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Development and Evaluation of a Human Skin Equivalent in a Semiautomatic Microfluidic Diffusion Chamber.
Tárnoki-Zách, Júlia; Mehes, Elod; Varga-Medveczky, Zsófia; Isai, Dona Greta; Barany, Nandor; Bugyik, Edina; Revesz, Zsolt; Paku, Sándor; Erdo, Franciska; Czirok, Andras.
Afiliação
  • Tárnoki-Zách J; Department of Biological Physics, Eotvos University, 1117 Budapest, Hungary.
  • Mehes E; Department of Biological Physics, Eotvos University, 1117 Budapest, Hungary.
  • Varga-Medveczky Z; Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, 1083 Budapest, Hungary.
  • Isai DG; Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
  • Barany N; First Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.
  • Bugyik E; First Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.
  • Revesz Z; Revesz Plasztika, 1125 Budapest, Hungary.
  • Paku S; First Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.
  • Erdo F; Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, 1083 Budapest, Hungary.
  • Czirok A; Department of Biological Physics, Eotvos University, 1117 Budapest, Hungary.
Pharmaceutics ; 13(6)2021 Jun 20.
Article em En | MEDLINE | ID: mdl-34202971
ABSTRACT
There is an increasing demand for transdermal transport measurements to optimize topical drug formulations and to achieve proper penetration profile of cosmetic ingredients. Reflecting ethical concerns the use of both human and animal tissues is becoming more restricted. Therefore, the focus of dermal research is shifting towards in vitro assays. In the current proof-of-concept study a three-layer skin equivalent using human HaCaT keratinocytes, an electrospun polycaprolactone mesh and a collagen-I gel was compared to human excised skin samples. We measured the permeability of the samples for 2% caffeine cream using a miniaturized dynamic diffusion cell ("skin-on-a-chip" microfluidic device). Caffeine delivery exhibits similar transport kinetics through the artificial skin and the human tissue after a rapid rise, a long-lasting high concentration steady state develops. This is markedly distinct from the kinetics measured when using cell-free constructs, where a shorter release was observable. These results imply that both the established skin equivalent and the microfluidic diffusion chamber can serve as a suitable base for further development of more complex tissue substitutes.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article