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Mesalazine controlled release oral pharmaceutical compositions

DC CAFC
  • US 6,773,720 B1
  • Filed: 12/13/2001
  • Issued: 08/10/2004
  • Est. Priority Date: 06/14/1999
  • Status: Expired due to Term
First Claim
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1. Controlled-release oral pharmaceutical compositions containing as an active ingredient 5-amino-salicylic acid, comprising:

  • a) an inner lipophilic matrix consisting of substances selected from the group consisting of unsaturated and/or hydrogenated fatty acid, salts, esters or amides thereof, fatty acid mono-, di- or triglycerids, waxes, ceramides, and cholesterol derivatives with melting points below 90°

    C., and wherein the active ingredient is dispersed both in said the lipophilic matrix and in the hydrophilic matrix;

    b) an outer hydrophilic matrix wherein the lipophilic matrix is dispersed, and said outer hydrophilic matrix consists of compounds selected from the group consisting of polymers or copolymers of acrylic or methacrylic acid, alkylvinyl polymers, hydroxyalkyl celluloses, carboxyalkyl celluloses, polysaccharides, dextrins, pectins, starches and derivatives, alginic acid, and natural or synthetic gums;

    c) optionally other excipients;

    wherein the active ingredient is present in an amount of 80 to 95% by weight of the total composition, and wherein the active ingredient is dispersed both in the lipophilic matrix and in the hydrophilic matrix.

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