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A new biological bone remodeling in silico model combined with advanced discretization methods

机译:结合先进离散化方法的新型计算机模拟生物学骨重建模型

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摘要

Bone remodeling remains a highly researched topic investigated by many strands of science. The main purpose of this work is formulating a new computational framework for biological simulation, extending the version of the bone remodeling model previously proposed by Komarova. Thus, considering only the biological aspect of the remodeling process, the action of osteoclasts and osteoblasts is taken into account as well as its impact on bone mass. It is conducted a spatiotemporal analysis of a remodeling cycle obtaining a dynamic behavior of bone cells very similar to the biological process already described in the literature. The numerical example used is based on bone images obtained with scanning electron microscopy. During simulation, it is possible to observe the variation of bone's architecture through isomaps. These maps are obtained through the combination of biological bone remodeling models with three distinct numerical techniques-finite element method (FEM), radial point interpolation method (RPIM), and natural neighbor radial point interpolation method (NNRPIM). A study combining these numerical techniques allows to compare their performance. Ultimately, this work supports the inclusion of meshless methods due to their smoother results and its easiness to be combined with medical images from CT scans and MRI.
机译:骨重塑仍然是许多科学研究的高度研究的话题。这项工作的主要目的是为生物学模拟制定新的计算框架,以扩展先前由Komarova提出的骨骼重塑模型的版本。因此,仅考虑重塑过程的生物学方面,就要考虑破骨细胞和成骨细胞的作用及其对骨量的影响。对重塑周期进行时空分析,以获得与文献中已描述的生物学过程非常相似的骨细胞动态行为。所使用的数值示例基于通过扫描电子显微镜获得的骨图像。在模拟过程中,可以通过等距线观察骨骼结构的变化。这些图是通过将生物骨骼重塑模型与三种不同的数值技术(有限元方法(FEM),径向点插值方法(RPIM)和自然邻域径向点插值方法(NNRPIM))相结合而获得的。结合这些数值技术的研究可以比较它们的性能。最终,这项工作支持无网格方法,因为它们具有更平滑的结果,并且易于与来自CT扫描和MRI的医学图像结合使用。

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