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Book of Abstracts - Ruhr-Universität Bochum

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P-33<br />

ISBOMC `10 5.7 – 9.7. 2010 <strong>Ruhr</strong>-<strong>Universität</strong> <strong>Bochum</strong><br />

The Research <strong>of</strong> the Interaction between Quercetin and Zirconium (IV) in<br />

Water-Ethanol Medium<br />

Olessya Loiko, a A.Khalitova, a B.Tuleuov, b A.Mashentseva *c<br />

a Karaganda State University, Faculty <strong>of</strong> Chemistry, Department <strong>of</strong> Chemistry, Universitetskaya 28,<br />

100000, Karaganda, Kazakhstan. b ISPH “Phytochemistry”,Gasalieva str.4 , 100000, Karaganda,<br />

Kazakhstan. c L.N.Gumilev Eurasian national university, Faculty <strong>of</strong> Chemistry, Department <strong>of</strong><br />

Chemistry, Munajtpasova 5, 010008, Astana, Kazakhstan.<br />

E-mail: olessya0905@gmail.com<br />

It’s known, that the search <strong>of</strong> new compounds with radioprotective, antioxidant and hepatoprotective<br />

activities is carried out among flavonoids; 1 because <strong>of</strong> their structural molecule uniqueness they can<br />

hamper not only oxidising processes, but also make transfer <strong>of</strong> energy and migration <strong>of</strong> elementary<br />

particles at the irradiation. At the same time, examples <strong>of</strong> individual flavonoids (rutin and quercetin)<br />

and their derivatives’ usage in the medical practice are single, despite their wide variety, accessibility<br />

<strong>of</strong> their production sources and relative availability.<br />

It is suggested that the biological activity <strong>of</strong> an organic ligand can be increased when co-coordinated<br />

or mixed with suitable metal ion, because <strong>of</strong> its ability to act as a free radical acceptor. 2 From the<br />

pharmacology point <strong>of</strong> view zirconium (IV) complexes are noted for their significant biological<br />

properties, namely antibacterial and antifungal activities. Information about mechanism <strong>of</strong> interaction<br />

between zirconium (IV) and quercetin will help to explain and predict biochemical activity <strong>of</strong> these<br />

components’ mixture in the medical product.<br />

The ability to form complex between quercetin and zirconium (IV) was studied in this work using<br />

spectrophotometer method. Quercetin zirconium (IV) complex is characterized by 3 absorption bands:<br />

in UV and visible parts <strong>of</strong> spectrum at 360 nm, 395 nm and 475 nm; the extension coefficients (ε)<br />

were calculated for these bands: 1042, 1045 and 2966 correspondingly. In the presence <strong>of</strong> metal ions,<br />

a bathochromic shift on 55 nm is observed in the absorption spectra <strong>of</strong> complex. Such bathochromic<br />

shift can be explained by the interaction <strong>of</strong> cobalt chloride with the free C3-oxo group <strong>of</strong> quercetin.<br />

Investigated complex was synthesized in the solid state. IR spectra <strong>of</strong> ligand and complex present<br />

evidence <strong>of</strong> the coordination between zirconium ions and oxo-group <strong>of</strong> quercetin. It can be noted that<br />

Zr-O frequencies appear at 559.78, 538.53 and 472.02cm -1 .<br />

As the result <strong>of</strong> made researches <strong>of</strong> complex formation between zirconium (IV) and quercetin, the<br />

influence <strong>of</strong> time, solvent and organic reagent concentration were studied. Studying the complex<br />

solubility, it was determined that the compound sufficiently dissolves in water-ethanol mixture. It has<br />

been shown, that if the content <strong>of</strong> ethanol is under 15%, the complex will fall in a precipitation. Using<br />

Jobs method it was established, that made compound has content, which formula is C30H18O15Zr. The<br />

stability constant <strong>of</strong> complex is (9,56 ± 0,01)·10 9 , this number shows that the complex is averagely<br />

stable. Complex forms at the room temperature.<br />

According to the PASS biocsreening calculation follow activities for the synthesized complex are<br />

antiparkinsonian, nootropic, cardioprotectant and creatine kinase inhibitor.<br />

References<br />

1. I.S. Vasil’eva, V.A. Paseshnichenko, The achievements <strong>of</strong> Biological Chemistry, 2000, 3, 153-156.<br />

2. M.Y. Morandi, J. Pourahmad, Free Radic. Biol. Med. 2003, 34, 243‐250.<br />

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