Novel Bioactive Co(II), Cu(II), Ni(II) and Zn(II) Complexes with Schiff Base Ligand Derived from Histidine and 1,3-Indandione: Synthesis, Structural Elucidation, Biological Investigation and Docking Analysis

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • V.V. Dhayabaran
  • T.D. Prakash
  • R. Renganathan
  • E. Friehs
  • D.W. Bahnemann

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OriginalspracheEnglisch
Seiten (von - bis)135-150
Seitenumfang16
FachzeitschriftJournal of fluorescence
Jahrgang27
Ausgabenummer1
PublikationsstatusVeröffentlicht - 1 Jan. 2017

Abstract

Novel bioactive complexes of Co(II), Cu(II), Ni(II) and Zn(II) metal ions with Schiff base ligand derived from histidine and 1,3-indandione were synthesized and thoroughly characterized by various analytical and spectral techniques. The biological investigations were carried out to examine the efficiency of the binding interaction of all the complexes with calf thymus DNA (CT-DNA). The binding properties were studied and evaluated quantitatively by K b and K sq values using UV-visible, fluorescence spectroscopy and voltammetric techniques. The experimental results revealed that the mode of binding of all the complexes with CT-DNA is via intercalation. It is further verified by viscosity measurements and thermal denaturation experiments. From the results of the cleavage study with pUC19 DNA it is inferred that all the complexes possess excellent cleaving ability. The present investigation proved that the binding interaction of all the complexes are significantly strong and the order of binding strength of the complexes is [Ni(L) 2] (K b = 3.11 × 10 6 M −1) > [Co(L) 2] (K b = 2.89 × 10 6 M −1) > [Cu(L) 2] (K b = 2.64 × 10 6 M −1) > [Zn(L) 2] (K b = 2.41 × 10 5 M −1). The complexes were also screened for antibacterial and anticandidal activity. The in vitro cytotoxicity of the ligand and complexes on the NIH/3 T3 mouse fibroblast cell lines were examined using CellTiter-Blue® (CTB) Cell viability assay, which unveiled that all the complexes exhibit more potent activities against NIH/3 T3 cells. Among all the complexes [Zn(L) 2] complex showed the maximum efficiency.

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Novel Bioactive Co(II), Cu(II), Ni(II) and Zn(II) Complexes with Schiff Base Ligand Derived from Histidine and 1,3-Indandione: Synthesis, Structural Elucidation, Biological Investigation and Docking Analysis. / Dhayabaran, V.V.; Prakash, T.D.; Renganathan, R. et al.
in: Journal of fluorescence, Jahrgang 27, Nr. 1, 01.01.2017, S. 135-150.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Novel Bioactive Co(II), Cu(II), Ni(II) and Zn(II) Complexes with Schiff Base Ligand Derived from Histidine and 1,3-Indandione: Synthesis, Structural Elucidation, Biological Investigation and Docking Analysis",
abstract = "Novel bioactive complexes of Co(II), Cu(II), Ni(II) and Zn(II) metal ions with Schiff base ligand derived from histidine and 1,3-indandione were synthesized and thoroughly characterized by various analytical and spectral techniques. The biological investigations were carried out to examine the efficiency of the binding interaction of all the complexes with calf thymus DNA (CT-DNA). The binding properties were studied and evaluated quantitatively by K b and K sq values using UV-visible, fluorescence spectroscopy and voltammetric techniques. The experimental results revealed that the mode of binding of all the complexes with CT-DNA is via intercalation. It is further verified by viscosity measurements and thermal denaturation experiments. From the results of the cleavage study with pUC19 DNA it is inferred that all the complexes possess excellent cleaving ability. The present investigation proved that the binding interaction of all the complexes are significantly strong and the order of binding strength of the complexes is [Ni(L) 2] (K b = 3.11 × 10 6 M −1) > [Co(L) 2] (K b = 2.89 × 10 6 M −1) > [Cu(L) 2] (K b = 2.64 × 10 6 M −1) > [Zn(L) 2] (K b = 2.41 × 10 5 M −1). The complexes were also screened for antibacterial and anticandidal activity. The in vitro cytotoxicity of the ligand and complexes on the NIH/3 T3 mouse fibroblast cell lines were examined using CellTiter-Blue{\textregistered} (CTB) Cell viability assay, which unveiled that all the complexes exhibit more potent activities against NIH/3 T3 cells. Among all the complexes [Zn(L) 2] complex showed the maximum efficiency. ",
keywords = "Amino acid, Cytotoxicity, DNA interaction, Docking studies, M(II) complexes, Schiff base",
author = "V.V. Dhayabaran and T.D. Prakash and R. Renganathan and E. Friehs and D.W. Bahnemann",
note = "Funding information: The authors sincerely thank the UGC, New Delhi, India for the financial support under major research project (UGC File No. 42-238/2013 (SR)), the Principal and management of Bishop Heber College, Tiruchirappalli, Tamilnadu, India for their constant encouragement and for providing the necessary facilities. The authors also gratefully acknowledge SAIF, IIT, Chennai and CRDI, Lucknow for providing analytical instrument facility.",
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TY - JOUR

T1 - Novel Bioactive Co(II), Cu(II), Ni(II) and Zn(II) Complexes with Schiff Base Ligand Derived from Histidine and 1,3-Indandione: Synthesis, Structural Elucidation, Biological Investigation and Docking Analysis

AU - Dhayabaran, V.V.

AU - Prakash, T.D.

AU - Renganathan, R.

AU - Friehs, E.

AU - Bahnemann, D.W.

N1 - Funding information: The authors sincerely thank the UGC, New Delhi, India for the financial support under major research project (UGC File No. 42-238/2013 (SR)), the Principal and management of Bishop Heber College, Tiruchirappalli, Tamilnadu, India for their constant encouragement and for providing the necessary facilities. The authors also gratefully acknowledge SAIF, IIT, Chennai and CRDI, Lucknow for providing analytical instrument facility.

PY - 2017/1/1

Y1 - 2017/1/1

N2 - Novel bioactive complexes of Co(II), Cu(II), Ni(II) and Zn(II) metal ions with Schiff base ligand derived from histidine and 1,3-indandione were synthesized and thoroughly characterized by various analytical and spectral techniques. The biological investigations were carried out to examine the efficiency of the binding interaction of all the complexes with calf thymus DNA (CT-DNA). The binding properties were studied and evaluated quantitatively by K b and K sq values using UV-visible, fluorescence spectroscopy and voltammetric techniques. The experimental results revealed that the mode of binding of all the complexes with CT-DNA is via intercalation. It is further verified by viscosity measurements and thermal denaturation experiments. From the results of the cleavage study with pUC19 DNA it is inferred that all the complexes possess excellent cleaving ability. The present investigation proved that the binding interaction of all the complexes are significantly strong and the order of binding strength of the complexes is [Ni(L) 2] (K b = 3.11 × 10 6 M −1) > [Co(L) 2] (K b = 2.89 × 10 6 M −1) > [Cu(L) 2] (K b = 2.64 × 10 6 M −1) > [Zn(L) 2] (K b = 2.41 × 10 5 M −1). The complexes were also screened for antibacterial and anticandidal activity. The in vitro cytotoxicity of the ligand and complexes on the NIH/3 T3 mouse fibroblast cell lines were examined using CellTiter-Blue® (CTB) Cell viability assay, which unveiled that all the complexes exhibit more potent activities against NIH/3 T3 cells. Among all the complexes [Zn(L) 2] complex showed the maximum efficiency.

AB - Novel bioactive complexes of Co(II), Cu(II), Ni(II) and Zn(II) metal ions with Schiff base ligand derived from histidine and 1,3-indandione were synthesized and thoroughly characterized by various analytical and spectral techniques. The biological investigations were carried out to examine the efficiency of the binding interaction of all the complexes with calf thymus DNA (CT-DNA). The binding properties were studied and evaluated quantitatively by K b and K sq values using UV-visible, fluorescence spectroscopy and voltammetric techniques. The experimental results revealed that the mode of binding of all the complexes with CT-DNA is via intercalation. It is further verified by viscosity measurements and thermal denaturation experiments. From the results of the cleavage study with pUC19 DNA it is inferred that all the complexes possess excellent cleaving ability. The present investigation proved that the binding interaction of all the complexes are significantly strong and the order of binding strength of the complexes is [Ni(L) 2] (K b = 3.11 × 10 6 M −1) > [Co(L) 2] (K b = 2.89 × 10 6 M −1) > [Cu(L) 2] (K b = 2.64 × 10 6 M −1) > [Zn(L) 2] (K b = 2.41 × 10 5 M −1). The complexes were also screened for antibacterial and anticandidal activity. The in vitro cytotoxicity of the ligand and complexes on the NIH/3 T3 mouse fibroblast cell lines were examined using CellTiter-Blue® (CTB) Cell viability assay, which unveiled that all the complexes exhibit more potent activities against NIH/3 T3 cells. Among all the complexes [Zn(L) 2] complex showed the maximum efficiency.

KW - Amino acid

KW - Cytotoxicity

KW - DNA interaction

KW - Docking studies

KW - M(II) complexes

KW - Schiff base

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U2 - 10.1007/s10895-016-1941-x

DO - 10.1007/s10895-016-1941-x

M3 - Article

VL - 27

SP - 135

EP - 150

JO - Journal of fluorescence

JF - Journal of fluorescence

SN - 1053-0509

IS - 1

ER -