US4167558A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Novel sustained release tablet formulations
Assignee: Hoffmann La Roche Inc
•
Filing: 1978-11-06
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Granted: 1979-09-11
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Expires: 1998-11-06
Abstract
Abstract A novel sustained release formulation for the preparation of tablets for oral administration is disclosed. The formulation is hydrodynamically balanced to be buoyant in gastric juice thereby remaining in the stomach for an extended period of time.
Inventors
- 👤 Prabhakar R. Sheth
- 👤 Jacques L. Tossounian
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 15:49
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/0012; A61K9/0053; A61K9/0065
Claims Analysis
Total Claims: 3
Claim 1
Independent Claim
153 words
A sustained release pharmaceutical tablet containing as the active ingredient acetylsalicylic acid, said tablet being hydrodynamically balanced so that, upon contact with gastric fluid, said tablet acquires and maintains a bulk density of less than one thereby being buoyant in said fluid and remaining buoyant in the gastric fluid of the stomach until substantially all of the acetylsalicylic acid contained therein has been released therefrom, said tablet comprising a homogeneous mixture of acetylsalicylic acid, from about 0% to about 80% by weight of therapeutically inert, pharmaceutically acceptable adjunct materials, and from about 20% by weight to about 75% by weight of one or a mixture of hydrocolloids selected from the group consisting of methyl cellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose and sodium carboxymethylcellulose to provide, upon contact with gastric fluid, a water impermeable barrier on the surface of said tablet, said tablet being compressed to a hardness of from about 5 to about 6 S.C.U.
Claim 2
Dependent Claim
153 words
A sustained release pharmaceutical tablet containing as the active ingredient acetylsalicylic acid, said tablet being hydrodynamically balanced so that, upon contact with gastric fluid, said tablet acquires and maintains a bulk density of less than one thereby being buoyant in said fluid and remaining buoyant in the gastric fluid of the stomach until substantially all of the acetylsalicylic acid contained therein has been released therefrom, said tablet comprising a homogeneous mixture of acetylsalicylic acid, from about 0% to about 80% by weight of therapeutically inert, pharmaceutically acceptable adjunct materials, and from about 20% by weight to about 75% by weight of one or a mixture of hydrocolloids selected from the group consisting of methyl cellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose and sodium carboxymethylcellulose to provide, upon contact with gastric fluid, a water impermeable barrier on the surface of said tablet, said tablet being compressed to a hardness of from about 5 to about 6 S.C.U.
Claim 3
Dependent Claim
14 words
The sustained release tablet in accordance with claim 1 wherein said hydrocolloid is hydroxypropylmethylcellulose.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-09-10 | 1983-03-12 | 1983-09-11 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-09-10 | 1987-03-12 | 1987-09-11 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-09-10 | 1991-03-12 | 1991-09-11 | $7700.00 | Window Closed / Lapsed |