Development and qualification of 3 L scale-down model for large scale vaccine process on vero cell culture using microcarriers

被引:0
|
作者
Huang, Renjing [1 ]
Wang, Kai [1 ]
Flamm, Matthew H. [2 ]
Vazquez, Jorge [3 ]
Gercke, Chris [1 ]
Ton, Christopher [4 ]
Whitmer, Travis [1 ]
Mathis, Pamela K. [5 ]
Ploeger, Kristin J. M. [1 ]
Rameez, Shahid [1 ]
机构
[1] Merck & Co Inc, Bioproc Drug Subst Commercializat, West Point, PA 19486 USA
[2] Merck & Co Inc, Appl Math & Modeling, West Point, PA 19486 USA
[3] Merck & Co Inc, Ctr Math Sci, West Point, PA 19486 USA
[4] Merck & Co Inc, Vaccine Proc Dev, West Point, PA 19486 USA
[5] Merck & Co Inc, Global Qual Large Mol Analyt Sci, West Point, PA 19486 USA
关键词
cell culture; computational fluid dynamics; multivariate data analysis; process characterization; scale-down model; Vero cells; ANIMAL-CELLS; DAMAGE; PLATFORM;
D O I
10.1002/bit.28785
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Scale-down models (SDM) are pivotal tools for process understanding and improvement to accelerate the development of vaccines from laboratory research to global commercialization. In this study, a 3 L SDM representing a 50 L scale Vero cell culture process of a live-attenuated virus vaccine using microcarriers was developed and qualified based on the constant impeller power per volume principle. Both multivariate data analysis (MVDA) and the traditional univariate data analysis showed comparable and equivalent cell growth, metabolic activity, and product quality results across scales. Computational fluid dynamics simulation further confirmed similar hydrodynamic stress between the two scales. Overview of kinetics and modeling approach for scale-down model development and qualification. image
引用
收藏
页码:3402 / 3414
页数:13
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