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使用离子色谱与高分辨率(Orbitrap)质谱联用技术对饮用水中卤乙酸、溴酸盐和茅草枯进行靶向定量模式比较

Targeted Quantitation Mode Comparison of Haloacetic Acids, Bromate, and Dalapon in Drinking Water Using Ion Chromatography Coupled to High-Resolution (Orbitrap) Mass Spectrometry.

作者信息

Huang Beibei, Rohrer Jeffrey

机构信息

Thermo Fisher Scientific, 1214 Oakmead Parkway, Sunnyvale, CA 94085, United States.

Thermo Fisher Scientific, 1214 Oakmead Parkway, Sunnyvale, CA 94085, United States.

出版信息

J Chromatogr A. 2020 Sep 18;1630:461538. doi: 10.1016/j.chroma.2020.461538.

Abstract

A highly selective, sensitive, and simple analytical method for identification and quantification of nine haloacetic acids, bromate, and dalapon has been developed. This method uses ion chromatography (IC) coupled with electrospray ionization-high-resolution mass spectrometry (IC-ESI-HRMS) to directly analyze water samples on a high capacity anion-exchange column, eliminating the need for sample pretreatment/derivatization. Our study compared the following three types of targeted quantitation experiments using a quadrupole-orbitrap hybrid mass spectrometer, full-scan MS with data-dependent tandem mass spectrometry (full MS/dd-MS with inclusion list), targeted selected ion monitoring (SIM) with data-dependent tandem mass spectrometry (t-SIM/dd-MS), and parallel reaction monitoring (PRM). Sensitivity, linearity, accuracy, and precision were validated following the guidelines of U.S. EPA Method 557. Single laboratory lowest concentration minimum reporting levels (LCMRLs) for the analytes using three different acquisition modes ranged from 0.0011 to 0.18 μg/L. All three quantitation modes showed good linearity for the eleven analytes with coefficients of determination of 0.9981- 0.9993. This IC-ESI-HRMS method was successfully applied to the analysis of commercial bottled water, tap water from San Francisco Bay Area, and the same tap water that has been through a filtered drinking water faucet. Both t-SIM/dd-MS and PRM modes were sensitive to confirm the trace-level presence of all nine HAAs, bromate, and dalapon in the tap water sample. Full-scan HRMS data acquisition provided the benefits of simultaneous data collection for both targeted and non-targeted components, and thus, suitability for simultaneous quantification of an unlimited number of compounds. Data-dependent MS/MS (dd-MS) product-ion spectra were used for confirmation. All three modes showed good quantitative performance and obtained similar values. Single laboratory precision and accuracy data are presented for three water matrices: reagent water, laboratory synthetic sample matrix (LSSM), and tap water. Single laboratory precision was 0.078- 8.04%, and accuracy was in the range 70-130% for the three MS modes.

摘要

已开发出一种用于鉴定和定量九种卤乙酸、溴酸盐和茅草枯的高选择性、灵敏且简便的分析方法。该方法采用离子色谱(IC)与电喷雾电离高分辨率质谱联用(IC-ESI-HRMS),在高容量阴离子交换柱上直接分析水样,无需进行样品预处理/衍生化。我们的研究使用四极杆-轨道阱混合质谱仪比较了以下三种靶向定量实验:全扫描质谱与数据依赖串联质谱联用(全MS/dd-MS,带包含列表)、靶向选择离子监测(t-SIM)与数据依赖串联质谱联用(t-SIM/dd-MS)以及平行反应监测(PRM)。按照美国环保署方法557的指南对灵敏度、线性、准确度和精密度进行了验证。使用三种不同采集模式时,各分析物的单实验室最低浓度最低报告水平(LCMRL)范围为0.0011至0.18μg/L。所有三种定量模式对11种分析物均显示出良好的线性,决定系数为0.9981至0.9993。这种IC-ESI-HRMS方法成功应用于商业瓶装水、旧金山湾区自来水以及经过过滤饮用水龙头的同一自来水的分析。t-SIM/dd-MS和PRM模式均灵敏地确认了自来水中所有九种卤乙酸、溴酸盐和茅草枯的痕量存在。全扫描HRMS数据采集具有同时收集靶向和非靶向成分数据的优点,因此适用于同时定量无限数量的化合物。数据依赖MS/MS(dd-MS)产物离子光谱用于确认。所有三种模式均显示出良好的定量性能并获得了相似的值。给出了三种水基质(试剂水、实验室合成样品基质(LSSM)和自来水)的单实验室精密度和准确度数据。三种质谱模式的单实验室精密度为0.078%至8.04%,准确度在70%至130%范围内。

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