首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >A fully automated approach for the analysis of 37 psychoactive substances in raw wastewater based on on-line solid phase extraction-liquid chromatography-tandem mass spectrometry
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A fully automated approach for the analysis of 37 psychoactive substances in raw wastewater based on on-line solid phase extraction-liquid chromatography-tandem mass spectrometry

机译:基于在线固相提取 - 液相色谱 - 串联质谱法的原料废水中37例精神活性分析的全自动方法

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摘要

This work presents a multi-residue method for the simultaneous determination of 37 legal and illicit psychoactive substances in wastewater, including the most common illicit drugs (cocaine-related compounds, amphetamine-type stimulants, hallucinogens, opiates/opioids, and cannabinoids), new psychoactive substances (two synthetic cathinones, the synthetic opioid AH-7921, and the arylcyclohexylamine methoxetamine), and legal but controlled psychoactive substances (stimulants, benzodiazepines, antidepressants, sedatives, antipsychotics, and hypnotics). To this end a fully automated analytical approach based on solid phase extraction coupled in series to liquid chromatography tandem mass spectrometry detection (on-line SPE- LC-MS/MS) was used. The methodology developed was validated in terms of linearity, recovery, repeatability, and sensitivity in wastewater. Method linearity was between 0.1 ng/L (or the analyte limit of quantification if higher) and 2,000 ng/L (10,250 ng/L in the case of caffeine). Absolute recoveries were variable (between 5% and 132%), depending on the analyte. However, the use of isotopically labeled compounds corrected for analyte losses during the extraction process and matrix effects (relative recoveries within the range of 80-120%). Repeatability of the method was satisfactory for all analytes, with RSD values lower than 13% for most compounds. Limits of detection and quantification in wastewater were below 7 and 23 ng/L, respectively, for all analytes except lormetazepam (10 and 32 ng/L), caffeine (13 and 44 ng/L), and the cannabinoids 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (18 and 61 ng/L) and 11-hydroxy-Delta(9)- tetrahydrocannabinol (69 and 228 ng/L). The method was applied to the analysis of wastewater samples collected daily in Barcelona for one week. Twenty-five of the 37 analytes were detected in the samples analyzed. Average concentrations ranged from 7 ng/L in the case of zolpidem to 54 mu g/L in the case of caffeine. (C) 2018 Elsevier B.V. All rights reserved.
机译:该工作提出了一种多残留方法,用于同时测定废水中的37种法律和非法精神活性物质,包括最常见的非法药物(可卡因相关的化合物,安非他明型兴奋剂,幻肽,阿片类药物和大麻素),新的精神活性物质(两种合成天然阴茎,合成阿片类药物AH-7921和芳基己酰胺甲氧酰胺),以及法律但受控的精神活性物质(兴奋剂,苯二氮卓类动物,抗抑郁药,镇静剂,抗精神病药和催眠药)。为此,基于固相萃取的全自动分析方法串联耦合到液相色谱串联质谱检测(在线SPE-LC-MS / MS)。在废水中的线性,恢复,可重复性和敏感性方面验证了开发的方法。方法线性度为0.1ng / L(或者在咖啡因的情况下的定量分析物限制)和2,000ng / L(10,250ng / L)。取决于分析物,绝对回收是可变的(5%和132%)。然而,在提取过程和基质效应期间使用同位素标记的化合物以进行分析物损失(相对回收率在80-120%的范围内)。对于所有分析物,该方法的可重复性令人满意,对于大多数化合物,RSD值低于13%。除了Lormetazepam(10和32 ng / L),咖啡因(13和44 ng / L)外,废水中的检测和定量限制分别低于7和23 ng / L,咖啡因(13和44 ng / L),以及大麻素11-NOR-9 -Carboxy-Delta(9)-Tetrahydrocannabol(18和61 ng / L)和11-羟基 - δ(9) - 四氢甘油醛(69和228 ng / L)。该方法应用于每天在巴塞罗那收集的废水样品一周的分析。在分析的样品中检测到37种分析物中的25个分析物中的25个。在咖啡因的情况下,平均浓度范围为7 ng / L至54μg/ l。 (c)2018年elestvier b.v.保留所有权利。

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