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Computational simulation modelling of bioreactor configurations for regenerating human bladder

Author

Listed:
  • Seokwon Pok
  • Dhananjay V. Dhane
  • Sundararajan V. Madihally

Abstract

The objective of this study was to investigate a bioreactor suitable for human bladder regeneration. Simulations were performed using the computational fluid dynamic tools. The thickness of the bladder scaffold was 3 mm, similar to the human bladder, and overall hold-up volume within the spherical shape scaffold was 755 ml. All simulations were performed using (i) Brinkman equation on porous regions using the properties of 1% chitosan–1% gelatin structures, (ii) Michaelis–Menten type rate law nutrient consumption for smooth muscle cells (SMCs) and (iii) Mackie–Meares relationship for determining effective diffusivities. Steady state simulations were performed using flow rates from 0.5 to 5 ml/min. Two different inlet shapes: (i) straight entry at the centre (Design 1) and (ii) entry with an expansion (Design 2) were simulated to evaluate shear stress distribution. Also, mimicking bladder shape of two inlets (Design 3) was tested. Design 2 provided the uniform shear stress at the inlet and nutrient distribution, which was further investigated for the effect of scaffold locations within the reactor: (i) attached with a 3-mm open channel (Design 2-A), (ii) flow through with no open channel (Design 2-B) and (iii) porous structure suspended in the middle with 1.5-mm open channel on either side (Design 2-C). In Design 2-A and 2-C, fluid flow occurred by diffusion dominant mechanisms. Furthermore, the designed bioreactor is suitable for increased cell density of SMCs. These results showed that increasing the flow rate is necessary due to the decreased permeability at cell densities similar to the human bladder.

Suggested Citation

  • Seokwon Pok & Dhananjay V. Dhane & Sundararajan V. Madihally, 2013. "Computational simulation modelling of bioreactor configurations for regenerating human bladder," Computer Methods in Biomechanics and Biomedical Engineering, Taylor & Francis Journals, vol. 16(8), pages 840-851, August.
  • Handle: RePEc:taf:gcmbxx:v:16:y:2013:i:8:p:840-851
    DOI: 10.1080/10255842.2011.641177
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