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Multi-residue analysis of pharmaceuticals in Belgian surface water: a novel screening-to-quantification approach using large-volume injection liquid chromatography coupled to high-resolution mass spectrometry

机译:比利时地表水中药物的多残留分析:使用大体积注射液相色谱与高分辨率质谱联用的新型筛选 - 定量方法

摘要

The ever growing number of emerging micropollutants such as pharmaceuticals requests rapid and sensitive full-spectrum analytical techniques. Time-of-flight highresolution mass spectrometry (TOF-HRMS) is a promising alternative for the state-ofthe- art MS/MS instruments because of its ability to simultaneously screen towards a virtually unlimited list of suspect compounds and to perform target quantification. The challenge for such suspect screening is to develop a strategy which minimizes the false negative rate without restraining numerous false positives. At the same time, omitting laborious sample enrichment through large-volume injection ultraperformance liquid chromatography (LVI-UPLC) is advantageous avoiding selective preconcentration. A novel suspect screening strategy was developed using LVI-UPLC-TOF-MS aiming the detection of 69 multi-class pharmaceuticals in surface water without the a priori availability of analytical standards. As a novel approach, the screening takes into account the signal intensity-dependent accurate mass error, hereby assuring the detection of 95% of pharmaceuticals present in surface water. Subsequently, the validation and applicability of the full-spectrum method for target quantification of the 69 pharmaceuticals in surface water is discussed. Analysis of five Belgian river water samples revealed the occurrence of 17 pharmaceuticals in a concentration range of 17 ng L-1 up to 3.1 μg L-1.
机译:越来越多的新兴微污染物(例如药物)需要快速而灵敏的全光谱分析技术。飞行时间高分辨率质谱(TOF-HRMS)是最先进的MS / MS仪器的有希望的替代品,因为它能够同时筛选几乎无限的可疑化合物列表并进行目标定量。这种可疑筛查面临的挑战是制定一种在不限制大量假阳性的情况下将假阴性率降至最低的策略。同时,通过大体积进样超高效液相色谱(LVI-UPLC)省去了费力的样品富集工作,有利于避免选择性预浓缩。使用LVI-UPLC-TOF-MS开发了一种新颖的可疑物筛查策略,旨在在无需事先获得分析标准的情况下检测地表水中的69种多类药物。作为一种新颖的方法,筛选考虑了信号强度相关的精确质量误差,从而确保了对地表水中存在的95%药物的检测。随后,讨论了用于地表水中69种药物目标定量的全谱方法的验证和适用性。对五个比利时河水样品的分析显示,在浓度范围为17 ng L-1至3.1μgL-1的情况下,存在17种药物。

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