AU3345197A - Stable drug form for oral administration with benzimidazole derivatives as active ingredient and process for the preparation thereof - Google Patents
Stable drug form for oral administration with benzimidazole derivatives as active ingredient and process for the preparation thereofInfo
- Publication number
- AU3345197A AU3345197A AU33451/97A AU3345197A AU3345197A AU 3345197 A AU3345197 A AU 3345197A AU 33451/97 A AU33451/97 A AU 33451/97A AU 3345197 A AU3345197 A AU 3345197A AU 3345197 A AU3345197 A AU 3345197A
- Authority
- AU
- Australia
- Prior art keywords
- drug form
- preparation
- stable drug
- oral administration
- active ingredient
- 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5084—Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs
Abstract
The invention relates to a stable drug form which is for oral administration and comprises: (a) a core comprising one or more active ingredients which are not to be released until after they have passed through the stomach, together with conventional pharmaceutical adjuvants, (b) an intermediate layer applied to the core, and (c) an external layer which is resistant to gastric juice. The intermediate layer in (b) is in the form of a reactive layer comprising a polymeric layered material which is partly neutralised with alkalis, is resistant to gastric juice and has cation-exchanger capacity. A process for the preparation of the stable drug form is also disclosed.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19626045A DE19626045C2 (en) | 1996-06-28 | 1996-06-28 | A stable dosage form for oral administration containing omeprazole as the active ingredient and methods of making the same |
DE19626045 | 1996-06-28 | ||
PCT/EP1997/003387 WO1998000114A2 (en) | 1996-06-28 | 1997-06-27 | Stable drug form for oral administration with benzimidazole derivatives as active ingredient and process for the preparation thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
AU3345197A true AU3345197A (en) | 1998-01-21 |
Family
ID=7798347
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU34388/97A Abandoned AU3438897A (en) | 1996-06-28 | 1997-06-27 | Stable drug form for oral administration and process for the preparation thereof |
AU33451/97A Abandoned AU3345197A (en) | 1996-06-28 | 1997-06-27 | Stable drug form for oral administration with benzimidazole derivatives as active ingredient and process for the preparation thereof |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU34388/97A Abandoned AU3438897A (en) | 1996-06-28 | 1997-06-27 | Stable drug form for oral administration and process for the preparation thereof |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0934058B1 (en) |
JP (1) | JP4641075B2 (en) |
AT (1) | ATE247457T1 (en) |
AU (2) | AU3438897A (en) |
CA (1) | CA2258918C (en) |
DE (2) | DE19626045C2 (en) |
DK (1) | DK0934058T3 (en) |
ES (1) | ES2205243T3 (en) |
PT (1) | PT934058E (en) |
WO (2) | WO1998000115A2 (en) |
ZA (2) | ZA975827B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2004258984B2 (en) * | 2003-07-23 | 2011-02-10 | Santarus, Inc. | Immediate-release formulation of acid-labile pharmaceutical compositions |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6489346B1 (en) | 1996-01-04 | 2002-12-03 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
US5840737A (en) | 1996-01-04 | 1998-11-24 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
SE9704869D0 (en) * | 1997-12-22 | 1997-12-22 | Astra Ab | New pharmaceutical formulaton II |
UA73092C2 (en) * | 1998-07-17 | 2005-06-15 | Брістол-Майерс Сквібб Компані | Tablets with enteric coating and method for their manufacture |
PT1105105E (en) | 1998-08-12 | 2006-07-31 | Altana Pharma Ag | METHOD OF ORAL ADMINISTRATION FOR PYRIDIN-2-ILMETILSULFINYL-1H-BENZIMIDAZOIS |
DE19845358A1 (en) * | 1998-10-02 | 2000-04-06 | Roehm Gmbh | Coated drug forms with controlled drug delivery |
IL130602A0 (en) | 1999-06-22 | 2000-06-01 | Dexcel Ltd | Stable benzimidazole formulation |
US6420473B1 (en) * | 2000-02-10 | 2002-07-16 | Bpsi Holdings, Inc. | Acrylic enteric coating compositions |
AR030557A1 (en) | 2000-04-14 | 2003-08-27 | Jagotec Ag | A TABLET IN MULTI-MAP OF CONTROLLED RELEASE AND TREATMENT METHOD |
US7316819B2 (en) * | 2001-03-08 | 2008-01-08 | Unigene Laboratories, Inc. | Oral peptide pharmaceutical dosage form and method of production |
KR100479637B1 (en) * | 2002-02-01 | 2005-03-31 | 한국화학연구원 | Oral dosage form comprising Lansoprazole and preparation method for the same |
DE10235475B4 (en) * | 2002-08-02 | 2006-04-27 | Ratiopharm Gmbh | Medicaments containing a benzimidazole compound in admixture with microcrystalline cellulose and process for their preparation |
RU2332237C2 (en) | 2002-08-02 | 2008-08-27 | Рациофарм Гмбх | Pharmaceutical drug containing benzymidazol derivative mixed with microcrystal cellulose, and method of its obtaining |
US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
PE20050496A1 (en) * | 2003-07-24 | 2005-06-12 | Smithkline Beecham Corp | FILMS THAT DISSOLVE BY ORAL ROUTE |
EP1721604A4 (en) * | 2004-03-04 | 2008-04-30 | Takeda Pharmaceutical | Stable capsule preparation |
US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
MX2007008141A (en) * | 2005-01-03 | 2007-12-10 | Lupin Ltd | Pharmaceutical composition of acid labile substances. |
DE102005032806A1 (en) * | 2005-07-12 | 2007-01-18 | Röhm Gmbh | Use of a partially neutralized, anionic (meth) acrylate copolymer as a coating for the preparation of a dosage form with a release of active ingredient at reduced pH values |
DE102006006532B4 (en) * | 2006-02-10 | 2007-11-08 | Biogenerics Pharma Gmbh | Pharmaceutical preparation |
WO2008135090A1 (en) | 2007-05-07 | 2008-11-13 | Evonik Röhm Gmbh | Solid dosage forms comprising an enteric coating with accelerated drug release |
DE102008056312A1 (en) | 2008-11-07 | 2010-05-12 | Biogenerics Pharma Gmbh | Use of micro-tablets as food and feed additive |
DE102010052847A1 (en) * | 2010-11-29 | 2012-05-31 | Temmler Werke Gmbh | Process for the preparation of a PPI-containing pharmaceutical preparation |
US8951996B2 (en) * | 2011-07-28 | 2015-02-10 | Lipocine Inc. | 17-hydroxyprogesterone ester-containing oral compositions and related methods |
JP5934835B2 (en) * | 2013-03-08 | 2016-06-15 | 富士フイルム株式会社 | Enteric granules and pharmaceutical compositions |
US10076494B2 (en) | 2016-06-16 | 2018-09-18 | Dexcel Pharma Technologies Ltd. | Stable orally disintegrating pharmaceutical compositions |
WO2019199488A1 (en) * | 2018-04-12 | 2019-10-17 | Bpsi Holdings Llc | Acidifying coatings and disintegration-resistant substrates coated therewith |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57171428A (en) * | 1981-04-13 | 1982-10-22 | Sankyo Co Ltd | Preparation of coated solid preparation |
JPS584730A (en) * | 1981-06-29 | 1983-01-11 | Shin Etsu Chem Co Ltd | Enteric coating composition and its preparation |
GB2189698A (en) * | 1986-04-30 | 1987-11-04 | Haessle Ab | Coated omeprazole tablets |
DE3822095A1 (en) * | 1988-06-30 | 1990-01-04 | Klinge Co Chem Pharm Fab | NEW MEDICAMENT FORMULATION AND METHOD FOR THE PRODUCTION THEREOF |
IT1230576B (en) * | 1988-10-20 | 1991-10-28 | Angeli Inst Spa | ORAL PHARMACEUTICAL FORMULATIONS WITH SELECTIVE LIBERATION IN THE COLON |
US5225202A (en) * | 1991-09-30 | 1993-07-06 | E. R. Squibb & Sons, Inc. | Enteric coated pharmaceutical compositions |
JPH0733659A (en) * | 1992-07-17 | 1995-02-03 | Yoshitomi Pharmaceut Ind Ltd | Antiulcer agent-containing pharmaceutical preparation |
AU4513393A (en) * | 1992-07-17 | 1994-02-14 | Astra Aktiebolag | Pharmaceutical composition containing antiulcer agent |
SE9302395D0 (en) * | 1993-07-09 | 1993-07-09 | Ab Astra | NEW PHARMACEUTICAL FORMULATION |
-
1996
- 1996-06-28 DE DE19626045A patent/DE19626045C2/en not_active Expired - Fee Related
-
1997
- 1997-06-27 JP JP50383698A patent/JP4641075B2/en not_active Expired - Fee Related
- 1997-06-27 ES ES97929304T patent/ES2205243T3/en not_active Expired - Lifetime
- 1997-06-27 AU AU34388/97A patent/AU3438897A/en not_active Abandoned
- 1997-06-27 WO PCT/EP1997/003388 patent/WO1998000115A2/en active Application Filing
- 1997-06-27 DK DK97929304T patent/DK0934058T3/en active
- 1997-06-27 WO PCT/EP1997/003387 patent/WO1998000114A2/en active IP Right Grant
- 1997-06-27 AT AT97929304T patent/ATE247457T1/en active
- 1997-06-27 AU AU33451/97A patent/AU3345197A/en not_active Abandoned
- 1997-06-27 PT PT97929304T patent/PT934058E/en unknown
- 1997-06-27 DE DE59710629T patent/DE59710629D1/en not_active Expired - Lifetime
- 1997-06-27 EP EP97929304A patent/EP0934058B1/en not_active Expired - Lifetime
- 1997-06-27 CA CA002258918A patent/CA2258918C/en not_active Expired - Fee Related
- 1997-06-30 ZA ZA9705827A patent/ZA975827B/en unknown
- 1997-06-30 ZA ZA9705828A patent/ZA975828B/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2004258984B2 (en) * | 2003-07-23 | 2011-02-10 | Santarus, Inc. | Immediate-release formulation of acid-labile pharmaceutical compositions |
Also Published As
Publication number | Publication date |
---|---|
CA2258918C (en) | 2005-11-22 |
DE59710629D1 (en) | 2003-09-25 |
EP0934058B1 (en) | 2003-08-20 |
ATE247457T1 (en) | 2003-09-15 |
JP4641075B2 (en) | 2011-03-02 |
ES2205243T3 (en) | 2004-05-01 |
DE19626045A1 (en) | 1998-01-08 |
PT934058E (en) | 2004-01-30 |
WO1998000115A3 (en) | 1998-02-26 |
WO1998000114A3 (en) | 1998-02-26 |
EP0934058A2 (en) | 1999-08-11 |
WO1998000115A2 (en) | 1998-01-08 |
JP2000514051A (en) | 2000-10-24 |
CA2258918A1 (en) | 1998-01-08 |
DE19626045C2 (en) | 1998-12-03 |
AU3438897A (en) | 1998-01-21 |
ZA975827B (en) | 1998-01-30 |
DK0934058T3 (en) | 2003-12-01 |
WO1998000114A2 (en) | 1998-01-08 |
ZA975828B (en) | 1998-01-30 |
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