Miniaturized Forced Degradation of Therapeutic Proteins and ADCs by Agitation-Induced Aggregation Using Orbital Shaking of Microplates.
Antibody drug conjugate(s) (ADC)
Forced conditions
Formulation
High throughput technology(s)
Interfacial stress
Mechanical stress
Monoclonal antibody(s)
Physical stability
Protein aggregation
Journal
Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R
Informations de publication
Date de publication:
05 2022
05 2022
Historique:
received:
01
06
2021
revised:
19
09
2021
accepted:
19
09
2021
pubmed:
27
9
2021
medline:
21
4
2022
entrez:
26
9
2021
Statut:
ppublish
Résumé
Microplate-based formulation screening is a powerful approach to identify stabilizing excipients for therapeutic proteins while reducing material requirements. However, this approach is sometimes not representative of studies conducted in relevant container closures. The present study aimed to identify critical parameters for a microplate-based orbital shaking method to screen biotherapeutic formulations by agitation-induced aggregation. For this purpose, an in-depth methodological study was conducted using different shakers, microplates, and plate seals. Aggregation was monitored by size exclusion chromatography, turbidity, and backgrounded membrane imaging. Both shaker quality and liquid-seal contact had substantial impacts on aggregation during shaking and resulted in non-uniform sample treatment when parameters were not suitably selected. The well volume to fill volume ratio (V
Identifiants
pubmed: 34563536
pii: S0022-3549(21)00497-4
doi: 10.1016/j.xphs.2021.09.027
pii:
doi:
Substances chimiques
Excipients
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1401-1413Informations de copyright
Copyright © 2021 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript.