Baz-Lomba J A, Löve Arndís Sue-Ching, Reid Malcolm J, Ólafsdóttir Kristín, Thomas Kevin V
Norwegian Institute for Water Research, Gaustadalléen 21, NO-0349 Oslo, Norway.
University of Iceland, Department of Pharmacology and Toxicology, Hofsvallagata 53, 107 Reykjavík, Iceland.
J Chromatogr A. 2018 Jan 5;1531:32-38. doi: 10.1016/j.chroma.2017.11.051. Epub 2017 Nov 22.
This article presents a novel approach for the analysis of 13 drugs in wastewater for use in wastewater-based epidemiology (WBE) studies. Sample preparation remains one of the principal bottlenecks in modern high-throughput analysis by ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The proposed methodology is based on the micro-extraction of small volumes (1 ml) of wastewater using a HLB 96-well microplate and both large volume injection (LVI) and post-loop mixing injection (PLM). With this configuration, the limits of quantification (LOQ) were below the reported environmental concentrations of the target compounds in wastewater. Furthermore, both the complexity of collecting, transporting and storing the wastewater sample, sample preparation time, cost and amount of solvent used are all diminished, enhancing the suitability of this methodology for future WBE studies. A new workflow is also proposed in order to create a virtual specimen library bank for WBE by using high-resolution mass spectrometry (HRMS). The method was validated and the limits of quantification were between 0.2 and 6.3 ng L. The relative standard deviations (RSD) for a standard mixture at 200 ng L (n = 6) was between 3.4 and 14.4% while the recoveries for the 13 drug target residues (DTR) were between 92 and 110%. The developed and validated method was finally successfully applied to 10 wastewater samples collected from Oslo, Norway.
本文提出了一种用于分析废水中13种药物的新方法,可用于基于废水的流行病学(WBE)研究。在通过超高效液相色谱-串联质谱(UHPLC-MS/MS)进行的现代高通量分析中,样品制备仍然是主要瓶颈之一。所提出的方法基于使用HLB 96孔微孔板对小体积(1毫升)废水进行微萃取,并结合大体积进样(LVI)和环后混合进样(PLM)。采用这种配置,定量限(LOQ)低于报道的废水中目标化合物的环境浓度。此外,废水样品的采集、运输和储存的复杂性、样品制备时间、成本以及所用溶剂量均有所降低,提高了该方法对未来WBE研究的适用性。还提出了一种新的工作流程,以便通过使用高分辨率质谱(HRMS)为WBE创建一个虚拟标本库。该方法经过验证,定量限在0.2至6.3纳克/升之间。200纳克/升标准混合物(n = 6)的相对标准偏差(RSD)在3.4%至14.4%之间,而13种药物目标残留物(DTR)的回收率在92%至110%之间。最终,所开发并经验证的方法成功应用于从挪威奥斯陆采集的10个废水样品。