Determination of 89 drugs and other micropollutants in unfiltered wastewater and freshwater by LC-MS/MS: an alternative sample preparation approach

被引:42
作者
Asimakopoulos, Alexandros G. [1 ,2 ]
Kannan, Pranav [2 ]
Higgins, Sean [2 ]
Kannan, Kurunthachalam [2 ,3 ,4 ,5 ]
机构
[1] Norwegian Univ Sci & Technol NTNU, Dept Chem, N-7491 Trondheim, Norway
[2] New York State Dept Hlth, Wadsworth Ctr, Empire State Plaza,POB 509, Albany, NY 12201 USA
[3] King Abdulaziz Univ, Fac Sci, Dept Biochem, Jeddah 21589, Saudi Arabia
[4] King Abdulaziz Univ, King Fahd Med Res Ctr, Expt Biochem Unit, Jeddah 21589, Saudi Arabia
[5] SUNY Albany, Dept Environm Hlth Sci, Sch Publ Hlth, Empire State Plaza,POB 509, Albany, NY 12201 USA
基金
美国国家科学基金会;
关键词
Drugs; Narcotics; Micropollutants; Wastewater; Freshwater; Illicit drugs; SOLID-PHASE EXTRACTION; MULTI-RESIDUE DETERMINATION; HYDROXYBENZOIC ACID-ESTERS; A DIGLYCIDYL ETHERS; ILLICIT DRUGS; HUMAN URINE; PSYCHOACTIVE PHARMACEUTICALS; EMERGING CONTAMINANTS; TREATMENT PLANTS; LIQUID;
D O I
10.1007/s00216-017-0561-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A liquid chromatography-triple quadrupole-tandem mass spectrometry (LC-qQq-MS/MS) method was developed for simultaneous determination of 89 legal neuropsychiatric pharmaceuticals and illicit drugs (both parent compounds and metabolites) and other micropollutants in unfiltered wastewater and freshwater. The target chemicals fall under the classes of amphetamine-type stimulants, cocaine compounds, opiates and opioids, benzodiazepines, lysergic compounds, antipsychotics, anesthetics, antiepileptics, antidepressants, sympathomimetics, cannabinoids, blood thinners, antihistamines, beta-blockers, caffeine derivatives, nicotine derivatives, z-drugs, new designer drugs, and Alzheimer medications. The sample preparation procedure was designed for unfiltered wastewater and freshwater without the need to separate the particulate matter (if any) from the aqueous phase prior to extraction. Samples were pre-concentrated by rotary evaporation in the presence of a solvent. Method precision (absolute values; N = 6 replicate analyses at the fortification level of 50 ng, k = 6 days) for 87 out of 89 target analytes ranged from 2.8 to 34% (RSD %). The limits of detection ranged from 0.11 to 202 ng L-1, and the matrix effects ranged from +16 to -84%. A total of 10 samples, 8 wastewater, 1 drinking water, and 1 lake water, were collected from New York State, USA, and were analyzed for the target compounds to demonstrate the applicability of the developed method. This is the first study to report the analysis of multiple classes of pharmaceuticals, illicit drugs, and other micropollutants in unfiltered wastewater.
引用
收藏
页码:6205 / 6225
页数:21
相关论文
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