Inclusion complexes of ferrocene uracil derivatives with cyclodextrins: solubilization and binding ability (CROSBI ID 717968)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Gazdek, Nika ; Drobac, Dunja ; Usenik, Andrea ; Halasz, Ivan ; Maračić, Silvija ; Lapić, Jasmina ; Raić-Malić, Silvana ; Djaković, Senka ; Tomišić, Vladislav ; Frkanec, Ruža ; Frkanec, Leo ;
engleski
Inclusion complexes of ferrocene uracil derivatives with cyclodextrins: solubilization and binding ability
Recent research shows that ferrocene uracil derivatives have biological activity. However, their high lipophilicity limits the application. It is known that cyclodextrins show abillity to improve drug water solubility by binding the hidrophobic moiety of the molecule inside of its cavity, such as ferrocene.2 Ferrocene shows different binding orientations as well as binding constants for alpha, beta and gama cyclodextrine in water.3 Environment of ferrocene can influence their binding to cyclodextrines. Therefore, we researched various ferocene uracyl derivatives with different R’, R groups and studied their binding ability with α-cyclodextrin, β- cyclodextrin, γ-cyclodextrin and modified (2- hydroxypropyl)-β-cyclodextrin in water. Characterisation was preformed using UV-Vis spectroscopy. Titrations were used to calculate binding constants that show range between.
complex ; ferrocene uracil ; cyclodextrin
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Podaci o prilogu
12-12.
2021.
objavljeno
Podaci o matičnoj publikaciji
Supramolecular chemistry 2021 : Book of abstracts
Frkanec, Leo ; Tomišić, Vladislav
Zagreb: Institut Ruđer Bošković
978-953-7941-39-0
Podaci o skupu
4. simpozij supramolekulske kemije
predavanje
10.12.2021-10.12.2021
Zagreb, Hrvatska