Agha Nezha Ahmad, Feyerabend Frank, Mihailova Boriana, Heidrich Stefanie, Bismayer Ulrich, Willumeit-Römer Regine
Helmholtz-Zentrum Geesthacht, Institute of Material Research, Division of Metallic Biomaterials, Max-Planck-Str. 1, 21502 Geesthacht.
University of Hamburg, Department of Earth Sciences, Grindelallee 48, 20146 Hamburg, Germany.
Mater Sci Eng C Mater Biol Appl. 2016 Jan 1;58:817-25. doi: 10.1016/j.msec.2015.09.067. Epub 2015 Sep 18.
Magnesium and its alloys have considerable potential for orthopedic applications. During the degradation process the interface between material and tissue is continuously changing. Moreover, too fast or uncontrolled degradation is detrimental for the outcome in vivo. Therefore in vitro setups utilizing physiological conditions are promising for the material/degradation analysis prior to animal experiments. The aim of this study is to elucidate the influence of inorganic salts contributing to the blood buffering capacity on degradation. Extruded pure magnesium samples were immersed under cell culture conditions for 3 and 10 days. Hank's balanced salt solution without calcium and magnesium (HBSS) plus 10% of fetal bovine serum (FBS) was used as the basic immersion medium. Additionally, different inorganic salts were added with respect to concentration in Dulbecco's modified Eagle's medium (DMEM, in vitro model) and human plasma (in vivo model) to form 12 different immersion media. Influences on the surrounding environment were observed by measuring pH and osmolality. The degradation interface was analyzed by electron-induced X-ray emission (EIXE) spectroscopy, including chemical-element mappings and electron microprobe analysis, as well as Fourier transform infrared reflection micro-spectroscopy (FTIR).
镁及其合金在骨科应用方面具有相当大的潜力。在降解过程中,材料与组织之间的界面不断变化。此外,过快或不受控制的降解对体内结果不利。因此,利用生理条件的体外实验装置对于在动物实验之前进行材料/降解分析很有前景。本研究的目的是阐明有助于血液缓冲能力的无机盐对降解的影响。将挤压纯镁样品在细胞培养条件下浸泡3天和10天。不含钙和镁的汉克斯平衡盐溶液(HBSS)加10%胎牛血清(FBS)用作基本浸泡培养基。此外,根据杜尔贝科改良伊格尔培养基(DMEM,体外模型)和人血浆(体内模型)中的浓度添加不同的无机盐,以形成12种不同的浸泡培养基。通过测量pH值和渗透压来观察对周围环境的影响。通过电子诱导X射线发射(EIXE)光谱分析降解界面,包括化学元素映射和电子微探针分析,以及傅里叶变换红外反射显微光谱(FTIR)。