Polymeric biomaterials with engineered degradation

被引:76
作者
Deshayes, Stephanie [1 ]
Kasko, Andrea M. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
enzymolysis; hydrolysis; oxidation; photolysis; polymeric biomaterials; stimuli-sensitive polymers; degradation; bioengineering; RING-OPENING POLYMERIZATION; TYROSINE-DERIVED POLYCARBONATES; PHOTOLABILE PROTECTING GROUPS; CRITICAL SOLUTION TEMPERATURE; UNCAGING CROSS-SECTIONS; PH-RESPONSIVE POLYMERS; DRUG-DELIVERY; CONTROLLED-RELEASE; ACID-LABILE; INTRACELLULAR DELIVERY;
D O I
10.1002/pola.26765
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymeric biomaterials are widely used as carriers for cells and therapeutic agents. Until recently, most research has been limited to a relatively narrow number of monomers and chemistries. A fundamental challenge in developing clinically relevant polymeric biomaterials is to independently control their chemical and physical properties across multiple scales in both time and space. Control over a biomaterial's chemical and physical properties is critical to recapitulate the complex cascades of signals and complex microenvironments found in nature. Typically, dynamically responsive biomaterials either degrade in the presence of a stimulus (i.e., water induces hydrolysis) or experience a change in solubility on application of the stimulus (i.e., temperature induces gelation via lower critical solution temperature LCST). This highlight discusses recent advances in stimulated and controlled degradation of polymeric biomaterials. The goal of this review is to provide a broad overview of physiologically relevant stimuli used to control the degradation of a wide range of polymeric biomaterials with varying architectures and physical forms. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3531-3566
引用
收藏
页码:3531 / 3566
页数:36
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