Electrophoretic deposition of nano structured hydroxyapatite coating on AZ91 magnesium alloy implants with different surface treatments

被引:101
作者
Rojaee, Ramin [1 ]
Fathi, Mohammadhossein [1 ,2 ]
Raeissi, Keyvan [3 ]
机构
[1] Isfahan Univ Technol, Dept Mat Engn, Biomat Res Grp, Esfahan 8415683111, Iran
[2] Isfahan Univ Med Sci, Dent Mat Res Ctr, Esfahan, Iran
[3] Isfahan Univ Technol, Dept Mat Engn, Esfahan 8415683111, Iran
关键词
Magnesium; Bio-degradable implant; Nanostructured hydroxyapatite; Electrophoretic deposition; Micro arc oxidation; Fluoride conversion coating; VITRO CORROSION BEHAVIOR; BIOACTIVITY EVALUATION; STAINLESS-STEEL; SPECTRA; MGF2; BIOCOMPATIBILITY; NANOPARTICLES; DEGRADATION; RESISTANCE; OXIDATION;
D O I
10.1016/j.apsusc.2013.08.108
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bio-absorbable magnesium (Mg) based alloys have been introduced as innovative orthopedic implants during recent years. It has been specified that rapid degradation of Mg based alloys in physiological environment should be restrained in order to be utilized in orthopedic trauma fixation and vascular intervention. In this developing field of healthcare materials, micro-arc oxidation (MAO), and MgF2 conversion coating were exploited as surface pre-treatment of AZ91 magnesium alloy to generate a nanostructured hydroxyapatite (n-HAp) coating via electrophoretic deposition (EPD) method. X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and transmission electron microscopy (TEM) techniques were used to characterize the obtained powder and coatings. The potentiodynamic polarization tests were carried out to evaluate the corrosion behavior of the coated and uncoated specimens, and in vitro bioactivity evaluation were performed in simulated body fluid. Results revealed that the MAO/n-HAp coated AZ91 Mg alloy samples with a rough topography and lower corrosion current density leads to a lower Mg degradation rate accompanied by high bioactivity. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:664 / 673
页数:10
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