Development of PDMS microbioreactor with well-defined and homogenous culture environment for chondrocyte 3-D culture

被引:89
作者
Wu, Min-Hsien
Urban, Jill P. G.
Cui, Zheng
Cui, Zhan Feng [1 ]
机构
[1] Univ Oxford, Dept Engn Sci, Oxford OX1 2JD, England
[2] Univ Oxford, Dept Physiol Anat & Genet, Oxford OX1 2JD, England
[3] Rutherford Appleton Lab, Cent Microstruct Facil, Didcot, Oxon, England
关键词
microbioreactors; microfluidic devices; PDMS; perfusion culture; chondrocytes;
D O I
10.1007/s10544-006-9597-y
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Perfusion cell culture is believed to provide a stable culture environment due to the continuous supply of nutrients and removal of waste. However, the culture scales used in most cases were large, where the culture conditions can not be regarded as homogenous because of chemical gradients. To improve this, the concept of miniaturization is applied to 3-D cell culture. In this study, a simple perfusion microbioreactor was developed based on mass transport simulation to find out the reasonable culture scales with relatively lower chemical gradients. Besides, PDMS surface was treated with surfactant solution to reduce non-specific serum protein adsorption, which keeps the culture conditions steady. Chondrocyte 3-D culture using the proposed microbioreactors was compared with similar perfusion culture with a larger culture scale. Results showed that surfactant-treated PDMS surface could reduce serum protein adsorption by 85% over the native one. Also, microbioreactors were proved to provide a stable culture environment (e.g. pH) over the culture period. Cell culture scale of 200 mu m thick culture construct was justified to have relatively lower chemical gradients than the larger scale perfusion culture. As a whole, the proposed culture system is capable of providing a well-defined and homogenous culture environment.
引用
收藏
页码:331 / 340
页数:10
相关论文
共 45 条
[1]   PREVENTION OF PROTEIN ADSORPTION AND PLATELET-ADHESION ON SURFACES BY PEO PPO PEO TRIBLOCK COPOLYMERS [J].
AMIJI, M ;
PARK, K .
BIOMATERIALS, 1992, 13 (10) :682-692
[2]   Fabrication of topologically complex three-dimensional microfluidic systems in PDMS by rapid prototyping [J].
Anderson, JR ;
Chiu, DT ;
Jackman, RJ ;
Cherniavskaya, O ;
McDonald, JC ;
Wu, HK ;
Whitesides, SH ;
Whitesides, GM .
ANALYTICAL CHEMISTRY, 2000, 72 (14) :3158-3164
[3]   Metabolism of the intervertebral disc: Effects of low levels of oxygen, glucose, and pH on rates of energy metabolism of bovine nucleus pulposus cells [J].
Bibby, SRS ;
Jones, DA ;
Ripley, RM ;
Urban, JPG .
SPINE, 2005, 30 (05) :487-496
[4]   Prototype of a novel autonomous perfusion chamber for long-term culturing and in situ investigation of various cell types [J].
Blau, AW ;
Ziegler, CM .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2001, 50 (01) :15-27
[5]   Gentle cell trapping and release on a microfluidic chip by in situ alginate hydrogel formation [J].
Braschler, T ;
Johann, R ;
Heule, M ;
Metref, L ;
Renaud, P .
LAB ON A CHIP, 2005, 5 (05) :553-559
[6]   Dynamic osmotic loading of chondrocytes using a novel microfluidic device [J].
Chao, PG ;
Tang, ZL ;
Angelini, E ;
West, AC ;
Costa, KD ;
Hung, CT .
JOURNAL OF BIOMECHANICS, 2005, 38 (06) :1273-1281
[7]   Diffusion of gases in silicone polymers: Molecular dynamics simulations [J].
Charati, SG ;
Stern, SA .
MACROMOLECULES, 1998, 31 (16) :5529-5535
[8]   Microfabricated platform for studying stem cell fates [J].
Chin, VI ;
Taupin, P ;
Sanga, S ;
Scheel, J ;
Gage, FH ;
Bhatia, SN .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 88 (03) :399-415
[9]   Human neural stem cell growth and differentiation in a gradient-generating microfluidic device [J].
Chung, BG ;
Flanagan, LA ;
Rhee, SW ;
Schwartz, PH ;
Lee, AP ;
Monuki, ES ;
Jeon, NL .
LAB ON A CHIP, 2005, 5 (04) :401-406
[10]   Perfusion increases cell content and matrix synthesis in chondrocyte three-dimensional cultures [J].
Davisson, T ;
Sah, RL ;
Ratcliffe, A .
TISSUE ENGINEERING, 2002, 8 (05) :807-816