Biocompatible in situ-forming glycopolypeptide hydrogels

被引:0
|
作者
SHI Shun [1 ,2 ,3 ]
YU ShuangJiang [1 ,3 ]
LI Gao [1 ,2 ,3 ]
HE ChaoLiang [1 ,2 ,3 ]
CHEN XueSi [1 ,2 ,3 ]
机构
[1] CAS Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
[2] College of Applied Chemistry and Engineering, University of Science and Technology of China
[3] Jilin Biomedical Polymers Engineering Laboratory
基金
中国国家自然科学基金;
关键词
in situ-forming; hydrogels; glycopolypeptide; tissue engineering; horseradish peroxidase;
D O I
暂无
中图分类号
O648.17 [凝胶及软胶];
学科分类号
070304 ; 081704 ;
摘要
A lack of biological activity hinders the application of synthetic hydrogels in tissue engineering and regenerative medicine.However, the use of glycopolypeptides in hydrogel synthesis may provide the materials with the desired biological activities.Herein, we prepared three in situ-forming hydrogels from various phenol-functionalized glycopolypeptides. The gelation time,mechanical properties, degradation properties, and biocompatibility of the hydrogels were assessed. Gelation time ranged from 11 to 380s, depending on the concentration of horseradish peroxidase. The galactose-modified polypeptide hydrogel showed the highest storage modulus with an obvious stress relaxation phenomenon. The prepared hydrogels exhibited good degradation properties and compatibility to cells and tissues. Furthermore, the rate of immune cell accumulation around the mannosemodified polypeptide hydrogel was the fastest among the hydrogels.
引用
收藏
页码:992 / 1004
页数:13
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