Journal
JOURNAL OF MOLECULAR LIQUIDS
Volume 318, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.molliq.2020.114308
Keywords
Binary solvent; Cyclodextrin; Inclusion complexation; Polyphenol; Thermodynamics; Solvation; Stability
Funding
- Vietnam National Foundation for Science and Technology Development (NAFOSTED) [104.06-2017.329]
- RFBR [19-53-54004]
- VAST [19-53-54004]
- Ministry of Science and Higher Education of the Russian Federation [FZZW-2020-0009]
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In this work, the solubility of rutin was first obtained in the water-ethanol solvents with small composition of co-solvent in the mixture at 25 degrees C. The results showed that the solubility of rutin improved with increasing ethanol content in the studied range 0-0.1 mol. fr. Solvation of hydroxypropyl-beta-cydodextrin in binary solvents was first studied by the method of interfacial distribution of the substance between two immiscible phases. It was found that when moving hydroxypropyl-beta-cydodextrin from water to the water-ethanol solvent, a decrease in the solvation of hydroxypropyl-beta-cydodextrin was observed. Complexation between rutin and beta-cyclodextrin or hydroxypropyl-fi-cydodextrin was also studied in water and in the water-ethanol solvents. In the aqueous solution containing hydroxypropyl-beta-cyclodextrin, the solubility of rutin was improved significantly and better than in the solution containing beta-cyclodextrin. The stability of (rutin-hydroxypropyl-beta-cyclodextrin) complex decreased with increasing the ethanol content and was determined by the sum of solvation of rutin (Delta(tr)G(Rut)) and hydroxypropyl-beta-cyclodextrin (Delta(tr)G(Rut)). This effect was also observed for the complexation reaction be- tween quercetin and hydroxypropyl-beta-cydodextrin in our previous study. (C) 2020 Elsevier B.V. All rights reserved.
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