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Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute

Bioengineered autologous skin substitutes (BASS) technology is an emerging field for skin burn therapy. However, further studies on BASS characterization, viability against standard procedures for wound healing, and protocol optimization are necessary for the improvement of BASS technology for clini...

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Autores principales: García-Valdivia, Marta, Quiñones-Vico, María I., Ortega-Llamas, Laura, Fernández-González, Ana, Ubago-Rodríguez, Ana, Sanabria-de la Torre, Raquel, Arias-Santiago, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220084/
https://www.ncbi.nlm.nih.gov/pubmed/35740473
http://dx.doi.org/10.3390/biomedicines10061453
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author García-Valdivia, Marta
Quiñones-Vico, María I.
Ortega-Llamas, Laura
Fernández-González, Ana
Ubago-Rodríguez, Ana
Sanabria-de la Torre, Raquel
Arias-Santiago, Salvador
author_facet García-Valdivia, Marta
Quiñones-Vico, María I.
Ortega-Llamas, Laura
Fernández-González, Ana
Ubago-Rodríguez, Ana
Sanabria-de la Torre, Raquel
Arias-Santiago, Salvador
author_sort García-Valdivia, Marta
collection PubMed
description Bioengineered autologous skin substitutes (BASS) technology is an emerging field for skin burn therapy. However, further studies on BASS characterization, viability against standard procedures for wound healing, and protocol optimization are necessary for the improvement of BASS technology for clinical use. The aim of this study is to evaluate the effect of common antiseptics for clinical use in BASS, focusing on cell viability, inflammatory cytokine pattern, and epithelium and skin barrier integrity, in order to establish the most adequate treatment for wound care after BASS grafting. Human keratinocytes (hKT) and dermal fibroblasts (hDF) were isolated from foreskin samples and integrated into hyaluronic acid-based BASS. The following antiseptics were applied every 48 h: ethanol (70%), chlorhexidine digluconate (1%), sodium hypochlorite (0.02%), povidone iodine (100 mg/mL), and polyhexanide (0.1%), during a follow-up of 16 days. Sodium hypochlorite was the only treatment that showed a high cell viability percentage throughout the evaluation time compared to other antiseptic treatments, as well as a similar cytokine secretion pattern as control BASS. No significant differences were found regarding epidermal barrier function. These findings point towards sodium hypochlorite being the least aggressive antiseptic treatment for BASS post-transplantation wound care.
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spelling pubmed-92200842022-06-24 Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute García-Valdivia, Marta Quiñones-Vico, María I. Ortega-Llamas, Laura Fernández-González, Ana Ubago-Rodríguez, Ana Sanabria-de la Torre, Raquel Arias-Santiago, Salvador Biomedicines Article Bioengineered autologous skin substitutes (BASS) technology is an emerging field for skin burn therapy. However, further studies on BASS characterization, viability against standard procedures for wound healing, and protocol optimization are necessary for the improvement of BASS technology for clinical use. The aim of this study is to evaluate the effect of common antiseptics for clinical use in BASS, focusing on cell viability, inflammatory cytokine pattern, and epithelium and skin barrier integrity, in order to establish the most adequate treatment for wound care after BASS grafting. Human keratinocytes (hKT) and dermal fibroblasts (hDF) were isolated from foreskin samples and integrated into hyaluronic acid-based BASS. The following antiseptics were applied every 48 h: ethanol (70%), chlorhexidine digluconate (1%), sodium hypochlorite (0.02%), povidone iodine (100 mg/mL), and polyhexanide (0.1%), during a follow-up of 16 days. Sodium hypochlorite was the only treatment that showed a high cell viability percentage throughout the evaluation time compared to other antiseptic treatments, as well as a similar cytokine secretion pattern as control BASS. No significant differences were found regarding epidermal barrier function. These findings point towards sodium hypochlorite being the least aggressive antiseptic treatment for BASS post-transplantation wound care. MDPI 2022-06-19 /pmc/articles/PMC9220084/ /pubmed/35740473 http://dx.doi.org/10.3390/biomedicines10061453 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 Article
García-Valdivia, Marta
Quiñones-Vico, María I.
Ortega-Llamas, Laura
Fernández-González, Ana
Ubago-Rodríguez, Ana
Sanabria-de la Torre, Raquel
Arias-Santiago, Salvador
Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute
title Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute
title_full Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute
title_fullStr Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute
title_full_unstemmed Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute
title_short Cytotoxicity, Epidermal Barrier Function and Cytokine Evaluation after Antiseptic Treatment in Bioengineered Autologous Skin Substitute
title_sort cytotoxicity, epidermal barrier function and cytokine evaluation after antiseptic treatment in bioengineered autologous skin substitute
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220084/
https://www.ncbi.nlm.nih.gov/pubmed/35740473
http://dx.doi.org/10.3390/biomedicines10061453
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