Postpolymerization Modifications of Alkene-Functional Polycarbonates for the Development of Advanced Materials Biomaterials

被引:43
作者
Thomas, Anthony W. [1 ]
Dove, Andrew P. [1 ]
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
关键词
degradable polymers; drug delivery; functional carbonates; postpolymerization modification; tissue scaffolds; RING-OPENING POLYMERIZATION; AMPHIPHILIC BLOCK-COPOLYMERS; 6-MEMBERED CYCLIC CARBONATE; TRIMETHYLENE CARBONATE; BIODEGRADABLE POLYMERS; EPSILON-CAPROLACTONE; ALIPHATIC POLYCARBONATES; GLYCOL CHITOSAN; DRUG-DELIVERY; IN-VITRO;
D O I
10.1002/mabi.201600310
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Functional aliphatic polycarbonates have attracted significant attention as materials for use as biomedical polymers in recent years. The incorporation of pendent functionality offers a facile method of modifying materials postpolymerization, thus enabling functionalities not compatible with ring-opening polymerization (ROP) to be introduced into the polymer. In particular, polycarbonates bearing alkene-terminated functional groups have generated considerable interest as a result of their ease of synthesis, and the wide range of materials that can be obtained by performing simple postpolymerization modifications on this functionality, for example, through radical thiol-ene addition, Michael addition, and epoxidation reactions. This review presents an in-depth appraisal of the methods used to modify alkene-functional polycarbonates postpolymerization, and the diversity of practical applications for which these materials and their derivatives have been used.
引用
收藏
页码:1762 / 1775
页数:14
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