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Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies

Nanotopographical TiO(2) films (including nanorod, nanotip, and nanowire topographies) were successfully fabricated on the metallic Ti surface via hydrothermal treatment and then underwent Ag plasma immersion ion implantation to incorporate Ag with TiO(2). The surface morphology, phase component, an...

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Autores principales: Li, Jinhua, Qiao, Yuqin, Zhu, Hongqin, Meng, Fanhao, Liu, Xuanyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4106954/
https://www.ncbi.nlm.nih.gov/pubmed/25075186
http://dx.doi.org/10.2147/IJN.S63807
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author Li, Jinhua
Qiao, Yuqin
Zhu, Hongqin
Meng, Fanhao
Liu, Xuanyong
author_facet Li, Jinhua
Qiao, Yuqin
Zhu, Hongqin
Meng, Fanhao
Liu, Xuanyong
author_sort Li, Jinhua
collection PubMed
description Nanotopographical TiO(2) films (including nanorod, nanotip, and nanowire topographies) were successfully fabricated on the metallic Ti surface via hydrothermal treatment and then underwent Ag plasma immersion ion implantation to incorporate Ag with TiO(2). The surface morphology, phase component, and chemical composition before and after Ag–PIII were characterized. In view of the potential clinical applications, both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus were used to estimate their antimicrobial effect. The nanostructured TiO(2) films on a Ti surface exhibit a better bacteriostatic effect on both microbes compared to the pristine Ti. The nanotopographies of the TiO(2) films affect the nucleation, growth, and distribution of Ag nanoparticles in the films during Ag–PIII process. The Ag nanoparticles are completely embedded into the nanorod film while partially exposed out of the nanotip and nanowire films, which account for the significant differences in the release behaviors of Ag ions in vitro. However, no significant difference exists in their antimicrobial activity against both microbes. The antimicrobial actions of the Ag@TiO(2) system described here consist of two methods – the contact-killing action and the release-killing action. Nevertheless, based on the observed results, the contact-killing action should be regarded as the main method to destroy microbes for all the Ag plasma-modified TiO(2) nanofilms. This study provides insight to optimize the surface design of Ti-based implants to acquire more effective antimicrobial surfaces to meet clinical applications.
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spelling pubmed-41069542014-07-29 Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies Li, Jinhua Qiao, Yuqin Zhu, Hongqin Meng, Fanhao Liu, Xuanyong Int J Nanomedicine Original Research Nanotopographical TiO(2) films (including nanorod, nanotip, and nanowire topographies) were successfully fabricated on the metallic Ti surface via hydrothermal treatment and then underwent Ag plasma immersion ion implantation to incorporate Ag with TiO(2). The surface morphology, phase component, and chemical composition before and after Ag–PIII were characterized. In view of the potential clinical applications, both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus were used to estimate their antimicrobial effect. The nanostructured TiO(2) films on a Ti surface exhibit a better bacteriostatic effect on both microbes compared to the pristine Ti. The nanotopographies of the TiO(2) films affect the nucleation, growth, and distribution of Ag nanoparticles in the films during Ag–PIII process. The Ag nanoparticles are completely embedded into the nanorod film while partially exposed out of the nanotip and nanowire films, which account for the significant differences in the release behaviors of Ag ions in vitro. However, no significant difference exists in their antimicrobial activity against both microbes. The antimicrobial actions of the Ag@TiO(2) system described here consist of two methods – the contact-killing action and the release-killing action. Nevertheless, based on the observed results, the contact-killing action should be regarded as the main method to destroy microbes for all the Ag plasma-modified TiO(2) nanofilms. This study provides insight to optimize the surface design of Ti-based implants to acquire more effective antimicrobial surfaces to meet clinical applications. Dove Medical Press 2014-07-16 /pmc/articles/PMC4106954/ /pubmed/25075186 http://dx.doi.org/10.2147/IJN.S63807 Text en © 2014 Li et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed.
spellingShingle Original Research
Li, Jinhua
Qiao, Yuqin
Zhu, Hongqin
Meng, Fanhao
Liu, Xuanyong
Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies
title Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies
title_full Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies
title_fullStr Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies
title_full_unstemmed Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies
title_short Existence, release, and antibacterial actions of silver nanoparticles on Ag–PIII TiO(2) films with different nanotopographies
title_sort existence, release, and antibacterial actions of silver nanoparticles on ag–piii tio(2) films with different nanotopographies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4106954/
https://www.ncbi.nlm.nih.gov/pubmed/25075186
http://dx.doi.org/10.2147/IJN.S63807
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