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Evaluation of photochemotherapeutic potential of a few oxo-bridged dimeric Fe(III) compounds having Salen-type ligands

Das, D and Raza, MK and Goswami, TK (2020) Evaluation of photochemotherapeutic potential of a few oxo-bridged dimeric Fe(III) compounds having Salen-type ligands. In: Polyhedron, 186 .

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Official URL: https://doi.org/10.1016/j.poly.2020.114614

Abstract

Four oxo-bridged dimeric Fe(III) complexes, viz. (µ-O){Fe(L)}2 (1�4), where L is N,�-bis(naphtalidene)-ethylenediamine, (H2L1 in 1); N,�-bis(naphtalidene)-1,2-phenylenediamine, (H2L2 in 2); N,�-bis(naphtalidene)-4-nitro-1,2-phenylenediamine (H2L3 in 3) and N,�-bis(naphtalidene)-4-carboxyl-1,2-phenylenediamine, (H2L4 in 4) were synthesized for their potential application as photochemotherapeutic agents in low energy visible light. The solid-state structure of complex 2 was confirmed by X-ray crystallography. The complexes bind to human serum albumin (HSA) reversibly in a pH dependent manner, which could be a potential carrier of the molecules in blood plasma. They also bind to calf-thymus (ct) DNA with considerable affinity. In vitro cellular experiments show that the complexes display significant photo-enhanced cytotoxicity in human cervical cancer (HeLa) and human breast cancer (MCF-7 and MDA-MB-231) cells with low dark toxicity. ICP-MS analysis show that the complexes enter HeLa cells in a dose-dependent manner. Flow cytometric and confocal microscopic experiments demonstrate that the complexes kill cancer cells on exposure to visible light primarily via apoptosis through the generation of reactive oxygen species (ROS). © 2020 Elsevier Ltd

Item Type: Journal Article
Publication: Polyhedron
Publisher: Elsevier Ltd
Additional Information: The copyright for this article belongs to Elsevier Ltd
Keywords: Apoptosis; Crystal structure; HSA binding; Iron(III) complexes; Photocytotoxicity; ROS generation
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 05 Nov 2021 06:41
Last Modified: 05 Nov 2021 06:41
URI: http://eprints.iisc.ac.in/id/eprint/65846

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