Department of Pharmaceutical Sciences, Merck & Co., Inc., Kenilworth, New Jersey 07033.
Department of Pharmaceutical Sciences, Merck & Co., Inc., Kenilworth, New Jersey 07033.
J Pharm Sci. 2019 Nov;108(11):3609-3615. doi: 10.1016/j.xphs.2019.07.005. Epub 2019 Jul 23.
Research on pharmaceutical pediatric powder-for-suspension formulations mainly focuses on chemical and physical stability of the active pharmaceutical ingredient. However, the chemical stability of excipients could also play a key role in governing the quality and performance of the product. The suspending agents that are added into formulations to suspend the active pharmaceutical ingredient particles are critical to ensure the suspension dose accuracy. In this article, we investigate the chemical stability of the suspending agent-xanthan gum-in the presence of other excipients, particularly commonly used acid modifiers (i.e., citric acid, malic acid, succinic acid, and fumaric acid) in pediatric powder-for-suspension formulations. We observed that some of the acid modifiers catalyze cross-linking of xanthan gum during accelerated stability studies in powder blends, which significantly decreases the viscosity of the corresponding constituted suspension, resulting in poor suspendability and dose inaccuracy. Furthermore, we found that the cross-linking of xanthan gum is acid-dependent and that a careful selection of acid modifiers can mitigate the degradation issues of xanthan gum. Finally, we characterized the cross-linked xanthan gum using Fourier transform infrared spectroscopy and solid-state nuclear magnetic resonance and discussed the possible degradation mechanisms.
关于药物儿童混悬剂配方的研究主要集中在活性药物成分的化学和物理稳定性上。然而,赋形剂的化学稳定性也可能对产品的质量和性能起着关键作用。混悬剂是添加到配方中以悬浮活性药物成分颗粒的物质,对于确保混悬剂量的准确性至关重要。在本文中,我们研究了在其他赋形剂存在的情况下,混悬剂-黄原胶的化学稳定性,特别是在儿科混悬剂配方中常用的酸改性剂(如柠檬酸、苹果酸、琥珀酸和富马酸)。我们观察到,在粉末混合物的加速稳定性研究中,一些酸改性剂会催化黄原胶的交联,这会显著降低相应构成的混悬液的粘度,导致混悬剂的混悬稳定性差和剂量不准确。此外,我们发现黄原胶的交联是酸依赖性的,并且可以通过仔细选择酸改性剂来减轻黄原胶的降解问题。最后,我们使用傅里叶变换红外光谱和固态核磁共振对交联黄原胶进行了表征,并讨论了可能的降解机制。