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一种用于超粘弹性材料表征的遗传算法优化框架:在人体关节软骨中的应用。

A genetic algorithm optimization framework for the characterization of hyper-viscoelastic materials: application to human articular cartilage.

作者信息

Allen Piers, Cox Sophie C, Jones Simon, Espino Daniel M

机构信息

Physical Sciences for Health CDT, Department of Chemistry, University of Birmingham, Birmingham, UK.

School of Chemical Engineering, University of Birmingham, Birmingham, UK.

出版信息

R Soc Open Sci. 2024 Jun 26;11(6):240383. doi: 10.1098/rsos.240383. eCollection 2024 Jun.

Abstract

This study aims to develop an automated framework for the characterization of materials which are both hyper-elastic and viscoelastic. This has been evaluated using human articular cartilage (AC). AC (26 tissue samples from 5 femoral heads) underwent dynamic mechanical analysis with a frequency sweep from 1 to 90 Hz. The conversion from a frequency- to time-domain hyper-viscoelastic material model was approximated using a modular framework design where finite element analysis was automated, and a genetic algorithm and interior point technique were employed to solve and optimize the material approximations. Three orders of approximation for the Prony series were evaluated at = 1, 3 and 5 for 20 and 50 iterations of a genetic cycle. This was repeated for 30 simulations of six combinations of the above all with randomly generated initialization points. There was a difference between = 1 and = 3/5 of approximately ~5% in terms of the error estimated. During unloading the opposite was seen with a 10% error difference between = 5 and 1. A reduction of ~1% parameter error was found when the number of generations increased from 20 to 50. In conclusion, the framework has proved effective in characterizing human AC.

摘要

本研究旨在开发一种用于表征超弹性和粘弹性材料的自动化框架。已使用人体关节软骨(AC)对此进行了评估。AC(来自5个股骨头的26个组织样本)进行了动态力学分析,频率范围为1至90 Hz。使用模块化框架设计将近频域到时域的超粘弹性材料模型进行近似,其中有限元分析是自动化的,并采用遗传算法和内点技术来求解和优化材料近似值。在遗传循环的20次和50次迭代中,对Prony级数的三个近似阶数在α = 1、3和5时进行了评估。对上述六种组合的30次模拟重复此操作,所有模拟均具有随机生成的初始化点。就估计误差而言,α = 1与α = 3/5之间存在约5%的差异。在卸载过程中,情况相反,α = 5与α = 1之间的误差差异为10%。当代数从20增加到50时,发现参数误差降低了约1%。总之,该框架已证明在表征人体AC方面是有效的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/11296198/ad9afcc2e656/rsos.240383.f001.jpg

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