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Predicting muscle tissue response from calibrated component models and histology-based finite element models
Ramachandra Kuravi1, Kay Leichsenring2, Robin Trostorf2
1Empa, Swiss Federal Laboratories for Materials Science and Technology, Überlandstrasse 129, CH-8600, Dübendorf, Switzerland; ETH Zurich, Institute for Mechanical Systems, Leonhardstrasse 21, CH-8092, Zürich, Switzerland.
Predicting skeletal muscle tissue mechanics from its components is possible within limits. While orders of magnitude and qualitative behavior are captured, deviations highlight missing model components and experimental data gaps in multiscale approaches.
Area of Science:
- Biomechanics
- Biomaterials Science
- Tissue Engineering
Background:
- Skeletal muscle is a complex, anisotropic soft biological tissue.
- Hierarchical organization of muscle fibers and extracellular matrix (ECM) influences mechanical properties.
- Previous work established 3D finite element models and experimental data on decellularized ECM properties.
Purpose of the Study:
- To calibrate a constitutive model of the skeletal muscle ECM using an inverse finite element procedure.
- To validate the predictive model through supplementary biaxial tensile tests on fresh and decellularized tissues.
- To assess the predictability of composite tissue response from individual component characteristics.
Main Methods:
- Development of 3D finite element models from histological sections.
- Decellularization of fresh tissue samples to obtain ECM properties.
- Inverse finite element analysis to calibrate ECM constitutive model.
- Biaxial tensile testing of fresh and decellularized tissues for validation.
Main Results:
- The predictive strategy matched orders of magnitude of tissue response.
- Qualitative mechanical behavior across various load cases was largely captured.
- Deviations between predicted and experimental results were observed, indicating limitations.
Conclusions:
- Predicting skeletal muscle tissue response from individual cell and ECM characteristics is feasible but limited.
- Existing models may lack crucial components or require more comprehensive experimental data.
- Bottom-up multiscale modeling approaches for skeletal muscle require further refinement.
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