Synthesis of cationic poly(4-vinylpyridine)-functionalized colloidal particles by emulsion polymerization with reactive block copolymer for protein adsorption

被引:12
作者
Cao, Jinxin [1 ,2 ]
Pan, Xiaodi [1 ,2 ]
Huang, Wei [1 ,2 ]
Wang, Yingjie [1 ,2 ]
Hua, Daoben [1 ,2 ]
Zhu, Xiulin [2 ]
Liang, Hongjun [3 ]
机构
[1] Soochow Univ, Sch Radiat Med & Protect, Coll Med, Suzhou 215123, Peoples R China
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn, Suzhou 215123, Peoples R China
[3] Colorado Sch Mines, Dept Met & Mat Engn, Golden, CO 80401 USA
关键词
Polymeric colloids; Poly(4-vinylpyridine); Protein adsorption; Emulsion polymerization; Block copolymer; SPHERICAL POLYELECTROLYTE BRUSHES; LATEX-PARTICLES; RADICAL POLYMERIZATION; MICROSPHERES; ALBUMIN;
D O I
10.1016/j.jcis.2012.05.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
We report here a novel protein sequestration method using polymeric colloidal particles prepared by emulsion polymerization with reactive block copolymers. Specifically, poly(4-vinyl-N-ethylpyridine bromide)block-polymethylacrylate block copolymers were synthesized from reversible addition-fragmentation chain transfer polymerization and used as emulsifiers for emulsion polymerization of poly(4-vinyl-N-ethylpyridine bromide)-functionalized polymeric colloidal particles. The particles have high and stable zeta potentials when dispersed in solution, regardless of pH variations. As a result, the polymeric colloids demonstrate a high affinity for oppositely charged proteins, even though the isoelectric points of proteins may vary greatly. We show here that BSA can be sequestered highly efficiently with a maximum binding capacity (similar to 900 mg/g). The adsorbed protein is easily released, and the polymeric colloids are regenerated after washing with a buffer solution of high ionic strength. These properties may prompt this type of novel macromolecule-functionalized colloids to be utilized for effective protein adsorption and separation. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:137 / 142
页数:6
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