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An itraconazole exhibiting increased solubility, the method of preparation of it and the pharmaceutical composition for oral administration containing the same

机译:表现出增加的溶解度的伊曲康唑,其制备方法和包含其的口服药物组合物

摘要

B AN ITRACONAZOL SHOWING INCREASED SOLUBILITY, THE METHOD OF PREPARING THE SAME AND THE PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION CONTAINING THE SAME D, in which the particle diameter of itraconazole, the insoluble drug, is thus reduced and crystalline, thus being transformed and crystalline crystalline in amorphic, increasing water solubility and dissolution rate. The improved itraconazole is a drug administered orally.
机译:依他康唑的溶解性增加,制备相同药物的方法和包含该的口服给药的药物组合物,其中伊曲康唑(不溶性药物)的粒径减小并结晶,因此被转化和无定形的晶体,增加水溶性和溶解速度。改进的伊曲康唑是口服药物。

著录项

  • 公开/公告号BR9810124A

    专利类型

  • 公开/公告日2000-08-08

    原文格式PDF

  • 申请/专利权人 DONG-A PHARMACEUTICAL CO. LTD;

    申请/专利号BR19989810124

  • 发明设计人 CHA BONG-JIN;OH JUN-GYO;KIM SU-EON;

    申请日1998-06-16

  • 分类号C07D403/14;A61K31/41;

  • 国家 BR

  • 入库时间 2022-08-22 01:57:08

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