Polysorbate stability: Effects of packaging materials, buffers, counterions, and pH

Polysorbates, widely used excipients in drug formulations, present a stability challenge due to complex degradation processes. This study investigates the hydrolysis of polysorbate (PS) under temperature stress (50 °C), focusing on the impact of primary packaging materials (glass vs. plastic vials), buffers (histidine and acetic acid), counterions (chloride vs. malate), and pH (4-7). Our findings reveal that leachables from plastic vials inhibit PS degradation in both histidine and acetic acid buffers. Kinetic parameters derived from sigmoidal fitting suggest distinct degradation mechanisms for each buffer. Furthermore, the malate counterion with histidine displays inhibitory effects on PS hydrolysis. Principal component analysis was employed to identify key factors. These results highlight the critical role of excipients and packaging in PS stability, providing valuable insights for biopharmaceutical formulation development and a deeper understanding of PS degradation complexities.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2024-09-13
DOI
https://doi.org/10.1016/j.ijpharm.2024.124598
Citations
4
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
0.69

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article

Polysorbate stability: Effects of packaging materials, buffers, counterions, and pH

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4 citations
International Journal of Pharmaceutics
biodegradable polymer synthesis and properties
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article

Polysorbate stability: Effects of packaging materials, buffers, counterions, and pH

Stane Pajk, Janez Mravljak, Miha Kastelic, Blaž Lebar, Mitja Zidar, Tinkara Lekić, Pija Košir
article en
4 citations

Abstract

Polysorbates, widely used excipients in drug formulations, present a stability challenge due to complex degradation processes. This study investigates the hydrolysis of polysorbate (PS) under temperature stress (50 °C), focusing on the impact of primary packaging materials (glass vs. plastic vials), buffers (histidine and acetic acid), counterions (chloride vs. malate), and pH (4-7). Our findings reveal that leachables from plastic vials inhibit PS degradation in both histidine and acetic acid buffers. Kinetic parameters derived from sigmoidal fitting suggest distinct degradation mechanisms for each buffer. Furthermore, the malate counterion with histidine displays inhibitory effects on PS hydrolysis. Principal component analysis was employed to identify key factors. These results highlight the critical role of excipients and packaging in PS stability, providing valuable insights for biopharmaceutical formulation development and a deeper understanding of PS degradation complexities.

International Journal of PharmaceuticsVol. 665
University of Ljubljana (SI), Slovenian Centre of Excellence for Space Sciences and Technologies (SI), Novartis (Slovenia) (SI)
Novartis, Javna Agencija za Raziskovalno Dejavnost RS
Openalex Percentile: Top 34%
biodegradable polymer synthesis and properties
0.69
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