Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/112067
Title: Comparative stability study of polysorbate 20 and polysorbate 80 related to oxidative degradation
Author(s): Kozuch, Benedykt
Weber, Johanna
Buske, JuliaLook up in the Integrated Authority File of the German National Library
Mäder, KarstenLook up in the Integrated Authority File of the German National Library
Garidel, PatrickLook up in the Integrated Authority File of the German National Library
Diederichs, TimLook up in the Integrated Authority File of the German National Library
Issue Date: 2023
Type: Article
Language: English
Abstract: The surfactants polysorbate 20 (PS20) and polysorbate 80 (PS80) are utilized to stabilize protein drugs. However, concerns have been raised regarding the degradation of PSs in biologics and the potential impact on product quality. Oxidation has been identified as a prevalent degradation mechanism under pharmaceutically relevant conditions. So far, a systematic stability comparison of both PSs under pharmaceutically relevant conditions has not been conducted and little is known about the dependence of oxidation on PS concentration. Here, we conducted a comparative stability study to investigate (i) the different oxidative degradation propensities between PS20 and PS80 and (ii) the impact of PS concentration on oxidative degradation. PS20 and PS80 in concentrations ranging from 0.1 mg⋅mL−1 to raw material were stored at 5, 25, and 40 °C for 48 weeks in acetate buffer pH 5.5 and water, respectively. We observed a temperature-dependent oxidative degradation of the PSs with strong (40 °C), moderate (25 °C), and weak/no degradation (5 °C). Especially at elevated temperatures such as 40 °C, fast oxidative PS degradation processes were detected. In this case study, a stronger degradation and earlier onset of oxidation was observed for PS80 in comparison to PS20, detected via the fluorescence micelle assay. Additionally, degradation was found to be strongly dependent on PS concentration, with significantly less oxidative processes at higher PS concentrations. Iron impurities, oxygen in the vial headspaces, and the pH values of the formulations were identified as the main contributing factors to accelerate PS oxidation.
URI: https://opendata.uni-halle.de//handle/1981185920/114025
http://dx.doi.org/10.25673/112067
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Journal Title: Pharmaceutics
Publisher: MDPI
Publisher Place: Basel
Volume: 15
Issue: 9
Original Publication: 10.3390/pharmaceutics15092332
Appears in Collections:Open Access Publikationen der MLU

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