首页> 外文期刊>Journal of Environmental Science and Health. Part B, Pesticides, Food Contaminants and Agricultural Wastes >Validation of reliable and selective methods for direct determination of glyphosate and aminomethylphosphonic acid in milk and urine using LC-MS/MS
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Validation of reliable and selective methods for direct determination of glyphosate and aminomethylphosphonic acid in milk and urine using LC-MS/MS

机译:使用LC-MS / MS验证直接测定牛奶和尿液中草甘膦和氨基甲基膦酸的可靠且选择性的方法

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Simple high-throughput procedures were developed for the direct analysis of glyphosate [N-(phosphonomethyl)glycine] and aminomethylphosphonic acid (AMPA) in human and bovine milk and human urine matrices. Samples were extracted with an acidified aqueous solution on a high-speed shaker. Stable isotope labeled internal standards were added with the extraction solvent to ensure accurate tracking and quantitation. An additional cleanup procedure using partitioning with methylene chloride was required for milk matrices to minimize the presence of matrix components that can impact the longevity of the analytical column. Both analytes were analyzed directly, without derivatization, by liquid chromatography tandem mass spectrometry using two separate precursor-to-product transitions that ensure and confirm the accuracy of the measured results. Method performance was evaluated during validation through a series of assessments that included linearity, accuracy, precision, selectivity, ionization effects and carryover. Limits of quantitation (LOQ) were determined to be 0.1 and 10 μg/L (ppb) for urine and milk, respectively, for both glyphosate and AMPA. Mean recoveries for all matrices were within 89-107% at three separate fortification levels including the LOQ. Precision for replicates was ≤7.4% relative standard deviation (RSD) for milk and ≤11.4% RSD for urine across all fortification levels. All human and bovine milk samples used for selectivity and ionization effects assessments were free of any detectable levels of glyphosate and AMPA. Some of the human urine samples contained trace levels of glyphosate and AMPA, which were background subtracted for accuracy assessments. Ionization effects testing showed no significant biases from the matrix. A successful independent external validation was conducted using the more complicated milk matrices to demonstrate method transferability.
机译:开发了一种简单的高通量方法,可直接分析人奶,牛乳和人尿基质中的草甘膦[N-(膦酰基甲基)甘氨酸]和氨基甲基膦酸(AMPA)。在高速振荡器上,用酸化的水溶液萃取样品。稳定同位素标记的内标与萃取溶剂一起添加,以确保准确的跟踪和定量。对于牛奶基质,还需要使用二氯甲烷进行额外的净化程序,以最大程度地减少可能影响分析柱寿命的基质成分。通过液相色谱串联质谱法使用两个独立的前体到产物的跃迁来直接分析两种分析物,而无需衍生化,以确保并确认测量结果的准确性。在验证过程中,通过一系列评估来评估方法的性能,这些评估包括线性,准确性,精密度,选择性,电离效应和残留。对于草甘膦和AMPA,尿和牛奶的定量限(LOQ)分别确定为0.1和10μg/ L(ppb)。在包括LOQ在内的三个单独的设防水平下,所有基质的平均回收率均在89-107%之内。在所有设防水平上,牛奶的重复精度为相对标准偏差(RSD)≤7.4%,尿液的RSD≤11.4%。用于选择性和电离效应评估的所有人乳和牛乳样品均不含任何可检测到的草甘膦和AMPA水平。一些人类尿液样本中含有痕量的草甘膦和AMPA,将其扣除背景以进行准确性评估。电离效应测试表明基质没有明显的偏差。使用更复杂的牛奶基质进行了成功的独立外部验证,以证明方法的可移植性。

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