Scale-down studies for assessing the impact of different stress parameters on growth and product quality during animal cell culture

Abstract Two series of reproducible fed-batch bench scale cultures have been undertaken, one series simulating the impact of spatial variations in pH and nutrients as found at commercial scale on performance, the other, the impact of fluid dynamic stresses associated with agitation. The first was unsuccessful because, somewhat surprisingly, the use of a peristaltic pump to circulate cells and medium through different spatial environments always led to a similar reduction in culture time and resulting product titre compared to uncirculated controls. This fall was sufficient to essentially mask other effects. In the second, even at maximum specific energy dissipation rates up to ∼160 times > with laminar extensional flow and ∼25 times > with turbulent flow compared to typical commercial conditions, no significant effects were observed on cell growth and viability. Most importantly, in all of the cases studied, product quality was unaffected compared to controls. In addition, it is suggested that because of the possibility of cell line specific behaviour and the relationship between damage to entities and the Kolmogorov scale of turbulence, sensitivity to fluid dynamic stresses is best studied in turbulent bench scale bioreactors.

[1]  Sven-Olof Enfors,et al.  Studies of insufficient mixing in bioreactors: Effects of limiting oxygen concentrations and short term oxygen starvation on Penicillium chrysogenum , 1988 .

[2]  C. McFarlane,et al.  Scale-down model to simulate spatial pH variations in large-scale bioreactors. , 2001, Biotechnology and bioengineering.

[3]  A. Nienow Reactor Engineering in Large Scale Animal Cell Culture , 2006, Cytotechnology.

[4]  W. H. Scott The effect of potential large-scale bioreactor environmental heterogeneities during fed-batch culture on the performance of an industrially-relevant GS-CHO cell culture, producing an IgG antibody , 2011 .

[5]  S. Sutera,et al.  Flow-induced trauma to blood cells. , 1977, Circulation research.

[6]  A. Nienow,et al.  Control of pH in large-scale, free suspension animal cell bioreactors: alkali addition and pH excursions. , 1999, Biotechnology and bioengineering.

[7]  Zhongqi Zhang,et al.  Mass spectrometry for structural characterization of therapeutic antibodies. , 2009, Mass spectrometry reviews.

[8]  Hongcheng Liu,et al.  Heterogeneity of monoclonal antibodies. , 2008, Journal of pharmaceutical sciences.

[9]  J. Piret,et al.  Production of a self-activating CBM-factor X fusion protein in a stable transformed Sf9 insect cell line using high cell density perfusion culture , 2004, Cytotechnology.

[10]  J. Chalmers,et al.  Physiological responses of CHO cells to repetitive hydrodynamic stress , 2009, Biotechnology and bioengineering.

[11]  D. Volkin,et al.  Origin of the Isoelectric Heterogeneity of Monoclonal Immunoglobulin h1B4 , 1993, Pharmaceutical Research.

[12]  Ruben Godoy-Silva,et al.  Evaluation of the effect of chronic hydrodynamical stresses on cultures of suspensed CHO‐6E6 cells , 2009, Biotechnology and bioengineering.

[13]  D. E. Leng,et al.  Immiscible Liquid–Liquid Systems , 2004 .

[14]  M Al-Rubeai,et al.  Estimation of disruption of animal cells by laminar shear stress , 1992, Biotechnology and bioengineering.

[15]  Joey Pollastrini,et al.  Response of a concentrated monoclonal antibody formulation to high shear , 2009, Biotechnology and bioengineering.

[16]  R. Dwek,et al.  A rapid high-resolution high-performance liquid chromatographic method for separating glycan mixtures and analyzing oligosaccharide profiles. , 1996, Analytical biochemistry.

[17]  Julie Varley,et al.  The response of GS-NS0 myeloma cells to single and multiple pH perturbations. , 2002, Biotechnology and bioengineering.

[18]  H. Kataoka,et al.  Dynamic deformation and recovery response of red blood cells to a cyclically reversing shear flow: Effects of frequency of cyclically reversing shear flow and shear stress level. , 2006, Biophysical journal.

[19]  Ruben Godoy-Silva,et al.  Acute hydrodynamic forces and apoptosis: A complex question , 2007, Biotechnology and bioengineering.

[20]  Xiaoyu Luo,et al.  Blood flow and damage by the roller pumps during cardiopulmonary bypass , 2005 .

[21]  Nigel Jenkins,et al.  Modifications of therapeutic proteins: challenges and prospects , 2007, Cytotechnology.

[22]  S. Hagen,et al.  Do protein molecules unfold in a simple shear flow? , 2006, Biophysical journal.

[23]  E. L. Paul,et al.  Handbook of Industrial Mixing , 2003 .

[24]  J. Chalmers,et al.  Fabrication and use of a transient contractional flow device to quantify the sensitivity of mammalian and insect cells to hydrodynamic forces , 2002, Biotechnology and bioengineering.

[25]  H. Chang,et al.  Limited Use of Centritech Lab II Centrifuge in Perfusion Culture of rCHO Cells for the Production of Recombinant Antibody , 2008, Biotechnology progress.

[26]  R. Elsworth,et al.  Submerged culture of hamster kidney cells in a stainless steel vessel , 1965 .

[27]  O. Merten Constructive improvement of the ultrasonic separation device ADI 1015 , 2000, Cytotechnology.

[28]  P Dunnill,et al.  Action of shear on enzymes: Studies with alcohol dehydrogenase , 1979, Biotechnology and bioengineering.

[29]  Reed J. Harris,et al.  Effect of Copper Sulfate on Performance of a Serum‐Free CHO Cell Culture Process and the Level of Free Thiol in the Recombinant Antibody Expressed , 2008, Biotechnology progress.

[30]  Alvin W Nienow,et al.  The scale-up of microbial batch and fed-batch fermentation processes. , 2007, Advances in applied microbiology.

[31]  B G Thompson,et al.  Effect of feed zone in fed‐batch fermentations of Saccharomyces cerevisiae , 1992, Biotechnology and bioengineering.

[32]  Margit Jeschke,et al.  Determination of the Origin of Charge Heterogeneity in a Murine Monoclonal Antibody , 2000, Pharmaceutical Research.

[33]  M. D. Johnson,et al.  Very large scale suspension cultures of mammalian cells. , 1985, Developments in biological standardization.