Gastric-retentive oral drug dosage forms for controlled release of highly soluble drugs
Abstract
The invention relates to medicaments freely or very readily soluble in water, and are produced in unit dosage form by incorporating into hydrophilic polymers consisting of a high molecular weight which swell when water embedded polymeric matrices. The dosage form may be a single tablet or two or three tablets retained in a capsule of gelatin only. This oral formulation is intended to be retained in the stomach and regulated manner diffuses the medicament containing the gastric cavity. With this method of administration, the drug is released from the matrix in gastric fluid by solution-diffusion. Once it reaches a sufficient size, the swollen polymeric matrix remains in the gastric cavity for several hours if the drug has been administered to the patient while nourishes, and remains long enough to allow a substantially complete release of the drug before it produces a significant erosion of the matrix. The swellable matrix reduces gastric fluid access to the drug thus limits the release rate of the drug. This procedure together with the delay spread by the selection of the specific polymers and polymer molecular weights give other variables result cone speed controlled sustained drug release in the gastric environment.
Term
No projected expiry on record.
- Priority
- Filed
- Granted
- Today
26 members in 11 offices
Priority claims2
| Document | Office | Kind | Date |
|---|---|---|---|
| 87050997 | United States of America | A | |
| 9811302 | United States of America | W |
Members26
| Document | Office | Kind | |
|---|---|---|---|
| CA2290624A1 | Canada | A1 | |
| WO9855107A1 | World Intellectual Property Organization (WIPO) | A1 | |
| AU8138698A | Australia | A | |
| EP0998271A1 | European Patent Office (EPO) | A1 | |
| JP2000513028A | Japan | A | |
| HK1027298A1 | Hong Kong, China | A1 | |
| AU729529B2 | Australia | B2 | |
| US2001018070A1 | United States of America | A1 | |
| US6340475B2 | United States of America | B2 | |
| US2002051820A1 | United States of America | A1 | |
| US2003039688A1 | United States of America | A1 | |
| CA2364845A1 | Canada | A1 | |
| US6635280B2 | United States of America | B2 | |
| EP0998271B1 | European Patent Office (EPO) | B1 | |
| AT302597TThis record | Austria | T | |
| ATE302597T1 | Austria | T1 | |
| DE69831335D1 | Germany | D1 | |
| PT998271E | Portugal | E | |
| ES2248908T3 | Spain | T3 | |
| DE69831335T2 | Germany | T2 | |
| CA2290624C | Canada | C | |
| CA2364845C | Canada | C | |
| JP4083818B2 | Japan | B2 | |
| EP0998271B3 | European Patent Office (EPO) | B3 | |
| ES2248908T7 | Spain | T7 | |
| DE69831335T3 | Germany | T3 |
1 legal event, as the office reported them to INPADOC
Events
| Event | Code | |
|---|---|---|
| Publication of translation of european patent specificationUEP | UEP |
Numbers
- Application
- 98931204
Titles2
- German
- IM MAGEN VERWEILENDE ORALE DOSIERUNGSFORMEN VON WASSERLÖSLICHEN ARZNEISTOFFEN MIT KONTROLLIERTER FREISETZUNG
- English
- MAGNIFYING ORAL DOSAGE FORMS OF WATER-SOLUBLE MEDICAMENTS WITH CONTROLLED RELEASE
Classification
- CPC, 5
- A61K9/0065
- A61K9/2013
- A61K9/2031
- A61K9/205
- A61K9/2054
- IPC, 13
- A61K31 136
- A61K31 155
- A61K31 335
- A61K31 341
- A61K31 40
- A61K31 4365
- A61K31 70
- A61K47 36
- A61K47 38
- A61K9 00
- A61K9 20
- A61K9 22
- A61K9 26