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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

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assigned zero fluid pressure boundary conditions to allow for free-draining of fluid. The<br />

finite element analysis was carried out with FEBio<br />

(http://mrl.sci.utah.edu/software/febio). Due to the high computational cost of the large<br />

degree of freedom biphasic analyses, simulations were conducted on a node of the<br />

SDSC Trestles cluster made available through XSEDE, Extreme Science and<br />

Engineering Discovery Environment (http:www.xsede.org). Utilized computing nodes<br />

contained 4 8-core 2.4 GHz AMD Magny-Cours processors, 64 GB of memory, and 160<br />

GB of SSD scratch space for fast file I/O. During post-processing, change in volumeaveraged<br />

cell effective strain, effective stress, total fluid flux and overall RVE 3 rd<br />

principal stress response were evaluated using PostView<br />

(http://mrl.sci.utah.edu/software/postview).<br />

4. RESULTS<br />

Volume averaged chondrocyte effective strain was up to 9.5% for the single cell case<br />

and varied from 9.5 to 15.5% for the 11 cell case (Figure 2). Cellular fluid flux vector<br />

fields also exhibited variations as more cells were introduced to the RVE, meriting<br />

further quantitative investigation (Figure 3). As calculated using the volume averaged<br />

3 rd principal stress results throughout the 10 second simulation, the normalized RMS<br />

difference between the single and 11 cell RVEs was only 1.5%. For reference and<br />

considering the utilized computational resource (see Methods), the single cell analysis<br />

required 3.33 hours of wall clock time (106.5 CPU hours) while the 11 cell case<br />

required 3.9 hours (125.17 CPU hours).<br />

5. DISCUSSION<br />

This study was successful in predicting single and eleven cell mechanics subject to the<br />

provided assumptions. Regarding aspects of cell health and function, preliminary results<br />

highlight that for a given point in the cartilage, neighboring cells may behave differently<br />

as predicted by anatomically realistic representation of chondrocyte distribution. While<br />

quantitative differences were indeed found for single versus eleven cell volume<br />

averaged effective strain results (Figure 2a), qualitative results were also observed for<br />

both the cell strain contours (Figure 2b and 2c) and the fluid flux vector field (Figure 3).<br />

These results highlight the potential for cellular interactions when anatomically based<br />

Figure 3. Fluid flux vector field in the cell(s) of the (a) single and (b) eleven cell<br />

models. Results are plotted at 10 seconds into the simulation. Note the potential<br />

influence of neighboring cells in the eleven cell model.

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