Sustained-release pharmaceutical tablet and process for preparation thereof

Claim 2

A sustained-release pharmaceutical tablet consisting essentially of (A) from about 35% to about 85% by weight of a plurality of encapsulated pellets each consisting essentially of (a) from about 30% to about 98% by weight of a sugar-starch bead which is coated with (b) from about 1% to about 70% by weight of a first coat consisting of from about 75% to about 99% by weight of theophylline an orally administrable drug and from about 1% to about 25% by weight of a water-soluble drug-binding substance selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose and hydroxypropyl methycellulose and (c) from about 1% to about 15% by weight of a second coat consisting essentially of from about 1% to about 10% by weight of a water-soluble film-forming substance selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose and hydroxypropyl methylcellulose, from about 1% to about 60% by weight of a water-insoluble film-forming substance consisting of ethylcellulose and from about 30% to about 98% by weight of a dusting powder selected from the group consisting of talc, silicon dioxide and titanium dioxide, which encapsulated pellets are blended and compressed into tablet form with (B) from about 15% to about 65% by weight of a compressible tableting mixture consisting essentially of from about 20% to about 40% by weight of a diluent selected from the group consisting of the monosaccharides and the disaccharides, from about 30% to about 50% by weight of a diluent-binder consisting of microcrystalline cellulose, from about 10% to about 30% by weight of a binder consisting of ethyl cellulose, and from about 5% to about 20% by weight of a hydrophobic lubricant selected from the group consisting of hydrogenated vegetable oil, stearic acid, magnesium stearate and calcium sterate.

Claim 3

A sustained-release pharmaceutical tablet according to claim 1 wherein the water-soluble drug-binding substance is polyvinylpyrrolidone, the water-soluble film-forming substance is polyvinylpyrrolidone, the water-insoluble film-forming substance is ethylcellulose, the dusting powder is talc, the diluent is lactose, and the hydrophobic lubricant is hydrogenated vegetable oil.

Claim 4

A sustained-release pharmaceutical tablet according to claim 2 wherein the second coat contains about 2% by weight of polyvinylpyrrolidone and about 46% by weight of ethylcellulose, the encapsulated pellets contain about 56% by weight of theophylline, and the tablet contains about 77% by weight of encapsulated pellets.

Claim 5

A sustained-release pharmaceutical tablet according to claim 2 wherein the second coat contains about 2% by weight of polyvinylpyrrolidone and about 2% by weight of ethylcellulose, the encapsulated pellets contain about 56.8% by weight of theophylline, and the tablet contains about 76% by weight of encapsulated pellets.

Claim 6

The process of preparing a sustained-release pharmaceutical tablet which comprises blending and compressing into tablet form a mixture consisting essentially of (A) from about 35% to about 85% by weight of a plurality of encapsulated pellets each consisting essentially of (a) from about 30% to about 98% by weight of a sugar-starch bead which is coated with (b) from about 1% to about 70% by weight of a first coat consisting of from about 75% to about 99% by weight of theophylline an orally administrable drug and from about 1% to about 25% by weight of a water-soluble drug-binding substance selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose and hydroxypropyl methylcelluose and (c) from about 1% to about 15% by weight of a second coat consisting essentially of from about 1% to about 10% by weight of a water-soluble film-forming substance selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose and hydroxypropyl methylcellulose, from about 1% to about 60% by weight of a water-insoluble film-forming substance consisting of ethylcellulose and from about 30% to about 98% by weight of a dusting powder selected from the group consisting of talc, silicon dioxide and titanium dioxide; wherein the first coat is formed by simultaneously applying the drug in powder form by dusting and the water-soluble drug-binding substance as a solution in a non-aqueous solvent by spraying and the second coat is formed by simultaneously applying the water-soluble film-forming substance and the water-insoluble film-forming substance as a solution in a nonaqueous solvent by spraying and the dusting powder by dusting; and (B) from about 15% to about 65% by weight of a compressible tableting mixture consisting essentially of from about 20% to about 40% by weight of a diluent selected from the group consisting of the monosaccharides and the disaccharides, from about 30% to about 50% by weight of a diluent-binder consisting of microcrystalline cellulose, from about 10% to about 30% by weight of a binder consisting of ethylcellulose, and from about 5% to about 20% by weight of a hydrophobic lubricant selected from the group consisting of hydrogenated vegetable oil, stearic acid, magnesium stearate and calcium stearate.

Claim 7

The process of preparing a sustained-release pharmaceutical tablet which comprises blending and compressing into tablet form a mixture consisting essentially of (A) from about 35% to about 85% by weight of a plurality of encapsulated pellets each consisting essentially of (a) from about 30% to about 98% by weight of a sugar-starch bead which is coated with (b) from about 1% to about 70% by weight of a first coat consisting of from about 75% to about 99% by weight of theophylline an orally administrable drug and from about 1% to about 25% by weight of a water-soluble drug-binding substance selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose and hydroxypropyl methylcelluose and (c) from about 1% to about 15% by weight of a second coat consisting essentially of from about 1% to about 10% by weight of a water-soluble film-forming substance selected from the group consisting of polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose and hydroxypropyl methylcellulose, from about 1% to about 60% by weight of a water-insoluble film-forming substance consisting of ethylcellulose and from about 30% to about 98% by weight of a dusting powder selected from the group consisting of talc, silicon dioxide and titanium dioxide; wherein the first coat is formed by simultaneously applying the drug in powder form by dusting and the water-soluble drug-binding substance as a solution in a non-aqueous solvent by spraying and the second coat is formed by simultaneously applying the water-soluble film-forming substance and the water-insoluble film-forming substance as a solution in a nonaqueous solvent by spraying and the dusting powder by dusting; and (B) from about 15% to about 65% by weight of a compressible tableting mixture consisting essentially of from about 20% to about 40% by weight of a diluent selected from the group consisting of the monosaccharides and the disaccharides, from about 30% to about 50% by weight of a diluent-binder consisting of microcrystalline cellulose, from about 10% to about 30% by weight of a binder consisting of ethylcellulose, and from about 5% to about 20% by weight of a hydrophobic lubricant selected from the group consisting of hydrogenated vegetable oil, stearic acid, magnesium stearate and calcium stearate.

Claim 8

The process according to claim 5 wherein the water-soluble drug-binding substance is polyvinylpyrrolidone, the water-soluble film-forming substance is polyvinylpyrrolidone, the water-insoluble film-forming substance is ethylcellulose, the dusting powder is talc, the diluent is lactose, and the hydrophobic lubricant is hydrogenated vegetable oil.

Claim 9

The process according to claim 6 wherein the second coat contains about 2% by weight of polyvinylpyrolidone and about 46% by weight of ethylcellulose, the encapsulated pellets contain about 56% by weight of theophylline, and the tablet contains about 77% by weight of encapsulated pellets.

Claim 10

The process according to claim 6 wherein the second coat contains about 2% by weight of polyvinylpyrrolidone and about 2% by weight of ethylcellulose, the encapsulated pellets contain about 56.8% by weight of theophylline, and the tablet contains about 76% by weight of encapsulated pellets.