| Literature DB >> 25298633 |
Neda Dadgar1, Maedeh Koohi Moftakhari Esfahani2, Sepideh Torabi1, Seyed Ebrahim Alavi2, Azim Akbarzadeh2.
Abstract
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.Entities:
Keywords: Artemisinin; Breast cancer; Cytotoxicity; Drug delivery; Nanoliposome
Year: 2013 PMID: 25298633 PMCID: PMC4175706 DOI: 10.1007/s12291-013-0389-x
Source DB: PubMed Journal: Indian J Clin Biochem ISSN: 0970-1915