Semi-continuous scale-down models for clone and operating parameter screening in perfusion bioreactors.


Journal

Biotechnology progress
ISSN: 1520-6033
Titre abrégé: Biotechnol Prog
Pays: United States
ID NLM: 8506292

Informations de publication

Date de publication:
05 2019
Historique:
received: 05 10 2018
revised: 07 01 2019
accepted: 13 02 2019
pubmed: 19 2 2019
medline: 16 4 2020
entrez: 19 2 2019
Statut: ppublish

Résumé

Perfusion cell culture, confined traditionally to the production of fragile molecules, is currently gaining broader attention in the biomanufacturing of therapeutic proteins. The development of these processes is made difficult by the limited availability of appropriate scale-down models. This is due to the continuous operation that requires complex control and cell retention capacity. For example, the determination of an optimal perfusion and bleed rate for continuous cell culture is often performed in scale-down bioreactors and requires a substantial amount of time and effort. To increase the experimental throughput and decrease the required workload, a semi-continuous procedure, referred to as the VCD

Identifiants

pubmed: 30773840
doi: 10.1002/btpr.2790
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2790

Informations de copyright

© 2019 American Institute of Chemical Engineers.

Auteurs

Jean-Marc Bielser (JM)

Biotech Process Sciences, Merck Biopharma, Vevey, Switzerland.
Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering, ETH Zürich, Zürich, Switzerland.

Jakub Domaradzki (J)

Biotech Process Sciences, Merck Biopharma, Vevey, Switzerland.

Jonathan Souquet (J)

Biotech Process Sciences, Merck Biopharma, Vevey, Switzerland.

Hervé Broly (H)

Biotech Process Sciences, Merck Biopharma, Vevey, Switzerland.

Massimo Morbidelli (M)

Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering, ETH Zürich, Zürich, Switzerland.

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Classifications MeSH