Photoreconfigurable Polymers for Biomedical Applications: Chemistry and Macromolecular Engineering

被引:63
作者
Zhu, Congcong [1 ]
Ninh, Chi [1 ]
Bettinger, Christopher J. [1 ,2 ,3 ]
机构
[1] Carnegie Mellon Univ, Dept Mat Sci & Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
[3] McGowan Inst Regenerat Med, Pittsburgh, PA 15219 USA
基金
美国安德鲁·梅隆基金会;
关键词
METAL-METAL BONDS; TRANSFER RADICAL POLYMERIZATION; NEAR-INFRARED LIGHT; PHOTOLABILE PROTECTING GROUPS; CROSS-LINKED HYDROGELS; SHAPE-MEMORY POLYMER; P-HYDROXYPHENACYL; RESPONSIVE POLYMERS; PHOTODEGRADABLE HYDROGELS; CATALYTIC DEPROTECTION;
D O I
10.1021/bm500990z
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
Stimuli-responsive polymers play an important role in many biomedical technologies. Light responsive polymers are particularly desirable because the parameters of irradiated light and diverse photoactive chemistries produce a large number of combinations between functional materials and associated stimuli. This Review summarizes recent advances in utilizing photoactive chemistries in macromolecules for prospective use in biomedical applications. Special focus is granted to selection criterion when choosing photofunctional groups. Synthetic strategies to incorporate these functionalities into polymers and networks with different topologies are also highlighted herein. Prospective applications of these materials are discussed including programmable matrices for controlled release, dynamic scaffolds for tissue engineering, and functional coatings for medical devices. The article concludes by summarizing the state of the art in photoresponsive polymers for biomedical applications including current challenges and future opportunities.
引用
收藏
页码:3474 / 3494
页数:21
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