Synthesis of temperature and pH-responsive crosslinked micelles from polypeptide-based graft copolymer

被引:26
|
作者
Zhao, Changwen [1 ]
He, Pan [1 ,2 ]
Xiao, Chunsheng [1 ,2 ]
Gao, Xiaoye [1 ,2 ]
Zhuang, Xiuli [1 ]
Chen, Xuesi [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly(N-isopropylacrylamide); Poly(L-glutamic acid); Self-assembly; Cross linked micelles; AQUEOUS-SOLUTION PROPERTIES; BLOCK-COPOLYMERS; TRIBLOCK COPOLYMER; DRUG-DELIVERY; MICELLIZATION; FABRICATION; POLYMERIZATION; POLYMERS; VESICLES; PEG;
D O I
10.1016/j.jcis.2011.04.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A polypeptide-based double hydrophilic graft copolymer was synthesized by the sequential grafting of poly(N-isopropylacrylamide) (PNIPAM) and 2-hydroxyethyl methacrylate (HEMA) onto poly(L-glutamic acid) (PGA) backbone. The copolymers were sensitive to both temperature and pH. The phase transition and aggregation behaviors of the graft copolymers in aqueous solutions were investigated by the turbidity measurements and dynamic laser scattering (DLS). The light transmittance decrease of the copolymers at temperature above lower critical solution temperature (LCST) was remarkably weakened at pH around 6.5 due to the coil to alpha helix change of PGA chain induced by pH. The copolymers can self-assembly into micelles with PNIPAM cores in the aqueous solution at pH 8.0 and 60 degrees C. Subsequently, polymerization of HEMA led to the facile preparation of crosslinked micelles, which were observed directly by transmission electron microscopy (TEM). The temperature controlled shrinkage behaviors of crosslinked micelles highly depended on the pH values of the solution. The crosslinked micelles aggregated at pH 5.0 due to the increased hydrophobic interactions among them induced by the protonation of PGA component. These crosslinked micelles have promising applications as intelligent drug delivery vehicles. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:436 / 442
页数:7
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