Virus study for continuous low pH viral inactivation inside a coiled flow inverter.


Journal

Biotechnology and bioengineering
ISSN: 1097-0290
Titre abrégé: Biotechnol Bioeng
Pays: United States
ID NLM: 7502021

Informations de publication

Date de publication:
04 2019
Historique:
received: 27 06 2018
revised: 06 09 2018
accepted: 26 10 2018
pubmed: 20 11 2018
medline: 22 4 2020
entrez: 20 11 2018
Statut: ppublish

Résumé

Continuous processing for the production of monoclonal antibodies (mAb) gains more and more importance. Several solutions exist for all the necessary production steps, leading to the possibility to build fully continuous processes. Low pH viral inactivation is a part of the standard platform process for mAb production. Consequently, Klutz et al. introduced the coiled flow inverter (CFI) as a tool for continuous low pH viral inactivation. Besides theoretical calculations of viral reduction, no viral clearance study has been presented so far. In addition, the validation of continuous viral clearance is often neglected in the already existing studies for continuous processing. This study shows in detail the development and execution of a virus study for continuous low pH viral inactivation inside a CFI. The concept presented is also valid for adaptation to other continuous viral clearance steps. The development of this concept includes the technical rationale for an experimental setup, a valid spiking procedure, and finally a sampling method. The experimental results shown represent a viral study using xenotropic murine leukemia virus as a model virus. Two different protein A (ProtA) chromatography setups with varying pH levels were tested. In addition, one of these setups was tested against a batch experiment utilizing the same process material. The results show that sufficient low pH viral inactivation (decadic logarithm reduction value >4) was achieved in all experiments. Complete viral inactivation took place within the first 14.5 min for both continuous studies and the batch study, hence showing similar results. This study therefore represents a successful virus study concept and experiment for a continuous viral inactivation step. Moreover, it was shown that the transfer from batch results to the continuous process is possible. This is accomplished by the narrow residence time distribution of the CFI, showing how close the setup approaches the ideal plug flow and with that batch operation.

Identifiants

pubmed: 30450694
doi: 10.1002/bit.26872
doi:

Substances chimiques

Antibodies, Monoclonal 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

857-869

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Laura David (L)

Invite GmbH, Biotech, Leverkusen, Germany.

Benjamin Maiser (B)

Bayer AG, Engineering & Technology, Leverkusen, Germany.

Martin Lobedann (M)

Invite GmbH, Biotech, Leverkusen, Germany.

Peter Schwan (P)

Bayer AG, Engineering & Technology, Leverkusen, Germany.

Michael Lasse (M)

Charles River Laboratories Germany GmbH, Biologics Testing Solutions, Cologne, Germany.

Horst Ruppach (H)

Charles River Laboratories Germany GmbH, Biologics Testing Solutions, Cologne, Germany.

Gerhard Schembecker (G)

BCI, Plant and Process Design, Dortmund, TU Dortmund University, Germany.

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Classifications MeSH