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Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies
Preclinical research remains hampered by an inadequate representation of human tissue environments which results in inaccurate predictions of a drug candidate’s effects and target’s suitability. While human 2D and 3D cell cultures and organoids have been extensively improved to mimic the precise str...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316928/ https://www.ncbi.nlm.nih.gov/pubmed/35890312 http://dx.doi.org/10.3390/pharmaceutics14071417 |
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author | Fernandez-Carro, Estibaliz Angenent, Maricke Gracia-Cazaña, Tamara Gilaberte, Yolanda Alcaine, Clara Ciriza, Jesús |
author_facet | Fernandez-Carro, Estibaliz Angenent, Maricke Gracia-Cazaña, Tamara Gilaberte, Yolanda Alcaine, Clara Ciriza, Jesús |
author_sort | Fernandez-Carro, Estibaliz |
collection | PubMed |
description | Preclinical research remains hampered by an inadequate representation of human tissue environments which results in inaccurate predictions of a drug candidate’s effects and target’s suitability. While human 2D and 3D cell cultures and organoids have been extensively improved to mimic the precise structure and function of human tissues, major challenges persist since only few of these models adequately represent the complexity of human tissues. The development of skin-on-chip technology has allowed the transition from static 3D cultures to dynamic 3D cultures resembling human physiology. The integration of vasculature, immune system, or the resident microbiome in the next generation of SoC, with continuous detection of changes in metabolism, would potentially overcome the current limitations, providing reliable and robust results and mimicking the complex human skin. This review aims to provide an overview of the biological skin constituents and mechanical requirements that should be incorporated in a human skin-on-chip, permitting pharmacological, toxicological, and cosmetic tests closer to reality. |
format | Online Article Text |
id | pubmed-9316928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93169282022-07-27 Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies Fernandez-Carro, Estibaliz Angenent, Maricke Gracia-Cazaña, Tamara Gilaberte, Yolanda Alcaine, Clara Ciriza, Jesús Pharmaceutics Review Preclinical research remains hampered by an inadequate representation of human tissue environments which results in inaccurate predictions of a drug candidate’s effects and target’s suitability. While human 2D and 3D cell cultures and organoids have been extensively improved to mimic the precise structure and function of human tissues, major challenges persist since only few of these models adequately represent the complexity of human tissues. The development of skin-on-chip technology has allowed the transition from static 3D cultures to dynamic 3D cultures resembling human physiology. The integration of vasculature, immune system, or the resident microbiome in the next generation of SoC, with continuous detection of changes in metabolism, would potentially overcome the current limitations, providing reliable and robust results and mimicking the complex human skin. This review aims to provide an overview of the biological skin constituents and mechanical requirements that should be incorporated in a human skin-on-chip, permitting pharmacological, toxicological, and cosmetic tests closer to reality. MDPI 2022-07-06 /pmc/articles/PMC9316928/ /pubmed/35890312 http://dx.doi.org/10.3390/pharmaceutics14071417 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Fernandez-Carro, Estibaliz Angenent, Maricke Gracia-Cazaña, Tamara Gilaberte, Yolanda Alcaine, Clara Ciriza, Jesús Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies |
title | Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies |
title_full | Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies |
title_fullStr | Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies |
title_full_unstemmed | Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies |
title_short | Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies |
title_sort | modeling an optimal 3d skin-on-chip within microfluidic devices for pharmacological studies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316928/ https://www.ncbi.nlm.nih.gov/pubmed/35890312 http://dx.doi.org/10.3390/pharmaceutics14071417 |
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