27.12.2012 Views

ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

analysis of the large-scale human motion, due to the reduced number of degrees of<br />

freedom; however, the lack of volume, internal fibers and pressure distribution limits<br />

the ability to investigate muscles’ biomechanics. To overcome these constraints, a 3D<br />

FE solver to simulate both passive behaviour of biological soft tissues and muscle<br />

contraction has been developed by our team [3].<br />

The 3D FE model is geometrically reconstructed from medical imaging, obtained from<br />

non-invasive scanning techniques, such as CT or MRI. However, depending on the<br />

medical imaging technique, there are some biological tissues that cannot be identified<br />

on medical images, either due to a lack of contrast or due to their small size and/or<br />

thickness. Unlike 1D models of a muscle-tendon system used in the lumped-parameter<br />

model, the accuracy of the mechanical response of a FE simulation is strongly driven by<br />

the accuracy of modelling of tiny details such as muscle membranes, which cannot be<br />

seen and/or identified from the most usual medical imaging techniques.<br />

In conclusion, it is difficult to identify and reconstruct from medical images thin<br />

membranes, such as fascia and aponeurosis. However, these connective tissues play a<br />

paramount role in the biomechanics of muscles and musculo-skeletal systems [4, 5]. In<br />

this study, we aim to investigate the role of membranes during isometric contraction of<br />

a human triceps surae muscle, evaluating mostly the generated forces at Achilles tendon,<br />

with and without considering the existence of membranes.<br />

3. MECHANICAL MODELING<br />

In brief, our FE solver is based on the hyperelastic behaviour of almost incompressible<br />

soft tissues, with a total Lagrangian formulation and a fully implicit time integration<br />

scheme [3]. Due to the incompressibility character of the biological soft tissues, a mixed<br />

type displacement-pressure (u/p) FE formulation was implemented. A muscle has the<br />

ability to develop internal forces and thus to produce internal work as a result of muscle<br />

fibers’ contraction. Therefore, the stress state in a muscle must be seen as the result of a<br />

superposition of passive and active parts [6], i.e.<br />

total pas act<br />

σ = σ + σ , (1)<br />

f f f<br />

total pas<br />

act<br />

where σ f , σ f and σ f are the total, the passive and the active Cauchy stress<br />

component along muscle fiber direction.<br />

3.1 Passive material behaviour<br />

Hyperelastic materials are assumed to be governed by a constitutive law linking the 2 nd<br />

Piola-Kirchhoff stress tensor S and the right Cauchy-Green strain tensor C , by means<br />

of a strain energy potential density W , which plays the role of a stress potential, i.e.,<br />

2 W ∂<br />

S = , (2)<br />

∂C<br />

where the strain energy potential W for almost incompressible materials is given by [7],<br />

k 2 1<br />

2<br />

W = W ( C) + ( J −1) − ( p − pɶ<br />

)<br />

2 2k<br />

. (3)<br />

The first term is related with the hyperelastic constitutive model and is a function of the<br />

2<br />

3<br />

isochoric strain tensor<br />

J −<br />

C = C and the second term represents the strain energy

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!