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In Vitro Metabolism of Quaternary Ammonium Compounds and Confirmation in Human Urine by Liquid Chromatography Ion-Mobility High-Resolution Mass Spectrometry.
Belova, Lidia; Musatadi, Mikel; Gys, Celine; Roggeman, Maarten; den Ouden, Fatima; Olivares, Maitane; van Nuijs, Alexander L N; Poma, Giulia; Covaci, Adrian.
Afiliación
  • Belova L; Toxicological Centre, University of Antwerp, Antwerp 2610, Belgium.
  • Musatadi M; Department of Analytical Chemistry, University of the Basque Country (UPV/EHU), Leioa 48940, Spain.
  • Gys C; Research Centre for Experimental Marine Biology and Biotechnology, University of the Basque Country (PiE-UPV/EHU), Plentzia 48620, Spain.
  • Roggeman M; Toxicological Centre, University of Antwerp, Antwerp 2610, Belgium.
  • den Ouden F; Toxicological Centre, University of Antwerp, Antwerp 2610, Belgium.
  • Olivares M; Toxicological Centre, University of Antwerp, Antwerp 2610, Belgium.
  • van Nuijs ALN; Department of Analytical Chemistry, University of the Basque Country (UPV/EHU), Leioa 48940, Spain.
  • Poma G; Research Centre for Experimental Marine Biology and Biotechnology, University of the Basque Country (PiE-UPV/EHU), Plentzia 48620, Spain.
  • Covaci A; Toxicological Centre, University of Antwerp, Antwerp 2610, Belgium.
Environ Sci Technol ; 2024 Sep 12.
Article en En | MEDLINE | ID: mdl-39264360
ABSTRACT
Quaternary ammonium compounds (QACs) are high-production chemicals used as cleaning and disinfecting agents. Due to their ubiquitous presence in the environment and several toxic effects described, human exposure to these chemicals gained increasing attention in recent years. However, very limited data on the biotransformation of QACs is available, hampering exposure assessment. In this study, three QACs (dimethyl dodecyl ammonium, C10-DDAC; benzyldimethyl dodecylammonium, C12-BAC; cetyltrimethylammonium, C16-ATMAC) commonly detected in indoor microenvironments were incubated with human liver microsomes and cytosol (HLM/HLC) simulating Phase I and II metabolism. Thirty-one Phase I metabolites were annotated originating from 19 biotransformation reactions. Four metabolites of C10-DDAC were described for the first time. A detailed assessment of experimental fragmentation spectra allowed to characterize potential oxidation sites. For each annotated metabolite, drift-tube ion-mobility derived collision cross section (DTCCSN2) values were reported, serving as an additional identification parameter and allowing the characterization of changes in DTCCSN2 values following metabolism. Lastly, eight metabolites, including four metabolites of both C12-BAC and C10-DDAC, were confirmed in human urine samples showing high oxidation states through introduction of up to four oxygen atoms. This is the first report of higher oxidized C10-DDAC metabolites in human urine facilitating future biomonitoring studies on QACs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Environ Sci Technol Año: 2024 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Environ Sci Technol Año: 2024 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos