Antisolvent crystallization of a cardiotonic drug in ionic liquids: Effect of mixing on the crystal properties

被引:20
作者
Jacqueline, Resende de Azevedo [1 ]
Fabienne, Espitalier [1 ]
Jean-Jacques, Letourneau [1 ]
Ines, Re Maria [1 ]
机构
[1] Univ Toulouse, Ctr RAPSODEE, Campus Jarlard, F-81013 Albi 09, France
关键词
Poorly water-soluble chug; Ionic liquids; Antisolvent crystallization; Dissolution enhancement; PRECIPITATION PROCESS; POLYMORPHIC DESIGN; SOLVENTS;
D O I
10.1016/j.jcrysgro.2016.12.057
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
LASSBio-294 (3,4-methylenedioxybenzoyl-2-thienylhydrazon) is a poorly soluble drug which has been proposed to have major advantages over other cardiotonic drugs. Poorly water soluble drugs present limited bioavailability due to their low solubility and dissolution rate. An antisolvent crystallization processing can improve the dissolution rate by decreasing the crystals particle size. However, LASSBio-294 is also poorly soluble in organic solvents and this operation is limited. In order to open new perspectives to improve dissolution rate, this work has investigated LASSBio-294 in terms of its antisolvent crystallization in 1-ethyl-3-methylimidazolium methyl phosphonate [emim][CH3O(H)PO2] as solvent and water as antisolvent. Two modes of mixing are tested in stirred vessel with different pre-mixers (Roughton or T-mixers) in order to investigate the mixing effect on the crystal properties (crystalline structure, particle size distribution, residual solvent and in vitro dissolution rate). Smaller drug particles with unchanged crystalline structure were obtained. Despite the decrease of the elementary particles size, the recrystallized particles did not achieve a better dissolution profile. However, this study was able to highlight a certain number of findings such as the impact of the hydrodynamic conditions on the crystals formation and the presence of a gel phase limiting the dissolution rate.
引用
收藏
页码:29 / 34
页数:6
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