Nie Haichen, Xu Wei, Ren Jie, Taylor Lynne S, Marsac Patrick J, John Christopher T, Byrn Stephen R
Department of Industrial and Physical Pharmacy, Purdue University , 575 Stadium Mall Drive, West Lafayette, Indiana 47907, United States.
Preformulation Sciences, Merck & Co., Inc. , 770 Sumneytown Pike, West Point, Pennsylvania 19486, United States.
Mol Pharm. 2016 Oct 3;13(10):3541-3552. doi: 10.1021/acs.molpharmaceut.6b00630. Epub 2016 Sep 7.
Excipient-induced salt disproportionation (conversion from salt form to free form) in the solid state during storage or manufacturing is a severe formulation issue that can negatively influence product performance. However, the role of excipient properties on salt disproportionation and mechanisms of proton transfer between salt and excipients are still unclear. Moreover, knowledge about the formation of disproportionation products and the consequent impact of these reactions products on the disproportionation process is still inadequate. In the present study, three commonly used lubricants (sodium stearate, calcium stearate, and magnesium stearate) were mixed with a hydrochloride salt as binary mixtures to examine their different capabilities for inducing salt disproportionation at a stressed storage condition (40 °C/65% RH). The overall objective of this research is to explore factors influencing the kinetics and extent of disproportionation including surface area, alkalinity, hygroscopicity, formation of new species, etc. In addition, we also aim to clarify the reaction mechanism and proton transfer between the model salt and stearates to provide insight into the in situ formed reaction products. We found that the properties of stearates significantly affect the disproportionation process in the initial stage of storage, while properties of the reaction products negatively affect the hygroscopicity of the powder mixture promoting disproportionation during longer-term storage. In addition, lubrication difference among three stearates was evaluated by performing compaction studies. The findings of this study provide an improved understanding of the proton transfer mechanism between the ionized form of an active pharmaceutical ingredient and excipients in solid dosage forms. It also provides pragmatic information for formulation scientists to select appropriate lubricants and other excipients, and to design robust formulations.
在储存或生产过程中,辅料诱导的盐在固态下的歧化(从盐形式转化为游离形式)是一个严重的制剂问题,会对产品性能产生负面影响。然而,辅料性质对盐歧化的作用以及盐与辅料之间质子转移的机制仍不清楚。此外,关于歧化产物的形成以及这些反应产物对歧化过程的后续影响的知识仍然不足。在本研究中,将三种常用润滑剂(硬脂酸钠、硬脂酸钙和硬脂酸镁)与一种盐酸盐作为二元混合物混合,以研究它们在加速储存条件(40°C/65%相对湿度)下诱导盐歧化的不同能力。本研究的总体目标是探索影响歧化动力学和程度的因素,包括表面积、碱性、吸湿性、新物种的形成等。此外,我们还旨在阐明模型盐与硬脂酸盐之间的反应机制和质子转移,以深入了解原位形成的反应产物。我们发现,硬脂酸盐的性质在储存初期显著影响歧化过程,而反应产物的性质在长期储存期间对促进歧化的粉末混合物的吸湿性产生负面影响。此外,通过进行压片研究评估了三种硬脂酸盐之间的润滑差异。本研究的结果有助于更好地理解固体剂型中活性药物成分的离子化形式与辅料之间的质子转移机制。它还为制剂科学家选择合适的润滑剂和其他辅料以及设计稳健的制剂提供了实用信息。