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Cytotoxicity and Dna/Bsa Binding Ability of Copper(Ii) Complexes With Dimethylbithiazole Publisher



Abedi A1 ; Lighvan ZM2 ; Ostad SN3
Authors
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Authors Affiliations
  1. 1. Department of Chemistry, North Tehran Branch, Islamic Azad University, Tehran, 19585-936, Iran
  2. 2. Department of Chemistry, Isfahan University of Technology, Isfahan, 84156/83111, Iran
  3. 3. Department of Toxicology and Pharmacology, Tehran University of Medical Sciences, Tehran, 14155/6451, Iran

Source: Monatshefte fur Chemie Published:2016


Abstract

The interaction of two copper(II) complexes [Cu(dmbt)2NO3](NO3) and [CuCl(dmbt)(μ-Cl)]2 with calf-thymus DNA has been explored by using absorption, emission, and thermal denaturation. Both complexes illustrate high interaction ability with calf-thymus DNA, with intrinsic binding constants Kb of 1.7 × 105 and 1.4 × 105 M−1 at 298 K, respectively, which is in the range of those found for typical classical intercalators. The intermolecular interaction between Cu complexes and bovine serum albumin (BSA) under imitated physiological conditions was investigated using UV–Vis and fluorescence. Tryptophan quenching experiment showed that both complexes bind BSA strongly, with dynamic quenching constants of 1.16 × 105 M−1 s−1 and 1.64 × 105 M−1 s−1, respectively, at 298 K, and a single class of binding site for the complexes on BSA. Both Cu complexes were also used for in vitro cytotoxicity evaluation against four cultures, NIH-3T3, Caco-2, HT-29, and T47D by MTT assay. Interestingly, nitrate contained complex illustrated no toxicity on normal cell line (NIH-3T3), with twice antitumor activity against colon carcinoma (HT-29), comparing with cisplatin. Graphical abstract: [Figure not available: see fulltext.] © 2016, Springer-Verlag Wien.