Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54269
Title: Physical properties and biological activities of hesperetin and naringenin in complex with methylated p-cyclodextrin
Authors: Waratchada Sangpheak
Jintawee Kicuntod
Roswitha Schuster
Thanyada Rungrotmongkol
Peter Wolschann
Nawee Kungwan
Helmut Viernstein
Monika Mueller
Piamsook Pongsawasdi
Keywords: Chemistry
Issue Date: 29-Dec-2015
Abstract: © 2015 Sangpheak et al; licensee Beilstein-Institut. The aim of this work is to improve physical properties and biological activities of the two flavanones hesperetin and naringenin by complexation with β-cyclodextrin (β-CD) and its methylated derivatives (2,6-di-O-methyl-β-cyclodextrin, DM-β-CD and randomly methylated-β-CD, RAMEB). The free energies of inclusion complexes between hesperetin with cyclodextrins (β-CD and DM-β-CD) were theoretically investigated by molecular dynamics simulation. The free energy values obtained suggested a more stable inclusion complex with DM-β-CD. The vdW force is the main guest-host interaction when hesperetin binds with CDs. The phase solubility diagram showed the formation of a soluble complex of ALtype, with higher increase in solubility and stability when hesperetin and naringenin were complexed with RAMEB. Solid complexes were prepared by freeze-drying, and the data from differential scanning calorimetry (DSC) confirmed the formation of inclusion complexes. The data obtained by the dissolution method showed that complexation with RAMEB resulted in a better release of both flavanones to aqueous solution. The flavanones-β-CD/DM-β-CD complexes demonstrated a similar or a slight increase in anti-inflammatory activity and cytotoxicity towards three different cancer cell lines. The overall results suggested that solubilities and bioactivities of both flavanones were increased by complexation with methylated β-CDs.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84961848296&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54269
ISSN: 18605397
Appears in Collections:CMUL: Journal Articles

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