Pharmaceutical cocrystallization: Engineering a remedy for caffeine hydration

被引:608
作者
Trask, AV
Motherwell, WDS
Jones, W
机构
[1] Univ Cambridge, Dept Chem, Pfizer Inst Pharmaceut Mat Sci, Cambridge CB2 1EW, England
[2] Cambridge Crystallog Data Ctr, Cambridge CB2 1EZ, England
关键词
D O I
10.1021/cg0496540
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A systematic crystal engineering study was performed on the model pharmaceutical compound caffeine to prepare a cocrystal that, unlike caffeine, is physically stable at all relative humidities (RH). Six cocrystal materials containing caffeine with one of several dicarboxylic acids are described herein. Methods of cocrystallization included solution growth, neat solid-state grinding, and grinding with solvent-drop addition. Crystal structures are reported for a total of five cocrystals containing caffeine (with oxalic acid, malonic acid, maleic acid, and glutaric acid), including two recently reported polymorphic caffeine cocrystals. In each of these structures, a predicted intermolecular hydrogen-bonding motif is observed. The stability with respect to RH is evaluated for the six cocrystal materials. The cocrystal with oxalic acid exhibits complete stability to humidity over a period of several weeks. Other cocrystals demonstrate lesser degrees of stability with respect to humidity.
引用
收藏
页码:1013 / 1021
页数:9
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