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3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses

[Image: see text] Three-dimensional (3D) printing technology has been proved to be a powerful tool for the free-form fabrication of titanium (Ti) implants. However, the surface quality of 3D printed Ti implants is not suitable for clinical application directly. Therefore, surface modification of 3D...

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Autores principales: Yu, Mingzhi, Wan, Yi, Ren, Bing, Wang, Hongwei, Zhang, Xiao, Qiu, Cheng, Liu, Anqi, Liu, Zhanqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745418/
https://www.ncbi.nlm.nih.gov/pubmed/33344827
http://dx.doi.org/10.1021/acsomega.0c04373
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author Yu, Mingzhi
Wan, Yi
Ren, Bing
Wang, Hongwei
Zhang, Xiao
Qiu, Cheng
Liu, Anqi
Liu, Zhanqiang
author_facet Yu, Mingzhi
Wan, Yi
Ren, Bing
Wang, Hongwei
Zhang, Xiao
Qiu, Cheng
Liu, Anqi
Liu, Zhanqiang
author_sort Yu, Mingzhi
collection PubMed
description [Image: see text] Three-dimensional (3D) printing technology has been proved to be a powerful tool for the free-form fabrication of titanium (Ti) implants. However, the surface quality of 3D printed Ti implants is not suitable for clinical application directly. Therefore, surface modification of 3D printed Ti implants is required in order to achieve good biocompatibility and osseointegration. In this study, a novel surface modification method of 3D printed Ti–6Al–4V implants has been proposed, which combined acid etching with hydrothermal treatment to construct micro/nanostructures. Polished TC4 sheets (P), electron beam melting Ti sheets (AE), and micro/nanostructured Ti sheets (AMH) were used in this study to evaluate the effects of different surface morphologies on cellular responses. The surface morphology and 3D topography after treatment were detected via scanning electron microscopy and laser scanning microscopy. The results illustrated that a hierarchical structure comprising micro-valleys and nanowires with a surface roughness of 14.388 μm was successfully constructed. Compared with group P samples, the hydrophilicity of group AMH samples significantly increased with a reduced water contact angle from 54.9° to 4.5°. Cell culture experiments indicated that the micro/nanostructures on the material surface could enhance the cell adhesion and proliferation of MC3T3s. The microstructure could enhance bone-to-implant contact, and the nanostructure could directly interact with some cell membrane receptors. Overall, this study proposes a new strategy to construct micro/nanostructures on the surface of 3D printed Ti–6Al–4V implants and may further serve as a potential modification method for better osteogenesis ability.
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spelling pubmed-77454182020-12-18 3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses Yu, Mingzhi Wan, Yi Ren, Bing Wang, Hongwei Zhang, Xiao Qiu, Cheng Liu, Anqi Liu, Zhanqiang ACS Omega [Image: see text] Three-dimensional (3D) printing technology has been proved to be a powerful tool for the free-form fabrication of titanium (Ti) implants. However, the surface quality of 3D printed Ti implants is not suitable for clinical application directly. Therefore, surface modification of 3D printed Ti implants is required in order to achieve good biocompatibility and osseointegration. In this study, a novel surface modification method of 3D printed Ti–6Al–4V implants has been proposed, which combined acid etching with hydrothermal treatment to construct micro/nanostructures. Polished TC4 sheets (P), electron beam melting Ti sheets (AE), and micro/nanostructured Ti sheets (AMH) were used in this study to evaluate the effects of different surface morphologies on cellular responses. The surface morphology and 3D topography after treatment were detected via scanning electron microscopy and laser scanning microscopy. The results illustrated that a hierarchical structure comprising micro-valleys and nanowires with a surface roughness of 14.388 μm was successfully constructed. Compared with group P samples, the hydrophilicity of group AMH samples significantly increased with a reduced water contact angle from 54.9° to 4.5°. Cell culture experiments indicated that the micro/nanostructures on the material surface could enhance the cell adhesion and proliferation of MC3T3s. The microstructure could enhance bone-to-implant contact, and the nanostructure could directly interact with some cell membrane receptors. Overall, this study proposes a new strategy to construct micro/nanostructures on the surface of 3D printed Ti–6Al–4V implants and may further serve as a potential modification method for better osteogenesis ability. American Chemical Society 2020-12-04 /pmc/articles/PMC7745418/ /pubmed/33344827 http://dx.doi.org/10.1021/acsomega.0c04373 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Yu, Mingzhi
Wan, Yi
Ren, Bing
Wang, Hongwei
Zhang, Xiao
Qiu, Cheng
Liu, Anqi
Liu, Zhanqiang
3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses
title 3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses
title_full 3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses
title_fullStr 3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses
title_full_unstemmed 3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses
title_short 3D Printed Ti–6Al–4V Implant with a Micro/Nanostructured Surface and Its Cellular Responses
title_sort 3d printed ti–6al–4v implant with a micro/nanostructured surface and its cellular responses
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745418/
https://www.ncbi.nlm.nih.gov/pubmed/33344827
http://dx.doi.org/10.1021/acsomega.0c04373
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