Mechanical Engineering Department, McGill University, Montreal, Quebec H3G 1A4, Canada.
Division of Orthopaedics, Department of Surgery, McGill University, Montreal, Quebec H3G 1A4, Canada.
Acta Biomater. 2017 Nov;63:350-368. doi: 10.1016/j.actbio.2017.09.013. Epub 2017 Sep 18.
Porous biomaterials can be additively manufactured with micro-architecture tailored to satisfy the stringent mechano-biological requirements imposed by bone replacement implants. In a previous investigation, we introduced structurally porous biomaterials, featuring strength five times stronger than commercially available porous materials, and confirmed their bone ingrowth capability in an in vivo canine model. While encouraging, the manufactured biomaterials showed geometric mismatches between their internal porous architecture and that of its as-designed counterpart, as well as discrepancies between predicted and tested mechanical properties, issues not fully elucidated. In this work, we propose a systematic approach integrating computed tomography, mechanical testing, and statistical analysis of geometric imperfections to generate statistical based numerical models of high-strength additively manufactured porous biomaterials. The method is used to develop morphology and mechanical maps that illustrate the role played by pore size, porosity, strut thickness, and topology on the relations governing their elastic modulus and compressive yield strength. Overall, there are mismatches between the mechanical properties of ideal-geometry models and as-manufactured porous biomaterials with average errors of 49% and 41% respectively for compressive elastic modulus and yield strength. The proposed methodology gives more accurate predictions for the compressive stiffness and the compressive strength properties with a reduction of the average error to 11% and 7.6%. The implications of the results and the methodology here introduced are discussed in the relevant biomechanical and clinical context, with insight that highlights promises and limitations of additively manufactured porous biomaterials for load-bearing bone replacement implants.
In this work, we perform mechanical characterization of load-bearing porous biomaterials for bone replacement over their entire design space. Results capture the shift in geometry and mechanical properties between as-designed and as-manufactured biomaterials induced by additive manufacturing. Characterization of this shift is crucial to ensure appropriate manufacturing of bone replacement implants that enable biological fixation through bone ingrowth as well as mechanical property harmonization with the native bone tissue. In addition, we propose a method to include manufacturing imperfections in the numerical models that can reduce the discrepancy between predicted and tested properties. The results give insight into the use of structurally porous biomaterials for the design and additive fabrication of load-bearing implants for bone replacement.
多孔生物材料可以通过微结构的添加制造来制造,以满足骨替代植入物所施加的严格的机械生物学要求。在之前的研究中,我们引入了结构多孔生物材料,其强度比市售多孔材料强五倍,并在体内犬模型中证实了其骨内生长能力。虽然令人鼓舞,但制造的生物材料显示出其内部多孔结构与其设计对应物之间的几何不匹配,以及预测和测试的机械性能之间的差异,这些问题尚未完全阐明。在这项工作中,我们提出了一种系统的方法,该方法结合了计算机断层扫描、机械测试和几何缺陷的统计分析,为高强度增材制造多孔生物材料生成基于统计的数值模型。该方法用于生成形貌和力学图谱,说明了孔径、孔隙率、支柱厚度和拓扑结构对控制其弹性模量和抗压屈服强度的关系的作用。总体而言,理想几何模型的力学性能与制造的多孔生物材料之间存在不匹配,抗压弹性模量和屈服强度的平均误差分别为 49%和 41%。所提出的方法对压缩刚度和抗压强度特性的预测更为准确,平均误差降低到 11%和 7.6%。讨论了相关生物力学和临床背景下结果和提出的方法的意义,强调了增材制造多孔生物材料在承载骨替代植入物中的潜力和局限性。
在这项工作中,我们对用于骨替代的承载多孔生物材料进行了整个设计空间的力学特性研究。结果捕捉到了增材制造引起的设计和制造生物材料之间的几何形状和机械性能的转变。这种转变的特性对于确保适当制造骨替代植入物至关重要,这些植入物可以通过骨内生长实现生物学固定,并与天然骨组织的机械性能协调一致。此外,我们提出了一种在数值模型中包含制造缺陷的方法,可以减少预测和测试性能之间的差异。结果深入了解了结构多孔生物材料在用于骨替代的承载植入物的设计和增材制造中的应用。