Quercetin (QCT) has a variety of pharmacological effects, such as antioxidant, antibacterial, anticancer, anticardiovascular and antiaging effects. However, its poor water solubility, stability and bioavailability limit its applications. The special structure of cyclodextrins and their derivatives with a hydrophobic inner cavity and hydrophilic outer wall can load a variety of hydrophobic drugs of a suitable size and shape, thereby improving the stability and solubility of these molecules. In this study, an inclusion complex of quercetin and sulfobutylether-β-cyclodextrin was prepared. It was characterized FT-IR, UV, H NMR, XRD, DSC, and SEM analysis, which revealed the successful formation of the inclusion complex. biological activity estimations were carried out and the results indicated that the inclusion complex displayed higher antioxidative and antibacterial properties compared with free QCT. In addition, the mechanisms of inclusion were explored using H NMR analysis and docking calculations, thus providing a theoretical basis for obtaining an inclusion complex.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10951979 | PMC |
http://dx.doi.org/10.1039/d3ra08936c | DOI Listing |
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