Department of Obstetrics, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.
Colloids Surf B Biointerfaces. 2011 Nov 1;88(1):58-62. doi: 10.1016/j.colsurfb.2011.06.003. Epub 2011 Jun 25.
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°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.
聚(乳酸-共-乙醇酸)-共包裹的磁性纳米粒子(PLGA MNPs)通过水包油包水(W/O/W)乳化法被制备为阿霉素(DOX)的载体(PLGA-DOX MNPs)。使用透射电子显微镜(TEM)和振动采样磁强计(VSM)测量 PLGA-DOX MNPs 的特性。结果发现,所合成的纳米粒子呈球形,平均粒径为 100±20nm,聚集程度低,具有良好的磁响应性。同时,通过改变 PLGA 和 DOX 颗粒的进料重量比,可以实现纳米粒子的药物含量和包封效率。这些 PLGA-DOX MNPs 在缓冲溶液中于 37°C 时也表现出 DOX 的持续释放。此外,通过 MTT 测定法测定载药纳米粒子对体外细胞毒性的影响,通过 Annexin V-FITC 凋亡检测试剂盒检测细胞凋亡。结果表明,PLGA-DOX MNPs 保留了显著的抗肿瘤活性。因此,PLGA-DOX MNPs 可能被认为是癌症化疗的一种有前途的药物传递系统。