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Crystal Structures, Stability, and Solubility Evaluation of a 2:1 Diosgenin–Piperazine Cocrystal

机译:晶体结构,稳定性和溶解度评估为2:1迪斯本素 - 哌嗪烯库

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A cocrystal of diosgenin with piperazine in 2:1 stoichiometry was successfully synthesized. The solid form was prepared by liquid assisted grinding, slurry and crystallization methods. The cocrystal was characterized by powder X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, Fourier transform infrared spectroscopy, and structure determined by single crystal X-ray diffraction, the hydrogen bonds formed into fish bone structure along the [010] direction and all the molecules packed into 3D layer structure along a axis. After formation of cocrystal, the solubility of diosgenin was improved, and the solubility value in 0.2% SDS solution was approximately 1.5 times as large as that of the parent material. Graphic Abstract
机译:成功地合成了2:1化学计量中哌嗪的二氧吡啶蛋白蛋白的共聚物。通过液体辅助研磨,浆料和结晶方法制备固体形式。通过粉末X射线衍射,差分扫描量热法,热重分析,傅里叶变换红外光谱,以及由单晶X射线衍射确定的结构,沿着[010]方向和所有的鱼骨结构确定的结构沿轴填充到3D层结构中的分子。在形成Cocrystal后,改善了Diosgenin的溶解度,0.2%SDS溶液中的溶解度值约为母体材料的1.5倍。图形摘要

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