EventsThe 17th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session b. Bioorganic, Medicinal and Natural Products of the event The 17th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2013
Citation
Stanislaw Kowalski, Marcin Lukasiewicz, Enhancement of flavonols water solubility by cyclodextrin inclusion complex formation - case study, in Proceedings of The 17th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2013, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-17-b005
Share
Email
Facebook
Twitter
LinkedIn

Enhancement of flavonols water solubility by cyclodextrin inclusion complex formation - case study

image
1. Univeristy of Agriculture in Krakow, Faculty of Food Technology
Abstract
The phenomenon of solubility increasing of nonpolar flavonol antioxidant – quercetin (QC) in water solutions containing β-cyclodextrin (CD) was studied. Complexation of QC by CD was investigated using phase solubility study. It allows to estimate the apparent formation constant for 1:1 host-guest complex. Additionally thermodynamic properties were evaluated as well showing spontaneous exothermic process of complex formation. Two solubility models were also employ to verify their applicability to predict QC concentration in solution. Those models included modified Apelbalt and Buchowski-Ksiazczak equations. In order to investigate the antioxidant properties of ternary systems QC/CD/water a radical scavenging activity using stable radical of DPPH was performed. Experiments indicated that antioxidant activity is temperature and CD concentration-dependent. It was shown that complexation may inhibit the radical scavenging by QC or changing the scavenging stoichiometry.
Keywords
cyclodextrin
inclusion complexes
thermodynamics
solubility modelling
Manuscript
Oxalate-Assisted Synthesis of Nano Cobalt Oxide
Biopolymer-Supported Iron Oxide Nanocomposite: Preparation and Catalytic Application in the Synthesis of Benzodiazepine Derivatives