Abstract

A new mononuclear Pt(II) complex, [Pt(DMP)(DIP)]Cl2.H2O, in which DMP is 4,4-dimethyl-2,2-bipyridine and DIP is 4,7-diphenyl-1,10-phenantroline, has been synthesized and characterized by physicochemical and spectroscopic methods. The binding interaction of this complex with calf thymus DNA (CT-DNA) was investigated using fluorimetry, spectrophotometry, circular dichroism, viscosimetry and cyclic voltametry (CV). UV-VIS spectrum showed 4 nm bathochromic shift of the absorption band at 280 nm along with significant hypochromicity for the absorption band of the complex. The intrnisic binding constant (K b = 2 × 104 M−1) is more in keeping with intercalators and suggests this binding mode. The viscosity measurements showed that the complex-DNA interaction can be hydrophobic and confirm intercalation. Moreover, the complex induced detectable changes in the CD spectrum of CT-DNA. The fluorescence studies revealed that the probable quenching mechanism of fluorescence of the complex by CT-DNA is static quenching. The thermodynamic parameters (ΔH > 0 and ΔS > 0) showed that main interaction with hydrogenic forces occurred that is intercalation mode. Also, CV results confirm this mode because, with increasing the CT-DNA concentration, shift to higher potential was observed.

Highlights

  • During the recent years, only some platinum compounds such as cisplatin, carboplatin, and more recently nedaplatin and oxaliplatin have been known as antitumor compounds in clinical treatments; the research in this field is still increasing [1,2,3,4,5]

  • We report the results of an investigation of the interaction with calf thymus DNA of the complex [Pt(DMP)(DIP)]Cl2·H2O

  • We investigate synthesis and characterization of new platinum(II) complex, and binding with calf thymus DNA (CT-DNA) was studied

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Summary

Introduction

Only some platinum compounds such as cisplatin, carboplatin, and more recently nedaplatin and oxaliplatin have been known as antitumor compounds in clinical treatments; the research in this field is still increasing [1,2,3,4,5]. McFadyen et al [13] synthesized a range of Pt(II) complexes containing substituted phenanthroline ligands and showed that the complex [Pt(en)(3,4,7,8-Me4phen)]Cl2 was two or three times more active than the corresponding phen-based complex [Pt(en)(phen)]Cl2, against murine leukemia cell lines. In this context, we report the results of an investigation of the interaction with calf thymus DNA of the complex [Pt(DMP)(DIP)]Cl2·H2O. UV spectrophotometry, fluorescence method, dynamic viscosity measurements circular dichroism, and cyclic voltametry studies have been preferred because small molecule-DNA interaction may be experimentally monitored by changes in the intensity and position of the spectroscopic peak responses or changes in dynamic viscosity of DNA

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