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Preparation Method of the Inclusion Complex of Peracetylated Cyclodextrin and Water-Soluble Drugs formed in Supercritical Carbon Dioxide and Use Thereof

机译:全乙酰化环糊精与超临界二氧化碳形成的水溶性药物包合物的制备方法及其用途

摘要

PURPOSE: A method for manufacturing an inclusion complex of peracetylated cyclodextrin or heptakis(2,3,6-tri-O-acetyl) cyclodextrin and soluble drugs is provided to enhance inclusion rate and to apply in oral administration. CONSTITUTION: A method for manufacturing an inclusion complex of peracetylated cyclodextrin and soluble drugs comprises: a step of stirring peracetylated cyclodextrin(PAc-CD) and soluble drugs to form an inclusion; a step of removing supercritical carbon dioxide. Peraceylated cyclodextrin is PAc-alpha-CD, PAc-beta-CD, or PAc-gamma-CD. A pharmaceutical composition contains the inclusion complex.
机译:目的:提供了一种制造过乙酰化环糊精或七(2,3,6-三-O-乙酰基)环糊精与可溶性药物的包合物的方法,以提高包合率并应用于口服。组成:一种过乙酰化环糊精与可溶性药物包合物的制备方法,包括:搅拌过乙酰化环糊精(PAc-CD)与可溶性药物形成包合物的步骤;去除超临界二氧化碳的步骤。过酰基化的环糊精是PAc-α-CD,PAc-β-CD或PAc-γ-CD。药物组合物包含包合物。

著录项

  • 公开/公告号KR101245469B1

    专利类型

  • 公开/公告日2013-03-25

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20100015496

  • 发明设计人 임권택;

    申请日2010-02-22

  • 分类号A61K31/4245;A61K47/40;A61P9;

  • 国家 KR

  • 入库时间 2022-08-21 16:25:31

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