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PERORAL ACTIVE AGENT SUSPENSION AND PROCESS FOR ITS PREPARATION

机译:口服活性剂的停药及其制备方法

摘要

The present invention relates to a physiologically inert suspension of an NSAID-type drug substance with a suspect particle size spectrum, in particular Meloxicam, in a stable dispersion medium, so that the suspension does not have to be containing a small amount of highly dispersed silica, wherein the three-dimensional siloidal structure is formed by introducing a high shear force of silica into the dispersion medium, and the suspension also contains a small amount of hydrophilic polymers soluble in the dispersion medium. and NSAIDs, especially Meloxicam, for use in the preparation of such suspensions. price. SHE
机译:本发明涉及在稳定的分散介质中具有可疑粒径谱的NSAID型药物的生理惰性悬浮液,特别是美洛昔康,从而该悬浮液不必包含少量高度分散的二氧化硅,其中三维二氧化硅结构是通过将二氧化硅的高剪切力引入分散介质中而形成的,并且悬浮液还包含少量可溶于分散介质中的亲水性聚合物。非甾体抗炎药,尤其是美洛昔康,用于制备这种悬浮液。价钱。她

著录项

  • 公开/公告号HU0102036A2

    专利类型

  • 公开/公告日2002-03-28

    原文格式PDF

  • 申请/专利权人 BOEHRINGER INGELHEIM PHARMA KG;

    申请/专利号HU20010002036

  • 发明设计人 SCHMELMER VEIT;TUERCK DIETRICH;

    申请日1999-03-23

  • 分类号A61K9/00;

  • 国家 HU

  • 入库时间 2022-08-22 00:45:17

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