表面带电脂质体载药及对小鼠体内弓形虫的作用
SURFACE CHARGED LIPOSOMES AS DRUG CARRIERS AND IN VIVO TESTS OF MICE INFECTED WITH TOXOPLASMA
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摘要: 表面电性是脂质体重要性质之一,本文用1,8-ANS作为探剂,采用荧光法和电泳法测定脂质体的表面电位。离子性药物的包封率及渗漏速度受脂质体表面电性影响,实验表明,脂质体表面电性和药物离子电性相反时,包封率高,渗漏速度慢。以小鼠感染弓形虫做模型,进行体内试验,证明脂质体载药显著优于游离药物的治疗效果。因弓形虫是细胞内寄生的原虫,凡有利于药物入胞的方法,可提高其疗效。此种模型试验简便、准确,其结果对载抗癌药脂质体研究可以借鉴。Abstract: The surface charge is one of the most important properties of liposomes. In this paper surface potential of liposomes was measured by fluorimetry using 1,8-ANS as a probe and by microelectrophoresis. The encapsulation efficiency and leakage rate of ionic drugs were influenced by the surface charge of liposomes. Higher encapsulation efficiency and lower leakage rate were resulted, if the surface charge of liposomes was opposite to the ionic charge of encapsulated drug.Mice infected with toxoplasma were used as a model. In in vivo test, liposomedrug was compared with the free drug. The. average survival days of groups of liposome-drugs were much longer than that of the group of free drugs.Mouse infected with toxoplasma is a simple, convenient and accurate model for measuring the biological activation of liposome-drugs.
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