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Design and evaluation of a skin-on-a-chip pumpless microfluidic device
The development of microfluidic culture technology facilitates the progress of study of cell and tissue biology. This technology expands the understanding of pathological and physiological changes. A skin chip, as in vitro model, consisting of normal skin tissue with epidermis and dermis layer (full...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232512/ https://www.ncbi.nlm.nih.gov/pubmed/37258538 http://dx.doi.org/10.1038/s41598-023-34796-3 |
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author | Mohamadali, Marjan Ghiaseddin, Ali Irani, Shiva Amirkhani, Mohammad Amir Dahmardehei, Mostafa |
author_facet | Mohamadali, Marjan Ghiaseddin, Ali Irani, Shiva Amirkhani, Mohammad Amir Dahmardehei, Mostafa |
author_sort | Mohamadali, Marjan |
collection | PubMed |
description | The development of microfluidic culture technology facilitates the progress of study of cell and tissue biology. This technology expands the understanding of pathological and physiological changes. A skin chip, as in vitro model, consisting of normal skin tissue with epidermis and dermis layer (full thickness) was developed. Polydimethylsiloxane microchannels with a fed-batched controlled perfusion feeding system were used to create a full-thick ex-vivo human skin on-chip model. The design of a novel skin-on-a-chip model was reported, in which the microchannel structures mimic the architecture of the realistic vascular network as nutrients transporter to the skin layers. Viabilities of full-thick skin samples cultured on the microbioreactor and traditional tissue culture plate revealed that a precise controlled condition provided by the microfluidic enhanced tissue viability at least for seven days. Several advantages in skin sample features under micro-scale-controlled conditions were found such as skin mechanical strength, water adsorption, skin morphology, gene expression, and biopsy longevity. This model can provide an in vitro environment for localizing drug delivery and transdermal drug diffusion studies. The skin on the chip can be a valuable in vitro model for representing the interaction between drugs and skin tissue and a realistic platform for evaluating skin reaction to pharmaceutical materials and cosmetic products. |
format | Online Article Text |
id | pubmed-10232512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102325122023-06-02 Design and evaluation of a skin-on-a-chip pumpless microfluidic device Mohamadali, Marjan Ghiaseddin, Ali Irani, Shiva Amirkhani, Mohammad Amir Dahmardehei, Mostafa Sci Rep Article The development of microfluidic culture technology facilitates the progress of study of cell and tissue biology. This technology expands the understanding of pathological and physiological changes. A skin chip, as in vitro model, consisting of normal skin tissue with epidermis and dermis layer (full thickness) was developed. Polydimethylsiloxane microchannels with a fed-batched controlled perfusion feeding system were used to create a full-thick ex-vivo human skin on-chip model. The design of a novel skin-on-a-chip model was reported, in which the microchannel structures mimic the architecture of the realistic vascular network as nutrients transporter to the skin layers. Viabilities of full-thick skin samples cultured on the microbioreactor and traditional tissue culture plate revealed that a precise controlled condition provided by the microfluidic enhanced tissue viability at least for seven days. Several advantages in skin sample features under micro-scale-controlled conditions were found such as skin mechanical strength, water adsorption, skin morphology, gene expression, and biopsy longevity. This model can provide an in vitro environment for localizing drug delivery and transdermal drug diffusion studies. The skin on the chip can be a valuable in vitro model for representing the interaction between drugs and skin tissue and a realistic platform for evaluating skin reaction to pharmaceutical materials and cosmetic products. Nature Publishing Group UK 2023-05-31 /pmc/articles/PMC10232512/ /pubmed/37258538 http://dx.doi.org/10.1038/s41598-023-34796-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mohamadali, Marjan Ghiaseddin, Ali Irani, Shiva Amirkhani, Mohammad Amir Dahmardehei, Mostafa Design and evaluation of a skin-on-a-chip pumpless microfluidic device |
title | Design and evaluation of a skin-on-a-chip pumpless microfluidic device |
title_full | Design and evaluation of a skin-on-a-chip pumpless microfluidic device |
title_fullStr | Design and evaluation of a skin-on-a-chip pumpless microfluidic device |
title_full_unstemmed | Design and evaluation of a skin-on-a-chip pumpless microfluidic device |
title_short | Design and evaluation of a skin-on-a-chip pumpless microfluidic device |
title_sort | design and evaluation of a skin-on-a-chip pumpless microfluidic device |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232512/ https://www.ncbi.nlm.nih.gov/pubmed/37258538 http://dx.doi.org/10.1038/s41598-023-34796-3 |
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