Chen Xiaoming, Griesser Ulrich J, Te Ruth L, Pfeiffer Ralph R, Morris Kenneth R, Stowell Joseph G, Byrn Stephen R
Department of Industrial and Physical Pharmacy, School of Pharmacy and Pharmacal Sciences, Purdue University, 575 Stadium Mall Drive, West Lafayette, IN 47906-2051, USA.
J Pharm Biomed Anal. 2005 Jul 15;38(4):670-7. doi: 10.1016/j.jpba.2005.02.017. Epub 2005 Mar 17.
Indomethacin was used as a model compound to investigate acid-base reactions of solid materials, a common type of drug-excipient interaction. In a typical experiment, 500 mg of pure alpha-form indomethacin were mixed with 500 mg of sodium bicarbonate. The mixture was kept at 40 degrees C and at several relative humidities. The reaction was monitored by IR spectroscopy, X-ray powder diffraction, and solid-state NMR. At 40 degrees C and 80% RH, the reaction is nearly complete after 300 h. As observed by IR spectroscopy, the characteristic peaks of alpha-indomethacin disappear during the course of the reaction with the appearance of the characteristic peaks of the salt product, sodium indomethacin trihydrate. Solid-state NMR spectra and X-ray powder diffraction patterns of the reaction mixtures confirm the transformation of the mixtures to sodium indomethacin trihydrate; the reduced peak intensities in the diffraction patterns of the product relative to the initial mixtures indicate the formation of a microcrystalline product. A change in the reaction rate of sodium bicarbonate with alpha-indomethacin is observed when the mixtures are stored at different relative humidities. At 40 degrees C and 66% RH, the reaction of sodium bicarbonate with alpha-indomethacin is about 86% complete after 500 h. No detectable reaction was observed for sodium bicarbonate with the alpha form of indomethacin at 40 degrees C and 11% RH after 15 months. The combination of these solid-state characterization techniques is demonstrated to be essential to detect and monitor acid-base reactions in solid materials, which are impossible to monitor using solution-chemistry methods. The reaction kinetics at 66% RH fits the Jander equation very well, which is consistent with a diffusion-controlled mechanism.
吲哚美辛被用作模型化合物来研究固体材料的酸碱反应,这是一种常见的药物-辅料相互作用类型。在一个典型的实验中,将500毫克纯α型吲哚美辛与500毫克碳酸氢钠混合。混合物在40摄氏度和几种相对湿度下保存。通过红外光谱、X射线粉末衍射和固态核磁共振对反应进行监测。在40摄氏度和80%相对湿度下,300小时后反应几乎完成。如通过红外光谱观察到的,α-吲哚美辛的特征峰在反应过程中消失,同时出现了盐产物三水合吲哚美辛钠的特征峰。反应混合物的固态核磁共振谱和X射线粉末衍射图谱证实了混合物向三水合吲哚美辛钠的转变;产物衍射图谱中相对于初始混合物的峰强度降低表明形成了微晶产物。当混合物在不同相对湿度下储存时,观察到碳酸氢钠与α-吲哚美辛的反应速率发生变化。在40摄氏度和66%相对湿度下,500小时后碳酸氢钠与α-吲哚美辛的反应约完成86%。在40摄氏度和11%相对湿度下,15个月后未观察到碳酸氢钠与α型吲哚美辛有可检测到的反应。事实证明,这些固态表征技术的组合对于检测和监测固体材料中的酸碱反应至关重要,而使用溶液化学方法是无法监测这些反应的。66%相对湿度下的反应动力学非常符合扬德方程,这与扩散控制机制一致。