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通过 microCT 密度计算和纳米压痕测试评估再生和未受伤的小鼠趾骨杨氏模量的差异。

Evaluating differences in Young's Modulus of regenerated and uninjured mouse digit bone through microCT density-based calculation and nanoindentation testing.

机构信息

Department of Biological & Agricultural Engineering, Louisiana State University, 149 E.B. Doran Building, Baton Rouge, LA 70803, USA.

Department of Surgery, Tulane School of Medicine, 1430 Tulane Ave, New Orleans, LA 70112, USA.

出版信息

J Biomech. 2022 Oct;143:111271. doi: 10.1016/j.jbiomech.2022.111271. Epub 2022 Aug 27.

Abstract

The mouse digit tip amputation model is an excellent model of bone regeneration, but its size and shape present an obstacle for biomechanical testing. As a result, assessing the structural quality of the regenerated bone in this model has focused on mineral density and bone architecture analysis. Here we describe an image-processing based method for assessment of mechanical properties in the regenerated digit by using micro-computed tomography mineral density data to calculate spatially discrete Young's modulus values throughout the entire distal third phalange. Further, we validate this method through comparison to nanoindentation-measured values for Young's modulus. Application to a set of regenerated and unamputated digits shows that regenerated bone has a lower Young's modulus compared to the uninjured digit, with a similar trend for experimental hardness values. Importantly, this method heightens the utility of the digit regeneration model, allows for more impactful treatment evaluation using the model, and introduces an analysis platform that can be used for other bones that do not conform to a standard long-bone model.

摘要

鼠标指尖截断模型是一种优秀的骨再生模型,但它的大小和形状对生物力学测试构成了障碍。因此,评估该模型中再生骨的结构质量主要集中在矿物质密度和骨结构分析上。在这里,我们描述了一种基于图像处理的方法,通过使用微计算机断层扫描矿物质密度数据来计算整个远端第三指骨的空间离散杨氏模量值,从而评估再生指尖的力学性能。此外,我们通过与纳米压痕测量的杨氏模量值进行比较来验证该方法。将该方法应用于一组再生和未截肢的指尖,结果表明再生骨的杨氏模量比未受伤的指尖低,实验硬度值也有类似的趋势。重要的是,这种方法提高了指尖再生模型的实用性,允许在该模型中进行更有影响力的治疗评估,并引入了一个分析平台,可用于其他不符合标准长骨模型的骨骼。

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引用本文的文献

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Age-Dependent Changes in Bone Architecture, Patterning, and Biomechanics During Skeletal Regeneration.
Front Cell Dev Biol. 2021 Oct 13;9:749055. doi: 10.3389/fcell.2021.749055. eCollection 2021.

本文引用的文献

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Front Cell Dev Biol. 2021 Oct 13;9:749055. doi: 10.3389/fcell.2021.749055. eCollection 2021.
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