Steric exclusion chromatography of lentiviral vectors using hydrophilic cellulose membranes.

Depletion potential Lentiviral vector purification Polyethylene glycol Steric exclusion chromatography

Journal

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

Informations de publication

Date de publication:
05 Jul 2022
Historique:
received: 23 02 2022
revised: 11 05 2022
accepted: 12 05 2022
pubmed: 23 5 2022
medline: 22 6 2022
entrez: 22 5 2022
Statut: ppublish

Résumé

Enveloped viral vectors like lentiviral vectors pose purification challenges due to their low stability. A gentle purification method is considered one of the major bottlenecks for lentiviral vector bioprocessing. To overcome these challenges, a promising method is steric exclusion chromatography which has been used to purify a variety of target molecules. In this study, we successfully identified optimal process parameters for steric exclusion chromatography to purify lentiviral vectors. Lentiviral vector particle recoveries and infectious recoveries of 86% and 88%, respectively, were achieved. The process parameters optimal for steric exclusion chromatography were determined as follows: polyethylene glycol with a molecular weight of 4000 Da, a polyethylene glycol concentration of 12.5%, and a flow rate of 7 mL⋅min

Identifiants

pubmed: 35598541
pii: S0021-9673(22)00341-7
doi: 10.1016/j.chroma.2022.463148
pii:
doi:

Substances chimiques

Polyethylene Glycols 3WJQ0SDW1A
Cellulose 9004-34-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

463148

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

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

Jennifer J Labisch (JJ)

Lab Essentials Applications Development, Sartorius Stedim Biotech GmbH, Göttingen, Lower Saxony, Germany; Institute of Technical Chemistry, Leibniz University Hannover, Hanover, Lower Saxony, Germany. Electronic address: jennifer.labisch@sartorius.com.

Meriem Kassar (M)

Lab Essentials Applications Development, Sartorius Stedim Biotech GmbH, Göttingen, Lower Saxony, Germany; Karlsruhe Institute of Technology, Institute of Process Engineering and Life Sciences, Biomolecular Separation Engineering, Karlsruhe, Baden-Württemberg, Germany.

Franziska Bollmann (F)

Marketing Separation Technologies, Sartorius Stedim Biotech GmbH, Göttingen, Lower Saxony, Germany.

Angela Valentic (A)

Karlsruhe Institute of Technology, Institute of Process Engineering and Life Sciences, Biomolecular Separation Engineering, Karlsruhe, Baden-Württemberg, Germany.

Jürgen Hubbuch (J)

Karlsruhe Institute of Technology, Institute of Process Engineering and Life Sciences, Biomolecular Separation Engineering, Karlsruhe, Baden-Württemberg, Germany.

Karl Pflanz (K)

Lab Essentials Applications Development, Sartorius Stedim Biotech GmbH, Göttingen, Lower Saxony, Germany.

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