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Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation
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 un...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537708/ https://www.ncbi.nlm.nih.gov/pubmed/37765302 http://dx.doi.org/10.3390/pharmaceutics15092332 |
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author | Kozuch, Benedykt Weber, Johanna Buske, Julia Mäder, Karsten Garidel, Patrick Diederichs, Tim |
author_facet | Kozuch, Benedykt Weber, Johanna Buske, Julia Mäder, Karsten Garidel, Patrick Diederichs, Tim |
author_sort | Kozuch, Benedykt |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10537708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105377082023-09-29 Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation Kozuch, Benedykt Weber, Johanna Buske, Julia Mäder, Karsten Garidel, Patrick Diederichs, Tim Pharmaceutics Article 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. MDPI 2023-09-16 /pmc/articles/PMC10537708/ /pubmed/37765302 http://dx.doi.org/10.3390/pharmaceutics15092332 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kozuch, Benedykt Weber, Johanna Buske, Julia Mäder, Karsten Garidel, Patrick Diederichs, Tim Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation |
title | Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation |
title_full | Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation |
title_fullStr | Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation |
title_full_unstemmed | Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation |
title_short | Comparative Stability Study of Polysorbate 20 and Polysorbate 80 Related to Oxidative Degradation |
title_sort | comparative stability study of polysorbate 20 and polysorbate 80 related to oxidative degradation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10537708/ https://www.ncbi.nlm.nih.gov/pubmed/37765302 http://dx.doi.org/10.3390/pharmaceutics15092332 |
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