Miniature Bioreactors for Rapid Bioprocess Development of Mammalian Cell Culture

Authors

  • Mohd Helmi Sani Department of Industrial Biotechnology, Faculty of Biosciences and Bioengineering, Universiti Teknologi Malaysia, 81310 UTM Johor Bahru, Johor, Malaysia
  • Frank Baganz Department of Biochemical Engineering, Faculty of Engineering Sciences, University College London, Torrington Place, WC1E 7JE, United Kingdom

DOI:

https://doi.org/10.11113/jt.v59.1569

Abstract

At present, there are a number of commercial small scale shaken systems available on the market with instrumented controllable microbioreactors such as Micro–24 Microreactor System (Pall Corporation, Port Washington, NY) and M2P Biolector, (M2P Labs GmbH, Aachen, Germany). The Micro–24 system is basically an orbital shaken 24–well plate that operates at working volume 3 – 7 mL with 24 independent reactors (deep wells, shaken and sparged) running simultaneously. Each reactor is designed as single use reactor that has the ability to continuously monitor and control the pH, DO and temperature. The reactor aeration is supplied by sparging air from gas feeds that can be controlled individually. Furthermore, pH can be controlled by gas sparging using either dilute ammonia or carbon dioxide directly into the culture medium through a membrane at the bottom of each reactor. Chen et al., (2009) evaluated the Micro–24 system for the mammalian cell culture process development and found the Micro–24 system is suitable as scaledown tool for cell culture application. The result showed that intra-well reproducibility, cell growth, metabolites profiles and protein titres were scalable with 2 L bioreactors.

References

Bareither, R., and Pollard, D. 2011. A Review of Advanced Small-scale

Parallel Bioreactor Technology for Accelerated Process Development:

Current State and Future Need. Biotechnology Progress. 27(1): 2–14.

Barrett, T. A., Wu, A., Zhang, H., Levy, M. S., and Lye, G. J. 2010. Microwell

Engineering Characterization for Mammalian Cell Culture Process

Development. Biotechnology and Bioengineering. 105 (2): 260–275.

Betts, J. I., and Baganz, F. 2006. Miniature Bioreactors: Current Practices and

Future Opportunities. Microbial Cell Factories. 5(21).

Chen, A., Chitta, R., Chang, D., and Anianullah, A. 2009. Twenty-four Well

Plate Miniature Bioreactor System as a Scale-Down Model for Cell

Culture Process Development. Biotechnology and Bioengineering. 102:

(1): 148–160.

Doig, S. Baganz, F. and Lye, G. 2006. High Throughput Screening and Process

Optimisation. In: Ratledge, C. Kristiansen and B. Kristiansen, eds. Basic

Biotechnology. Cambridge: Cambridge University Press.

Funke, M., Buchenauer, A., Schnakenberg, U., Mokwa, W., Diederichs, S.,

Mertens, A., Müller, C., Kensy, F., and Büchs, J. 2010. Microfluidic

Biolector-Microfluidic Bioprocess Control in Microtiter Plates.

Biotechnology and Bioengineering. 107(3): 497–505.

Ge, X., Hanson, M., Shen, H., Kostov, Y., Brorson, K. A., Frey, D. D.,

Moreira, A. R., and Rao, G. 2006. Validation of an Optical Sensor-based

High-Throughput Bioreactor System for Mammalian Cell Culture.

Journal of Biotechnology. 122(3): 293–306.

Gill, N. K., Appleton, M., Baganz, F., and Lye, G. J. 2008a. Design and

Characterisation of a Miniature Stirred Bioreactor System for Parallel

Microbial Fermentations. Biochemical Engineering Journal. 39(1): 164–

Hanson, M. A., Rao, G. 2010. Biominiaturization of bioreactors. In:

Encyclopedia of Industrial Biotechnology: Bioprocess, Bioseperation and

Cell Technology, Flickinger, M. C., John Wiley and Sons, Inc.

Legmann, R., Schreyer, H. B., Combs, R. G., McCormick, E. L., Russo, A. P.,

and Rodgers, S. T. 2009. A Predictive High-throughput Scale-down

Model of Monoclonal Antibody Production In CHO Cells. Biotechnology

and Bioengineering. 104(6): 1107–1120.

Lye, G. J., Ayazi-Shamlou, P., Baganz, F., Dalby, P. A., and Woodley, J. M.

Accelerated Design of Bioconversion Processes Using Automated

Microscale Processing Techniques. Trends in Biotechnology. 21(1): 29–

Micheletti, M., and Lye, G. J. 2006. Microscale Bioprocess Optimisation.

Current Opinion in Biotechnology. 17(6): 611–618.

Micheletti, M., Barrett, T., Doig, S. D., Baganz, F., Levy, M. S., Woodley, J.

M., and Lye, G. J. 2006. Fluid Mixing in Shaken Bioreactors:

Implications for Scale-up Predictions from Microlitre-scale Microbial

And Mammalian Cell Cultures. Chemical Engineering Science. 61(9):.

–2949.

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Published

2012-09-14

How to Cite

Miniature Bioreactors for Rapid Bioprocess Development of Mammalian Cell Culture. (2012). Jurnal Teknologi, 59(1). https://doi.org/10.11113/jt.v59.1569