4.6 Article

Simultaneous determination of estrogenic and androgenic hormones in water by isotope dilution gas chromatography-tandem mass spectrometry

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1218, Issue 12, Pages 1668-1676

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2011.01.068

Keywords

Estrogens; Androgens; Drinking water; Wastewater; Surface water

Funding

  1. Australian Research Council [LP0989365]
  2. Australian Research Council [LP0989365] Funding Source: Australian Research Council

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A rapid gas chromatography-tandem mass spectrometry (GC-MS/MS) analytical method was developed for the simultaneous analysis of 7 estrogenic hormones (17 alpha-estradiol, 17 beta-estradiol, estrone, mestranol, 17 alpha-ethynylestradiol, levonorgestrel, estriol) and 5 androgenic hormones (testosterone, androsterone, etiocholanolone, dihydrotestosterone, androstenedione) in aqueous matrices. This method is unique in its inclusion of all 12 of these estrogens and androgens and is of particular value due to its very short chromatographic run time of 15 min. The use of isotope dilution for all analytes ensures the accurate quantification, accounting for analytical variabilities that may be introduced during sample processing and instrumental analysis. Direct isotopically labelled analogues were used for 8 of the 12 hormones and satisfactory isotope standards were identified for the remaining 4 hormones. Method detection levels (MDLs) were determined to describe analyte concentrations sufficient to provide a signal with 99% certainty of detection. The established MDLs for most analytes were 1-5 ng L-1 in a variety of aqueous matrices. However, slightly higher MDLs were observed for etiocholanolone, androstenedione, testosterone, levonorgestrel and dihydrotestosterone in some aqueous matrices. Sample matrices were observed to have only a minor impact on MDLs and the method validation confirmed satisfactory method stability over intra-day and inter-day analyses of surface water and tertiary treated effluent samples. (C) 2011 Elsevier B.V. All rights reserved.

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