Enhancing Biopolymer Hydrogel Functionality through Interpenetrating Networks

被引:220
作者
Dhand, Abhishek P. [1 ]
Galarraga, Jonathan H. [1 ]
Burdick, Jason A. [1 ]
机构
[1] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
HYALURONIC-ACID; MECHANICAL-PROPERTIES; CROSS-LINKING; SEMIINTERPENETRATING NETWORK; STEM-CELLS; PHOTOCROSSLINKABLE GELATIN; SODIUM ALGINATE; EXTREMELY TOUGH; IPN HYDROGELS; SILK FIBROIN;
D O I
10.1016/j.tibtech.2020.08.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Traditional hydrogels are strong candidates for biomedical applications; however, they may suffer from drawbacks such as weak mechanics, static properties, and an inability to fully replicate aspects of the cellular microenvironment. These challenges can be addressed through the incorporation of second networks to form interpenetrating polymer network (IPN) hydrogels. The objective of this review is to establish clear trends on the enhanced functionality achieved by incorporating secondary networks into traditional, biopolymer-based hydrogels. These include mechanical reinforcement, ?smart? systems that respond to external stimuli, and the ability to tune cell? material interactions. Through attention to network structure and chemistry, IPN hydrogels may advance to meet challenging criteria for a wide range of biomedical fields.
引用
收藏
页码:519 / 538
页数:20
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