共晶
结晶
化学
戊二酸
共晶体系
琥珀酸
溶解度
吡拉西坦
化学工程
结晶学
成核
Crystal(编程语言)
材料科学
溶解
差示扫描量热法
晶体生长
有机化学
热力学
分子
氢键
物理
工程类
药理学
医学
合金
作者
Lin Bian,Haiping Zhao,Hongxun Hao,Qiuxiang Yin,Songgu Wu,Junbo Gong,Weibing Dong
标识
DOI:10.1002/ceat.201200720
摘要
Abstract An efficient and reliable approach to discover new pharmaceutical cocrystals in the early development stage is proposed and used to develop cocrystals of piracetam with some aliphatic diacids. A 1:1 cocrystal of piracetam and glutaric acid was screened by a mechanochemical method and identified by powder X‐ray diffraction and differential scanning calorimetry. Followed by solution crystallization, this cocrystal was reproduced. To better understand the mechanism of cocrystal formation in solution crystallization, process analytical technologies including focused beam reflectance measurement, attenuated total reflectance‐Fourier transform infrared, and particle vision measurement were applied to investigate the cocrystallization process of piracetam with glutaric acid. The mechanism of cocrystal formation during solution‐mediated phase transformation is discussed in detail.
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