Polymorphs of praziquantel-succinic acid cocrystal: Crystal structure, thermodynamic relationship, and improved pharmaceutical performance

被引:4
|
作者
Wang, Lin [1 ]
Xie, Qihuang [2 ]
Shi, Xiaoju [3 ]
Zhu, Yujing [2 ]
Li, Shuyan [1 ]
Ji, Fang [1 ]
Yu, Jing [1 ]
Li, Duanxiu [2 ]
Zhang, Hailu [2 ,4 ]
机构
[1] Jiangsu Vocat Coll Agr & Forestry, Jurong 212400, Peoples R China
[2] Chinese Acad Sci, Suzhou Inst Nanotech & Nanobion, Lab Pharmaceut Solid State Chem, Suzhou 215123, Peoples R China
[3] Suzhou Vocat Hlth Coll, Suzhou 215009, Peoples R China
[4] Wuhan Univ Sci & Technol, Interdisciplinary Inst NMR & Mol Sci NMR X, Sch Chem & Chem Engn, State Key Lab Refractories & Met, Wuhan 430081, Peoples R China
基金
中国国家自然科学基金;
关键词
Pharmaceutical cocrystal; Cocrystal polymorphs; Praziquantel; Thermodynamic relationship; Pharmaceutical performance; PHYSICOCHEMICAL PROPERTIES; SOLUBILITY; CRYSTALLIZATION; PROGRAM;
D O I
10.1016/j.molstruc.2024.138124
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Polymorphism is a ubiquitous phenomenon of critical significance for the pharmaceutical industry, yet reports on cocrystal polymorphs are scarce. This study elucidates the crystal structure of the praziquantel (PZQ)-succinic acid (SUC) cocrystal polymorph, alpha-PZQ-SUC. The dominant supramolecular interaction in the cocrystal polymorph is the O - H center dot center dot center dot O hydrogen bond between SUC and PZQ, consistent with the supramolecular interaction in the previously reported beta-PZQ-SUC polymorph. Comprehensive analysis, including thermal analysis, theoretical calculations, and solvent-mediated polymorphic transformation experiments, established a monotropic relationship between the two polymorphs, with alpha-PZQ-SUC demonstrating greater stability than beta-PZQ-SUC. Both alpha-PZQ-SUC and beta-PZQ-SUC enhance the solubility and dissolution behavior of PZQ, indicating their suitability for pharmaceutical applications based on improved pharmaceutical performance.
引用
收藏
页数:7
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