Analysis of Environmental Protection Agency priority endocrine disruptor hormones and bisphenol A in tap, surface and wastewater by online concentration liquid chromatography tandem mass spectrometry

被引:59
作者
Goeury, Ken [1 ,2 ]
Duy, Sung Vo [1 ]
Munoz, Gabriel [1 ]
Prevost, Michele [2 ]
Sauve, Sebastien [1 ]
机构
[1] Univ Montreal, Dept Chem, Montreal, PQ, Canada
[2] Ecole Polytech Montreal, Dept Civil Geol & Min Engn, Montreal, PQ, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
US EPA-priority hormones and bisphenol A; Large volume on-line solid phase extraction; UHPLC-MS/MS; Drinking water; surface water; and wastewater; Method validation and quality control; Matrix effects; SOLID-PHASE EXTRACTION; SEWAGE-TREATMENT PLANTS; PERSONAL CARE PRODUCTS; STEROID SEX-HORMONES; EMERGING CONTAMINANTS; SYNTHETIC ESTROGENS; RIVER-BASIN; PHARMACEUTICALS; FATE; DERIVATIZATION;
D O I
10.1016/j.chroma.2019.01.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The list of endocrine disrupting compounds (EDCs) defined under U.S. EPA Method 539 was recently expanded to include additional hormones and bisphenol A (BPA). Here, we validated a fast and robust alternative method compliant with Method 539.1 requirements in diverse water matrixes (i.e., ultra-pure water, tap water, surface water, and wastewater influent and effluent). Automated large volume injection solid phase extraction (SPE) coupled on-line to ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) was investigated for this purpose. The surveyed molecules included 13 EPA-priority hormones (testosterone, progesterone, medroxyprogesterone, levonorgestrel, norethindrone, androstenedione, estrone, beta-estradiol, alpha-estradiol, equilin, equilenin, ethinylestradiol, estriol) and BPA. Combinations of ionization source and mobile phases were optimized for improved sensitivity. Suitable chromatographic performances were obtained and the implementation of an on-line SPE washing step consecutive to sample loading was investigated. On-line SPE extraction efficiencies in acceptable ranges (64-79%) and detection limits in the order of nanogram per liter or sub-nanogram per liter were obtained. The linearity range extended over 2-3 orders of magnitude, with determination coefficients (R-2) typically > 0.9980. Robust precision and trueness complying with acceptance criteria (70-130%) were obtained for the scope of analytes/matrix combinations. Limited internal standard variations were also observed across samples (+/- 18%), well within the +/- 50% acceptance criterion. The method was successfully applied to field-collected samples in Canada and summed EDC concentrations were reported in the range of 0.80-2.8 ng L-1, 6.8-19 ng L-1, 260-790 ng L-1, and 37-360 ng L(-1)in tap water, surface water, effluent and influent wastewater samples, respectively. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 98
页数:12
相关论文
共 79 条
  • [1] Determination of steroid sex hormones in water and urine matrices by stir bar sorptive extraction and liquid chromatography with diode array detection
    Almeida, C.
    Nogueira, J. M. F.
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 41 (04) : 1303 - 1311
  • [2] Derivatization of ethinylestradiol with dansyl chloride to enhance electrospray ionization: Application in trace analysis of ethinylestradiol in rhesus monkey plasma
    Anari, MR
    Bakhtiar, R
    Zhu, B
    Huskey, S
    Franklin, RB
    Evans, DC
    [J]. ANALYTICAL CHEMISTRY, 2002, 74 (16) : 4136 - 4144
  • [3] Monitoring natural and synthetic estrogens at activated sludge sewage treatment plants and in a receiving river water
    Baronti, C
    Curini, R
    D'Ascenzo, G
    Di Corcia, A
    Gentili, A
    Samperi, R
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (24) : 5059 - 5066
  • [4] Simultaneous Detection of 13 Endocrine Disrupting Chemicals in Water by a Combination of SPE-BSTFA Derivatization and GC-MS in Transboundary Rivers (France-Belgium)
    Ben Sghaier, Rafika
    Net, Sopheak
    Ghorbel-Abid, Ibtissem
    Bessadok, Salma
    Le Coz, Maiwen
    Ben Hassan-Chehimi, Dalila
    Trabelsi-Ayadi, Malika
    Tackx, Michele
    Ouddane, Baghdad
    [J]. WATER AIR AND SOIL POLLUTION, 2017, 228 (01)
  • [5] Standardized Procedure for the Simultaneous Determination of the Matrix Effect, Recovery, Process Efficiency, and Internal Standard Association
    Bienvenu, Jean-Francois
    Provencher, Gilles
    Belanger, Patrick
    Berube, Rene
    Dumas, Pierre
    Gagne, Sehastien
    Gaudreau, Eric
    Fleury, Normand
    [J]. ANALYTICAL CHEMISTRY, 2017, 89 (14) : 7560 - 7568
  • [6] Per- and polyfluoroalkyl substances in source and treated drinking waters of the United States
    Boone, J. Scott
    Vigo, Craig
    Boone, Tripp
    Byrne, Christian
    Ferrario, Joseph
    Benson, Robert
    Donohue, Joyce
    Simmons, Jane Ellen
    Kolpin, Dana W.
    Furlong, Edward T.
    Glassmeyer, Susan T.
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2019, 653 : 359 - 369
  • [7] Treatment of estrogens and androgens in dairy wastewater by a constructed wetland system
    Cai, Kai
    Elliott, Christopher T.
    Phillips, Debra H.
    Scippo, Marie-Louise
    Muller, Marc
    Connolly, Lisa
    [J]. WATER RESEARCH, 2012, 46 (07) : 2333 - 2343
  • [8] Endocrine Disruptors: From Endocrine to Metabolic Disruption
    Casals-Casas, Cristina
    Desvergne, Beatrice
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, VOL 73, 2011, 73 : 135 - 162
  • [9] Development of a sensitive and robust online dual column liquid chromatography-tandem mass spectrometry method for the analysis of natural and synthetic estrogens and their conjugates in river water and wastewater
    Celic, Mira
    Insa, Sara
    Skrbic, Biljana
    Petrovic, Mira
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2017, 409 (23) : 5427 - 5440
  • [10] Fully-automated on-line solid phase extraction coupled to high-performance liquid chromatography-tandem mass spectrometric analysis at sub-ng/L levels of selected estrogens in surface water and wastewater
    Ciofi, L.
    Fibbi, D.
    Chiuminatto, U.
    Coppini, E.
    Checchini, L.
    Del Bubba, M.
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2013, 1283 : 53 - 61