Mardal Marie, Kinyua Juliet, Ramin Pedram, Miserez Bram, Van Nuijs Alexander L N, Covaci Adrian, Meyer Markus R
Department of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Saarland University, Homburg, Germany.
Toxicological Center, Department of Pharmaceutical Sciences, University of Antwerp, Antwerp, Belgium.
Drug Test Anal. 2017 Jan;9(1):106-114. doi: 10.1002/dta.1957. Epub 2016 Feb 17.
Monitoring population drug use through wastewater-based epidemiology (WBE) is a useful method to quantitatively follow trends and estimate total drug consumption in communities. Concentrations of drug biomarkers might be low in wastewater due to dilution; and therefore analysis of pooled urine (PU) is useful to detect consumed drugs and identify targets of illicit drugs use. The aims of the study were (1) to screen PU and urinated soil (US) samples collected at festivals for illicit drug excretion products using hyphenated techniques; (2) to develop and validate a hydrophilic interaction liquid chromatography - mass spectrometry / mass spectrometry (HILIC-MS/MS) method of quantifying urinary targets of identified drugs in wastewater; and (3) to conduct a 24 h stability study, using PU and US to better reflect the chemical environment for targets in wastewater. Cocaine (COC) and ecstasy-like compounds were the most frequently detected illicit drugs; an analytical method was developed to quantify their excretion products. Hydroxymethoxymethamphetamine (HMMA), 3,4-methylenedioxymethamphetamine (MDMA), 3,4-methylenedioxyamphetamine (MDA), HMMA sulfate (HMMA-S), benzoylecgonine (BE), and cocaethylene (CE) had 85-102% of initial concentration after 8 h of incubation, whereas COC and ecgonine methyl ester (EME) had 74 and 67% after 8 h, respectively. HMMA showed a net increase during 24 h of incubation (107% ± 27, n = 8), possibly due to the cleavage of HMMA conjugates, and biotransformation of MDMA. The results suggest HMMA as analytical target for MDMA consumption in WBE, due to its stability in wastewater and its excretion as the main phase I metabolite of MDMA. Copyright © 2016 John Wiley & Sons, Ltd.
通过基于污水的流行病学(WBE)监测人群药物使用情况,是一种定量追踪趋势并估算社区药物总消费量的有用方法。由于稀释作用,污水中药物生物标志物的浓度可能较低;因此,分析混合尿液(PU)有助于检测已消费的药物并确定非法药物使用的目标人群。本研究的目的是:(1)使用联用技术筛查在节日期间收集的PU和尿渍土壤(US)样本中的非法药物排泄产物;(2)开发并验证一种亲水作用液相色谱 - 质谱/质谱(HILIC-MS/MS)方法,用于定量污水中已鉴定药物的尿液目标物;(3)使用PU和US进行24小时稳定性研究,以更好地反映污水中目标物的化学环境。可卡因(COC)和摇头丸类化合物是最常检测到的非法药物;开发了一种分析方法来定量其排泄产物。羟甲氧基甲基苯丙胺(HMMA)、3,4-亚甲基二氧基甲基苯丙胺(MDMA)、3,4-亚甲基二氧基苯丙胺(MDA)、硫酸羟甲氧基甲基苯丙胺(HMMA-S)、苯甲酰芽子碱(BE)和可口乙酮(CE)在孵育8小时后,初始浓度保留率为85 - 102%,而COC和芽子碱甲酯(EME)在8小时后的保留率分别为74%和67%。HMMA在孵育24小时期间呈现净增加(107% ± 27,n = 8),这可能是由于HMMA共轭物的裂解以及MDMA的生物转化。结果表明,HMMA可作为WBE中MDMA消费的分析目标物,因为它在污水中具有稳定性,并且作为MDMA的主要I相代谢产物排泄。版权所有© 2016 John Wiley & Sons, Ltd.