Characterization of a Monoclonal Antibody Cell Culture Production Process Using a Quality by Design Approach

被引:40
作者
Horvath, Brian [1 ]
Mun, Melissa [1 ]
Laird, Michael W. [1 ]
机构
[1] Genentech Inc, BioProc Dev US, Late Stage Cell Culture, San Francisco, CA 94080 USA
关键词
Quality by Design; Chinese hamster ovary; Monoclonal antibody; Process characterization; Process validation; Ion-exchange chromatography; PARAMETERS;
D O I
10.1007/s12033-010-9267-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The goal of quality by design (QbD) in cell culture manufacturing is to develop manufacturing processes which deliver products with consistent critical quality attributes (CQAs). QbD approaches can lead to better process understanding through the use of process parameter risk ranking and statistical design of experiments (DOE). The QbD process starts with an analysis of process parameter risk with respect to CQAs and key performance indicators (KPIs). Initial DOE study designs and their factor test ranges are based on the outcomes of the process parameter risk ranking exercises. Initial DOE studies screen factors for significant influences on CQAs as well as characterize responses for process KPIs. In the case study provided here, multifactor process characterization studies using a scale-down model resulted in significant variation in charge heterogeneity of a monoclonal antibody (MAb) as measured by ion-exchange chromatography (IEC). Iterative DOE studies, using both screening and response surface designs, were used to narrow the operating parameter ranges so that charge heterogeneity could be controlled to an acceptable level. The data from the DOE studies were used to predict worst-case conditions, which were then verified by testing at those conditions. Using the approach described here, multivariate process parameter ranges were identified that yield acceptable CQA levels and that still provide operational flexibility for manufacturing.
引用
收藏
页码:203 / 206
页数:4
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