首页> 外国专利> Solid instant-release form of administration, process for preparing such form of administration and use of therapeutic active substances when preparing such solid instant-release form of administration

Solid instant-release form of administration, process for preparing such form of administration and use of therapeutic active substances when preparing such solid instant-release form of administration

机译:固体速释剂型,制备这种剂型的方法以及在制备这种固体速释剂型时治疗活性物质的用途

摘要

In the present invention, there is disclosed a solid instant-release form of administration comprising therapeutic active substances or concentrates of active substance in an envelope composed of auxiliary substances wherein the active substances or concentrates of active substances have gel-forming properties in aqueous media such that when the active substances are dissolved in water or aqueous systems at concentrations of less than 20% they increase the viscosity of the solution to a value of more than 5 mPa.s, wherein the instant-release form has a diameter of more than 10 microns and releases active substance by more than 70 percent within a period of one hour and wherein the active substances or concentrates of the active substances are enclosed within a primary envelope formed by auxiliary substances that inhibit or compensate gel formation. There is also disclosed a process for preparing the above-described solid instant-release form of administration, said preparation process comprising mixing, granulation, spray drying, spray solidification or press granulation of active substances or concentrates of active substances with auxiliary substances being selected from the group consisting of macromolecular substances from the group consisting of sugars, salts of fatty acids, fats, waxes, surfactants, silicates or highly dispersed silicon dioxide.
机译:在本发明中,公开了固体速释剂型,其包括由辅助物质组成的包膜中的治疗活性物质或活性物质浓缩物,其中活性物质或活性物质浓缩物在水性介质中具有凝胶形成性质。当活性物质以小于20%的浓度溶于水或水性体系时,它们将溶液的粘度增加到大于5 mPa.s的值,其中速释形式的直径大于10在一小时内,可释放超过70%的活性物质,其中活性物质或活性物质的浓缩物被封闭在由抑制或补偿凝胶形成的辅助物质形成的初级包膜内。还公开了制备上述固体速释形式的给药方法,所述制备方法包括将活性物质或活性物质浓缩物与选自以下的辅助物质混合,制粒,喷雾干燥,喷雾固化或压制粒化。由大分子物质组成的组,其选自糖,脂肪酸盐,脂肪,蜡,表面活性剂,硅酸盐或高度分散的二氧化硅。

著录项

  • 公开/公告号CZ298897B6

    专利类型

  • 公开/公告日2008-03-05

    原文格式PDF

  • 申请/专利权人 HEIDELBERG PHARMA HOLDING GMBH;

    申请/专利号CZ19980002320

  • 申请日1997-01-24

  • 分类号A61K9/20;A61K9;A61K9/22;A61K31;A61K31/70;A61K31/7042;A61K31/7052;A61K31/706;A61K31/7064;A61K31/7068;A61K31/7072;A61K45;A61K47/30;A61K47/36;A61K47/38;A61K47/48;A61P9;A61P9/06;A61P9/08;A61P29;A61P31;A61P31/12;A61P31/14;A61P35;A61P37;A61P37/02;A61P43;

  • 国家 CZ

  • 入库时间 2022-08-21 20:08:28

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