Comparison of supercritical fluid chromatography-tandem mass spectrometry and liquid chromatography-tandem mass spectrometry for the stereoselective analysis of chlorfenvinphos and dimethylvinphos in tobacco

被引:2
|
作者
Yang, Fei [1 ]
Cui, Haozhe [2 ]
Wang, Chunqiong [3 ]
Wang, Ying [1 ]
Zhu, Wenjing [4 ]
Deng, Huimin [1 ]
Liu, Shanshan [1 ]
Bian, Zhaoyang [1 ]
Lu, Junli [1 ]
Tang, Gangling [1 ]
Ji, Yuan [5 ]
机构
[1] China Natl Tobacco Qual Supervis & Test Ctr, Zhengzhou 450001, Peoples R China
[2] Univ Sheffield, Dept Mol Biol & Biotechnol, Sheffield, England
[3] Yunnan Tobacco Qual Supervis & Test Stn, Kunming, Peoples R China
[4] Guizhou Tobacco Qual Supervis & Test Stn, Guiyang, Peoples R China
[5] Shandong Inst Food & Drug Control, Jinan 250101, Peoples R China
关键词
chlorfenvinphos; dimethylvinphos; reversed-phase liquid chromatography-tandem mass spectrometry; stereoselective separation; supercritical fluid chromatography-tandem mass spectrometry; PESTICIDE-RESIDUES; MEVINPHOS; QUECHERS; ISOMERS; CIS;
D O I
10.1002/jssc.202300449
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This study used reversed-phase liquid chromatography-tandem mass spectrometry and supercritical fluid chromatography-tandem mass spectrometry for determination of the stereoisomers of chlorfenvinphos and dimethylvinphos in tobacco. Tobacco samples were extracted and purified with a modified quick, easy, cheap, effective, rugged, and safe technique using spherical carbon. The performance of both methodologies was comprehensively compared in terms of methods validation parameters (separation efficiency, linearity, selectivity, recovery, repeatability, sensitivity, matrix effect, etc.). Under optimized conditions, the calibration curves of the stereoisomers of chlorfenvinphos and dimethylvinphos in the range of 10-500 ng/mL showed excellent linearity with R-2 & GE; 0.997 in both methods. The adequate recoveries of analytes from three different spiked tobaccos were obtained using reversed-phase liquid chromatography-tandem mass spectrometry (86.1-95.7%) as well as supercritical fluid chromatography-tandem mass spectrometry (86.5-94.0%). The relative standard deviations for spiked samples were all below 7.0%. Compared with supercritical fluid chromatography-tandem mass spectrometry, lower matrix effects and LODs can be obtained in reversed-phase liquid chromatography-tandem mass spectrometry.
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页数:12
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