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Validation of the 3D Skin Comet assay using full thickness skin models: Transferability and reproducibility

Author: Reisinger, K. · Blatz, V. · Brinkmann, J. · Downs, T.R. · Fischer, A. · Henkler, F. · Hoffmann, S. · Krul, C. · Liebsch, M. · Luch, A. · Pirow, R. · Reus, A.A. · Schulz, M. · Pfuhler, S.
Source:Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 827, 27-41
Identifier: 787778
doi: doi:10.1016/j.mrgentox.2018.01.003
Keywords: Biology · Comet assay · Dermal exposure · DNA damage · In vitro genotoxicity · Phenion®FT · Skin · 7,12 dimethylbenz[a]anthracene · Aphidicolin · Cadmium chloride · Cyclohexanone · Ethylnitrosourea · Fallic acid propyl ester · Mitomycin · Phthalic acid bis(2 ethylhexyl) ester · Cell isolation · Controlled study · Cytotoxicity test · Genotoxicity assay · Human · Human tissue · Predictive value · Priority journal · Reproducibility · Validation study · Biomedical Innovation · Healthy Living · Life Triskelion BV · RAPID - Risk Analysis for Products in Development TARA - Toxicology and Risk Assessment · ELSS - Earth, Life and Social Sciences


Recently revised OECD Testing Guidelines highlight the importance of considering the first site-of-contact when investigating the genotoxic hazard. Thus far, only in vivo approaches are available to address the dermal route of exposure. The 3D Skin Comet and Reconstructed Skin Micronucleus (RSMN) assays intend to close this gap in the in vitro genotoxicity toolbox by investigating DNA damage after topical application. This represents the most relevant route of exposure for a variety of compounds found in household products, cosmetics, and industrial chemicals. The comet assay methodology is able to detect both chromosomal damage and DNA lesions that may give rise to gene mutations, thereby complementing the RSMN which detects only chromosomal damage. Here, the comet assay was adapted to two reconstructed full thickness human skin models: the EpiDerm™- and Phenion® Full-Thickness Skin Models. First, tissue-specific protocols for the isolation of single cells and the general comet assay were transferred to European and US-American laboratories. After establishment of the assay, the protocol was then further optimized with appropriate cytotoxicity measurements and the use of aphidicolin, a DNA repair inhibitor, to improve the assay's sensitivity. In the first phase of an ongoing validation study eight chemicals were tested in three laboratories each using the Phenion® Full-Thickness Skin Model, informing several validation modules. Ultimately, the 3D Skin Comet assay demonstrated a high predictive capacity and good intra- and inter-laboratory reproducibility with four laboratories reaching a 100% predictivity and the fifth yielding 70%. The data are intended to demonstrate the use of the 3D Skin Comet assay as a new in vitro tool for following up on positive findings from the standard in vitro genotoxicity test battery for dermally applied chemicals, ultimately helping to drive the regulatory acceptance of the assay. To expand the database, the validation will continue by testing an additional 22 chemicals. © 2018 The Authors Chemicals/CAS: 7,12 dimethylbenz[a]anthracene, 57-97-6; aphidicolin, 38966-21-1; cadmium chloride, 10108-64-2; cyclohexanone, 108-94-1; ethylnitrosourea, 759-73-9; eugenol, 97-53-0; gallic acid propyl ester, 121-79-9; mitomycin, 1404-00-8, 50-07-7, 74349-48-7; phthalic acid bis(2 ethylhexyl) ester, 117-81-7