Effect of pressure up to 5.5 GPa on dry powder samples of chlorpropamide form-A

被引:49
作者
Boldyreva, Elena V.
Dmitriev, Vladimir
Hancock, Bruno C.
机构
[1] Novosibirsk State Univ, Novosibirsk 630090, Russia
[2] RAS, SB, Inst Solid State Chem, Novosibirsk 630128, Russia
[3] Pfizer Inc, Groton, CT 06340 USA
[4] European Synchrotron Radiat Facil, Swiss Norwegian Beamlines, F-38043 Grenoble, France
基金
俄罗斯基础研究基金会;
关键词
pressure; polymorphism; polymorphic transformation; X-ray powder diffraction; chlorpropamide;
D O I
10.1016/j.ijpharm.2006.07.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of pressure up to 5.5 GPa on a dry powder sample of chlorpropamide (4-chloro-N-((propylamino)-carbonyl)-benzenesulfonamide), form-A (sp. gr. P2(1)2(1)2(1), a = 9.066 angstrom, b = 5.218 angstrom, c = 26.604 angstrom), was studied in situ in a Merrill-Bassett diamond anvil cell using high-resolution Xray powder diffraction (a synchrotron radiation source at SNBLESRF, Grenoble). No evidence of the polymorphic transformation of chlorpropamide form-A to form-C was observed. The A-C polymorphic transition on tabletting previously reported by Otsuka et al. (1989) is therefore likely to be due to local heating effects. Similarly, the phase transitions of form-A reported by Cao (2002) to be induced by pressure applied to a sample in its saturated ethanol solution (at 0.9 and at 2.0 GPa) would appear to be solvent-mediated. In the dry sample, a phase transition may be supposed to occur at pressures above 4 GPa, but this requires further studies. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 57
页数:7
相关论文
共 33 条
[11]   New software for searching the Cambridge Structural Database and visualizing crystal structures [J].
Bruno, IJ ;
Cole, JC ;
Edgington, PR ;
Kessler, M ;
Macrae, CF ;
McCabe, P ;
Pearson, J ;
Taylor, R .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2002, 58 :389-397
[12]  
Burger A, 1975, SCI PHARM, V43, P152
[13]  
Cao W., 2002, THESIS PURDUE U
[14]  
CHAN HK, 1985, DRUG DEV IND PHARM, V11, P315, DOI 10.3109/03639048509056874
[15]  
de Villiers Melgardt M., 1999, Acta Pharmaceutica (Zagreb), V49, P79
[16]   Pressure-induced formation of a solvate of paracetamol [J].
Fabbiani, FPA ;
Allan, DR ;
Dawson, A ;
David, WIF ;
McGregor, PA ;
Oswald, IDH ;
Parsons, S ;
Pulham, CR .
CHEMICAL COMMUNICATIONS, 2003, (24) :3004-3005
[17]   An exploration of the polymorphism of piracetam using high pressure [J].
Fabbiani, FPA ;
Allan, DR ;
Parsons, S ;
Pulham, CR .
CRYSTENGCOMM, 2005, 7 :179-186
[18]   High-pressure recrystallisation - a route to new polymorphs and solvates of acetamide and parabanic acid [J].
Fabbiani, FPA ;
Allan, DR ;
Marshall, WG ;
Parsons, S ;
Pulham, CR ;
Smith, RI .
JOURNAL OF CRYSTAL GROWTH, 2005, 275 (1-2) :185-192
[19]   High-pressure recrystallisation - a route to new polymorphs and solvates [J].
Fabbiani, FPA ;
Allan, DR ;
David, WIF ;
Moggach, SA ;
Parsons, S ;
Pulham, CR .
CRYSTENGCOMM, 2004, 6 :504-511
[20]   Raman observation of a new (ζ) polymorph of glycine? [J].
Goryainov, SV ;
Boldyreva, E ;
Kolesnik, EN .
CHEMICAL PHYSICS LETTERS, 2006, 419 (4-6) :496-500