Evaluation of ceramic passive samplers using a mixed-mode strong cation-exchange sorbent to monitor polar contaminants in river water

被引:3
作者
Cliville-Cabre, Pol [1 ]
Lacorte, Silvia [2 ]
Borrull, Francesc [1 ]
Fontanals, Nuria [1 ]
Marce, Rosa Maria [1 ]
机构
[1] Univ Rovira & Virgili, Dept Analyt Chem & Organ Chem, Sescelades Campus,Marcel li Domingo 1, Tarragona 43007, Spain
[2] IDAEA CSIC, Dept Environm Chem, Jordi Girona 18, Barcelona 08034, Spain
关键词
Ceramic passive samplers; Mixed-mode strong cation-exchange sorbent; River water; Therapeutic and illicit drugs; Liquid chromatography-tandem mass; spectrometry; SOLID-PHASE EXTRACTION; PERSONAL CARE PRODUCTS; ILLICIT DRUGS; SURFACE-WATER; WASTE-WATER; ORGANIC-COMPOUNDS; EMERGING CONTAMINANTS; IN-SITU; PHARMACEUTICALS; ABUSE;
D O I
10.1016/j.chroma.2023.464348
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Although most of the analytical methods developed for the monitoring of contaminants in environmental waters are based on discrete grab sampling, an alternative of increasing interest is the use of passive sampling. Methods based on passive sampling provide the sampling and pre-concentration of the analytes in-situ, which makes the sample treatment less time consuming and costly than using discrete grab sampling. In this study, ceramic passive samplers (CPSs) using mixed-mode strong cation-exchange sorbent (Oasis MCX) as retention phase were evaluated for the determination of a group of 21 therapeutic and illicit drugs and some of their metabolites in river water samples that were determined by liquid chromatography-tandem mass spectrometry. After assessing the stability of the analytes, the CPSs were calibrated for 9 days with bottled water and river water, obtaining, for the 19 stable compounds, sample rates (Rs) ranging between 0.180 and 1.767 mL/day and diffusion coefficients (De) between 2.02E-8 and 2.81E-7 cm2/s. Once calibrated, CPSs were deployed for the determination of contaminants in the Ebre River, with good reproducibility, and some of the analytes were determined, including amongst others, gabapentin at 76 ng/L, caffeine at 203 ng/L or diclofenac amine at 57 ng/L. The passive sampling method herein presented is simple and feasible and allows the time-integrated analysis of pharmaceuticals and drugs at trace levels in river water. This study opens the possibility of using other mixed-mode sorbents or other types of sorbents as retaining phase on CPSs for the determination of very polar contaminants in water.
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页数:7
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