Promethazine determination in plasma samples by using carbon paste electrode modified with molecularly imprinted polymer (MIP): Coupling of extraction, preconcentration and electrochemical determination

被引:70
|
作者
Alizadeh, Taher [1 ]
Akhoundian, Maedeh [1 ]
机构
[1] Univ Mohaghegh Ardabili, Dept Appl Chem, Fac Sci, Ardebil, Iran
关键词
Promethazine; Molecularly imprinted polymer; Voltammetric determination; Carbon paste modified electrode; PERFORMANCE LIQUID-CHROMATOGRAPHY; PHARMACEUTICAL FORMULATIONS; PHENOTHIAZINE DRUGS; VOLTAMMETRIC SENSOR; HPLC METHOD; HYDROCHLORIDE; ENANTIOMERS; SEPARATION; ASSAY; ELECTROPHORESIS;
D O I
10.1016/j.electacta.2010.05.037
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A promethazine (PMZ) molecularly imprinted polymer (MIP) and a non-imprinted polymer (NIP) were synthesized by two different formulations of methacrylic acid-ethylene glycol dimethacrylate (MAA-EGDMA) and vinyl benzene-divinyl benzene (VB-DVB). Then, the MIPs were used to modify the carbon paste electrode (CP). The response difference between MIP-CP and NIP-CP electrodes, containing VB-DVB polymer, was higher than that for MIP-CP and NIP-CP modified with polymer of MM-EGDMA, indicating the lower nonselective surface adsorption property of the VB-DVB based MIP. The MIP, incorporated in the carbon paste electrode, functioned as selectively recognition element and pre-concentrator agent for PMZ determination. The prepared electrode was used for PMZ measurement by the three steps procedure including analyte extraction in the electrode, electrode washing and electrochemical measurement of PMZ. It was shown that the electrode washing, after PMZ extraction, led to enhanced selectivity. Square wave voltammetry (SWV) for PMZ determination by proposed electrode was proved to be better than that of differential pulse voltammetry. Some parameters, effective on the electrode response, were optimized and then a calibration curve was plotted. Two dynamic linear range of 7 x 10(-9) to 4 x 10(-7) and 4 x 10(-7) to 7 x 10(-6) mol L-1 were obtained. The detection limit of the method was calculated equal to 3.2 x 10(-9) mol L-1. This method was used successful for PMZ determination in blood serum sample. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5867 / 5873
页数:7
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