Literature DB >> 7764531

Monoclonal antibody process development using medium concentrates.

T A Bibila1, C S Ranucci, K Glazomitsky, B C Buckland, J G Aunins.   

Abstract

A fed-batch process using concentrated medium was evaluated for its ability to improve cell culture longevity and final monoclonal antibody (MAb) titers for two monoclonal antibody producing cell lines. It was found to result in up to 7-fold increases in final antibody titers compared to batch culture controls. Although the development cell line specific fed-batch protocols is critical to the development of cost-efficient large-scale production processes, the use of complete medium concentrates provided us with a quick and simple method for producing large quantities of antibodies in the early stages of process development, thus accelerating early work on purification process development, analytical development, biochemical characterization, and safety studies. Insights gained from the concentrated medium fed-batch approach were valuable for the development of refined, cell line specific feeding strategies yielding final MAb titers on the order of 1-2 g/L. Process development data on the effects of inhibitory growth byproducts, medium osmolarity, and the mode of nutrient feed addition on culture longevity and MAb production and information on culture metabolic behavior were successfully incorporated in the development of the optimized fed-batch protocols.

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Year:  1994        PMID: 7764531     DOI: 10.1021/bp00025a011

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  18 in total

1.  Continuous, high capacity reconstitution of nutrient media from concentrated intermediates.

Authors:  D W Jayme; J M Kubiak; T A Battistoni; D J Cady
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

2.  Basal medium development for serum-free culture: a historical perspective.

Authors:  D Jayme; T Watanabe; T Shimada
Journal:  Cytotechnology       Date:  1997-01       Impact factor: 2.058

3.  Alteration of mammalian cell metabolism by dynamic nutrient feeding.

Authors:  W Zhou; J Rehm; A Europa; W S Hu
Journal:  Cytotechnology       Date:  1997-07       Impact factor: 2.058

4.  Apoptosis and nutrition: Involvement of amino acid transport system in repression of hybridoma cell death.

Authors:  F Franěk; K Chládková-Šrámková
Journal:  Cytotechnology       Date:  1995-01       Impact factor: 2.058

5.  Discrimination among IgG1-kappa monoclonal antibodies produced by two cell lines using charge state distributions in nanoESI-TOF mass spectra.

Authors:  Leila Zamani; Jessica Lindholm; Leopold L Ilag; Sven P Jacobsson
Journal:  J Am Soc Mass Spectrom       Date:  2009-02-27       Impact factor: 3.109

6.  Analysis of the use of fortified medium in continuous culture of mammalian cells.

Authors:  A Gambhir; C Zhang; A Europa; W S Hu
Journal:  Cytotechnology       Date:  1999-11       Impact factor: 2.058

7.  Introduction to animal cell culture technology-past, present and future.

Authors:  O-W Merten
Journal:  Cytotechnology       Date:  2006-08-03       Impact factor: 2.058

8.  Effect of hypoosmotic pressure on cell growth and antibody production in recombinant Chinese hamster ovary cell culture.

Authors:  M S Lee; G M Lee
Journal:  Cytotechnology       Date:  2001-07       Impact factor: 2.058

9.  Influence of osmolarity and pH increase to achieve a reduction of monoclonal antibodies aggregates in a production process.

Authors:  R Franco; G Daniela; M Fabrizio; G Ilaria; H Detlev
Journal:  Cytotechnology       Date:  1999-01       Impact factor: 2.058

10.  Amino acids metabolism by VO 208 hybridoma cells: some aspects of the culture process and medium composition influence.

Authors:  A Martial-Gros; J L Goergen; J M Engasser; A Marc
Journal:  Cytotechnology       Date:  2001-10       Impact factor: 2.058

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