Cargando…
Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies
Epidermal growth factor (EGF) can be efficiently used in wound healing process; but the main obstacle of its clinical use is its susceptibility to proteolysis and maintaining its effective concentration in the site of action. In this study, chitosan nanoparticles containing EGF is formulated using a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190615/ https://www.ncbi.nlm.nih.gov/pubmed/36734307 http://dx.doi.org/10.1049/nbt2.12116 |
_version_ | 1785043311880306688 |
---|---|
author | Montazeri, Samaneh Rastegari, Ali Mohammadi, Zohreh Nazari, Mahboobeh Yousefi, Maryam Samadi, Fatemeh Yazdi Najafzadeh, Somayeh Aghsami, Mehdi |
author_facet | Montazeri, Samaneh Rastegari, Ali Mohammadi, Zohreh Nazari, Mahboobeh Yousefi, Maryam Samadi, Fatemeh Yazdi Najafzadeh, Somayeh Aghsami, Mehdi |
author_sort | Montazeri, Samaneh |
collection | PubMed |
description | Epidermal growth factor (EGF) can be efficiently used in wound healing process; but the main obstacle of its clinical use is its susceptibility to proteolysis and maintaining its effective concentration in the site of action. In this study, chitosan nanoparticles containing EGF is formulated using a simple method to increase its stability in physiological pH as well as protect its biological activity and effectiveness in wound healing process. Nanoparticles with different ratios of chitosan/EGF were prepared and evaluated in vitro and in vivo. Obtained results showed nanoparticles with 2:1 ratio of chitosan/EGF were able to release 80% of encapsulated protein after 12 h. Cell proliferation study demonstrated that prepared nanoparticles could protect EGF functionality in physiological pH. In vivo results showed that nanoparticles with 2:1 ratio of chitosan/EGF could significantly accelerate the wound closure‐rate, re‐epithelialisation and collagen deposition. In conclusion, the designed nanoparticles in optimal ratio can be considered as a potential vehicle for EGF delivery to wounds with the aim of improving healing process. |
format | Online Article Text |
id | pubmed-10190615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101906152023-05-18 Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies Montazeri, Samaneh Rastegari, Ali Mohammadi, Zohreh Nazari, Mahboobeh Yousefi, Maryam Samadi, Fatemeh Yazdi Najafzadeh, Somayeh Aghsami, Mehdi IET Nanobiotechnol Original Research Epidermal growth factor (EGF) can be efficiently used in wound healing process; but the main obstacle of its clinical use is its susceptibility to proteolysis and maintaining its effective concentration in the site of action. In this study, chitosan nanoparticles containing EGF is formulated using a simple method to increase its stability in physiological pH as well as protect its biological activity and effectiveness in wound healing process. Nanoparticles with different ratios of chitosan/EGF were prepared and evaluated in vitro and in vivo. Obtained results showed nanoparticles with 2:1 ratio of chitosan/EGF were able to release 80% of encapsulated protein after 12 h. Cell proliferation study demonstrated that prepared nanoparticles could protect EGF functionality in physiological pH. In vivo results showed that nanoparticles with 2:1 ratio of chitosan/EGF could significantly accelerate the wound closure‐rate, re‐epithelialisation and collagen deposition. In conclusion, the designed nanoparticles in optimal ratio can be considered as a potential vehicle for EGF delivery to wounds with the aim of improving healing process. John Wiley and Sons Inc. 2023-02-03 /pmc/articles/PMC10190615/ /pubmed/36734307 http://dx.doi.org/10.1049/nbt2.12116 Text en © 2023 The Authors. IET Nanobiotechnology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Montazeri, Samaneh Rastegari, Ali Mohammadi, Zohreh Nazari, Mahboobeh Yousefi, Maryam Samadi, Fatemeh Yazdi Najafzadeh, Somayeh Aghsami, Mehdi Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies |
title | Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies |
title_full | Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies |
title_fullStr | Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies |
title_full_unstemmed | Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies |
title_short | Chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: In vitro and in vivo studies |
title_sort | chitosan nanoparticle loaded by epidermal growth factor as a potential protein carrier for wound healing: in vitro and in vivo studies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10190615/ https://www.ncbi.nlm.nih.gov/pubmed/36734307 http://dx.doi.org/10.1049/nbt2.12116 |
work_keys_str_mv | AT montazerisamaneh chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT rastegariali chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT mohammadizohreh chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT nazarimahboobeh chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT yousefimaryam chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT samadifatemehyazdi chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT najafzadehsomayeh chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies AT aghsamimehdi chitosannanoparticleloadedbyepidermalgrowthfactorasapotentialproteincarrierforwoundhealinginvitroandinvivostudies |