首页> 外国专利> A Solid Pharmaceutical composition containing a water soluble Taxoide and a Cyclodextrin, its solutions in aqueous Solvents for usoparenteral, a process for its preparationA method for preventing the self Aggregation and precipitation of a premature Taxoide Group delpaclita

A Solid Pharmaceutical composition containing a water soluble Taxoide and a Cyclodextrin, its solutions in aqueous Solvents for usoparenteral, a process for its preparationA method for preventing the self Aggregation and precipitation of a premature Taxoide Group delpaclita

机译:包含水溶性紫杉醇和环糊精的固体药物组合物,其在非胃肠外用水性溶剂中的溶液,其制备方法防止过早的紫杉醇酯delpaclita的自聚集和沉淀的方法

摘要

Water soluble solid pharmaceutical ingredients, including an aqueous solution of taxonomic sterols and cyclopentanediol and their solutions, are used as steroids: (a) as an active ingredient, it contains taxonomic sterols, such as paclitaxel and small taxonomic sterols, widely distributed, with large surface area, amoxicillin, preferably liaofeihua, It may exist in the form of salt or multi-form hydrate or solution, for example, the solution made of conetano and (b) contains fine acetyl gamma cyclopentadiol or hydroxypropyl beta cyclopentadiol (hereinafter referred to as cyclopentadiol), which can split the epidermis, AMOLIN, and preferably liofilizada,the weight ratio being between the mentioned taxoid and the cyclodextrininated from 1:25 to 1: 250; C) and eventually contain other auxiliary materials soluble in water and usually used in medicines intended for parenteral administration. In particular, the pharmaceutical composition contains as active ingredient paclitaxel and acetyl-gamma-cyclodextrin in a weight ratio of 1: 100 to 1: 150,or docetaxel and hydroxypropyl-beta-cyclodextrin in a weight ratio of 1:25 to 1: 100. The pharmaceutical composition may contain as cyclodextrin any of the following components: acetyl-gamma-cyclodextrin with an acetylation degree comprised between about 2 and about 12 groups per cyclodextrin ring, acetyl-gamma-cyclodextrin with an acetylation degree of approximately 8 gruposacetyl per cyclodextrin ring, hydroxy-propyl-beta-cyclodextrin with a degree of substitution between about 2 and about 10 hydroxypropyl groups per cyclodextrin ring,hydroxy-propyl-beta-cyclodextrin with a degree of substitution between about 4 and about 6 hydroxypropyl groups per cyclodextrin ring. A process for preparing a pharmaceutical composition in solid and instantaneously soluble state as mentioned above, and its solutions in aqueous solvents for parenteral use, process in which: a) dissolves
机译:水溶性固体药物成分,包括生物分类固醇和环戊二醇的水溶液及其溶液,均用作类固醇:(a)作为活性成分,它包含生物分类固醇,例如紫杉醇和小型生物分类固醇,分布广泛,具有较大的表面积,阿莫西林,优选廖非花,可以盐或多种形式的水合物或溶液形式存在,例如,由十六烷和(b)制得的溶液含有细乙酰基γ-环戊二醇或羟丙基β-环戊二醇(以下简称“环戊二醇),其可以将表皮,AMOLIN和优选地利菲利扎达分裂,重量比在所述紫杉醇和环糊精之间为1:25至1:250; C),并最终含有其他可溶于水的辅助材料,通常用于肠胃外给药的药物。特别地,该药物组合物包含重量比为1:100至1:150的紫杉醇和乙酰基-γ-环糊精,或重量比为1:25至1:100的紫杉萜和羟丙基-β-环糊精作为活性成分。药物组合物可包含以下任何成分作为环糊精:每个环糊精环的乙酰化度为约2至约12个基团的乙酰基-γ-环糊精,每个环糊精的乙酰化度为约8个古丙基的乙酰基-γ-环糊精。环,每个环糊精环的取代度为约2至约10个羟丙基的羟丙基-β-环糊精,每个环糊精环的取代度为约4至约6个羟丙基的羟丙基-β-环糊精。如上所述的固体和瞬时可溶状态的药物组合物的制备方法及其在肠胃外使用的水性溶剂中的溶液,其中a)溶解

著录项

  • 公开/公告号AR015482A1

    专利类型

  • 公开/公告日2001-05-02

    原文格式PDF

  • 申请/专利权人 THISSEN LABORATOIRES S.A.;

    申请/专利号AR1998P105607

  • 发明设计人

    申请日1998-11-06

  • 分类号A61K31/337;A61K47/48;A61K47/40;A61P35/00;

  • 国家 AR

  • 入库时间 2022-08-22 01:26:23

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