AUTHOR=Henneberger Luise , Huchthausen Julia , König Maria , Menge Alina , Wojtysiak Niklas , Escher Beate I. 

TITLE=Experimental exposure assessment of designed chemical mixtures in cell-based in vitro bioassays

JOURNAL=Frontiers in Environmental Chemistry

VOLUME=3

YEAR=2022

URL=https://www.frontiersin.org/journals/environmental-chemistry/articles/10.3389/fenvc.2022.1018162

DOI=10.3389/fenvc.2022.1018162

ISSN=2673-4486

ABSTRACT=<p>Cell-based bioassays are useful tools for the effect assessment of complex mixtures, but so far exposure assessment has not been performed for mixtures of chemicals. In the present study, cytotoxicity and activation of oxidative stress response were measured for three designed chemical mixtures with up to twelve components. The measurements of biological responses were complemented by concentration measurements using solid-phase microextraction to derive the freely dissolved concentrations of the mixtures (<italic>C</italic><sub>free,mix</sub>). The tested mixtures showed slightly higher cytotoxic effects than predicted by the concentration addition model. Nominal and freely dissolved effect concentrations of the mixtures were very similar (within a factor of 1.5), but nominal concentrations (<italic>C</italic><sub>nom</sub>) and <italic>C</italic><sub>free</sub> of the individual mixture components were only similar for the hydrophilic chemicals (e.g., caffeine, coumarin, lamotrigine). For hydrophobic (e.g., fluoranthene) and acidic chemicals (e.g., diclofenac, naproxen) <italic>C</italic><sub>free</sub> was up to 648 times lower than <italic>C</italic><sub>nom</sub>. Chemicals were dosed in equipotent nominal concentration ratios and therefore contributed equally to the detected effects. Hydrophilic chemicals with low potency dominated <italic>C</italic><sub>nom,mix</sub> (up to 95%) and <italic>C</italic><sub>free,mix</sub> (up to 99%). Several mixture components (e.g., diclofenac, ibuprofen, naproxen and warfarin) showed increasing free fractions with increasing <italic>C</italic><sub>nom,mix</sub> and therefore also a concentration-dependent contribution to <italic>C</italic><sub>free,mix</sub>. Based on the findings of this study, we concluded that <italic>C</italic><sub>nom,mix</sub> will be sufficient for evaluating the toxicity of mixtures that contain chemicals with diverse physicochemical properties at low concentration levels. In contrast, for risk assessment purposes and quantitative <italic>in vitro</italic> to <italic>in vivo</italic> extrapolations, <italic>C</italic><sub>free,mix</sub> is a better parameter because the <italic>in vitro</italic> responses can be related to freely dissolved concentrations in human plasma.</p>