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Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface

[Image: see text] Zirconia has become an excellent choice of dental implants because of its excellent mechanical strength, aesthetic, and biocompatibility. Although some studies have shown ultraviolet (UV) irradiation is effective to photofunctionalize dental zirconia that can improve osteoblastic f...

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Autores principales: Han, Aifang, Ding, Hao, Tsoi, James Kit Hon, Imazato, Satoshi, Matinlinna, Jukka P., Chen, Zhuofan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081443/
https://www.ncbi.nlm.nih.gov/pubmed/32201799
http://dx.doi.org/10.1021/acsomega.9b04123
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author Han, Aifang
Ding, Hao
Tsoi, James Kit Hon
Imazato, Satoshi
Matinlinna, Jukka P.
Chen, Zhuofan
author_facet Han, Aifang
Ding, Hao
Tsoi, James Kit Hon
Imazato, Satoshi
Matinlinna, Jukka P.
Chen, Zhuofan
author_sort Han, Aifang
collection PubMed
description [Image: see text] Zirconia has become an excellent choice of dental implants because of its excellent mechanical strength, aesthetic, and biocompatibility. Although some studies have shown ultraviolet (UV) irradiation is effective to photofunctionalize dental zirconia that can improve osteoblastic function, the scattered information has not identified the most effective exposure time and wavelength of UV. Herein, this study has investigated the effects of UV irradiation on zirconia after UV-A (365 nm) or UV-C (243 nm) photofunctionalization for different times (15 min, 3 and 24 h). After irradiation, the zirconia surface was analyzed by color spectrophotometry, scanned electron microscopy (SEM), energy-dispersive X-ray spectrometry, water contact angle (WCA) with goniometer, and X-ray diffraction. Osteoblastic (MC3T3-E1) cells were cultured on zirconia discs and evaluated with a CCK-8 test kit for cell proliferation (3 h and 1 day) and with alkaline phosphatase (ALP) activity (14 days). Significant color change (ΔE) was observed by irradiating with UV-C for 15 min (1.99), 3 h (1.92), and 24 h (3.35), whereas only minute changes were observed with UV-A (respectively, ΔE: 0.18, 0.14, 0.57). No surface textural changes were observed nor a monoclinic phase was detected on both the UV-A and UV-C irradiated samples. UV-C significantly decreased the C/Zr ratios and WCA, with irradiating for 24 h presenting the lowest values, and it was the only condition to give significantly higher ALP activity at 14 days (p < 0.05) and CCK-8 values for 1 day culture (p < 0.05). It is concluded that UV-C (but not UV-A) irradiation can significantly change the aesthetic in color, and only prolonged 24 h UV-C irradiation can enhance MC3T3-E1 cell adhesion on zirconia by photofunctionalization.
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spelling pubmed-70814432020-03-20 Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface Han, Aifang Ding, Hao Tsoi, James Kit Hon Imazato, Satoshi Matinlinna, Jukka P. Chen, Zhuofan ACS Omega [Image: see text] Zirconia has become an excellent choice of dental implants because of its excellent mechanical strength, aesthetic, and biocompatibility. Although some studies have shown ultraviolet (UV) irradiation is effective to photofunctionalize dental zirconia that can improve osteoblastic function, the scattered information has not identified the most effective exposure time and wavelength of UV. Herein, this study has investigated the effects of UV irradiation on zirconia after UV-A (365 nm) or UV-C (243 nm) photofunctionalization for different times (15 min, 3 and 24 h). After irradiation, the zirconia surface was analyzed by color spectrophotometry, scanned electron microscopy (SEM), energy-dispersive X-ray spectrometry, water contact angle (WCA) with goniometer, and X-ray diffraction. Osteoblastic (MC3T3-E1) cells were cultured on zirconia discs and evaluated with a CCK-8 test kit for cell proliferation (3 h and 1 day) and with alkaline phosphatase (ALP) activity (14 days). Significant color change (ΔE) was observed by irradiating with UV-C for 15 min (1.99), 3 h (1.92), and 24 h (3.35), whereas only minute changes were observed with UV-A (respectively, ΔE: 0.18, 0.14, 0.57). No surface textural changes were observed nor a monoclinic phase was detected on both the UV-A and UV-C irradiated samples. UV-C significantly decreased the C/Zr ratios and WCA, with irradiating for 24 h presenting the lowest values, and it was the only condition to give significantly higher ALP activity at 14 days (p < 0.05) and CCK-8 values for 1 day culture (p < 0.05). It is concluded that UV-C (but not UV-A) irradiation can significantly change the aesthetic in color, and only prolonged 24 h UV-C irradiation can enhance MC3T3-E1 cell adhesion on zirconia by photofunctionalization. American Chemical Society 2020-03-05 /pmc/articles/PMC7081443/ /pubmed/32201799 http://dx.doi.org/10.1021/acsomega.9b04123 Text en Copyright © 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 Han, Aifang
Ding, Hao
Tsoi, James Kit Hon
Imazato, Satoshi
Matinlinna, Jukka P.
Chen, Zhuofan
Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface
title Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface
title_full Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface
title_fullStr Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface
title_full_unstemmed Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface
title_short Prolonged UV-C Irradiation is a Double-Edged Sword on the Zirconia Surface
title_sort prolonged uv-c irradiation is a double-edged sword on the zirconia surface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081443/
https://www.ncbi.nlm.nih.gov/pubmed/32201799
http://dx.doi.org/10.1021/acsomega.9b04123
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