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In Vitro DNA/BSA Binding, Anticancer and Normal Cell Activity of Pd(II) Complexes: Substitution Behaviour and Computational Study
Author(s) -
Mukherjee Subhajit,
Mitra Ishani,
B. Venkata P. Reddy,
Das Payel,
Misini Bashkim,
Linert Wolfgang,
Moi Sankar Ch.
Publication year - 2018
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201800211
Subject(s) - chemistry , hela , ligand (biochemistry) , cysteine , stereochemistry , cytotoxicity , linkage isomerism , in vitro , biochemistry , enzyme , receptor , metal , organic chemistry
In the aspect of an effective palladium based anticancer drug design, Pd(II) complexes [Pd(MAMP)Cl 2 ], C1 ; [Pd(MAMP)(H 2 O) 2 ]x 2 , C2 ; [Pd(MAMP)(L‐cys)]x, C3 ; [Pd(MAMP)(N‐ac‐L‐cys)], C4 ; [Pd(MAMP)(DL‐meth)]x 2 , C5 ; and [Pd(MAMP)(DL‐pen)]x, C6 (where x=ClO 4 − /NO 3 − ) have been synthesised and characterised where 2‐[(methylamino)methyl]pyridine (MAMP) has been considered as carrier ligand and chloride, aqua, L‐cysteine (L‐cys), N‐acetyl‐L‐cysteine (N‐ac‐L‐cys), DL‐methionine (DL‐meth) and DL‐penicillamine (DL‐pen) are selected as leaving group. DNA as well as protein binding ability of the complexes has been investigated with CT‐DNA and BSA and the related binding parameters have been evaluated. Kinetic investigation for the reactions of Pd(II)‐diaqua complex C2 with four selected sulfur containing bio‐molecules have been carried out under pseudo first order condition. In addition, theoretical investigation has also been considered for structural optimisation, frontier molecular orbital mapping, TD‐DFT and NBO analysis. To get an insight into the cytotoxicity, the complexes have been treated on three different cancer cell lines (A549, HeLa, Hep G2) which reveal comparable anticancer activity of the reported complexes with the clinically acquainted anticancer drug Cisplatin. Very less complex initiated reactive oxygen species (ROS) with low degree of cell death in two different non‐tumour cell lines (L6 myotubes and HEK 293) indicate minimum normal cell toxicity of the complexes.