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Catch-up validation study of an in vitro skin irritation test method based on an open source reconstructed epidermis (phase I).

Zugehörigkeit
Henkel AG & Co. KGaA, Henkelstr. 67, 40589 Düsseldorf, Germany. Electronic address: karsten.mewes@henkel.com.
Mewes, K. R.;
Zugehörigkeit
Henkel AG & Co. KGaA, Henkelstr. 67, 40589 Düsseldorf, Germany.
Fischer, A.;
Zugehörigkeit
Goethe-University, Medical School, Department of Dermatology, Venereology and Allergology, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Zöller, N. N.;
Zugehörigkeit
Goethe-University, Medical School, Department of Dermatology, Venereology and Allergology, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Laubach, V.;
Zugehörigkeit
Goethe-University, Medical School, Department of Dermatology, Venereology and Allergology, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Bernd, A.;
Zugehörigkeit
VITO NV Flemish Institute for Technological Research, Environmental Risk and Health Unit, Boeretang 200, 2400 Mol, Belgium.
Jacobs, A.;
Zugehörigkeit
VITO NV Flemish Institute for Technological Research, Environmental Risk and Health Unit, Boeretang 200, 2400 Mol, Belgium.
van Rompay, A.;
Zugehörigkeit
Bundesinstitut für Risikobewertung (BfR), Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.
Liebsch, Manfred;
Zugehörigkeit
Bundesinstitut für Risikobewertung (BfR), Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.
Pirow, Ralph;
Zugehörigkeit
Henkel AG & Co. KGaA, Henkelstr. 67, 40589 Düsseldorf, Germany.
Petersohn, D.

We have developed a new in vitro skin irritation test based on an open source reconstructed epidermis (OS-REp) with openly accessible protocols for tissue production and test performance. Due to structural, mechanistic and procedural similarity, a blinded catch-up validation study for skin irritation according to OECD Performance Standards (PS) was conducted in three laboratories to promote regulatory acceptance, with OS-REp models produced at a single production site only. While overall sensitivity and predictive capacity met the PS requirements, overall specificity was only 57%. A thorough analysis of the test results led to the assumption that some of the false-positive classifications could have been evoked by volatile skin-irritating chemicals tested in the same culture plate as the non-irritants falsely predicted as irritants. With GC/MS and biological approaches the cross-contamination effect was confirmed and the experimental set-up adapted accordingly. Retesting of the affected chemicals with the improved experimental set-up and otherwise identical protocol resulted in correct classifications as non-irritants. Taking these re-test results into account, 93% overall sensitivity, 70% specificity and 82% accuracy was achieved, which is in accordance with the OECD PS. A sufficient reliability of the method was indicated by a within-laboratory-reproducibility of 85-95% and a between-laboratory-reproducibility of 90%.

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