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   <subfield code="a">Influence of various cyclodextrins on the stability of hydrocortisone 17-butyrate in aqueous solution</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[In Chun, Bo Kim]</subfield>
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   <subfield code="a">The stabilizing effects of α-, β-, γ- and dimethyl-β-cyclodextrins (α-, β-, γ-and DM-β-CyDs) on the degradation of hydrocortisone 17-butyrate (HC-17B) in aqueous solution was investigated. HC-17B underwent a facile hydroxide ion-catalyzed rearrangement to the less active 21-butyrate ester by the apparent first-order kinetics, and maximum stability of HC-17B was obtained at around, pH 4.0. The stability of HC-17B was increased by inclusion complexation with α-, γ- and DM-β-CyD in the pH range of 2.0-8.0 examined, whereas β-CyD accelerated the degradation of HC-17B at the pH higher than 5.0. The effects of ionic strength, solvent, temperature and CyD concentration were also investigated. Stability constants and apparent degradation rate constants of HC-17B-γ-CyD and HC-17B-DM-β-CyD complexes were determined kinetically on the basis of 1∶1 complexation. The results suggested that the inclusion complexation with γ-CyD or DM-β-CyD was most useful means to enhance the stability of the steroid.</subfield>
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