Effects of concentration of Ag nanoparticles on surface structure and in vitro biological responses of oxide layer on pure titanium via plasma electrolytic oxidation

被引:48
作者
Shin, Kin Ryong [1 ]
Kim, Yeon Sung [1 ]
Kim, Gye Won [1 ]
Yang, Hae Woong [2 ]
Ko, Young Gun [2 ]
Shin, Dong Hyuk [1 ]
机构
[1] Hanyang Univ, Dept Mat Sci & Engn, Ansan 425791, South Korea
[2] Yeungnam Univ, Sch Mat Sci & Engn, Gyongsan 712749, South Korea
基金
新加坡国家研究基金会;
关键词
Plasma electrolytic oxidation; Ag nanoparticles; Bacteria; Simulated body fluid; Osteoblast; ELECTROCHEMICAL SYNTHESIS; SILVER NANOPARTICLES; INFECTIONS; SCALE;
D O I
10.1016/j.apsusc.2015.04.161
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
This study was to investigate how Ag nanoparticles with various concentrations affect the surface structure and in vitro biological properties of oxide layers on the pure titanium produced by a plasma electrolytic oxidation (PEO) process. For this aim, PEO processes were carried out at an AC current density of 100 mA/cm(2) for 300 s in potassium pyrophosphate (K4P2O7) electrolytes containing 0, 0.1, 0.3 and 0.5 g/lAg nanoparticles. Structural investigations using scanning electron microscopy evidenced that the oxide layers showed the successful incorporation of Ag nanoparticles, and the topographical deformation of the porous surface was found when the concentration of Ag nanoparticles was more than 0.1 g/l. Based on the anti-bacterial activity of all oxide layers, the Ag nanoparticles uniformly spread were of considerable importance in triggering the disinfection of E. coli bacteria. The bone forming abilities and cell (MC3T3-E1) proliferation rates of oxide layers produced in electrolytes containing 0 and 0.1 g/l Ag nanoparticles were higher than those containing 0.3 and 0.5 g/lAg nanoparticles. Consequently, the oxide layer on pure titanium via PEO process in the electrolyte with 0.1 g/l Ag nanoparticles exhibited better the bioactivity accompanying the anti-bacterial activity. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:574 / 582
页数:9
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