Tuning selectivity in cation-exchange chromatography applied for monoclonal antibody separations, part 1: Alternative mobile phases and fine tuning of the separation.

Cation-exchange chromatography Method development Monoclonal antibody Salt gradient Salt-mediated pH gradient pH gradient

Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
10 May 2019
Historique:
received: 18 12 2018
revised: 07 02 2019
accepted: 18 02 2019
pubmed: 27 2 2019
medline: 30 7 2019
entrez: 27 2 2019
Statut: ppublish

Résumé

Cation exchange chromatography (CEX) of therapeutic monoclonal antibodies is generally performed with either salt gradient (MES buffer + NaCl) or using commercial pH gradient buffer. The goal of this study was to find out some alternative buffer systems for CEX separation of mAbs, which may offer alternative selectivity, while maintaining similar peak shapes. Among the new buffers that were tested, (N-morpholino)ethanesulfonic acid (MES) / 1,3-diamino-2-propanol (DAP), and citric acid / 2-(cyclohexylamino)ethanesulfonic acid (CHES) systems were particularly promising, especially when combining them with a moderate salt gradient of NaCl. This two buffer system provides an equivalent or slightly better separation than the standard, mobile phases for therapeutic mAbs. It was also demonstrated that working with salt-mediated pH gradients, allows to extend the possibilities in method development, since the concentration of salt in the mobile phase has a significant impact on selectivity. Using HPLC modeling software (Drylab), it was possible to successfully develop CEX methods for authentic mAb samples within only 6 h, by optimizing the gradient steepness and salt concentration in the B eluent.

Identifiants

pubmed: 30807918
pii: S0731-7085(18)32855-3
doi: 10.1016/j.jpba.2019.02.024
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
Buffers 0
Cations 0
Sodium Chloride 451W47IQ8X

Types de publication

Journal Article

Langues

eng

Pagination

138-147

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Evelin Farsang (E)

Department of Analytical Chemistry, University of Pannonia, Egyetem u. 10, 8200 Veszprém, Hungary.

Amarande Murisier (A)

School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, CMU - Rue Michel Servet, 1, 1211 Geneva 4, Switzerland.

Krisztián Horváth (K)

Department of Analytical Chemistry, University of Pannonia, Egyetem u. 10, 8200 Veszprém, Hungary.

Alain Beck (A)

Center of Immunology Pierre Fabre, 5 Avenue Napoléon III, BP 60497, 74160 Saint-Julien-en-Genevois, France.

Róbert Kormány (R)

Egis Pharmaceuticals Plc., Keresztúri út 30-38, Budapest 1106, Hungary.

Davy Guillarme (D)

School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, CMU - Rue Michel Servet, 1, 1211 Geneva 4, Switzerland.

Szabolcs Fekete (S)

School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, CMU - Rue Michel Servet, 1, 1211 Geneva 4, Switzerland. Electronic address: szabolcs.fekete@unige.ch.

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Classifications MeSH