Monolithic molecular imprinted polymer fiber for recognition and solid phase microextraction of ephedrine and pseudoephedrine in biological samples prior to capillary electrophoresis analysis

被引:78
作者
Deng, Dong-Li [1 ,2 ]
Zhang, Ji-You [1 ]
Chen, Chen [1 ]
Hou, Xiao-Ling [2 ]
Su, Ying-Ying [1 ]
Wu, Lan [1 ]
机构
[1] Sichuan Univ, Analyt & Testing Ctr, Chengdu 610064, Peoples R China
[2] Sichuan Univ, Coll Chem, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
Capillary electrophoresis; Molecular imprinting; Solid phase microextraction; Ephedrine; Pseudoephedrine; MICELLAR ELECTROKINETIC CHROMATOGRAPHY; INDUCED FLUORESCENCE DETECTION; SENSITIVE DETERMINATION; ZONE-ELECTROPHORESIS; HERBAL STIMULANT; EXTRACTION; PERFORMANCE; URINE; CYCLODEXTRIN; SPECTROMETRY;
D O I
10.1016/j.chroma.2011.11.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel capillary electrophoresis (CE) method coupled with monolithic molecular imprinted polymer (MIP) fiber based solid phase microextraction (SPME) was developed for selective and sensitive determination of ephedrine (E) and pseudoephedrine (PE). With in situ polymerization in a silica capillary mold and E as template, the MIP fibers could be produced in batch reproducibly and each fiber was available for 50 extraction cycles without significant decrease in extraction ability. Using the MIP fiber under optimized extraction conditions, CE detection limits of E and PE were greatly lowered from 0.20 to 0.00096 mu g/mL and 0.12 to 0.0011 mu g/mL, respectively. Analysis of urine and serum samples by the MIP-SPME-CE method was also performed, with results indicating that E and PE could be selectively extracted. The recoveries and relative standard deviations (RSDs) for sample analysis were found in the range of 91-104% and 3.8-9.1%, respectively. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 200
页数:6
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