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Rapid intensification of an established CHO cell fed‐batch process

Currently, the mammalian biomanufacturing industry explores process intensification (PI) to meet upcoming demands of biotherapeutics while keeping production flexible but, more importantly, as economic as possible. However, intensified processes often require more development time compared with conv...

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Autores principales: Schulze, Markus, Niemann, Julia, Wijffels, Rene H., Matuszczyk, Jens, Martens, Dirk E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286570/
https://www.ncbi.nlm.nih.gov/pubmed/34542245
http://dx.doi.org/10.1002/btpr.3213
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author Schulze, Markus
Niemann, Julia
Wijffels, Rene H.
Matuszczyk, Jens
Martens, Dirk E.
author_facet Schulze, Markus
Niemann, Julia
Wijffels, Rene H.
Matuszczyk, Jens
Martens, Dirk E.
author_sort Schulze, Markus
collection PubMed
description Currently, the mammalian biomanufacturing industry explores process intensification (PI) to meet upcoming demands of biotherapeutics while keeping production flexible but, more importantly, as economic as possible. However, intensified processes often require more development time compared with conventional fed‐batches (FBs) preventing their implementation. Hence, rapid and efficient, yet straightforward strategies for PI are needed. In this study we demonstrate such a strategy for the intensification of an N‐stage FB by implementing N‐1 perfusion cell culture and high inoculum cell densities resulting in a robust intensified FB (iFB). Furthermore, we show successful combination of such an iFB with the addition of productivity enhancers, which has not been reported so far. The conventional CHO cell FB process was step‐wise improved and intensified rapidly in multi‐parallel small‐scale bioreactors using N‐1 perfusion. The iFBs were performed in 15 and 250 ml bioreactors and allowed to evaluate the impact on key process indicators (KPI): the space–time yield (STY) was successfully doubled from 0.28 to 0.55 g/L d, while product quality was maintained. This gain was generated by initially increasing the inoculation density, thus shrinking process time, and second supplementation with butyric acid (BA), which reduced cell growth and enhanced cell‐specific productivity from ~25 to 37 pg/(cell d). Potential impacts of PI on cell metabolism were evaluated using flux balance analysis. Initial metabolic differences between the standard and intensified process were observed but disappeared quickly. This shows that PI can be achieved rapidly for new as well as existing processes without introducing sustained changes in cellular and metabolic behavior.
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spelling pubmed-92865702022-07-19 Rapid intensification of an established CHO cell fed‐batch process Schulze, Markus Niemann, Julia Wijffels, Rene H. Matuszczyk, Jens Martens, Dirk E. Biotechnol Prog RESEARCH ARTICLES Currently, the mammalian biomanufacturing industry explores process intensification (PI) to meet upcoming demands of biotherapeutics while keeping production flexible but, more importantly, as economic as possible. However, intensified processes often require more development time compared with conventional fed‐batches (FBs) preventing their implementation. Hence, rapid and efficient, yet straightforward strategies for PI are needed. In this study we demonstrate such a strategy for the intensification of an N‐stage FB by implementing N‐1 perfusion cell culture and high inoculum cell densities resulting in a robust intensified FB (iFB). Furthermore, we show successful combination of such an iFB with the addition of productivity enhancers, which has not been reported so far. The conventional CHO cell FB process was step‐wise improved and intensified rapidly in multi‐parallel small‐scale bioreactors using N‐1 perfusion. The iFBs were performed in 15 and 250 ml bioreactors and allowed to evaluate the impact on key process indicators (KPI): the space–time yield (STY) was successfully doubled from 0.28 to 0.55 g/L d, while product quality was maintained. This gain was generated by initially increasing the inoculation density, thus shrinking process time, and second supplementation with butyric acid (BA), which reduced cell growth and enhanced cell‐specific productivity from ~25 to 37 pg/(cell d). Potential impacts of PI on cell metabolism were evaluated using flux balance analysis. Initial metabolic differences between the standard and intensified process were observed but disappeared quickly. This shows that PI can be achieved rapidly for new as well as existing processes without introducing sustained changes in cellular and metabolic behavior. John Wiley & Sons, Inc. 2021-09-25 2022 /pmc/articles/PMC9286570/ /pubmed/34542245 http://dx.doi.org/10.1002/btpr.3213 Text en © 2021 The Authors. Biotechnology Progress published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle RESEARCH ARTICLES
Schulze, Markus
Niemann, Julia
Wijffels, Rene H.
Matuszczyk, Jens
Martens, Dirk E.
Rapid intensification of an established CHO cell fed‐batch process
title Rapid intensification of an established CHO cell fed‐batch process
title_full Rapid intensification of an established CHO cell fed‐batch process
title_fullStr Rapid intensification of an established CHO cell fed‐batch process
title_full_unstemmed Rapid intensification of an established CHO cell fed‐batch process
title_short Rapid intensification of an established CHO cell fed‐batch process
title_sort rapid intensification of an established cho cell fed‐batch process
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9286570/
https://www.ncbi.nlm.nih.gov/pubmed/34542245
http://dx.doi.org/10.1002/btpr.3213
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