Hong Chao, Xie Yan, Yao Yashu, Li Guowen, Yuan Xiurong, Shen Hongyi
Research Center for Health and Nutrition, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
Pharm Res. 2015 Jan;32(1):47-60. doi: 10.1007/s11095-014-1443-y. Epub 2014 Jun 18.
To develop a streamlined strategy for pharmaceutical cocrystal preparation without knowledge of the stoichiometric ratio by preparing and characterizing the cocrystals of myricetin (MYR) with four cocrystal coformers (CCF).
An approach based on the phase solubility diagram (PSD) was used for MYR cocrystals preparation and the solid-state properties were characterized by differential scanning calorimetry (DSC), fourier transform-infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), and scanning electron microscopy (SEM). The ternary phase diagram (TPD) was constructed by combining the PSD and nuclear magnetic resonance (NMR) data. After that, the TPD was verified by traditional methods. The dissolution of MYR in the four cocrystals and pure MYR within three different media were also evaluated.
A simple research method for MYR cocrystal preparation was obtained as follows: first, the PSD of MYR and CCF was constructed and analyzed; second, by transforming the curve in the PSD to a TPD, a region of pure cocrystals formation was exhibited, and then MYR cocrystals were prepared and identified by DSC, FT-IR, PXRD, and SEM; third, with the composition of the prepared cocrystal from NMR, the TPD of the MYR-CCF-Solvent system was constructed. The powder dissolution data showed that the solubility and dissolution rate of MYR was significantly enhanced by the cocrystals.
A novel strategy for pharmaceutical cocrystals preparation without knowledge of the stoichiometric ratio based on the TPD was established and MYR cocrystals were successfully prepared. The present study provides a systematic approach for pharmaceutical cocrystal generation, which benefits the development and application of cocrystal technology in drug delivery.
通过制备杨梅素(MYR)与四种共晶形成剂(CCF)的共晶并对其进行表征,开发一种无需了解化学计量比的药物共晶制备简化策略。
采用基于相溶解度图(PSD)的方法制备MYR共晶,并通过差示扫描量热法(DSC)、傅里叶变换红外光谱法(FT-IR)、粉末X射线衍射法(PXRD)和扫描电子显微镜法(SEM)对其固态性质进行表征。通过结合PSD和核磁共振(NMR)数据构建三元相图(TPD)。之后,用传统方法对TPD进行验证。还评估了MYR在四种共晶以及纯MYR在三种不同介质中的溶出情况。
获得了一种制备MYR共晶的简单研究方法,具体如下:首先,构建并分析MYR和CCF的PSD;其次,通过将PSD中的曲线转换为TPD,展示出纯共晶形成区域,然后用DSC、FT-IR、PXRD和SEM制备并鉴定MYR共晶;第三,根据NMR得到的制备共晶的组成,构建MYR-CCF-溶剂体系的TPD。粉末溶出数据表明,共晶显著提高了MYR的溶解度和溶出速率。
建立了一种基于TPD的无需了解化学计量比的药物共晶制备新策略,并成功制备了MYR共晶。本研究为药物共晶的生成提供了一种系统方法,有利于共晶技术在药物递送中的开发和应用。