Cell Culture and Tissue Engineering
Optimizing capacity utilization by large scale 3000 L perfusion in seed train bioreactors
Article first published online: 17 JAN 2013
DOI: 10.1002/btpr.1672
Copyright © 2012 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Pohlscheidt, M., Jacobs, M., Wolf, S., Thiele, J., Jockwer, A., Gabelsberger, J., Jenzsch, M., Tebbe, H. and Burg, J. (2013), Optimizing capacity utilization by large scale 3000 L perfusion in seed train bioreactors. Biotechnol Progress, 29: 222–229. doi: 10.1002/btpr.1672
Publication History
- Issue published online: 4 FEB 2013
- Article first published online: 17 JAN 2013
- Accepted manuscript online: 5 DEC 2012 11:42PM EST
- Manuscript Revised: 20 NOV 2012
- Manuscript Received: 21 SEP 2012
Funded by
- Technical Development department in Penzberg, Germany
- Helmholtz Institute, Braunschweig, Germany
- Abstract
- Article
- References
- Cited By
Keywords:
- perfusion;
- cell culture;
- large scale;
- seed train;
- inclined settler
Abstract
Increasing capacity utilization and lowering manufacturing costs are critical for pharmaceutical companies to improve their competitiveness in a challenging environment. Development of next generation cell lines, improved media formulations, application of mature technologies and innovative operational strategies have been deployed to improve yields and capacity utilization. This article describes a large-scale perfusion strategy for the N-1 seed train bioreactor that was successfully applied to achieve higher inoculation cell densities in the production culture. The N-1 perfusion at 3,000-L scale, utilizing a inclined settler, achieved cell densities of up to 158 × 105 cell mL−1 at perfusion rates of 2950 L day−1 and a retention efficiency of >85%. This approach increased inoculation cell densities and decreased cultivation times by ∼20% in a CHO-based, fed-batch antibody manufacturing process while providing comparable culture performance, productivity, and product quality. The strategy therefore yielded significant increase in capacity utilization and concomitant cost improvement in a large scale cGMP facility. Details of the strategy, the cell retention device, and the cell culture performance are described in this article. © 2012 American Institute of Chemical Engineers Biotechnol. Prog., 2013

1520-6033/asset/BTPR_left.gif?v=1&s=a5be2ff5a0fe6ccdaad74a6d128c142e5f71a8da)
1520-6033/asset/BTPR_right.gif?v=1&s=992d113a3e61fc9d3571812359165df86cf830e4)
