Department of Pharmaceutics, University of Minnesota , Minneapolis, Minnesota 55455, USA.
Mol Pharm. 2011 Jun 6;8(3):982-9. doi: 10.1021/mp200043u. Epub 2011 May 16.
The water of crystallization released during dehydration of dibasic calcium phosphate dihydrate (DCPD) mediated the cocrystal formation between carbamazepine (CBZ) and nicotinamide (NMA) in intact tablets. The dehydration of DCPD, the disappearance of the reactants (CBZ and NMA) and the appearance of the product (CBZ-NMA cocrystal) were simultaneously monitored by quantitative powder X-ray diffractometry. In a second model system, the water of crystallization released by the dehydration of DCPD caused the chemical decomposition of aspirin. Salicylic acid, one of the decomposition products, reacted with CBZ to form CBZ-salicylic acid cocrystal in tablets. This is the first report of cocrystal formation in intact tablets, demonstrating water mediated noncovalent synthesis in a multicomponent matrix. While the potential implications of such transformations, on both the mechanical and biopharmaceutical properties, can be profound, their characterization, using conventional solution based analytical techniques, can be challenging.
在二水磷酸氢钙(DCPD)脱水过程中释放的结晶水介导了卡马西平(CBZ)和烟酰胺(NMA)在完整片剂中的共晶形成。定量粉末 X 射线衍射法同时监测了 DCPD 的脱水、反应物(CBZ 和 NMA)的消失和产物(CBZ-NMA 共晶)的出现。在第二个模型系统中,DCPD 脱水释放的结晶水导致阿司匹林发生化学分解。作为分解产物之一的水杨酸与 CBZ 反应,在片剂中形成 CBZ-水杨酸共晶。这是在完整片剂中形成共晶的首次报道,证明了多组分基质中水分介导的非共价合成。虽然这种转变对机械和药物特性的潜在影响可能是深远的,但使用传统的基于溶液的分析技术对其进行表征可能具有挑战性。