Scale-up of continuous multicolumn chromatography for the protein a capture step: From bench to clinical manufacturing

被引:20
|
作者
Oetes, Ozan [1 ]
Flato, Hendrik [1 ]
Ramirez, Daniel Vazquez [1 ]
Badertscher, Britta [2 ]
Bisschops, Marc [3 ]
Capito, Florian [1 ]
机构
[1] Sanofi Aventis Deutschland GmbH, Bioproc Dev, Ind Pk Hochst, D-65926 Frankfurt, Germany
[2] Pall Schweiz AG, Schafergweg 16, CH-4057 Basel, Switzerland
[3] Pall Medistad BV, Nijverheidsweg 1, NL-1671 GC Medemblik, Netherlands
关键词
Multi-column chromatography; Downstream processing; Continuous chromatography; Upscale; COUNTER-CURRENT CHROMATOGRAPHY; MOVING-BED CHROMATOGRAPHY; ANTIBODY PURIFICATION; AFFINITY-CHROMATOGRAPHY; DESIGN;
D O I
10.1016/j.jbiotec.2018.07.022
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
The awareness about implementing continuous processing for biopharmaceutical products has significantly increased throughout the recent years not only at developmental scale but also for phase I supply in clinical trial manufacturing. In this study, we focused on upscaling continuous protein A chromatography from lab to pilot scale using the Cadence (TM) BioSMB PD and the Cadence (TM) BioSMB Process 80 system, respectively. Additionally, we evaluated hardware and software capability whilst running the system for 10 days non-stop using feed from a perfusion bioreactor. In terms of product quality and removal of impurities, comparable data was obtained regarding lab scale and production scale. Compared to batch mode, productivity was increased by 400 to 500%. Furthermore, the system worked accurately during the whole trial, proving its potential for the implementation into a hybrid or an end-to-end continuous process.
引用
收藏
页码:168 / 174
页数:7
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