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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Integrated identification/confirmatory and targeted analysis of epoxyeicosatrienosic acids in human serum by LC-TOF MS and automated on-line SPE-LC-QqQ MS/MS
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Integrated identification/confirmatory and targeted analysis of epoxyeicosatrienosic acids in human serum by LC-TOF MS and automated on-line SPE-LC-QqQ MS/MS

机译:通过LC-TOF MS和自动在线SPE-LC-QqQ MS / MS对人血清中环氧二十碳三烯酸进行综合鉴定/确证和靶向分析

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摘要

A combined strategy is here proposed for qualitative/quantitative targeted analysis of epoxyeicosa-trienoic acids (EETs) in human serum. Identification of EET regioisomers was initially carried out by LC-TOF MS in high accuracy mode under optimum conditions for chromatographic separation of the four isomers with an isocratic method using 40:40:20 (v/v/v) methanol-acetonitrile-water containing 0.02% acetic acid. Confirmatory analysis was supported on MS/MS experiments using the hybrid QqTOF mass analyzer by targeted fragmentation of the precursor ion fitting with the molecular formula C_(20)H_(32)O_3 (319.2279 m/z). Identification of selective fragment ions in high accuracy mode enabled the localization of the epoxy functional group and, therefore, the assignation of chromatographic peaks to each EET isomer. After qualitative analysis, an automated method was developed for analysis of EETs in human serum by direct analysis using an on-line platform based on SPE-LC-QqQ MS/MS in selected reaction monitoring. Recovery factors estimated with a dual-cartridge configuration were above 87% for all metabolites either using non-spiked and spiked serum at three different concentrations. Precision, calculated as within-laboratory repeatability and expressed as relative standard deviation, ranged from 2.5 to 9.9% with detection limits below 0.15 ng mL~(-1). The optimization of the method was completed with a stability study under different conditions to assess the suited conditions for analysis of EET intermediate metabolites. Finally, concentration ranges of EETs were measured in nine healthy individuals.
机译:本文提出了一种组合策略,用于人血清中环氧二十碳三烯酸(EET)的定性/定量靶向分析。 EET区域异构体的鉴定最初是通过LC-TOF MS在高精度条件下进行的,该条件是采用等度方法,使用40:40:20(v / v / v)甲醇-乙腈-水等度色谱法分离四种异构体的最佳条件0.02%乙酸。 MS / MS实验使用混合QqTOF质量分析仪通过对分子式为C_(20)H_(32)O_3(319.2279 m / z)的前体离子拟合进行有针对性的碎裂来支持验证性分析。以高精度模式鉴定选择性碎片离子可实现环氧基官能团的定位,因此可将色谱峰分配给每个EET异构体。在定性分析之后,开发了一种自动方法,用于在选定的反应监测中使用基于SPE-LC-QqQ MS / MS的在线平台直接分析,通过直接分析来分析人血清中的EET。使用三种浓度的非加标和加标血清,用双药筒配置估算的所有代谢物的回收率均高于87%。精密度以实验室内重复性计算,并表示为相对标准偏差,范围为2.5%至9.9%,检测限低于0.15 ng mL〜(-1)。该方法的优化通过在不同条件下的稳定性研究完成,以评估适合分析EET中间代谢物的条件。最后,在9名健康个体中测量了EET的浓度范围。

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