Hattori Yusuke, Sato Maiko, Otsuka Makoto
Research Institute of Pharmaceutical Sciences, Faculty of Pharmacy, Musashino University, Tokyo, Japan.
J Pharm Pharmacol. 2015 Nov;67(11):1512-8. doi: 10.1111/jphp.12461. Epub 2015 Aug 19.
Objectives of this study are investigating the initial dissolution kinetics of the cocrystal of carbamazepine (CBZ) with nicotinamide (NIC) and understanding its initial dissolution process.
Cocrystal solids of CBZ with NIC were prepared by co-milling and solvent evaporation methods. The formation of cocrystal solid was verified via X-ray diffraction measurement. Dissolution tests of the solids were performed using an original flow cell and ultraviolet-visible spectroscopic detector. The spectra monitored in situ were analyzed to determine the dissolved compounds separately using the classical least squares regression method. The initial dissolution profiles were interpreted using simultaneous model of dissolution and phase changes.
In the initial dissolution, CBZ in the cocrystal structure dissolved in water and it was suggested that CBZ reached a metastable intermediate state simultaneously with dissolution. The cocrystal solid prepared by solvent evaporation provided a higher rate constant of the phase change than that prepared by co-milling. Our results thus support the use of evaporation as the method of choice to produce ordered cocrystal structures.
We suggest that CBZ forms dihydrate during the dissolution process; however, during the initial phase of dissolution, CBZ changes to a metastable intermediate phase.
本研究的目的是研究卡马西平(CBZ)与烟酰胺(NIC)共晶的初始溶解动力学,并了解其初始溶解过程。
通过共研磨和溶剂蒸发法制备了CBZ与NIC的共晶固体。通过X射线衍射测量验证了共晶固体的形成。使用原始流通池和紫外可见光谱检测器对固体进行溶解测试。使用经典最小二乘回归法对原位监测的光谱进行分析,以分别确定溶解的化合物。使用溶解和相变的同步模型解释初始溶解曲线。
在初始溶解过程中,共晶结构中的CBZ溶解于水中,并且表明CBZ在溶解的同时达到了亚稳态中间状态。通过溶剂蒸发制备的共晶固体比通过共研磨制备的共晶固体提供了更高的相变速率常数。因此,我们的结果支持使用蒸发作为制备有序共晶结构的首选方法。
我们认为CBZ在溶解过程中形成二水合物;然而,在溶解的初始阶段,CBZ转变为亚稳态中间相。