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Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation

Zirconia is a superior implant material owing to its high mechanical strength, durable corrosion resistance, superior aesthetic effect and excellent biocompatibility. However, the bioactivity of zirconia surfaces remains a great challenge for implant osseointegration. A titania (TiO(2)) coating was...

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Autores principales: Tang, Shuang, Wang, Yan, Zong, Zhenyu, Ding, Ning, Zhang, Zutai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393212/
https://www.ncbi.nlm.nih.gov/pubmed/36003530
http://dx.doi.org/10.3389/fbioe.2022.945869
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author Tang, Shuang
Wang, Yan
Zong, Zhenyu
Ding, Ning
Zhang, Zutai
author_facet Tang, Shuang
Wang, Yan
Zong, Zhenyu
Ding, Ning
Zhang, Zutai
author_sort Tang, Shuang
collection PubMed
description Zirconia is a superior implant material owing to its high mechanical strength, durable corrosion resistance, superior aesthetic effect and excellent biocompatibility. However, the bioactivity of zirconia surfaces remains a great challenge for implant osseointegration. A titania (TiO(2)) coating was innovatively synthesized on the surface of zirconia by infiltration in a suspension of zirconium oxychloride and titania for dense sintering. Subsequently, the coating was subjected to ultraviolet (UV) light to enhance the biological inertness of zirconia. Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and contact angle analysis were conducted to confirm the surface characteristics. Afterwards, in vitro assessments of cell adhesion, proliferation and osteogenic differentiation of MC3T3-E1 cells were performed. Zirconia samples were implanted into rat femurs to assess biocompatibility and host tissue response in vivo. Micro-CT evaluation and histological testing were conducted. After UV irradiation, the content of hydroxyl groups and hydrophilicity of TiO(2)-modified zirconia were significantly increased. The results of in vitro experiments showed that TiO(2)-modified zirconia subjected to UV light could promote cell proliferation and spreading, enhance ALP activity and the degree of mineralization, and upregulate osteogenesis-related genes. Furthermore, in vivo assessments confirmed that UV-irradiated TiO(2)-modified zirconia implants maximized the promotion of osseointegration. TiO(2)-modified zirconia after UV treatment will have broad clinical application prospects in improving the osseointegration of zirconia implants.
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spelling pubmed-93932122022-08-23 Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation Tang, Shuang Wang, Yan Zong, Zhenyu Ding, Ning Zhang, Zutai Front Bioeng Biotechnol Bioengineering and Biotechnology Zirconia is a superior implant material owing to its high mechanical strength, durable corrosion resistance, superior aesthetic effect and excellent biocompatibility. However, the bioactivity of zirconia surfaces remains a great challenge for implant osseointegration. A titania (TiO(2)) coating was innovatively synthesized on the surface of zirconia by infiltration in a suspension of zirconium oxychloride and titania for dense sintering. Subsequently, the coating was subjected to ultraviolet (UV) light to enhance the biological inertness of zirconia. Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and contact angle analysis were conducted to confirm the surface characteristics. Afterwards, in vitro assessments of cell adhesion, proliferation and osteogenic differentiation of MC3T3-E1 cells were performed. Zirconia samples were implanted into rat femurs to assess biocompatibility and host tissue response in vivo. Micro-CT evaluation and histological testing were conducted. After UV irradiation, the content of hydroxyl groups and hydrophilicity of TiO(2)-modified zirconia were significantly increased. The results of in vitro experiments showed that TiO(2)-modified zirconia subjected to UV light could promote cell proliferation and spreading, enhance ALP activity and the degree of mineralization, and upregulate osteogenesis-related genes. Furthermore, in vivo assessments confirmed that UV-irradiated TiO(2)-modified zirconia implants maximized the promotion of osseointegration. TiO(2)-modified zirconia after UV treatment will have broad clinical application prospects in improving the osseointegration of zirconia implants. Frontiers Media S.A. 2022-08-08 /pmc/articles/PMC9393212/ /pubmed/36003530 http://dx.doi.org/10.3389/fbioe.2022.945869 Text en Copyright © 2022 Tang, Wang, Zong, Ding and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Tang, Shuang
Wang, Yan
Zong, Zhenyu
Ding, Ning
Zhang, Zutai
Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
title Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
title_full Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
title_fullStr Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
title_full_unstemmed Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
title_short Enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
title_sort enhanced osteogenic activity of titania-modified zirconia implant by ultraviolet irradiation
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393212/
https://www.ncbi.nlm.nih.gov/pubmed/36003530
http://dx.doi.org/10.3389/fbioe.2022.945869
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