Evaluation of criteria for bioreactor comparison and operation standardization for mammalian cell culture
Author(s) -
Platas Barradas Oscar,
Jandt Uwe,
Minh Phan Linh Da,
Villanueva Mario E.,
Schaletzky Martin,
Rath Alexander,
Freund Susann,
Reichl Udo,
Skerhutt Eva,
Scholz Sebastian,
Noll Thomas,
Sandig Volker,
Pörtner Ralf,
Zeng AnPing
Publication year - 2012
Publication title -
engineering in life sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.547
H-Index - 57
eISSN - 1618-2863
pISSN - 1618-0240
DOI - 10.1002/elsc.201100163
Subject(s) - bioreactor , impeller , biochemical engineering , consistency (knowledge bases) , chemostat , process (computing) , process engineering , process development , standardization , work (physics) , computer science , biological system , microbiology and biotechnology , biology , engineering , mechanical engineering , artificial intelligence , botany , operating system , genetics , bacteria
Development of bioprocesses with mammalian cell culture deals with different bioreactor types and scales. The bioreactors might be intended for generation of cell inoculum and production, research, process development, validation, or transfer purposes. During these activities, not only the difficulty of up and downscaling might lead to failure of consistency in cell growth, but also the use of different bioreactor geometries and operation conditions. In such cases, criteria for bioreactor design and process transfer should be carefully evaluated in order to select appropriate cultivation parameters. In this work, power input, mixing time, impeller tip speed, and R eynolds number have been compared systematically for the cultivation of the human cell line AGE 1. HN within three partner laboratories using five different bioreactor systems. Proper operation ranges for the bioreactors were identified using the maximal cell‐specific growth rate ( μ max ) as indicator. Common optimum values for process transfer criteria were found in these geometrically different bioreactors, in which deviations of μ max between cultivation systems can be importantly reduced. The data obtained in this work are used for process standardization and comparability of results obtained in different bioreactor systems, i.e. to guarantee lab‐to‐lab consistency for systems biology approaches using mammalian cells.
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