首页> 外文期刊>International journal of environmental analytical chemistry >Simultaneous multi-residue pesticide analysis in soil samples with ultra-high-performance liquid chromatography-tandem mass spectrometry using QuEChERS and pressurised liquid extraction methods
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Simultaneous multi-residue pesticide analysis in soil samples with ultra-high-performance liquid chromatography-tandem mass spectrometry using QuEChERS and pressurised liquid extraction methods

机译:使用QuEChERS和加压液体萃取方法的超高效液相色谱-串联质谱法同时分析土壤样品中的多残留农药

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To assess soil contamination, it is important to be able to measure different classes of pesticides simultaneously. For this reason we developed a sensitive ultra-high-performance liquid chromatography-tandem mass spectrometry method for the simultaneous analysis of 25 pesticides in soil samples. Multi-class pesticides (triazines, phenylureas, phenoxy acid pesticides etc.) were analysed using a single mass spectrometry method with a fast polarity switching option, allowing the analysis of 19 compounds in the positive ionisation mode and six compounds in the negative ionisation mode. Extraction of pesticides from soil samples was performed employing a pressurised liquid extraction (PLE) and a quick, easy, cheap, effective, rugged and safe (QuEChERS) procedure, recently developed for the extraction of multi-residue pesticides from food matrices. The extraction efficiency, performance and recoveries of these two procedures were evaluated and compared. In addition, we studied the effect of matrix on signal suppression or enhancement. Isotope-labelled internal standards (ILIS) were used to compensate the suppression or enhancement of signal intensities in the extracted samples. The method was validated using reference soil material (EUROSOIL 7) spiked with 50 mu g/kg of each pesticide. The average recovery by PLE varied between 65.1% and 122.2% with RSDs of 1.7-23.4%. QuEChERS provided better recoveries for most of the pesticides, the extraction recovery ranging from 79.4% to 113.3% with RSDs of 1.0-12.2%. Limits of quantification for all target compounds were within a range of 0.1-2.9 mu g/kg.
机译:要评估土壤污染,重要的是能够同时测量不同类别的农药。因此,我们开发了一种灵敏的超高效液相色谱-串联质谱法,用于同时分析土壤样品中的25种农药。使用具有快速极性切换选项的单一质谱方法分析了多类农药(三嗪,苯脲,苯氧基酸农药等),可以分析正电离模式下的19种化合物和负电离模式下的六种化合物。使用加压液体萃取(PLE)和快速,简便,廉价,有效,坚固而安全的(QuEChERS)程序从土壤样品中萃取农药,最近已开发出可从食品基质中萃取多种残留农药的方法。评价并比较了这两种方法的提取效率,性能和回收率。此外,我们研究了矩阵对信号抑制或增强的影响。同位素标记的内标(ILIS)用于补偿提取样品中信号强度的抑制或增强。使用掺有50μg / kg每种农药的参考土壤材料(EUROSOIL 7)验证了该方法。 PLE的平均回收率在65.1%和122.2%之间,RSD为1.7-23.4%。 QuEChERS为大多数农药提供了更好的回收率,萃取回收率从79.4%到113.3%,RSD为1.0-12.2%。所有目标化合物的定量限在0.1-2.9μg / kg的范围内。

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