Details

Autor(en) / Beteiligte

• Sindhuja, Elangovan
• Ramesh, Rengan
• Dharmaraj, Nallasamy
• Liu, Yu

Titel

DNA/protein interaction and cytotoxicity of palladium(II) complexes of thiocarboxamide ligands

Ist Teil von

• Inorganica Chimica Acta, 2014-05, Vol.416, p.1-12

Ort / Verlag

Elsevier B.V

Erscheinungsjahr

2014

Quelle

ScienceDirect

Beschreibungen/Notizen

• Synthesis and characterisation of Pd(II) thiocarboxamide complexes. Modification of the ligands significantly affects the DNA/protein binding behavior of the complexes. All the complexes behave as potential antioxidant agents. The in vitro cytotoxicity against two human cancer cell lines are evaluated. •Four Pd(II) thiocarboxamide complexes have been synthesized and structurally characterized.•The complexes bind to DNA and bovine serum albumin proteins via intercalation.•Complexes show excellent antioxidant activity.•Promising in vitro cytotoxicity results against HeLa and MCF-7 cancer cells. Four planar palladium(II) complexes with general formula [Pd(Cl)(L)(PPh3)] (HL=N-substituted pyridine-2-thiocarboxamide) have been synthesized and characterized by analytical, spectral (IR, UV–Vis and 1H, 13C and 31P NMR) and single crystal X-ray methods. Crystal structure of all the complexes indicated a mono negative bidentate coordination of thiocarboxamide ligands to the palladium center via pyridine nitrogen and thiol sulfur and reveals a square planar geometry. The interaction of palladium(II) thiocarboxamide complexes with calf thymus DNA (CT-DNA) studied by absorption and emission spectroscopic methods revealed that complexes 5–8 could interact with CT-DNA through intercalation. Further, the interaction of the palladium complexes with bovine serum albumin (BSA) was investigated using UV–Vis, fluorescence and synchronous fluorescence methods. The tryptophan and tyrosine residues in BSA as model protein was quenched by the complexes in a static quenching process. The radical scavenging ability of all the complexes was accessed by in vitro antioxidant assays involving DPPH radical, hydroxyl radical, nitric oxide radical and ABTS radicals and was found to be excellent. Further, the anti-cancer activity of complexes 5–8 against HeLa, MCF-7 and NIH-3T3 cell line has been studied. Though the complexes 5, 6 and 8 showed more potent anticancer activity than cisplatin, complex 5 was found to be superior.