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A genetic algorithm optimization framework for the characterization of hyper-viscoelastic materials: application to human articular cartilage.
Allen, Piers; Cox, Sophie C; Jones, Simon; Espino, Daniel M.
Afiliação
  • Allen P; Physical Sciences for Health CDT, Department of Chemistry, University of Birmingham, Birmingham, UK.
  • Cox SC; School of Chemical Engineering, University of Birmingham, Birmingham, UK.
  • Jones S; Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
  • Espino DM; Department of Mechanical Engineering, University of Birmingham, Birmingham, UK.
R Soc Open Sci ; 11(6): 240383, 2024 Jun.
Article em En | MEDLINE | ID: mdl-39100168
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 N = 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 N = 1 and N = 3/5 of approximately ~5% in terms of the error estimated. During unloading the opposite was seen with a 10% error difference between N = 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: R Soc Open Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: R Soc Open Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido