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首页> 外文期刊>Analytical and bioanalytical chemistry >Direct determination of glyphosate, glufosinate, and AMPA in soybean and corn by liquid chromatography/tandem mass spectrometry
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Direct determination of glyphosate, glufosinate, and AMPA in soybean and corn by liquid chromatography/tandem mass spectrometry

机译:液相色谱/串联质谱法直接测定大豆和玉米中的草甘膦,草铵膦和AMPA

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Glyphosate, glufosinate, and aminomethylphosphonic acid (AMPA) are amphoteric, low mass, high water soluble, and do not have chromophore. They are very difficult to be retained on a reversed phase HPLC and detected by UV or fluorescence detectors. A liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed to determine these analytes in soybean and corn using a reversed phase with weak anion-exchange and cation-exchange mixed-mode Acclaim (TM) Trinity (TM) Q1 column. The sample was shaken with water containing ethylenediaminetetraacetic acid disodium salt (Na(2)EDTA) and acetic acid for 10 min to precipitate protein and extract the analytes into the solution. The supernatant was passed thru an Oasis HLB SPE to retain suspended particulates and non-polar interferences. The sample was directly injected and analyzed in 6 min by LC-MS/MS with no sample concentration or derivatization steps. Three isotopically labeled internal standards corresponding to each analyte were used to counter matrix suppression effect. Linearity of the detector response with a minimum coefficient of determination (R (2)) of more than 0.995 was demonstrated in the range of 10 to 1000 ng/mL for each analyte. Accuracy (recovery %) and precision (relative standard deviation or RSD %) were evaluated at the fortification levels of 0.1, 0.5, and 2 mu g/g in seven replicates in both soybean and corn samples.
机译:草甘膦,草铵膦和氨基甲基膦酸(AMPA)是两性的,质量低,水溶性高,并且没有发色团。它们很难保留在反相HPLC上,很难用UV或荧光检测器检测。开发了一种液相色谱/串联质谱(LC-MS / MS)方法,使用具有弱阴离子交换和阳离子交换混合模式Acclaim(TM)Trinity(TM)Q1的反相色谱法测定大豆和玉米中的这些分析物柱。将样品与含有乙二胺四乙酸二钠盐(Na(2)EDTA)和乙酸的水一起振摇10分钟,以沉淀蛋白质并将分析物提取到溶液中。使上清液通过Oasis HLB SPE,以保留悬浮颗粒和非极性干扰。直接进样并在6分钟内通过LC-MS / MS进行分析,没有样品浓缩或衍生化步骤。对应于每种分析物的三种同位素标记的内标用于抵消基质抑制作用。在每种分析物的10到1000 ng / mL范围内,最小测定系数(R(2))大于0.995的检测器响应呈线性关系。在强化水平为0.1、0.5和2μg / g的情况下,在大豆和玉米样品中进行了7次重复分析,评估了准确性(回收率%)和精密度(相对标准偏差或RSD%)。

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