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The effect of an autologous cellular gel-matrix integrated implant system on wound healing
BACKGROUND: This manuscript reports the production and preclinical studies to examine the tolerance and efficacy of an autologous cellular gel-matrix integrated implant system (IIS) aimed to treat full-thickness skin lesions. METHODS: The best concentration of fibrinogen and thrombin was experimenta...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907325/ https://www.ncbi.nlm.nih.gov/pubmed/20565787 http://dx.doi.org/10.1186/1479-5876-8-59 |
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author | Weinstein-Oppenheimer, Caroline R Aceituno, Alexis R Brown, Donald I Acevedo, Cristian Ceriani, Ricardo Fuentes, Miguel A Albornoz, Fernando Henríquez-Roldán, Carlos F Morales, Patricio Maclean, Claudio Tapia, Sergio M Young, Manuel E |
author_facet | Weinstein-Oppenheimer, Caroline R Aceituno, Alexis R Brown, Donald I Acevedo, Cristian Ceriani, Ricardo Fuentes, Miguel A Albornoz, Fernando Henríquez-Roldán, Carlos F Morales, Patricio Maclean, Claudio Tapia, Sergio M Young, Manuel E |
author_sort | Weinstein-Oppenheimer, Caroline R |
collection | PubMed |
description | BACKGROUND: This manuscript reports the production and preclinical studies to examine the tolerance and efficacy of an autologous cellular gel-matrix integrated implant system (IIS) aimed to treat full-thickness skin lesions. METHODS: The best concentration of fibrinogen and thrombin was experimentally determined by employing 28 formula ratios of thrombin and fibrinogen and checking clot formation and apparent stability. IIS was formed by integrating skin cells by means of the in situ gelification of fibrin into a porous crosslinked scaffold composed of chitosan, gelatin and hyaluronic acid. The in vitro cell proliferation within the IIS was examined by the MTT assay and PCNA expression. An experimental rabbit model consisting of six circular lesions was utilized to test each of the components of the IIS. Then, the IIS was utilized in an animal model to cover a 35% body surface full thickness lesion. RESULTS: The preclinical assays in rabbits demonstrated that the IIS was well tolerated and also that IIS-treated rabbit with lesions of 35% of their body surface, exhibited a better survival rate (p = 0,06). CONCLUSION: IIS should be further studied as a new wound dressing which shows promising properties, being the most remarkable its good biological tolerance and cell growth promotion properties. |
format | Text |
id | pubmed-2907325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29073252010-07-21 The effect of an autologous cellular gel-matrix integrated implant system on wound healing Weinstein-Oppenheimer, Caroline R Aceituno, Alexis R Brown, Donald I Acevedo, Cristian Ceriani, Ricardo Fuentes, Miguel A Albornoz, Fernando Henríquez-Roldán, Carlos F Morales, Patricio Maclean, Claudio Tapia, Sergio M Young, Manuel E J Transl Med Research BACKGROUND: This manuscript reports the production and preclinical studies to examine the tolerance and efficacy of an autologous cellular gel-matrix integrated implant system (IIS) aimed to treat full-thickness skin lesions. METHODS: The best concentration of fibrinogen and thrombin was experimentally determined by employing 28 formula ratios of thrombin and fibrinogen and checking clot formation and apparent stability. IIS was formed by integrating skin cells by means of the in situ gelification of fibrin into a porous crosslinked scaffold composed of chitosan, gelatin and hyaluronic acid. The in vitro cell proliferation within the IIS was examined by the MTT assay and PCNA expression. An experimental rabbit model consisting of six circular lesions was utilized to test each of the components of the IIS. Then, the IIS was utilized in an animal model to cover a 35% body surface full thickness lesion. RESULTS: The preclinical assays in rabbits demonstrated that the IIS was well tolerated and also that IIS-treated rabbit with lesions of 35% of their body surface, exhibited a better survival rate (p = 0,06). CONCLUSION: IIS should be further studied as a new wound dressing which shows promising properties, being the most remarkable its good biological tolerance and cell growth promotion properties. BioMed Central 2010-06-17 /pmc/articles/PMC2907325/ /pubmed/20565787 http://dx.doi.org/10.1186/1479-5876-8-59 Text en Copyright ©2010 Weinstein-Oppenheimer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Weinstein-Oppenheimer, Caroline R Aceituno, Alexis R Brown, Donald I Acevedo, Cristian Ceriani, Ricardo Fuentes, Miguel A Albornoz, Fernando Henríquez-Roldán, Carlos F Morales, Patricio Maclean, Claudio Tapia, Sergio M Young, Manuel E The effect of an autologous cellular gel-matrix integrated implant system on wound healing |
title | The effect of an autologous cellular gel-matrix integrated implant system on wound healing |
title_full | The effect of an autologous cellular gel-matrix integrated implant system on wound healing |
title_fullStr | The effect of an autologous cellular gel-matrix integrated implant system on wound healing |
title_full_unstemmed | The effect of an autologous cellular gel-matrix integrated implant system on wound healing |
title_short | The effect of an autologous cellular gel-matrix integrated implant system on wound healing |
title_sort | effect of an autologous cellular gel-matrix integrated implant system on wound healing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907325/ https://www.ncbi.nlm.nih.gov/pubmed/20565787 http://dx.doi.org/10.1186/1479-5876-8-59 |
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