Dadgar Neda, Koohi Moftakhari Esfahani Maedeh, Torabi Sepideh, Alavi Seyed Ebrahim, Akbarzadeh Azim
Department of Agricultural Biotechnology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Pilot Nanobiotechnology, Pasteur Institute of Iran, No 358, 12 Farvardin Street, Jomhoori Avenue, 13169-43551 Tehran, Iran.
Indian J Clin Biochem. 2014 Oct;29(4):501-4. doi: 10.1007/s12291-013-0389-x. Epub 2013 Oct 1.
This study is aimed to investigate the nanoliposomal artemisinin preparation, and its implementation on breast cancer cells. Side effects have been one of the common challenges of drug usage, as well as cancer treatment. In order to reduce such effects, nanotechnology has been a great help. Nanoliposomes are provided through reverse phase evaporation. In this method, certain proportions of phosphatidylcholine, cholesterol and artemisinin were mixed together. Besides, the obtained formulation was pegylated by using polyethylene glycol 2000 in order to increase its stability and solubility. The mean diameter of non-pegylated and pegylated liposomal artemisinin was determined by Zeta sizer system. The percent of drug released from liposome was performed by dialysis. The encapsulation efficiency of both formulations was estimated by spectrophotometry method. As a result, encapsulation and drug release of nanoliposomal formulation were more than the pegylation of the same formulation. In addition, this study indicated that cytotoxicity effect of pegylated nanoliposomal artemisinin was more, in comparison with nanoliposomal artemisinin.
本研究旨在探究纳米脂质体青蒿素制剂及其对乳腺癌细胞的作用。副作用一直是药物使用以及癌症治疗中常见的挑战之一。为了减少此类影响,纳米技术起到了很大的帮助。纳米脂质体通过逆相蒸发法制备。在该方法中,将一定比例的磷脂酰胆碱、胆固醇和青蒿素混合在一起。此外,为了提高其稳定性和溶解性,使用聚乙二醇2000对所得制剂进行聚乙二醇化。通过Zeta粒度分析仪系统测定未聚乙二醇化和聚乙二醇化脂质体青蒿素的平均直径。通过透析测定脂质体中药物的释放百分比。采用分光光度法估算两种制剂的包封率。结果表明,纳米脂质体制剂的包封率和药物释放率均高于相同制剂的聚乙二醇化产物。此外,本研究表明,与纳米脂质体青蒿素相比,聚乙二醇化纳米脂质体青蒿素的细胞毒性作用更强。