KMID : 0369819970270030233
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Jorunal of Korean Pharmaceutical Sciences 1997 Volume.27 No. 3 p.233 ~ p.239
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Dissolution of Glibenclamide Polymorphs
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¼Õ¿µÅÃ/Sohn YT
¾öº¸¿µ/Um BY
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Abstract
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Glibenclamide is a second generation sulfonylurea that is orally active as a hypoglycemic drug. It exists as a crystalline powder which is sparingly soluble in water. It was investigated that the potential of glibenclamide to exhibit polymorphism. Three polymorphic modifications (form 1, form 2 and form 3) and three pseudopolymorphic modifications (form 4, form 5 and form 6) were obtained by crystallization from different organic solvents. The isolated crystal forms were characterized by differential scanning calorimetry(DSC), thermogravimetric analysis(TGA) and X-ray crystallography powder diffraction studies. Form 1 was the most stable and melt at $175.4^{\circ}C$ ¼ö½Ä À̹ÌÁö. Form 2 was metastable and melt at $151.0^{\circ}C$ ¼ö½Ä À̹ÌÁö. Form 3 was a new polymorphic modification because it was different from form 1 and form 2 in X-ray crystallography powder diffraction data. Form 4 was a 1 : 7(toluene : glibenclamide) toluene solvate; form 5 was a 1 : 5(toluene : glibenclamide) toluene solvate; form 6 was a 3 : 8(pentanol : glibenclamide) pentanol solvate. All forms were stable in 3-month storage under 0% or 100% humidity condition. The dissolution rate of form 4 was highest; those of form 2, form 3, form 1, form 5 and form 6 followed.
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KEYWORD
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Glibenclamide, DSC, TGA, Dissolution, Polymorphism
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