Preparation and evaluation of a novel molecularly imprinted polymer coating for selective extraction of indomethacin from biological samples by electrochemically controlled in-tube solid phase microextraction

被引:42
作者
Asiabi, Hamid [1 ]
Yamini, Yadollah [1 ]
Seidi, Shahram [2 ]
Ghahramanifard, Fazel [2 ]
机构
[1] Tarbiat Modares Univ, Dept Chem, POB 14115-175, Tehran, Iran
[2] KN Toosi Univ Technol, Dept Analyt Chem, Fac Chem, Tehran, Iran
关键词
Electrochemically controlled; In-tube solid phase microextraction; Indomethacin; Molecularly imprinted polymer; Polypyrrole; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; MONOLITHIC CAPILLARY; AMINO-ACIDS; POLYPYRROLE; CHEMISTRY; SILICA; FIBERS; DEVICE; DRUGS;
D O I
10.1016/j.aca.2016.01.060
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the present work, an automated on-line electrochemically controlled in-tube solid-phase microextraction (EC-in-tube SPME) coupled with HPLC-UV was developed for the selective extraction and preconcentration of indomethacin as a model analyte in biological samples. Applying an electrical potential can improve the extraction efficiency and provide more convenient manipulation of different properties of the extraction system including selectivity, clean-up, rate, and efficiency. For more enhancement of the selectivity and applicability of this method, a novel molecularly imprinted polymer coated tube was prepared and applied for extraction of indomethacin. For this purpose, nanostructured copolymer coating consisting of polypyrrole doped with ethylene glycol dimethacrylate was prepared on the inner surface of a stainless-steel tube by electrochemical synthesis. The characteristics and application of the tubes were investigated. Electron microscopy provided a cross linked porous surface and the average thickness of the MIP coating was 45 mm. Compared with the non-imprinted polymer coated tubes, the special selectivity for indomethacin was discovered with the molecularly imprinted coated tube. Moreover, stable and reproducible responses were obtained without being considerably influenced by interferences commonly existing in biological samples. Under the optimal conditions, the limits of detection were in the range of 0.07-2.0 mg L-1 in different matrices. This method showed good linearity for indomethacin in the range of 0.1-200 mg L-1, with coefficients of determination better than 0.996. The inter-and intra-assay precisions (RSD%, n = 3) were respectively in the range of 3.5-8.4% and 2.3-7.6% at three concentration levels of 7, 70 and 150 mg L-1. The results showed that the proposed method can be successfully applied for selective analysis of indomethacin in biological samples. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:76 / 85
页数:10
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