Taste-masked pharmaceutical compositions with gastrosoluble pore-formers
First Claim
1. A pharmaceutical composition comprising a plurality of taste-masked particles, wherein the task-masked particles comprise:
- (a) a drug-containing core particle; and
(b) a taste-masking membrane on said drug-containing core particle comprising a combination of a water-insoluble polymer and a gastrosoluble inorganic or organic pore-former at a ratio ranging from about 95/5 to about 50/50 having a thickness of from about 5% to about 50% based on the weight of the coated particle and an average particle size of not more than about 400 μ
m wherein the composition exhibits acceptable taste-masking when the composition is placed in the oral cavity for 60 seconds and the composition releases not less than about 60% of the dose in 30 min when tested for dissolution using United States Pharmacopoeia Apparatus 2 (paddles @ 50 rpm in 900 mL of pH 1.2 buffer).
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Abstract
There is provided a method for preparing an orally disintegrating tablet (ODT) composition comprising microparticles of one or more taste-masked active pharmaceutical ingredient(s), rapidly-dispersing microgranules, and other optional, pharmaceutically acceptable excipients wherein the ODT disintegrates on contact with saliva in the buccal cavity forming a smooth, easy-to-swallow suspension. Furthermore, the microparticles (crystals, granules, beads or pellets containing the active), coated with a taste-masking membrane comprising a water-insoluble polymer and one or more gastrosoluble inorganic or organic pore-formers (practically insoluble in water and saliva, but soluble in an acidic buffer), exhibit acceptable taste-masking when placed in the oral cavity and provide rapid, substantially-complete release of the dose on entry into the stomach.
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Citations
25 Claims
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1. A pharmaceutical composition comprising a plurality of taste-masked particles, wherein the task-masked particles comprise:
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(a) a drug-containing core particle; and
(b) a taste-masking membrane on said drug-containing core particle comprising a combination of a water-insoluble polymer and a gastrosoluble inorganic or organic pore-former at a ratio ranging from about 95/5 to about 50/50 having a thickness of from about 5% to about 50% based on the weight of the coated particle and an average particle size of not more than about 400 μ
m wherein the composition exhibits acceptable taste-masking when the composition is placed in the oral cavity for 60 seconds and the composition releases not less than about 60% of the dose in 30 min when tested for dissolution using United States Pharmacopoeia Apparatus 2 (paddles @ 50 rpm in 900 mL of pH 1.2 buffer). - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16)
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17. A method of manufacturing a pharmaceutical composition comprising:
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a) preparing core particles comprising an active pharmaceutical ingredient; and
b) coating the core particles by applying a membrane comprising a mixture of water-insoluble polymer and a gastrosoluble organic or inorganic pore former present at a ratio of from about 95/5 to about 50/50, the membrane coating comprising from about 5% to about 50% based on the total weight of the coated particles, wherein the composition exhibits the following properties;
1) acceptable taste-masking when the composition is placed in the oral cavity for 60 seconds; and
2) releases not less than about 60% of the active in 30 min when tested for dissolution using United States Pharmacopoeia Apparatus 2 (paddles @ 50 rpm in 900 mL of pH 1.2 buffer). - View Dependent Claims (18, 19, 20, 21, 22, 23, 24, 25)
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Specification