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Synthesis of trimethoprim metal complexes: Spectral, electrochemical, thermal, DNA-binding and surface morphology studies

  • Nihat Demirezen
  • , Derya Tarinç
  • , Duygu Polat
  • , Mustafa Çeşme
  • , Ayşegül Gölcü*
  • , Mehmet Tümer
  • *Bu çalışma için yazışmadan sorumlu yazar

Araştırma sonucu: Dergiye katkıMakalebilirkişi

41 Atıf (Scopus)

Özet

Complexes of trimethoprim (TMP), with Cu(II), Zn(II), Pt(II), Ru(III) and Fe(III) have been synthesized. Then, these complexes have been characterized by spectroscopic techniques involving UV-vis, IR, mass and 1H NMR. CHN elemental analysis, electrochemical and thermal behavior of complexes have also been investigated. The electrochemical properties of all complexes have been investigated by cyclic voltammetry (CV) using glassy carbon electrode. The biological activity of the complexes has been evaluated by examining their ability to bind to calf-thymus DNA (CT DNA) with UV spectroscopy and cyclic voltammetry. UV studies of the interaction of the complexes with DNA have shown that these compounds can bind to CT DNA. The binding constants of the complexes with CT DNA have also been calculated. The cyclic voltammograms of the complexes in the presence of CT DNA have shown that the complexes can bind to CT DNA by both the intercalative and the electrostatic binding mode. The antimicrobial activity of these complexes has been evaluated against three Gram-positive and four Gram-negative bacteria. Antifungal activity against two different fungi has been evaluated and compared with the reference drug TMP. Almost all types of complexes show excellent activity against all type of bacteria and fungi. The morphology of the CT DNA, TMP, metal ions and metal complexes has been investigated by scanning electron microscopy (SEM). To get the SEM images, the interaction of compounds with CT DNA has been studied by means of differential pulse voltammetry (DPV) at CT DNA modified pencil graphite electrode (PGE). The decrease in intensity of the guanine oxidation signals has been used as an indicator for the interaction mechanism.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)243-255
Sayfa sayısı13
DergiSpectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
Hacim94
DOI'lar
Yayın durumuYayınlandı - Ağu 2012
Harici olarak yayınlandıEvet

Finansman

The authors wish to thank TUBITAK (Project No.: 109T020 ), KSU (Project No.: 2009/4-12 and Project No.: 2010/5-19 ) for the financial supports and Prof. Dr. Metin Dıgrak (Department of Biology, Faculty of Science and Letters, University of Kahramanmaras Sutcu Imam, Campuse of Avsar, 46100 Kahramanmaras, Turkey) for antimicrobial studies.

FinansörlerFinansör numarası
TUBITAK109T020
Kansas State University2009/4-12, 2010/5-19

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