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Scale transitions in bone elasticity from the nanometer level up to cortical and trabecular bone

机译:从纳米水平的骨骼弹性转变为皮质和小梁骨

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Our goal, the prediction of the anisotropic elastic properties of bone on the basis of an appropriate description of its hierarchical organization, has been a research challenge for decades. However (cited from, p. 177), "so far", in 2001, "no one has developed a theory of bone structure that can satisfactorily explain its mechanical behavior on the basis of its internal structure and composition." This drawback seems to result from an insufficient nanostructural representation of the extracellular bone matrix or ultrastructure, defined at a characteristic length of 5 to 10 microns. We derived the morphology governing the ultrastructural elasticity from ultrasonic and chemical experiments, through energy considerations. Here we show how to integrate this morphology and the microporosity into a unified continuum micromechanics model, based on intrinsic stiffness values for bone mineral, collagen, non-mineral matter, and marrow, which are valid for all types of mineralized tissues in vertebrates. The volume fractions of the phases (mineral, collagen, microporosity), representing the composition of different tissues, serve as model input. Predicted elasticity tensors (output of the model) agree very well with experimental data.
机译:我们的目标是在其分层组织的适当描述的基础上预测骨骼的各向异性弹性特性,几十年来挑战。然而,2001年,“到目前为止,”迄今为止,“迄今为止”,“没有人开发出骨骼结构理论,可以在其内部结构和组成的基础上令人满意地解释其机械行为。”该缺点似乎是由细胞外骨基质或超微结构的不足表示的不足,以5至10微米的特征长度定义。通过能量考虑,我们通过能量考虑来源于超声波和化学实验的超微结构弹性的形态。在这里,我们展示了如何基于骨矿物,胶原蛋白,非矿物质和骨髓的内在刚度值将这种形态和微孔集成为统一的连续内微机械模型,这对于脊椎动物中的所有类型的矿化组织有效。相阶段的体积分数(矿物质,胶原蛋白,微孔率),代表不同组织的组成,用作模型输入。预测弹性张量(模型的输出)与实验数据非常吻合。

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