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Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells
Chronic wounds not only lower the quality of patient's life significantly, but also present a huge financial burden for the healthcare systems around the world. Treatment of larger wounds often requires the use of more complex materials, which can ensure a successful renewal or replacement of d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466929/ https://www.ncbi.nlm.nih.gov/pubmed/31024901 http://dx.doi.org/10.3389/fchem.2019.00217 |
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author | Maver, Tina Mohan, Tamilselvan Gradišnik, Lidija Finšgar, Matjaž Stana Kleinschek, Karin Maver, Uroš |
author_facet | Maver, Tina Mohan, Tamilselvan Gradišnik, Lidija Finšgar, Matjaž Stana Kleinschek, Karin Maver, Uroš |
author_sort | Maver, Tina |
collection | PubMed |
description | Chronic wounds not only lower the quality of patient's life significantly, but also present a huge financial burden for the healthcare systems around the world. Treatment of larger wounds often requires the use of more complex materials, which can ensure a successful renewal or replacement of damaged or destroyed tissues. Despite a range of advanced wound dressings that can facilitate wound healing, there are still no clinically used dressings for effective local pain management. Herein, alginate (ALG) and carboxymethyl cellulose (CMC), two of the most commonly used materials in the field of chronic wound care, and combination of ALG-CMC were used to create a model wound dressing system in the form of multi-layered thin solid films using the spin-assisted layer-by-layer (LBL) coating technique. The latter multi-layer system was used to incorporate and study the release kinetics of analgesic drugs such as diclofenac and lidocaine at physiological conditions. The wettability, morphology, physicochemical and surface properties of the coated films were evaluated using different surface sensitive analytical tools. The influence of in situ incorporated drug molecules on the surface properties (e.g., roughness) and on the proliferation of human skin cells (keratinocytes and skin fibroblasts) was further evaluated. The results obtained from this preliminary study should be considered as the basis for the development “real” wound dressing materials and for 3D bio-printing applications. |
format | Online Article Text |
id | pubmed-6466929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64669292019-04-25 Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells Maver, Tina Mohan, Tamilselvan Gradišnik, Lidija Finšgar, Matjaž Stana Kleinschek, Karin Maver, Uroš Front Chem Chemistry Chronic wounds not only lower the quality of patient's life significantly, but also present a huge financial burden for the healthcare systems around the world. Treatment of larger wounds often requires the use of more complex materials, which can ensure a successful renewal or replacement of damaged or destroyed tissues. Despite a range of advanced wound dressings that can facilitate wound healing, there are still no clinically used dressings for effective local pain management. Herein, alginate (ALG) and carboxymethyl cellulose (CMC), two of the most commonly used materials in the field of chronic wound care, and combination of ALG-CMC were used to create a model wound dressing system in the form of multi-layered thin solid films using the spin-assisted layer-by-layer (LBL) coating technique. The latter multi-layer system was used to incorporate and study the release kinetics of analgesic drugs such as diclofenac and lidocaine at physiological conditions. The wettability, morphology, physicochemical and surface properties of the coated films were evaluated using different surface sensitive analytical tools. The influence of in situ incorporated drug molecules on the surface properties (e.g., roughness) and on the proliferation of human skin cells (keratinocytes and skin fibroblasts) was further evaluated. The results obtained from this preliminary study should be considered as the basis for the development “real” wound dressing materials and for 3D bio-printing applications. Frontiers Media S.A. 2019-04-09 /pmc/articles/PMC6466929/ /pubmed/31024901 http://dx.doi.org/10.3389/fchem.2019.00217 Text en Copyright © 2019 Maver, Mohan, Gradišnik, Finšgar, Stana Kleinschek and Maver. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Maver, Tina Mohan, Tamilselvan Gradišnik, Lidija Finšgar, Matjaž Stana Kleinschek, Karin Maver, Uroš Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells |
title | Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells |
title_full | Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells |
title_fullStr | Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells |
title_full_unstemmed | Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells |
title_short | Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells |
title_sort | polysaccharide thin solid films for analgesic drug delivery and growth of human skin cells |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466929/ https://www.ncbi.nlm.nih.gov/pubmed/31024901 http://dx.doi.org/10.3389/fchem.2019.00217 |
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