Book of Abstracts - Ruhr-Universität Bochum
Book of Abstracts - Ruhr-Universität Bochum
Book of Abstracts - Ruhr-Universität Bochum
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
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 />
91