Lebar Blaž, Lekić Tinkara, Košir Pija, Kastelic Miha, Zidar Mitja, Mravljak Janez, Pajk Stane
Novartis Pharmaceutical Manufacturing LLC, Verovškova ulica 57, 1000, Ljubljana, Slovenia; Faculty of Pharmacy, University of Ljubljana, Aškerčeva cesta 7, 1000, Ljubljana, Slovenia.
Novartis Pharmaceutical Manufacturing LLC, Verovškova ulica 57, 1000, Ljubljana, Slovenia.
Int J Pharm. 2024 Nov 15;665:124598. doi: 10.1016/j.ijpharm.2024.124598. Epub 2024 Sep 13.
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.
聚山梨酯是药物制剂中广泛使用的辅料,由于其复杂的降解过程,对稳定性构成挑战。本研究考察了聚山梨酯(PS)在温度胁迫(50°C)下的水解情况,重点关注一级包装材料(玻璃瓶与塑料瓶)、缓冲液(组氨酸和乙酸)、抗衡离子(氯离子与苹果酸根离子)和pH值(4 - 7)的影响。我们的研究结果表明,塑料瓶中的可浸出物在组氨酸和乙酸缓冲液中均能抑制PS的降解。通过S形拟合得到的动力学参数表明,每种缓冲液的降解机制不同。此外,组氨酸与苹果酸根离子对PS水解具有抑制作用。采用主成分分析来确定关键因素。这些结果突出了辅料和包装在PS稳定性中的关键作用,为生物制药制剂开发提供了有价值的见解,并加深了对PS降解复杂性的理解。