Your browser doesn't support javascript.
loading
Suitability of different reconstructed human skin models in the skin and liver Chip2 microphysiological model to investigate the kinetics and first-pass skin metabolism of the hair dye, 4-amino-2-hydroxytoluene.
Brandmair, Katrin; Tao, Thi-Phuong; Gerlach, Silke; Przibilla, Julia; Schepky, Andreas; Marx, Uwe; Hewitt, Nicola J; Kühnl, Jochen; Maschmeyer, Ilka.
Afiliación
  • Brandmair K; Beiersdorf AG, Unnastraße 48, D-20253, Hamburg, Germany.
  • Tao TP; TissUse GmbH, Oudenarder Str. 16, D-13347, Berlin, Germany.
  • Gerlach S; Beiersdorf AG, Unnastraße 48, D-20253, Hamburg, Germany.
  • Przibilla J; Pharmacelsus GmbH, Science Park 2, D-66123, Saarbrücken, Germany.
  • Schepky A; Beiersdorf AG, Unnastraße 48, D-20253, Hamburg, Germany.
  • Marx U; TissUse GmbH, Oudenarder Str. 16, D-13347, Berlin, Germany.
  • Hewitt NJ; Cosmetics Europe, Avenue Herrmann-Debroux 40, 1160, Auderghem, Belgium.
  • Kühnl J; Beiersdorf AG, Unnastraße 48, D-20253, Hamburg, Germany.
  • Maschmeyer I; TissUse GmbH, Oudenarder Str. 16, D-13347, Berlin, Germany.
J Appl Toxicol ; 44(3): 333-343, 2024 Mar.
Article en En | MEDLINE | ID: mdl-37699698
The HUMIMIC skin-liver Chip2 microphysiological systems model using the epidermal model, EpiDerm™, was reported previously to mimic application route-dependent metabolism of the hair dye, 4-amino-2-hydroxytoluene (AHT). Therefore, we evaluated the use of alternative skin models-SkinEthic™, EpiDermFT™ and PhenionFT™-for the same purpose. In static incubations, AHT permeation was similar using SkinEthic™ and EpiDerm™ models. Older Day 21 (D21) SkinEthic™ models with a thicker stratum corneum did not exhibit a greater barrier to AHT (overall permeation was the same in D17 and D21 models). All epidermal models metabolised AHT, with the EpiDerm™ exhibiting higher N-acetylation than SkinEthic™ models. AHT metabolism by D21 SkinEthic™ models was lower than that by D17 SkinEthic™ and EpiDerm™ models, thus a thicker stratum corneum was associated with fewer viable cells and a lower metabolic activity. AHT permeation was much slower using PhenionFT™ compared to epidermal models and better reflected permeation of AHT through native human skin. This model also extensively metabolised AHT to N-acetyl-AHT. After a single topical or systemic application of AHT to Chip2 model with PhenionFT™, medium was analysed for parent and metabolites over 5 days. The first-pass metabolism of AHT was demonstrated, and the introduction of a wash step after 30 min decreased the exposure to AHT and its metabolites by 33% and 40%-43%, respectively. In conclusion, epidermal and FT skin models used in the Chip2 can mimic the first-pass skin metabolism of AHT. This highlights the flexibility of the Chip2 to incorporate different skin models according to the purpose.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cresoles / Tinturas para el Cabello Límite: Humans Idioma: En Revista: J Appl Toxicol Año: 2024 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cresoles / Tinturas para el Cabello Límite: Humans Idioma: En Revista: J Appl Toxicol Año: 2024 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido