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US4540566A Expired / Lapsed US ⏱️ 0.0 years remaining

Prolonged release drug dosage forms based on modified low viscosity grade hydroxypropylmethylcellulose

Assignee: Forest Laboratories LLC
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Filing: 1984-04-02
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Granted: 1985-09-10
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Expires: 2004-04-02
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Abstract

Abstract A carrier base material combined with a therapeutically active medicament and shaped and compressed to a solid unit dosage form having a controlled and prolonged release pattern upon administration, the carrier base material being a mixture of one or more nonionic cellulose ethers and an anionic surfactant, and wherein at least one of the cellulose ethers is a modified hydroxypropylmethylcellulose having a number average molecular weight of less than 50,000 and has been modified by successive or concurrent exposure to moisture and air.

Inventors

  • 👤 Stanley S. Davis
  • 👤 Norman G. Gaylord

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 14:52
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/20; A61K9/2004; A61K9/2013; A61K9/2022; A61K9/205; A61K9/2054

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 84 words
A carrier base material combined with a therapeutically active medicament and shaped and compressed to a solid unit dosage form having a controlled and prolonged release pattern upon administration, the carrier base material being a mixture of one or more water-soluble nonionic cellulose ethers and an anionic surfactant, and wherein at least one of the cellulose ethers is a modified hydroxypropylmethylcellulose having a number average molecular weight of less than 50,000 and has been modified by successive or concurrent exposure to moisture and air.
Claim 2
Dependent Claim 84 words
A carrier base material combined with a therapeutically active medicament and shaped and compressed to a solid unit dosage form having a controlled and prolonged release pattern upon administration, the carrier base material being a mixture of one or more water-soluble nonionic cellulose ethers and an anionic surfactant, and wherein at least one of the cellulose ethers is a modified hydroxypropylmethylcellulose having a number average molecular weight of less than 50,000 and has been modified by successive or concurrent exposure to moisture and air.
Claim 3
Dependent Claim 23 words
A composition according to claim 1 wherein the hydroxypropylmethylcellulose has a methoxyl content of 28-30 weight-% and a hydroxypropoxyl content of 7.5-12 weight-%.
Claim 4
Dependent Claim 19 words
A composition according to claim 1 wherein the anionic surfactant is an alkali metal salt of an organic sulfate.
Claim 5
Dependent Claim 23 words
A composition according to claim 3 wherein the organic sulfate is selected from the group consisting of C 8 -C 24 alcohol sulfates.
Claim 6
Dependent Claim 17 words
A composition according to claim 3 wherein the organic sulfate is the sulfate of an ethoxylated compound.
Claim 7
Dependent Claim 19 words
A composition according to claim 1 wherein the anionic surfactant is an alkali metal salt of an organic sulfonate.
Claim 8
Dependent Claim 14 words
A composition according to claim 6 wherein the organic sulfonate is an aryl sulfonate.
Claim 9
Dependent Claim 14 words
A composition according to claim 6 wherein the organic sulfonate is a dialkyl sulfosuccinate.
Claim 10
Independent Claim 91 words
A method for the preparation of a therapeutically active solid unit dosage form having a controlled and prolonged release pattern upon administration, consisting of compressing and shaping a mixture of a therapeutically active medicament and a carrier base material consisting of a mixture of one or more water-soluble nonionic cellulose ethers and an anionic surfactant, and wherein at least one of the cellulose ethers is a modified hydroxypropylmethylcellulose having a number average molecular weight of less that 50,000 and has been modified by successive or concurrent exposure to moisture and air.
Claim 11
Independent Claim 91 words
A method for the preparation of a therapeutically active solid unit dosage form having a controlled and prolonged release pattern upon administration, consisting of compressing and shaping a mixture of a therapeutically active medicament and a carrier base material consisting of a mixture of one or more water-soluble nonionic cellulose ethers and an anionic surfactant, and wherein at least one of the cellulose ethers is a modified hydroxypropylmethylcellulose having a number average molecular weight of less that 50,000 and has been modified by successive or concurrent exposure to moisture and air.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-09-09 1989-03-11 1989-09-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-09-09 1993-03-11 1993-09-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-09-09 1997-03-11 1997-09-10 $7700.00 Window Closed / Lapsed

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