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Rapid Determination of Organonitrogen, Organophosphorus and Carbamate Pesticides in Tea by Ultrahigh-Performance Liquid Chromatography–Tandem Mass Spectrometry (UPLC-MS/MS)

机译:超高效液相色谱-串联质谱法(UPLC-MS / MS)快速测定茶叶中的有机氮,有机磷和氨基甲酸酯类农药

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摘要

A rapid and effective multiresidue method has been developed for the determination of 18 pesticide residues (selected from organonitrogen, organophosphorus, and carbamate pesticides) in tea by ultrahigh-performance liquid chromatography–tandem mass spectrometry. Tea samples were extracted with acetonitrile and purified by a novel multilayer solid-phase extraction cartridge—Cleanet TPT. Evaluation of the influence of the mobile phase on the ionization efficiency, resolution, and sensitivity was carried out by comparing the acetonitrile–water and methanol–water with different modifiers. The recoveries of all the pesticides varied from 70 to 110 % with a relative standard deviation of less than 15 %, and the determination coefficient for each pesticide was R 2>0.99. Matrix-matched standard calibration curve was used to reduce errors associated with matrix-induced enhancement or suppression effects. The limit of detection for all targeted pesticides ranged from 0.03 to 1.5 μg/kg. Applicability ofthis analytical approach was confirmed by successful determination of tea samples from different regions of China.
机译:建立了一种快速有效的多残留方法,通过超高效液相色谱-串联质谱法测定茶叶中的18种农药残留(选自有机氮,有机磷和氨基甲酸酯农药)。茶样品用乙腈萃取,并通过新型多层固相萃取柱Cleanet TPT纯化。通过将乙腈-水和甲醇-水与不同的改性剂进行比较,评估了流动相对电离效率,分离度和灵敏度的影响。所有农药的回收率在70%至110%之间,相对标准偏差小于15%,每种农药的测定系数为R 2> 0.99。使用基质匹配的标准校准曲线来减少与基质诱导的增强或抑制作用相关的误差。所有目标农药的检出限为0.03至1.5μg/ kg。通过成功测定中国不同地区的茶叶样品,证实了这种分析方法的适用性。

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