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Biological Performance of Electrospun Polymer Fibres

The evaluation of biological responses to polymeric scaffolds are important, given that the ideal scaffold should be biocompatible, biodegradable, promote cell adhesion and aid cell proliferation. The primary goal of this research was to measure the biological responses of cells against various poly...

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Autores principales: Hall Barrientos, Ivan Joseph, MacKenzie, Graeme R., Wilson, Clive G., Lamprou, Dimitrios A., Coats, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384992/
https://www.ncbi.nlm.nih.gov/pubmed/30682805
http://dx.doi.org/10.3390/ma12030363
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author Hall Barrientos, Ivan Joseph
MacKenzie, Graeme R.
Wilson, Clive G.
Lamprou, Dimitrios A.
Coats, Paul
author_facet Hall Barrientos, Ivan Joseph
MacKenzie, Graeme R.
Wilson, Clive G.
Lamprou, Dimitrios A.
Coats, Paul
author_sort Hall Barrientos, Ivan Joseph
collection PubMed
description The evaluation of biological responses to polymeric scaffolds are important, given that the ideal scaffold should be biocompatible, biodegradable, promote cell adhesion and aid cell proliferation. The primary goal of this research was to measure the biological responses of cells against various polymeric and collagen electrospun scaffolds (polycaprolactone (PCL) and polylactic acid (PLA) polymers: PCL–drug, PCL–collagen–drug, PLA–drug and PLA–collagen–drug); cell proliferation was measured with a cell adhesion assay and cell viability using 5-bromo-2′-deoxyuridine (BrdU) and resazurin assays. The results demonstrated that there is a distinct lack of growth of cells against any irgasan (IRG) loaded scaffolds and far greater adhesion of cells against levofloxacin (LEVO) loaded scaffolds. Fourteen-day studies revealed a significant increase in cell growth after a 7-day period. The addition of collagen in the formulations did not promote greater cell adhesion. Cell viability studies revealed the levels of IRG used in scaffolds were toxic to cells, with the concentration used 475 times higher than the EC(50) value for IRG. It was concluded that the negatively charged carboxylic acid group found in LEVO is attracting positively charged fibronectin, which in turn is attracting the cell to adhere to the adsorbed proteins on the surface of the scaffold. Overall, the biological studies examined in this paper are valuable as preliminary data for potential further studies into more complex aspects of cell behaviour with polymeric scaffolds.
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spelling pubmed-63849922019-02-23 Biological Performance of Electrospun Polymer Fibres Hall Barrientos, Ivan Joseph MacKenzie, Graeme R. Wilson, Clive G. Lamprou, Dimitrios A. Coats, Paul Materials (Basel) Article The evaluation of biological responses to polymeric scaffolds are important, given that the ideal scaffold should be biocompatible, biodegradable, promote cell adhesion and aid cell proliferation. The primary goal of this research was to measure the biological responses of cells against various polymeric and collagen electrospun scaffolds (polycaprolactone (PCL) and polylactic acid (PLA) polymers: PCL–drug, PCL–collagen–drug, PLA–drug and PLA–collagen–drug); cell proliferation was measured with a cell adhesion assay and cell viability using 5-bromo-2′-deoxyuridine (BrdU) and resazurin assays. The results demonstrated that there is a distinct lack of growth of cells against any irgasan (IRG) loaded scaffolds and far greater adhesion of cells against levofloxacin (LEVO) loaded scaffolds. Fourteen-day studies revealed a significant increase in cell growth after a 7-day period. The addition of collagen in the formulations did not promote greater cell adhesion. Cell viability studies revealed the levels of IRG used in scaffolds were toxic to cells, with the concentration used 475 times higher than the EC(50) value for IRG. It was concluded that the negatively charged carboxylic acid group found in LEVO is attracting positively charged fibronectin, which in turn is attracting the cell to adhere to the adsorbed proteins on the surface of the scaffold. Overall, the biological studies examined in this paper are valuable as preliminary data for potential further studies into more complex aspects of cell behaviour with polymeric scaffolds. MDPI 2019-01-24 /pmc/articles/PMC6384992/ /pubmed/30682805 http://dx.doi.org/10.3390/ma12030363 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hall Barrientos, Ivan Joseph
MacKenzie, Graeme R.
Wilson, Clive G.
Lamprou, Dimitrios A.
Coats, Paul
Biological Performance of Electrospun Polymer Fibres
title Biological Performance of Electrospun Polymer Fibres
title_full Biological Performance of Electrospun Polymer Fibres
title_fullStr Biological Performance of Electrospun Polymer Fibres
title_full_unstemmed Biological Performance of Electrospun Polymer Fibres
title_short Biological Performance of Electrospun Polymer Fibres
title_sort biological performance of electrospun polymer fibres
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384992/
https://www.ncbi.nlm.nih.gov/pubmed/30682805
http://dx.doi.org/10.3390/ma12030363
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