Development of gold nanoparticles modified screen-printed carbon electrode for the analysis of thiram, disulfiram and their derivative in food using ultra-high performance liquid chromatography

被引:65
作者
Charoenkitamorn, Kanokwan [1 ]
Chailapakul, Orawon [1 ,3 ]
Siangproh, Weena [2 ]
机构
[1] Chulalongkorn Univ, Fac Sci, Dept Chem, Electrochem & Opt Spect Res Unit, Bangkok 10330, Thailand
[2] Srinakharinwirot Univ, Fac Sci, Dept Chem, Bangkok 10110, Thailand
[3] Chulalongkorn Univ, Natl Ctr Excellent Petr Petrochem & Adv Mat, Bangkok 10330, Thailand
关键词
Dithiocarbamates; Fungicides; Screen-printed carbon electrode; Gold nanoparticles; Simultaneous determination; Ultra-high performance liquid chromatography; CAPILLARY ELECTROPHORETIC DETERMINATION; ELECTROCHEMICAL DETECTION; VOLTAMMETRIC DETERMINATION; DITHIOCARBAMATE FUNGICIDE; VEGETABLE SAMPLES; RESIDUE ANALYSIS; PESTICIDES; ZIRAM; ACID; DIMETHYLDITHIOCARBAMATE;
D O I
10.1016/j.talanta.2014.09.020
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
For the first time, gold nanoparticles (AuNPs) modified screen-printed carbon electrode (SPCE) was developed as working electrode in ultra-high performance liquid chromatography (UHPLC) coupled with electrochemical detection (UHPLC-ED) for simultaneous determination of thiram, disulfiram, and N,N-diethyl-N',N'-dimethylthiuram disulfide, their derivative compound. The separation was performed in reversed-phase mode using C18 column, mobile phase consisting of 55:45 (v/v) ratio of 0.05 M phosphate buffer solution (pH 5) and acetonitrile at a flow rate of 1.5 mL min(-1). For the detection part, the amperometric detection was chosen with a detection potential of 1.2 V vs. Ag/AgCl. Under the optimal conditions, the good linear relationship was obtained in the range of 0.07-15, 0.07-12, and 0.5-15 mu g mL(-1) (correlation coefficient more than 0.9900) for thiram, N,N-diethyl-N',N'-dimethylthiuram disulfide, and disulfiram, respectively. The limits of detection (LODs) of thiram, N,N-diethyl-N',N'-dimethylthiuram disulfide, and disulfiram were 0.022, 0.023, and 0.165 mu g mL-1, respectively. Moreover, this method was successfully applied for the detection of these compounds in real samples (apple, grape and lettuce) with the recoveries ranging from 94.3% to 108.8%. To validate this developed method, a highly quantitative agreement was clearly observed compared to standard UHPLC-UV system. Therefore, the proposed electrode can be effectively used as an alternative electrode in UHPLC-ED for rapid, selective, highly sensitive, and simultaneous determination of thiram, disulfiram, and N,N-diethyl-N',N'-dimethylthiuram disulfide. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:416 / 423
页数:8
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