4.7 Article

A sensitive, robust method for determining natural and synthetic hormones in surface and wastewaters by continuous solid-phase extraction-gas chromatography-mass spectrometry

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 29, Issue 35, Pages 53619-53632

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-022-19577-1

Keywords

Natural and synthetic hormones; Water; Continuous solid-phase extraction; Microwave-assisted derivatization; Gas chromatography-mass spectrometry

Funding

  1. Consejeria de Economia, Conocimiento, Empresas y Universidad, Regional Government of Andalucia, Spain [PY20181211]
  2. EU FEDER funds
  3. Research Programme of the University of Jaen (Plan 2019-2020)
  4. CRUE-CSIC agreement
  5. Springer Nature

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Steroidal estrogens have become a serious threat to the environment and living organisms. Scientists have developed a sensitive method using continuous solid-phase extraction and gas chromatography-mass spectrometry to detect estrogens at very low concentrations. This method is highly sensitive, accurate, and environmentally friendly.
Over recent decades, steroidal estrogens have become an emerging and very serious issue as they pose a serious threat to living organisms, soil, plants, and water resources in general. Estrogens have therefore been the subject of considerable scientific attention in order to develop new methodologies for its determination, being able of detecting them at very low concentrations. Those procedures minimize or eliminate the consumption of organic solvents and reagents that may be incompatible with the environment. In this respect, we developed a sensitive, selective method for the simultaneous determination of thirteen natural and synthetic hormones present at the nanogram-per-liter level in various types of water by using continuous solid-phase extraction in combination with gas chromatography and mass spectrometry (GC-MS). The target analytes were preferentially sorbed on an Oasis HLB sorbent column (80 mg) and eluted with acetone (600 mu L) for derivatization with a mixture of 70 mu L of N,O-bis(trimethylsilyl) trifluoroacetamide and trimethylchlorosilane and 35 mu L of petroleum ether in a household microwave oven at 200 W for 4 min. Under optimum conditions, the ensuing method exhibited good linearity (r >= 0.998), good precision (RSD <= 7%), high recoveries (92-103%), and low detection limits (0.01-0.3 ng L-1). The method outperforms existing alternatives in robustness, sensitivity, throughput, flexibility-it allows both estrogens, progestogens, and androgens to be determined simultaneously-and compliance with the principles of Green Chemistry. It was successfully used to analyze various types of water samples (mineral, tap, well, pond, swimming pool, river, and waste) that were found to contain four estrogens (estrone, 17 beta-estradiol, 17 alpha-ethinylestradiol, and hexestrol), two progestogens (testosterone, dihydrotestosterone), and one progestogen (progesterone) at concentrations ranging from 3.0 to 110 ng L-1.

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