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FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management

Successful treatments for acute and chronic skin wounds remain challenging. The goal of this proof-of-concept study was to assess the technical feasibility and safety of a novel wound treatment solution, FastSkin(®), in a pig model. FastSkin(®) was prepared from skin micrografts patterned in blood u...

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Autores principales: di Summa, Pietro G., Di Marzio, Nicola, Jafari, Paris, Jaconi, Marisa E., Nesic, Dobrila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607178/
https://www.ncbi.nlm.nih.gov/pubmed/37892702
http://dx.doi.org/10.3390/jcm12206564
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author di Summa, Pietro G.
Di Marzio, Nicola
Jafari, Paris
Jaconi, Marisa E.
Nesic, Dobrila
author_facet di Summa, Pietro G.
Di Marzio, Nicola
Jafari, Paris
Jaconi, Marisa E.
Nesic, Dobrila
author_sort di Summa, Pietro G.
collection PubMed
description Successful treatments for acute and chronic skin wounds remain challenging. The goal of this proof-of-concept study was to assess the technical feasibility and safety of a novel wound treatment solution, FastSkin(®), in a pig model. FastSkin(®) was prepared from skin micrografts patterned in blood using acoustic waves. Upon coagulation, the graft was transferred on a silicone sheet and placed on wounds. Six full-thickness wounds were created at the back of two pigs and treated with either FastSkin(®), split-thickness skin graft (positive control), a gauze coverage (negative control, NC1), or blood patterned without micrografts (negative control, NC2). Silicone sheets were removed after 7, 14, and 21 days. Wound healing was monitored for six weeks and evaluated macroscopically for re-epithelialization and morphometrically for residual wound area and wound contraction. Tissue regeneration was assessed with histology after six weeks. Re-epithelialization was faster in wounds covered with FastSkin(®) treatments compared to NC2 and in NC2 compared to NC1. Importantly, an enhanced collagen organization was observed in FastSkin(®) in contrast to NC treatments. In summary, two clinically approved skin wound treatments, namely micrografting and blood clot graft, were successfully merged with sound-induced patterning of micrografts to produce an autologous, simple, and biologically active wound treatment concept.
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spelling pubmed-106071782023-10-28 FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management di Summa, Pietro G. Di Marzio, Nicola Jafari, Paris Jaconi, Marisa E. Nesic, Dobrila J Clin Med Article Successful treatments for acute and chronic skin wounds remain challenging. The goal of this proof-of-concept study was to assess the technical feasibility and safety of a novel wound treatment solution, FastSkin(®), in a pig model. FastSkin(®) was prepared from skin micrografts patterned in blood using acoustic waves. Upon coagulation, the graft was transferred on a silicone sheet and placed on wounds. Six full-thickness wounds were created at the back of two pigs and treated with either FastSkin(®), split-thickness skin graft (positive control), a gauze coverage (negative control, NC1), or blood patterned without micrografts (negative control, NC2). Silicone sheets were removed after 7, 14, and 21 days. Wound healing was monitored for six weeks and evaluated macroscopically for re-epithelialization and morphometrically for residual wound area and wound contraction. Tissue regeneration was assessed with histology after six weeks. Re-epithelialization was faster in wounds covered with FastSkin(®) treatments compared to NC2 and in NC2 compared to NC1. Importantly, an enhanced collagen organization was observed in FastSkin(®) in contrast to NC treatments. In summary, two clinically approved skin wound treatments, namely micrografting and blood clot graft, were successfully merged with sound-induced patterning of micrografts to produce an autologous, simple, and biologically active wound treatment concept. MDPI 2023-10-16 /pmc/articles/PMC10607178/ /pubmed/37892702 http://dx.doi.org/10.3390/jcm12206564 Text en © 2023 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
di Summa, Pietro G.
Di Marzio, Nicola
Jafari, Paris
Jaconi, Marisa E.
Nesic, Dobrila
FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management
title FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management
title_full FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management
title_fullStr FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management
title_full_unstemmed FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management
title_short FastSkin(®) Concept: A Novel Treatment for Complex Acute and Chronic Wound Management
title_sort fastskin(®) concept: a novel treatment for complex acute and chronic wound management
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607178/
https://www.ncbi.nlm.nih.gov/pubmed/37892702
http://dx.doi.org/10.3390/jcm12206564
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