首页> 外国专利> ENCAPSULATION AND DEAGGREGATION OF POLYENE ANTIBIOTICS USING POLY(ETHYLENE GLYCOL)-PHOSPHOLIPID MICELLES

ENCAPSULATION AND DEAGGREGATION OF POLYENE ANTIBIOTICS USING POLY(ETHYLENE GLYCOL)-PHOSPHOLIPID MICELLES

机译:聚乙烯醇-磷脂胶束对聚乙烯抗菌剂的包封和去胶

摘要

Amphotericin B (or other hydrophobic compound) is encapsulated in a deaggregated form in micelles of monomethoxy poly(ethylene glycol)-phospholipid (as specifically exemplified, the phospholipid is 1,2 di-stearoyl-sn-glycero-3-phosphatidyl ethanolamine) formed by solvent evaporation. Advantageously, the hydration of the dried drug-polymer film is carried at between about 25° C. and about 80° C. The micelles can be reconstituted with the Amphotericin B (or other hydrophobic compound) in a deaggregated state and safely used in therapy for fungal infections of humans or animals, especially for systemic fungal infections, or other desired application. The polyene micellar formulations described herein are reduced in toxicity as compared with those polyene formulations in which there is significant occurrence of aggregated polyenes.
机译:将两性霉素B(或其他疏水性化合物)以解聚形式封装在形成的单甲氧基聚(乙二醇)-磷脂(具体示例为磷脂是1,2-二硬脂酰基-sn-甘油-3-磷脂酰乙醇胺)的胶束中通过溶剂蒸发。有利地,干燥的药物-聚合物膜的水合作用在约25℃至约80℃之间进行。所述胶束可以用两性霉素B(或其他疏水性化合物)以解聚状态重构并安全地用于治疗中。用于人或动物的真菌感染,特别是用于全身性真菌感染或其他所需的应用。与其中显着发生聚集多烯的那些多烯制剂相比,本文所述的多烯胶束制剂的毒性降低。

著录项

  • 公开/公告号US2009148509A1

    专利类型

  • 公开/公告日2009-06-11

    原文格式PDF

  • 申请/专利权人 GLEN S. KWON;

    申请/专利号US20080238298

  • 发明设计人 GLEN S. KWON;

    申请日2008-09-25

  • 分类号A61K31/7048;A61K9/127;

  • 国家 US

  • 入库时间 2022-08-21 19:36:52

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