298
24. Sokolova R, Ramesova S, Kocabova J et al
(2016) On the difference in decomposition of taxifolin and luteolin vs. fisetin and
quercetin in aqueous media. Monatsh Chem
147:1375–1383. https://doi.org/10.1007/
s00706-016-1737-3
25. Szejtli J (1998) Introduction and general overview of cyclodextrin chemistry. Chem Rev
98:1743–1753
26. Kaifer AE, Gomez-Kaifer M (1999)
Supramolecular electrochemistry. Wiley-VCH,
Weinheim
27. Hromadova M, Sokolova R (2011)
Electrochemical reactions of organic molecules in the presence of cyclodextrins. Curr
Org Chem 15:2950–2956. https://doi.
org/10.2174/138527211798357119
28. Pospisil L, Trskova R, Colombini MP et al
(1998) Inclusion complexes of atrazine with
alfa-, beta- and gamma-cyclodextrins, evidence by polarographic kinetic currents. J
Incl Phen 31:57–70. https://doi.org/10.102
3/A:1007924517198
29. Amatore C, Buriez O, Labbe E et al (2008)
Supramolecular effects of cyclodextrins on the
electrochemical reduction and reactivity of
aromatic carbonyl compounds. J Electroanal
Chem
621(2):134–145.
https://doi.
org/10.1016/j.jelechem.2007.07.029
30. Diamantis DA, Ramesova S, Chatzigiannis
CM et al (2018) Exploring the oxidation
and iron binding profile of a cyclodextrin
encapsulated quercetin complex unveiled a
controlled complex dissociation through a
chemical stimulus. Biochim Biophys Acta
Gen Subjects 1862:1913–1924. https://doi.
org/10.1016/j.bbagen.2018.06.006
31. Matsue T, Osa T, Evans DH (1984)
Determination of some physical constants of cyclodextrin complexes by electrochemical methods. J Incl Phenom Mol
Recognit Chem 2:547–554. https://doi.
org/10.1007/978-94-009-5376-5_58
32. Ramesova S, Sokolova R, Degano I et al (2011)
The influence of the host-guest interaction on
the oxidation of natural flavonoid dyes. Collect
Czech Chem Commun 76:1651–1667.
https://doi.org/10.1135/cccc2011106
33. Kellici
TF,
Chatziathanasiadou
MV,
Diamantis D et al (2016) Mapping the
interactions and bioactivity of quercetin(2-hydroxypropyl)-beta-cyclodextrin
complex. Int J Pharm 511:303–311. https://doi.
org/10.1016/j.ijpharm.2016.07.008
Romana Sokolová and Ilaria Degano
24. Sokolova R, Ramesova S, Kocabova J et al
(2016) On the difference in decomposition of taxifolin and luteolin vs. fisetin and
quercetin in aqueous media. Monatsh Chem
147:1375–1383. https://doi.org/10.1007/
s00706-016-1737-3
25. Szejtli J (1998) Introduction and general overview of cyclodextrin chemistry. Chem Rev
98:1743–1753
26. Kaifer AE, Gomez-Kaifer M (1999)
Supramolecular electrochemistry. Wiley-VCH,
Weinheim
27. Hromadova M, Sokolova R (2011)
Electrochemical reactions of organic molecules in the presence of cyclodextrins. Curr
Org Chem 15:2950–2956. https://doi.
org/10.2174/138527211798357119
28. Pospisil L, Trskova R, Colombini MP et al
(1998) Inclusion complexes of atrazine with
alfa-, beta- and gamma-cyclodextrins, evidence by polarographic kinetic currents. J
Incl Phen 31:57–70. https://doi.org/10.102
3/A:1007924517198
29. Amatore C, Buriez O, Labbe E et al (2008)
Supramolecular effects of cyclodextrins on the
electrochemical reduction and reactivity of
aromatic carbonyl compounds. J Electroanal
Chem
621(2):134–145.
https://doi.
org/10.1016/j.jelechem.2007.07.029
30. Diamantis DA, Ramesova S, Chatzigiannis
CM et al (2018) Exploring the oxidation
and iron binding profile of a cyclodextrin
encapsulated quercetin complex unveiled a
controlled complex dissociation through a
chemical stimulus. Biochim Biophys Acta
Gen Subjects 1862:1913–1924. https://doi.
org/10.1016/j.bbagen.2018.06.006
31. Matsue T, Osa T, Evans DH (1984)
Determination of some physical constants of cyclodextrin complexes by electrochemical methods. J Incl Phenom Mol
Recognit Chem 2:547–554. https://doi.
org/10.1007/978-94-009-5376-5_58
32. Ramesova S, Sokolova R, Degano I et al (2011)
The influence of the host-guest interaction on
the oxidation of natural flavonoid dyes. Collect
Czech Chem Commun 76:1651–1667.
https://doi.org/10.1135/cccc2011106
33. Kellici
TF,
Chatziathanasiadou
MV,
Diamantis D et al (2016) Mapping the
interactions and bioactivity of quercetin(2-hydroxypropyl)-beta-cyclodextrin
complex. Int J Pharm 511:303–311. https://doi.
org/10.1016/j.ijpharm.2016.07.008
Romana Sokolová and Ilaria Degano
