首页> 美国卫生研究院文献>Springer Open Choice >A new analytical framework for multi-residue analysis of chemically diverse endocrine disruptors in complex environmental matrices utilising ultra-performance liquid chromatography coupled with high-resolution tandem quadrupole time-of-flight mass spectrometry
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A new analytical framework for multi-residue analysis of chemically diverse endocrine disruptors in complex environmental matrices utilising ultra-performance liquid chromatography coupled with high-resolution tandem quadrupole time-of-flight mass spectrometry

机译:利用超高效液相色谱与高分辨率串联四极杆飞行时间质谱联用对复杂环境基质中化学多样性内分泌干扰物进行多残留分析的新分析框架

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摘要

This manuscript presents a comprehensive analytical framework for identification and quantification of chemically diverse endocrine disrupting chemicals (EDCs) used in personal care and consumer products in diverse solid and liquid environmental matrices with an ultimate goal of evaluating public exposure to EDCs via water fingerprinting. Liquid chromatography coupled with tandem quadrupole time-of-flight mass spectrometry (UHPLC-ESI-MS/MS) was used for targeted analysis of selected EDCs as well as to identify and quantify a few metabolites using post-acquisition data mining. Solid-phase extraction (SPE) was applied to liquid matrices in order to reduce matrix effects and provide required sample concentration and ultimately, high sensitivity and selectivity of measurements. SPE recoveries in liquid samples ranged from 49 to 140% with method quantification limits not exceeding 1 ng L−1 for the majority of EDCs. Microwave-assisted extraction (MAE) was applied to solid samples and when followed by SPE, it permitted the analysis of EDCs in digested sludge. MAE/SPE recoveries varied from 11 to 186% and MQLs between 0.03 and 8.1 ng g−1 with the majority of compounds showing MQLs below 2 ng g−1. Mass error for quantifier and qualifier ions was below 5 ppm when analysing river water and effluent wastewater and below 10 ppm when analysing influent wastewater and solid samples. The method was successfully applied to environmental samples, with 33 EDCs identified and quantified in wastewater and receiving waters. In addition, several EDCs were found in digested sludge, which confirms that for a more comprehensive understanding of exposure patterns and environmental impact, analysis of solids cannot be neglected. Finally, post-acquisition data mining permitted the identification and quantification of a metabolite of BPA and the identification of a metabolite of 4-Cl-3-methylphenol. >Graphical abstract
机译:该手稿提供了一个综合的分析框架,用于鉴定和量化在各种固体和液体环境基质中用于个人护理和消费品的化学多样性内分泌干扰化学物质(EDC),其最终目标是通过水指纹评估公众对EDC的暴露程度。液相色谱与串联四极杆飞行时间质谱(UHPLC-ESI-MS / MS)一起用于选定EDC的目标分析,并使用采集后数据挖掘来鉴定和量化一些代谢物。固相萃取(SPE)应用于液体基质,以减少基质效应并提供所需的样品浓度,并最终提供高灵敏度和测量选择性。对于大多数EDC,液体样品中SPE的回收率介于49%至140%之间,方法定量限不超过1 ng L -1 。微波辅助萃取(MAE)用于固体样品,然后进行固相萃取,可以分析消化污泥中的EDC。 MAE / SPE回收率在11%至186%之间,MQL在0.03至8.1ng g -1 之间,大多数化合物的MQL在2ng g -1 以下。分析河水和废水时定量子和定性离子的质量误差低于5 ppm,分析进水废水和固体样品时的质量误差低于10 ppm。该方法已成功应用于环境样品,在废水和接收水中鉴定并定量了33种EDC。此外,在消化的污泥中发现了几种EDC,这证实了要更全面地了解暴露方式和环境影响,不能忽略对固体的分析。最后,采集后的数据挖掘允许对BPA代谢物进行鉴定和定量,以及对4-Cl-3-甲基苯酚的代谢物进行鉴定。 <!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> >图形摘要<!- fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题a7->ᅟ

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