Iron-Gold Composites for Biodegradable Implants: In Vitro Investigation on Biodegradation and Biomineralization

被引:6
作者
Rabeeh, V. P. Muhammad [1 ]
Rahim, Shebeer A. A. [2 ]
Parambath, Sijina Kinattingara [3 ]
Rajanikant, G. K. [3 ]
Hanas, T. [1 ,2 ]
机构
[1] Natl Inst Technol Calicut, Sch Mat Sci & Engn, Nanomat Res Lab, Kozhikode 673601, India
[2] Natl Inst Technol Calicut, Dept Mech Engn, Kozhikode 673601, India
[3] Natl Inst Technol Calicut, Sch Biotechnol, Kozhikode 673601, India
关键词
composite; powder metallurgy; biodegradableimplant; In vitro; biometal; biomineralization; PURE IRON; FE-PD; DEGRADATION; ALLOYS; BIOCOMPATIBILITY; CORROSION; CYTOCOMPATIBILITY; MICROSTRUCTURE; EVOLUTION; PHOSPHATE;
D O I
10.1021/acsbiomaterials.3c00513
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The biocompatibility and biodegradation of iron (Fe)make it asuitable candidate for developing biodegradable metallic implants.However, the degradation rate of Fe in a physiological environmentis extremely slow and needs to be enhanced to a rate compatible withtissue growth. Incorporating noble metals improves the Fe degradationrate by forming galvanic couples. This study incorporated gold (Au)into Fe at very low concentrations of 1.25 and 2.37 mu g/g toimprove the degradation rate. The electrochemical corrosion test ofthe samples revealed that the Au-containing samples showed a four-timeand nine-time faster degradation rate than pure Fe. Furthermore, theimmersion test and long-term electrochemical impedance spectroscopyconducted in simulated body fluid (SBF) revealed that the Au-incorporatedsamples exhibited increased bioactivity and degraded faster than pureFe. Integrating nanogold into a Fe matrix increased the in situ formationof hydroxyapatite on the sample's surface and did not causetoxicity to L929-murine fibroblast cells. It is suggested that Fe-Aucomposites with low concentrations of Au can be used to tailor thebiodegradation rate and promote the biomineralization of Fe-basedimplants in the physiological environment.
引用
收藏
页码:4255 / 4268
页数:14
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