首页> 外国专利> SOLID PHARMACEUTICAL PREPARATION COMPOSITION COMPRISING LIQUID OR SEMI-SOLID ACTIVE INGREDIENT AND POROUS CELLULOSE AGGREGATE PARTICLE

SOLID PHARMACEUTICAL PREPARATION COMPOSITION COMPRISING LIQUID OR SEMI-SOLID ACTIVE INGREDIENT AND POROUS CELLULOSE AGGREGATE PARTICLE

机译:包含液体或半固体活性成分和多孔纤维素聚集颗粒的固体药物制剂组合物

摘要

PROBLEM TO BE SOLVED: To obtain a solid pharmaceutical preparation composition preventing bleeding of a liquid ingredient and having good tableting and disintegrating properties in a solid pharmaceutical preparation comprising the liquid or semisolid active ingredient by using a porous cellulose aggregate having a large intraparticle pore volume.;SOLUTION: This solid pharmaceutical preparation composition is characterized as comprising an active ingredient which is liquid or semisolid at normal temperature and the porous cellulose aggregate. Furthermore, the porous cellulose aggregate has a secondary aggregate structure in which cellulose primary particles are aggregated and ≥0.265 cm3/g intraparticle pore volume, contains I type crystals, has 30 μm average particle diameter, 1.3-20 m2/g specific surface area and 44° angle of repose and disintegrates in water.;COPYRIGHT: (C)2005,JPO&NCIPI
机译:解决的问题:通过使用具有大的颗粒内孔体积的多孔纤维素聚集体,获得在包含液体或半固体活性成分的固体药物制剂中防止液体成分渗出并且具有良好的压片和崩解性质的固体药物制剂组合物。 ;解决方案:该固体药物制剂组合物的特征在于包含在常温下为液体或半固体的活性成分和多孔纤维素聚集体。此外,多孔纤维素聚集体具有二级聚集体结构,其中纤维素初级颗粒聚集,并且颗粒内孔体积为≥0.265cm 3 / g,包含I型晶体,平均颗粒>30μm。直径1.3-20 m 2 / g比表面积和<44°水中的静止角和崩解角。;版权所有:(C)2005,JPO&NCIPI

著录项

  • 公开/公告号JP2005255616A

    专利类型

  • 公开/公告日2005-09-22

    原文格式PDF

  • 申请/专利权人 ASAHI KASEI CHEMICALS CORP;

    申请/专利号JP20040069663

  • 申请日2004-03-11

  • 分类号A61K47/38;A61J3/06;A61J3/10;A61K9/20;

  • 国家 JP

  • 入库时间 2022-08-21 22:36:11

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