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Process for preparing crystalline particles of fluticasone, beclomethasone, salmeterol and salbutamol

机译:制备氟替卡松,倍氯米松,沙美特罗和沙丁胺醇的晶体颗粒的方法

摘要

The present invention relates to a novel process for preparing crystalline particles of substance which comprises mixing a solution of the substance in a liquid solvent with a liquid anti-solvent for said substance, which liquid anti-solvent is miscible with the liquid solvent, characterised in that the resultant crystalline particles generated are harvested by a process which comprises: (i) mixing a first liquid phase formed from the resultant suspension of crystalline substance in solvent/anti-solvent mixture with a third liquid which is immiscible with said solvent/anti-solvent mixture or a component thereof thereby forming a second liquid phase and which is a non-solvent for the substance such that the substance is segregated into the second liquid phase; (ii) separating the two phases; and (iii) separating the crystalline particles of substance from the second liquid phase.
机译:本发明涉及一种制备物质结晶颗粒的新方法,该方法包括将物质在液体溶剂中的溶液与用于该物质的液体反溶剂混合,该液体反溶剂可与液体溶剂混溶,其特征在于:通过以下方法收集产生的所得结晶颗粒:(i)将由所得结晶物质在溶剂/反溶剂混合物中形成的悬浮液形成的第一液相与与所述溶剂/抗溶剂不混溶的第三液体混合。溶剂混合物或其组分从而形成第二液相,并且是该物质的非溶剂,使得该物质被分离成第二液相; (ii)将两个阶段分开; (iii)从第二液相中分离出物质的结晶颗粒。

著录项

  • 公开/公告号EP1438023B1

    专利类型

  • 公开/公告日2006-03-01

    原文格式PDF

  • 申请/专利权人 GLAXO GROUP LTD;

    申请/专利号EP20020770107

  • 发明设计人 MCLOUGHLIN MARTIN JOHN;

    申请日2002-10-23

  • 分类号A61K9/14;

  • 国家 EP

  • 入库时间 2022-08-21 21:30:23

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