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生物反应器中施加于三维工程细胞系统的微流体动力学环境预测。

Prediction of the micro-fluid dynamic environment imposed to three-dimensional engineered cell systems in bioreactors.

作者信息

Boschetti Federica, Raimondi Manuela Teresa, Migliavacca Francesco, Dubini Gabriele

机构信息

Laboratory of Biological Structure Mechanics, Department of Structural Engineering and Bioengineering, Politecnico di Milano, Piazza L. da Vinci 32, 20133 Milan, Italy.

出版信息

J Biomech. 2006;39(3):418-25. doi: 10.1016/j.jbiomech.2004.12.022.

DOI:10.1016/j.jbiomech.2004.12.022
PMID:16389082
Abstract

Bioreactors allowing culture medium perfusion overcome diffusion limitations associated with static culturing and provide flow-mediated mechanical stimuli. The hydrodynamic stress imposed to cells will depend not only on the culture medium flow rate, but also on the scaffold three-dimensional (3D) micro-architecture. We developed a CFD model of the flow of culture medium through a 3D scaffold of homogeneous geometry, with the aim of predicting the shear stress acting on cells as a function of parameters that can be controlled during the scaffold fabrication process, such as the scaffold porosity and the pore size, and during the cell culture, such as the medium flow rate and the diameter of the perfused scaffold section. We built three groups of models corresponding to three pore sizes: 50, 100 and 150 microm. Each group was made of four models corresponding to 59%, 65%, 77%, and 89% porosity. A commercial finite-element code was used to set up and solve the problem and to analyze the results. The mode value of shear stress varied between 2 and 5 mPa, and was obtained for a circular scaffold of 15.5 mm diameter, perfused by a flow rate of 0.5 ml/min. The simulations showed that the pore size is a variable strongly influencing the predicted shear stress level, whereas the porosity is a variable strongly affecting the statistical distribution of the shear stresses, but not their magnitude. Our results provide a basis for the completion of more exhaustive quantitative studies to further assess the relationship between perfusion, at known micro-fluid dynamic conditions, and tissue growth in vitro.

摘要

允许培养基灌注的生物反应器克服了与静态培养相关的扩散限制,并提供了流动介导的机械刺激。施加给细胞的流体动力应力不仅取决于培养基流速,还取决于支架的三维(3D)微结构。我们开发了一种计算流体动力学(CFD)模型,用于模拟培养基在具有均匀几何形状的3D支架中的流动,目的是预测作用于细胞的剪切应力,该应力是支架制造过程中可控制参数(如支架孔隙率和孔径)以及细胞培养过程中(如培养基流速和灌注支架部分的直径)的函数。我们构建了三组对应于三种孔径(50、100和150微米)的模型。每组由四个对应于59%、65%、77%和89%孔隙率的模型组成。使用商业有限元代码来设置和解决问题并分析结果。剪切应力的模态值在2至5毫帕之间变化,对于直径为15.5毫米、流速为0.5毫升/分钟灌注的圆形支架可获得该值。模拟结果表明,孔径是强烈影响预测剪切应力水平的变量,而孔隙率是强烈影响剪切应力统计分布但不影响其大小的变量。我们的结果为完成更详尽的定量研究提供了基础,以进一步评估在已知微流体动力学条件下灌注与体外组织生长之间的关系。

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