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Thermal and in Situ X-ray Diffraction Analysis of a Dimorphic Co-Crystal, 1:1 Caffeine-Glutaric Acid

机译:双晶共晶体1:1咖啡因-戊二酸的热和原位X射线衍射分析

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Spurred by the enormous interest in co-crystals from the pharmaceutical industry, many novel co-crystals of active pharmaceutical ingredients have been discovered in recent years, and this has in turn led to an increasing number of reports on polymorphs of co-crystals. Hence, a thorough characterization and understanding of co-crystal polymorphs is a valuable step during drug development. The purpose of this study is to perform in situ structural analysis and to determine thermodynamic stability of a dimorphic co-crystal system, 1:1 caffeine glutaric acid (CA-GA, Forms I and II). We performed thermal and structural characterizations by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), hot-stage microscopy (HSM), and slurry and in situ variable temperature X-ray diffraction (VTXRD). For completeness, we have also redetermined crystal structures of CA GA Forms I and II at 180 K using single crystal X-ray diffraction. Our results revealed that Form II is stable and Form I is metastable at ambient conditions. Further, the results suggest that the dimorphs are enantiotropically related and the transition temperature is estimated to be 79 degrees C.
机译:在制药业对共晶体的巨大兴趣的刺激下,近年来发现了许多新型的活性药物成分的共晶体,这反过来导致了有关共晶体多晶型物的报道越来越多。因此,对共晶多晶型物进行彻底的表征和理解是药物开发过程中的重要步骤。这项研究的目的是进行原位结构分析,并确定双晶共结晶系统1:1咖啡因戊二酸(CA-GA,形式I和II)的热力学稳定性。我们通过差示扫描量热法(DSC),热重分析(TGA),热台显微镜(HSM)以及浆料和原位可变温度X射线衍射(VTXRD)进行了热和结构表征。为完整起见,我们还使用单晶X射线衍射重新确定了CA GA I和II型CA GA的晶体结构。我们的结果表明,在环境条件下,晶型II是稳定的,晶型I是亚稳的。此外,结果表明,双晶型与对映体有关,并且转变温度估计为79℃。

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