Multi-residue analysis of drugs of abuse in wastewater and surface water by solid-phase extraction and liquid chromatography-positive electrospray ionisation tandem mass spectrometry

被引:219
作者
Baker, David R. [2 ]
Kasprzyk-Hordern, Barbara [1 ,2 ]
机构
[1] Univ Bath, Dept Chem, Fac Sci, Bath BA2 7AY, Avon, England
[2] Univ Huddersfield, Dept Chem & Biol Sci, Sch Appl Sci, Huddersfield HD1 3DH, W Yorkshire, England
关键词
Illicit drugs; Drugs of abuse; Precursors; UPLC; Wastewater; Surface water; Environment; LC-MS/MS; Sewage; Crack cocaine; SPE; Pharmaceuticals; Multi-residue; ILLICIT DRUGS; STIMULATORY DRUGS; METABOLITES; COCAINE; PHARMACEUTICALS; URINE; REMOVAL; BELGIUM; SAMPLES; MS/MS;
D O I
10.1016/j.chroma.2011.01.060
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new-multi residue method was developed for the environmental monitoring of 65 stimulants, opiod and morphine derivatives, benzodiazepines, antidepressants, dissociative anaesthetics, drug precursors, human urine indicators and their metabolites in wastewater and surface water. The proposed analytical methodology offers rapid analysis for a large number of compounds, with low limits of quantification and utilises only one solid-phase extraction-ultra performance liquid chromatography-positive electrospray ionisation tandem mass spectrometry (SPE-LC-MS/MS) method, thus overcoming the drawbacks of previously published procedures. The method employed solid phase extraction with the usage of Oasis MCX sorbent and subsequent ultra performance liquid chromatography-positive electrospray ionisation tandem mass spectrometry. The usage of a 1.7 mu m particle size column (1 mm x 150 mm) resulted in very low flow rates (0.04 mL min(-1)), and as a consequence gave good sensitivity, low mobile phase consumption and short retention times for all compounds (from 2.9 to 23.1 min). High SPE recoveries (>60%) were obtained for the majority of compounds. The mean correlation coefficients of the calibration curves were typically higher than 0.997 and showed good linearity in the range 0-1000 mu g L-1. The method limits of detection ranged from 0.1 ng L-1 for compounds including cocaine, benzoylecgonine, norbenzoylecgonine and 2-oxo-3-hydroxy-LSD to 100 ng L-1 for caffeine. Method quantification limits ranged from 0.5 to 154.2 ng L-1. Intra-and inter-day repeatabilities were on average less than 10%. The method accuracy range was within -33.1 to 30.1%. The new multi-residue method was used to analyse drugs of abuse in wastewater and river water in the UK environment. Of the targeted 65 compounds, 46 analytes were detected at levels above the method quantification limit (MQL) in wastewater treatment plant (WWTP) influent, 43 in WWTP effluent and 36 compounds in river water. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1620 / 1631
页数:12
相关论文
共 45 条
[1]  
[Anonymous], 2002, OFFICIAL J EUROPEAN
[2]  
[Anonymous], 2009, STAT DRUGS PROBL EUR
[3]   The occurrence of illicit and therapeutic pharmaceuticals in wastewater effluent and surface waters in Nebraska [J].
Bartelt-Hunt, Shannon L. ;
Snow, Daniel D. ;
Damon, Teyona ;
Shockley, Johnette ;
Hoagland, Kyle .
ENVIRONMENTAL POLLUTION, 2009, 157 (03) :786-791
[4]   Analysis of llicit and illicit drugs in waste, surface and lake water samples using large volume direct injection high performance liquid chromatography - Electrospray tandem mass spectrometry (HPLC-MS/MS) [J].
Berset, Jean-Daniel ;
Brenneisen, Rudolf ;
Mathieu, Christoph .
CHEMOSPHERE, 2010, 81 (07) :859-866
[5]   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 [J].
Bijlsma, Lubertus ;
Sancho, Juan V. ;
Pitarch, Elena ;
Ibanez, Maria ;
Hernandez, Felix .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (15) :3078-3089
[6]   Trace determination of cannabinoids and opiates in wastewater and surface waters by ultra-performance liquid chromatography-tandem mass spectrometry [J].
Boleda, M. Rosa ;
Galceran, M. Teresa ;
Ventura, Francesc .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1175 (01) :38-48
[7]   Using environmental analytical data to estimate levels of community consumption of illicit drugs and abused pharmaceuticals [J].
Bones, Jonathan ;
Thomas, Kevin V. ;
Paull, Brett .
JOURNAL OF ENVIRONMENTAL MONITORING, 2007, 9 (07) :701-707
[8]   Identification and measurement of illicit drugs and their metabolites in urban wastewater by liquid chromatography-tandem mass spectrometry [J].
Castiglioni, Sara ;
Zuccato, Ettore ;
Crisci, Elisabetta ;
Chiabrando, Chiara ;
Fanelli, Roberto ;
Bagnati, Renzo .
ANALYTICAL CHEMISTRY, 2006, 78 (24) :8421-8429
[9]   Eliminating Solid Phase Extraction with Large-Volume Injection LC/MS/MS: Analysis of Illicit and Legal Drugs and Human Urine Indicators in US Wastewaters [J].
Chiaia, Aurea C. ;
Banta-Green, Cale ;
Field, Jennifer .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (23) :8841-8848
[10]  
Daughton C.G., 2001, PHARM PERSONAL CARE