novel formulation and method of synthesis |
US201615318599A | 2016-12-13 | 2016-12-13 | |
US16/288,650 US20190192660A1 (en) | 2010-12-29 | 2019-02-28 | 18f-fluciclovine compositions in citrate buffers |
US16/997,188 US11534494B2 (en) | 2011-12-21 | 2020-08-19 | Formulation and method of synthesis |
US17/557,755 US20220111052A1 (en) | 2011-12-21 | 2021-12-21 | Eluent solution |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/997,188 Division US11534494B2 (en) | 2011-12-21 | 2020-08-19 | Formulation and method of synthesis |
Publications (1)
Publication Number | Publication Date |
---|---|
US20220111052A1 true US20220111052A1 (en) | 2022-04-14 |
Family
ID=74259817
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/997,188 Active 2033-02-05 US11534494B2 (en) | 2011-12-21 | 2020-08-19 | Formulation and method of synthesis |
US17/557,755 Pending US20220111052A1 (en) | 2011-12-21 | 2021-12-21 | Eluent solution |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/997,188 Active 2033-02-05 US11534494B2 (en) | 2011-12-21 | 2020-08-19 | Formulation and method of synthesis |
Country Status (1)
Country | Link |
---|---|
US (2) | US11534494B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113019279A (en) * | 2021-03-11 | 2021-06-25 | 山西医科大学第一医院 | Automatic synthesis device for preparing radiopharmaceuticals and using method thereof |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1356827A1 (en) | 2002-04-24 | 2003-10-29 | Mallinckrodt Inc. | Method for obtaining a 2-18F-fluor-2-deoxy-D-glucose (18F-FDG)-solution |
US7993626B2 (en) | 2007-01-11 | 2011-08-09 | Immunomedics, Inc. | Methods and compositions for F-18 labeling of proteins, peptides and other molecules |
CN100418585C (en) | 2003-07-24 | 2008-09-17 | 伯拉考成像股份公司 | Stable radiopharmaceutical compositions and methods for preparation |
GB0422004D0 (en) | 2004-10-05 | 2004-11-03 | Amersham Plc | Method of deprotection |
WO2007001958A2 (en) | 2005-06-23 | 2007-01-04 | Emory University | Stereoselective synthesis of amino acid analogs for tumor imaging |
AU2006319987B2 (en) | 2005-11-29 | 2012-09-06 | Nihon Medi-Physics Co., Ltd. | Precursor compound of radioactive halogen labeled organic compound |
KR101317258B1 (en) | 2006-05-11 | 2013-10-14 | 니혼 메디피직스 가부시키가이샤 | Process for production of radioactive fluorine-labeled organic compound |
CN101563107B (en) | 2006-12-21 | 2012-07-11 | 日本医事物理股份有限公司 | Radioactive diagnostic imaging agent |
EP2119458B9 (en) | 2007-02-13 | 2013-08-21 | Nihon Medi-Physics Co., Ltd. | Method for production of radiation diagnostic imaging agent |
SG178393A1 (en) * | 2009-08-14 | 2012-03-29 | Univ Pennsylvania | Single diastereomers of 4-fluoroglutamine and methods fo their preparation and use |
WO2012089594A1 (en) | 2010-12-29 | 2012-07-05 | Ge Healthcare Limited | Eluent solution |
GB201117785D0 (en) | 2011-10-14 | 2011-11-30 | Ge Healthcare Ltd | Improved radiosynthesis method |
RU2623163C2 (en) | 2011-12-21 | 2017-06-22 | ДжиИ ХЕЛТКЕР ЛИМИТЕД | Composition 18f- flutsiklovina in citrate buffers |
GB201205703D0 (en) | 2012-03-30 | 2012-05-16 | Ge Healthcare Ltd | Synthon composition |
GB201214220D0 (en) | 2012-08-09 | 2012-09-19 | Ge Healthcare Ltd | Radiosynthesis |
-
2020
- 2020-08-19 US US16/997,188 patent/US11534494B2/en active Active
-
2021
- 2021-12-21 US US17/557,755 patent/US20220111052A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
US11534494B2 (en) | 2022-12-27 |
US20210030878A1 (en) | 2021-02-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3766522B1 (en) | Automated method for the preparation of 18f-fluciclovine compositions | |
US10023525B2 (en) | Preparation of 18F-fluciclovine | |
JP2022136074A (en) | Novel formulation and method of synthesis | |
EP2793954B1 (en) | 18f-fluciclovine compositions in citrate buffers | |
US20220111052A1 (en) | Eluent solution | |
US20180177900A1 (en) | Radiolabelling Process | |
US20220001034A1 (en) | Novel formulation and method of synthesis | |
GB2561122B (en) | Composition comprising [18F]-Fluciclovine | |
NZ624250B2 (en) | 18f-fluciclovine compositions in citrate buffers | |
NZ624250A (en) | 18f-fluciclovine compositions in citrate buffers |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STPP | Information on status: patent application and granting procedure in general |
Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |