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Itraconazole formulation for oral administration

机译:伊曲康唑口服制剂

摘要

PROBLEM TO BE SOLVED: To develop an itraconazole preparation having a high biological utilization factor, by improving dissolubility of the itraconazole in a gastric digestive juice comprising an acidic liquid.;SOLUTION: This itraconazole preparation for oral administration is produced by spraying/coating fine particles having an average particle diameter of 10-60 m as nuclear particles with a mixture solution of the itraconazole and an enteric polymer, and then controlling an average particle diameter of an obtained coated powder to be 50-120 m. Thus, the preparation which is improved in the dissolubility in the gastric digestive juice is produced.;COPYRIGHT: (C)2006,JPO&NCIPI
机译:解决的问题:通过改善伊曲康唑在包含酸性液体的胃消化液中的溶解性,来开发具有高生物利用度的伊曲康唑制剂;溶液:该伊曲康唑口服制剂是通过将细颗粒喷雾/包衣制备的。将具有平均粒径为10-60m的核颗粒与伊曲康唑和肠溶性聚合物的混合溶液混合,然后将获得的包衣粉末的平均粒径控制为50-120m。因此,制备了在胃消化液中的溶解性得到改善的制剂。;版权所有:(C)2006,JPO&NCIPI

著录项

  • 公开/公告号JP4342426B2

    专利类型

  • 公开/公告日2009-10-14

    原文格式PDF

  • 申请/专利权人 科研製薬株式会社;

    申请/专利号JP20040338572

  • 发明设计人 大島 孝雄;薗田 良一;大熊 盛之;

    申请日2004-11-24

  • 分类号A61K31/496;A61K9/14;A61K9/20;A61K47/34;A61K47/36;A61K47/38;A61K47/26;A61P31/10;

  • 国家 JP

  • 入库时间 2022-08-21 19:43:11

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