首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Validation and use of a fast sample preparation method and liquid chromatography-tandem mass spectrometry in analysis of ultra-trace levels of 98 organophosphorus pesticide and carbamate residues in a total diet study involving diversified food types
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Validation and use of a fast sample preparation method and liquid chromatography-tandem mass spectrometry in analysis of ultra-trace levels of 98 organophosphorus pesticide and carbamate residues in a total diet study involving diversified food types

机译:在涉及多种食品类型的总饮食研究中,快速样品制备方法和液相色谱-串联质谱法在分析痕量98种有机磷农药和氨基甲酸酯残留量中的验证和应用

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This paper reports a comprehensive sensitive multi-residue liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for detection, identification and quantitation of 73 pesticides and their related products, a total of 98 analytes, belonging to organophosphorus pesticides (OPPs) and carbamates, in foods. The proposed method makes use of a modified QuEChERS (quick, easy, cheap, effective, rigged, and safe) procedure that combines isolation of the pesticides and sample clean-up in a single step. Analysis is performed by liquid chromatography-electrospray ionization-tandem mass spectrometry operated in the multiple reaction monitoring (MRM) mode, acquiring two specific precursor-product ion transitions per target compound. Two main fragment ions for each pesticide were obtained to achieve the identification according to the SANCO guidelines 10684/2009. The method was validated with various food samples, including edible oil, meat, egg, cheese, chocolate, coffee, rice, tree nuts, citric fruits, vegetables, etc. No significant matrix effect was observed for tested pesticides, therefore, matrix-matched calibration was not necessary. Calibration curves were linear and covered from 1 to 20μgL~(-1) for all compounds studied. The average recoveries, measured at 10μgkg~(-1), were in the range 70-120% for all of the compounds tested with relative standard deviations below 20%, while a value of 10μgkg~(-1) has been established as the method limit of quantitation (MLOQ) for all target analytes. Similar trueness and precision results were also obtained for spiking at 200μgkg~(-1). Expanded uncertainty values were in the range 21-27% while the HorRat ratios were below 1. The method has been successfully applied to the analysis of 700 food samples in the course of a baseline monitoring study of OPPs and carbamates.
机译:本文报告了一种综合灵敏的多残留液相色谱-串联质谱(LC-MS / MS)方法,用于检测,鉴定和定量73种农药及其相关产品,总共98种分析物,属于有机磷农药(OPP)和氨基甲酸酯,在食物中。所提出的方法利用了改良的QuEChERS(快速,简便,便宜,有效,操纵和安全)程序,该程序将农药的分离和样品净化步骤结合在一起。通过在多反应监测(MRM)模式下操作的液相色谱-电喷雾电离-串联质谱进行分析,每个目标化合物获得两个特定的前体产物离子跃迁。根据SANCO指南10684/2009,获得了每种农药的两个主要碎片离子,以实现鉴定。该方法已在各种食品样品中得到验证,包括食用油,肉,蛋,奶酪,巧克力,咖啡,大米,坚果,柠檬酸水果,蔬菜等。对于测试农药,未观察到明显的基质效应,因此基质匹配无需校准。所有研究化合物的校准曲线均为线性,覆盖范围为1至20μgL〜(-1)。对于所有测试化合物,相对标准偏差低于20%,在10μgkg〜(-1)下测得的平均回收率在70-120%的范围内,而将10μgkg〜(-1)的值确定为所有目标分析物的方法定量限(MLOQ)。对于200μgkg〜(-1)的加标也获得了相似的真实性和精密度结果。当HorPat比率低于1时,扩展的不确定性值在21-27%的范围内。该方法已在OPP和氨基甲酸酯的基线监测研究过程中成功应用于700个食品样品的分析。

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