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Optimization and establishment of QuEChERS based method for determination of propoxycarbazone and its metabolite in food commodities by liquid chromatography coupled to tandem mass spectrometry

机译:基于QuEChERS的液相色谱-串联质谱法测定食品中丙氧卡巴zone及其代谢物的方法的建立

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摘要

This study reports a method for propoxycarbazone pesticide determination including its metabolite in food commodities (lettuce, beetroot, soybean meal and honey). Both compounds were extracted, and samples cleaned using a buffered QuEChERS (Quick, Easy, Cheap, Effective, Rugged and Safe) method based on the AOAC Official Method, followed by ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). Both matrix-matched calibration curves showed good linearity (R-2 =0.99) within the tested ranges. Method performance was assessed on the basis of recovery and intra/inter-day precision studies at spiked concentrations of 10 (25) and 50 mu g/kg (n=5). Mean recovery rates were between 73 and 110%, while precision studies, assessed by relative standard deviation (RSD), were = 20%. The limits of quantification (LOQ) were established as 10 or 25 mu g/kg, depending on the matrix, which are low enough for monitoring residues at regulated maximum residue levels.
机译:这项研究报告了一种测定丙氧卡巴zone农药的方法,包括食品中的代谢产物(生菜,甜菜根,豆粕和蜂蜜)。提取两种化合物,并使用基于AOAC官方方法的QuEChERS(快速,简便,廉价,有效,坚固和安全)方法对样品进行清洗,然后采用高效液相色谱-串联质谱(UHPLC-MS /多发性硬化症)。两种基质匹配的校准曲线在测试范围内均显示出良好的线性(R-2 = 0.99)。在回收浓度和日内/日间精密度研究的基础上,以加标浓度10(25)和50μg / kg(n = 5)评估方法性能。平均回收率在73%至110%之间,而通过相对标准偏差(RSD)评估的精密度研究则≤20%。定量限(LOQ)被确定为10或25μg / kg,这取决于基质,其低到足以以规定的最大残留量监测残留物。

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