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Process for preparing a pharmaceutical composition in the form of microspheres with prolonged release of an active princu00ecpio water-soluble, and microspheres

机译:具有延长的活性princ u00ecpio水溶性微丸形式的微球形式的药物组合物的制备方法和微球

摘要

"Process for the preparation of a pharmaceutical composition in the form of microspheres with prolonged release of an active princu00ecpio water-soluble, and microspheres.The present invention relates to a process for the preparation of a pharmaceutical composition in the form of microspheres with prolonged release of an active ingredient a water-soluble.Characterized by the fact that he understands the succession of the following steps: dissolution of the active principle in a suitable amount of water.Emulsification of the aqueous solution of the active principle thus obtained with a solution of a copolymer matrix D, 1 - lactu00eddeo - Co glicolu00eddeo, of an average molecular weight of between 40000 and 80.000 and having a ratio of lactic acid / glycolic acid ranging from 50 / 50 and 80 / 20, dissolved in a chlorinated hydrocarbon, leading to a first emulsion microfina and homogeneous.Emulsification of that first emulsion thus obtained in an external aqueous phase, containing a surfactant, an agent increases the viscosity and osmotic agent.Evaporation of the solvent extraction to obtain microspheres that recovers after filtration, washing and drying.The invention is also object microspheres, which can be obtained by the implementation of this process.Presenting a continuous release of an active principle over a period of more than two months, with advantage for a period of at least three months.
机译:具有延长的活性princ水溶性水溶性微球形式的药物组合物的制备方法和微球。本发明涉及以微球形式的药物组合物的制备方法。的特点是他了解以下步骤的连续性:将活性成分溶解在适量的水中,由此乳化了活性成分的水溶液共聚物基质D的溶液,其平均分子量为40000至80.000,且乳酸/乙醇酸之比为50 // 50至80 //的1-乳酸-Co glicol-葡聚糖20,溶于氯代烃中,产生第一乳液微细粉且均质。如此得到的第一乳液在外部水相中的乳化表面活性剂,增加黏度的试剂和渗透剂。蒸发溶剂萃取液得到微球,过滤,洗涤和干燥后可回收。本发明也是目的微球,可通过实施该方法获得。在两个多月的时间里发布有效原则,至少三个月。

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