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Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing
Wound care is an integral part of effective recovery. However, its associated financial burden on national health services globally is significant enough to warrant further research and development in this field. In this study, multifunctional polymer wafers were prepared, which provide antibacteria...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968014/ https://www.ncbi.nlm.nih.gov/pubmed/36839805 http://dx.doi.org/10.3390/pharmaceutics15020483 |
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author | Man, Ernest Easdon, Claire McLellan, Iain Yiu, Humphrey H. P. Hoskins, Clare |
author_facet | Man, Ernest Easdon, Claire McLellan, Iain Yiu, Humphrey H. P. Hoskins, Clare |
author_sort | Man, Ernest |
collection | PubMed |
description | Wound care is an integral part of effective recovery. However, its associated financial burden on national health services globally is significant enough to warrant further research and development in this field. In this study, multifunctional polymer wafers were prepared, which provide antibacterial activity, high cell viability, high swelling capacity and a thermally stable medium which can be used to facilitate the delivery of therapeutic agents. The purpose of this polymer wafer is to facilitate wound healing, by creating nanosilver particles within the polymer matrix itself via a one-pot synthesis method. This study compares the use of two synthetic agents in tandem, detailing the effects on the morphology and size of nanosilver particles. Two synthetic methods with varying parameters were tested, with one method using silver nitrate, calcium chloride and sodium alginate, whilst the other included aloe vera gel as an extra component, which serves as another reductant for nanosilver synthesis. Both methods generated thermally stable alginate matrices with high degrees of swelling capacities (400–900%) coupled with interstitially formed nanosilver of varying shapes and sizes. These matrices exhibited controlled nanosilver release rates which were able to elicit antibacterial activity against MRSA, whilst maintaining an average cell viability value of above 90%. Based on the results of this study, the multifunctional polymer wafers that were created set the standard for future polymeric devices for wound healing. These polymer wafers can then be further modified to suit specific types of wounds, thereby allowing this multifunctional polymer wafer to be applied to different wounding scenarios. |
format | Online Article Text |
id | pubmed-9968014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99680142023-02-27 Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing Man, Ernest Easdon, Claire McLellan, Iain Yiu, Humphrey H. P. Hoskins, Clare Pharmaceutics Article Wound care is an integral part of effective recovery. However, its associated financial burden on national health services globally is significant enough to warrant further research and development in this field. In this study, multifunctional polymer wafers were prepared, which provide antibacterial activity, high cell viability, high swelling capacity and a thermally stable medium which can be used to facilitate the delivery of therapeutic agents. The purpose of this polymer wafer is to facilitate wound healing, by creating nanosilver particles within the polymer matrix itself via a one-pot synthesis method. This study compares the use of two synthetic agents in tandem, detailing the effects on the morphology and size of nanosilver particles. Two synthetic methods with varying parameters were tested, with one method using silver nitrate, calcium chloride and sodium alginate, whilst the other included aloe vera gel as an extra component, which serves as another reductant for nanosilver synthesis. Both methods generated thermally stable alginate matrices with high degrees of swelling capacities (400–900%) coupled with interstitially formed nanosilver of varying shapes and sizes. These matrices exhibited controlled nanosilver release rates which were able to elicit antibacterial activity against MRSA, whilst maintaining an average cell viability value of above 90%. Based on the results of this study, the multifunctional polymer wafers that were created set the standard for future polymeric devices for wound healing. These polymer wafers can then be further modified to suit specific types of wounds, thereby allowing this multifunctional polymer wafer to be applied to different wounding scenarios. MDPI 2023-02-01 /pmc/articles/PMC9968014/ /pubmed/36839805 http://dx.doi.org/10.3390/pharmaceutics15020483 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 Man, Ernest Easdon, Claire McLellan, Iain Yiu, Humphrey H. P. Hoskins, Clare Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing |
title | Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing |
title_full | Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing |
title_fullStr | Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing |
title_full_unstemmed | Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing |
title_short | Exploration of Nanosilver Calcium Alginate-Based Multifunctional Polymer Wafers for Wound Healing |
title_sort | exploration of nanosilver calcium alginate-based multifunctional polymer wafers for wound healing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968014/ https://www.ncbi.nlm.nih.gov/pubmed/36839805 http://dx.doi.org/10.3390/pharmaceutics15020483 |
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