DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes

Three Schiff base Cu(II) complexes, (N,N’-bis(acetylacetone)propylenediimine) copper(II) complex, [Cu(acac2pn)] (1), (N,N'-bis-(benzoylacetone) propylenediimine)copper(II) complex, [Cu(phacac2pn)] (2) and (N,N’-bis- -(trifluoroacetylacetone)propylenediimine)copper(II) complex, [Cu(tfacac2pn)] (...

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Main Authors: Mijatović Aleksandar, Caković Angelina Z., Lolić Aleksandar, Sretenović Snežana, Živanović Marko N., Šeklić Dragana S., Bogojeski Jovana, Petrović Biljana V.
Format: Article
Language:English
Published: Serbian Chemical Society 2023-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:https://doiserbia.nb.rs/img/doi/0352-5139/2023/0352-51392300063M.pdf
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author Mijatović Aleksandar
Caković Angelina Z.
Lolić Aleksandar
Sretenović Snežana
Živanović Marko N.
Šeklić Dragana S.
Bogojeski Jovana
Petrović Biljana V.
author_facet Mijatović Aleksandar
Caković Angelina Z.
Lolić Aleksandar
Sretenović Snežana
Živanović Marko N.
Šeklić Dragana S.
Bogojeski Jovana
Petrović Biljana V.
author_sort Mijatović Aleksandar
collection DOAJ
description Three Schiff base Cu(II) complexes, (N,N’-bis(acetylacetone)propylenediimine) copper(II) complex, [Cu(acac2pn)] (1), (N,N'-bis-(benzoylacetone) propylenediimine)copper(II) complex, [Cu(phacac2pn)] (2) and (N,N’-bis- -(trifluoroacetylacetone)propylenediimine)copper(II) complex, [Cu(tfacac2pn)] (3), were used to investigate the interactions with calf thymus DNA (ct-DNA) and bovine serum albumin (BSA) using the electronic absorption and spectroscopic fluorescence methods. UV–Vis absorption studies showed that studied complexes interact with DNA molecule and exhibit moderate binding affinity. Fluorescence studies of complexes 1–3 also showed a possibility for DNA intercalation as well as a relatively high binding ability toward BSA. Among the tested complexes, the highest affinity for DNA and BSA molecules was shown by complex 1. Cytotoxic analyses, performed on human colorectal carcinoma HCT-116 and healthy lung fibroblast MRC-5 cell lines, showed that complex 2 exhibited activity on both cell lines, while complexes 1 and 3 did not show any activity.
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spelling doaj.art-dbe49eebf62a46faa66c818ba9c4dafa2024-04-10T10:17:11ZengSerbian Chemical SocietyJournal of the Serbian Chemical Society0352-51391820-74212023-01-0188121307131710.2298/JSC230614063M0352-51392300063MDNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexesMijatović Aleksandar0Caković Angelina Z.1https://orcid.org/0000-0003-3909-4211Lolić Aleksandar2https://orcid.org/0000-0002-5354-9019Sretenović Snežana3https://orcid.org/0009-0002-0515-7931Živanović Marko N.4https://orcid.org/0000-0002-8833-8035Šeklić Dragana S.5https://orcid.org/0000-0002-2093-5335Bogojeski Jovana6Petrović Biljana V.7https://orcid.org/0000-0001-7914-6026University of Belgrade, Faculty of Mining and Geology, Belgrade, SerbiaUniversity of Kragujevac, Faculty of Science, KragujevacUniversity of Belgrade, Faculty of Chemistry, BelgradeUniversity of Kragujevac, Faculty of Medicinal Science, Department of Internal medicine, Kragujevac, SerbiaUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Kragujevac, SerbiaUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Kragujevac, SerbiaUniversity of Kragujevac, Faculty of Science, KragujevacUniversity of Kragujevac, Faculty of Science, KragujevacThree Schiff base Cu(II) complexes, (N,N’-bis(acetylacetone)propylenediimine) copper(II) complex, [Cu(acac2pn)] (1), (N,N'-bis-(benzoylacetone) propylenediimine)copper(II) complex, [Cu(phacac2pn)] (2) and (N,N’-bis- -(trifluoroacetylacetone)propylenediimine)copper(II) complex, [Cu(tfacac2pn)] (3), were used to investigate the interactions with calf thymus DNA (ct-DNA) and bovine serum albumin (BSA) using the electronic absorption and spectroscopic fluorescence methods. UV–Vis absorption studies showed that studied complexes interact with DNA molecule and exhibit moderate binding affinity. Fluorescence studies of complexes 1–3 also showed a possibility for DNA intercalation as well as a relatively high binding ability toward BSA. Among the tested complexes, the highest affinity for DNA and BSA molecules was shown by complex 1. Cytotoxic analyses, performed on human colorectal carcinoma HCT-116 and healthy lung fibroblast MRC-5 cell lines, showed that complex 2 exhibited activity on both cell lines, while complexes 1 and 3 did not show any activity.https://doiserbia.nb.rs/img/doi/0352-5139/2023/0352-51392300063M.pdfantitumormechanismcell linebiomoleculeaffinitydrug design
spellingShingle Mijatović Aleksandar
Caković Angelina Z.
Lolić Aleksandar
Sretenović Snežana
Živanović Marko N.
Šeklić Dragana S.
Bogojeski Jovana
Petrović Biljana V.
DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes
Journal of the Serbian Chemical Society
antitumor
mechanism
cell line
biomolecule
affinity
drug design
title DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes
title_full DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes
title_fullStr DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes
title_full_unstemmed DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes
title_short DNA/BSA interactions and cytotoxic studies of tetradentate N,N,O,O Schiff base copper(II) complexes
title_sort dna bsa interactions and cytotoxic studies of tetradentate n n o o schiff base copper ii complexes
topic antitumor
mechanism
cell line
biomolecule
affinity
drug design
url https://doiserbia.nb.rs/img/doi/0352-5139/2023/0352-51392300063M.pdf
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