Bridging Oxidative Defense and DNA Disruption: Methyl Piperazine Metal Complexes as Multifunctional Therapeutics.
TL;DR
Compound 6b showed higher cytotoxic efficiency than the complexes, which subsequently increased the lipophilic character and favored its permeation through the lipid surface of the cell, aiding in inhibiting cell growth easily and demonstrating the bioactivity of the Cu(II) complex (6b) as a potential therapeutic agent.
Abstract
INTRODUCTION Novel Co(II), Cu(II), and Zn(II) complexes of Schiff base ligand with N2O2 donor sites were synthesized from 5-((4-methylpyrazin-1(4)-yl)methyl)isophthalaldehyde and subsequently condensed with Phenylpropanolamine (PPA).
Materials And Methods
FT-IR, UV-Visible, NMR (1H), and mass spectrometry established the structure of synthesized compounds. In addition, susceptibility, thermal analysis, powder XRD, and cyclic voltammetry were also performed. The interaction between the final compounds and CT-DNA was investigated using UV-visible absorption spectroscopy. In addition, cytotoxic studies were performed in the HeLa cell line using the MTT assay.
Results
The Co(II) complex demonstrated a high-spin octahedral geometry with a [ML(H2O)2] stoichiometry, whereas the Cu(II) and Zn(II) complexes (6a and 6b) were found to have square-planar geometries with a (ML) stoichiometry. Agarose gel electrophoresis demonstrated that the Cu(II) complex (6c) effectively hydrolyzed and cleaved CT-DNA and also showed enhanced free-radical scavenging ability compared to the standard, ascorbic acid. The Cu(II) complex displayed superior potency in inhibiting the proliferation of the HeLa cancer cell line (IC50: 6.12 μg/mL) relative to the standard drug cisplatin.
Discussion
Compound 6b showed higher cytotoxic efficiency than the complexes, which subsequently increased the lipophilic character and favored its permeation through the lipid surface of the cell, aiding in inhibiting cell growth easily. The results of cytotoxicity experiments also matched well with the order of CT-DNA binding affinities: 6b > 6a > 6c.
Conclusion
The current work demonstrates the bioactivity of the Cu(II) complex (6b) as a potential therapeutic agent.