Conclusion
This paper has focused upon potential replacements for animal origin medium components which exhibit comparable biological performance in cell culture systems but eliminate concerns regarding introduction of adventitious contaminants. Nutrient media devoid of components derived from animals are commercially available. Similar strategies may be exploited to modify customized formulations to generate protein-free and even biochemically-defined second generation media to support cellular proliferation and biological production.
Practical considerations for development and quality assurance of nutrient media demand comparable emphasis on process controls for media manufacture. Careful maintenance of facilities and equipment, environmental controls and monitoring, design and control of manufacturing processes, and validated equipment sanitization are required to ensure final product integrity.
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References
Jayme DW and Blackman KE (1985) Culture media for propagation of mammalian cells, viruses and other biologicals, In: Advances in Biotechnological Processes, 5: 1–30 (Liss) New York
Ham RG and McKeehan WG (1979) Media and growth requirements, In: Methodsin Enzymology 58: 44–93
Bader F, Davis G. Dinowitz M. Garfinkle B, Harvey J, Kozak R. Lubiniecki A. Rubino M, Schubert D, Wiebe M and Woollett G (1998) Assessment of risk of bovine spongiform encephalopathy in pharmaceutical products, part 1, BioPharm 11: 20–32.
Gibcobri, Products & Reference Guide (1997/1998).
Young SP and Garner C (1990) Delivery of iron to human cells by bovine transferrin, Biochem J., 265: 587–591.
Keenan J and Clynes M (1996) Replacement of transferrin by simple iron compounds for MDCK cells grown and subcultured in serum-free medium, In Vitro Cell Dev. Biol-Animal, 32: 451–453
Kovar J and Franek F (1987) Iron compounds at high concentrations enable hybridoma growth in a protein-free medium, Biotechnol. Lett. 9: 259–264.
Sauer P, Burky J, Wesson M and Sternard H (1997) Investigating alternatives to transferrin, In: Process development and production issues in monoclonal antibody manufacturing, Waterside Monoclonal Conference, April 1997, Norfolk, VA.
Fike RM, Pfohl JL, Epstein DA, Jayme DW and Weiss SA (1991) Hybridoma growth and monoclonal antibody production in protein-free hybridoma medium BioPharmocolugy 4: 26–29.
Gorfien SF, Dzimian JL, Tilkins ML, Godwin GP and Fike RM (in press) Recombinant protein production by CHO cells cultured in a chemically defined medium, In: Animal Cell Technology: Basic & Applied Aspects.
Price PJ and Evege E K (1997) Serum-free medium without animal components for virus production, Focus, 19: 67–69.
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© 1999 Kluwer Academic Publishers
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Jayme, D.W., Smith, S.R. (1999). Options to Eliminate Animal-Derived Components of Cell Culture Media. In: Kitagawa, Y., Matsuda, T., Iijima, S. (eds) Animal Cell Technology: Basic & Applied Aspects., vol 1. Springer, Dordrecht. https://doi.org/10.1007/0-306-46865-4_34
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DOI: https://doi.org/10.1007/0-306-46865-4_34
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