Literature DB >> 20730770

Characterization of cell-banking parameters for the cryopreservation of mammalian cell lines in 100-mL cryobags.

Rüdiger Heidemann1, Svenja Lünse, Doan Tran, Chun Zhang.   

Abstract

This article describes a cell banking process for rBHK cell lines in 100-mL cryobags. As the use of larger volume cell banks requires greater cell numbers and longer preparation time, extensive characterization of key process parameters beyond the conventional ranges was performed to support a cGMP banking process. All experiments were conducted using two recombinant BHK21 cell lines, one of them cotransfected with Hsp70. The results show that the entire cell banking process for these BHK cell lines can be performed at room temperature. A DMSO exposure time up to 5 h either directly in a bioreactor or in shaker flasks did not result in any significant negative effect after cell thaw, when the cryocontainers were frozen immediately after filling. Extensive characterization did not indicate any significant apoptotic effects after thaw. However, the Hsp70 cotransfected cell line did show a slightly better protection from potential cryopreservation-induced apoptosis. Surprisingly, it was found that cells transferred into cryobags showed a low recovery rate after thaw if the incubation time exceeded 1.5 h before freezing. Additional experiments confirmed that the DMSO exposure time inside the cryocontainer in contrast to the DMSO exposure in a reactor or shaker flasks is much more critical. The cryobag cell banking process should therefore be performed within a 1(1/2)-2 h window; a banking process for vials should not exceed 2(1/2) h. (c) 2010 American Institute of Chemical Engineers

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Year:  2010        PMID: 20730770     DOI: 10.1002/btpr.427

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


  8 in total

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2.  GMP cryopreservation of large volumes of cells for regenerative medicine: active control of the freezing process.

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Journal:  Stem Cell Rev Rep       Date:  2021-11-10       Impact factor: 6.692

4.  A Method to Efficiently Cryopreserve Mammalian Cells on Paper Platforms.

Authors:  Muhammedin Deliorman; Pavithra Sukumar; Roaa Alnemari; Mohammad A Qasaimeh
Journal:  Bio Protoc       Date:  2020-09-20

5.  Very high density of Chinese hamster ovary cells in perfusion by alternating tangential flow or tangential flow filtration in WAVE Bioreactor™-part II: Applications for antibody production and cryopreservation.

Authors:  Marie-Françoise Clincke; Carin Mölleryd; Puneeth K Samani; Eva Lindskog; Eric Fäldt; Kieron Walsh; Véronique Chotteau
Journal:  Biotechnol Prog       Date:  2013-05-21

6.  Bioprocessing of cryopreservation for large-scale banking of human pluripotent stem cells.

Authors:  Yan Li; Teng Ma
Journal:  Biores Open Access       Date:  2012-10

7.  A scale down process for the development of large volume cryopreservation.

Authors:  Peter Kilbride; G John Morris; Stuart Milne; Barry Fuller; Jeremy Skepper; Clare Selden
Journal:  Cryobiology       Date:  2014-09-16       Impact factor: 2.487

8.  Spatial considerations during cryopreservation of a large volume sample.

Authors:  Peter Kilbride; Stephen Lamb; Stuart Milne; Stephanie Gibbons; Eloy Erro; James Bundy; Clare Selden; Barry Fuller; John Morris
Journal:  Cryobiology       Date:  2016-05-30       Impact factor: 2.487

  8 in total

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