Department of Pharmaceutics, College of Pharmacy, University of Minnesota-Twin Cities, 9-177 WDH, 308 Harvard Street Southeast, Minneapolis, Minnesota 55455, United States.
Department of Chemistry, X-Ray Crystallographic Laboratory, LeClaire-Dow Chemical Instrumentation Facility, University of Minnesota-Twin Cities, 207 Pleasant Street SE, Minneapolis, Minnesota 55455, United States.
Mol Pharm. 2020 Oct 5;17(10):3915-3929. doi: 10.1021/acs.molpharmaceut.0c00661. Epub 2020 Sep 22.
Levothyroxine sodium pentahydrate (LSP; CHINNaO·5HO) gradually loses one molecule of water of crystallization as the water vapor pressure is decreased from 90% to 15% RH (40 °C), a behavior characteristic of nonstoichiometric hydrates. LSP loses four molecules of water of crystallization to form levothyroxine sodium monohydrate (LSM; CHINNaO·HO) under realistic storage conditions (40 °C/0% RH for 3 h). The crystal structure of LSP was determined following which the specimen was partially dehydrated to form LSM. The crystal structure of LSM provided insight into its potential for high reactivity. Thus, its presence in a drug product is undesirable. In LSP-oxalic acid mixtures stored in a hermetic container at 40 °C, there was moisture transfer from drug to excipient. Synchrotron X-ray diffractometry revealed dehydration of LSP resulting in LSM, while anhydrous oxalic acid transformed to its dihydrate. In formulations of LSP, chemical degradation of levothyroxine sodium may be preceded by its partial dehydration.
五水合左甲状腺素钠(LSP;CHINNaO·5HO)在水蒸气压力从 90%降至 15%RH(40°C)的过程中,会逐渐失去一个结晶水分子,这种行为是非化学计量水合物的特征。LSP 在实际储存条件下(40°C/0%RH 持续 3 小时)会失去四个结晶水分子,形成左甲状腺素钠一水合物(LSM;CHINNaO·HO)。在确定 LSP 的晶体结构后,对其进行部分脱水以形成 LSM。LSM 的晶体结构提供了其高反应性的潜在信息。因此,它在药物产品中是不理想的。在 40°C 下储存在密封容器中的 LSP-草酸混合物中,药物会向赋形剂转移水分。同步加速器 X 射线衍射揭示了 LSP 的脱水导致 LSM 的形成,而无水草酸则转化为其二水合物。在 LSP 的配方中,左甲状腺素钠的化学降解可能先于其部分脱水。