Coupling curvature-dependent and shear stress-stimulated neotissue growth in dynamic bioreactor cultures: a 3D computational model of a complete scaffold

被引:55
作者
Guyot, Y. [1 ,2 ]
Papantoniou, I. [1 ,3 ]
Luyten, F. P. [1 ,3 ]
Geris, L. [1 ,2 ,4 ]
机构
[1] Katholieke Univ Leuven, Div Skeletal Tissue Engn, Prometheus, Onderwijs Navorsing 1 8,Herestr 49,PB 813, B-3000 Louvain, Belgium
[2] Univ Liege, Biomech Res Unit, Chemin Chevreuils 1 BAT 52-3, B-4000 Liege, Belgium
[3] Katholieke Univ Leuven, Skeletal Biol & Engn Res Ctr, Onderwijs Navorsing 1 8,Herestr 49,PB 813, B-3000 Louvain, Belgium
[4] Katholieke Univ Leuven, Dept Mech Engn, Biomech Sect, Celestijnenlaan 300C,PB 2419, B-3001 Leuven, Belgium
基金
欧洲研究理事会;
关键词
3D neotissue growth; Shear stress influence; Fluid flow; Bioreactor; Numerical modeling; TISSUE-ENGINEERED CONSTRUCTS; STEM-CELL DIFFERENTIATION; HUMAN BONE-MARROW; FLUID-DYNAMICS; MECHANICAL STIMULATION; PRESSURE-DROP; PORE GEOMETRY; FLOW-THROUGH; PERFUSION; OPTIMIZATION;
D O I
10.1007/s10237-015-0753-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The main challenge in tissue engineering consists in understanding and controlling the growth process of in vitro cultured neotissues toward obtaining functional tissues. Computational models can provide crucial information on appropriate bioreactor and scaffold design but also on the bioprocess environment and culture conditions. In this study, the development of a 3D model using the level set method to capture the growth of a microporous neotissue domain in a dynamic culture environment (perfusion bioreactor) was pursued. In our model, neotissue growth velocity was influenced by scaffold geometry as well as by flow- induced shear stresses. The neotissue was modeled as a homogenous porous medium with a given permeability, and the Brinkman equation was used to calculate the flow profile in both neotissue and void space. Neotissue growth was modeled until the scaffold void volume was filled, thus capturing already established experimental observations, in particular the differences between scaffold filling under different flow regimes. This tool is envisaged as a scaffold shape and bioprocess optimization tool with predictive capacities. It will allow controlling fluid flow during long-term culture, whereby neotissue growth alters flow patterns, in order to provide shear stress profiles and magnitudes across the whole scaffold volume influencing, in turn, the neotissue growth.
引用
收藏
页码:169 / 180
页数:12
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