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.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ijpharm.2013.06.026DOI Listing

Publication Analysis

Top Keywords

polymorph acetohexamide
8
form
5
crystallization polymorph
4
acetohexamide
4
acetohexamide 2-hydroxybutyl-β-cyclodextrin
4
solution
4
2-hydroxybutyl-β-cyclodextrin solution
4
solution form
4
form high
4
high aqueous
4

Similar Publications

Article Synopsis
  • Controlling drug crystallization is crucial in pre-formulation studies, and new methods, particularly using tailored additives, are gaining popularity.* -
  • Hydrophilic cyclodextrins (CDs) serve as effective additives that influence drug crystallization through host-guest interactions, impacting both solution and solid state forms.* -
  • The review highlights recent advancements in using CDs for crystal engineering, showcasing their ability to detect new polymorphs and modify crystal shape, as well as create stable amorphous drug/CD complexes under humid conditions.*
View Article and Find Full Text PDF

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.

View Article and Find Full Text PDF

Recent advances in crystallographic computing have made it possible to solve by powder diffraction methods structures that have not been possible to solve by single-crystal methods. Although there is vast improvement in the quality of data obtained from high-intensity synchrotron radiation, we found that surprisingly reliable results can be obtained from conventional laboratory sources. In this article we examine the application of Monte Carlo/simulated annealing methods for the determination of structures ranging in complexity from 9 to 15 degrees of freedom.

View Article and Find Full Text PDF

Infrared data determined for known polymorphic forms and some new derivatives of acetohexamide and related compounds support the view that acetohexamide polymorphs exhibit keto-enol tautomerism. They indicate that type A polymorphs exist in the enol form, probably stabilized by intramolecular bonding between an O-H and S = O group to form a six-membered ring. Type B polymorphs exist in the keto form with the urea carbonyl group intermolecularly bonded to a sulphonamide N-H.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!