期刊
COLLOIDS AND SURFACES B-BIOINTERFACES
卷 88, 期 1, 页码 58-62出版社
ELSEVIER
DOI: 10.1016/j.colsurfb.2011.06.003
关键词
Doxorubicin; Poly(lactide-co-glycolide); Drug carrier; Magnetic
资金
- Science and Technology Committee of Shanghai [074119647, 1052nm01200]
- Health Bureau of Shanghai [2007147]
The poly(lactide-co-glycolide)-coated magnetic nanoparticles (PLGA MNPs) were prepared as carriers of doxorubicin (PLGA-DOX MNPs) through water-in-oil-in-water (W/O/W) emulsification method. The characteristics of PLGA-DOX MNPs were measured by using transmission electron microscopy (TEM) and vibrating-sampling magnetometry (VSM). It was found that the synthesized nanoparticles were spherical in shape with an average size of 100 +/- 20 nm, low aggregation and good magnetic responsivity. Meanwhile, the drug content and encapsulation efficiency of nanoparticles can be achieved by varying the feed weight ratios of PLGA and DOX particles. These PLGA-DOX MNPs also demonstrated sustained release of DOX at 37 degrees C in buffer solution. Besides, influence of drug-loaded nanoparticles on in vitro cytotoxicity was determined by MTT assay, while cellular apoptosis was detected by Annexin V-FITC apoptosis detection kit. The results showed that PLGA-DOX MNPs retained significant antitumor activities. Therefore, PLGA-DOX MNPs might be considered a promising drug delivery system for cancer chemotherapy. (C) 2011 Elsevier B.V. All rights reserved.
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