Self-Healing Supramolecular Self-Assembled Hydrogels Based on Poly(L-glutamic acid)

被引:164
|
作者
Li, Guifei [1 ]
Wu, Jie [1 ]
Wang, Bo [1 ]
Yan, Shifeng [1 ]
Zhang, Kunxi [1 ]
Ding, Jianxun [2 ]
Yin, Jingbo [1 ]
机构
[1] Shanghai Univ, Sch Mat Sci & Engn, Shanghai 200444, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
SHAPE-MEMORY; CELL; PROTEIN; CHOLESTEROL; GENERATION; SCAFFOLDS; DELIVERY; BEHAVIOR; RELEASE; MATRIX;
D O I
10.1021/acs.biomac.5b01287
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Self-healing polymeric hydrogels have the capability to recover their structures and functionalities upon injury, which are extremely attractive in emerging biomedical applications. This research reports a new kind of self-healing polypeptide hydrogels based on self-assembly between cholesterol (Chol)-modified triblock poly(L-glutamic acid)-block-poly(ethylene glycol)-block-poly(L-glutamic acid) ((PLGA-b-PEG-b-PLGA)-g-Chol) and beta-cydodextrin (beta-CD)-modified poly(L-glutamic acid) (PLGA-g-beta-CD). The hydrogel formation relied on the host and guest linkage between beta-CD and Chol. This study demonstrates the influences of polymer concentration and beta-CD/Chol molar ratio on viscoelastic behavior of the hydrogels. The results showed that storage modulus was highest at polymer concentration of 15% w/v and beta-CD/ Chol molar ratio of 1:1. The effect of the PLGA molecular weight in (PLGA-b-PEG-b-PLGA)-g-Chol on viscoelastic behavior, mechanical properties and in vitro degradation of the supramolecular hydrogels was also studied. The hydrogels showed outstanding self-healing capability and good cytocompatibility. The multilayer structure was constructed using hydrogels with self-healing ability. The developed hydrogels provide a fascinating glimpse for the applications in tissue engineering.
引用
收藏
页码:3508 / 3518
页数:11
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