Multiplug filtration cleanup method with multi-walled carbon nanotubes for the analysis of malachite green, diethylstilbestrol residues, and their metabolites in aquatic products by liquid chromatography-tandem mass spectrometry

被引:23
|
作者
Qin, Yuhong [1 ]
Zhang, Jingru [1 ]
Li, Yanjie [1 ]
Han, Yongtao [1 ]
Zou, Nan [1 ]
Jiang, Yanbin [2 ]
Shan, Jihao [3 ]
Pan, Canping [1 ]
机构
[1] China Agr Univ, Beijing Adv Innovat Ctr Food Nutr & Human Hlth, Dept Appl Chem, Coll Sci, 2 Yuanmingyuan West Rd, Beijing 100193, Peoples R China
[2] China Anim Dis Control Ctr CADC, Maizidian St Bldg 20, Beijing 100125, Peoples R China
[3] Chinese Acad Agr Sci, Inst Agroprod Proc Sci & Technol, 2 Yuanmingyuan West Rd, Beijing 100193, Peoples R China
关键词
Multiple-walled carbon nanotubes; Multiplug filtration cleanup; Aquaculture; Residue analysis; LEUCOMALACHITE GREEN; PESTICIDE-RESIDUES; HPLC-DAD; EXTRACTION; QUECHERS; VALIDATION; WATER;
D O I
10.1007/s00216-016-9686-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The food safety supervision in aquatic products has raised public concern in recent years. In this study, a liquid chromatographic-tandem mass spectrometric (LC-MS/MS) method for the simultaneous quantification and identification of four residues of the ever widely used analytes (including malachite green, leucomalachite green, diethylstilbestrol, and dienestrol) in aquaculture samples was developed. For sample preparation, a modified QuEChERS (quick, easy, cheap, effective, rugged, and safe) method was used, which was initially developed for pesticide residue analysis. For cleanup procedure, low-temperature cleanup method was combined with multiplug filtration cleanup (m-PFC) method based on multi-walled carbon nanotubes (MWCNTs). The volume of water, extraction solvent, cleanup sorbents, and m-PFC procedure were optimized for carp, striped bass, and giant salamander matrices. It was validated by analyzing four residues in each matrix spiked at three concentration levels of 0.5, 5, and 50 mu g/kg (n = 5). The method was successfully validated according to the 2002/657/EC guidelines. After optimization, spike recoveries were within 73-106 % and < 15 % relative standard deviations (RSDs) for all analytes in the tested matrices. Limits of quantification (LOQs) for the proposed method ranged from 0.10 to 0.50 mu g/kg. Matrix-matched calibrations were performed with the coefficients of determination > 0.998 between concentration levels of 0.5 and 200 mu g/kg. The developed method was successfully applied to the determination of residues in market samples.
引用
收藏
页码:5801 / 5809
页数:9
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