Determination of endocrine-disrupting compounds in drinking waters by fast liquid chromatography-tandemmass spectrometry

被引:38
作者
Magi, Emanuele [1 ]
Scapolla, Carlo [1 ]
Di Carro, Marina [1 ]
Liscio, Camilla [1 ]
机构
[1] Univ Genoa, Dept Chem & Ind Chem, I-16146 Genoa, Italy
来源
JOURNAL OF MASS SPECTROMETRY | 2010年 / 45卷 / 09期
关键词
endocrine-disrupting compounds; drinking waters; polar organic chemical integrative samplers; liquid chromatography-tandem mass spectrometry; SEWAGE-TREATMENT PLANTS; MASS-SPECTROMETRY; ORGANIC CONTAMINANTS; BISPHENOL-A; ESTROGENS; ALKYLPHENOL; SURFACTANTS; EXTRACTION; CHEMICALS; HORMONES;
D O I
10.1002/jms.1781
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Growing attention has been recently paid to safety of food and drinking water, making necessary the adoption of policies for water sources protection and the development of sensitive and rapid analytical methods to identify micropollutants. Endocrine-disrupting compounds (EDCs) have emerged as a major issue as they alter the functioning of the endocrine system. Since ingestion of EDCs via food is considered the major exposure route, there is a growing interest in understanding EDC fate during drinking water treatment and in monitoring potential contamination of surface waters and groundwaters. In this work, a fast liquid chromatography-electrospray ionization-tandem mass spectrometry method was developed for the determination of 4-n-nonylphenol (NP), bisphenol A (BPA), estrone (E1), 17 beta-estradiol (E2) and 17 alpha-ethinylestradiol (EE2) in drinking waters. In the literature analytical articles seldom provide details regarding fragmentation pathways. In this paper spectra of the five EDCs in negative ESI were interpreted with the support of accurate mass spectra acquired by a quadrupole time-of-flight instrument; fragmentation pathways were also proposed. The chromatographic separation of EDCs was optimized on a Pinnacle DB Biphenylic column with awater-acetonitrile gradient. Quantitative analysis was performed in multiple reaction monitoring (MRM) mode using bisphenol A-d(16) (BPA-d(16)) as internal standard; calibration curves showed good correlation coefficients (0.9989-0.9997). All figures of merit of the method were satisfactory; limits of detection were in the range 0.2-0.4 ng/ml. The method was applied to the determination of the analytes in waters sampled by polar organic chemical integrative samplers in a drinking water treatment plant. Rather low concentration of BPA, NP and E1 were measured in the inlet, while none of the considered EDCs was detected in the outlet. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1003 / 1011
页数:9
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