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一种将利福平和异烟肼包裹于脂质体中的简单技术。

A simple technique for entrapping rifampicin and isoniazid into liposomes.

作者信息

Wasserman M, Beltrán R M, Quintana F O, Mendoza P M, Orozco L C, Rodriguez G

出版信息

Tubercle. 1986 Jun;67(2):83-90. doi: 10.1016/0041-3879(86)90001-2.

DOI:10.1016/0041-3879(86)90001-2
PMID:3775868
Abstract

A method for the preparation of liposomes loaded with rifampicin and isoniazid is described. Optimal conditions were established; the lipid suspension was mixed with the aqueous solution of the drugs and was sonicated in a bath for 30 min at 50 degrees C. The optimum composition tested was phosphatidyl choline, cholesterol and cardiolipin in a molar ratio of 7:2:1. The separation of unloaded drug was performed by centrifugation through three successive Sephadex G-25 columns. The liposomes were multilamellar vesicles with a size ranging from 100-300 nm. The drugs were trapped in concentrations from 6.5-9.5 mg/ml. This method is suitable for preparation of liposomes in small laboratories.

摘要

描述了一种制备负载利福平和异烟肼的脂质体的方法。确定了最佳条件;将脂质悬浮液与药物水溶液混合,并在50℃的水浴中超声处理30分钟。测试的最佳组成为摩尔比为7:2:1的磷脂酰胆碱、胆固醇和心磷脂。通过连续通过三个葡聚糖G-25柱进行离心来分离未负载的药物。脂质体为多层囊泡,大小范围为100 - 300nm。药物的包封浓度为6.5 - 9.5mg/ml。该方法适用于小型实验室制备脂质体。

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A simple technique for entrapping rifampicin and isoniazid into liposomes.一种将利福平和异烟肼包裹于脂质体中的简单技术。
Tubercle. 1986 Jun;67(2):83-90. doi: 10.1016/0041-3879(86)90001-2.
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Antimicrob Agents Chemother. 1997 Jun;41(6):1211-4. doi: 10.1128/AAC.41.6.1211.