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首页> 外文期刊>Crystal growth & design >Turning Liquid Propofol into Solid (without Freezing It): Thermodynamic Characterization of Pharmaceutical Cocrystals Built with a Liquid Drug
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Turning Liquid Propofol into Solid (without Freezing It): Thermodynamic Characterization of Pharmaceutical Cocrystals Built with a Liquid Drug

机译:将液体丙泊酚变成固体(不冻结):用液体药物构建的药物共晶体的热力学表征

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摘要

Most drugs are delivered as crystalline solids, but some widely used pharmaceutical ingredients cannot be crystallized at ambient conditions: propofol, one of the most widely used anesthetic agents in the world is a liquid. Here we stabilize propofol in a crystalline phase by cocrystallization, and we thoroughly characterize the structural and thermodynamic properties of the new materials. Ternary solubility diagrams of a liquid pharmaceutical ingredient cocrystallized with a solid coformer are presented and analyzed for the first time. It is shown that, when equilibrated with the solid cocrsytal, the concentration of propofol in water is kept constant in a wide range of starting compositions.
机译:大多数药物以结晶固体形式提供,但某些广泛使用的药物成分无法在环境条件下结晶:异丙酚是世界上使用最广泛的麻醉剂之一。在这里,我们通过共结晶将丙泊酚稳定在结晶相中,并彻底表征了新材料的结构和热力学性质。首次显示并分析了与固体共形成剂共结晶的液体药物成分的三元溶解度图。结果表明,当与固态苯甲醛平衡时,水中丙泊酚的浓度在各种起始组合物中均保持恒定。

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