| Literature DB >> 25962790 |
Valérie Girard1, Nicolas-Julian Hilbold2, Candy K S Ng3, Laurence Pegon4, Wael Chahim5, Fabien Rousset6, Vincent Monchois7.
Abstract
The development and optimization of a purification process of monoclonal antibodies based on two continuous chromatography steps for capture and intermediate purification are presented. The two chromatography steps were individually optimized using either batch chromatography or sequential multicolumn chromatography (SMCC). Proprietary simulation software was used to optimize SMCC and to evaluate the potential gains compared with batch chromatography. The SMCC recipes provided by the simulation software were evaluated experimentally. A good correlation was found between the simulated results and experimental observations. Significant gains were observed on the productivity, buffer consumption and the volume of resin required for SMCC over batch chromatography. Based on these results, a chained process from the capture to polishing steps was implemented. This chained process demonstrated significantly better performance compared with the batch equivalent while satisfying the specifications. The expected positive impact provided by implementing continuous chromatography is also discussed.Keywords: Antibody purification; Continuous biomanufacturing; Continuous bioprocessing; Continuous chromatography; Downstream processing; Monoclonal antibody
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Year: 2015 PMID: 25962790 DOI: 10.1016/j.jbiotec.2015.04.026
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307