Email updates

Keep up to date with the latest news and content from BMC Proceedings and BioMed Central.

This article is part of the supplement: 22nd European Society for Animal Cell Technology (ESACT) Meeting on Cell Based Technologies

Open Access Meeting abstract

Evaluation of a disposable stirred tank bioreactor for cultivation of mammalian cells

Alexander Hähnel1, Benjamin Pütz3, Kai Iding2, Tabea Niediek2, Frank Gudermann3 and Dirk Lütkemeyer12*

Author Affiliations

1 Institute for Protein Characterisation, Faculty of Engineering and Mathematics, University of Applied Sciences, Bielefeld, Germany

2 BIBITEC GmbH, Bielefeld, Germany

3 Institute of Technical Analytics, Faculty of Engineering and Mathematics, University of Applied Sciences, Bielefeld, Germany

For all author emails, please log on.

BMC Proceedings 2011, 5(Suppl 8):P54  doi:10.1186/1753-6561-5-S8-P54


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/5/S8/P54


Published:22 November 2011

© 2011 Hähnel et al; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Disposable bioreactors are increasingly gaining acceptance for cell culture applications due to a number of advantages including ease of use and reduced labour costs, less requirements for utilities such as steam and purified water. In addition, the system requires no cleaning or cleaning validation and only a reduced clean room footprint. Integrated ready to use pre-sterilised disposable sensors for pH and dO2 monitoring are expected to reduce the risk of contamination compared to conventional electrodes. Accordingly, a disposable pre-sterilised and therefore ready-to-use 200 L bioreactor featuring optical sensors for dO2 and pH has been evaluated for suspension culture of CHO cells in protein free media.

Materials and methods

Several fed-batch cultivations with a maximum cultivation time of 9 days were performed as follows.

Cells: Recombinant CHO cell lines producing monoclonal antibodies

Media: MAM-PF2, Bioconcept, Allschwil, Switzerland

Feed and medium from Teutocell, Bielefeld, Germany

Both media are chemically defined and protein free.

Feeds: Different commercial available amino acid concentrates, glucose and glutamine

Bioreactor: BIOSTAT® CultiBag STR 200 L, Sartorius Stedim biotech, Göttingen, Germany

Parameter control: Agitation of the culture was performed by a pre-installed magnetic driven stirrer with two 3-blade impellers at 80 rpm, pH-adjustment via adding CO2 to the overlay stream and dO2 was controlled via aeration of pure oxygen through the ring-sparger.

Results

Maximum cell densities between 5.0 x 106 and 1.3 x 107 cells/mL with viabilities between 85 % and 100 % were achieved. Results of one typical fed-batch cultivation are shown in figure 1.

thumbnailFigure 1. Cell growth and viability during a fed-batch cultivation of CHO cells in the 200 L disposable bioreactor.

The cell densities depended more on the medium performance and feeding strategy than on the bioreactor-features itself. At a cell density of 1.3 x 107 cells/mL the volume flow of pure oxygen was at a rate of 0.85 L/min. In regard to the system’s maximum flow rate of 20 L/min, the throughput of oxygen most likely would not become a bottleneck of even higher cell densities. Detailed comparison of the optical pH and dO2 probes with their conventional counterparts revealed a reliable concordant performance.

Conclusion

The disposable BIOSTAT® CultiBag STR 200 L bioreactor is a reliable cultivation system for high cell density operations above 107 cells/mL with mammalian cells. The usually installed ring-sparger supplies a sufficient amount of gas into the liquid phase and still offers adequate reserves. In direct comparison the optical sensors correlated excellently with the conventional electrodes. External pH-testing and recalibration is mandatory to compensate for the drift of the pH-sensor. The reactor’s overall performance is convincing in this field of operation, which is mainly due to its ease of use combined with the low utilisation of space. The set up procedure can be done in less than three hours which is remarkable compared with stainless steel bio-reactors and the advantage in prevention of cross-contaminants during changeover of campaigns is preeminent.

Acknowlegement

The supply of materials by Dr. Greller and Mrs. Noack (Sartorius Stedim Biotech GmbH) is greatly acknowledged.