Diastereoselective metabolism of homomenthyl salicylate (homosalate)

  • Homosalate (HMS) is a salicylate UV filter broadly used in sunscreens and personal care products. The aim of this study was the collection of human toxicokinetic data on HMS as a tool for risk assessment. For this purpose, metabolism and urinary excretion after a single oral HMS dose (98.2–149.1 \(\mu\)g (kg body weight)\(^{−1}\)) were investigated in four volunteers (two male, two female). As commercial products generally contain a mixture of \(\it cis-\) and \(\it trans\)-HMS, both \(\it cis-\)rich and \(\it trans\)-rich isomer mixtures were studied to investigate possible differences in metabolism. Initial metabolite screening tentatively identified six oxidative metabolite subgroups, of which hydroxylated and carboxylic acid metabolites were studied in more detail. Unchanged parent HMS and the previously identified HMS metabolites 5-((2-hydroxybenzoyl)oxy)-3,3-dimethylcyclohexane-1-carboxylic acid (HMS-CA) and 3-hydroxy-3,5,5-trimethylcyclohexyl 2-hydroxybenzoate (3OH-HMS), respectively, were quantified separately as \(\it cis-\) and \(\it trans\)-isomers via authentic standards by isotope dilution analysis. In addition, further alkyl-hydroxylated and carboxylic acid metabolites were investigated semi-quantitatively. Peak concentrations in urine were reached 1.5–6.3 h post-dose and more than 80 % of each of the quantitatively investigated metabolites (and at least 70 % of the semi-quantitatively investigated metabolites) was excreted within the first 24 h. Plasma and urine data indicated that oral bioavailability of \(\it cis-\)HMS was one order of magnitude below that of \(\it trans\)-HMS. Furthermore, the mean total urinary excretion fraction (\(F_{ue}\)) for the metabolites derived from \(\it trans\)-HMS (6.4 %) was two orders of magnitude higher than for the metabolites derived from \(\it cis-\)HMS (0.045 %). Our data proves diastereoselectivity in toxicokinetics of \(\it cis-\) and \(\it trans\)-HMS, emphasizing the necessity to address isomer ratios in future studies including HMS exposure and risk assessments.

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Metadaten
Author:Katharina E. EbertORCiDGND, Peter GriemGND, Tobias WeißORCiDGND, Thomas BrüningORCiDGND, Heiko HayenORCiDGND, Holger M. KochORCiDGND, Daniel BuryORCiDGND
URN:urn:nbn:de:hbz:294-103717
DOI:https://doi.org/10.1016/j.envint.2022.107637
Parent Title (English):Environment international
Subtitle (English):identification of relevant human exposure biomarkers
Publisher:Elsevier Science
Place of publication:Amsterdam, Niederlande
Document Type:Article
Language:English
Date of Publication (online):2023/11/10
Date of first Publication:2022/11/17
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:Open Access Fonds
Homosalate; Human biomonitoring; Metabolism; Oral dose; Sunscreen; Ultraviolet filter
Volume:170
Issue:Article 107637
First Page:107637-1
Last Page:107637-14
Note:
Article Processing Charge funded by the Deutsche Forschungsgemeinschaft (DFG) and the Open Access Publication Fund of Ruhr-Universität Bochum.
Institutes/Facilities:Institut für Prävention und Arbeitsmedizin der Deutschen Gesetzlichen Unfallversicherung
Dewey Decimal Classification:Technik, Medizin, angewandte Wissenschaften / Medizin, Gesundheit
open_access (DINI-Set):open_access
Licence (English):License LogoCreative Commons - CC BY-NC-ND 4.0 - Attribution-NonCommercial-NoDerivatives 4.0 International