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用于细胞递送的可注射双网络水凝胶的构建

Construction of Injectable Double-Network Hydrogels for Cell Delivery.

作者信息

Yan Yan, Li Mengnan, Yang Di, Wang Qian, Liang Fuxin, Qu Xiaozhong, Qiu Dong, Yang Zhenzhong

机构信息

College of Materials Science and Opto-electronic Technology, University of Chinese Academy of Sciences , Beijing 100049, China.

State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.

出版信息

Biomacromolecules. 2017 Jul 10;18(7):2128-2138. doi: 10.1021/acs.biomac.7b00452. Epub 2017 Jun 5.

Abstract

Herein we present a unique method of using dynamic cross-links, which are dynamic covalent bonding and ionic interaction, for the construction of injectable double-network (DN) hydrogels, with the objective of cell delivery for cartilage repair. Glycol chitosan and dibenzaldhyde capped poly(ethylene oxide) formed the first network, while calcium alginate formed the second one, and in the resultant DN hydrogel, either of the networks could be selectively removed. The moduli of the DN hydrogel were significantly improved compared to that of the parent single-network hydrogels and were tunable by changing the chemical components. In situ 3D cell encapsulation could be easily performed by mixing cell suspension to the polymer solutions and transferred through a syringe needle before sol-gel transition. Cell proliferation and mediated differentiation of mouse chondrogenic cells were achieved in the DN hydrogel extracellular matrix.

摘要

在此,我们提出了一种独特的方法,即利用动态交联(动态共价键合和离子相互作用)来构建可注射双网络(DN)水凝胶,目的是用于细胞递送以修复软骨。乙二醇壳聚糖和二苯甲醛封端的聚环氧乙烷形成第一个网络,而海藻酸钙形成第二个网络,在所得的DN水凝胶中,任一网络都可以被选择性去除。与母体单网络水凝胶相比,DN水凝胶的模量显著提高,并且可以通过改变化学成分进行调节。通过将细胞悬液与聚合物溶液混合,并在溶胶-凝胶转变之前通过注射器针头转移,可轻松实现原位3D细胞封装。在DN水凝胶细胞外基质中实现了小鼠软骨生成细胞的增殖和介导分化。

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