Your browser doesn't support javascript.
loading
2D µ-Particle Image Velocimetry and Computational Fluid Dynamics Study Within a 3D Porous Scaffold.
Campos Marin, A; Grossi, T; Bianchi, E; Dubini, G; Lacroix, D.
Afiliación
  • Campos Marin A; Insigneo Institute for in silico Medicine, Department of Mechanical Engineering, University of Sheffield, Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UK.
  • Grossi T; Laboratory of Biological Structure Mechanics, Politecnico di Milano, Milan, Italy.
  • Bianchi E; Laboratory of Biological Structure Mechanics, Politecnico di Milano, Milan, Italy.
  • Dubini G; Laboratory of Biological Structure Mechanics, Politecnico di Milano, Milan, Italy.
  • Lacroix D; Insigneo Institute for in silico Medicine, Department of Mechanical Engineering, University of Sheffield, Pam Liversidge Building, Mappin Street, Sheffield, S1 3JD, UK. D.Lacroix@sheffield.ac.uk.
Ann Biomed Eng ; 45(5): 1341-1351, 2017 05.
Article en En | MEDLINE | ID: mdl-27957607
Transport properties of 3D scaffolds under fluid flow are critical for tissue development. Computational fluid dynamics (CFD) models can resolve 3D flows and nutrient concentrations in bioreactors at the scaffold-pore scale with high resolution. However, CFD models can be formulated based on assumptions and simplifications. µ-Particle image velocimetry (PIV) measurements should be performed to improve the reliability and predictive power of such models. Nevertheless, measuring fluid flow velocities within 3D scaffolds is challenging. The aim of this study was to develop a µPIV approach to allow the extraction of velocity fields from a 3D additive manufacturing scaffold using a conventional 2D µPIV system. The µ-computed tomography scaffold geometry was included in a CFD model where perfusion conditions were simulated. Good agreement was found between velocity profiles from measurements and computational results. Maximum velocities were found at the centre of the pore using both techniques with a difference of 12% which was expected according to the accuracy of the µPIV system. However, significant differences in terms of velocity magnitude were found near scaffold substrate due to scaffold brightness which affected the µPIV measurements. As a result, the limitations of the µPIV system only permits a partial validation of the CFD model. Nevertheless, the combination of both techniques allowed a detailed description of velocity maps within a 3D scaffold which is crucial to determine the optimal cell and nutrient transport properties.
Asunto(s)
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Reología / Simulación por Computador / Reactores Biológicos / Nanopartículas / Modelos Teóricos Tipo de estudio: Prognostic_studies Idioma: En Revista: Ann Biomed Eng Año: 2017 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Reología / Simulación por Computador / Reactores Biológicos / Nanopartículas / Modelos Teóricos Tipo de estudio: Prognostic_studies Idioma: En Revista: Ann Biomed Eng Año: 2017 Tipo del documento: Article