Development of a Scale Down Cell Culture Model Using Multivariate Analysis as a Qualification Tool

被引:43
作者
Tsang, Valerie Liu [1 ]
Wang, Angela X. [1 ]
Yusuf-Makagiansar, Helena [1 ]
Ryll, Thomas [1 ]
机构
[1] Biogen Idec Inc, Cell Culture Dev, Res Triangle Pk, NC 27709 USA
关键词
multivariate analysis; quality by design; process characterization; scale down model; bioreactor scaling; MONOCLONAL-ANTIBODY PRODUCTION; ELEVATED PCO(2); DESIGN SPACE; QUALITY; FERMENTATION; OSMOLALITY; METABOLISM; PROTEIN;
D O I
10.1002/btpr.1819
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
In characterizing a cell culture process to support regulatory activities such as process validation and Quality by Design, developing a representative scale down model for design space definition is of great importance. The manufacturing bioreactor should ideally reproduce bench scale performance with respect to all measurable parameters. However, due to intrinsic geometric differences between scales, process performance at manufacturing scale often varies from bench scale performance, typically exhibiting differences in parameters such as cell growth, protein productivity, and/or dissolved carbon dioxide concentration. Here, we describe a case study in which a bench scale cell culture process model is developed to mimic historical manufacturing scale performance for a late stage CHO-based monoclonal antibody program. Using multivariate analysis (MVA) as primary data analysis tool in addition to traditional univariate analysis techniques to identify gaps between scales, process adjustments were implemented at bench scale resulting in an improved scale down cell culture process model. Finally we propose an approach for small scale model qualification including three main aspects: MVA, comparison of key physiological rates, and comparison of product quality attributes. (c) 2013 American Institute of Chemical Engineers Biotechnol. Prog., 30:152-160, 2014
引用
收藏
页码:152 / 160
页数:9
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