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Effects of Nanoliposomal and Pegylated Nanoliposomal Artemisinin in Treatment of Breast Cancer

机译:纳米脂质体和聚乙二醇化纳米脂质体青蒿素在乳腺癌治疗中的作用

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摘要

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.
机译:这项研究旨在研究纳米脂质体青蒿素的制备及其在乳腺癌细胞上的实现。副作用一直是药物使用以及癌症治疗的常见挑战之一。为了减少这种影响,纳米技术已经有了很大的帮助。通过反相蒸发提供纳米脂质体。用这种方法,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,通过使用聚乙二醇2000将所得制剂聚乙二醇化以增加其稳定性和溶解性。非聚乙二醇化和聚乙二醇化脂质体青蒿素的平均直径通过Zeta sizer系统测定。从脂质体释放的药物的百分比通过透析进行。通过分光光度法估计两种制剂的包封效率。结果,纳米脂质体制剂的包封和药物释放远大于相同制剂的聚乙二醇化。此外,这项研究表明,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大。

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