Biomolecule-functionalized polymer brushes

被引:159
作者
Jiang, Hui [1 ]
Xu, Fu-Jian [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Key Lab Carbon Fiber & Funct Polymers, State Key Lab Chem Resource Engn,Minist Educ, Beijing 100029, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
TRANSFER RADICAL POLYMERIZATION; POLY(ACRYLIC ACID) BRUSHES; SURFACE-INITIATED ATRP; HIGH-CAPACITY; COVALENT IMMOBILIZATION; POLYETHYLENE-GLYCOL; POLY(2-HYDROXYETHYL METHACRYLATE); PROTEIN IMMOBILIZATION; TEMPERATURE SENSITIVITY; POLYCAPROLACTONE FILMS;
D O I
10.1039/c2cs35453e
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Functional polymer brushes have been utilized extensively for the immobilization of biomolecules, which is of crucial importance for the development of biosensors and biotechnology. Recent progress in polymerization methods, in particular surface-initiated atom transfer radical polymerization (ATRP), has provided a unique means for the design and synthesis of new biomolecule-functionalized polymer brushes. This current review summarizes such recent research activities. The different preparation strategies for biomolecule immobilization through polymer brush spacers are described in detail. The functional groups of the polymer brushes used for biomolecule immobilization include epoxide, carboxylic acid, hydroxyl, aldehyde, and amine groups. The recent research activities indicate that functional polymer brushes become versatile and powerful spacers for immobilization of various biomolecules to maximize their functionalities. This review also demonstrates that surface-initiated ATRP is used more frequently than other polymerization methods in the designs of new biomolecule-functionalized polymer brushes.
引用
收藏
页码:3394 / 3426
页数:33
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