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Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds

Background: Electrospun fibers are widely studied in regenerative medicine for their ability to mimic the extracellular matrix (ECM) and provide mechanical support. In vitro studies indicated that cell adhesion and migration is superior on smooth poly(L-lactic acid) (PLLA) electrospun scaffolds and...

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Autores principales: Ravindran Girija, Aswathy, Strudwick, Xanthe, Balasubramanian, Sivakumar, Palaninathan, Vivekanandan, Nair, Sakthikumar Dasappan, Cowin, Allison J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056316/
https://www.ncbi.nlm.nih.gov/pubmed/36986741
http://dx.doi.org/10.3390/pharmaceutics15030880
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author Ravindran Girija, Aswathy
Strudwick, Xanthe
Balasubramanian, Sivakumar
Palaninathan, Vivekanandan
Nair, Sakthikumar Dasappan
Cowin, Allison J.
author_facet Ravindran Girija, Aswathy
Strudwick, Xanthe
Balasubramanian, Sivakumar
Palaninathan, Vivekanandan
Nair, Sakthikumar Dasappan
Cowin, Allison J.
author_sort Ravindran Girija, Aswathy
collection PubMed
description Background: Electrospun fibers are widely studied in regenerative medicine for their ability to mimic the extracellular matrix (ECM) and provide mechanical support. In vitro studies indicated that cell adhesion and migration is superior on smooth poly(L-lactic acid) (PLLA) electrospun scaffolds and porous scaffolds once biofunctionalized with collagen. Methods: The in vivo performance of PLLA scaffolds with modified topology and collagen biofunctionalization in full-thickness mouse wounds was assessed by cellular infiltration, wound closure and re-epithelialization and ECM deposition. Results: Early indications suggested unmodified, smooth PLLA scaffolds perform poorly, with limited cellular infiltration and matrix deposition around the scaffold, the largest wound area, a significantly larger panniculus gape, and lowest re-epithelialization; however, by day 14, no significant differences were observed. Collagen biofunctionalization may improve healing, as collagen-functionalized smooth scaffolds were smallest overall, and collagen-functionalized porous scaffolds were smaller than non-functionalized porous scaffolds; the highest re-epithelialization was observed in wounds treated with collagen-functionalized scaffolds. Conclusion: Our results suggest that limited incorporation of smooth PLLA scaffolds into the healing wound occurs, and that altering surface topology, particularly by utilizing collagen biofunctionalization, may improve healing. The differing performance of the unmodified scaffolds in the in vitro versus in vivo studies demonstrates the importance of preclinical testing.
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spelling pubmed-100563162023-03-30 Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds Ravindran Girija, Aswathy Strudwick, Xanthe Balasubramanian, Sivakumar Palaninathan, Vivekanandan Nair, Sakthikumar Dasappan Cowin, Allison J. Pharmaceutics Article Background: Electrospun fibers are widely studied in regenerative medicine for their ability to mimic the extracellular matrix (ECM) and provide mechanical support. In vitro studies indicated that cell adhesion and migration is superior on smooth poly(L-lactic acid) (PLLA) electrospun scaffolds and porous scaffolds once biofunctionalized with collagen. Methods: The in vivo performance of PLLA scaffolds with modified topology and collagen biofunctionalization in full-thickness mouse wounds was assessed by cellular infiltration, wound closure and re-epithelialization and ECM deposition. Results: Early indications suggested unmodified, smooth PLLA scaffolds perform poorly, with limited cellular infiltration and matrix deposition around the scaffold, the largest wound area, a significantly larger panniculus gape, and lowest re-epithelialization; however, by day 14, no significant differences were observed. Collagen biofunctionalization may improve healing, as collagen-functionalized smooth scaffolds were smallest overall, and collagen-functionalized porous scaffolds were smaller than non-functionalized porous scaffolds; the highest re-epithelialization was observed in wounds treated with collagen-functionalized scaffolds. Conclusion: Our results suggest that limited incorporation of smooth PLLA scaffolds into the healing wound occurs, and that altering surface topology, particularly by utilizing collagen biofunctionalization, may improve healing. The differing performance of the unmodified scaffolds in the in vitro versus in vivo studies demonstrates the importance of preclinical testing. MDPI 2023-03-08 /pmc/articles/PMC10056316/ /pubmed/36986741 http://dx.doi.org/10.3390/pharmaceutics15030880 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
Ravindran Girija, Aswathy
Strudwick, Xanthe
Balasubramanian, Sivakumar
Palaninathan, Vivekanandan
Nair, Sakthikumar Dasappan
Cowin, Allison J.
Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds
title Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds
title_full Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds
title_fullStr Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds
title_full_unstemmed Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds
title_short Collagen Functionalization of Polymeric Electrospun Scaffolds to Improve Integration into Full-Thickness Wounds
title_sort collagen functionalization of polymeric electrospun scaffolds to improve integration into full-thickness wounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056316/
https://www.ncbi.nlm.nih.gov/pubmed/36986741
http://dx.doi.org/10.3390/pharmaceutics15030880
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