Finite element study of scaffold architecture design and culture conditions for tissue engineering

被引:254
作者
Olivares, Andy L. [2 ]
Marshal, Elia [2 ]
Planell, Josep A. [2 ]
Lacroix, Damien [1 ]
机构
[1] Inst Bioengn Catalonia, Biomechan & Mechanobiol Grp, Barcelona 08028, Spain
[2] Tech Univ Catalonia UPC, Dept Mat Sci, Barcelona 08028, Spain
关键词
Tissue engineering; Scaffold; Rapid prototyping; Computational fluid dynamics; Finite element; STRUCTURE LIBRARY; SHEAR-STRESS; PART; DIFFERENTIATION; BONE; SIMULATION; PERFUSION; FLOW; FABRICATION; STIMULI;
D O I
10.1016/j.biomaterials.2009.07.041
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tissue engineering scaffolds provide temporary mechanical support for tissue regeneration and transfer global mechanical load to mechanical stimuli to cells through its architecture. In this study the interactions between scaffold pore morphology, mechanical stimuli developed at the cell microscopic level, and culture conditions applied at the macroscopic scale are studied on two regular scaffold structures. Gyroid and hexagonal scaffolds of 55% and 70% porosity were modeled in a finite element analysis and were submitted to an inlet fluid flow or compressive strain. A mechanoregulation theory based on scaffold shear strain and fluid shear stress was applied for determining the influence of each structures on the mechanical stimuli on initial conditions. Results indicate that the distribution of shear stress induced by fluid perfusion is very dependent on pore distribution within the scaffold. Gyroid architectures provide a better accessibility of the fluid than hexagonal structures. Based on the mechanoregulation theory, the differentiation process in these structures was more sensitive to inlet fluid flow than axial strain of the scaffold. This study provides a computational approach to determine the mechanical stimuli at the cellular level when cells are cultured in a bioreactor and to relate mechanical stimuli with cell differentiation. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6142 / 6149
页数:8
相关论文
共 29 条
[1]   Framework for optimal design of porous scaffold microstructure by computational simulation of bone regeneration [J].
Adachi, T ;
Osako, Y ;
Tanaka, M ;
Hojo, M ;
Hollister, SJ .
BIOMATERIALS, 2006, 27 (21) :3964-3972
[2]   Dynamic shear stress in parallel-plate flow chambers [J].
Bacabac, RG ;
Smit, TH ;
Cowin, SC ;
Van Loon, JJWA ;
Nieuwstadt, FTM ;
Heethaar, R ;
Klein-Nulend, J .
JOURNAL OF BIOMECHANICS, 2005, 38 (01) :159-167
[3]   Prediction of the micro-fluid dynamic environment imposed to three-dimensional engineered cell systems in bioreactors [J].
Boschetti, F ;
Raimondi, MT ;
Migliavacca, F ;
Dubini, G .
JOURNAL OF BIOMECHANICS, 2006, 39 (03) :418-425
[4]   Simulation of tissue differentiation in a scaffold as a function of porosity, Young's modulus and dissolution rate: Application of mechanobiological models in tissue engineering [J].
Byrne, Damien P. ;
Lacroix, Damien ;
Planell, Josep A. ;
Kelly, Daniel J. ;
Prendergast, Patrick J. .
BIOMATERIALS, 2007, 28 (36) :5544-5554
[5]   CORRELATIONS BETWEEN MECHANICAL-STRESS HISTORY AND TISSUE DIFFERENTIATION IN INITIAL FRACTURE-HEALING [J].
CARTER, DR ;
BLENMAN, PR ;
BEAUPRE, GS .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1988, 6 (05) :736-748
[6]   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
[7]   Development of a tissue engineering scaffold structure library for rapid prototyping. Part 1: Investigation and classification [J].
C.M. Cheah ;
C.K. Chua ;
K.F. Leong ;
S.W. Chua .
The International Journal of Advanced Manufacturing Technology, 2003, 21 (4) :291-301
[8]   Development of a tissue engineering scaffold structure library for rapid prototyping. Part 2: Parametric library and assembly program [J].
C.M. Cheah ;
C.K. Chua ;
K.F. Leong ;
S.W. Chua .
The International Journal of Advanced Manufacturing Technology, 2003, 21 (4) :302-312
[9]   Magnitudes of local stress and strain along bony surfaces predict the course and type of fracture healing [J].
Claes, LE ;
Heigele, CA .
JOURNAL OF BIOMECHANICS, 1999, 32 (03) :255-266
[10]  
Cowin S. C., 2002, Journal of Musculoskeletal & Neuronal Interactions, V2, P256