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Analytical and Bioanalytical Chemistry

, Volume 411, Issue 25, pp 6767–6775 | Cite as

Screening for estrogen active nonylphenols in surface waters by planar solid phase extraction–planar yeast estrogen screen

  • Dinah Schick
  • Claudia OelligEmail author
Research Paper
  • 79 Downloads

Abstract

Nonylphenols (NP) are ubiquitous in the environment and show toxic effects and estrogenic activity. According to the corresponding framework directive in the field of water quality, isomers of NP (including 4-n-NP and branched 4-NP) are classified as priority hazardous substances and are regulated as a group of chain and ring isomers with a maximum acceptable concentration of 2 μg/L in inland and other surface waters. This study presents a new sensitive and innovative screening approach for estrogen active NP based on high-performance thin-layer chromatography. NP were focused in a single target zone on thin-layer plates by planar solid phase extraction (pSPE) and detected by a planar yeast estrogen screen (pYES) on the basis of their estrogenic activity. The mean limits of detection and quantitation were 14 and 26 ng per zone, respectively. After liquid–liquid extraction of water samples with dichloromethane, the mean recovery was close to 100% (relative standard deviation of 21% or less), and estrogen active NP were detectable down to 1 μg/L. Thus, pSPE–pYES provides both the detection and the quantitation of estrogenic NP in surface waters at the maximum acceptable concentration. Application of the approach on extracts of surface waters showed the use of pSPE–pYES for environmental samples, and no complex and time-consuming clean-up of the extracts was required. Estrogenic NP were not detectable in any of the investigated surface waters by means of the screening approach presented.

Keywords

Nonylphenols Estrogen active compounds Surface waters High-performance thin-layer chromatography Planar solid phase extraction Planar yeast estrogen screen 

Notes

Acknowledgements

The authors thank Merck (Darmstadt, Germany) for support with HPTLC plates and S. Buchinger (German Federal Institute of Hydrology, Koblenz, Germany), for providing the yeast cells. The authors also thank R. Kölling-Paternoga and T. Brune (Department of Yeast Genetics and Fermentation Technology, Institute of Food Science and Biotechnology, University of Hohenheim, Stuttgart, Germany) for preparation and storage of the cryogenic stock and the preparation of the yeast agar plates, and Wilfried Mitschang and Susan Bairaktar for their experimental work for their bachelor theses. Additionally, the authors thank W. Schwack (University of Gießen, Gießen, Germany) for helpful discussions.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no competing interests.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Institute of Food ChemistryUniversity of HohenheimStuttgartGermany

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