Synthesis and characterization of well-defined PAA-PEG multi-responsive hydrogels by ATRP and click chemistry

被引:12
|
作者
Zhou, Chao [1 ]
Qian, Shan-shan [1 ]
Li, Xia-jun [2 ]
Yao, Fang [1 ]
Forsythe, John S. [3 ]
Fu, Guo-dong [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
[2] Southeast Univ, Sch Publ Hlth, Nanjing 210009, Jiangsu, Peoples R China
[3] Monash Univ, Dept Mat Engn, Clayton, Vic 3800, Australia
基金
中国国家自然科学基金;
关键词
MOLECULAR THERMODYNAMIC THEORY; POLY(ACRYLIC ACID) HYDROGELS; AMPHIPHILIC MODEL NETWORKS; PHASE-TRANSITION; ACRYLIC-ACID; POLYMER; PH; BEHAVIOR; CONETWORKS; DENDRIMERS;
D O I
10.1039/c4ra09438g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multi-responsive poly(acrylic acid)-poly(ethylene glycol) (PAA-PEG) hydrogels with well-defined crosslinking structures were synthesized using atom transfer radical polymerization (ATRP) and copper-catalyzed 1,3-dipolar azide-alkyne cycloaddition (CuAAC) techniques. The well-defined PAA-PEG hydrogels with different degrees of crosslinking were produced from controlling the molecular weight of the PAA and PEG chains. The prepared multi-responsive hydrogels exhibit regular physical and mechanical properties by adjusting the pH and Ca2+ ion secondary crosslinking. With increasing pH, the swelling ratio of the well-defined multi-responsive PAA-PEG hydrogels increased remarkably. Furthermore, the well-defined PAA-PEG hydrogels with Ca2+ secondary crosslinking possessed a significantly higher crosslinking density as reflected by the lower swelling ratio, higher storage modulus, higher electrical conductivity and thermal stability. An in vitro cell viability assay also indicated that well-defined multi-responsive PAA-PEG hydrogels are biocompatible and have potential for implantable biomaterials.
引用
收藏
页码:54631 / 54640
页数:10
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