Probing synergistic interplay between bio-inspired peptidomimetic chitosan-copper complexes and doxorubicin.

A Pandit, L Khare, D Jahagirdar, A Srivastav, R Jain, P Dandekar

Journal: International journal of biological macromolecules 2021;161():1475-1483

PMID: 32750482

Abstract

The current investigation reports a novel and facile method for modification of low molecular weight chitosan (Cs) with guanidine moieties, aimed at enhancing its cellular interaction and thus augmenting its cellular internalization. Guadinylated chitosan-copper (Cs-Gn-Cu) chelates, based on copper-nitrogen co-ordination, were established. Characterization of chelates was conducted using H NMR, C NMR, XPS, XRD, TGA-DTA, and GPC techniques. Anticancer activity of formed chelates was confirmed against A549 cells using MTT assay. Experimental outcomes, for the first time, have provided an empirical evidence for synergistic interaction between the chelated polymer (Cs-Gn-Cu) and the established anti-cancer agent, Doxorubicin (Dox), based on analysis by the Chou Talalay method and estimation of their combination indices. ROS induction was demonstrated as the mechanism of action of the chelated polymer, which supplemented rapid destruction of cancerous cells by Dox. These findings strongly advocate the need for harnessing unexplored potential of these innovative metal polymer chelates in cases of Dox resistant lung cancer, wherein the polymeric system itself would serve as an anti-cancer agent.

Copyright © 2020 Elsevier B.V. All rights reserved.

Address: Department of Chemical Engineering, Institute of Chemical Technology, Matunga, Mumbai-19, India.; Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Matunga, Mumbai-19, India.; Department of Chemical Engineering, Institute of Chemical Technology, Matunga, Mumbai-19, India. Electronic address: [email protected].; Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Matunga, Mumbai-19, India. Electronic address: [email protected].

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