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Published in

SAGE Publications, European Journal of Mass Spectrometry, 6(26), p. 400-408, 2020

DOI: 10.1177/1469066720973412

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UV-visible photodegradation of naproxen in water – Structural elucidation of photoproducts and potential toxicity

Journal article published in 2020 by Noemi Cazzaniga, Zsuzsanna Varga, Edith Nicol ORCID, Stéphane Bouchonnet ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The UV-visible photodegradation of Naproxen (6-methoxy-α-methyl-2-naphthaleneacetic acid, CAS: 22204-53-1), one of the most used and detected non-steroidal anti-inflammatory drugs (NSAIDs) in the world, and its ecotoxicological consequences were investigated in an aqueous medium. The photo-transformation products were analyzed and the structures of photoproducts were elucidated using gas chromatography coupled with tandem mass spectrometry (GC-MS/MS) and high-performance liquid chromatography coupled with ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry (LC-FTICR-MS). Seven photoproducts were detected and characterized, photo-transformation mechanisms have been postulated to rationalize their formation under irradiation. In silico Q.S.A.R. (Quantitative Structure-Activity Relationship) toxicity predictions were performed with the Toxicity Estimation Software Tool (T.E.S.T.) and in vitro assays were carried out on Vibrio fischeri bacteria. Some of the obtained photoproducts exhibit higher potential toxicity than Naproxen itself but the whole toxicity of the irradiated solution is not of major concern.