Impact of virus-antibody interactions on viral clearance in anion exchange chromatography.

Anion exchange chromatography (AEX) Electrostatic interactions Minute Virus of Mice (MVM) Molecular Operating Environment (MOE) Virus removal

Journal

Journal of chromatography. A
ISSN: 1873-3778
Titre abrégé: J Chromatogr A
Pays: Netherlands
ID NLM: 9318488

Informations de publication

Date de publication:
06 Dec 2020
Historique:
received: 24 08 2020
revised: 16 10 2020
accepted: 17 10 2020
pubmed: 1 11 2020
medline: 2 12 2020
entrez: 31 10 2020
Statut: ppublish

Résumé

Viral clearance is an important performance metric for the downstream process of monoclonal antibodies (mAbs) due to its impact on patient safety. Anion exchange chromatography (AEX) has been well-accepted in the industry as one of the workhorse techniques for removing viruses, and is considered to be able to achieve high log clearance values under most operating conditions. However, it is not uncommon for viral clearance results on AEX to fall below the desired level despite operating under conditions that should achieve high clearance levels according to conventional wisdom of how this mode of chromatography operates. In this study, a design of experiment (DoE) approach was used to develop a more fundamental understanding of viral clearance during AEX chromatography using Minute Virus of Mice (MVM) on POROS HQ resin. Load pH, conductivity and virus concentration were evaluated as design factors for three mAbs with varying physical and chemical properties. The hydrophobicity and surface charge distributions of the molecules were found to be the most significant factors in influencing viral clearance performance, and the viral clearance trends did not seem to fit with conventional wisdom. To explain this seemingly unconventional behavior, we propose a new mechanism that suggests that interactions between the mAb and the virus have a major contribution on retention of the virus on the resin. This furthered understanding may help improve the predictability, performance and robustness of viral clearance during AEX chromatography.

Identifiants

pubmed: 33128974
pii: S0021-9673(20)30909-2
doi: 10.1016/j.chroma.2020.461635
pii:
doi:

Substances chimiques

Anions 0
Antibodies, Monoclonal 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

461635

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jessica Hung (J)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA.

Shing Fung Lam (SF)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA.

Zhijun Tan (Z)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA. Electronic address: zhijun.tan@bms.com.

Derek Choy (D)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA.

Naresh Chennamsetty (N)

Biologics Analytical Development and Attribute Science, Bristol-Myers Squibb, New Brunswick, NJ, USA.

Angela Lewandowski (A)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA.

Wenbin Qi (W)

Thermo Fisher Scientific, Waltham, MA, USA.

Moira Lynch (M)

Thermo Fisher Scientific, Waltham, MA, USA.

Sanchayita Ghose (S)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA.

Zheng Jian Li (ZJ)

Biologics Process Development, Bristol-Myers Squibb, Devens, MA, USA.

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Classifications MeSH