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Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates
A combination of [Formula: see text] nanotube array (TON) and controlled drug release system is employed to provide enhanced surface properties of titanium implants. Electrochemical anodization process is used to generate TON for introducing, vancomycin, an effective antibacterial drug against Staph...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124201/ https://www.ncbi.nlm.nih.gov/pubmed/35597786 http://dx.doi.org/10.1038/s41598-022-12332-z |
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author | Nowruzi, Fateme Imani, Rana Faghihi, Shahab |
author_facet | Nowruzi, Fateme Imani, Rana Faghihi, Shahab |
author_sort | Nowruzi, Fateme |
collection | PubMed |
description | A combination of [Formula: see text] nanotube array (TON) and controlled drug release system is employed to provide enhanced surface properties of titanium implants. Electrochemical anodization process is used to generate TON for introducing, vancomycin, an effective antibacterial drug against Staphylococcus aureus. TON loaded vancomycin is then coated with a number of layers of 10% gelatin using spin coating technique. The gelatin film is reinforced with graphene oxide (GO) nanoparticles to improve the surface bioactivity. The surface of the samples is characterized by field emission electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), and contact angle measurement. The results illustrate that the TON was constructed and vancomycin molecules are successfully loaded. The drug release study shows that the amount of released vancomycin is controlled by the thickness of gelatin layers. With an increase in gelatin film layers from 3 to 7, the release of vancomycin in the burst release phase decreased from 58 to 31%, and sustained release extended from 10 to 17 days. The addition of GO nanoparticles seems to reduce drug release in from 31 to 22% (burst release phase) and prolonged drug release (from 17 to 19 days). MTT assay indicates that samples show no cytotoxicity, and combination of GO nanoparticles with gelatin coating could highly promote MG63 cell proliferation. Soaking the samples in SBF solution after 3 and 7 days demonstrates that hydroxy apatite crystals were deposited on the TON surface with GO-gelatin coating more than surface of TON with gelatin. Moreover, based on the results of disc diffusion assay, both samples (loaded with Vancomycin and coated with gelatin and gelatin-GO) with the inhibition zones equaled to 20 mm show effective antibacterial properties against S. aureus. The evidence demonstrates that titania nanotube loaded with vancomycin and coated with gelatin-GO has a great potential for general applicability to the orthopedic implant field. |
format | Online Article Text |
id | pubmed-9124201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91242012022-05-23 Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates Nowruzi, Fateme Imani, Rana Faghihi, Shahab Sci Rep Article A combination of [Formula: see text] nanotube array (TON) and controlled drug release system is employed to provide enhanced surface properties of titanium implants. Electrochemical anodization process is used to generate TON for introducing, vancomycin, an effective antibacterial drug against Staphylococcus aureus. TON loaded vancomycin is then coated with a number of layers of 10% gelatin using spin coating technique. The gelatin film is reinforced with graphene oxide (GO) nanoparticles to improve the surface bioactivity. The surface of the samples is characterized by field emission electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDS), and contact angle measurement. The results illustrate that the TON was constructed and vancomycin molecules are successfully loaded. The drug release study shows that the amount of released vancomycin is controlled by the thickness of gelatin layers. With an increase in gelatin film layers from 3 to 7, the release of vancomycin in the burst release phase decreased from 58 to 31%, and sustained release extended from 10 to 17 days. The addition of GO nanoparticles seems to reduce drug release in from 31 to 22% (burst release phase) and prolonged drug release (from 17 to 19 days). MTT assay indicates that samples show no cytotoxicity, and combination of GO nanoparticles with gelatin coating could highly promote MG63 cell proliferation. Soaking the samples in SBF solution after 3 and 7 days demonstrates that hydroxy apatite crystals were deposited on the TON surface with GO-gelatin coating more than surface of TON with gelatin. Moreover, based on the results of disc diffusion assay, both samples (loaded with Vancomycin and coated with gelatin and gelatin-GO) with the inhibition zones equaled to 20 mm show effective antibacterial properties against S. aureus. The evidence demonstrates that titania nanotube loaded with vancomycin and coated with gelatin-GO has a great potential for general applicability to the orthopedic implant field. Nature Publishing Group UK 2022-05-21 /pmc/articles/PMC9124201/ /pubmed/35597786 http://dx.doi.org/10.1038/s41598-022-12332-z Text en © The Author(s) 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 Nowruzi, Fateme Imani, Rana Faghihi, Shahab Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
title | Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
title_full | Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
title_fullStr | Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
title_full_unstemmed | Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
title_short | Effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
title_sort | effect of electrochemical oxidation and drug loading on the antibacterial properties and cell biocompatibility of titanium substrates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124201/ https://www.ncbi.nlm.nih.gov/pubmed/35597786 http://dx.doi.org/10.1038/s41598-022-12332-z |
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