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Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds
Non-healing wounds have placed an enormous stress on both patients and healthcare systems worldwide. Severe complications induced by these wounds can lead to limb amputation or even death and urgently require more effective treatments. Electrospun scaffolds have great potential for improving wound h...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686307/ https://www.ncbi.nlm.nih.gov/pubmed/33235239 http://dx.doi.org/10.1038/s41598-020-76971-w |
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author | Abdullah, Turdimuhammad Gauthaman, Kalamegam Mostafavi, Azadeh Alshahrie, Ahmed Salah, Numan Morganti, Pierfrancesco Chianese, Angelo Tamayol, Ali Memic, Adnan |
author_facet | Abdullah, Turdimuhammad Gauthaman, Kalamegam Mostafavi, Azadeh Alshahrie, Ahmed Salah, Numan Morganti, Pierfrancesco Chianese, Angelo Tamayol, Ali Memic, Adnan |
author_sort | Abdullah, Turdimuhammad |
collection | PubMed |
description | Non-healing wounds have placed an enormous stress on both patients and healthcare systems worldwide. Severe complications induced by these wounds can lead to limb amputation or even death and urgently require more effective treatments. Electrospun scaffolds have great potential for improving wound healing treatments by providing controlled drug delivery. Previously, we developed fibrous scaffolds from complex carbohydrate polymers [i.e. chitin-lignin (CL) gels]. However, their application was limited by solubility and undesirable burst drug release. Here, a coaxial electrospinning is applied to encapsulate the CL gels with polycaprolactone (PCL). Presence of a PCL shell layer thus provides longer shelf-life for the CL gels in a wet environment and sustainable drug release. Antibiotics loaded into core–shell fibrous platform effectively inhibit both gram-positive and -negative bacteria without inducting observable cytotoxicity. Therefore, PCL coated CL fibrous gel platforms appear to be good candidates for controlled drug release based wound dressing applications. |
format | Online Article Text |
id | pubmed-7686307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76863072020-11-27 Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds Abdullah, Turdimuhammad Gauthaman, Kalamegam Mostafavi, Azadeh Alshahrie, Ahmed Salah, Numan Morganti, Pierfrancesco Chianese, Angelo Tamayol, Ali Memic, Adnan Sci Rep Article Non-healing wounds have placed an enormous stress on both patients and healthcare systems worldwide. Severe complications induced by these wounds can lead to limb amputation or even death and urgently require more effective treatments. Electrospun scaffolds have great potential for improving wound healing treatments by providing controlled drug delivery. Previously, we developed fibrous scaffolds from complex carbohydrate polymers [i.e. chitin-lignin (CL) gels]. However, their application was limited by solubility and undesirable burst drug release. Here, a coaxial electrospinning is applied to encapsulate the CL gels with polycaprolactone (PCL). Presence of a PCL shell layer thus provides longer shelf-life for the CL gels in a wet environment and sustainable drug release. Antibiotics loaded into core–shell fibrous platform effectively inhibit both gram-positive and -negative bacteria without inducting observable cytotoxicity. Therefore, PCL coated CL fibrous gel platforms appear to be good candidates for controlled drug release based wound dressing applications. Nature Publishing Group UK 2020-11-24 /pmc/articles/PMC7686307/ /pubmed/33235239 http://dx.doi.org/10.1038/s41598-020-76971-w Text en © The Author(s) 2020, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Abdullah, Turdimuhammad Gauthaman, Kalamegam Mostafavi, Azadeh Alshahrie, Ahmed Salah, Numan Morganti, Pierfrancesco Chianese, Angelo Tamayol, Ali Memic, Adnan Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
title | Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
title_full | Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
title_fullStr | Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
title_full_unstemmed | Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
title_short | Sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
title_sort | sustainable drug release from polycaprolactone coated chitin-lignin gel fibrous scaffolds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686307/ https://www.ncbi.nlm.nih.gov/pubmed/33235239 http://dx.doi.org/10.1038/s41598-020-76971-w |
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