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PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing
Application of growth factors at wound site has improved the efficiency and quality of healing. Basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) induce proliferation of various cells in wound healing. Delivery of growth factor from controlled release systems protec...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915706/ https://www.ncbi.nlm.nih.gov/pubmed/31844069 http://dx.doi.org/10.1038/s41598-019-55214-7 |
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author | Vijayan, Amritha A., Sabareeswaran Kumar, G. S. Vinod |
author_facet | Vijayan, Amritha A., Sabareeswaran Kumar, G. S. Vinod |
author_sort | Vijayan, Amritha |
collection | PubMed |
description | Application of growth factors at wound site has improved the efficiency and quality of healing. Basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) induce proliferation of various cells in wound healing. Delivery of growth factor from controlled release systems protect it from degradation and also result in sustained delivery of it at the site of injury. The goal of the study was to develop a Polyethylene glycol (PEG) cross-linked cotton-like chitosan scaffold (CS-PEG-H) by freeze-drying method and chemically conjugate heparin to the scaffold to which the growth factors can be electrostatically bound and evaluate its wound healing properties in vitro and in vivo. The growth factor containing scaffolds induced increased proliferation of HaCaT cells, increased neovascularization and collagen formation seen by H and E and Masson’s trichrome staining. Immunohistochemistry was performed using the Ki67 marker which increased proliferation of cells in growth factor containing scaffold treated group. Frequent dressing changes are a major deterrent to proper wound healing. Our system was found to release both VEGF and bFGF in a continuous manner and attained stability after 7 days. Thus our system can maintain therapeutic levels of growth factor at the wound bed thereby avoiding the need for daily applications and frequent dressing changes. Thus, it can be a promising candidate for wound healing. |
format | Online Article Text |
id | pubmed-6915706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69157062019-12-18 PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing Vijayan, Amritha A., Sabareeswaran Kumar, G. S. Vinod Sci Rep Article Application of growth factors at wound site has improved the efficiency and quality of healing. Basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) induce proliferation of various cells in wound healing. Delivery of growth factor from controlled release systems protect it from degradation and also result in sustained delivery of it at the site of injury. The goal of the study was to develop a Polyethylene glycol (PEG) cross-linked cotton-like chitosan scaffold (CS-PEG-H) by freeze-drying method and chemically conjugate heparin to the scaffold to which the growth factors can be electrostatically bound and evaluate its wound healing properties in vitro and in vivo. The growth factor containing scaffolds induced increased proliferation of HaCaT cells, increased neovascularization and collagen formation seen by H and E and Masson’s trichrome staining. Immunohistochemistry was performed using the Ki67 marker which increased proliferation of cells in growth factor containing scaffold treated group. Frequent dressing changes are a major deterrent to proper wound healing. Our system was found to release both VEGF and bFGF in a continuous manner and attained stability after 7 days. Thus our system can maintain therapeutic levels of growth factor at the wound bed thereby avoiding the need for daily applications and frequent dressing changes. Thus, it can be a promising candidate for wound healing. Nature Publishing Group UK 2019-12-16 /pmc/articles/PMC6915706/ /pubmed/31844069 http://dx.doi.org/10.1038/s41598-019-55214-7 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Vijayan, Amritha A., Sabareeswaran Kumar, G. S. Vinod PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
title | PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
title_full | PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
title_fullStr | PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
title_full_unstemmed | PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
title_short | PEG grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
title_sort | peg grafted chitosan scaffold for dual growth factor delivery for enhanced wound healing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915706/ https://www.ncbi.nlm.nih.gov/pubmed/31844069 http://dx.doi.org/10.1038/s41598-019-55214-7 |
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