A 1:1 pharmaceutical cocrystal of myricetin in combination with uncommon piracetam conformer: X-ray single crystal analysis and mechanochemical synthesis

被引:46
|
作者
Sowa, Michal [1 ]
Slepokura, Katarzyna [2 ]
Matczak-Jon, Ewa [1 ]
机构
[1] Wroclaw Univ Technol, Dept Chem, PL-50370 Wroclaw, Poland
[2] Univ Wroclaw, Fac Chem, PL-50383 Wroclaw, Poland
关键词
Myricetin; Piracetam; Cocrystals; Solvent-drop grinding; Mechanochemistry; X-ray crystallography; CO-CRYSTALS; EXPLORATION; MECHANISM; RAMAN; CELL;
D O I
10.1016/j.molstruc.2013.10.071
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
Combination of two Active Pharmaceutical Ingredients, myricetin and piracetam, yields a 1:1 cocrystal characterized by X-ray single-crystal and powder diffraction, Raman spectroscopy, H-1 NMR, thermal analysis (DSC and TG-DTA) methods. Constituents of the cocrystalline phase were also investigated in terms of Hirshfeld surfaces. Compounds in their neutral forms cocrystallize in the Pna2(1) space group of orthorhombic system. Notably, piracetam adopts an uncommon conformation, not encountered in its cocrystals previously described. In the crystal lattice, a three-dimensional hydrogen-bonded network is observed, including formation of a 2D molecular scaffolding motif. A scale-up procedure is readily available with use of solvent-drop grinding method, in which application of a variety of common solvents leads to formation of the cocrystal, as confirmed by XRPD and Raman spectroscopy. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:114 / 121
页数:8
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