Institute of Chemical Technology, Prague, Faculty of Food and Biochemical Technology, Department of Food Chemistry and Analysis, Technicka 3, 166 28 Prague 6, Czech Republic.
J Chromatogr A. 2010 Jan 29;1217(5):648-59. doi: 10.1016/j.chroma.2009.11.098. Epub 2009 Dec 4.
In this study, the potential of ultra-high-performance liquid chromatography coupled with the time-of-flight mass spectrometry (UHPLC-TOF MS) to enable rapid and comprehensive analysis of 212 pesticide residues in QuEChERS extracts obtained from four plant matrices has been investigated. Method optimization is discussed in detail. In addition to molecular adducts, also fragment ions were provided for all target pesticides, thus obtaining at least three identification points required by European Decision 2002/657/EC was achieved. To get maximum information on analytes present in the extracts, each sample was examined within two injections, the first in a positive and the next one in a negative ionization mode. Under UHPLC conditions, both analyses were completed within 24min. For more than 96% of pesticides involved in this study, the limit of quantification was < or =10micro/kg. As a part of the work, strategy enabling screening of non-target pesticides and their metabolites is demonstrated on analysis of real-life samples.
本研究旨在探索超高效液相色谱-飞行时间质谱(UHPLC-TOF MS)在快速、全面分析四种植物基质中 QuEChERS 提取液中 212 种农药残留方面的潜力。文中详细讨论了方法优化问题。除了分子加合物之外,还为所有目标农药提供了碎片离子,从而满足了欧洲 2002/657/EC 号决定中规定的至少三个鉴定点的要求。为了从提取物中获得最大的分析物信息量,每个样品在两次进样中进行检测,第一次为正离子模式,第二次为负离子模式。在 UHPLC 条件下,两次分析均在 24 分钟内完成。对于本研究涉及的 96%以上的农药,定量限均<或=10μg/kg。作为工作的一部分,还展示了一种能够在分析实际样品时筛选非目标农药及其代谢物的策略。