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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
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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.

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

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