RU98108032A - NEW LIQUID STABLE COMPOSITIONS BASED ON PARACETAMOL AND METHOD FOR PRODUCING THEM - Google Patents
NEW LIQUID STABLE COMPOSITIONS BASED ON PARACETAMOL AND METHOD FOR PRODUCING THEMInfo
- Publication number
- RU98108032A RU98108032A RU98108032/14A RU98108032A RU98108032A RU 98108032 A RU98108032 A RU 98108032A RU 98108032/14 A RU98108032/14 A RU 98108032/14A RU 98108032 A RU98108032 A RU 98108032A RU 98108032 A RU98108032 A RU 98108032A
- Authority
- RU
- Russia
- Prior art keywords
- paracetamol
- stable liquid
- new stable
- compositions based
- liquid compositions
- Prior art date
Links
- RZVAJINKPMORJF-UHFFFAOYSA-N p-acetaminophenol Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 title claims 31
- 229960005489 paracetamol Drugs 0.000 title claims 31
- 239000000203 mixture Substances 0.000 title claims 29
- 239000007788 liquid Substances 0.000 title claims 28
- 238000004519 manufacturing process Methods 0.000 title 1
- BQJCRHHNABKAKU-KBQPJGBKSA-N Morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 claims 5
- 239000003125 aqueous solvent Substances 0.000 claims 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 4
- 229930014694 morphine Natural products 0.000 claims 4
- 229960005181 morphine Drugs 0.000 claims 4
- 125000003396 thiol group Chemical group [H]S* 0.000 claims 4
- 150000000996 L-ascorbic acids Chemical group 0.000 claims 3
- 230000000202 analgesic Effects 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 239000000243 solution Substances 0.000 claims 3
- OROGSEYTTFOCAN-DNJOTXNNSA-N Codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 claims 2
- 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 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- -1 alkali metal ascorbates Chemical class 0.000 claims 2
- 239000002260 anti-inflammatory agent Substances 0.000 claims 2
- 229940121363 anti-inflammatory agents Drugs 0.000 claims 2
- 235000010323 ascorbic acid Nutrition 0.000 claims 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 150000002894 organic compounds Chemical group 0.000 claims 2
- 239000002516 radical scavenger Substances 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- CIWBSHSKHKDKBQ-DUZGATOHSA-N (+)-Ascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims 1
- VHJLVAABSRFDPM-UHFFFAOYSA-N 1,4-dimercaptobutane-2,3-diol Chemical compound SCC(O)C(O)CS VHJLVAABSRFDPM-UHFFFAOYSA-N 0.000 claims 1
- DTTDXHDYTWQDCS-UHFFFAOYSA-N 1-phenylcyclohexan-1-ol Chemical class C=1C=CC=CC=1C1(O)CCCCC1 DTTDXHDYTWQDCS-UHFFFAOYSA-N 0.000 claims 1
- LLSKXGRDUPMXLC-UHFFFAOYSA-N 1-phenylpiperidine Chemical class C1CCCCN1C1=CC=CC=C1 LLSKXGRDUPMXLC-UHFFFAOYSA-N 0.000 claims 1
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 claims 1
- KDHYZCWXWUZIPR-UHFFFAOYSA-N 2-phenyl-1H-azepine Chemical class N1C=CC=CC=C1C1=CC=CC=C1 KDHYZCWXWUZIPR-UHFFFAOYSA-N 0.000 claims 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N 3-Mercaptopropane-1,2-diol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 claims 1
- 229960004308 ACETYLCYSTEINE Drugs 0.000 claims 1
- 229960002433 Cysteine Drugs 0.000 claims 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 claims 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
- FBPFZTCFMRRESA-KAZBKCHUSA-N D-Mannitol Natural products OC[C@@H](O)[C@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KAZBKCHUSA-N 0.000 claims 1
- CIWBSHSKHKDKBQ-MVHIGOERSA-N D-ascorbic acid Chemical compound OC[C@@H](O)[C@@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-MVHIGOERSA-N 0.000 claims 1
- RWSXRVCMGQZWBV-WDSKDSINSA-N Glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 claims 1
- 229960003180 Glutathione Drugs 0.000 claims 1
- 108010024636 Glutathione Proteins 0.000 claims 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N Inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims 1
- 229960000367 Inositol Drugs 0.000 claims 1
- DKYWVDODHFEZIM-UHFFFAOYSA-N Ketoprofen Chemical group OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 claims 1
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 claims 1
- 235000000069 L-ascorbic acid Nutrition 0.000 claims 1
- 239000002211 L-ascorbic acid Substances 0.000 claims 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims 1
- 229960004635 Mesna Drugs 0.000 claims 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N Thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N Thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Vitamin C Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 239000001961 anticonvulsive agent Substances 0.000 claims 1
- 239000002111 antiemetic agent Substances 0.000 claims 1
- 229960005070 ascorbic acid Drugs 0.000 claims 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M buffer Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims 1
- 239000007853 buffer solution Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 229960004126 codeine Drugs 0.000 claims 1
- ZNEWHQLOPFWXOF-UHFFFAOYSA-N coenzyme M Chemical compound OS(=O)(=O)CCS ZNEWHQLOPFWXOF-UHFFFAOYSA-N 0.000 claims 1
- 239000008139 complexing agent Substances 0.000 claims 1
- 239000003246 corticosteroid Substances 0.000 claims 1
- 235000018417 cysteine Nutrition 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000011261 inert gas Substances 0.000 claims 1
- 229960000991 ketoprofen Drugs 0.000 claims 1
- 239000000594 mannitol Substances 0.000 claims 1
- 235000010355 mannitol Nutrition 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 238000007911 parenteral administration Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000000600 sorbitol Substances 0.000 claims 1
- 239000003029 tricyclic antidepressant agent Substances 0.000 claims 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N β-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 claims 1
Claims (27)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9609858A FR2751875B1 (en) | 1996-08-05 | 1996-08-05 | NOVEL STABLE LIQUID FORMULATIONS BASED ON PARACETAMOL AND THEIR METHOD OF PREPARATION |
FR9609858 | 1996-08-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU98108032A true RU98108032A (en) | 2000-05-20 |
RU2192249C2 RU2192249C2 (en) | 2002-11-10 |
Family
ID=9494820
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU98108032/14A RU2192249C2 (en) | 1996-08-05 | 1997-08-05 | Paracetamol-base liquid stable composition and method of its preparing |
Country Status (23)
Country | Link |
---|---|
US (1) | US6028222A (en) |
EP (1) | EP0858329B1 (en) |
JP (2) | JP5060681B2 (en) |
KR (1) | KR100521235B1 (en) |
CN (1) | CN1133426C (en) |
AP (1) | AP957A (en) |
AT (1) | ATE241972T1 (en) |
AU (1) | AU742576B2 (en) |
BR (1) | BR9702362A (en) |
CA (1) | CA2233924C (en) |
CZ (1) | CZ298427B6 (en) |
DE (1) | DE69722580T2 (en) |
DK (1) | DK0858329T3 (en) |
ES (1) | ES2201316T3 (en) |
FR (1) | FR2751875B1 (en) |
HU (1) | HU226117B1 (en) |
MX (1) | MX9802734A (en) |
NZ (1) | NZ330136A (en) |
OA (1) | OA10678A (en) |
PL (1) | PL193104B1 (en) |
PT (1) | PT858329E (en) |
RU (1) | RU2192249C2 (en) |
WO (1) | WO1998005314A1 (en) |
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EP0620001A1 (en) * | 1993-04-16 | 1994-10-19 | McNEIL-PPC, INC. | Aqueous pharmaceutical suspension and process for preparation thereof |
DE4327462A1 (en) * | 1993-08-16 | 1995-02-23 | Carl Heinrich Dr Weischer | N-Acetyl-p-aminophenol derivatives for controlling pain |
JPH07206689A (en) * | 1994-01-21 | 1995-08-08 | Barnett Lab Ltd | Curing composition and use of this composition for curing crapulence |
SK96196A3 (en) * | 1994-01-24 | 1997-03-05 | Procter & Gamble | Process for solubilizing difficultly soluble pharmaceutical actives |
US5510389A (en) * | 1994-03-02 | 1996-04-23 | The Procter & Gamble Company | Concentrated acetaminophen solution compositions |
JPH09286724A (en) * | 1996-04-19 | 1997-11-04 | Takeda Chem Ind Ltd | Liquid stablizer for oral administration |
-
1996
- 1996-08-05 FR FR9609858A patent/FR2751875B1/en not_active Expired - Fee Related
-
1997
- 1997-08-05 PT PT97936739T patent/PT858329E/en unknown
- 1997-08-05 AP APAP/P/1998/001223A patent/AP957A/en active
- 1997-08-05 AT AT97936739T patent/ATE241972T1/en active
- 1997-08-05 DE DE69722580T patent/DE69722580T2/en not_active Expired - Lifetime
- 1997-08-05 CA CA2233924A patent/CA2233924C/en not_active Expired - Lifetime
- 1997-08-05 US US09/051,246 patent/US6028222A/en not_active Expired - Lifetime
- 1997-08-05 EP EP97936739A patent/EP0858329B1/en not_active Expired - Lifetime
- 1997-08-05 BR BR9702362-0A patent/BR9702362A/en not_active IP Right Cessation
- 1997-08-05 NZ NZ330136A patent/NZ330136A/en not_active IP Right Cessation
- 1997-08-05 WO PCT/FR1997/001452 patent/WO1998005314A1/en active IP Right Grant
- 1997-08-05 ES ES97936739T patent/ES2201316T3/en not_active Expired - Lifetime
- 1997-08-05 DK DK97936739T patent/DK0858329T3/en active
- 1997-08-05 CN CNB971913714A patent/CN1133426C/en not_active Expired - Lifetime
- 1997-08-05 AU AU39451/97A patent/AU742576B2/en not_active Expired
- 1997-08-05 RU RU98108032/14A patent/RU2192249C2/en active
- 1997-08-05 JP JP50768698A patent/JP5060681B2/en not_active Expired - Lifetime
- 1997-08-05 KR KR1019980702453A patent/KR100521235B1/en not_active IP Right Cessation
- 1997-08-05 HU HU9901893A patent/HU226117B1/en unknown
- 1997-08-05 PL PL326069A patent/PL193104B1/en unknown
- 1997-08-05 CZ CZ0104898A patent/CZ298427B6/en not_active IP Right Cessation
-
1998
- 1998-04-03 MX MX9802734A patent/MX9802734A/en unknown
- 1998-04-03 OA OA9800039A patent/OA10678A/en unknown
-
2010
- 2010-04-28 JP JP2010104213A patent/JP5122604B2/en not_active Expired - Lifetime
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