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Validation study for in vitro skin irritation test using reconstructed human skin equivalents constructed by layer-by-layer cell coating technology.

Takami AkagiTomomi YamadaHiromi MiyazakiHiroyuki TaguchiHidefumi IkedaMasakazu KatohSimona MuraPatrick CouvreurPaninee ChetprayoonRawiwan ManiratanachoteHiroaki YoshidaHiroharu AjiroKoji HashimotoTakao AshikagaHajime KojimaMitsuru Akashi
Published in: Journal of applied toxicology : JAT (2023)
The aim of this study is to validate an in vitro skin irritation test (SIT) using three-dimensional reconstructed human epidermal (RhE) skin equivalents prepared by layer-by-layer (LbL) method (LbL-3D Skin) in a series of inter-laboratory studies. The goal of these validation studies is to evaluate the ability of this in vitro test to reliably discriminate skin irritant from non-irritant chemicals, as defined by OECD and UN GHS. This me-too validation study is to assess the within- and between-laboratory reproducibility, as well as the predictive capacity, of the LbL-3D Skin SIT in accordance with performance standards for OECD TG 439. The developed skin model, LbL-3D Skin had a highly differentiated epidermis and dermis, similar to the Validated Reference Methods (VRM) and native human skin. The quality parameters (cell survival in controls, tissue integrity and barrier function) were similar to VRM and in accordance with OECD TG 439. The LbL-3D Skin SIT validation study was performed by three participating laboratories, and consisted of three independent tests using 20 reference chemicals. The results obtained with the LbL-3D Skin demonstrated high within-laboratory and between-laboratory reproducibility, as well as high accuracy for use as a stand-alone assay to distinguish skin irritants from non-irritants. The predictive potency of LbL-3D Skin SIT using total 54 test chemicals were comparable to those in other RhE models in OECD TG 439. The validation study demonstrated that LbL-3D Skin has proven to be a robust and reliable method for predicting skin irritation.
Keyphrases
  • soft tissue
  • wound healing
  • endothelial cells
  • high throughput
  • quality improvement