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Synthesis, Characterization and Dna Binding Studies of a New Ibuprofen–Platinum(Ii) Complex Publisher Pubmed



Shiri F1, 2 ; Hadidi S3, 4 ; Rahiminasrabadi M1, 2 ; Ahmadi F5, 6 ; Ganjali MR7, 8 ; Ehrlich H9
Authors
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Authors Affiliations
  1. 1. Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
  2. 2. Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran
  3. 3. Inorganic Chemistry Department, Faculty of Chemistry, Razi University, Kermanshah, Iran
  4. 4. Medical Biology Research Center (MBRC), Kermanshah University of Medical Sciences, Kermanshah, Iran
  5. 5. Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Medicinal Chemistry, School of Pharmacy-International Campus, Iran University of Medical Sciences, Tehran, Iran
  7. 7. Center of Excellence in Electrochemistry, University of Tehran, Tehran, Iran
  8. 8. Biosensor Research Centre, Endocrinology & Metabolism Molecular and Cellular Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. IESEM, TU Bergakademie, Freiberg, Germany

Source: Journal of Biomolecular Structure and Dynamics Published:2020


Abstract

The study is focused on the synthesis of a novel complex of ibuprofen and Platinum(II). The formation of the product was characterized through analytical tools including Fourier-transform infrared spectroscopy, proton nuclear magnetic resonance, ultraviolet–visible spectroscopy, mass spectrometry as well as density functional theory. Using the continuous variation method, the stoichiometry of Pt(HIb)2(Cl)2 binding on DNA (ct-DNA) determines as a single class of binding. Based on the results of Stern–Volmer analysis on the fluorescence quenching data, the quenching mechanism was determined to be static in nature. The studies indicated that the complex could bind DNA molecules via groove binding for four major reasons. Initially, the complex–DNA binding constant determined based on spectrophotometric data were found to be comparable to those of groove-binding drugs. In addition, the competitive fluorimetric based on the applications of Hoechst 33258 proved the ability of Pt(HIb)2(Cl)2 to displace with Hoechst in its DNA-bounded form, reflecting the competition between Pt(HIb)2(Cl)2 and Hoechst for groove binding. Further, no considerable changes were observed in the intensity of the methylene blue (MB)-DNA system after adding the Pt(HIb)2(Cl)2 complex, reflecting the stability of MB molecules in the DNA helix and a non-intercalative bonds of Pt(HIb)2(Cl)2 interaction on DNA. Finally, minor changes in the viscosity of DNA in the presence of Pt(HIb)2(Cl)2, indicated that changes in the length of DNA in the presence of the complex are negligible, supporting the assumption of DNA groove-binding. Also induced CD spectral changes and docking simulations were in favor of the groove mechanism for the Pt(HIb)2(Cl)2–DNA binding. Communicated by Ramaswamy H. Sarma. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
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