Article ID Journal Published Year Pages File Type
1407004 Journal of Molecular Structure 2008 6 Pages PDF
Abstract

The interaction between spironolactone (Sp) and hydroxypropyl-β-cyclodextrin (HPβCD) has been investigated in aqueous solution and in the solid state. Phase solubility studies indicate that the complex is formed with possible stoichiometry of 1:1 and association constant of 9806 M−1. Differential scanning calorimetry (DSC) gave evidence for the formation of the complex. The details of Sp/HPβCD molecular interaction were analyzed by Fourier transform infrared (FTIR) and Raman spectroscopy. The characterization studies confirmed that the CO groups of the six-member ring and acetylthio group of Sp interacts with the hydroxyl groups inside and outside the cavity of HPβCD through formation of hydrogen bonds.

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
, , , ,