Online monitoring and control of upstream cell culture process using 1D and 2D-LC with SegFlow interface
- PMID: 34185315
- DOI: 10.1002/bit.27873
Online monitoring and control of upstream cell culture process using 1D and 2D-LC with SegFlow interface
Abstract
The biopharmaceutical industry is transitioning from currently deployed batch-mode bioprocessing to a highly efficient and agile next-generation bioprocessing with the adaptation of continuous bioprocessing, which reduces capital investment and operational costs. Continuous bioprocessing, aligned with FDA's quality-by-design platform, is designed to develop robust processes to deliver safe and effective drugs. With the deployment of knowledge-based operations, product quality can be built into the process to achieve desired critical quality attributes (CQAs) with reduced variability. To facilitate next-generation continuous bioprocessing, it is essential to embrace a fundamental shift-in-paradigm from "quality-by-testing" to "quality-by-design," which requires the deployment of process analytical technologies (PAT). With the adaptation of PAT, a systematic approach of process and product understanding and timely process control are feasible. Deployment of PAT tools for real-time monitoring of CQAs and feedback control is critical for continuous bioprocessing. Given the current deficiency in PAT tools to support continuous bioprocessing, we have integrated Infinity 2D-LC with a post-flow-splitter in conjunction with the SegFlow autosampler to the bioreactors. With this integrated system, we have established a platform for online measurements of titer and CQAs of monoclonal antibodies as well as amino acid analysis of bioreactor cell culture.
Keywords: 2D-LC; SegFlow; continuous bioprocessing; monoclonal antibody (mAb); process analytical technology (PAT); quality by design (QbD).
© 2021 Wiley Periodicals LLC.
References
REFERENCES
-
- Allison, G. , Cain, Y. T. , Cooney, C. , Garcia, T. , Bizjak, T. G. , Holte, O. , Jagota, N. , Komas, B. , Korakianiti, E. , Kourti, D. , Madurawe, R. , Morefield, E. , Montgomery, F. , Nasr, M. , Randolph, W. , Robert, J. L. , Rudd, D. , & Zezza, D. (2015). Regulatory and quality considerations for continuous manufacturing. Journal of Pharmaceutical Sciences, 104(3), 803-812. https://doi.org/10.1002/jps.24324
-
- Alper, J. (2019). Continuous manufacturing for the modernization of pharmaceutical production. Proceedings of a workshop, National Academies of Sciences, Engineering, and Medicine; Division on Earth and Life Studies; Board on Chemical Sciences and Technology. Washington, DC: National Academies Press. https://doi.org/10.17226/25340
-
- Bayer, K. (2014). Brief note on the development of biotechnology. Food Technology and Biotechnology, 52(1), 13-15.
-
- Bhambure, R. , Kumar, K. , & Rathore, A. S. (2011). High-throughput process development for biopharmaceutical drug substances. Trends in Biotechnology, 29(3), 127-135. https://doi.org/10.1016/j.tibtech.2010.12.001
-
- Brühlmann, D. , Jordan, M. , Hemberger, J. , Sauer, M. , Stettler, M. , & Broly, H. (2015). Tailoring recombinant protein quality by rational media design. Biotechnology Progress, 31(3), 615-629. https://doi.org/10.1002/btpr.2089
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