UV-enhanced bioactivity and cell response of micro-arc oxidized titania coatings

被引:209
作者
Han, Yong [1 ]
Chen, Donghui [1 ]
Sun, Jifeng [1 ]
Zhang, Yumei [2 ]
Xu, Kewei [1 ]
机构
[1] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
[2] Fourth Mil Med Univ, Sch Stomatol, Xian 710032, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
UV-light; titania coating; bioactivity; cell response; micro-arc oxidation;
D O I
10.1016/j.actbio.2008.03.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Using ultraviolet (UV) irradiation of micro-arc oxidized (MAO) titania coating in distilled water for 0.5 and 2 h, we have achieved an enhanced bioactivity and cell response to titania surface. The MAO coating appears porous and predominantly consists of nanocrystallized anatase TiO2. Compared with the MAO coating, the UV-irradiated coatings do not exhibit any obvious change in surface roughness, morphology, grain size and phase component; however, they have more abundant basic Ti-OH groups and become more hydrophilic because the water contact angle decreases significantly from 17.9 +/- 0.8 degrees to 0 degrees. In simulated body fluid (SBF), bonelike apatite-forming ability is significantly stronger on the UV-irradiated coatings than the MAO coating. SaOS-2 human osteoblast-like cell attachment, proliferation and alkaline phosphatase of the cell are greater on the UV-irradiated coatings relative to the MAO coating. UV irradiation of titania results in the conversion of Ti4+ to Ti3+ and the generation of oxygen vacancies, which could react with the absorbed water to form basic Ti-OH groups. The enhanced bioactivity and cell response of the UV-irradiated coatings are proven to result from abundant Ti-OH groups on the coating surfaces. After storing the UV-irradiated coatings in the dark for two weeks, the basic Ti-OH groups on the coatings slightly decrease in amount and can induce apatite formation after a short period of SBF immersion, and show relative long-term stability. (C) 2008 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1518 / 1529
页数:12
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