The design of new drug delivery systems has been widely sought after. The stability,
solubility, and difficulty of targeting active sites for new drugs have always been challenging …

Cyclodextrins (CDs) are cyclic oligosaccharides, consisting of glucopyranose units, which
are able to form host–guest inclusion complexes with lipophilic molecules. The ability of CD …

Introduction: Recently, the entrapment of hydrophobic drugs in the form of water-soluble
drug–cyclodextrin (CD) complex in liposomes has been investigated as a new strategy to …

Cyclodextrins have been widely applied to the pharmaceutical field due to their ability to
include hydrophobic molecules in their cavity and to mask certain physicochemical …

Liposomes loaded with drug–cyclodextrin complexes are widely used as drug delivery
systems, especially for species with low aqueous solubility and stability. Investigation of the …

Complexation with cyclodextrins (CDs) has been widely and successfully used in
pharmaceutical field, mainly for enhancing solubility, stability and bioavailability of a variety …

A novel concept in drug delivery discussed here, takes advantage of certain properties of the
drug “containers” cyclodextrins and liposomes to combine them into a single system thus …

The aim of this study was to investigate the effect of hydroxypropyl-β-cyclodextrin (HPβCD),
widely used as a solubility enhancer, on liposomal formulations. To this end, HPβCD was …

For some years cyclodextrins and their hydrophilic derivatives have been described in the
literature as solubilizers capable of enhancing the loading capacity of liposomes and …

Cyclodextrins (CDs) are cyclic oligosaccharides able to improve drug water solubility and
stability by forming CD/drug inclusion complexes. To further increase drug entrapment and …