The kinetic direct peptide reactivity assay (kDPRA): Intra- and inter-laboratory reproducibility in a seven-laboratory ring trial
Language English Country Germany Media print-electronic
Document type Journal Article
- Keywords
- GHS sub-classification, alternative methods, peptide reactivity, predictivity, risk assessment, skin sensitization,
- MeSH
- Animal Testing Alternatives methods MeSH
- Biological Assay methods MeSH
- Kinetics MeSH
- Skin Diseases chemically induced MeSH
- Laboratories standards MeSH
- Humans MeSH
- Reproducibility of Results MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
While the skin sensitization hazard of substances can be identified using non-animal methods, the classification of potency into UN GHS sub-categories 1A and 1B remains challenging. The kinetic direct peptide reactivity assay (kDPRA) is a modification of the DPRA wherein the reaction kinetics of a test substance towards a synthetic cysteine-containing peptide are evaluated. For this purpose, several concentrations of the test substance are incubated with the synthetic peptide for several incubation times. The reaction is stopped by addition of monobromobimane, which forms a fluorescent complex with the free cysteine of the model peptide. The relative remaining non-depleted amount of peptide is determined. Kinetic rate constants are derived from the depletion vs concentration and time matrix and used to distinguish between UN GHS sub-category 1A sensitizers and test substances in sub-category 1B/not classified test substances. In this study, we present a ring trial of the kDPRA with 24 blind-coded test substances in seven laboratories. The intra- and inter-laboratory reproducibility were 96% and 88%, respectively (both for differentiating GHS Cat 1A sensitizers from GHS Cat 1B/not classified). Following an independent peer review, the kDPRA was considered to be acceptable for the identification of GHS Cat 1A skin sensitizers. Besides GHS Cat 1A identification, the kDPRA can be used as part of a defined approach(es) with a quantitative data integration procedure for skin sensitization potency assessment. For this aim, next to reproducibility of classification, the quantitative reproducibility and variability of the rate constants were quantified in this study.
BASF SE Experimental Toxicology and Ecology Ludwigshafen Germany
Charles River Laboratories Den Bosch BV The Netherlands
Givaudan Schweiz AG Kemptthal Switzerland
Institute for In Vitro Sciences Inc Gaithersburg MD USA
L'Oréal Research and Innovation Aulnay sous Bois France
National Institute of Public Health Centre of Toxicology and Health Safety Prague Czech Republic
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