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Toxicol Appl Pharmacol. 2013 Oct 15;272(2):529-41. doi: 10.1016/j.taap.2013.07.003. Epub 2013 Jul 19.

An epidermal equivalent assay for identification and ranking potency of contact sensitizers.

Author information

1
Department of Dermatology, VU University Medical Centre, Dept of Oral Cell Biology, ACTA, Amsterdam, The Netherlands. Electronic address: S.Gibbs@VUMC.nl.

Abstract

The purpose of this study was to explore the possibility of combining the epidermal equivalent (EE) potency assay with the assay which assesses release of interleukin-18 (IL-18) to provide a single test for identification and classification of skin sensitizing chemicals, including chemicals of low water solubility or stability. A protocol was developed using different 3D-epidermal models including in house VUMC model, epiCS® (previously EST1000™), MatTek EpiDerm™ and SkinEthic™ RHE and also the impact of different vehicles (acetone:olive oil 4:1, 1% DMSO, ethanol, water) was investigated. Following topical exposure for 24h to 17 contact allergens and 13 non-sensitizers a robust increase in IL-18 release was observed only after exposure to contact allergens. A putative prediction model is proposed from data obtained from two laboratories yielding 95% accuracy. Correlating the in vitro EE sensitizer potency data, which assesses the chemical concentration which results in 50% cytotoxicity (EE-EC50) with human and animal data showed a superior correlation with human DSA05 (μg/cm(2)) data (Spearman r=0.8500; P value (two-tailed)=0.0061) compared to LLNA data (Spearman r=0.5968; P value (two-tailed)=0.0542). DSA05=induction dose per skin area that produces a positive response in 5% of the tested population Also a good correlation was observed for release of IL-18 (SI-2) into culture supernatants with human DSA05 data (Spearman r=0.8333; P value (two-tailed)=0.0154). This easily transferable human in vitro assay appears to be very promising, but additional testing of a larger chemical set with the different EE models is required to fully evaluate the utility of this assay and to establish a definitive prediction model.

KEYWORDS:

2-mercaptobenzothiazole; 4-nitrobenzyl bromide; C-OH; CA; DMF; DMSO; DNCB; DSA(05) (μg/cm(2)); DiSFeB; Dipartimento di Scienze Farmacologiche e Biomolecolari; EE; EUG; Epidermal equivalent; GLC; GXL; HBA; IL-18; In vitro; Irritant; LAC; MBT; NBB; PHL; PPD; Potency; RES; SDS; Sensitizer; VU University Medical Centre; VUMC; cinnamaldehyde; cinnamic alcohol; dimethylformamide; dimethylsulfoxide; dinitrochlorobenzene; epidermal equivalent; eugenol; glycerol; glyoxal; hydroxybenzoic acid; induction dose per skin area (DSA) that produces a positive response in 5% of the tested population; interleukin-18; lactic acid; p-phenylendiamine; phenol; resorcinol; sodium dodecyl sulphate

PMID:
23876969
DOI:
10.1016/j.taap.2013.07.003
[Indexed for MEDLINE]
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