High-pressure studies of pharmaceuticals: An exploration of the behavior of piracetam

被引:122
作者
Fabbiani, Francesca P. A.
Allan, David R.
David, William I. F.
Davidson, Alistair J.
Lennie, Alistair R.
Parsons, Simon
Pulham, Colin R.
Warren, John E.
机构
[1] Rutherford Appleton Lab, CCLRC, ISIS, Neutron Facil, Didcot OX11 0QX, Oxon, England
[2] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[3] Univ Edinburgh, Ctr Sci Extreme Conditions, Edinburgh EH9 3JJ, Midlothian, Scotland
[4] CCLRC, Daresbury Lab, Warrington WA4 4AD, Cheshire, England
关键词
D O I
10.1021/cg0607710
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The structural response of the nootropic drug piracetam (2-oxo-pyrrolidineacetamide) to both direct compression and high-pressure recrystallization from aqueous solution is reported. Crystals obtained by these methods have been characterized in situ by single-crystal X-ray diffraction. Compression of form II between pressures of 0.45-0.70 GPa caused a reversible, single-crystal to single-crystal transition to give a new polymorph, form V. Crystallization from a dilute aqueous solution of piracetam at a pressure of 0.6 GPa via crystallization of high-pressure ice-VI resulted in the formation of a previously unreported dihydrate. The molecular packing arrangements of these new structures are compared with the known polymorphs and hydrates of piracetam. This study highlights how the systematic variation of pressure is a powerful method for the exploration of polymorphism and solvate formation and has the potential to add a further dimension to polymorph screening of pharmaceuticals.
引用
收藏
页码:1115 / 1124
页数:10
相关论文
共 78 条
[71]  
TERMINASSIAN L, 1992, J THERM ANAL CALORIM, V38, P181
[72]   An up-to-date approach to drug polymorphism [J].
Toscani, S .
THERMOCHIMICA ACTA, 1998, 321 (1-2) :73-79
[73]   Supercritical carbon dioxide treatment as a method for polymorph preparation of deoxycholic acid [J].
Tozuka, Y ;
Kawada, D ;
Oguchi, T ;
Yamamoto, K .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 263 (1-2) :45-50
[74]   Crystalline solids [J].
Vippagunta, SR ;
Brittain, HG ;
Grant, DJW .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 48 (01) :3-26
[75]   Crystal engineering of pharmaceutical co-crystals from polymorphic active pharmaceutical ingredients [J].
Vishweshwar, P ;
McMahon, JA ;
Peterson, ML ;
Hickey, MB ;
Shattock, TR ;
Zaworotko, MJ .
CHEMICAL COMMUNICATIONS, 2005, (36) :4601-4603
[76]   Effect of pressure on the crystal structure of salicylaldoxime-I, and the structure of salicylaldoxime-II at 5.93 GPa [J].
Wood, Peter A. ;
Forgan, Ross S. ;
Henderson, David ;
Parsons, Simon ;
Pidcock, Elna ;
Tasker, Peter A. ;
Warren, John E. .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2006, 62 (06) :1099-1111
[77]   Physical characterization of polymorphic drugs: an integrated characterization strategy [J].
Yu, L ;
Reutzel, SM ;
Stephenson, GA .
PHARMACEUTICAL SCIENCE & TECHNOLOGY TODAY, 1998, 1 (03) :118-127
[78]  
2003, CHEM ENG NEWS, V81, P32