Literature DB >> 1366723

A comparison of different culture methods for hybridoma propagation and monoclonal antibody production.

C P Marquis1, C Harbour, J P Barford, K S Low.   

Abstract

A major variable to consider in the production of biologicals from mammalian cell cultures is the mode of operation, be it a batch, continuous, perfusion, fed-batch or other production method. The final choice must consider a number of fundamental and economic issues. Here we present some antibody production data from different cell lines using different modes of production and discuss the important factors for consideration in choosing a production strategy. It was found that the productivity of batch cultures was lower than that obtained in continuous and perfused cultures, but that productivity could be improved by implementing suitable feeding strategies. The antibody productivity of one cell line, MCL1, during exponential phase was not affected by media type or glucose level. The maximum productivity of two cell lines in continuous culture was found to occur at dilution rates below the maximum, from 0.019 to 0.030 hr-1.

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Year:  1990        PMID: 1366723     DOI: 10.1007/bf00148812

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  12 in total

1.  Batch production and growth kinetics of hybridomas.

Authors:  O W Merten
Journal:  Cytotechnology       Date:  1988-02       Impact factor: 2.058

2.  Continuous hybridoma growth and monoclonal antibody production in hollow fiber reactors-separators.

Authors:  G L Altshuler; D M Dziewulski; J A Sowek; G Belfort
Journal:  Biotechnol Bioeng       Date:  1986-05       Impact factor: 4.530

3.  A radial flow hollow fiber bioreactor for the large-scale culture of mammalian cells.

Authors:  J P Tharakan; P C Chau
Journal:  Biotechnol Bioeng       Date:  1986-03       Impact factor: 4.530

4.  A kinetic analysis of hybridoma growth and metabolism in batch and continuous suspension culture: effect of nutrient concentration, dilution rate, and pH.

Authors:  W M Miller; H W Blanch; C R Wilke
Journal:  Biotechnol Bioeng       Date:  1988-10-05       Impact factor: 4.530

5.  Flow effects on the viability and lysis of suspended mammalian cells.

Authors:  Anne McQueen; Eliane Meilhoc; James E Bailey
Journal:  Biotechnol Lett       Date:  1987-12       Impact factor: 2.461

6.  Blood grouping with monoclonal antibodies.

Authors:  C Harbour; A Fletcher
Journal:  Dev Biol Stand       Date:  1987

7.  Automated production of monoclonal antibodies in a cytostat.

Authors:  S Fazekas de St Groth
Journal:  J Immunol Methods       Date:  1983-02-25       Impact factor: 2.303

8.  High-Density culture of mouse-human hybridoma in serum-free defined medium.

Authors:  Y Takazawa; M Tokashiki; H Murakami; K Yamada; H Omura
Journal:  Biotechnol Bioeng       Date:  1988-02-05       Impact factor: 4.530

9.  Monoclonal antibodies specific for blood groups A and B.

Authors:  A Fletcher; C Harbour; R de Zwart
Journal:  Aust J Exp Biol Med Sci       Date:  1984-08

10.  High yields from microcarrier cultures by medium perfusion.

Authors:  M Butler; T Imamura; J Thomas; W G Thilly
Journal:  J Cell Sci       Date:  1983-05       Impact factor: 5.285

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  1 in total

1.  Increase of hybridoma productivity using an original dialysis culture system.

Authors:  B Mathiot; A Perani; D Dumas; M Maugras; J Didelon; J F Stoltz
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

  1 in total

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