Simultaneous determination of cyflumetofen and its main metabolite residues in samples of plant and animal origin using multi-walled carbon nanotubes in dispersive solid-phase extraction and ultrahigh performance liquid chromatography-tandem mass spectrometry

被引:89
|
作者
Li, Minmin [1 ,2 ]
Liu, Xingang [1 ]
Dong, Fengshou [1 ]
Xu, Jun [1 ]
Kong, Zhiqiang [2 ]
Li, Yuanbo [1 ]
Zheng, Yongquan [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China
[2] Chinese Acad Agr Sci, Inst Agroprod Proc Sci & Technol, Beijing 100193, Peoples R China
基金
中国国家自然科学基金;
关键词
Cyflumetofen; Metabolites; WMCNTs; Plant origin; Animal origin; UPLC-MS/MS; MULTIRESIDUE ANALYSIS; PESTICIDE-RESIDUES; TOXICITY; VEGETABLES; FRUITS; DRUGS; WATER; GAS;
D O I
10.1016/j.chroma.2013.05.052
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid and effective method for the simultaneous determination of cyflumetofen and its main metabolite residues in samples of plant and animal origin (tomato, apple, eggplant, soybean, green tea, fish, and pork liver) was developed using ultrahigh performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Samples were extracted with acetonitrile and cleaned-up with multi-walled carbon nanotubes (MWCNTs). The determination of the presence of target compounds was achieved in less than 4.0 min using an electrospray ionization source in the positive mode (ESI+) for cyflumetofen and 2-(trifluoromethyl) benzamide (B-3) and the negative mode (ESI-) for alpha,alpha,alpha-trifluoro-o-toluic acid (B-1). The entire method was validated by evaluating the repeatability, linearity, precision, trueness, and matrix effect. Average recoveries of the analytes were in the range of 79.3-117.6% with relative standard deviation values below 7.6%. Limits of quantification (LOQs) ranged from 0.7 to 9.8 mu g kg(-1), which were lower than the maximum residue limits (MRLs) for the cyflumetofen found in foods in Japan. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 103
页数:9
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