Effect of Pore Architecture on Oxygen Diffusion in 3D Scaffolds for Tissue Engineering

被引:34
作者
Ahn, Geunseon [1 ]
Park, Jeong Hun [1 ]
Kang, Taeyun [1 ]
Lee, Jin Woo [4 ]
Kang, Hyun-Wook [3 ]
Cho, Dong-Woo [1 ,2 ]
机构
[1] Pohang Univ Sci & Technol POSTECH, Dept Mech Engn, Pohang 790784, Kyeongbuk, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Div Integrat Biosci & Biotechnol, Pohang 790784, Kyeongbuk, South Korea
[3] Wake Forest Univ, Wake Forest Inst Regenerat Med, Winston Salem, NC 27157 USA
[4] Univ Texas Austin, Dept Mech Engn, Austin, TX 78712 USA
来源
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME | 2010年 / 132卷 / 10期
关键词
three-dimensional scaffolds; pore architecture; oxygen diffusion; projection-based microstereolithography (pMSTL) system; sacrificial molding process; SOLID FREEFORM FABRICATION; CARTILAGINOUS CONSTRUCTS; GRADIENTS; POROSITY;
D O I
10.1115/1.4002429
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The aim of this study was to maximize oxygen diffusion within a three-dimensional scaffold in order to improve cell viability and proliferation. To evaluate the effect of pore architecture on oxygen diffusion, we designed a regular channel shape with uniform diameter, referred to as cylinder shaped, and a new channel shape with a channel diameter gradient, referred to as cone shaped. A numerical analysis predicted higher oxygen concentration in the cone-shaped channels than in the cylinder-shaped channels, throughout the scaffold. To confirm these numerical results, we examined cell proliferation and viability in 2D constructs and 3D scaffolds. Cell culture experiments revealed that cell proliferation and viability were superior in the constructs and scaffolds with cone-shaped channels. [DOI: 10.1115/1.4002429]
引用
收藏
页码:1 / 5
页数:5
相关论文
共 16 条
[1]
Development of a bi-pore scaffold using indirect solid freeform fabrication based on microstereolithography technology [J].
Kang, Hyun-Wook ;
Rhie, Jong-Won ;
Cho, Dong-Woo .
MICROELECTRONIC ENGINEERING, 2009, 86 (4-6) :941-944
[2]
Development of an indirect solid freeform fabrication process based on microstereolithography for 3D porous scaffolds [J].
Kang, Hyun-Wook ;
Seol, Young-Joon ;
Cho, Dong-Woo .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2009, 19 (01)
[3]
Diffusion in musculoskeletal tissue engineering scaffolds: Design issues related to porosity, permeability, architecture, and nutrient mixing [J].
Karande, TS ;
Ong, JL ;
Agrawal, CM .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (12) :1728-1743
[4]
Novel approach to fabricate keratin sponge scaffolds with controlled pore size and porosity [J].
Katoh, K ;
Tanabe, T ;
Yamauchi, K .
BIOMATERIALS, 2004, 25 (18) :4255-4262
[5]
Determination of oxygen gradients in engineered tissue using a fluorescent sensor [J].
Kellner, K ;
Liebsch, G ;
Klimant, I ;
Wolfbeis, OS ;
Blunk, T ;
Schulz, MB ;
Göpferich, A .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 80 (01) :73-83
[6]
Development of nano- and microscale composite 3D scaffolds using PPF/DEF-HA and micro-stereolithography [J].
Lee, Jin Woo ;
Ahn, GeunSeon ;
Kim, Dae Shick ;
Cho, Dong-Woo .
MICROELECTRONIC ENGINEERING, 2009, 86 (4-6) :1465-1467
[7]
Solid freeform fabrication of three-dimensional scaffolds for engineering replacement tissues and organs [J].
Leong, KF ;
Cheah, CM ;
Chua, CK .
BIOMATERIALS, 2003, 24 (13) :2363-2378
[8]
Heterogeneous proliferation within engineered cartilaginous tissue: The role of oxygen tension [J].
Lewis, MC ;
MacArthur, BD ;
Malda, J ;
Pettet, G ;
Please, CP .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 91 (05) :607-615
[9]
Biodegradable polymer scaffolds with well-defined interconnected spherical pore network [J].
Ma, PX ;
Choi, JW .
TISSUE ENGINEERING, 2001, 7 (01) :23-33
[10]
The effect of PEGT/PBT scaffold architecture on the composition of tissue engineered cartilage [J].
Malda, J ;
Woodfield, TBF ;
van der Vloodt, F ;
Wilson, C ;
Martens, DE ;
Tramper, J ;
van Blitterswijk, CA ;
Riesle, J .
BIOMATERIALS, 2005, 26 (01) :63-72