Platform development for high‐throughput optimization of perfusion processes: Part I: Implementation of cell bleeds in microwell plates
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Wiley
2024
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| _version_ | 1867004709076729856 |
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| author | Marie Dorn Kerensa Klottrup‐Rees Ken Lee Martina Micheletti |
| author_facet | Marie Dorn Kerensa Klottrup‐Rees Ken Lee Martina Micheletti Marie Dorn Kerensa Klottrup‐Rees Ken Lee Martina Micheletti |
| collection | Wiley Open Access |
| contents | Platform development for high‐throughput optimization of perfusion processes: Part I: Implementation of cell bleeds in microwell plates Marie Dorn Kerensa Klottrup‐Rees Ken Lee Martina Micheletti Biotechnology and Bioengineering AbstractThe promise of continuous processing to increase yields and improve product quality of biopharmaceuticals while decreasing the manufacturing footprint is transformative. Developing and optimizing perfusion operations requires screening various parameters, which is expensive and time‐consuming when using benchtop bioreactors. Scale‐down models (SDMs) are the most feasible option for high‐throughput data generation and condition screening. However, new SDMs mimicking perfusion are required, enabling experiments to be run in parallel. In this study, a method using microwell plates (MWP) operating in semi‐perfusion mode with an implemented cell bleed step is presented. A CHO cell line was cultivated in a 24‐well MWP (Vw = 1.2 mL) and grown at four high cell density (HCD) setpoints. Quasi steady‐state condition was obtained by manually performing cell bleeds followed by a total medium exchange after centrifugation. Further, two HCD setpoints were scaled up (VW = 30 mL), comparing a squared six‐well deepwell plate (DWP) to shake flasks (SF). This evaluation showed comparable results between systems (DWP vs. SF) and scales (MWP vs. DWP + SF). The results show that the well‐plate‐based methods are suitable to perform HCD and quasi steady‐state cultivations providing a robust solution to industrially relevant challenges such as cell clone and media selection. 10.1002/bit.28682 http://creativecommons.org/licenses/by/4.0/ |
| doi_str_mv | 10.1002/bit.28682 |
| format | Artículo Open Access |
| id | wiley_oa_10_1002_bit_28682 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by/4.0/ |
| publishDate | 2024 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | Platform development for high‐throughput optimization of perfusion processes: Part I: Implementation of cell bleeds in microwell plates Marie Dorn Kerensa Klottrup‐Rees Ken Lee Martina Micheletti Biotechnology and Bioengineering Platform development for high‐throughput optimization of perfusion processes: Part I: Implementation of cell bleeds in microwell plates Marie Dorn Kerensa Klottrup‐Rees Ken Lee Martina Micheletti Biotechnology and Bioengineering AbstractThe promise of continuous processing to increase yields and improve product quality of biopharmaceuticals while decreasing the manufacturing footprint is transformative. Developing and optimizing perfusion operations requires screening various parameters, which is expensive and time‐consuming when using benchtop bioreactors. Scale‐down models (SDMs) are the most feasible option for high‐throughput data generation and condition screening. However, new SDMs mimicking perfusion are required, enabling experiments to be run in parallel. In this study, a method using microwell plates (MWP) operating in semi‐perfusion mode with an implemented cell bleed step is presented. A CHO cell line was cultivated in a 24‐well MWP (Vw = 1.2 mL) and grown at four high cell density (HCD) setpoints. Quasi steady‐state condition was obtained by manually performing cell bleeds followed by a total medium exchange after centrifugation. Further, two HCD setpoints were scaled up (VW = 30 mL), comparing a squared six‐well deepwell plate (DWP) to shake flasks (SF). This evaluation showed comparable results between systems (DWP vs. SF) and scales (MWP vs. DWP + SF). The results show that the well‐plate‐based methods are suitable to perform HCD and quasi steady‐state cultivations providing a robust solution to industrially relevant challenges such as cell clone and media selection. 10.1002/bit.28682 http://creativecommons.org/licenses/by/4.0/ |
| title | Platform development for high‐throughput optimization of perfusion processes: Part I: Implementation of cell bleeds in microwell plates |
| topic | Biotechnology and Bioengineering |
| url | https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/bit.28682 |