Method for delivering dosage form for diltiazem

Claim 1

A method for delivering diltiazem to a recipient in need thereof, which method comprises: (a) admitting orally into the recipient a device comprising: (1) a wall surrounding and forming a compartment, which compartment comprises: (A) a diltiazem composition comprising from 70 wt % to 96 wt % of a member selected from the group consisting of diltiazem and its pharmaceutically acceptable salts, from 0.5 wt % to 15 wt % of polyacrylic acid comprising a 2,500,000 to 4,000,000 molecular weight, from 0.5 wt % to 20 wt % of a poly(ethylene oxide) comprising a 4,000,000 to 5,500,000 molecular weight, and from 0.5 wt % to 20 wt % of a poly(vinyl pyrrolidone) comprising a 35,000 to 40,000 molecular weight; (B) a push composition comprising from 70 wt % to 95 wt % of poly(ethylene oxide) comprising a 6,200,000 to 7,500,000 molecular weight, from 1 wt % to 20 wt % of an osmagent, and from 1 wt % to 15 wt % of a hydroxypropylmethylcellulose comprising a 9,000 to 16,000 molecular weight; (2) at least one passageway in the wall; and, (b) delivering diltiazem by the device imbibing fluid through the wall into the compartment to cause the diltiazem composition to form a dispensable composition and to cause the push composition to push the diltiazem composition through the passageway for delivering diltiazem to the recipient.

Claim 2

A method for delivering diltiazem to a recipient in need thereof, which method comprises: (a) admitting orally into the recipient a device comprising: (1) a wall surrounding and forming a compartment, which compartment comprises: (A) a diltiazem composition comprising from 70 wt % to 96 wt % of a member selected from the group consisting of diltiazem and its pharmaceutically acceptable salts, from 0.5 wt % to 15 wt % of polyacrylic acid comprising a 2,500,000 to 4,000,000 molecular weight, from 0.5 wt % to 20 wt % of a poly(ethylene oxide) comprising a 4,000,000 to 5,500,000 molecular weight, and from 0.5 wt % to 20 wt % of a poly(vinyl pyrrolidone) comprising a 35,000 to 40,000 molecular weight; (B) a push composition comprising from 70 wt % to 95 wt % of poly(ethylene oxide) comprising a 6,200,000 to 7,500,000 molecular weight, from 1 wt % to 20 wt % of an osmagent, and from 1 wt % to 15 wt % of a hydroxypropylmethylcellulose comprising a 9,000 to 16,000 molecular weight; (2) at least one passageway in the wall; and, (b) delivering diltiazem by the device imbibing fluid through the wall into the compartment to cause the diltiazem composition to form a dispensable composition and to cause the push composition to push the diltiazem composition through the passageway for delivering diltiazem to the recipient.

Claim 3

A method for delivering diltiazem to a recipient in need thereof, which method comprises: (a) admitting orally into the recipient a dosage form comprising: (1) a wall comprising at least in part a composition, which composition comprises a member selected from the group consisting of a cellulose ester, cellulose ether, cellulose ester-ether, cellulose acylate, cellulose diacylate, cellulose acetate, cellulose diacetate and cellulose triacetate, which wall surrounds; (2) a compartment; (3) an osmotic core in the compartment, which core comprises from 30 mg to 500 mg of a member selected from the group consisting of diltiazem and its pharmaceutically acceptable salts, wherein the salt is a member selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, lactate, citrate, tartrate, malate, maleate, fumarate, ascorbate, gluconate, aspartatate, and salicylate; (4) means in the wall for delivering diltiazem from the dosage form, said means comprising a leached passageway formed in the wall when the dosage form is in the recipient, and, (b) delivering from the osmotic core from 30 mg up to 500 mg of diltiazem through the leached passageway to the recipient over 24 hours.

Claim 4

A method for delivering diltiazem to a recipient in need thereof, which method comprises: (a) admitting orally into the recipient a dosage form comprising: (1) a wall comprising at least in part a composition, which composition comprises a member selected from the group consisting of a cellulose ester, cellulose ether, cellulose ester-ether, cellulose acylate, cellulose diacylate, cellulose acetate, cellulose diacetate and cellulose triacetate, which wall surrounds; (2) a compartment; (3) an osmotic core in the compartment, which core comprises from 30 mg to 500 mg of a member selected from the group consisting of diltiazem and its pharmaceutically acceptable salts, wherein the salt is a member selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, lactate, citrate, tartrate, malate, maleate, fumarate, ascorbate, gluconate, aspartatate, and salicylate; (4) means in the wall for delivering diltiazem from the dosage form, said means comprising a leached passageway formed in the wall when the dosage form is in the recipient, and, (b) delivering from the osmotic core from 30 mg up to 500 mg of diltiazem through the leached passageway to the recipient over 24 hours.