One-step synthesis of mussel-inspired molecularly imprinted magnetic polymer as stationary phase for chip-based open tubular capillary electrochromatography enantioseparation

被引:54
作者
Wang, Xiao-Ni [1 ]
Liang, Ru-Ping [1 ]
Meng, Xiang-Ying [1 ]
Qiu, Jian-Ding [1 ]
机构
[1] Nanchang Univ, Dept Chem, Nanchang, Peoples R China
基金
中国国家自然科学基金;
关键词
Molecularly imprinted polymer; Enantioseparation; Polydopamine; Magnetic nanoparticles; PDMS microchip; RECOGNITION PROPERTIES; ASCORBIC-ACID; URIC-ACID; SURFACE; NANOPARTICLES; SEPARATION; EXTRACTION; NANOTUBES; PROTEINS;
D O I
10.1016/j.chroma.2014.08.044
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A facile approach for preparation of molecularly imprinted polymers was developed and successfully used as chiral stationary phase for rapid enantioseparation by open tubular capillary electrochromatography (OT-CEC). In this work, molecularly imprinted polymers were one-step prepared employing Fe3O4 nanoparticles (NPs) as the supporting substrate and dopamine as the functional monomer. By simply mixing Fe3O4 NPs with template molecules in a weak alkaline solution of dopamine, a thin adherent polydopamine (PDA) film imprinted with template molecules was formed by the self-polymerization of dopamine on the surface of Fe3O4 NPs. After extracting the embedded template molecules, the produced imprinted Fe3O4@PDA NPs are of three dimensional shape of template molecules favoring high binding capacity and magnetism property for easy manipulation. The imprinted Fe3O4@PDA NPs prepared with L-tryptophan, L-tyrosine, Gly-L-Phe or s-ofloxacin as template molecules were packed in the PDMS microchannel via magnetic field as novel stationary phase for the successful enantioseparation of corresponding target analysts. In addition, the imprinted Fe3O4@PDA NPs-based OT-CEC system exhibited excellent reproducibility, stability and repeatability, which provides a powerful protocol for separation enantiomers within a short analytical time and opens up a promising avenue for high-throughput screening of chiral compounds. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:301 / 308
页数:8
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