Water and Soil Quality Research Group, Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18-26, 08034, Barcelona, Spain.
Water and Soil Quality Research Group, Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18-26, 08034, Barcelona, Spain; Department of Aquatic Sciences and Assessment, Swedish University of Agricultural Sciences, Box 7050, SE-750 07 Uppsala, Sweden.
J Chromatogr A. 2018 Nov 16;1576:80-89. doi: 10.1016/j.chroma.2018.09.038. Epub 2018 Sep 18.
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- Δ-tetrahydrocannabinol (18 and 61 ng/L) and 11-hydroxy-Δ- 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 μg/L in the case of caffeine.
本工作提出了一种同时测定废水中 37 种法定和非法精神活性物质的多残留方法,包括最常见的非法药物(可卡因相关化合物、苯丙胺类兴奋剂、致幻剂、阿片类药物/类阿片类药物和大麻素)、新精神活性物质(两种合成卡西酮、合成阿片类药物 AH-7921 以及芳基环己基胺甲氧基乙基),以及合法但受管制的精神活性物质(兴奋剂、苯二氮䓬类、抗抑郁药、镇静剂、抗精神病药和催眠药)。为此,采用了一种基于固相萃取串联液相色谱串联质谱检测(在线 SPE-LC-MS/MS)的全自动分析方法。所开发的方法在废水的线性、回收率、重复性和灵敏度方面进行了验证。方法的线性范围在 0.1ng/L(或更高的分析物定量下限)和 2000ng/L(咖啡因的情况下为 10250ng/L)之间。绝对回收率因分析物而异,在 5%至 132%之间变化。然而,使用同位素标记化合物可校正提取过程中的分析物损失和基质效应(相对回收率在 80-120%范围内)。对于大多数化合物,方法的重复性令人满意,相对标准偏差值低于 13%。除了氯硝西泮(10 和 32ng/L)、咖啡因(13 和 44ng/L)以及大麻素 11-去甲-9-羧酸-Δ-四氢大麻酚(18 和 61ng/L)和 11-羟基-Δ-四氢大麻酚(69 和 228ng/L)外,所有分析物在废水中的检出限和定量限均低于 7 和 23ng/L。该方法应用于在巴塞罗那每天收集的一周废水样品的分析。在所分析的样品中检测到 37 种分析物中的 25 种。平均浓度范围从佐匹克隆的 7ng/L 到咖啡因的 54μg/L。