Metal-Based Molecular Compounds: Structure, Analytical Properties, dsDNA Binding Studies and In Vitro Antiproliferative Activity on Selected Cancer Cell Lines

Mustafa Çeşme*, Ayşegül Gölcü

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

In this work, to contribute to research in the area of new chemotherapeutic agents, we attempted at obtaining new metal-based compounds as alternatives to the existing metal-based anticancer drugs. In this context, Cu(II), Zn(II) and Pt(II) metal-based complexes of pharmaceutically active compound, effective antineoplastic methotrexate (MTX), were synthesized, and their structures were elucidated by analytical (melting point, elemental analysis, conductivity, and solubility), spectroscopic (UV-Vis, IR, 1H NMR, LC-MS and ICP-OES) and thermal (TGA, DTA) methods. UV-Vis spectroscopy examined interactions of MTX pharmaceutically active substances and their metal-based compounds with the fish sperm double-stranded DNA (FS-dsDNA). Regarding the data obtained from spectroscopic measurements, it is understood that all compounds interact with FS-dsDNA. The antiproliferative activity of the active agent MTX and the newly synthesized metal-based compounds was investigated on C6 and He-La cells in comparison to the active anticancer agents present in the market using real-time cell analyzer with four different concentrations. Also, interactions of all compounds obtained with the double-stranded FS-dsDNA were studied using pencil graphite electrode (PGE) by monitoring changes in the signal of the guanine base. The associated surface morphology was examined by differential pulse voltammetry (DPV) and scanning electron microscopy (SEM) techniques.

Original languageEnglish
Pages (from-to)392-410
Number of pages19
JournalPharmaceutical Chemistry Journal
Volume53
Issue number5
DOIs
Publication statusPublished - 1 Aug 2019

Bibliographical note

Publisher Copyright:
© 2019, Springer Science+Business Media, LLC, part of Springer Nature.

Funding

The authors are grateful to the TUBITAK (Project No. 112T721, COST/CM1105) and KSU (Project No. 2011/8-6D) for support. We would like to thank Prof. Dr. Ibrahim Demirtas (Cankiri Karatekin University) for his valuable help and support for anticancer activity tests.

FundersFunder number
TUBITAK112T721, COST/CM1105
Kennesaw State University2011/8-6D

    Keywords

    • differential pulse voltammetry (DPV); anticancer; xCELLigence
    • drug – DNA interaction
    • metal-based drugs
    • methotrexate
    • pencil graphite electrode (PGE)

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