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亲水作用液相色谱-串联质谱法测定环境样品中经对溴苯甲酰溴柱前衍生后的甲基膦酸和烷基甲基膦酸

Hydrophilic interaction liquid chromatography-tandem mass spectrometry methylphosponic and alkyl methylphosphonic acids determination in environmental samples after pre-column derivatization with p-bromophenacyl bromide.

作者信息

Baygildiev T M, Rodin I A, Stavrianidi A N, Braun A V, Lebedev A T, Rybalchenko I V, Shpigun O A

机构信息

Chemistry Department, Lomonosov Moscow State University, 119991 Moscow, Russia.

Chemistry Department, Lomonosov Moscow State University, 119991 Moscow, Russia.

出版信息

J Chromatogr A. 2016 Apr 15;1442:19-25. doi: 10.1016/j.chroma.2016.03.001. Epub 2016 Mar 3.

Abstract

Once exposed to the environment organophosphate nerve agents readily degrade by rapid hydrolysis to the corresponding alkyl methylphosphonic acids which do not exist in nature. These alkyl methylphosphonic acids are finally slowly hydrolyzed to methylphosphonic acid. Methylphosphonic acid is the most stable hydrolysis product of organophosphate nerve agents, persisting in environment for a long time. A highly sensitive method of methylphosphonic acid and alkyl methylphosphonic acids detection in dust and ground mixed samples has been developed and validated. The fact that alkyl methylphosphonic acids unlike methylphosphonic acid did not react with p-bromophenacyl bromide under chosen conditions was discovered. This allowed simultaneous chromatographic separation and mass spectrometric detection of derivatized methylphosphonic acid and underivatized alkyl methylphosphonic acids using HILIC-MS/MS method. Very simple sample pretreatment with high recoveries for each analyte was developed. Methylphosphonic acid pre-column derivate and alkyl methylphosphonic acids were detected using tandem mass spectrometry with electrospray ionization after hydrophilic interaction liquid chromatography separation. The developed approach allows achieving ultra-low detection limits: 200 pg mL(-1) for methylphosphonic acid, 70 pg mL(-1) for ethyl methylphosphonic acid, 8 pg mL(-1) for i-propyl methylphosphonic acid, 8 pg mL(-1) for i-butyl methylphosphonic acid, 5 pg mL(-1) for pinacolyl methylphosphonic acid in the extracts of dust and ground mixed samples. This approach was successfully applied to the dust and ground mixed samples from decommissioned plant for the production of chemical weapons.

摘要

一旦暴露于环境中,有机磷酸酯神经毒剂会通过快速水解迅速降解为自然界中不存在的相应烷基甲基膦酸。这些烷基甲基膦酸最终会缓慢水解为甲基膦酸。甲基膦酸是有机磷酸酯神经毒剂最稳定的水解产物,会在环境中长时间存在。现已开发并验证了一种用于检测粉尘和地面混合样品中甲基膦酸和烷基甲基膦酸的高灵敏度方法。发现在选定条件下,与甲基膦酸不同,烷基甲基膦酸不与对溴苯甲酰溴反应。这使得能够使用亲水作用液相色谱-串联质谱法(HILIC-MS/MS)对衍生化的甲基膦酸和未衍生化的烷基甲基膦酸进行同时色谱分离和质谱检测。开发了一种非常简单的样品预处理方法,每种分析物的回收率都很高。在亲水作用液相色谱分离后,使用电喷雾电离串联质谱法检测甲基膦酸柱前衍生物和烷基甲基膦酸。所开发的方法能够实现超低检测限:粉尘和地面混合样品提取物中甲基膦酸的检测限为200 pg mL(-1),乙基甲基膦酸为70 pg mL(-1),异丙基甲基膦酸为8 pg mL(-1),异丁基甲基膦酸为8 pg mL(-1),频哪基甲基膦酸为5 pg mL(-1)。该方法已成功应用于化学武器生产退役工厂的粉尘和地面混合样品。

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