3-D computational modeling of media flow through scaffolds in a perfusion bioreactor

被引:268
作者
Porter, B
Zauel, R
Stockman, H
Guldberg, R
Fyhrie, D
机构
[1] Henry Ford Hosp, Ctr Bone & Joint, Dept Orthopaed Surg, Detroit, MI 48202 USA
[2] Georgia Inst Technol, Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[3] Sandia Natl Labs, Dept Geochem, Albuquerque, NM 87185 USA
基金
美国国家科学基金会;
关键词
fluid shear stress; bioreactor; scaffold; micro CT; imaging; computational fluid dynamics;
D O I
10.1016/j.jbiomech.2004.04.011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Media perfusion bioreactor systems have been developed to improve mass transport throughout three-dimensional (3-D) tissue-engineered constructs cultured in vitro. In addition to enhancing the exchange of nutrients and wastes, these systems simultaneously deliver flow-mediated shear stresses to cells seeded within the constructs. Local shear stresses are a function of media flow rate and dynamic viscosity, bioreactor configuration, and porous scaffold microarchitecture. We have used the Lattice-Boltzmann method to simulate the flow conditions within perfused cell-seeded cylindrical scaffolds. Microcomputed tomography imaging was used to define the scaffold micro architecture for the simulations, which produce a 3-D fluid velocity field throughout the scaffold porosity. Shear stresses were estimated at various media flow rates by multiplying the symmetric part of the gradient of the velocity field by the dynamic viscosity of the cell culture media. The shear stress algorithm was validated by modeling flow between infinite parallel plates and comparing the calculated shear stress distribution to the analytical solution. Relating the simulation results to perfusion experiments, an average surface shear stress of 5 x 10(-5) Pa was found to correspond to increased cell proliferation, while higher shear stresses were associated with upregulation of bone marker genes. This modeling approach can be used to compare results obtained for different perfusion bioreactor systems or different scaffold microarchitectures and may allow specific shear stresses to be determined that optimize the amount, type, or distribution of in vitro tissue growth. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:543 / 549
页数:7
相关论文
共 25 条
[1]   Fluid flow increases mineralized matrix deposition in 3D perfusion culture of marrow stromal osteloblasts in a dose-dependent manner [J].
Bancroft, GN ;
Sikavitsast, VI ;
van den Dolder, J ;
Sheffield, TL ;
Ambrose, CG ;
Jansen, JA ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12600-12605
[2]  
Botchwey EA, 2003, BIORHEOLOGY, V40, P299
[3]   Effects of medium perfusion rate on cell-seeded three-dimensional bone constructs in vitro [J].
Cartmell, SH ;
Porter, BD ;
García, AJ ;
Guldberg, RE .
TISSUE ENGINEERING, 2003, 9 (06) :1197-1203
[4]   On boundary conditions in lattice Boltzmann methods [J].
Chen, SY ;
Martinez, D ;
Mei, RW .
PHYSICS OF FLUIDS, 1996, 8 (09) :2527-2536
[5]  
COURNUBERT R, 1991, PHYS D, V47, P241
[6]   Mechanosensitivity of bone cells to oscillating fluid flow induced shear stress may be modulated by chemotransport [J].
Donahue, TLH ;
Haut, TR ;
Yellowley, CE ;
Donahue, HJ ;
Jacobs, CR .
JOURNAL OF BIOMECHANICS, 2003, 36 (09) :1363-1371
[7]   THE DIRECT EXAMINATION OF 3-DIMENSIONAL BONE ARCHITECTURE INVITRO BY COMPUTED-TOMOGRAPHY [J].
FELDKAMP, LA ;
GOLDSTEIN, SA ;
PARFITT, AM ;
JESION, G ;
KLEEREKOPER, M .
JOURNAL OF BONE AND MINERAL RESEARCH, 1989, 4 (01) :3-11
[8]   NEOCARTILAGE FORMATION INVITRO AND INVIVO USING CELLS CULTURED ON SYNTHETIC BIODEGRADABLE POLYMERS [J].
FREED, LE ;
MARQUIS, JC ;
NOHRIA, A ;
EMMANUAL, J ;
MIKOS, AG ;
LANGER, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (01) :11-23
[9]   Perfusion enhances functions of bone marrow stromal cells in three-dimensional culture [J].
Glowacki, J ;
Mizuno, S ;
Greenberger, JS .
CELL TRANSPLANTATION, 1998, 7 (03) :319-326
[10]   Effect of convection on osteoblastic cell growth and function in biodegradable polymer foam scaffolds [J].
Goldstein, AS ;
Juarez, TM ;
Helmke, CD ;
Gustin, MC ;
Mikos, AG .
BIOMATERIALS, 2001, 22 (11) :1279-1288