QuEChERS analytical approach for monitoring endocrine-disrupting chemicals in human urine.

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
S Callejas-Martos, E Eljarrat
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Abstract

This study introduces an analytical method for the determination of endocrine-disrupting chemicals (EDCs) in human urine samples, employing QuEChERS as a clean-up step for the first time in this biological matrix. Sample preparation was rigorously optimized through the evaluation of sample and final dilution volumes, balancing the need to reduce matrix interference without sacrificing sensitivity. High-performance liquid chromatography coupled with a triple quadrupole-time-of-flight mass spectrometer (HPLC-QTOF) was employed, enabling the detection of 13 target analytes (five OPEs, five phthalates, and three parabens' metabolites). Chromatographic separation was achieved in 16 min, and mass spectrometry parameters were fine-tuned to maximize signal sensitivity. The method was validated by assessing parameters such as selectivity, linearity, precision, accuracy, and sensitivity. Linearity of response was demonstrated for all of the compounds (r2 > 0.99), with method detection limits of 0.01-0.33 ng/mL and limits of quantification of 0.03-1.08 ng/mL. Accuracy ranged from 67 to 99% and inter- and intra-day precision were under 20%, for the majority of the analytes. The validated method was then applied to 39 human urine samples, confirming its reliability and practical utility for monitoring EDC exposure in urban populations. The highest concentrations were found in parabens, followed by phthalates and finally OPEs, with median values of 117, 43.5, and 25.4 ng/g of creatinine, respectively. The detection of all three EDC groups in 100% of the samples underscores the importance of this comprehensive analytical approach being capable of simultaneously assessing these contaminants in human biomonitoring studies.

用于监测人体尿液中内分泌干扰化学物质的QuEChERS分析方法。
本研究介绍了一种测定人类尿液样本中内分泌干扰化学物质(EDCs)的分析方法,首次在这种生物基质中采用QuEChERS作为清理步骤。通过评估样品和最终稀释体积,严格优化样品制备,在不牺牲灵敏度的情况下平衡减少基质干扰的需要。采用高效液相色谱联用三重四极杆飞行时间质谱仪(HPLC-QTOF)检测13种目标分析物(5种OPEs, 5种邻苯二甲酸酯和3种对羟基苯甲酸酯代谢物)。色谱分离在16分钟内完成,质谱参数微调以最大限度地提高信号灵敏度。通过评价方法的选择性、线性度、精密度、准确度和灵敏度等参数对方法进行了验证。所有化合物均呈线性关系(r2 > 0.99),方法检出限为0.01 ~ 0.33 ng/mL,定量限为0.03 ~ 1.08 ng/mL。对于大多数分析物,准确度范围为67%至99%,日间和日内精度低于20%。然后将该验证方法应用于39份人类尿液样本,证实了其在监测城市人群EDC暴露方面的可靠性和实用性。对羟基苯甲酸酯的浓度最高,其次是邻苯二甲酸酯,最后是OPEs,肌酐的中位数分别为117、43.5和25.4 ng/g。在100%的样品中检测到所有三种EDC组,强调了这种能够同时评估人类生物监测研究中这些污染物的综合分析方法的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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