CA2521276A1 - Fermentation process for the preparation of pravastatin - Google Patents
Fermentation process for the preparation of pravastatin Download PDFInfo
- Publication number
- CA2521276A1 CA2521276A1 CA002521276A CA2521276A CA2521276A1 CA 2521276 A1 CA2521276 A1 CA 2521276A1 CA 002521276 A CA002521276 A CA 002521276A CA 2521276 A CA2521276 A CA 2521276A CA 2521276 A1 CA2521276 A1 CA 2521276A1
- Authority
- CA
- Canada
- Prior art keywords
- compactin
- pravastatin
- concentration
- substantially pure
- fermentation
- 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.)
- Abandoned
Links
- 229960002965 pravastatin Drugs 0.000 title claims abstract description 69
- TUZYXOIXSAXUGO-UHFFFAOYSA-N Pravastatin Natural products C1=CC(C)C(CCC(O)CC(O)CC(O)=O)C2C(OC(=O)C(C)CC)CC(O)C=C21 TUZYXOIXSAXUGO-UHFFFAOYSA-N 0.000 title claims abstract description 61
- TUZYXOIXSAXUGO-PZAWKZKUSA-N pravastatin Chemical compound C1=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(O)=O)[C@H]2[C@@H](OC(=O)[C@@H](C)CC)C[C@H](O)C=C21 TUZYXOIXSAXUGO-PZAWKZKUSA-N 0.000 title claims abstract description 55
- 230000004151 fermentation Effects 0.000 title claims abstract description 15
- 238000000855 fermentation Methods 0.000 title claims abstract description 14
- 238000002360 preparation method Methods 0.000 title abstract description 5
- AJLFOPYRIVGYMJ-INTXDZFKSA-N mevastatin Chemical compound C([C@H]1[C@@H](C)C=CC2=CCC[C@@H]([C@H]12)OC(=O)[C@@H](C)CC)C[C@@H]1C[C@@H](O)CC(=O)O1 AJLFOPYRIVGYMJ-INTXDZFKSA-N 0.000 claims abstract description 77
- AJLFOPYRIVGYMJ-UHFFFAOYSA-N SJ000287055 Natural products C12C(OC(=O)C(C)CC)CCC=C2C=CC(C)C1CCC1CC(O)CC(=O)O1 AJLFOPYRIVGYMJ-UHFFFAOYSA-N 0.000 claims abstract description 73
- BOZILQFLQYBIIY-UHFFFAOYSA-N mevastatin hydroxy acid Natural products C1=CC(C)C(CCC(O)CC(O)CC(O)=O)C2C(OC(=O)C(C)CC)CCC=C21 BOZILQFLQYBIIY-UHFFFAOYSA-N 0.000 claims abstract description 73
- VGMFHMLQOYWYHN-UHFFFAOYSA-N Compactin Natural products OCC1OC(OC2C(O)C(O)C(CO)OC2Oc3cc(O)c4C(=O)C(=COc4c3)c5ccc(O)c(O)c5)C(O)C(O)C1O VGMFHMLQOYWYHN-UHFFFAOYSA-N 0.000 claims abstract description 72
- 238000000034 method Methods 0.000 claims abstract description 62
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 16
- 244000005700 microbiome Species 0.000 claims description 16
- 235000012054 meals Nutrition 0.000 claims description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
- 238000004128 high performance liquid chromatography Methods 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 10
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 9
- 239000008103 glucose Substances 0.000 claims description 9
- 239000013587 production medium Substances 0.000 claims description 9
- 244000068988 Glycine max Species 0.000 claims description 8
- 235000010469 Glycine max Nutrition 0.000 claims description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 208000035150 Hypercholesterolemia Diseases 0.000 claims description 6
- 235000012343 cottonseed oil Nutrition 0.000 claims description 6
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 239000011780 sodium chloride Substances 0.000 claims description 6
- 240000008042 Zea mays Species 0.000 claims description 5
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 5
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 5
- 238000013019 agitation Methods 0.000 claims description 5
- 235000005822 corn Nutrition 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 4
- 238000012258 culturing Methods 0.000 claims description 3
- 159000000000 sodium salts Chemical class 0.000 claims description 3
- 241000187747 Streptomyces Species 0.000 claims description 2
- 241000178285 Streptomyces carbophilus Species 0.000 claims 2
- 230000033444 hydroxylation Effects 0.000 abstract description 5
- 238000005805 hydroxylation reaction Methods 0.000 abstract description 5
- 230000000813 microbial effect Effects 0.000 abstract description 5
- 239000012535 impurity Substances 0.000 abstract description 3
- XUKUURHRXDUEBC-SXOMAYOGSA-N (3s,5r)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoic acid Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-SXOMAYOGSA-N 0.000 description 11
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 10
- 239000002609 medium Substances 0.000 description 7
- -1 as well as Chemical compound 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 102100029077 3-hydroxy-3-methylglutaryl-coenzyme A reductase Human genes 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000001888 Peptone Substances 0.000 description 4
- 108010080698 Peptones Proteins 0.000 description 4
- 235000019319 peptone Nutrition 0.000 description 4
- CABVTRNMFUVUDM-VRHQGPGLSA-N (3S)-3-hydroxy-3-methylglutaryl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C[C@@](O)(CC(O)=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 CABVTRNMFUVUDM-VRHQGPGLSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 108090000895 Hydroxymethylglutaryl CoA Reductases Proteins 0.000 description 3
- 235000012000 cholesterol Nutrition 0.000 description 3
- 229910000160 potassium phosphate Inorganic materials 0.000 description 3
- 235000011009 potassium phosphates Nutrition 0.000 description 3
- 238000011218 seed culture Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 108010030975 Polyketide Synthases Proteins 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- ZGGHKIMDNBDHJB-NRFPMOEYSA-M (3R,5S)-fluvastatin sodium Chemical compound [Na+].C12=CC=CC=C2N(C(C)C)C(\C=C\[C@@H](O)C[C@@H](O)CC([O-])=O)=C1C1=CC=C(F)C=C1 ZGGHKIMDNBDHJB-NRFPMOEYSA-M 0.000 description 1
- KJTLQQUUPVSXIM-ZCFIWIBFSA-M (R)-mevalonate Chemical compound OCC[C@](O)(C)CC([O-])=O KJTLQQUUPVSXIM-ZCFIWIBFSA-M 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 101710158485 3-hydroxy-3-methylglutaryl-coenzyme A reductase Proteins 0.000 description 1
- 241000187362 Actinomadura Species 0.000 description 1
- XUKUURHRXDUEBC-KAYWLYCHSA-N Atorvastatin Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-KAYWLYCHSA-N 0.000 description 1
- XUKUURHRXDUEBC-UHFFFAOYSA-N Atorvastatin Natural products C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CCC(O)CC(O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000235555 Cunninghamella Species 0.000 description 1
- KJTLQQUUPVSXIM-UHFFFAOYSA-N DL-mevalonic acid Natural products OCCC(O)(C)CC(O)=O KJTLQQUUPVSXIM-UHFFFAOYSA-N 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- PCZOHLXUXFIOCF-UHFFFAOYSA-N Monacolin X Natural products C12C(OC(=O)C(C)CC)CC(C)C=C2C=CC(C)C1CCC1CC(O)CC(=O)O1 PCZOHLXUXFIOCF-UHFFFAOYSA-N 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- RYMZZMVNJRMUDD-UHFFFAOYSA-N SJ000286063 Natural products C12C(OC(=O)C(C)(C)CC)CC(C)C=C2C=CC(C)C1CCC1CC(O)CC(=O)O1 RYMZZMVNJRMUDD-UHFFFAOYSA-N 0.000 description 1
- 235000019764 Soybean Meal Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000187180 Streptomyces sp. Species 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000003529 anticholesteremic agent Substances 0.000 description 1
- 230000003143 atherosclerotic effect Effects 0.000 description 1
- 229960005370 atorvastatin Drugs 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- VQODGRNSFPNSQE-DVTGEIKXSA-N betamethasone phosphate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)COP(O)(O)=O)(O)[C@@]1(C)C[C@@H]2O VQODGRNSFPNSQE-DVTGEIKXSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 229960005110 cerivastatin Drugs 0.000 description 1
- SEERZIQQUAZTOL-ANMDKAQQSA-N cerivastatin Chemical compound COCC1=C(C(C)C)N=C(C(C)C)C(\C=C\[C@@H](O)C[C@@H](O)CC(O)=O)=C1C1=CC=C(F)C=C1 SEERZIQQUAZTOL-ANMDKAQQSA-N 0.000 description 1
- 150000005829 chemical entities Chemical class 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 208000029078 coronary artery disease Diseases 0.000 description 1
- 231100000433 cytotoxic Toxicity 0.000 description 1
- 230000001472 cytotoxic effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- AIUDWMLXCFRVDR-UHFFFAOYSA-N dimethyl 2-(3-ethyl-3-methylpentyl)propanedioate Chemical class CCC(C)(CC)CCC(C(=O)OC)C(=O)OC AIUDWMLXCFRVDR-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940096118 ella Drugs 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229960003765 fluvastatin Drugs 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 238000009655 industrial fermentation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229960004844 lovastatin Drugs 0.000 description 1
- PCZOHLXUXFIOCF-BXMDZJJMSA-N lovastatin Chemical compound C([C@H]1[C@@H](C)C=CC2=C[C@H](C)C[C@@H]([C@H]12)OC(=O)[C@@H](C)CC)C[C@@H]1C[C@@H](O)CC(=O)O1 PCZOHLXUXFIOCF-BXMDZJJMSA-N 0.000 description 1
- QLJODMDSTUBWDW-UHFFFAOYSA-N lovastatin hydroxy acid Natural products C1=CC(C)C(CCC(O)CC(O)CC(O)=O)C2C(OC(=O)C(C)CC)CC(C)C=C21 QLJODMDSTUBWDW-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229950009116 mevastatin Drugs 0.000 description 1
- 239000013586 microbial product Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229940066779 peptones Drugs 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229940096701 plain lipid modifying drug hmg coa reductase inhibitors Drugs 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- VWBQYTRBTXKKOG-IYNICTALSA-M pravastatin sodium Chemical class [Na+].C1=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC([O-])=O)[C@H]2[C@@H](OC(=O)[C@@H](C)CC)C[C@H](O)C=C21 VWBQYTRBTXKKOG-IYNICTALSA-M 0.000 description 1
- 229960001495 pravastatin sodium Drugs 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229960002855 simvastatin Drugs 0.000 description 1
- RYMZZMVNJRMUDD-HGQWONQESA-N simvastatin Chemical compound C([C@H]1[C@@H](C)C=CC2=C[C@H](C)C[C@@H]([C@H]12)OC(=O)C(C)(C)CC)C[C@@H]1C[C@@H](O)CC(=O)O1 RYMZZMVNJRMUDD-HGQWONQESA-N 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- OOLLAFOLCSJHRE-ZHAKMVSLSA-N ulipristal acetate Chemical compound C1=CC(N(C)C)=CC=C1[C@@H]1C2=C3CCC(=O)C=C3CC[C@H]2[C@H](CC[C@]2(OC(C)=O)C(C)=O)[C@]2(C)C1 OOLLAFOLCSJHRE-ZHAKMVSLSA-N 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
- C07C69/33—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with hydroxy compounds having more than three hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/62—Carboxylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/14—All rings being cycloaliphatic
- C07C2602/26—All rings being cycloaliphatic the ring system containing ten carbon atoms
- C07C2602/28—Hydrogenated naphthalenes
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The invention relates to a fermentation process for the preparation of substantially pure pravastatin. The process provides a method of producing pravastatin by microbial hydroxylation of compactin (ML-236B) by maintaining a concentration of compactin at not less than 300 ~g /ml during the process. The process produces substantially pure pravastatin with reduced related impurities. The invention also relates to pharmaceutical compositions that include the substantially pure pravastatin.
Description
FERMENTATION PROCESS
FOR THE PREPARATION OF PRAVASTATIN
Field of the Invention The field of invention relates to a fermentation process for the preparation of substantially pure pravastatin. ~ The process provides a method of producing pravastatin by microbial hydroxylation of compactin (ML-236B) by maintaining a concentration of compactin at not less than 300 ~,g /ml during the process. The process produces substantially pure pravastatin with reduced related impurities. The invention also relates to pharmaceutical compositions that include the substantially pure pravastatin.
l0 Background of the Invention Hypercholesterolemia or elevated plasma cholesterol level has long been recognized as a major risk factor for atherosclerotic disease, and specifically for coronary heart disease. The biosynthesis of cholesterol is a major contributing factor to hypercholesterolemia. In the rate determining step of the biosyxithesis of cholesterol, 15 HMG-CoA reductase catalyzes the conversion of HMG-CoA to mevalonate. It was expected that plasma cholesterol could be reduced as a result of inhibition of HMG-CoA
reductase because more than 70% of the total input of body cholesterol is derived from de novo synthesis in humans.
Pravastatin, simvastatin, lovastatin, mevastatin, atorvastatin, fluvastatin, 20 cerivastatin and derivatives and analogues thereof are known as HMG-CoA
reductase inhibitors, and are used as antihypercholesterolemic agents.
During the past two decades, 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase) has been extensively studied. In 1975, compactin (ML-236B), a potent inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase was 25 discovered in the culture broth of Pehcilliufra citr~iyauf~a. After a thorough screening of hundreds of microbial products, as well as, chemically or biologically modified derivatives of ML-236B, pravastatin sodium was chosen as a candidate for development.
Pravastatin sodimn was chosen because of its stronger and more tissue-selective activity than the prototype compound.
Presently, the most economically feasible process for making pravastatin is by the microbial hydroxylation of compactin at C-6 position. Microbial hydroxylation of compactin to pravastatin can be accomplished to various extents with molds belonging to different genera, such as Mucof° Rlaizopus, Syncepl2alastruna, Cunninghamella, Mortie~ella and with filamentous bacteria belonging to different genera, such as Nocaf-dia, Actinomadura, Streptomyces, as described in various patents [U.S. Patent Nos.
5,179,013;
4,448,979; 4,346,227; 4,537,859; U.S. Patent Applications US2002/0081675A1;
US200110026934A1; Japanese Patent No. 58-10572; and European Patent No.
0605230].
The most common problem encountered in the commercial production of 1o pravastatin is that most microorganisms are not able to tolerate the compactin substrate fed even at low concentrations due to its cytotoxic effect. (Biotechnol. Bioeng., 42:815-820, 1993]. Taking into account the efficient manufacture of the active ingredient on an industrial scale, it is important to have a strain that is able to tolerate high concentrations of compactin, as well as, pravastatin.
15 Furthermore, the purity of the active ingredient is an important factor for the manufacturing of a safe and effective pharmaceutical product. Several structurally related products are sometimes produced during the fermentation processes, and often only one product is desired from a process, thereby requiring a method to control the ratio of these different analogues. A commercial process typically requires either exclusive or 2o predominant production of one product. V~hile the nature of polyketide synthase permits controlled biosynthesis of a single chemical entity, a significant number of polyketide synthases generate related products (J. Ind. Microbiol. Biotechnol., 27; 368-377, 2001).
However, the known methods of producing pravastatin are ill-suited for controlling the formation of these analogues.
25 Summary of the Invention In one general aspect there is provided a process for producing substantially pure pravastatin. The process includes culturing microorganisms under conditions capable of converting compactin to pravastatin by maintaining the concentration of compactin at a level of not less than about 300 ~.g /mL during the process.
30 The process is accomplished through the use of fermentation techniques known in the art, for example, the repeated fed-batch culture technique. The process may include periodically adding quantities of compactin in the culture broth during the fermentation to maintain the concentration of compactin at not less than about 300 ~,g /mL
during the process.
111 another embodiment, the concentration of compactin is maintained at a level within the range of about 300-900 ~,g /mL. This embodiment may result in an about 14-fold decrease in the amount of Impurity B of Formula III and an about 7-fold decrease in the amount of the compound of Formula IV.
The compactin used in this process may be in the form of a solution. The compactin solution may include soluble salts of compactin, for example, the sodium salt of to compactin. The compactin may be one or any of at least substantially purified compactin, semi-purified compactin and an intermediate compound produced during the synthesis of compactin.
The microorganisms may be any species of the genus S'tr~ept~rnyces. In one embodiment, the microorganism may be ~'ta~ept~nmyees eerrb~plailus. In other 15 embodiments, the microorganism may be a Stf-ept~rnyces ccrrb~p7ailus strain, variant or a mutant thereof.
The conditions capable of converting compactin to pravastatin include the fermentation production medium containing glucose at a concentration level of about 15-23 (g/L), Soya bean meal at a concentration level of about 25-38 (g/L), cottonseed meal at 2o a concentration level of about ?-4 (g/L), com steep liquor at a concentration level of about 5-8 (g/L), sodium chloride at a concentration level of about 5-6 (g/L) and calcium carbonate at a concentration level of about 2-3 (g/L).
The conditions capable of converting compactin to pravastatin may also include maintaining the temperature of the production medium at about 18 °C to about 50°C. In 25 another embodiment, the temperature is maintained at about 25 °C to about 30 °C.
The conditions capable of converting compactin to pravastatin may also include the maintenance of the pH of the production medium from about 5 to about 10.
In another embodiment, the pH is maintained from about 6 to about 8.5. In yet another embodiment, the pH may be maintained from about 7.3 to about 8Ø The conditions capable of converting compactin to pravastatin may also include agitation at about 100 to about 600 rpm. In one embodiment, the agitation may be at about 100 to about 350 rpm.
In one embodiment of the process, the percentage conversion of compactin to pravastatin is at least about 50% w/w as determined by HPLC. The percentage conversion may be at least about 65 to about 75% w/w, or at least about 70% w/w as determined by HPLC.
In another general aspect there is provided substantially pure pravastatin containing not more than about 0.12% w/w of Impurity B and not more than about 0.6%
w/w of 3"-hydroxy-pravastatin.
l0 In yet another general aspect there is provided a pharmaceutical composition that includes substantially pure pravastatin containing not more than about 0.12%
w/w of linpurity B and not more than about 0.6% w/w of 3"-hydroxy-pravastatin, and pharmaceutically acceptable excipients.
In another general aspect there is provided a method of treating 15 hypercholesterolemia. The method includes administering to a patient in need of treatment for hypercholesterolemia a pharmaceutical composition that includes substantially pure pravastatin containing not more than about 0.12% w/w of Impurity B
and not more than about 0.6% w/w of 3"-hydroxy-pravastatin, and other pharmaceutically acceptable excipients.
20 The details of one or more embodiments of the inventions are set forth in the description below. ~ther features, objects and advantages of the invention will be apparent from the description.
Detailed Description of the Invention The present invention provides an efficient process for the preparation of 25 substantially pure pravastatin of Formula I by microbial hydroxylation of compactin of Formula II. By maintaining the concentration of compactin at not less than 300 ~.g /ml throughout the process, the quantities of Impurity B and 3"-(S)-hydroxy pravastatin, of Formula III and IV respectively, are substantially reduced.
C02Na CH3 C02Na CHg H H OH
N ~ a H, OH H ; ', __. OH __. OH
H I .~ H H
O O
H I .. H
CH3 ~ CH3 13C.. H3C
H H
HO H
FORMULA I FORMULA II
H I H H OH H I H H OH
--~ OH ~ --~ OH
.~H H ~ .~H H
O O O O
I '~ H ~ OH ~ '' H OH
m>, H3G.~ H~ H >d< H3C.~ H~ H
HO H cH3 HO H CHg ~°~RI~iULA IIT ~"~ULA ~' Compactin is provided and contacted with whole cells of Strept~myces sp. under the conditions in which the microorganism converts compactin to pravastatin.
The process i5 may be carried out subsequent to or during the growth of the microorganism to be employed. The compactin substrate is placed in contact with the microorganisms and is converted to pravastatin. Compactin may be provided in the form of a solution comprising the sodium salt of compactin, and may be the purified, crude or intermediate stage of compactin.
2o The term "substantially pure pravastatin" as used herein is defined as pravastatin or a pharmaceutically acceptable salt thereof having a purity of not less than 99.3% w/w wherein the impurity B and 3"-hydroxypravastatin are not present at not more than about 0.12% w/w of Impurity B and not more than about 0.6% w/w of 3"-hydroxy-pravastatin as determined by HPLC.
25 The conversion of compactin to pravastatin can be done using fermentation techniques known in the art; for example, those of the types useful for large-scale industrial fermentation process, such as batch, fed-batch or continuous culture techniques.
For example, agitated liquid submerged culture techniques can be used.
The growth of the microorganism may be achieved through the use of an appropriate medium containing nutrients, such as carbon, nitrogen sources and trace elements, which are added to the culture medium. Suitable assimilable carbon sources include one or more of glucose, glycerol, maltose, dextrin, starch, sucrose etc. Suitable nitrogen sources include one or more of soybean meal, peptones, cottonseed meal, corn steep liquor, meat extract, yeast extract, ammonium sulfate, ammonium nitrate etc.
Suitable inorganic salts include one or more of sodium chloride, phosphates, calcium l0 carbonate etc.
Suitable seed medium may include glucose at concentrations of about 16-25 (g/L), I
Soya bean meal at concentrations of about 4-6 (g/L), peptone at concentrations of about 4-6 (g/L), potassium phosphate at concentrations of about 0.08-0.13 (g/L) and calcium carbonate at concentrations of about 4-6 (g/L). For example, the seed medium used can 15 comprise glucose at concentrations of about 20 (g/L), Soya bean meal at concentrations of about 5(g/L), peptone at concentrations of about 5 (g/L), potassium phosphate at concentrations of about 0.1 (g/L) and calcium carbonate at concentrations of about 5 (g/L).
Suitable production medium may include glucose at concentrations of about 15-(g/L), Soya bean aneal at concentrations of about 25-38 (g/L), cottonseed meal at 2o concentrations of about 2-4 (g/L), corn steep liquor at concentrations of about 5-8 (g/L), sodium chloride at concentrations of about 5-6 (g/L) and calcium carbonate at concentrations of about 2-3 (g/L). For example, the production medium used may include glucose at concentrations of about 18 (g/L), Soya bean meal at concentrations of about 30 (g/L), cottonseed meal at concentrations of about 3 (g/L), corn steep liquor at 25 concentrations of about 6 (g/L), sodium chloride at concentrations of about 6 (g/L) and calcium carbonate at concentrations of about 2.4 (g/L).
The incubation temperature can be about 18°C to about 50°C, for example, about 25°C to about 30°C or for example about 26°C to about 28°C. Suitable pH of the culture broth may range from about 5 to about 10, for example, about 6.0 to 8.5, or for example, 3o about 7.3 to about 8Ø The process may be carried out under aerobic conditions, such as by means of aeration and/or agitation. The fermentation broth may be agitated at about 100 to 600 rpm, for example, at about 100 to about 350 rpm or for example, at about 150 to 300 rpm.
The amount of compactin at the onset of the process can be, for example, in the range from about 300 ~,g/mL to about 1800 ~,g/mL of the culture medium, or for example, in the range of about 300 ~,g/mL to about 900 ~.g/mL.
The resulting substantially pure pravastatiri recovered from processes described herein contains not more than about 0.12% w/w of Impurity B and not more than about 0.6% w/w of 3"-hydroxy-pravastatin as determined by HPLC.
The substantially pure pravastatin can be formulated into a dosage form with other io pharmaceutically acceptable excipients. ~ptional excipients include, but are not limited to, one or more of colorants, diluents, lubricants, binders, disintergrants, and glidants.
Suitable dosage forms include one or more of tablets, capsules, dispersions, and liquids.
Any percentage of conversion of compactin to pravastatin can be practiced according to processes described herein, for example at least about 50% w/w, or for is example, at least about 60%w/w, or for example, about 65-75°/~ w/w.
While the present invention has been described in terms of its specific embodiments, certain modifications and equivalents will be apparent to those skilled in the art and are intended to be included within the scope of the present invention.
Examble 1: Bioconversion of Compactin to Pravastatin - ZJncontrolled Compactin 2o Concentration Level This example illustrates the bioconversion of compactin to pravastatin by Stf°ept~frayces ca~bophilus. The seed medium was inoculated with a slant culture at 28°C
for 2 days. 400 ml of mature seed culture was added to a 20 L production fermenter.
The components of the seed and production medium employed in these examples 25 are as follows:
A seed medium containing glucose 20 (g/L), Soya bean meal 5 (g/L), peptone 5 (g/L), potassium phosphate 0.1 (g/L) and calcium carbonate 5 (g/L) was inoculated with spores of Streptomyces sp. from a slant culture, and cultured at 500 rpm, 28°C for 2 days, to give a seed culture. 400 ml of this seed culture was added to 20-L
production fermenter _7-containing glucose 1 ~ (g/L), Soya bean meal 30, (g/L) cottonseed meal 3 (g/L), corn steep liquor 6 (g/L), sodium chloride 6 (g/L) and calcium carbonate 2.4 (g/L).
The medium was pre-sterilized at 121 °C for 30 minutes. After the growth of the microorganism, an initial shot of compactin was added to the fermenter to a level of 500 ~.g/ml and further cultured. Compactin was further added when the concentration of compactin level was less than 50 ~,g/ml. The rate of compactin bioconversion was monitored by HPLC. The percentage of conversion was calculated on the basis of compactin added and pravastatin produced. Concentrations (w/w) of Impurity B
and 3"S
hydroxy pravastatin were also determined by HPLC.
to The levels of impurity B and 3"S hydroxy pravastatin present were in the range of 0.9 to 1.27 °/~ w/w (Figure 1) and 1.84 to 2.96 % w/w (Figure 2), respectively, as determined by HPLC.
Example 2: Bioconversion of Compactin to Pravastatin - Controlled Compactin Concentration Level 15 The procedure of Example 1 was followed but the concentration of compactin was maintained between 300-900 ~g/ml throughout the batch as determined by HPLC.
Compactin was added when the concentration reached the lowest value in the range.
The concentration levels of impurity B and 3"S hydroxy pravastatin were in the range of 0.08 to 0.12% w/w and 0.4 to 0.6% w/w respectively. These values represent 2o about 14-fold and 7-fold lower impurity levels, respectively, as compared to the pravastatin obtained in Example 1 (Figures 1 and 2).
The resultant product of Example 2 was purified using an industrial scale recovery process detailed in PCT Patent Application W~ 01/44144. The purity of pravastatin obtained is about 99.4°/~ w/w as determined by HPLC.
25 Example 3: Kinetics of Compactin Bioconversion This example illustrates the kinetics of the conversion of compactin to pravastatin.
The medium and culture conditions employed were the same as in Example 1.
After 2 days of microorganism growth, presterilized compactin solution was added to the fermenter to a level of 300-900 ~,g/ml and further cultured. Compactin was further _g_ added so as to maintain the compactin concentration level at the prescribed range. The rate of compactin bioconversion at different time intervals was monitored for the next 6 days by HPLC. Percentage conversion was calculated on the basis of compactin charged and pravastatin produced. The concentration levels of Zinpurity B and 3"S
hydroxy pravastatin were also determined by HPLC. The data is provided in Figure 1 and Figure 2 respectively.
IMPURITY B
1.4 1.2 0.8 d ;~ 0.6 m 0.4 0 0.2 3"S HYDRO~PY PRAVASTATIN
c 2'.5 ~ 2 a 1.5 '° 1 0.5 v The results indicate that pravastatin is obtained with very low quantities of related compounds, Impurity B and 3"S hydroxy pravastatin, when the concentration of compactin was maintained between 300 and 900 ~,g/mL.
While several particular forms of the invention have been illustrated and described, it will be apparent that various modifications and combinations of the invention detailed in _ 9 ._ Days Uncontrolled C~ Controlled Days D Uncontrolled ~ Controlled the text can be made without departing from the spirit and scope of the invention. Further, it is contemplated that any single feature or any combination of optional features of the inventive variations described herein may be specifically excluded from the claimed invention and be so described as a negative limitation.
- to -
FOR THE PREPARATION OF PRAVASTATIN
Field of the Invention The field of invention relates to a fermentation process for the preparation of substantially pure pravastatin. ~ The process provides a method of producing pravastatin by microbial hydroxylation of compactin (ML-236B) by maintaining a concentration of compactin at not less than 300 ~,g /ml during the process. The process produces substantially pure pravastatin with reduced related impurities. The invention also relates to pharmaceutical compositions that include the substantially pure pravastatin.
l0 Background of the Invention Hypercholesterolemia or elevated plasma cholesterol level has long been recognized as a major risk factor for atherosclerotic disease, and specifically for coronary heart disease. The biosynthesis of cholesterol is a major contributing factor to hypercholesterolemia. In the rate determining step of the biosyxithesis of cholesterol, 15 HMG-CoA reductase catalyzes the conversion of HMG-CoA to mevalonate. It was expected that plasma cholesterol could be reduced as a result of inhibition of HMG-CoA
reductase because more than 70% of the total input of body cholesterol is derived from de novo synthesis in humans.
Pravastatin, simvastatin, lovastatin, mevastatin, atorvastatin, fluvastatin, 20 cerivastatin and derivatives and analogues thereof are known as HMG-CoA
reductase inhibitors, and are used as antihypercholesterolemic agents.
During the past two decades, 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase) has been extensively studied. In 1975, compactin (ML-236B), a potent inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase was 25 discovered in the culture broth of Pehcilliufra citr~iyauf~a. After a thorough screening of hundreds of microbial products, as well as, chemically or biologically modified derivatives of ML-236B, pravastatin sodium was chosen as a candidate for development.
Pravastatin sodimn was chosen because of its stronger and more tissue-selective activity than the prototype compound.
Presently, the most economically feasible process for making pravastatin is by the microbial hydroxylation of compactin at C-6 position. Microbial hydroxylation of compactin to pravastatin can be accomplished to various extents with molds belonging to different genera, such as Mucof° Rlaizopus, Syncepl2alastruna, Cunninghamella, Mortie~ella and with filamentous bacteria belonging to different genera, such as Nocaf-dia, Actinomadura, Streptomyces, as described in various patents [U.S. Patent Nos.
5,179,013;
4,448,979; 4,346,227; 4,537,859; U.S. Patent Applications US2002/0081675A1;
US200110026934A1; Japanese Patent No. 58-10572; and European Patent No.
0605230].
The most common problem encountered in the commercial production of 1o pravastatin is that most microorganisms are not able to tolerate the compactin substrate fed even at low concentrations due to its cytotoxic effect. (Biotechnol. Bioeng., 42:815-820, 1993]. Taking into account the efficient manufacture of the active ingredient on an industrial scale, it is important to have a strain that is able to tolerate high concentrations of compactin, as well as, pravastatin.
15 Furthermore, the purity of the active ingredient is an important factor for the manufacturing of a safe and effective pharmaceutical product. Several structurally related products are sometimes produced during the fermentation processes, and often only one product is desired from a process, thereby requiring a method to control the ratio of these different analogues. A commercial process typically requires either exclusive or 2o predominant production of one product. V~hile the nature of polyketide synthase permits controlled biosynthesis of a single chemical entity, a significant number of polyketide synthases generate related products (J. Ind. Microbiol. Biotechnol., 27; 368-377, 2001).
However, the known methods of producing pravastatin are ill-suited for controlling the formation of these analogues.
25 Summary of the Invention In one general aspect there is provided a process for producing substantially pure pravastatin. The process includes culturing microorganisms under conditions capable of converting compactin to pravastatin by maintaining the concentration of compactin at a level of not less than about 300 ~.g /mL during the process.
30 The process is accomplished through the use of fermentation techniques known in the art, for example, the repeated fed-batch culture technique. The process may include periodically adding quantities of compactin in the culture broth during the fermentation to maintain the concentration of compactin at not less than about 300 ~,g /mL
during the process.
111 another embodiment, the concentration of compactin is maintained at a level within the range of about 300-900 ~,g /mL. This embodiment may result in an about 14-fold decrease in the amount of Impurity B of Formula III and an about 7-fold decrease in the amount of the compound of Formula IV.
The compactin used in this process may be in the form of a solution. The compactin solution may include soluble salts of compactin, for example, the sodium salt of to compactin. The compactin may be one or any of at least substantially purified compactin, semi-purified compactin and an intermediate compound produced during the synthesis of compactin.
The microorganisms may be any species of the genus S'tr~ept~rnyces. In one embodiment, the microorganism may be ~'ta~ept~nmyees eerrb~plailus. In other 15 embodiments, the microorganism may be a Stf-ept~rnyces ccrrb~p7ailus strain, variant or a mutant thereof.
The conditions capable of converting compactin to pravastatin include the fermentation production medium containing glucose at a concentration level of about 15-23 (g/L), Soya bean meal at a concentration level of about 25-38 (g/L), cottonseed meal at 2o a concentration level of about ?-4 (g/L), com steep liquor at a concentration level of about 5-8 (g/L), sodium chloride at a concentration level of about 5-6 (g/L) and calcium carbonate at a concentration level of about 2-3 (g/L).
The conditions capable of converting compactin to pravastatin may also include maintaining the temperature of the production medium at about 18 °C to about 50°C. In 25 another embodiment, the temperature is maintained at about 25 °C to about 30 °C.
The conditions capable of converting compactin to pravastatin may also include the maintenance of the pH of the production medium from about 5 to about 10.
In another embodiment, the pH is maintained from about 6 to about 8.5. In yet another embodiment, the pH may be maintained from about 7.3 to about 8Ø The conditions capable of converting compactin to pravastatin may also include agitation at about 100 to about 600 rpm. In one embodiment, the agitation may be at about 100 to about 350 rpm.
In one embodiment of the process, the percentage conversion of compactin to pravastatin is at least about 50% w/w as determined by HPLC. The percentage conversion may be at least about 65 to about 75% w/w, or at least about 70% w/w as determined by HPLC.
In another general aspect there is provided substantially pure pravastatin containing not more than about 0.12% w/w of Impurity B and not more than about 0.6%
w/w of 3"-hydroxy-pravastatin.
l0 In yet another general aspect there is provided a pharmaceutical composition that includes substantially pure pravastatin containing not more than about 0.12%
w/w of linpurity B and not more than about 0.6% w/w of 3"-hydroxy-pravastatin, and pharmaceutically acceptable excipients.
In another general aspect there is provided a method of treating 15 hypercholesterolemia. The method includes administering to a patient in need of treatment for hypercholesterolemia a pharmaceutical composition that includes substantially pure pravastatin containing not more than about 0.12% w/w of Impurity B
and not more than about 0.6% w/w of 3"-hydroxy-pravastatin, and other pharmaceutically acceptable excipients.
20 The details of one or more embodiments of the inventions are set forth in the description below. ~ther features, objects and advantages of the invention will be apparent from the description.
Detailed Description of the Invention The present invention provides an efficient process for the preparation of 25 substantially pure pravastatin of Formula I by microbial hydroxylation of compactin of Formula II. By maintaining the concentration of compactin at not less than 300 ~.g /ml throughout the process, the quantities of Impurity B and 3"-(S)-hydroxy pravastatin, of Formula III and IV respectively, are substantially reduced.
C02Na CH3 C02Na CHg H H OH
N ~ a H, OH H ; ', __. OH __. OH
H I .~ H H
O O
H I .. H
CH3 ~ CH3 13C.. H3C
H H
HO H
FORMULA I FORMULA II
H I H H OH H I H H OH
--~ OH ~ --~ OH
.~H H ~ .~H H
O O O O
I '~ H ~ OH ~ '' H OH
m>, H3G.~ H~ H >d< H3C.~ H~ H
HO H cH3 HO H CHg ~°~RI~iULA IIT ~"~ULA ~' Compactin is provided and contacted with whole cells of Strept~myces sp. under the conditions in which the microorganism converts compactin to pravastatin.
The process i5 may be carried out subsequent to or during the growth of the microorganism to be employed. The compactin substrate is placed in contact with the microorganisms and is converted to pravastatin. Compactin may be provided in the form of a solution comprising the sodium salt of compactin, and may be the purified, crude or intermediate stage of compactin.
2o The term "substantially pure pravastatin" as used herein is defined as pravastatin or a pharmaceutically acceptable salt thereof having a purity of not less than 99.3% w/w wherein the impurity B and 3"-hydroxypravastatin are not present at not more than about 0.12% w/w of Impurity B and not more than about 0.6% w/w of 3"-hydroxy-pravastatin as determined by HPLC.
25 The conversion of compactin to pravastatin can be done using fermentation techniques known in the art; for example, those of the types useful for large-scale industrial fermentation process, such as batch, fed-batch or continuous culture techniques.
For example, agitated liquid submerged culture techniques can be used.
The growth of the microorganism may be achieved through the use of an appropriate medium containing nutrients, such as carbon, nitrogen sources and trace elements, which are added to the culture medium. Suitable assimilable carbon sources include one or more of glucose, glycerol, maltose, dextrin, starch, sucrose etc. Suitable nitrogen sources include one or more of soybean meal, peptones, cottonseed meal, corn steep liquor, meat extract, yeast extract, ammonium sulfate, ammonium nitrate etc.
Suitable inorganic salts include one or more of sodium chloride, phosphates, calcium l0 carbonate etc.
Suitable seed medium may include glucose at concentrations of about 16-25 (g/L), I
Soya bean meal at concentrations of about 4-6 (g/L), peptone at concentrations of about 4-6 (g/L), potassium phosphate at concentrations of about 0.08-0.13 (g/L) and calcium carbonate at concentrations of about 4-6 (g/L). For example, the seed medium used can 15 comprise glucose at concentrations of about 20 (g/L), Soya bean meal at concentrations of about 5(g/L), peptone at concentrations of about 5 (g/L), potassium phosphate at concentrations of about 0.1 (g/L) and calcium carbonate at concentrations of about 5 (g/L).
Suitable production medium may include glucose at concentrations of about 15-(g/L), Soya bean aneal at concentrations of about 25-38 (g/L), cottonseed meal at 2o concentrations of about 2-4 (g/L), corn steep liquor at concentrations of about 5-8 (g/L), sodium chloride at concentrations of about 5-6 (g/L) and calcium carbonate at concentrations of about 2-3 (g/L). For example, the production medium used may include glucose at concentrations of about 18 (g/L), Soya bean meal at concentrations of about 30 (g/L), cottonseed meal at concentrations of about 3 (g/L), corn steep liquor at 25 concentrations of about 6 (g/L), sodium chloride at concentrations of about 6 (g/L) and calcium carbonate at concentrations of about 2.4 (g/L).
The incubation temperature can be about 18°C to about 50°C, for example, about 25°C to about 30°C or for example about 26°C to about 28°C. Suitable pH of the culture broth may range from about 5 to about 10, for example, about 6.0 to 8.5, or for example, 3o about 7.3 to about 8Ø The process may be carried out under aerobic conditions, such as by means of aeration and/or agitation. The fermentation broth may be agitated at about 100 to 600 rpm, for example, at about 100 to about 350 rpm or for example, at about 150 to 300 rpm.
The amount of compactin at the onset of the process can be, for example, in the range from about 300 ~,g/mL to about 1800 ~,g/mL of the culture medium, or for example, in the range of about 300 ~,g/mL to about 900 ~.g/mL.
The resulting substantially pure pravastatiri recovered from processes described herein contains not more than about 0.12% w/w of Impurity B and not more than about 0.6% w/w of 3"-hydroxy-pravastatin as determined by HPLC.
The substantially pure pravastatin can be formulated into a dosage form with other io pharmaceutically acceptable excipients. ~ptional excipients include, but are not limited to, one or more of colorants, diluents, lubricants, binders, disintergrants, and glidants.
Suitable dosage forms include one or more of tablets, capsules, dispersions, and liquids.
Any percentage of conversion of compactin to pravastatin can be practiced according to processes described herein, for example at least about 50% w/w, or for is example, at least about 60%w/w, or for example, about 65-75°/~ w/w.
While the present invention has been described in terms of its specific embodiments, certain modifications and equivalents will be apparent to those skilled in the art and are intended to be included within the scope of the present invention.
Examble 1: Bioconversion of Compactin to Pravastatin - ZJncontrolled Compactin 2o Concentration Level This example illustrates the bioconversion of compactin to pravastatin by Stf°ept~frayces ca~bophilus. The seed medium was inoculated with a slant culture at 28°C
for 2 days. 400 ml of mature seed culture was added to a 20 L production fermenter.
The components of the seed and production medium employed in these examples 25 are as follows:
A seed medium containing glucose 20 (g/L), Soya bean meal 5 (g/L), peptone 5 (g/L), potassium phosphate 0.1 (g/L) and calcium carbonate 5 (g/L) was inoculated with spores of Streptomyces sp. from a slant culture, and cultured at 500 rpm, 28°C for 2 days, to give a seed culture. 400 ml of this seed culture was added to 20-L
production fermenter _7-containing glucose 1 ~ (g/L), Soya bean meal 30, (g/L) cottonseed meal 3 (g/L), corn steep liquor 6 (g/L), sodium chloride 6 (g/L) and calcium carbonate 2.4 (g/L).
The medium was pre-sterilized at 121 °C for 30 minutes. After the growth of the microorganism, an initial shot of compactin was added to the fermenter to a level of 500 ~.g/ml and further cultured. Compactin was further added when the concentration of compactin level was less than 50 ~,g/ml. The rate of compactin bioconversion was monitored by HPLC. The percentage of conversion was calculated on the basis of compactin added and pravastatin produced. Concentrations (w/w) of Impurity B
and 3"S
hydroxy pravastatin were also determined by HPLC.
to The levels of impurity B and 3"S hydroxy pravastatin present were in the range of 0.9 to 1.27 °/~ w/w (Figure 1) and 1.84 to 2.96 % w/w (Figure 2), respectively, as determined by HPLC.
Example 2: Bioconversion of Compactin to Pravastatin - Controlled Compactin Concentration Level 15 The procedure of Example 1 was followed but the concentration of compactin was maintained between 300-900 ~g/ml throughout the batch as determined by HPLC.
Compactin was added when the concentration reached the lowest value in the range.
The concentration levels of impurity B and 3"S hydroxy pravastatin were in the range of 0.08 to 0.12% w/w and 0.4 to 0.6% w/w respectively. These values represent 2o about 14-fold and 7-fold lower impurity levels, respectively, as compared to the pravastatin obtained in Example 1 (Figures 1 and 2).
The resultant product of Example 2 was purified using an industrial scale recovery process detailed in PCT Patent Application W~ 01/44144. The purity of pravastatin obtained is about 99.4°/~ w/w as determined by HPLC.
25 Example 3: Kinetics of Compactin Bioconversion This example illustrates the kinetics of the conversion of compactin to pravastatin.
The medium and culture conditions employed were the same as in Example 1.
After 2 days of microorganism growth, presterilized compactin solution was added to the fermenter to a level of 300-900 ~,g/ml and further cultured. Compactin was further _g_ added so as to maintain the compactin concentration level at the prescribed range. The rate of compactin bioconversion at different time intervals was monitored for the next 6 days by HPLC. Percentage conversion was calculated on the basis of compactin charged and pravastatin produced. The concentration levels of Zinpurity B and 3"S
hydroxy pravastatin were also determined by HPLC. The data is provided in Figure 1 and Figure 2 respectively.
IMPURITY B
1.4 1.2 0.8 d ;~ 0.6 m 0.4 0 0.2 3"S HYDRO~PY PRAVASTATIN
c 2'.5 ~ 2 a 1.5 '° 1 0.5 v The results indicate that pravastatin is obtained with very low quantities of related compounds, Impurity B and 3"S hydroxy pravastatin, when the concentration of compactin was maintained between 300 and 900 ~,g/mL.
While several particular forms of the invention have been illustrated and described, it will be apparent that various modifications and combinations of the invention detailed in _ 9 ._ Days Uncontrolled C~ Controlled Days D Uncontrolled ~ Controlled the text can be made without departing from the spirit and scope of the invention. Further, it is contemplated that any single feature or any combination of optional features of the inventive variations described herein may be specifically excluded from the claimed invention and be so described as a negative limitation.
- to -
Claims (25)
1. A process for producing substantially pure pravastatin, the process comprising culturing microorganisms under conditions capable of converting compactin to pravastatin by maintaining a concentration of compactin not less than 300 µg/mL
during the process.
during the process.
2. The process of claim 1, wherein the culturing of microorganisms comprises fermentation.
3. The process of claim 2, wherein the fermentation comprises a repeated fed-batch culture technique.
4. The process of claim 2, further comprising periodically adding quantities of compactin during the fermentation to maintain the concentration of compactin at not less than 300 µg/mL during the process.
5. The process of claim 4, wherein the concentration of compactin is maintained within the range of about 300-900 µg/mL.
6. The process of claim 4, wherein the compactin is in the form of a solution.
7. The process of claim 4, wherein the compactin comprises any soluble salt of compactor.
8. The process of claim 7, wherein the compactin solution comprises the sodium salt of compactin.
9. The process of claim 1, wherein the microorganism belongs to the Streptomyces genus.
10. The process of claim 9, wherein the microorganism is a Streptomyces carbophilus strain, variant or mutant thereof.
11. The process of claim 10, wherein the microorganism is a Streptomyces carbophilus strain.
12. The process of claim 1, wherein the conditions capable of converting compactin to pravastatin comprise a fermentation production medium comprising glucose at a concentration of about 15-23 (g/L), Soya bean meal at a concentration of about 38 (g/L), cottonseed meal at a concentration of about 2-4 (g/L), corn steep liquor at a concentration of about 5-8 (g/L), sodium chloride at a concentration of about 5-6 (g/L) and calcium carbonate at a concentration of about 2-3 (g/L).
13. The process of claim 12, wherein the conditions capable of converting compactin to pravastatin further comprise maintaining the temperature of the production medium at about 18°C to about 50°C.
14. The process of claim 13, wherein the temperature is maintained at about 25°C to about 30°C.
15. The process of claim 12, wherein the conditions capable of converting compactin to pravastatin further comprise maintaining pH of the production medium at about to about 10.
16. The process of claim 15, wherein the pH is maintained at about 6 to about 8.5.
17. The process of claim 15, wherein the pH is maintained at about 7.3 to about 8Ø
18. The process of claim 12, wherein the conditions capable of converting compactin to pravastatin further comprises agitation at about 100 to about 600 rpm.
19. The process of claim 18, wherein the agitation is at about 100 to about 350 rpm.
20. The process of claim 1, wherein at least 50% w/w of compactin is converted to pravastatin as determined by HPLC.
21. The process of claim 20, wherein the percentage conversion is at least about 65 to about 75% w/w.
22. The process of claim 20, wherein the percentage conversion is at least about 70%
w/w.
w/w.
23. Substantially pure pravastatin containing not more than about 0.12% w/w of the compound of Formula III and not more than about 0.6% w/w of 3"-hydroxy-pravastatin of the structure of Formula IV.
24. A pharmaceutical composition comprising substantially pure pravastatin, not more than about 0.12% w/w of the compound of Formula III, not more than about 0.6%
w/w of 3"-hydroxy-pravastatin of the structure of Formula IV, and pharmaceutically acceptable excipients.
w/w of 3"-hydroxy-pravastatin of the structure of Formula IV, and pharmaceutically acceptable excipients.
25. A method of treating hypercholesterolemia comprising administering to a patient in need of treatment for hypercholesterolemia a pharmaceutical composition comprising substantially pure pravastatin, not more than about 0.12% w/w of the compound of Formula III, not more than about 0.6% w/w of 3"-hydroxy-pravastatin of the structure of Formula IV, and pharmaceutically acceptable excipients.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN559DE2003 | 2003-04-01 | ||
IN559/DEL/2003 | 2003-04-01 | ||
PCT/IB2004/001003 WO2004087935A2 (en) | 2003-04-01 | 2004-04-01 | Fermentation process for the preparation of pravastatin |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2521276A1 true CA2521276A1 (en) | 2004-10-14 |
Family
ID=33104991
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002521276A Abandoned CA2521276A1 (en) | 2003-04-01 | 2004-04-01 | Fermentation process for the preparation of pravastatin |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1613760A2 (en) |
CA (1) | CA2521276A1 (en) |
WO (1) | WO2004087935A2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1953233A1 (en) | 2007-02-02 | 2008-08-06 | LEK Pharmaceuticals d.d. | Fermentation process for preparing pravastatin |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5942423A (en) * | 1995-06-07 | 1999-08-24 | Massachusetts Institute Of Technology | Conversion of compactin to pravastatin by actinomadura |
KR100210482B1 (en) * | 1997-04-10 | 1999-07-15 | 김종인 | Streptomyces exfoliatus yj-118 and process of pravastatin sodium |
SI20072A (en) * | 1998-09-18 | 2000-04-30 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | PROCEDURE OF PREPARATION OF INHIBITORS OF HMG-CoA REDUCTASE |
US6682913B1 (en) * | 1999-02-03 | 2004-01-27 | Institute For Drug Research Ltd. | Microbial process for preparing pravastatin |
JP3463875B2 (en) * | 2001-08-06 | 2003-11-05 | 三共株式会社 | How to purify pravastatin |
-
2004
- 2004-04-01 WO PCT/IB2004/001003 patent/WO2004087935A2/en not_active Application Discontinuation
- 2004-04-01 CA CA002521276A patent/CA2521276A1/en not_active Abandoned
- 2004-04-01 EP EP04725114A patent/EP1613760A2/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
WO2004087935A3 (en) | 2005-01-13 |
WO2004087935A2 (en) | 2004-10-14 |
EP1613760A2 (en) | 2006-01-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0833938B1 (en) | Reduction of ketone groups | |
JPH067176A (en) | Novel fermentation of triol acid i by mutagenic strain of aspergillus terreus | |
EP2019869B1 (en) | Fermentative production of lipstatin | |
US6682913B1 (en) | Microbial process for preparing pravastatin | |
AU774438B2 (en) | Microbial process for preparing pravastatin | |
JP3683606B2 (en) | Method for producing enzymatic hydroxylation of HMG-CoA reductase inhibitor and its intermediate | |
US5409820A (en) | Process for the production of lovastatin using Coniothyrium fuckelii | |
CA2521276A1 (en) | Fermentation process for the preparation of pravastatin | |
WO2008092950A1 (en) | Fermentation process for preparing pravastatin | |
EP0975789A1 (en) | Nitrogen feed in statin fermentation | |
US6197560B1 (en) | Metabolic controlled fermentation procedure for the manufacture of lovastatin hydroxy acid | |
JPH02245191A (en) | Preparation of 6-alpha-hydroxymethyl phobastatin | |
JP4045403B2 (en) | Method for producing hydroxy fatty acid and γ-lactone | |
US6500651B1 (en) | Metabolic controlled fermentation procedure for the manufacture of lovastatin hydroxy acid | |
US5639643A (en) | Preparation of 3-hydroxyphenylacetic acid | |
JP2004115380A (en) | New mevastatin derivative and method for producing the same | |
JP2004196680A (en) | New fki-0929 substance and its production method | |
EP1491522A1 (en) | Microbial process for preparing pravastatin | |
CA2572473A1 (en) | Sodium salt of pravastatin in crystalline form |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Dead |