首页> 外国专利> THE PREPARATION METHOD OF DOXORUBICIN-POLYBUTYLCYANOACRYLATE NANOPARTICLES

THE PREPARATION METHOD OF DOXORUBICIN-POLYBUTYLCYANOACRYLATE NANOPARTICLES

机译:阿霉素-聚氰基丙烯酸酯纳米颗粒的制备方法

摘要

A preparation method of doxorubicin-polybutylcyanoacrylate nanoparticles, whose steps are as follows: HCl solution react with doxorubicin hydrochloride powders, and stir the mixture to dissolve, followed by the addition of Dextran70, then a-butylcyanoacrylate, stir it till an orange opalescence appears, then adjust pH to 7; filter it over filter membrane of 0.45µm, and dry to give the nanoparticles. The DOX­PBCA-NP available from the invention can carry many drug including chemotherapeutics and gene drug, whose targeting property can significantly reduce the toxicity of drug, improve the therapeutic effect, reduce dose anddose frequency, improve patient compliance, increase the stability of gene drug against ribozyme, increase the drug concentration in cells and increase the action time.
机译:一种阿霉素-聚氰基丙烯酸丁酯纳米粒子的制备方法,其步骤如下:盐酸溶液与阿霉素盐酸盐粉末反应,搅拌使混合物溶解,然后加入右旋糖酐Dextran70,然后加入丙烯酸正丁酯,搅拌直至出现橙色乳白色,然后调节pH至7;用0.45μm的滤膜过滤,然后干燥得到纳米颗粒。可从本发明获得的DOXPBCA-NP可以携带许多药物,包括化学治疗药和基因药物,其靶向性质可以显着降低药物的毒性,改善治疗效果,减少剂量和剂量频率,改善患者依从性,增加基因药物针对药物的稳定性。核酶,增加细胞中的药物浓度并增加作用时间。

著录项

  • 公开/公告号WO2006015534A1

    专利类型

  • 公开/公告日2006-02-16

    原文格式PDF

  • 申请/专利权人 ZHANG YANGDE;

    申请/专利号WO2005CN01056

  • 发明设计人 ZHANG YANGDE;

    申请日2005-07-18

  • 分类号A61K9/51;A61K9/16;A61K31/704;A61K47/32;A61P35/00;

  • 国家 WO

  • 入库时间 2022-08-21 21:32:33

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