Laboratory of Analytical Chemistry, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zographou, 15771 Athens, Greece; Catalan Institute for Water Research (ICRA), Carrer Emili Grahit 101, 17003 Girona, Spain.
Laboratory of Analytical Chemistry, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zographou, 15771 Athens, Greece.
J Hazard Mater. 2020 Apr 5;387:121712. doi: 10.1016/j.jhazmat.2019.121712. Epub 2019 Nov 18.
This study presents the development and validation of a comprehensive quantitative target methodology for the analysis of 2316 emerging pollutants in water based on Ultra-Performance Liquid Chromatography Quadrupole-Time-Of-Flight Mass Spectrometry (UPLC-Q-ToF-HRMS/MS). Target compounds include pesticides, pharmaceuticals, drugs of abuse, industrial chemicals, doping compounds, surfactants and transformation products, among others. The method was validated for 195 analytes, chosen to be representative of the chemical space of the target list, enabling the assessment of the performance of the method. The method involves a generic sample preparation based on mixed mode solid phase extraction, a UPLC-QTOF-MS/MS screening method using Data Independent Acquisition (DIA) mode, which provides MS and MS/MS spectra simultaneously and an elaborate strong post-acquisition evaluation of the data. The processing method was optimized to provide a successful identification rate >95 % and to minimize the number of false positive results (< 5 %). Decision limit (CCα) and detection capability (CCβ) were also introduced in the validation scheme to provide more realistic metrics on the performance of a HRMS-based wide-scope screening method. A new system of identification points (IPs) based on the one described in the Commission Decision 2002/657/EC was applied to communicate the confidence level in the identification of the analytes. This system considers retention time, mass accuracy, isotopic fit and fragmentation; taking full advantage of the capacities of the HRMS instruments. Finally, 398 contaminants were detected and quantified in real wastewater.
本研究提出了一种基于超高效液相色谱四极杆飞行时间质谱(UPLC-Q-ToF-HRMS/MS)分析水中 2316 种新兴污染物的综合定量目标方法的开发和验证。目标化合物包括农药、药物、滥用药物、工业化学品、兴奋剂化合物、表面活性剂和转化产物等。该方法针对 195 种分析物进行了验证,这些分析物被选择为目标列表化学空间的代表性物质,以评估方法的性能。该方法涉及一种基于混合模式固相萃取的通用样品制备方法、一种使用数据非依赖性采集(DIA)模式的 UPLC-QTOF-MS/MS 筛选方法,该方法同时提供 MS 和 MS/MS 谱图,并对数据进行精心的强后采集评估。该处理方法经过优化,以提供>95%的成功识别率,并将假阳性结果的数量(<5%)降至最低。在验证方案中还引入了决策限(CCα)和检测能力(CCβ),以提供基于 HRMS 的宽范围筛选方法性能的更现实指标。应用了一种基于委员会决定 2002/657/EC 中描述的鉴定点(IP)系统,以传达对分析物鉴定置信水平的信息。该系统考虑保留时间、质量精度、同位素拟合和碎片化;充分利用 HRMS 仪器的能力。最后,在实际废水中检测和定量了 398 种污染物。