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Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility

BACKGROUND: Electrospun nanofibers based on Colocasia esculenta tuber (CET) protein are considered as a promising material for wound dressing applications. However, the use of these nanofibers in aqueous conditions has poor stability. The present study was performed to obtain insights into the cross...

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Autores principales: Wardhani, Riesca Ayu Kusuma, Asri, Lia A T W, Rachmawati, Heni, Khairurrijal, Khairurrijal, Purwasasmita, Bambang Sunendar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457767/
https://www.ncbi.nlm.nih.gov/pubmed/32922010
http://dx.doi.org/10.2147/IJN.S261483
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author Wardhani, Riesca Ayu Kusuma
Asri, Lia A T W
Rachmawati, Heni
Khairurrijal, Khairurrijal
Purwasasmita, Bambang Sunendar
author_facet Wardhani, Riesca Ayu Kusuma
Asri, Lia A T W
Rachmawati, Heni
Khairurrijal, Khairurrijal
Purwasasmita, Bambang Sunendar
author_sort Wardhani, Riesca Ayu Kusuma
collection PubMed
description BACKGROUND: Electrospun nanofibers based on Colocasia esculenta tuber (CET) protein are considered as a promising material for wound dressing applications. However, the use of these nanofibers in aqueous conditions has poor stability. The present study was performed to obtain insights into the crosslinked electrospun CET’s protein–chitosan (CS)–poly(ethylene oxide) (PEO) nanofibers and to evaluate their potential for wound dressing applications. METHODS: The electrospun nanofibers were crosslinked with glutaraldehyde (GA) vapor and heat treatment (HT) to enhance their physicochemical stability. The crosslinked nanofibers were characterized by protein profiles, morphology structures, thermal behavior, mechanical properties, and degradation behavior. Furthermore, the antibacterial properties and cytocompatibility were analyzed by antibacterial assessment and cell proliferation. RESULTS: The protein profiles of the electrospun CET’s protein–CS–PEO nanofibers before and after HT crosslinking contained one major bioactive protein with a molecular weight of 14.4 kDa. Scanning electron microscopy images of the crosslinked nanofibers indicated preservation of the structure after immersion in phosphate buffered saline. The crosslinked nanofibers resulted in higher ultimate tensile strength and lower ultimate strain compared to the non-crosslinked nanofibers. GA vapor crosslinking showed higher water stability compared to HT crosslinking. The in vitro antibacterial activity of the crosslinked nanofibers showed a stronger bacteriostatic effect on Staphylococcus aureus than on Escherichia coli. Human skin fibroblast cell proliferation on crosslinked GA vapor and HT nanofibers with 1% (w/v) CS and 2% (w/v) CET’s protein demonstrated the highest among all the other crosslinked nanofibers after seven days of cell culture. Cell proliferation and cell morphology results revealed that introducing higher CET’s protein concentration on crosslinked nanofibers could increase cell proliferation of the crosslinked nanofibers. CONCLUSION: These results are promising for the potential use of the crosslinked electrospun CET’s protein–CS–PEO nanofibers as bioactive wound dressing materials.
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spelling pubmed-74577672020-09-11 Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility Wardhani, Riesca Ayu Kusuma Asri, Lia A T W Rachmawati, Heni Khairurrijal, Khairurrijal Purwasasmita, Bambang Sunendar Int J Nanomedicine Original Research BACKGROUND: Electrospun nanofibers based on Colocasia esculenta tuber (CET) protein are considered as a promising material for wound dressing applications. However, the use of these nanofibers in aqueous conditions has poor stability. The present study was performed to obtain insights into the crosslinked electrospun CET’s protein–chitosan (CS)–poly(ethylene oxide) (PEO) nanofibers and to evaluate their potential for wound dressing applications. METHODS: The electrospun nanofibers were crosslinked with glutaraldehyde (GA) vapor and heat treatment (HT) to enhance their physicochemical stability. The crosslinked nanofibers were characterized by protein profiles, morphology structures, thermal behavior, mechanical properties, and degradation behavior. Furthermore, the antibacterial properties and cytocompatibility were analyzed by antibacterial assessment and cell proliferation. RESULTS: The protein profiles of the electrospun CET’s protein–CS–PEO nanofibers before and after HT crosslinking contained one major bioactive protein with a molecular weight of 14.4 kDa. Scanning electron microscopy images of the crosslinked nanofibers indicated preservation of the structure after immersion in phosphate buffered saline. The crosslinked nanofibers resulted in higher ultimate tensile strength and lower ultimate strain compared to the non-crosslinked nanofibers. GA vapor crosslinking showed higher water stability compared to HT crosslinking. The in vitro antibacterial activity of the crosslinked nanofibers showed a stronger bacteriostatic effect on Staphylococcus aureus than on Escherichia coli. Human skin fibroblast cell proliferation on crosslinked GA vapor and HT nanofibers with 1% (w/v) CS and 2% (w/v) CET’s protein demonstrated the highest among all the other crosslinked nanofibers after seven days of cell culture. Cell proliferation and cell morphology results revealed that introducing higher CET’s protein concentration on crosslinked nanofibers could increase cell proliferation of the crosslinked nanofibers. CONCLUSION: These results are promising for the potential use of the crosslinked electrospun CET’s protein–CS–PEO nanofibers as bioactive wound dressing materials. Dove 2020-08-25 /pmc/articles/PMC7457767/ /pubmed/32922010 http://dx.doi.org/10.2147/IJN.S261483 Text en © 2020 Wardhani et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wardhani, Riesca Ayu Kusuma
Asri, Lia A T W
Rachmawati, Heni
Khairurrijal, Khairurrijal
Purwasasmita, Bambang Sunendar
Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility
title Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility
title_full Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility
title_fullStr Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility
title_full_unstemmed Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility
title_short Physical–Chemical Crosslinked Electrospun Colocasia esculenta Tuber Protein–Chitosan–Poly(Ethylene Oxide) Nanofibers with Antibacterial Activity and Cytocompatibility
title_sort physical–chemical crosslinked electrospun colocasia esculenta tuber protein–chitosan–poly(ethylene oxide) nanofibers with antibacterial activity and cytocompatibility
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457767/
https://www.ncbi.nlm.nih.gov/pubmed/32922010
http://dx.doi.org/10.2147/IJN.S261483
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