Journal
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
Volume 233, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jpba.2023.115496
Keywords
Biopharmaceutical formulations; Monoclonal antibody; Excipients; Stability; Polysorbate 80; Degradation product
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This study investigated the stability of polysorbate 80 in different formulation buffers used in biopharmaceuticals, aiming to understand the influence of excipients on its degradation. The degradation of polysorbate 80 can affect the quality of drug products and lead to protein aggregation and particle formation. The study used different assays to monitor the degradation trend and found that excipients can impact the kinetics of degradation, with histidine buffer being more prone to degradation than acetate, phosphate, or citrate buffers.
A study on the polysorbate 80 stability in various formulation buffers commonly used in biopharmaceuticals was performed, to investigate the excipients influence on polysorbate 80 degradation. Polysorbate 80 is a common excipient in biopharmaceutical products. However, its degradation will potentially impact the drug product quality, and may trigger protein aggregation and particles formation. Due to the heterogeneity of the poly-sorbates and the mutual effects with other formulation compositions, the study of polysorbate degradation is challenging. Herein, a real-time stability study was designed and performed. The polysorbate 80 degradation trend was monitored by fluorescence micelle-based assay (FMA), reversed-phase-ultra-performance liquid chromatography-evaporative light scattering detector (RP-UPLC-ELSD) assay, and LC-MS assay. These assays provide orthogonal results to reveal both the micelle-forming capability and the compositional changes of polysorbate 80 in different buffer systems. The degradation occurred after a period of storage under 25 degrees C in different trend, which indicates the excipients could impact the degradation kinetics. Upon comparison, the degradation is prone to happen in histidine buffer than in acetate, phosphate or citrate buffers. LC-MS confirms oxidation as an independent degradation pathway with detection of the oxidative aldehyde. Thus, it is necessary to pay more attention to the excipients selection and their potential impact on polysorbate 80 stability to achieve longer shelf life for the biopharmaceuticals. Besides, the protective roles of several additives were figured out, which could be applied as potential industrial solutions to the polysorbate 80 degradation issues.
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