Landrigan Matthew D, Roeder Ryan K
Department of Aerospace and Mechanical Engineering, The University of Notre Dame, Notre Dame, IN 46556, USA.
J Biomech. 2009 Jun 19;42(9):1212-7. doi: 10.1016/j.jbiomech.2009.03.016. Epub 2009 Apr 25.
Accumulation of fatigue microdamage in cortical bone specimens is commonly measured by a modulus or stiffness degradation after normalizing tissue heterogeneity by the initial modulus or stiffness of each specimen measured during a preloading step. In the first experiment, the initial specimen modulus defined using linear elastic beam theory (LEBT) was shown to be nonlinearly dependent on the preload level, which subsequently caused systematic error in the amount and rate of damage accumulation measured by the LEBT modulus degradation. Therefore, the secant modulus is recommended for measurements of the initial specimen modulus during preloading. In the second experiment, different measures of mechanical degradation were directly compared and shown to result in widely varying estimates of damage accumulation during fatigue. After loading to 400,000 cycles, the normalized LEBT modulus decreased by 26% and the creep strain ratio decreased by 58%, but the normalized secant modulus experienced no degradation and histology revealed no significant differences in microcrack density. The LEBT modulus was shown to include the combined effect of both elastic (recovered) and creep (accumulated) strain. Therefore, at minimum, both the secant modulus and creep should be measured throughout a test to most accurately indicate damage accumulation and account for different damage mechanisms. Histology revealed indentation of tissue adjacent to roller supports, with significant sub-surface damage beneath large indentations, accounting for 22% of the creep strain on average. The indentation of roller supports resulted in inflated measures of the LEBT modulus degradation and creep. The results of this study suggest that investigations of fatigue microdamage in cortical bone should avoid the use of four-point bending unless no other option is possible.
通过在预加载步骤中测量每个标本的初始模量或刚度对组织异质性进行归一化后,皮质骨标本中疲劳微损伤的积累通常通过模量或刚度的降解来测量。在第一个实验中,使用线性弹性梁理论(LEBT)定义的初始标本模量被证明与预加载水平呈非线性相关,这随后导致了通过LEBT模量降解测量的损伤积累量和速率出现系统误差。因此,建议在预加载期间使用割线模量来测量初始标本模量。在第二个实验中,直接比较了不同的机械降解测量方法,结果表明这些方法在疲劳过程中对损伤积累的估计差异很大。加载至400,000次循环后,归一化的LEBT模量下降了26%,蠕变应变率下降了58%,但归一化的割线模量没有降解,组织学显示微裂纹密度没有显著差异。LEBT模量被证明包括弹性(恢复)应变和蠕变(积累)应变的综合影响。因此,至少在整个测试过程中应同时测量割线模量和蠕变,以最准确地指示损伤积累并考虑不同的损伤机制。组织学显示滚轮支撑附近的组织有压痕,大压痕下方有明显的亚表面损伤,平均占蠕变应变的22%。滚轮支撑的压痕导致LEBT模量降解和蠕变的测量值虚高。本研究结果表明,除非别无选择,否则对皮质骨疲劳微损伤的研究应避免使用四点弯曲。