Efficiency improvement of an antibody production process by increasing the inoculum density

被引:16
|
作者
Hecht, Volker [1 ]
Duvar, Sevim [1 ]
Ziehr, Holger [1 ]
Burg, Josef [2 ]
Jockwer, Alexander [2 ]
机构
[1] Fraunhofer Inst Toxicol & Expt Med ITEM, Pharmaceut Biotechnol Div, Braunschweig, Germany
[2] Roche Diagnost GmbH, Pharmaceut Biotech Prod & Dev, Penzberg, Germany
关键词
cell retention; perfusion; seed train; inocululation enhancement; CHO; CONTINUOUS FERMENTATION; PERFUSION CULTURE; CELLS;
D O I
10.1002/btpr.1887
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
Increasing economic pressure is the main driving force to enhance the efficiency of existing processes. We developed a perfusion strategy for a seed train reactor to generate a higher inoculum density for a subsequent fed batch production culture. A higher inoculum density can reduce culture duration without compromising product titers. Hence, a better capacity utilization can be achieved. The perfusion strategy was planned to be implemented in an existing large scale antibody production process. Therefore, facility and process constraints had to be considered. This article describes the initial development steps. Using a proprietary medium and a Chinese hamster ovary cell line expressing an IgG antibody, four different cell retention devices were compared in regard to retention efficiency and reliability. Two devices were selected for further process refinement, a centrifuge and an inclined gravitational settler. A concentrated feed medium was developed to meet facility constraints regarding maximum accumulated perfundate volume. A 2-day batch phase followed by 5 days of perfusion resulted in cell densities of 1.6 x 1010 cells L-1, a 3.5 fold increase compared to batch cultivations. Two reactor volumes of concentrated feed medium were needed to achieve this goal. Eleven cultivations were carried out in bench and 50 L reactors showing acceptable reproducibility and ease of scale up. In addition, it was shown that at least three perfusion phases can be combined within a repeated perfusion strategy. (c) 2014 American Institute of Chemical Engineers Biotechnol. Prog., 30:607-615, 2014
引用
收藏
页码:607 / 615
页数:9
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