RU2009127302A - Способ изготовления твердого, орально применимого фармацевтического состава - Google Patents
Способ изготовления твердого, орально применимого фармацевтического состава Download PDFInfo
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- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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Abstract
1. Твердый, орально применимый фармацевтический состав, содержащий гидролизованную форму 5-хлор-N-({(5S)-2-оксо-3-[4-(3-оксо-4-морфолинил)фенил]-1,3-оксазолидин-5-ил}метил)-2-тиофенкарбокс-амида (I). ! 2. Фармацевтический состав по п.1, содержащий действующее вещество (I) в кристаллической форме. ! 3. Фармацевтический состав по п.2, содержащий действующее вещество (I) в микрокристаллической форме. ! 4. Фармацевтический состав по одному из пп.1-3, отличающийся тем, что действующее вещество (I) содержится в концентрации от 1 до 60% в пересчете на общую массу препарата. ! 5. Фармацевтический состав по одному из пп.1-3, содержащий в качестве смачивающего средства лаурилсульфат натрия. ! 6. Фармацевтический состав по п.4, содержащий в качестве смачивающего средства лаурилсульфат натрия. !7. Фармацевтический состав по п.5, содержащий лаурилсульфат натрия в концентрации от 0,1 до 5% в пересчете на общую массу. ! 8. Фармацевтический состав по п.6, содержащий лаурилсульфат натрия в концентрации от 0,1 до 5% в пересчете на общую массу. ! 9. Фармацевтический состав по одному из пп.1-3 или 6-8, содержащий в качестве гидрофильного связующего гидроксипропилметилцеллюлозу. ! 10. Фармацевтический состав по п.4, содержащий в качестве гидрофильного связующего гидроксипропилметилцеллюлозу. ! 11. Фармацевтический состав по п.5, содержащий в качестве гидрофильного связующего гидроксипропилметилцеллюлозу. ! 12. Фармацевтический состав по п.9, содержащий гидроксипропилметилцеллюлозу в концентрации от 1 до 15% в пересчете на общую массу. ! 13. Фармацевтический состав по п.9, содержащий гидроксипропилметилцеллюлозу в концентрации от 1 до 15% в пересчете на общую массу. ! 14. Фармацевтич�
Claims (17)
1. Твердый, орально применимый фармацевтический состав, содержащий гидролизованную форму 5-хлор-N-({(5S)-2-оксо-3-[4-(3-оксо-4-морфолинил)фенил]-1,3-оксазолидин-5-ил}метил)-2-тиофенкарбокс-амида (I).
2. Фармацевтический состав по п.1, содержащий действующее вещество (I) в кристаллической форме.
3. Фармацевтический состав по п.2, содержащий действующее вещество (I) в микрокристаллической форме.
4. Фармацевтический состав по одному из пп.1-3, отличающийся тем, что действующее вещество (I) содержится в концентрации от 1 до 60% в пересчете на общую массу препарата.
5. Фармацевтический состав по одному из пп.1-3, содержащий в качестве смачивающего средства лаурилсульфат натрия.
6. Фармацевтический состав по п.4, содержащий в качестве смачивающего средства лаурилсульфат натрия.
7. Фармацевтический состав по п.5, содержащий лаурилсульфат натрия в концентрации от 0,1 до 5% в пересчете на общую массу.
8. Фармацевтический состав по п.6, содержащий лаурилсульфат натрия в концентрации от 0,1 до 5% в пересчете на общую массу.
9. Фармацевтический состав по одному из пп.1-3 или 6-8, содержащий в качестве гидрофильного связующего гидроксипропилметилцеллюлозу.
10. Фармацевтический состав по п.4, содержащий в качестве гидрофильного связующего гидроксипропилметилцеллюлозу.
11. Фармацевтический состав по п.5, содержащий в качестве гидрофильного связующего гидроксипропилметилцеллюлозу.
12. Фармацевтический состав по п.9, содержащий гидроксипропилметилцеллюлозу в концентрации от 1 до 15% в пересчете на общую массу.
13. Фармацевтический состав по п.9, содержащий гидроксипропилметилцеллюлозу в концентрации от 1 до 15% в пересчете на общую массу.
14. Фармацевтический состав по п.11, содержащий гидроксипропилметилцеллюлозу в концентрации от 1 до 15% в пересчете на общую массу.
15. Фармацевтический состав по п.1 в форме таблетки.
16. Фармацевтический состав по п.15 в форме быстро высвобождающей действующее вещество таблетки.
17. Фармацевтический состав по п.15 или 16, отличающийся тем, что таблетка покрыта лаком.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10355461.0 | 2003-11-27 | ||
DE10355461A DE10355461A1 (de) | 2003-11-27 | 2003-11-27 | Verfahren zur Herstellung einer festen, oral applizierbaren pharmazeutischen Zusammensetzung |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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RU2006122599/15A Division RU2379036C2 (ru) | 2003-11-27 | 2004-11-13 | Способ изготовления твердого, орально применимого фармацевтического состава |
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RU2009127302A true RU2009127302A (ru) | 2011-01-27 |
RU2493850C2 RU2493850C2 (ru) | 2013-09-27 |
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RU2006122599/15A RU2379036C2 (ru) | 2003-11-27 | 2004-11-13 | Способ изготовления твердого, орально применимого фармацевтического состава |
RU2009127302/15A RU2493850C2 (ru) | 2003-11-27 | 2009-07-16 | Способ изготовления твердого, орально применимого фармацевтического состава |
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RU2006122599/15A RU2379036C2 (ru) | 2003-11-27 | 2004-11-13 | Способ изготовления твердого, орально применимого фармацевтического состава |
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US (4) | US20080026057A1 (ru) |
EP (1) | EP1689370B2 (ru) |
JP (1) | JP4852423B2 (ru) |
KR (1) | KR101151117B1 (ru) |
CN (1) | CN1886120B (ru) |
AR (2) | AR047844A1 (ru) |
AT (1) | ATE385782T1 (ru) |
AU (1) | AU2004305226B2 (ru) |
BR (1) | BRPI0416404B8 (ru) |
CA (1) | CA2547113C (ru) |
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CU (1) | CU23551B7 (ru) |
CY (1) | CY1107369T1 (ru) |
DE (2) | DE10355461A1 (ru) |
DK (1) | DK1689370T4 (ru) |
EC (1) | ECSP066584A (ru) |
ES (1) | ES2300845T5 (ru) |
GT (1) | GT200400239A (ru) |
HK (1) | HK1099518A1 (ru) |
HN (1) | HN2004000490A (ru) |
HR (1) | HRP20080150T4 (ru) |
IL (1) | IL175860B2 (ru) |
MA (1) | MA28178A1 (ru) |
MY (1) | MY138386A (ru) |
NO (1) | NO340156B1 (ru) |
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PE (1) | PE20050666A1 (ru) |
PL (1) | PL1689370T5 (ru) |
PT (1) | PT1689370E (ru) |
RU (2) | RU2379036C2 (ru) |
SI (2) | SI1689370T2 (ru) |
TW (1) | TWI356702B (ru) |
UA (1) | UA85693C2 (ru) |
WO (1) | WO2005060940A2 (ru) |
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Families Citing this family (74)
Publication number | Priority date | Publication date | Assignee | Title |
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DE19962924A1 (de) | 1999-12-24 | 2001-07-05 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
DE10129725A1 (de) * | 2001-06-20 | 2003-01-02 | Bayer Ag | Kombinationstherapie substituierter Oxazolidinone |
DE10300111A1 (de) * | 2003-01-07 | 2004-07-15 | Bayer Healthcare Ag | Verfahren zur Herstellung von 5-Chlor-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)-phenyl]-1,3-oxazolidin-5-yl}-methyl)-2-thiophencarboxamid |
DE10355461A1 (de) | 2003-11-27 | 2005-06-23 | Bayer Healthcare Ag | Verfahren zur Herstellung einer festen, oral applizierbaren pharmazeutischen Zusammensetzung |
DE102004062475A1 (de) * | 2004-12-24 | 2006-07-06 | Bayer Healthcare Ag | Feste, oral applizierbare pharmazeutische Darreichungsformen mit modifizierter Freisetzung |
EP1685841A1 (en) | 2005-01-31 | 2006-08-02 | Bayer Health Care Aktiengesellschaft | Prevention and treatment of thromboembolic disorders |
DE102005045518A1 (de) | 2005-09-23 | 2007-03-29 | Bayer Healthcare Ag | 2-Aminoethoxyessigsäure-Derivate und ihre Verwendung |
KR101364400B1 (ko) | 2005-10-04 | 2014-02-17 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 5-클로로-n-({(5s)-2-옥소-3-[4-(3-옥소-4-모르폴리닐)-페닐]-1,3-옥사졸리딘-5-일}-메틸)-2-티오펜 카르복사미드의 신규 다형체 및 무정형 형태 |
DE102005047558A1 (de) * | 2005-10-04 | 2008-02-07 | Bayer Healthcare Ag | Kombinationstherapie substituierter Oxazolidinone zur Prophylaxe und Behandlung von cerebralen Durchblutungsstörungen |
DE102005047561A1 (de) * | 2005-10-04 | 2007-04-05 | Bayer Healthcare Ag | Feste, oral applizierbare pharmazeutische Darreichungsformen mit schneller Wirkstofffreisetzung |
DE102006007146A1 (de) | 2006-02-16 | 2007-08-23 | Bayer Healthcare Ag | Aminoacyl-Prodrugs |
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EP1685841A1 (en) | 2005-01-31 | 2006-08-02 | Bayer Health Care Aktiengesellschaft | Prevention and treatment of thromboembolic disorders |
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KR101364400B1 (ko) | 2005-10-04 | 2014-02-17 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 5-클로로-n-({(5s)-2-옥소-3-[4-(3-옥소-4-모르폴리닐)-페닐]-1,3-옥사졸리딘-5-일}-메틸)-2-티오펜 카르복사미드의 신규 다형체 및 무정형 형태 |
DE102005048824A1 (de) | 2005-10-10 | 2007-04-12 | Bayer Healthcare Ag | Behandlung und Prophylaxe von Mikroangiopathien |
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DE102006051625A1 (de) | 2006-11-02 | 2008-05-08 | Bayer Materialscience Ag | Kombinationstherapie substituierter Oxazolidinone |
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