Development of a solvent-free method for the simultaneous identification/quantification of drugs of abuse and their metabolites in environmental water by LC-MS/MS

被引:85
|
作者
Martinez Bueno, M. J. [1 ]
Ucles, S. [1 ]
Hernando, M. D. [1 ,2 ]
Fernandez-Alba, A. R. [1 ,3 ]
机构
[1] Univ Almeria, Dept Hydrogeol & Analyt Chem, Pesticide Residues Res Grp, La Canada De San Urbano 04120, Almeria, Spain
[2] Univ Alcala, Natl Reference Ctr Persistent Organ Pollutants, Madrid 28871, Spain
[3] Univ Alcala, Fdn IMDEA Agua, Madrid 28805, Spain
关键词
Direct injection; Illicit drugs; Metabolites; Environmental water; LC-QqLIT-MS/MS; Green analytical chemistry; SOLID-PHASE EXTRACTION; LIQUID-CHROMATOGRAPHY; ILLICIT DRUGS; WASTE-WATER; ORGANIC POLLUTANTS; STIMULATORY DRUGS; SPECTROMETRY; SURFACE; CONTAMINANTS; ONLINE;
D O I
10.1016/j.talanta.2011.03.051
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This work details a rapid analytical method using direct sample injection for the simultaneous identification/quantification of 22 drugs of abuse, including some of their major metabolites, in environmental samples. This has been developed using a hybrid triple quadrupole-linear ion trap-mass spectrometer (QqLIT). With the increasing sensitivity of today's tandem mass spectrometers, direct injection analysis of water samples has become an attractive alternative to traditional analytical protocols, which often include a preliminary pre-concentration step. What's more, this kind of analysis is in accordance with many of the main objectives of so-called green analytical chemistry, or environmentally friendly practice. The analytical performance of the LC-MS/MS method was evaluated in three different water matrices (surface water, influent and effluent wastewater). Data acquisition was carried out in selected reaction monitoring (SRM) mode under time-scheduled conditions, monitoring two SRM transitions for simultaneous identification/quantification of all target compounds in the samples. Additionally, an experiment was performed using the information-dependent acquisition (IDA) scan to carry out the identification of those analytes for which the second transition was present at a low intensity. Finally, the two methodologies developed were applied to real samples for evaluation. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 166
页数:10
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