Analysis of real-time mixture cytotoxicity data following repeated exposure using BK/TD models
Creators
- 1. Models for Toxicology and Ecotoxicology Unit, INERIS, Parc Technologique Alata, BP 2, 60550 Verneuil-en-Halatte (France)
- 2. ODESIA Neosciences, Sophia Antipolis, 400 route des chappes, 06903 Sophia Antipolis (France)
- 3. INRA, ToxAlim, 400 route des Chappes, BP, 167 06903 Sophia Antipolis, Cedex (France)
- 4. INRA, UMR 1402 INRA-AgroParisTech Ecosys, 78850 Thiverval Grignon (France)
- 5. AgroParisTech, UMR 1402 INRA-AgroParisTech Ecosys, 78850 Thiverval Grignon (France)
Description
Cosmetic products generally consist of multiple ingredients. Thus, cosmetic risk assessment has to deal with mixture toxicity on a long-term scale which means it has to be assessed in the context of repeated exposure. Given that animal testing has been banned for cosmetics risk assessment, in vitro assays allowing long-term repeated exposure and adapted for in vitro – in vivo extrapolation need to be developed. However, most in vitro tests only assess short-term effects and consider static endpoints which hinder extrapolation to realistic human exposure scenarios where concentration in target organs is varies over time. Thanks to impedance metrics, real-time cell viability monitoring for repeated exposure has become possible. We recently constructed biokinetic/toxicodynamic models (BK/TD) to analyze such data (Teng et al., 2015) for three hepatotoxic cosmetic ingredients: coumarin, isoeugenol and benzophenone-2. In the present study, we aim to apply these models to analyze the dynamics of mixture impedance data using the concepts of concentration addition and independent action. Metabolic interactions between the mixture components were investigated, characterized and implemented in the models, as they impacted the actual cellular exposure. Indeed, cellular metabolism following mixture exposure induced a quick disappearance of the compounds from the exposure system. We showed that isoeugenol substantially decreased the metabolism of benzophenone-2, reducing the disappearance of this compound and enhancing its in vitro toxicity. Apart from this metabolic interaction, no mixtures showed any interaction, and all binary mixtures were successfully modeled by at least one model based on exposure to the individual compounds. - Highlights: • We could predict cell response over repeated exposure to mixtures of cosmetics. • Compounds acted independently on the cells. • Metabolic interactions impacted exposure concentrations to the compounds.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2016.06.018Additional details
Identifiers
- DOI
- 10.1016/j.taap.2016.06.018;
- PII
- S0041-008X(16)30152-1;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 305
- Journal Page Range
- p. 118-126
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49038541
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ABUNDANCE; ANIMALS; BENZOPHENONE; BINARY MIXTURES; CONCENTRATION RATIO; CONSUMER PRODUCTS; COUMARIN; EXTRAPOLATION; HAZARDS; IMPEDANCE; IN VITRO; IN VIVO; LIVER CELLS; METABOLISM; ORGANS; RISK ASSESSMENT; TOXICITY
- Descriptors DEC
- ANIMAL CELLS; ANTICOAGULANTS; BODY; DIMENSIONLESS NUMBERS; DISPERSIONS; DRUGS; ESTERS; HEMATOLOGIC AGENTS; HETEROCYCLIC COMPOUNDS; HETEROCYCLIC OXYGEN COMPOUNDS; KETONES; LACTONES; MATHEMATICAL SOLUTIONS; MIXTURES; NUMERICAL SOLUTION; ORGANIC COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; PYRANS; SOMATIC CELLS
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.