Biotinylated thermoresponsive core cross-linked nanoparticles via RAFT polymerization and "click" chemistry

被引:18
作者
Lv, Wenhui [1 ]
Liu, Li [1 ]
Luo, Yan [1 ]
Wang, Xiaojuan [1 ]
Liu, Yuwei [1 ]
机构
[1] Nankai Univ, Inst Polymer Chem, Minist Educ, Key Lab Funct Polymer Mat, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
RAFT polymerization; Click" chemistry; Molecular recognition; Nanoparticles; Thermoresponsive; FRAGMENTATION TRANSFER POLYMERIZATION; BLOCK-COPOLYMERS; DRUG-DELIVERY; MICELLES; POLYMERS; POLY(N-ISOPROPYLACRYLAMIDES); NEOGLYCOPOLYMERS; BIOAVAILABILITY; BIOCONJUGATION; GLYCOPOLYMERS;
D O I
10.1016/j.jcis.2011.01.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A straightforward approach to the synthesis of "clickable" thermoresponsive core cross-linked (CCL) nanoparticles was developed. This approach was based on reversible addition-fragmentation chain transfer (RAFT) radical cross-linking polymerization of styrene and divinylbenzene with azide-functionalized poly(N-isopropylacrylamide) (PNIPAM-N-3) as macro chain transfer agent in a selective solvent. Spherical nanoparticles with a diameter of 12 nm were obtained after 24 h polymerization. When the lyophilized CCL nanoparticles were dispersed in THF, spherical nanoparticles were observed, confirming the stability of CCL nanoparticles. The transmission electron microscopy (TEM) studies demonstrated that spherical nanoparticles and wormlike structure coexisted in the aqueous solution. The CCL nanoparticles have a lower critical solution temperature (LCST) at about 29.6 degrees C, a little lower than that of PNIPAM homopolymer. Biotin molecules were conjugated to the surface of CCL nanoparticles via "click" chemistry in aqueous media. After bioconjugation, the LCST shifted to 28.3 degrees C. The bioavailability of biotin to protein avidin was evaluated by a 4'-hydroxyazobenzene-2-carboxylic acid/avidin (HABA/avidin) binding assay and TEM. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 23
页数:8
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