Process monitoring of polysaccharide deketalization for vaccine bioconjugation development using in situ analytical methodology.

PAT PCV Pharmaceuticals Pneumococcal conjugate vaccine Process analytical technology Real time analysis Spectroscopy Vaccine process development

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:
05 Feb 2022
Historique:
received: 16 09 2021
revised: 08 12 2021
accepted: 09 12 2021
pubmed: 21 12 2021
medline: 12 1 2022
entrez: 20 12 2021
Statut: ppublish

Résumé

Pneumococcal conjugate vaccines (PCVs) are formed by bioconjugation of a carrier protein to the purified capsular polysaccharide (Ps) from multiple serological strains of Streptococcus pneumoniae. The associated bioconjugation chemistry relies on initial selective modifications to the Ps backbone structure. Among these modifications, removal of a ketal functional group, termed deketalization, is one that is important for pharmaceutical PCV production. Herein, we report a process monitoring investigation into the deketalization of a polysaccharide relevant to PCV process development. We have applied process analytical technology (PAT) for in situ process monitoring to study the deketalization reaction in real time. We find that in situ FTIR spectroscopy elucidates multiple classes of reaction kinetics, one of which correlates strongly with the deketalization reaction of interest. This PAT approach to real time reaction monitoring offers the possibility of improved process monitoring in the pharmaceutical production of PCVs. To our knowledge, this report represents the first PAT investigation into Ps deketalization. Our findings suggest that broader application of PAT to the chemical modifications associated with PCV bioconjugation, as well as other pharmaceutically relevant bioconjugation processes, carries the power to enhance process understanding, control, and efficiency through real time process monitoring.

Identifiants

pubmed: 34929570
pii: S0731-7085(21)00644-0
doi: 10.1016/j.jpba.2021.114533
pii:
doi:

Substances chimiques

Carrier Proteins 0
Pneumococcal Vaccines 0
Polysaccharides 0
Vaccines, Conjugate 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114533

Informations de copyright

Copyright © 2021. 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

Justin P Lomont (JP)

Analytical Research & Development, MRL, Merck & Co., Inc, West Point, PA 19486, USA. Electronic address: justin.lomont@merck.com.

Nicole M Ralbovsky (NM)

Analytical Research & Development, MRL, Merck & Co., Inc, West Point, PA 19486, USA.

Christine Guza (C)

Process Research & Development, MRL, Merck & Co., Inc., West Point, PA 19486, USA.

Anumita Saha-Shah (A)

Analytical Research & Development, MRL, Merck & Co., Inc, West Point, PA 19486, USA.

Joseph Burzynski (J)

Process Research & Development, MRL, Merck & Co., Inc., West Point, PA 19486, USA.

Janelle Konietzko (J)

Process Research & Development, MRL, Merck & Co., Inc., West Point, PA 19486, USA.

Sheng-Ching Wang (SC)

Process Research & Development, MRL, Merck & Co., Inc., West Point, PA 19486, USA.

Patrick M McHugh (PM)

Process Research & Development, MRL, Merck & Co., Inc., West Point, PA 19486, USA.

Ian Mangion (I)

Analytical Research & Development, MRL, Merck & Co., Inc, West Point, PA 19486, USA.

Joseph P Smith (JP)

Analytical Research & Development, MRL, Merck & Co., Inc, West Point, PA 19486, USA. Electronic address: joseph.smith@merck.com.

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Classifications MeSH