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1.
Cytotechnology ; 64(6): 623-34, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22451075

ABSTRACT

By means of a model predictive control strategy it was possible to ensure a high batch-to-batch reproducibility in animal cell (CHO-cell) suspensions cultured for a recombinant therapeutic protein (EPO) production. The general control objective was derived by identifying an optimal specific growth rate taking productivity, protein quality and process controllability into account. This goal was approached indirectly by controlling the oxygen mass consumed by the cells which is related to specific biomass growth rate and cell concentration profile by manipulating the glutamine feed rate. Process knowledge represented by a classical model was incorporated into the model predictive control algorithm. The controller was employed in several cultivation experiments. During these cultivations, the model parameters were adapted after each sampling event to cope with changes in the process' dynamics. The ability to predict the state variables, particularly for the oxygen consumption, led to only moderate changes in the desired optimal operational trajectories. Hence, nearly identical oxygen consumption profiles, cell and protein titers as well as sialylation patterns were obtained for all cultivation runs.

2.
Biotechnol J ; 6(12): 1547-56, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21818861

ABSTRACT

Most discussions about stirred tank bioreactors for cell cultures focus on liquid-phase motions and neglect the importance of the gas phase for mixing, power input and especially CO(2) stripping. Particularly in large production reactors, CO(2) removal from the culture is known to be a major problem. Here, we show that stripping is mainly affected by the change of the gas composition during the movement of the gas phase through the bioreactor from the sparger system towards the headspace. A mathematical model for CO(2)-stripping and O(2)-mass transfer is presented taking gas-residence times into account. The gas phase is not moving through the reactor in form of a plug flow as often assumed. The model is validated by measurement data. Further measurement results are presented that show how the gas is partly recirculated by the impellers, thus increasing the gas-residence time. The gas-residence times can be measured easily with stimulus-response techniques. The results offer further insights on the gas-residence time distributions in stirred tank reactors.


Subject(s)
Bioreactors , Carbon Dioxide/chemistry , Cell Culture Techniques/instrumentation , Models, Biological , Models, Chemical , Animals , Cell Culture Techniques/methods , Computer Simulation , Physical Phenomena , Pilot Projects , Reproducibility of Results
3.
Biotechnol Lett ; 33(11): 2103-10, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21744145

ABSTRACT

Batch-to-batch reproducibility of animal cell cultures can significantly be enhanced using process control procedures. Most informative signals for advanced process control can be derived from the volume fractions of oxygen and carbon dioxide in the vent line of the reactors. Here we employed simple low-cost sensors, previously not considered for off-gas analysis at a laboratory-scale cell cultures, and compared them with a simultaneously used quadrupole mass spectrometer, i.e., the standard equipment. A decisive advantage is that the sensors did not need any calibration and are easy to use. We show that monitoring and advanced control of cell cultures can significantly be simplified using the devices tested here and that the same batch-to-batch reproducibility can be obtained with much less effort than before.


Subject(s)
Bioreactors , Biotechnology/methods , Cell Proliferation , Gases/chemistry , Animals , CHO Cells , Carbon Dioxide/metabolism , Cell Culture Techniques , Cricetinae , Cricetulus , Oxygen Consumption
4.
Biotechnol Lett ; 33(9): 1781-8, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21626417

ABSTRACT

A very simple but effective process control technique is proposed that leads to a high batch-to-batch reproducibility with respect to biomass concentration as well as the specific biomass growth rate profiles in E. coli fermentations performed during recombinant protein production. It makes use of the well-established temperature controllers in currently used fermenters, but takes its information from the difference between the controlled culture temperature T (cult) and the temperature T (coolin) of the coolant fed to the fermenter's cooling jacket as adjusted by the fermenter temperature controller. For process control purposes this measured difference is corrected regarding stirrer influences and cumulated before it is used as a new process control variable. As a spin-off of this control, it becomes possible to estimate online the oxygen mass transfer rates and the corresponding k(L)a values during the real cultivation process.


Subject(s)
Bioreactors/microbiology , Biotechnology/methods , Escherichia coli/metabolism , Recombinant Proteins/metabolism , Biomass , Escherichia coli/genetics , Escherichia coli/growth & development , Fermentation , Recombinant Proteins/genetics , Temperature
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