Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1407004 | Journal of Molecular Structure | 2008 | 6 Pages |
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.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Omid Rajabi, Farnoosh Tayyari, Roshanak Salari, Sayyed Faramarz Tayyari,