共晶
化学
溶解
拉莫三嗪
Crystal(编程语言)
盐(化学)
多态性(计算机科学)
结晶学
晶体结构
立体化学
结晶习性
结晶
有机化学
分子
氢键
基因
生物
基因型
神经科学
程序设计语言
生物化学
癫痫
计算机科学
作者
Jiaquan Li,Yangjia Huang,Qi An,Wenyu Li,Jianting Li,Hongji Liu,Dezhi Yang,Yang Lu,Zhengzheng Zhou
标识
DOI:10.1016/j.ijpharm.2022.122310
摘要
Multi-component pharmaceutical systems such as cocrystal and salt have gained popularity in academia and industry due to their ability to regulate the poor physicochemical properties of active pharmaceutical ingredients (APIs). However, different crystal states, namely polymorphs are becoming a key factor influencing future clinical drug safety. It remains an under explored field, particularly how to hit the polymorphs of multi-components system quickly and effectively. For the first time, a novel drug-drug salt of lamotrigine (LAM)-tolfenamic acid (TOL) with two polymorphs and two solvates were discovered in this study. Forms I and II exist in rhombohedral and block crystal morphologies, whereas methanol and ethanol solvates are crystallized as rods and flakes, respectively. Further physicochemical properties were characterized and compared between parent compounds and the four crystal forms. The apparent solubilities of the new four crystal forms were higher than TOL but lower than LAM. The intrinsic dissolution rates of all crystal forms at 37.0 °C followed a similar trend, and all crystal forms were non-hygroscopic (<1.0%). Two stable polymorphs provide a new choice for the further formulation development.
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