Cell Culture and Tissue Engineering
Enhanced productivity of NS0 cells in fed-batch culture with cholesterol nanoparticle supplementation
Article first published online: 20 APR 2011
DOI: 10.1002/btpr.608
Copyright © 2011 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Wu, Y., Ma, N., Wyslouzil, B. E., Chalmers, J. J., McCormick, E. and Casnocha, S. A. (2011), Enhanced productivity of NS0 cells in fed-batch culture with cholesterol nanoparticle supplementation. Biotechnol Progress, 27: 796–802. doi: 10.1002/btpr.608
Publication History
- Issue published online: 6 JUN 2011
- Article first published online: 20 APR 2011
- Accepted manuscript online: 21 MAR 2011 02:48PM EST
- Manuscript Revised: 9 FEB 2011
- Manuscript Received: 22 JUN 2010
Funded by
- Nanoscale Science and Engineering Center (NSEC). Grant Number: EEC-0425626
- Abstract
- Article
- References
- Cited By
Keywords:
- electrohydrodynamic spraying;
- NS0;
- cholesterol;
- nanoparticles;
- cell culture;
- monoclonal antibody
Abstract
NS0 cells are an important industrial cell line for the production of therapeutic monoclonal antibodies. Culturing these cells is challenging because they are cholesterol auxotrophs, and providing cholesterol to the cells is hampered by the low solubility of lipids in aqueous medium. Limited loading capacity, precipitation, instability, and toxicity are associated with traditional delivery methods that involve solvents or carrier molecules. In this work, nanoparticle cholesterol mixtures (NCM) were produced by electrohydrodynamic spraying and added directly to a cholesterol auxotroph NS0 cell line. Compared to a cholesterol-cyclodextrin solution and a commercial proprietary cholesterol solution, SyntheChol™ NS0 supplement, NCM is significantly less cytotoxic. In the fed batch cell culture process, product titer was increased by 32% when the NCM supplement replaced SyntheChol™ NS0 supplement. An even greater product titer improvement, 64%, was achieved when both NCM and SyntheChol™ NS0 supplements were used in the fed-batch process. © 2011 American Institute of Chemical Engineers Biotechnol. Prog., 2011

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