Electrochemical and biological behaviors of porous titania (TiO2) in simulated body fluids for implantation in human bodies

被引:41
作者
Badawy, Waheed A. [1 ]
Fathi, Ahlam M. [2 ]
El-Sherief, Rabab M. [1 ]
Fadl-Allah, Sahar A. [1 ]
机构
[1] Cairo Univ, Fac Sci, Dept Chem, Giza, Egypt
[2] Natl Res Ctr, Dept Phys Chem, Giza, Egypt
关键词
Adsorption; Biological compatibility; Bone implants; Calcium phosphate; Dental applications; Titanium oxide; ANODIC-OXIDATION; APATITE; FILM; BIOMATERIALS; TI6AL4V; ABILITY; ALLOYS; GROWTH; METAL; CP;
D O I
10.1016/j.jallcom.2008.08.061
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Porous titania, TiO2, films on Ti substrates were prepared electrochemically. The adsorption of biologically compatible ions, like calcium and phosphate ions, on the formed TiO2 films was investigated by elect to chemical impedance spectroscopy, EIS, and electron diffraction X-ray, EDX, techniques. The morphology of the formed oxide films and the adsorbed layers on their surfaces was investigated by the scanning electron microscopy, SEM. The experimental impedance data were fitted to theoretical data according to proposed equivalent circuit models. The impedance data fitting enabled the explanation of the structure of the oxide film and the adsorption phenomena occurred on its surface. The film characteristics under different conditions were discussed and the adsorption of Ca2+ and PO43- was explained. The results have shown that the oxide films formed potentiostatically on Ti in H2O2 containing H2SO4 are capable to adsorb biologically compatible ions. The adsorbed layer thickness was found to increase with the increase of concentration of calcium ions present in the ambient electrolyte. The biocompatibility of these materials depends essentially on the apatite-forming ability of TiO2 due to calcium ion incorporation in the adsorbed films. The formed oxide films with the relatively thick apatite-like adsorbed layer are good implants for bone surgeries and dental applications. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:911 / 916
页数:6
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