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同时采用超高压液相色谱-串联质谱法测定地表水和城市废水中的苯丙胺及苯丙胺类兴奋剂、可卡因及其代谢物以及一种大麻代谢物。

Simultaneous ultra-high-pressure liquid chromatography-tandem mass spectrometry determination of amphetamine and amphetamine-like stimulants, cocaine and its metabolites, and a cannabis metabolite in surface water and urban wastewater.

作者信息

Bijlsma Lubertus, Sancho Juan V, Pitarch Elena, Ibáñez Maria, Hernández Félix

机构信息

Research Institute for Pesticides and Water, University Jaume I, Castellón, Spain.

出版信息

J Chromatogr A. 2009 Apr 10;1216(15):3078-89. doi: 10.1016/j.chroma.2009.01.067. Epub 2009 Jan 29.

DOI:10.1016/j.chroma.2009.01.067
PMID:19201418
Abstract

An ultra-high-pressure liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method has been developed for the simultaneous quantification and confirmation of 11 basic/acidic illicit drugs and relevant metabolites in surface and urban wastewater at ng/L levels. The sample pre-treatment consisted of a solid-phase extraction using Oasis MCX cartridges. Analyte deuterated compounds were used as surrogate internal standards (except for norbenzoylecgonine and norcocaine) to compensate for possible errors resulting from matrix effects and those associated to the sample preparation procedure. After SPE enrichment, the selected drugs were separated within 6min under UHPLC optimized conditions. To efficiently combine UHPLC with MS/MS, a fast-acquisition triple quadrupole mass analyzer (TQD from Waters) in positive-ion mode (ESI+) was used. The excellent selectivity and sensitivity of the TQD analyzer in selected reaction monitoring mode allowed quantification and reliable identification at the LOQ levels. Satisfactory recoveries (70-120%) and precision (RSD<20%) were obtained for most compounds in different types of water samples, spiked at two concentration levels [limit of quantification (LOQ) and 10LOQ]. Thus, surface water was spiked at 30 ng/L and 300 ng/L (amphetamine and amphetamine-like stimulants), 10 ng/L and 100 ng/L (cocaine and its metabolites), 300 ng/L and 3000 ng/L (tetrahydrocannabinol-COOH). Recovery experiments in effluent and influent wastewater were performed at spiking levels of three and fifteen times higher than the levels spiked in surface water, respectively. The validated method was applied to urban wastewater samples (influent and effluent). The acquisition of three selected reaction monitoring transitions per analyte allowed positive findings to be confirmed by accomplishment of ion ratios between the quantification transition and two additional specific confirmation transitions. In general, drug consumption increased in the weekends and during an important musical event. The highest concentration levels were 27.5 microg/L and 10.5 microg/L, which corresponded to 3,4-methylenedioxymethamphetamine (MDMA, or ecstasy) and to benzoylecgonine (a cocaine metabolite), respectively. The wastewater treatment plants showed good removal efficiency (>99%) for low levels of illicit drugs in water, but some difficulties were observed when high drug levels were present in wastewaters.

摘要

已开发出一种超高压液相色谱-串联质谱(UHPLC-MS/MS)方法,用于同时定量和确证地表水中及城市废水中纳克/升水平的11种碱性/酸性非法药物及其相关代谢物。样品预处理包括使用Oasis MCX柱进行固相萃取。除去甲苯甲酰芽子碱和去甲可卡因外,分析物的氘代化合物用作替代内标,以补偿基质效应以及与样品制备过程相关的可能误差。经过固相萃取富集后,在超高效液相色谱优化条件下,选定的药物在6分钟内实现分离。为了有效地将超高效液相色谱与串联质谱联用,使用了正离子模式(电喷雾电离源,ESI+)下的快速采集三重四极杆质谱仪(沃特世公司的TQD)。TQD分析仪在选择反应监测模式下具有出色的选择性和灵敏度,能够在定量限水平进行定量和可靠鉴定。在不同类型的水样中,以两种浓度水平(定量限和10倍定量限)加标,大多数化合物获得了令人满意的回收率(70-120%)和精密度(相对标准偏差<20%)。因此,地表水加标的浓度分别为30纳克/升和300纳克/升(苯丙胺和苯丙胺类兴奋剂)、10纳克/升和100纳克/升(可卡因及其代谢物)、300纳克/升和3000纳克/升(四氢大麻酚-COOH)。在污水和进水废水的回收率实验中,加标水平分别比地表水中加标的水平高3倍和15倍。经验证的方法应用于城市废水样品(进水和出水)。每个分析物采集三个选择反应监测跃迁,通过定量跃迁与另外两个特定确证跃迁之间的离子比率来确证阳性结果。总体而言,周末和一场重要音乐活动期间药物消费量增加。最高浓度水平分别为27.5微克/升和10.5微克/升,分别对应于3,4-亚甲基二氧甲基苯丙胺(摇头丸)和苯甲酰芽子碱(一种可卡因代谢物)。污水处理厂对水中低水平的非法药物显示出良好的去除效率(>99%),但当废水中存在高药物水平时,观察到了一些困难。

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