Issue 53, 2020

In vitro anticancer activity of parent and nano-encapsulated samarium(iii) complex towards antimicrobial activity studies and FS-DNA/BSA binding affinity

Abstract

Based on the potential anticancer properties of lanthanide complexes, the anticancer activity of the Sm(III) complex containing a 2,2′-bipyridine ligand (bpy) and its interaction with FS-DNA (Fish-Salmon DNA) and BSA (Bovine Serum Albumin) were examined experimentally and by molecular docking in this paper. Absorption and fluorescence spectroscopic methods were used to define the thermodynamic parameters, binding constant (Kb), and the probable binding mechanism. It was concluded that the Sm complex interacts with FS-DNA through a minor groove with a Kb of 105 M−1. Also, the Kb for the BSA binding at 298 K was found to be 5.89 × 105 M−1, showing relatively a high tendency of the Sm complex to DNA and BSA. Besides, the Sm complex was docked to BSA and DNA by the autodock program. The results of the docking calculations were in good agreement with the experimental examinations. Additionally, the antifungal and antibacterial properties of this complex were investigated. The anticancer tests on the effect of the Sm complex, starch nano-encapsulation, and lipid nano-encapsulation in MCF-7 and A-549 cell lines were performed by the MTT method. It can be observed that the Sm complex and its nanocarriers presented a selective inhibitory effect on various cancer cell growths.

Graphical abstract: In vitro anticancer activity of parent and nano-encapsulated samarium(iii) complex towards antimicrobial activity studies and FS-DNA/BSA binding affinity

Article information

Article type
Paper
Submitted
16 6月 2020
Accepted
11 8月 2020
First published
28 8月 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 31979-31990

In vitro anticancer activity of parent and nano-encapsulated samarium(III) complex towards antimicrobial activity studies and FS-DNA/BSA binding affinity

S. Asadpour, Z. Aramesh-Boroujeni and S. Jahani, RSC Adv., 2020, 10, 31979 DOI: 10.1039/D0RA05280A

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