Poly(L-lactic acid)/Hydroxyapatite/Collagen Composite Coatings on AZ31 Magnesium Alloy for Biomedical Application
详细信息    查看全文 | 下载全文 | 推荐本文 |
  • 作者:WANG Zhen-linYAN Yu-huaWAN TaoYANG Hui
  • 会议时间:2014-04-21
  • 关键词:Poly(L-lactic acid) ; Hydroxyapatite ; Collagen ; Composite coating ; Magnesium alloy
  • 作者单位:WANG Zhen-lin,YANG Hui(College of Materials Science and Engineering, Chongqing University of Technology, Chongqing 400054, China)YAN Yu-hua,WAN Tao(Research Centre of Biomaterials and Engineering, Wuhan University of Technology, Wuhan 430070, China)
  • 母体文献:2014(重庆)国际表面工程论坛暨第十二届全国表面工程·电镀与精饰年会论文集
  • 会议名称:2014(重庆)国际表面工程论坛暨第十二届全国表面工程·电镀与精饰年会
  • 会议地点:重庆
  • 主办单位:中国表面工程协会
  • 语种:chi
摘要
Hydroxyapatite/collagen composite (HAC) was preliminarily fabricated by biomineralization, the bioactive poly(L-lactic acid)/HAC composite coatings were spin coated on AZ31 magnesium alloy using poly(L-lactic acid) solution mixed with HAC particles, the resultant materials and coatings were characterized in structure and properties, furthermore the in-vitro degradation behavior in 1.5-fold Hank's solution was investigated.The results show that HAC composite achieved chemical bonding between hydroxyapatite and collagen similar to natural bone, composite coatings on AZ31 magnesium alloy retained the bioactive functional groups of the componential materials and improved the corrosion resistance of Mg alloy, the mass fraction of HAC particles incorporated into the composite influenced the porous architecture and thus the corrosion resistance of the composite coating due to phase separation cause as well as volume concentration effects.Composite coatings curbed the sharp rising of pH value and inhibited the released Mg2+ from substrate to extensive degree, and the degradation behavior was supposed to be correlated to microstructure of the coating as well as the synergistic reactions among alkaline and acidic degraded products.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700