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采用混合模式固相萃取和四极杆飞行时间液质联用技术对废水中的非法药物进行筛选和选择性定量分析。

Screening and selective quantification of illicit drugs in wastewater by mixed-mode solid-phase extraction and quadrupole-time-of-flight liquid chromatography-mass spectrometry.

机构信息

Department of Analytical Chemistry, Nutrition and Food Sciences, IIAA-Institute for Food Analysis and Research, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain.

出版信息

Anal Chem. 2012 Feb 7;84(3):1708-17. doi: 10.1021/ac202989e. Epub 2012 Jan 12.

Abstract

For the first time, a mixed-mode solid-phase extraction with fractionation of basic analytes from neutral and acidic species during cartridge elution and liquid chromatography-quadrupole-time-of-flight mass spectrometry (LC-QTOF-MS) was combined for the quantitative determination of 24 illicit drugs and metabolites in urban sewage samples. The effects of several sample preparation and instrumental parameters in the sensitivity and selectivity of the quantitative method are thoroughly discussed. Under final working conditions, recoveries above 63% and 82% were attained for all species in raw and treated sewage, respectively; whereas, the limits of quantification of the method, defined for a signal-to-noise of 10 (S/N = 10), ranged from 2 to 50 ng L(-1). Sequential elution of mixed-mode cartridges allowed a significant reduction of matrix effects observed during electrospray ionization of basic drugs versus those measured for hydrophilic balance reversed-phase sorbents and the same mixed-mode polymer without fractionated elution. Analysis of raw wastewater samples confirmed the ubiquity of cocaine (COC), benzoylecgonine (BE), and 11-nor-9-carboxy-Δ(9)-tetrahydrocannabinol (THCCOOH) in this matrix. The capability of the above methodology to identify new illicit drugs and/or metabolites in sewage samples is also discussed. With this aim, a two step strategy is proposed. First, high-resolution MS chromatograms, acquired throughout each chromatographic run, are automatically searched against an in-house built database, a reduced list of candidate drugs is generated, and the corresponding extracted ion chromatograms are obtained. In a further LC run, the tandem mass spectrometry (MS/MS) spectra of unknown peaks are acquired using different collision energies and compared with those existing in public libraries, or interpreted, to assign the unknown peak to one of the previously selected candidates.

摘要

首次结合混合模式固相萃取,在柱洗脱过程中对碱性分析物进行分段,同时采用液相色谱-四极杆飞行时间质谱(LC-QTOF-MS),对城市污水样品中的 24 种非法药物和代谢物进行定量测定。本文深入探讨了几种样品前处理和仪器参数对定量方法的灵敏度和选择性的影响。在最终工作条件下,原始污水和处理污水中所有物质的回收率均高于 63%和 82%;而方法的定量限(S/N = 10 时的信号噪声比为 10)定义为 2 至 50ng/L。混合模式柱的顺序洗脱可显著降低电喷雾电离碱性药物时观察到的基质效应,与亲水平衡反相固定相吸附剂和相同的未分段洗脱混合模式聚合物相比,该效应显著降低。对原废水样品的分析证实了可卡因(COC)、苯甲酰古柯碱(BE)和 11-去甲-9-羧酸-Δ(9)-四氢大麻酚(THCCOOH)在该基质中的普遍性。还讨论了上述方法在污水样品中识别新的非法药物和/或代谢物的能力。为此,提出了两步策略。首先,在每个色谱运行过程中自动搜索高分辨 MS 色谱图,针对内部构建的数据库进行搜索,生成候选药物的简化列表,并获得相应的提取离子色谱图。在进一步的 LC 运行中,使用不同的碰撞能量获取未知峰的串联质谱(MS/MS)谱图,并与公共库中的谱图进行比较,或进行解释,将未知峰分配给之前选择的候选物之一。

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