Effect of organic acids on the solid-state polymorphic phase transformation of piracetam

被引:3
|
作者
Fan, Fanfan [1 ]
Xu, Shuyuan [1 ]
Guo, Minshan [1 ]
Cai, Ting [1 ,2 ,3 ]
机构
[1] China Pharmaceut Univ, Coll Pharm, Dept Pharmaceut, State Key Lab Nat Med, Nanjing 211198, Peoples R China
[2] China Pharmaceut Univ, Sch Engn, Dept Pharmaceut Engn, Nanjing 211198, Peoples R China
[3] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
Piracetam; Organic acids; Metastable polymorph; Solid-state phase transformation; Crystallization kinetics; DIFFUSIONLESS CRYSTAL-GROWTH; HIGH-PRESSURE; TRANSITION; FORMS; CRYSTALLIZATION; STABILITY; GLASS; EXPLORATION; NIFEDIPINE; MIXTURES;
D O I
10.1016/j.ijpharm.2023.123532
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Metastable polymorphs are frequently used in oral solid dosage forms to enhance the absorption of poorly watersoluble drug compounds. However, the solid phase transformation from the metastable polymorph to the thermodynamically stable polymorph during manufacturing or storage poses a major challenge for product development and quality control. Here, we report that low-content organic acids can exhibit distinct effects on the solid-state polymorphic phase transformation of piracetam (PCM), a nootropic drug used for memory enhancement. The addition of 1 mol% citric acid (CA) and tricarballylic acid (TA) can significantly inhibit the phase transformation of PCM Form I to Form II, while glutaric acid (GA) and adipic acid (AA) produce a minor effect. A molecular simulation shows that organic acid molecules can adsorb on the crystal surface of PCM Form I, thus slowing the movement of molecules from the metastable form to the stable form. Our study provides deeper insights into the mechanisms of solid-state polymorphic phase transformation of drugs in the presence of additives and facilitates opportunities for controlling the stability of metastable pharmaceuticals.
引用
收藏
页数:11
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