Literature DB >> 7765949

Repeated-batch cultures of baby hamster kidney cell aggregates in stirred vessels.

J L Moreira1, A S Feliciano, P C Santana, P E Cruz, J G Aunins, M J Carrondo.   

Abstract

Natural aggregates of Baby Hamster Kidney cells were grown in stirred vessels operated as repeated-batch cultures during more than 600 hours. Different protocols were applied to passaging different fractions of the initial culture: single cells, large size distributed aggregates and large aggregates. When single cells or aggregates with the same size distribution found in culture are used as inoculum, it is possible to maintain semi-continuous cultures during more than 600 hours while keeping cell growth and viability. These results suggest that aggregate culture in large scale might be feasible, since a small scale culture can easily be used as inoculum for larger vessels without noticeable modification of the aggregate characteristics. However, when only the large aggregates are used as inoculum, it was shown that much lower cell concentrations are obtained, cell viability in aggregates dropping to less than 60%. Under this 'selection' procedure, aggregates maintain a constant size, larger than under batch experiments, up to approximately 400 hours; after this time, aggregate size increases to almost twice the size expected from batch cultures.

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Year:  1994        PMID: 7765949     DOI: 10.1007/BF00762409

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


  20 in total

1.  Evaluation of a microcarrier process for large-scale cultivation of attenuated hepatitis A.

Authors:  B H Junker; F Wu; S Wang; J Waterbury; G Hunt; J Hennessey; J Aunins; J Lewis; M Silberklang; B C Buckland
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

2.  Extended expression of liver functions of hepatocytes in collagen-contained cell aggregates (cell packs).

Authors:  Y Hirai; K Takebe; M Nakajima; M Takashina; M Iizuka
Journal:  Cytotechnology       Date:  1991-07       Impact factor: 2.058

Review 3.  Environmental effects on protein glycosylation.

Authors:  C F Goochee; T Monica
Journal:  Biotechnology (N Y)       Date:  1990-05

4.  Evaluation of a hepatocyte-entrapment hollow fiber bioreactor: a potential bioartificial liver.

Authors:  S L Nyberg; R A Shatford; M V Peshwa; J G White; F B Cerra; W S Hu
Journal:  Biotechnol Bioeng       Date:  1993-01-20       Impact factor: 4.530

5.  Production of rabies vaccine by an industrial scale BHK 21 suspension cell culture process.

Authors:  T W Pay; A Boge; F J Menard; P J Radlett
Journal:  Dev Biol Stand       Date:  1985

6.  Expression of recombinant antibody and secreted alkaline phosphatase in mammalian cells. Influence of cell line and culture system upon production kinetics.

Authors:  A J Racher; J L Moreira; P M Alves; M Wirth; U H Weidle; H Hauser; M J Carrondo; J B Griffiths
Journal:  Appl Microbiol Biotechnol       Date:  1994-02       Impact factor: 4.813

7.  Studies of baby hamster kidney natural cell aggregation in suspended batch cultures.

Authors:  J L Moreira; P M Alves; J M Rodrigues; P E Cruz; J G Aunins; M J Carrondo
Journal:  Ann N Y Acad Sci       Date:  1994-11-30       Impact factor: 5.691

8.  High-level expression of recombinant human soluble thrombomodulin in serum-free medium by CHO-K1 cells.

Authors:  M Ogata; K Wakita; K Kimura; Y Marumoto; K Oh-i; S Shimizu
Journal:  Appl Microbiol Biotechnol       Date:  1993-01       Impact factor: 4.813

9.  Cultivation of anchorage-dependent animal cells in microsphere-induced aggregate culture.

Authors:  S Goetghebeur; W S Hu
Journal:  Appl Microbiol Biotechnol       Date:  1991-03       Impact factor: 4.813

10.  Influence of glucose and oxygen supply conditions on the oxygenation of multicellular spheroids.

Authors:  W Mueller-Klieser; J P Freyer; R M Sutherland
Journal:  Br J Cancer       Date:  1986-03       Impact factor: 7.640

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