乙二醇
胶束
化学
药物输送
聚合
高分子化学
环氧乙烷
氧化还原
动态光散射
共聚物
亚甲基
控制释放
泊洛沙姆
纳米凝胶
有机化学
材料科学
聚合物
水溶液
纳米颗粒
纳米技术
作者
Quang Nam Bui,Yi Li,Moon-Sun Jang,Đại Phú Huỳnh,Jung Hee Lee,Doo Sung Lee
出处
期刊:Macromolecules
[American Chemical Society]
日期:2015-06-03
卷期号:48 (12): 4046-4054
被引量:89
标识
DOI:10.1021/acs.macromol.5b00423
摘要
In this report, a redox- and pH-sensitive poly(β-amino ester)-grafted disulfide methylene oxide poly(ethylene glycol) (PAE-g-DSMPEG) was synthesized, and it showed not only a sharp pH-dependent assembly–disassembly transition but also a quick shell shading in a high concentration of reducing agent by Michael addition polymerization. 1H NMR, dynamic light scattering, and transition electron microscopy were combined to characterize the redox- and pH-responsiveness in various triggered conditions. The hydrophobic drug doxorubicin (DOX) was used as the model drug to investigate the encapsulation and delivery ability of polymeric micelles, in both in vitro and in vivo experiments. Notably, antitumor experiments in tumor-bearing mice showed that DOX-loaded polymeric micelles effectively enhanced the therapeutic efficacy in comparison to free-DOX. These results were further confirmed by histopathological examinations. Taken together, the results suggested that PAE-g-DSMPEG could be a potential hydrophobic drug delivery vehicle.
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