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Updated: Aug 16, 2026

Transport Properties of Ibuprofen Encapsulated in Cyclodextrin Nanosponge Hydrogels: A Proton HR-MAS NMR Spectroscopy Study
Published on: August 15, 2016
Amorphous water-soluble derivatives of cyclodextrins: nontoxic dissolution enhancing excipients
Abstract:
Dissolution properties of drugs may be improved by their conversion to an amorphous state or by complexation with cyclodextrins. The present report describes the preparation of cyclodextrin derivatives which are intrinsically amorphous, and water-soluble, and their use as complexation agents. Such derivatives were prepared by condensation of alpha-, beta-, or gamma-cyclodextrins with epoxides (propylene oxide, isobutylene oxide, epichlorohydrin, 1,4-butanediol diglycidyl ether). The condensation products effectively solubilized estradiol, progesterone, or testosterone in water; these solutions, upon freeze-drying, yielded solids which could be directly compressed to tablets which dissolve completely within minutes. Condensation products of cyclodextrins did not have any untoward or toxic effects when administered chronically to mice per os for a 16-week period.
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