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filingDate 2000-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d74987d4800126470083e26dbfe7b676
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_501a7a1e4e4d31d92afa8e50ff35f5f9
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publicationDate 2004-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2239457-C2
titleOfInvention Sustained-release pharmaceutical composition and method for its preparing
abstract FIELD: medicine, pharmacy. n SUBSTANCE: invention relates to polypeptide-base sustained-release pharmaceutical compositions, namely, water-insoluble salt of pharmaceutically active ionic peptide and counter ionic macromolecule-carrier. Peptide can represent a LHRH antagonist (luteinizing hormone-releasing hormone), such as cetrorelix, and macromolecule can represents anionic polysaccharide, such as carboxymethylcellulose. Salt is prepared using ion-exchange resins for separate removing counterions from peptide and macromolecule-carrier forms free ions of peptide/macromolecule. Then these free ions of peptide and macromolecules are mixed to form water-insoluble peptide-macromolecule salt. Invention provides expanding assortment of pharmaceutical agents of protein nature with sustained-release effect. n EFFECT: improved preparing method, valuable properties of composition. n 55 cl, 2 tbl, 2 dwg, 7 ex
priorityDate 1999-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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