Literature DB >> 7765113

High-density culture of FM-3A cells using a bioreactor with an external tangential-flow filtration device.

H Kawahara1, S Mitsuda, E Kumazawa, Y Takeshita.   

Abstract

A novel bioreactor system developed for high-density cultures of suspended mammalian cells is described using a tangential-flow filtration device outside the culture vessel to separate viable cells from spent medium. The filtration device is based on thin porous microfiltration membranes with a pore size of 0.20-0.65 microns. Because cells have a diameter of about 10-20 microns, they cannot permeate these membranes with the spent medium. So, allowing a perfusion culture to be created using this system. In most membrane filtration systems, clogging of the membranes has made long-term operation difficult. In this system, however, high pressure is not applied directly to the membrane, thus minimizing clogging. Also, clogging of the membrane was prevented by washing the membrane surface once a day, and increasing the membrane surface area. With this system, FM-3A cells were cultured and maintained at a high density of 3.0 x 10(7) cells/ml for two weeks, and a continuous culture was supported for as long as 34 days.

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Year:  1994        PMID: 7765113     DOI: 10.1007/BF00772196

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


  7 in total

1.  High density culture of hybridoma cells using a perfusion culture vessel with an external centrifuge.

Authors:  M Tokashiki; T Arai; K Hamamoto; K Ishimaru
Journal:  Cytotechnology       Date:  1990-05       Impact factor: 2.058

2.  Hybridoma perfusion systems: a comparison study.

Authors:  D de la Broise; M Noiseux; B Massie; R Lemieux
Journal:  Biotechnol Bioeng       Date:  1992-06-05       Impact factor: 4.530

3.  Use of tangential flow filtration in perfusion propagation of hybridoma cells for production of monoclonal antibodies.

Authors:  D Velez; L Miller; J D Macmillan
Journal:  Biotechnol Bioeng       Date:  1989-02-20       Impact factor: 4.530

4.  Cell culture on artificial capillaries: an approach to tissue growth in vitro.

Authors:  R A Knazek; P M Gullino; P O Kohler; R L Dedrick
Journal:  Science       Date:  1972-10-06       Impact factor: 47.728

5.  Spin filter culture: the propagation of mammalian cells in suspension.

Authors:  P Himmelfarb; P S Thayer; H E Martin
Journal:  Science       Date:  1969-05-02       Impact factor: 47.728

6.  Entrapment of animal cells for production of monoclonal antibodies and other biomolecules.

Authors:  K Nilsson; W Scheirer; O W Merten; L Ostberg; E Liehl; H W Katinger; K Mosbach
Journal:  Nature       Date:  1983-04-14       Impact factor: 49.962

7.  Microencapsulation of living cells and tissues.

Authors:  F Lim; R D Moss
Journal:  J Pharm Sci       Date:  1981-04       Impact factor: 3.534

  7 in total
  3 in total

1.  Mammalian cell retention devices for stirred perfusion bioreactors.

Authors:  S M Woodside; B D Bowen; J M Piret
Journal:  Cytotechnology       Date:  1998-11       Impact factor: 2.058

2.  Separation of CHO cells using hydrocyclones.

Authors:  Rodrigo C V Pinto; Ricardo A Medronho; Leda R Castilho
Journal:  Cytotechnology       Date:  2007-11-14       Impact factor: 2.058

3.  Very high density of CHO cells in perfusion by ATF or TFF in WAVE bioreactor™. Part I. Effect of the cell density on the process.

Authors:  Marie-Françoise Clincke; Carin Mölleryd; Ye Zhang; Eva Lindskog; Kieron Walsh; Véronique Chotteau
Journal:  Biotechnol Prog       Date:  2013-05-21
  3 in total

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