药物和疫苗的模型脂质体递送系统

F. Firdaus, Zeinab G. Khalil, R. Capon, M. Skwarczynski, I. Toth
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引用次数: 1

摘要

自从60年前脂质体被发现以来,就一直被用于药物输送。它们作为载体提供的优势已经被认识到,并被用于改善许多药物的输送和消除有害的副作用。脂质体输送已被用于抗癌药物、抗结核药物、各种疫苗的测试,仅举几例。方法研制了一系列添加胆固醇和聚乙二醇的脂质体制剂。用流式细胞术和共聚焦显微镜检测和分析了人前列腺癌上皮细胞(PC-3)和小鼠巨噬细胞对这些制剂的摄取情况。结果以卵磷脂酰甘油为主要脂质制备的阴离子小脂质体囊泡(≤200 nm)最容易被PC-3细胞和巨噬细胞吸收。结论制备的脂质体制剂可作为药物和疫苗递送的模型系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Model Liposomal Delivery System for Drugs and Vaccines
Background Liposomes have been used for drug delivery since their discovery 60-years-ago. The advantages they provide as carriers have been recognised and exploited to improve the delivery of numerous drugs and eliminate harmful side-effects. Liposomal delivery has been tested for anticancer drugs, anti-tuberculosis drugs, variety of vaccines, just to list a few. Methods We developed a series of liposomal formulations with the addition of cholesterol and polyethylene glycol. The uptake of these formulations by human epithelial prostate cancer (PC-3) cells and mouse macrophages was examined and analysed by flow cytometry and confocal microscopy. Results Among the liposomes tested, small anionic liposome vesicles (≤200 nm) prepared with egg phosphatidylglycerol as the main lipid were most effectively taken up by PC-3 cells and macrophages. Conclusion We produced a liposome formulation that can be used as a model system for the delivery of drugs and vaccines.
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