Ahmad Agha Nezha, Willumeit-Römer Regine, Laipple Daniel, Luthringer Bérengère, Feyerabend Frank
Division of Metallic Biomaterials, Institute of Material Research, Helmholtz-Zentrum Geesthacht, Geesthacht, Germany.
Division of Materials Physics, Institute of Material Research, Helmholtz-Zentrum Geesthacht, Geesthacht, Germany.
PLoS One. 2016 Jun 21;11(6):e0157874. doi: 10.1371/journal.pone.0157874. eCollection 2016.
Magnesium alloys have been identified as a new generation material of orthopaedic implants. In vitro setups mimicking physiological conditions are promising for material / degradation analysis prior to in vivo studies however the direct influence of cell on the degradation mechanism has never been investigated. For the first time, the direct, active, influence of human primary osteoblasts on magnesium-based materials (pure magnesium, Mg-2Ag and Mg-10Gd alloys) is studied for up to 14 days. Several parameters such as composition of the degradation interface (directly beneath the cells) are analysed with a scanning electron microscope equipped with energy dispersive X-ray and focused ion beam. Furthermore, influence of the materials on cell metabolism is examined via different parameters like active mineralisation process. The results are highlighting the influences of the selected alloying element on the initial cells metabolic activity.
镁合金已被确定为新一代骨科植入材料。在体内研究之前,模拟生理条件的体外实验装置对于材料/降解分析很有前景,然而,细胞对降解机制的直接影响从未被研究过。首次对人类原代成骨细胞对镁基材料(纯镁、Mg-2Ag和Mg-10Gd合金)长达14天的直接、积极影响进行了研究。使用配备能量色散X射线和聚焦离子束的扫描电子显微镜分析了几个参数,如降解界面(细胞正下方)的组成。此外,通过活性矿化过程等不同参数研究了材料对细胞代谢的影响。结果突出了所选合金元素对初始细胞代谢活性的影响。