Development and qualification of an automated capillary Western method for the identification of polysaccharide serotypes in pneumococcal conjugate vaccine (PCV).


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:
20 Jan 2024
Historique:
received: 27 02 2023
revised: 02 10 2023
accepted: 10 10 2023
medline: 6 12 2023
pubmed: 23 10 2023
entrez: 22 10 2023
Statut: ppublish

Résumé

Streptococcus pneumoniae bacterial infection causes mortality in both adults and infants. To mitigate the impact of the disease, several Pneumococcal conjugate vaccines (PCVs) have been manufactured for the U.S. market, including the recent approval of the 15-valent PCV Vaxneuvance™ from MSD. These vaccines demonstrate high efficacy for both the adult and pediatric dose. These PCVs contain multiple unique serotypes in the final, formulated vaccine product, and identifying a specific polysaccharide, in the presence of other serotypes, is a critical quality attribute that must be demonstrated through analytical testing. Here we describe the development and qualification of an identity assay using an automated capillary western system, called Simple Western, implementing a multi-valent system suitability sample (SSS) to determine individual polysaccharide components. The assay was optimized through rigorous analytical development and was successfully qualified for use in the clinical release of the PCV.

Identifiants

pubmed: 37866079
pii: S0731-7085(23)00557-5
doi: 10.1016/j.jpba.2023.115788
pii:
doi:

Substances chimiques

Pneumococcal Vaccines 0
Vaccines, Conjugate 0
Polysaccharides 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

115788

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors are employed by Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, a pharmaceutical company and may potentially own stock and/or hold stock options in Merck & Co., Inc., Rahway, NJ, USA. Funding for this research was provided by Merck Sharp and Dohme Corp., a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Auteurs

Alyssa Deiss (A)

Analytical Research Development, Merck & Co., Inc., Rahway, NJ, USA. Electronic address: alyssa.deiss@merck.com.

John W Loughney (JW)

Analytical Research Development, Merck & Co., Inc., Rahway, NJ, USA.

Richard R Rustandi (RR)

Analytical Research Development, Merck & Co., Inc., Rahway, NJ, USA.

Kimberly Vuolo (K)

Analytical Research Development, Merck & Co., Inc., Rahway, NJ, USA.

Megan A Mackey (MA)

Analytical Research Development, Merck & Co., Inc., Rahway, NJ, USA.

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Classifications MeSH