Structural polymorphism and solubility of medicinal drugs (Using Perindopril as an Example)

被引:0
|
作者
N. Yu. Bogdanov
K. A. Gorchakov
V. S. Puchnin
V. A. Stepanov
V. S. Khmelevskaya
机构
[1] National Nuclear Research University,Obninsk Institute for Nuclear Power Engineering, Moscow Engineering Physics Institute
来源
Crystallography Reports | 2011年 / 56卷
关键词
Dioxane; Crystallography Report; Perindopril; Polymor Phism; Chloride Methylene;
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学科分类号
摘要
The correlation between the structural polymorphism of perindopril salt C19H32N2O5 · C4H11N and its bioavailability has been investigated. During the crystallization of perindopril salt from an organic solvent, a low-symmetry perindopril polymorph is formed when the most polar solvent is used. It is shown that the dissolution rate in water, which is a measure of the bioavailability of any pharmaceutical product, is higher for the perindopril salt grown from the least polar solvent and that the structure has a monoclinic symmetry.
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页码:608 / 610
页数:2
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