Literature DB >> 7764677

Viable cell recycle with an inclined settler in the perfusion culture of suspended recombinant Chinese hamster ovary cells.

J A Searles1, P Todd, D S Kompala.   

Abstract

The perfusion culture of suspended mammalian cells requires a cell retention device, the best of which will retain all viable cells and reject all nonviable cells and debris. The inclined settler is a passive, simple, inexpensive, and easy-to-maintain device that has been shown in the past to selectively remove single nonviable cells of hybridoma cultures. In this work, we have demonstrated the preferential return of viable recombinant Chinese hamster ovary (CHO) cells through the use of a three-port settler maintained at lower temperatures and vibrated to reduce cell attachment and enhance cell return to the bioreactor. The residence time of CHO cells in the cooled, vibrated settler was determined by flow-cytometric discrimination of tracer recombinant CHO cells. Cells returning to the bioreactor through the underflow had an average residence time of 1.46 h in the settler. During perfusion cultures with cell densities above 10(6) cells/mL, cells seen to be stalled within the settler were easily dislodged by periodic air bubbling using a simple back-flushing procedure in which headspace gas was brought through the settler underflow port. The resuspended cells were returned to the bioreactor within an average of 32 min after bubbling. This study demonstrates that inclined sedimentation technology can be utilized to selectively recycle viable recombinant CHO cells with only a short retention time in an inclined settler.

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Year:  1994        PMID: 7764677     DOI: 10.1021/bp00026a600

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


  8 in total

1.  Stable expression of recombinant human coagulation factor XIII in protein-free suspension culture of Chinese hamster ovary cells.

Authors:  B H Chun; W G Bang; Y K Park; S K Woo
Journal:  Cytotechnology       Date:  2001-11       Impact factor: 2.058

2.  Dielectrophoretic forces can be safely used to retain viable cells in perfusion cultures of animal cells.

Authors:  A Docoslis; N Kalogerakis; L A Behie
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

3.  Long-term stable production of monocyte-colony inhibition factor (M-CIF) from CHO microcarrier perfusion cultures.

Authors:  D Kong; R Gentz; J Zhang
Journal:  Cytotechnology       Date:  1998-03       Impact factor: 2.058

4.  Increased production of a secreted glycoprotein in engineered CHO cells through amplification of a transcription factor.

Authors:  Venkata R M Mangalampalli; Mark C Mowry; Matthew L Lipscomb; Rohaizah I James; Alyssa K Johnson; Dhinakar S Kompala
Journal:  Cytotechnology       Date:  2002-01       Impact factor: 2.058

5.  Engineering Chinese hamster ovary (CHO) cells to achieve an inverse growth - associated production of a foreign protein, beta-galactosidase.

Authors:  F W Lee; C B Elias; P Todd; D S Kompala
Journal:  Cytotechnology       Date:  1998-11       Impact factor: 2.058

6.  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

7.  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

8.  Enhancing the functionality of a microscale bioreactor system as an industrial process development tool for mammalian perfusion culture.

Authors:  David J Sewell; Richard Turner; Ray Field; William Holmes; Rahul Pradhan; Christopher Spencer; Stephen G Oliver; Nigel Kh Slater; Duygu Dikicioglu
Journal:  Biotechnol Bioeng       Date:  2019-02-20       Impact factor: 4.530

  8 in total

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