发明名称 Sistema iii de liberação de droga
摘要 <p>A drug delivery system (DDS) for administration of a water soluble, cationic, and amphiphilic pharmaceutically active substance (API) which DDS comprises amorphous particles of <100 nm of a poorly water soluble complex of the API with a Na-salt of N-all-trans-retinoyl cysteic acid methyl ester and/or a Na-salt of N-13-cis-retinoyl cysteic acid methyl ester, which particles are entrapped in nanoparticles formed a Na-salt of N-all-trans-retinoyl cysteic acid methyl ester and/or a Na-salt of N-13-cis-retinoyl cysteic acid methyl ester, the w/w-ratio of Na-salt of N-alltrans-retinoyl cysteic acid methyl ester and/or a Na-salt of N-13-cis-retinoyl cysteic acid methyl ester to the complex is about 0.5:1 to about 20:1. A pharmaceutical composition comprising such a DDS. Methods for preparation of such a DDS and such a pharmaceutical composition. Use of such a DDS and pharmaceutical composition for treatment of cancer.</p>
申请公布号 BRPI0821739(A2) 申请公布日期 2015.06.16
申请号 BR2008PI21739 申请日期 2008.12.18
申请人 ARDENIA INVESTIMENTS 发明人 JULIAN ALEKSOV;IGOR LOKOT
分类号 A61K47/48;A61K9/14;A61P35/00 主分类号 A61K47/48
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