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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of beta-blockers and beta(2)-agonists in sewage by solid-phase extraction and liquid chromatography-tandem mass spectrometry
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Determination of beta-blockers and beta(2)-agonists in sewage by solid-phase extraction and liquid chromatography-tandem mass spectrometry

机译:固相萃取-液相色谱-串联质谱法测定污水中的β-受体阻滞剂和β(2)-激动剂

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A method using solid-phase extraction (SPE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed for the determination of 12 beta-blockers and beta(2)-agonists in wastewater samples. Extraction of the drugs was effected by an Oasis MCX cartridge with a strong cation resin adsorbent. Matrix coextractives were removed from the SPE cartridge by methanol prior to the elution of the drugs with a mixture of dichloromethane, 2-propranol, and ammonium hydroxide. The extract was analyzed by LC-MS/MS with electrospray ionization operating in the positive mode. Recovery of the 12 compounds was in most cases better than 85% at the fortification levels of 500 and 50 ng/L, with standard deviations between 3 and 7%. Based on a concentration factor of 250, the method detection limits ranged from 6 to 11 ng/L for the target compounds. No degradation of these drugs in spiked sewage effluent samples was observed over a storage period of 7 days at 4 degrees C in the dark. Many beta-blockers were detected in the 14 wastewater samples collected from seven Canadian sewage treatment plants; those occurring at the highest concentrations were atenolol, acebutolol, sotalol, and metroprolol, with overall median concentrations of 1370, 339, 282, and 257 ng/L, respectively. However, there was only a small decrease in the median concentrations of these P-blockers between the primary and final effluent, suggesting that these drugs are not easily removed by the sewage treatment processes. As a result of selective extraction and effective removal of coextractives, no matrix effect was observed for the samples during LC-MS/MS analyses. Crown Copyright (C) 2007 Published by Elsevier B.V. All rights reserved.
机译:已经开发出一种使用固相萃取(SPE)和液相色谱-串联质谱(LC-MS / MS)的方法来测定废水样品中的12种β-受体阻滞剂和β(2)-激动剂。药物的提取是通过带有强阳离子树脂吸附剂的Oasis MCX柱进行的。在用二氯甲烷,2-丙醇和氢氧化铵的混合物洗脱药物之前,先用甲醇从SPE柱中除去基质共提取物。提取物通过LC-MS / MS分析,电喷雾电离以正模式运行。在强化水平为500和50 ng / L的情况下,大多数情况下12种化合物的回收率优于85%,标准偏差为3%至7%。基于250的浓缩系数,目标化合物的方法检测极限范围为6到11 ng / L。在黑暗中于4摄氏度下储存7天,在加标的污水样品中未观察到这些药物的降解。在从加拿大七个污水处理厂收集的14个废水样本中检测到许多β受体阻滞剂。最高浓度的是阿替洛尔,醋丁酚,索他洛尔和甲硝酚,总中位数浓度分别为1370、339、282和257 ng / L。但是,这些P受体阻滞剂的主要排放物和最终排放物之间的中位浓度仅略有下降,这表明这些药物不易通过污水处理过程去除。选择性提取和有效去除共提取物的结果是,在LC-MS / MS分析期间未观察到样品的基质效应。 Crown版权所有(C)2007,Elsevier B.V.保留所有权利。

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