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Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application

Core-shell nanofibers with the ability to carry multiple drugs are attracting the attention to develop appropriate drug delivery systems for wounds dressing applications. In this study, biocompatible core-shell nanofibers have been designed as a promising dual-drug carrier with the capability of del...

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Autores principales: Kharaghani, Davood, Gitigard, Parastoo, Ohtani, Hijiri, Kim, Kyu Oh, Ullah, Sana, Saito, Yusuke, Khan, Muhammad Qamar, Kim, Ick Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718412/
https://www.ncbi.nlm.nih.gov/pubmed/31477774
http://dx.doi.org/10.1038/s41598-019-49132-x
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author Kharaghani, Davood
Gitigard, Parastoo
Ohtani, Hijiri
Kim, Kyu Oh
Ullah, Sana
Saito, Yusuke
Khan, Muhammad Qamar
Kim, Ick Soo
author_facet Kharaghani, Davood
Gitigard, Parastoo
Ohtani, Hijiri
Kim, Kyu Oh
Ullah, Sana
Saito, Yusuke
Khan, Muhammad Qamar
Kim, Ick Soo
author_sort Kharaghani, Davood
collection PubMed
description Core-shell nanofibers with the ability to carry multiple drugs are attracting the attention to develop appropriate drug delivery systems for wounds dressing applications. In this study, biocompatible core-shell nanofibers have been designed as a promising dual-drug carrier with the capability of delivering both water-soluble and organic solvent-soluble drugs simultaneously. With the aim of fabricating the core-shell nanofibers, the dipping method has been employed. For this propose, core nanofibers made from polyvinyl alcohol (PVA) were immersed in various concentrations of polyacrylonitrile (PAN) and cross-linked by dipping into ethanol. Diclofenac sodium salt (DSs) and gentamicin sulfate (GENs) have been loaded into the core and shell nanofibers as models of the drug, respectively. The morphology study of core-shell nanofibers showed that the concentrations between 1% w/w up to 2% w/w PAN/GENs, with deep penetration into the internal layers of PAV/DSs nanofibers could lead to the core-shell structure. The cytotoxicity results showed the competency of designed core-shell nanofibers for wound dressing application. Also, the release profile exhibits the controllable behavior of drug release.
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spelling pubmed-67184122019-09-17 Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application Kharaghani, Davood Gitigard, Parastoo Ohtani, Hijiri Kim, Kyu Oh Ullah, Sana Saito, Yusuke Khan, Muhammad Qamar Kim, Ick Soo Sci Rep Article Core-shell nanofibers with the ability to carry multiple drugs are attracting the attention to develop appropriate drug delivery systems for wounds dressing applications. In this study, biocompatible core-shell nanofibers have been designed as a promising dual-drug carrier with the capability of delivering both water-soluble and organic solvent-soluble drugs simultaneously. With the aim of fabricating the core-shell nanofibers, the dipping method has been employed. For this propose, core nanofibers made from polyvinyl alcohol (PVA) were immersed in various concentrations of polyacrylonitrile (PAN) and cross-linked by dipping into ethanol. Diclofenac sodium salt (DSs) and gentamicin sulfate (GENs) have been loaded into the core and shell nanofibers as models of the drug, respectively. The morphology study of core-shell nanofibers showed that the concentrations between 1% w/w up to 2% w/w PAN/GENs, with deep penetration into the internal layers of PAV/DSs nanofibers could lead to the core-shell structure. The cytotoxicity results showed the competency of designed core-shell nanofibers for wound dressing application. Also, the release profile exhibits the controllable behavior of drug release. Nature Publishing Group UK 2019-09-02 /pmc/articles/PMC6718412/ /pubmed/31477774 http://dx.doi.org/10.1038/s41598-019-49132-x 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
Kharaghani, Davood
Gitigard, Parastoo
Ohtani, Hijiri
Kim, Kyu Oh
Ullah, Sana
Saito, Yusuke
Khan, Muhammad Qamar
Kim, Ick Soo
Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application
title Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application
title_full Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application
title_fullStr Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application
title_full_unstemmed Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application
title_short Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application
title_sort design and characterization of dual drug delivery based on in-situ assembled pva/pan core-shell nanofibers for wound dressing application
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718412/
https://www.ncbi.nlm.nih.gov/pubmed/31477774
http://dx.doi.org/10.1038/s41598-019-49132-x
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