Chinese Journal of Chromatography ›› 2012, Vol. 30 ›› Issue (02): 146-153.DOI: 10.3724/SP.J.1123.2011.10012

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Evaluation of QuEChERS methods for the analysis of 66 organophosphorus pesticide residues in vegetables by liquid chromatography-tandem mass spectrometry

WANG Lianzhu1*, ZHOU Yu2, CHEN Yong1, WANG Ruilong1, LIN Zixu1, LIN Dejuan3, ZHENG Shaohui1   

  1. 1. Zhangzhou Entry-Exit Inspection and Quarantine Bureau, Zhangzhou 363100, China; 2. Xiamen Entry-Exit Inspection and Quarantine Bureau, Xiamen 361012, China; 3. Zhangzhou Normal University, Zhangzhou 363000, China
  • Received:2011-10-13 Revised:2011-12-05 Online:2012-02-28 Published:2012-03-22

Abstract: A comparison was made between the two versions of QuEChERS sample preparation method for the extraction of 66 organophosphorus pesticides (OPPS) in vegetables. The two QuEChERS methods were the original method without buffer published in 2003, and the AOAC Official Method 2007.01 with acetate buffer. The adsorption behaviors of primary secondary amine (PSA) sorbent and C18 sorbent on the OPPS were studied. The method of after-extraction addition was used to evaluate matrix effects for OPPS in matrix of broccoli, tomato, green soybean, radish and shallot during liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. As a result, the QuEChERS method with acetate buffer gave higher and more consistent recoveries for some of OPPS. The PSA sorbent and C18 sorbent can adsorb dibrom, so the QuEChERS method was not suitable for the analysis of dibrom. The maximum matrix effects were in the extracts of broccoli during LC-MS/MS analysis. In this article, OPPS were extracted using the QuEChERS method with acetate buffer, and analysed by LC-MS/MS under the optimized conditions with monitoring 132 MS/MS transitions of precursor ions (two for each pesticide) in one single run. Recoveries for all but dibrom at fortification levels of 10, 40, 80 μg/kg in broccoli, tomato, green soybean, radish and shallot ranged from 55% to 122% with relative standard deviations of 1.6%~18%. The limits of quantification (S/N≥10) were 0.1~8 μg/kg. Based on these results, the analytical method was proven to be highly efficient, robust and sensitive, and suitable for the monitoring of the maximum residue limits (MRLs) of 66 OPPS in vegetables.

Key words: adsorption, liquid chromatography-tandem mass spectrometry (LC-MS/MS), matrix effects, organophosphorus pesticides (OPPS), vegetable, QuEChERS