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作 者:陈丽凤[1] 张西臣[1] 杨永胜[1] 何宏轩 尹继刚[1] 杨举[1] 李建华[1]
机构地区:[1]解放军农牧大学寄生虫病学教研室
出 处:《中国寄生虫病防治杂志》1999年第2期117-119,共3页Chinese Journal of Parasitic Disease Control
基 金:吉林省科委基金
摘 要:用改良的冷冻融溶法制备出碘醚柳胺(Rafoxanide,Raf)脂质体定向剂,并对其药物特性进行了观察与测定。用Raf与聚乙烯吡咯烷酮(Polyvinylpyrolidone,PVP)共沉法解决了Raf在水性介质中不溶的问题,从而为制备该药脂质体创造了必要条件。采用单因素比较法优选出制备碘醚柳胺脂质体的最佳处方组成:药脂比为1∶27(w/w);Pc与Chol比为2∶1(mol/mol)。结果显示,用此法制备的脂质体包封率可高达58%;电镜下显示以多层脂质体为主,粒径大者4μm~6μm,小者0.1μm~1.0μm,后者约占60%。在室温条件下贮存75d后,其包封率由原来的56.97%下降到51.83%,表明用本法制备的脂质体具有良好稳定性。Rafoxanide(Raf) liposomes were prepared by modified freezethawing method. To improve solubility of Raf, Raf was made into Rafpolyvinylpyrrolidone(PVP) coprecipitate. Through singlefactor comparison, the optimal prescription selected was 127(w/w) for druglipid and 21(molmol) for lecithincholesterol. Under these conditions, the encapsulated rate of Rafliposomes was up to 58%. The size of Rafliposomes was observed and measured under electron microscope. The results indicated that most of vesicles were multilamellar and the size ranged from 0.1-6.0 m. To determine the stability, Rafliposomes were stored in room temperature for 75 days. The results showed that the encapsulated rate dropped from 56.97% to 51.83%, which indicated that Rafliposomes had a better stability.
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