共晶
化学
阿魏酸
苯甲酸
没食子酸
有机化学
活性成分
溶剂
溶解度
色谱法
分子
氢键
生物信息学
生物
抗氧化剂
作者
Shiying Yang,Qiwen Liu,Weiwen Ji,Qi An,Junke Song,Cheng Xing,Dezhi Yang,Li Zhang,Yang Lu,Guanhua Du
出处
期刊:Molecules
[MDPI AG]
日期:2022-03-21
卷期号:27 (6): 2022-2022
被引量:3
标识
DOI:10.3390/molecules27062022
摘要
Solvent-assisted grinding (SAG) and solution slow evaporation (SSE) methods are generally used for the preparation of cocrystals. However, even by using the same solvent, active pharmaceutical ingredient (API), and cocrystal coformer (CCF), the cocrystals prepared using the two methods above are sometimes inconsistent. In the present study, in the cocrystal synthesis of praziquantel (PRA) with polyhydroxy phenolic acid, including protocatechuic acid (PA), gallic acid (GA), and ferulic acid (FA), five different cocrystals were prepared using SAG and SSE. Three of the cocrystals prepared using the SAG method have the structural characteristics of carboxylic acid dimer, and two cocrystals prepared using the SSE method formed cocrystal solvates with the structural characteristics of carboxylic acid monomer. For phenolic acids containing only one phenolic hydroxyl group (ferulic acid), when preparing cocrystals with PRA by using SAG and SSE, the same product was obtained. In addition, the weak molecular interactions that were observed in the cocrystal are explained at the molecular level by using theoretical calculation methods. Finally, the in vitro solubility of cocrystals without crystal solvents and in vivo bioavailability of PRA-FA were evaluated to further understand the influence on the physicochemical properties of API for the introduction of CCF.
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