生物复合材料
材料科学
磷灰石
模拟体液
复合材料
复合数
结晶度
聚合物
生物活性玻璃
化学工程
扫描电子显微镜
工程类
作者
Xiaoyan Cao,Na Tian,Xiang Dong,Cheng‐Kung Cheng
出处
期刊:Polymers
[Multidisciplinary Digital Publishing Institute]
日期:2019-05-06
卷期号:11 (5): 812-812
被引量:6
标识
DOI:10.3390/polym11050812
摘要
The emergence of polylactide composites reinforced with bioresorbable silicate glass fibers has allowed for the long-term success of biodegradable polymers in load-bearing orthopedic applications. However, few studies have reported on the degradation behavior and bioactivity of such biocomposites. The aim of this work was to investigate the degradation behavior and in vitro bioactivity of a novel biocomposite pin composed of bioresorbable continuous glass fibers and poly-L-D-lactide in simulated body fluid for 78 weeks. As the materials degraded, periodic spiral delamination formed microtubes and funnel-shaped structures in the biocomposite pins. It was speculated that the direction of degradation, from both ends towards the middle of the fibers and from the surface through to the bulk of the polymer matrix, could facilitate bone healing. Following immersion in simulated body fluid, a bone-like apatite layer formed on the biocomposite pins which had a similar composition and structure to natural bone. The sheet- and needle-like apatite nanostructure was doped with sodium, magnesium, and carbonate ions, which acted to lower the Ca/P atomic ratio to less than the stoichiometric apatite and presented a calcium-deficient apatite with low crystallinity. These findings demonstrated the bioactivity of the new biocomposite pins in vitro and their excellent potential for load-bearing applications.
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