Dual thermal- and pH-responsive polypeptide-based hydrogels

被引:19
|
作者
Meng, Fan-dong [1 ]
Ni, Yun-xia [1 ]
Ji, Si-fan [1 ]
Fu, Xiao-hui [1 ]
Wei, Yu-han [1 ]
Sun, Jing [1 ]
Li, Zhi-bo [1 ]
机构
[1] Qingdao Univ Sci & Technol, Sch Polymer Sci & Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
pH-responsive; Thermal-responsive; Hydrogel; Polypeptide; SUPRAMOLECULAR HYDROGELS; GELATION; POLY(L-GLUTAMATE); DELIVERY;
D O I
10.1007/s10118-017-1959-9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Smart hydrogels have received increasing attention for their great potential for the applications in many fields. Herein, we report a facile approach to prepare a class of dual-responsive hydrogels assembled from synthetic statistical/block thermal-responsive copoly(L-glutamate)s copolymerized with poly(ethylene glycol), which were prepared by ring-opening polymerization (ROP) and post-modification strategy. The incorporation of oligo(ethylene glycol) (OEG) and glutamic acid residues offers the gels with thermal- and pH-responsive properties simultaneously. We have systematically studied the influence of both temperature and pH on the gelation behaviors of these copolymers. It is found that the increase of glutamic acid content and solution pH values can significantly suppress the gelation ability of the samples. Circular dichroism (CD) results show that the alpha-helix conformation appears to be the dominant secondary conformation. More interestingly, the gelation property of the block copolymer with statistical thermal-responsive copoly(L-glutamate)s shows greater dependence on pH as compared to that with block segments due to the distinct morphology of the self-assemblies. The obtained hydrogels exhibit pH-dependent and thermal-responsive gelation behaviors, which enable them as an ideal smart hydrogel system for biomedical applications.
引用
收藏
页码:1243 / 1252
页数:10
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