超高效液相色谱-串联质谱法测定3种谷物中砜吡草唑及其代谢物残留

    Determination of pyroxasulfone and its metabolites residues in three grains by UPLC-MS/MS

    • 摘要: 基于超高效液相色谱-串联质谱(UPLC-MS/MS)技术建立了可同时检测玉米、大豆和小麦中砜吡草唑及其4种代谢物M1、M3、M25和M28残留的分析方法。样品经体积分数为2%的甲酸乙腈溶液提取,50 mg C18、50 mg石墨化炭黑(GCB)吸附剂和100 mg无水硫酸镁净化,BEH-C18色谱柱分离,多重反应监测模式,UPLC-MS/MS检测,基质匹配外标法定量。结果表明:在0.0005~0.02 mg/L内,各化合物基质标准工作液的质量浓度与响应值的线性关系良好,相关系数(r)> 0.99。在0.01~0.1 mg/kg的添加水平下,各化合物的日内和日间平均回收率为76%~96%,相对标准偏差(RSD)为8.8%~9.9%,方法定量限(LOQ)为0.01 mg/kg,方法各指标符合农药残留分析的要求,可用于砜吡草唑及其代谢物残留的检测。

       

      Abstract: Based on the ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) technique, a residue analysis method was established for simultaneous determination of pyroxasulfone and its four metabolites (M1, M3, M25, M28) in maize, soybean and wheat. The samples were extracted by acetonitrile with 2%(V/V) formic acid, purified with 50 mg C18, 50 mg graphitized carbon black (GCB), and 100 mg magnesium sulfate anhydrous, separated on a BEH-C18 column, detected by UPLC-MS/MS in multiple reaction monitoring mode, and quantified with a matrix-matched external standard method. The results showed that the linear relation between the areas and the mass concentrations of all compounds was satisfied, given the correlation coefficient (r) above 0.99 within the concentration of 0.0005-0.02 mg/L. The average inter-day and intra-day recoveries of all compounds were 76%-96% with the relative standard deviations (RSD) of 8.8%-9.9% at the spiked levels of 0.01 to 0.1 mg/kg. The limits of quantification (LOQ) of the method were 0.01 mg/kg. The method validation parameters met the requirements of residue analysis, showing that it could be used for the detection of pyroxasulfone and its metabolites in the three crops.

       

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