首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Rapid IC-MS/MS determination of methylphosphonic acid in urine of rats exposed to organophosphorus nerve agents
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Rapid IC-MS/MS determination of methylphosphonic acid in urine of rats exposed to organophosphorus nerve agents

机译:快速IC-MS / MS测定尿液中尿液中甲基膦酸暴露于有机磷神经剂的大鼠

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摘要

A direct approach for the determination of a specific hydrolysis product of organophosphorus nerve agents such as methylphosphonic acid (MPA) in urine by ion chromatography and tandem mass spectrometry (IC-MS/MS) has been developed. The first advantage of the proposed approach is a rapid and simple sample preparation, which does not require a large sample volume, complicated and laborious preconcentration and derivatization steps, and takes less than 7 min per sample. The second advantage is the fast and selective IC determination of MPA carried out on a noncommercial anion exchanger based on a poly(styrene-co-divinylbenzene) (PS-DVB) substrate with a high degree of crosslinking and a covalently-bonded branched functional layer, which enables complete resolution of MPA from major urine matrix components and allows one to overcome matrix effects. Hyphenation of IC with tandem mass spectrometry results in highly sensitive and reliable MPA determination with the lowest detection limit (4 ng mL(-1)) reported so far for HPLC determination of MPA in urine. The proposed approach is successfully applied for the analysis of urine from rats exposed to nonlethal doses of organophosphorus nerve agents such as sarin, soman, and VR in up to 13 days after initial exposure, which shows the possibility to verify the nerve agent exposure after a long period of time.
机译:已经开发了通过离子色谱法测定尿液中尿液中甲基膦酸(MPa)如甲基膦酸(MPa)的特定水解产物的直接方法已经开发出来和串联质谱法(IC-MS / MS)。所提出的方法的第一个优点是一种快速简单的样品制剂,其不需要大的样品体积,复杂和艰苦的预浓缩步骤,并且每种样品小于7分钟。第二个优点是基于聚(苯乙烯 - 二二乙烯基苯)(PS-DVB)衬底,具有高度交联和共价键合的支链功能层,快速和选择性IC测定MPa在非商业阴离子交换器上进行的MPa。 ,这使得能够从主要尿矩阵组件中完成MPa,并允许一个人克服矩阵效应。通过串联质谱法的IC的连字符导致高度敏感和可靠的MPa测定,以迄今为止尿液中HPLC测定MPa的最低检测限(4ng mL(-1))。拟议的方法成功地应用于暴露于非致命剂量的有机磷神经药物如初始暴露后13天的大鼠尿液的尿液分析,这表明在a之后验证神经试剂暴露的可能性很长一段时间。

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