http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S60255719-A

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filingDate 1984-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8d7107a747cf56d1cf063dac71b87a9
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publicationDate 1985-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60255719-A
titleOfInvention Preparation of nifedipine sustained release pharmaceutical
abstract PURPOSE: To obtain the titled pharmaceutical useful as a remedy for angina pectoris, by incorporating and copulverizing a copulverized fine powdery composition obtained from a salt, e.g. magnesium silicate or Mg 2 CO 3 , etc. with casein and nifedipine with an enteric coating agent and a plasticizer, and dry granulating the resultant mixture. n CONSTITUTION: One or more selected from magnesium silicate, Mg 2 CO 3 , dried aluminum hydroxide gel, etc. are copulverized with casein and nifedipine to give a fine powdery composition, which is then incorporated with an enteric coating agent, e.g. cellulose acetate phthalate, a plasticizer, e.g. PEG, and copulverized. The resultant copulverized mixture is then dry granulated. A higher fatty acid ester e.g. sucrose ester of a fatty acid, may be further used in addition to the above-mentioned enteric coating agent and plasticizer for the above-mentioned fine powdery composition. Thus, the aimed solid nifedipine pharmaceutical having ready absorbability and sustained release property can be obtained without using an organic solvent. n COPYRIGHT: (C)1985,JPO&Japio
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priorityDate 1984-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 49.