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用于匹配部位研究矿物质质量分数和胶原纤维方向对板层骨轴向压入模量影响的计算和实验方法学。

Computational and experimental methodology for site-matched investigations of the influence of mineral mass fraction and collagen orientation on the axial indentation modulus of lamellar bone.

机构信息

Institute of Lightweight Design and Structural Biomechanics, Vienna University of Technology, Gusshausstrasse 27-29, A-1040 Vienna, Austria; Department of Applied Physics, Eindhoven University of Technology, P.O. Box 513, NL-5600 MB Eindhoven, The Netherlands.

出版信息

J Mech Behav Biomed Mater. 2013 Dec;28:195-205. doi: 10.1016/j.jmbbm.2013.07.004. Epub 2013 Jul 29.

Abstract

Relationships between mineralization, collagen orientation and indentation modulus were investigated in bone structural units from the mid-shaft of human femora using a site-matched design. Mineral mass fraction, collagen fibril angle and indentation moduli were measured in registered anatomical sites using backscattered electron imaging, polarized light microscopy and nano-indentation, respectively. Theoretical indentation moduli were calculated with a homogenization model from the quantified mineral densities and mean collagen fibril orientations. The average indentation moduli predicted based on local mineralization and collagen fibers arrangement were not significantly different from the average measured experimentally with nanoindentation (p=0.9). Surprisingly, no substantial correlation of the measured indentation moduli with tissue mineralization and/or collagen fiber arrangement was found. Nano-porosity, micro-damage, collagen cross-links, non-collagenous proteins or other parameters affect the indentation measurements. Additional testing/simulation methods need to be considered to properly understand the variability of indentation moduli, beyond the mineralization and collagen arrangement in bone structural units.

摘要

采用匹配部位设计,研究了人体股骨中段骨结构单位的矿化、胶原排列与压痕模量之间的关系。使用背散射电子成像、偏光显微镜和纳米压痕分别在已注册的解剖部位测量矿化物质分数、胶原纤维角和压痕模量。利用从定量矿化密度和平均胶原纤维取向计算得到的均匀化模型计算理论压痕模量。基于局部矿化和胶原纤维排列预测的平均压痕模量与通过纳米压痕实验测量的平均压痕模量没有显著差异(p=0.9)。令人惊讶的是,未发现测量的压痕模量与组织矿化和/或胶原纤维排列之间存在实质性相关性。纳米孔隙率、微损伤、胶原交联、非胶原蛋白或其他参数会影响压痕测量。需要考虑其他测试/模拟方法,以除骨结构单位的矿化和胶原排列外,更好地理解压痕模量的可变性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f086/3843116/27704fc8bd03/fx1.jpg

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