Development and Evaluation of a Human Skin Equivalent in a Semiautomatic Microfluidic Diffusion Chamber.

3D printed device electrospun mesh microfluidic diffusion chamber skin equivalent transepithelial transport kinetic

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
20 Jun 2021
Historique:
received: 21 04 2021
revised: 02 06 2021
accepted: 11 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34202971
pii: pharmaceutics13060910
doi: 10.3390/pharmaceutics13060910
pmc: PMC8235028
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Nemzeti Fejlesztési Ügynökség
ID : OTKA-FWF ANN 132225 to AC

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Auteurs

Júlia Tárnoki-Zách (J)

Department of Biological Physics, Eotvos University, 1117 Budapest, Hungary.

Elod Mehes (E)

Department of Biological Physics, Eotvos University, 1117 Budapest, Hungary.

Zsófia Varga-Medveczky (Z)

Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, 1083 Budapest, Hungary.

Dona Greta Isai (DG)

Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.

Nandor Barany (N)

First Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.

Edina Bugyik (E)

First Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.

Zsolt Revesz (Z)

Revesz Plasztika, 1125 Budapest, Hungary.

Sándor Paku (S)

First Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.

Franciska Erdo (F)

Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, 1083 Budapest, Hungary.

Andras Czirok (A)

Department of Biological Physics, Eotvos University, 1117 Budapest, Hungary.
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.

Classifications MeSH