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Crystallization of a new polymorph of acetohexamide from 2-hydroxybutyl-β-cyclodextrin solution: form VI with a high aqueous solubility.
- Source :
-
International journal of pharmaceutics [Int J Pharm] 2013 Sep 10; Vol. 453 (2), pp. 315-21. Date of Electronic Publication: 2013 Jun 21. - Publication Year :
- 2013
-
Abstract
- A new polymorph of acetohexamide (Form VI) was prepared via the formation of a complex with 2-hydoxybutyl-β-cyclodextrin (HB-β-CD) in aqueous solution. An alkaline solution of acetohexamide and HB-β-CD was adjusted to pH 4.0 by titration with hydrochloric acid. The resulting opaque solution was filtered through paper and allowed to stand at 4°C for 24h. The resulting precipitate was isolated on a filter and analyzed for polymorph content by powder X-ray diffractometry and thermal analysis. The diffraction pattern and thermal behavior of the precipitate was different from those of previously reported acetohexamide polymorphs (Forms I, III, IV and V), indicating that a new polymorph of the drug, i.e. Form VI was produced. This new polymorph was fairly stable against conversion to a stable form even at accelerated storage conditions. Crystalline Form VI was highly soluble in water and dissolved more rapidly than the other known polymorphs. This property was reflected in the blood concentrations of the drug after oral administration to rats.<br /> (Copyright © 2013 Elsevier B.V. All rights reserved.)
- Subjects :
- 2-Hydroxypropyl-beta-cyclodextrin
Acetohexamide blood
Acetohexamide pharmacokinetics
Animals
Crystallization
Hypoglycemic Agents blood
Hypoglycemic Agents pharmacokinetics
Male
Powder Diffraction
Rats
Rats, Wistar
Solubility
X-Ray Diffraction
Acetohexamide chemistry
Hypoglycemic Agents chemistry
beta-Cyclodextrins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3476
- Volume :
- 453
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- International journal of pharmaceutics
- Publication Type :
- Academic Journal
- Accession number :
- 23796835
- Full Text :
- https://doi.org/10.1016/j.ijpharm.2013.06.026