A practical approach in bioreactor scale-up and process transfer using a combination of constantP/Vand vvm as the criterion
Autor: | Rubin Jiang, Eric Brodean, Hao Chen, T. Craig Seamans, John Bowers, Kristin O'Neill, Sen Xu, Balrina Gupta, Linda Hoshan |
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Rok vydání: | 2017 |
Předmět: |
0106 biological sciences
0301 basic medicine Stripping (chemistry) Cell Survival Cell Count CHO Cells 01 natural sciences 03 medical and health sciences Bioreactors Cricetulus 010608 biotechnology Bioreactor Animals Process engineering Scaling Cells Cultured Sparging Cell Proliferation Mass transfer coefficient Chemistry business.industry Antibodies Monoclonal Carbon Dioxide Volumetric flow rate Oxygen 030104 developmental biology Volume (thermodynamics) Chemical engineering SCALE-UP business Biotechnology |
Zdroj: | Biotechnology Progress. 33:1146-1159 |
ISSN: | 8756-7938 |
DOI: | 10.1002/btpr.2489 |
Popis: | Bioreactor scale-up is a critical step in the production of therapeutic proteins such as monoclonal antibodies (MAbs). With the scale-up criterion such as similar power input per volume or O2 volumetric mass transfer coefficient ( kLa), adequate oxygen supply and cell growth can be largely achieved. However, CO2 stripping in the growth phase is often inadequate. This could cascade down to increased base addition and osmolality, as well as residual lactate increase and compromised production and product quality. Here we describe a practical approach in bioreactor scale-up and process transfer, where bioreactor information may be limited. We evaluated the sparger kLa and kLaCO2 (CO2 volumetric mass transfer coefficient) from a range of bioreactor scales (3-2,000 L) with different spargers. Results demonstrated that kLa for oxygen is not an issue when scaling from small-scale to large-scale bioreactors at the same gas flow rate per reactor volume (vvm). Results also showed that sparging CO2 stripping, kLaCO2, is dominated by the gas throughput. As a result, a combination of a minimum constant vvm air or N2 flow with a similar specific power was used as the general scale-up criterion. An equation was developed to determine the minimum vvm required for removing CO2 produced from cell respiration. We demonstrated the effectiveness of using such scale-up criterion with five MAb projects exhibiting different cell growth and metabolic characteristics, scaled from 3 to 2,000 L bioreactors across four sites. © 2017 American Institute of Chemical Engineers Biotechnol. Prog., 33:1146-1159, 2017. |
Databáze: | OpenAIRE |
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