A poly(L-lysine)-based hydrophilic star block co-polymer as a protein nanocarrier with facile encapsulation and pH-responsive release

被引:49
|
作者
Yan, Yunsong [2 ]
Wei, Daixu [1 ]
Li, Jiayan [2 ]
Zheng, Jinhong [2 ]
Shi, Ganggang [2 ]
Luo, Wenhong [2 ]
Pan, Ying [2 ]
Wang, Jinzhi [2 ]
Zhang, Lumian [2 ]
He, Xiaoying [2 ]
Liu, Daojun [2 ]
机构
[1] Natl Engn Res Ctr Nanotechnol, Shanghai 200241, Peoples R China
[2] Shantou Univ, Coll Med, Shantou 515041, Peoples R China
基金
中国国家自然科学基金;
关键词
Star block co-polymer; Drug delivery system; Poly(L-lysine); Insulin; Protein; POLY(ETHYLENE GLYCOL); POLYAMIDOAMINE DENDRIMERS; DELIVERY; MICROPARTICLES; MICROCAPSULES; MICELLES; CARRIER; DRUGS;
D O I
10.1016/j.actbio.2012.02.016
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A hydrophilic star block co-polymer was synthesized, characterized, and evaluated as a protein nanocarrier. The star block co-polymer was composed of a hyperbranched polyethylenimine (PEI) core, a poly(L-lysine) (PLL) inner shell, and a poly(ethylene glycol) (PEG) outer shell. The model protein insulin can be rapidly and efficiently encapsulated by the synthesized polymer in aqueous phosphate buffer at physiological pH. Complexation between PEI-PLL-b-PEG and insulin was investigated using native polyacryl-amide gel electrophoresis. The uptake of enhanced green fluorescent protein into Ad293 cells mediated by PEI-PLL-b-PEG was also investigated. The encapsulated insulin demonstrated sustained release at physiological pH and showed accelerated release when the pH was decreased. The insulin released from the star block co-polymer retained its chemical integrity and immunogenicity. (C) 2012 Acts Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2113 / 2120
页数:8
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