4.6 Article

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

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1591, 期 -, 页码 87-98

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2019.01.016

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

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. NSERC Industrial Chair on Drinking Water at Polytechnique Montreal
  3. Canadian Foundation for Innovation

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据