首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Simple and quick determination of analgesics and other contaminants of emerging concern in environmental waters by on-line solid phase extraction coupled to liquid chromatography-tandem mass spectrometry
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Simple and quick determination of analgesics and other contaminants of emerging concern in environmental waters by on-line solid phase extraction coupled to liquid chromatography-tandem mass spectrometry

机译:通过在线固相萃取-液相色谱-串联质谱联用技术快速简便地测定环境水中正在出现的止痛药和其他污染物

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摘要

A simple and quick analytical method has been developed for the determination of pharmaceutical compounds in water. An on-line solid-phase extraction (SPE) coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been optimized to determine 7 contaminants of emerging concern in environmental waters at ng L-1 levels. This procedure requires minimal sample handling and small sample volume (900 mu L) with a total running time of 18 min. Several SPE parameters were evaluated and optimized in order to achieve a high sample throughput. Therefore sample volume, carryover and reusability of the cartridges were evaluated. Performance characteristics were evaluated and good linearity was obtained (R-2 > 0.98). Recoveries were evaluated in spiked samples at three concentrations and the values ranged from 71 to 104%. Intra and inter-day precision was lower than 10 and 13% respectively. Limits of quantification were equal to or lower than 10 ng L-1, except for 1,7-dimethylxanthine (20 ng L-1) and ibuprofen (50 ng L-1). The method was applied to 20 environmental water samples, and ibuprofen was the compound most widely detected at concentrations up to 42.06 mu gL(-1), whereas the other compounds were detected in fewer samples at lower concentrations (up to 15.99 mu g L-1). (C) 2016 Elsevier B.V. All rights reserved.
机译:已经开发出一种简单而快速的分析方法来测定水中的药物化合物。在线固相萃取(SPE)结合液相色谱-串联质谱(LC-MS / MS)方法已得到优化,可确定ng L-1含量的7种环境水中新兴污染物。此过程需要最少的样品处理和较小的样品量(900μL),总运行时间为18分钟。评估并优化了几个SPE参数,以实现高样品通量。因此,评估了样品盒的样品量,残留量和可重复使用性。评价性能特征并获得良好的线性(R-2> 0.98)。在三种浓度的加标样品中评估回收率,其回收率范围为71%至104%。日内和日间精度分别低于10%和13%。除1,7-二甲基黄嘌呤(20 ng L-1)和布洛芬(50 ng L-1)外,定量限等于或低于10 ng L-1。该方法适用于20个环境水样品,布洛芬是浓度高达42.06μgL(-1)时检测最广泛的化合物,而其他化合物则以较低的浓度(高达15.99μg L- 1)。 (C)2016 Elsevier B.V.保留所有权利。

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