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Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation
BACKGROUND: Electrostimulation (ES) therapy for wound healing is limited in clinical use due to barriers such as cumbersome equipment and intermittent delivery of therapy. METHODS: We adapted a human skin xenograft model that can be used to directly examine the nanogenerator-driven ES (NG-ES) effect...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454068/ https://www.ncbi.nlm.nih.gov/pubmed/34544434 http://dx.doi.org/10.1186/s12951-021-01036-7 |
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author | Liu, Aiping Long, Yin Li , Jun Gu , Long Karim, Aos Wang, Xudong Gibson, Angela L. F. |
author_facet | Liu, Aiping Long, Yin Li , Jun Gu , Long Karim, Aos Wang, Xudong Gibson, Angela L. F. |
author_sort | Liu, Aiping |
collection | PubMed |
description | BACKGROUND: Electrostimulation (ES) therapy for wound healing is limited in clinical use due to barriers such as cumbersome equipment and intermittent delivery of therapy. METHODS: We adapted a human skin xenograft model that can be used to directly examine the nanogenerator-driven ES (NG-ES) effects on human skin in vivo—an essential translational step toward clinical application of the NG-ES technique for wound healing. RESULTS: We show that NG-ES leads to rapid wound closure with complete restoration of normal skin architecture within 7 days compared to more than 30 days in the literature. NG-ES accelerates the inflammatory phase of wound healing with more rapid resolution of neutrophils and macrophages and enhances wound bed perfusion with more robust neovascularization. CONCLUSION: Our results support the translational evaluation and optimization of the NG-ES technology to deliver convenient, efficient wound healing therapy for use in human wounds. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01036-7. |
format | Online Article Text |
id | pubmed-8454068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84540682021-09-21 Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation Liu, Aiping Long, Yin Li , Jun Gu , Long Karim, Aos Wang, Xudong Gibson, Angela L. F. J Nanobiotechnology Research BACKGROUND: Electrostimulation (ES) therapy for wound healing is limited in clinical use due to barriers such as cumbersome equipment and intermittent delivery of therapy. METHODS: We adapted a human skin xenograft model that can be used to directly examine the nanogenerator-driven ES (NG-ES) effects on human skin in vivo—an essential translational step toward clinical application of the NG-ES technique for wound healing. RESULTS: We show that NG-ES leads to rapid wound closure with complete restoration of normal skin architecture within 7 days compared to more than 30 days in the literature. NG-ES accelerates the inflammatory phase of wound healing with more rapid resolution of neutrophils and macrophages and enhances wound bed perfusion with more robust neovascularization. CONCLUSION: Our results support the translational evaluation and optimization of the NG-ES technology to deliver convenient, efficient wound healing therapy for use in human wounds. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01036-7. BioMed Central 2021-09-20 /pmc/articles/PMC8454068/ /pubmed/34544434 http://dx.doi.org/10.1186/s12951-021-01036-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Aiping Long, Yin Li , Jun Gu , Long Karim, Aos Wang, Xudong Gibson, Angela L. F. Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
title | Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
title_full | Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
title_fullStr | Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
title_full_unstemmed | Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
title_short | Accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
title_sort | accelerated complete human skin architecture restoration after wounding by nanogenerator-driven electrostimulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454068/ https://www.ncbi.nlm.nih.gov/pubmed/34544434 http://dx.doi.org/10.1186/s12951-021-01036-7 |
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