Literature DB >> 30298995

Shift to high-intensity, low-volume perfusion cell culture enabling a continuous, integrated bioprocess.

Matthew Gagnon1, Shashikant Nagre2, Wenge Wang1, Gregory W Hiller1.   

Abstract

In order to address the increasing demand for biologics, cell culture intensification using perfusion offers significantly higher productivities while also reducing manufacturing costs, especially when part of an integrated, continuous bioprocess. An initial study of a long-duration perfusion process using a cell-bleed to maintain a target cell density observed a 2.1-fold higher cell-specific productivity and a gradual decline in the culture growth rate when perfused at an overall lower rate. Subsequent studies sought an alternative process that largely reduced the overall volume of media needed by first perfusing at a high cell-specific perfusion rate (CSPR) to support a high cell density followed by continued perfusion at a low CSPR to promote a more productive stationary phase. This high intensity, low-volume perfusion (HILVOP) process achieved cumulative volumetric productivities of 1.5-1.6 g/L/day with two CHO cell lines. When compared to each cell line's respective commercial-ready, fed-batch process, a 3.1-3.8-fold productivity increase was demonstrated while yielding similar product quality. Furthermore, the higher productivity achieved with HILVOP used 6.6-12.3-fold less media than a similarly productive long-duration process.
© 2018 American Institute of Chemical Engineers Biotechnol. Prog., 34:1472-1481, 2018. © 2018 American Institute of Chemical Engineers.

Entities:  

Keywords:  CHO cells; HIPCOP; cell culture intensification; integrated bioprocess; perfusion

Mesh:

Year:  2018        PMID: 30298995     DOI: 10.1002/btpr.2723

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


  5 in total

1.  Engineering death resistance in CHO cells for improved perfusion culture.

Authors:  Michael A MacDonald; Matthias Nöbel; Verónica S Martínez; Kym Baker; Evan Shave; Peter P Gray; Stephen Mahler; Trent Munro; Lars K Nielsen; Esteban Marcellin
Journal:  MAbs       Date:  2022 Jan-Dec       Impact factor: 6.440

2.  Rapid development of clone-specific, high-performing perfusion media from established feed supplements.

Authors:  Patrick Mayrhofer; David Reinhart; Andreas Castan; Renate Kunert
Journal:  Biotechnol Prog       Date:  2019-11-11

3.  N-1 Perfusion Platform Development Using a Capacitance Probe for Biomanufacturing.

Authors:  Emily S C Rittershaus; Matthew S Rehmann; Jianlin Xu; Qin He; Charles Hill; Jeffrey Swanberg; Michael C Borys; Zheng-Jian Li; Anurag Khetan
Journal:  Bioengineering (Basel)       Date:  2022-03-22

4.  Online estimation of changing metabolic capacities in continuous Corynebacterium glutamicum cultivations growing on a complex sugar mixture.

Authors:  Peter Sinner; Marlene Stiegler; Oliver Goldbeck; Gerd M Seibold; Christoph Herwig; Julian Kager
Journal:  Biotechnol Bioeng       Date:  2021-12-11       Impact factor: 4.395

5.  Wide-surface pore microfiltration membrane drastically improves sieving decay in TFF-based perfusion cell culture and streamline chromatography integration for continuous bioprocessing.

Authors:  Nuno D S Pinto; Mark Brower
Journal:  Biotechnol Bioeng       Date:  2020-07-30       Impact factor: 4.395

  5 in total

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