Fang Liang, Richard Coralie AdÈle, Shi Galen Huaiqiu, Dong Xia, Rase Marissa, Wang Tingting
West Pharmaceutical Services, Inc., Exton, PA; and.
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN.
PDA J Pharm Sci Technol. 2021 Jul-Aug;75(4):317-331. doi: 10.5731/pdajpst.2020.012278. Epub 2021 Jan 15.
Previous studies have shown that parenteral formulation excipients can interact with the silicone oil in prefilled syringes, thereby causing variations in glide force that affect the performance of autoinjectors. Thus, it is crucial to control the glide force of the prefilled syringes to mitigate the potential risk of dose inaccuracies. This study provided a systematic understanding of the chemical interactions between the excipients, physical interactions between the excipients and the container, as well as their impact on the functional performance of prefilled syringes. The design of experiment approach used in this study generated statistically meaningful data, which confirmed that different excipients caused varying increase in glide force in siliconized prefilled syringes. The data indicated that poloxamer 188 can more effectively maintain stable glide forces during accelerated storage conditions compared with polysorbate 80. This finding was further enhanced using Hansen solubility parameters theory, which provided a fundamental understanding of the mechanisms behind the physical interactions. Chemical stability analysis of the surfactants suggested that degradation of excipients also impacts syringe functionality. In summary, the results revealed the unique interactions between parenteral pharmaceutical excipients and primary packaging systems and the physicochemical foundation behind them.
先前的研究表明,肠胃外制剂辅料可与预填充注射器中的硅油相互作用,从而导致滑动力发生变化,进而影响自动注射器的性能。因此,控制预填充注射器的滑动力以降低剂量不准确的潜在风险至关重要。本研究系统地了解了辅料之间的化学相互作用、辅料与容器之间的物理相互作用,以及它们对预填充注射器功能性能的影响。本研究中使用的实验设计方法产生了具有统计学意义的数据,证实了不同的辅料会使硅化预填充注射器的滑动力产生不同程度的增加。数据表明,与聚山梨酯80相比,泊洛沙姆188在加速储存条件下能更有效地保持稳定的滑动力。使用汉森溶解度参数理论进一步强化了这一发现,该理论提供了对物理相互作用背后机制的基本理解。表面活性剂的化学稳定性分析表明,辅料的降解也会影响注射器的功能。总之,结果揭示了肠胃外药物辅料与一级包装系统之间独特的相互作用及其背后的物理化学基础。