Photocytotoxicity and near-IR light DNA cleavage activity of oxovanadium(IV) Schiff base complexes having phenanthroline bases

被引:39
作者
Prasad, Puja [1 ]
Sasmal, Pijus K. [1 ]
Majumdar, Ritankar [2 ]
Dighe, Rajan R. [2 ]
Chakravarty, Akhil R. [1 ]
机构
[1] Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Dept Mol Reprod Dev & Genet, Bangalore 560012, Karnataka, India
关键词
Oxovanadium(IV) complex; Photocleavage of DNA; Photocytotoxicity Crystal structure; Schiff base; Phenanthroline bases; PHOTODYNAMIC THERAPY; RED-LIGHT; NUCLEASE ACTIVITY; VISIBLE-LIGHT; BINDING; 1,10-PHENANTHROLINE; PHOTOSENSITIZERS; PHOTOCLEAVAGE; DESIGN; CYTOTOXICITY;
D O I
10.1016/j.ica.2010.03.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Oxovanadium(IV) complexes [VO(L)(B)] (1-3), where H2L is a Schiff base ligand 2-(2-hydroxybenzylideneamino) phenol and B is 1,10-phenanthroline (phen for 1), dipyrido[3,2-d:2',3'-f]quinoxaline (dpq for 2) or dipyrido[3,2-a:2',3'-c]phenazine (dppz for 3), have been prepared, characterized and their DNA binding property and photo-induced DNA cleavage activity studied. Complex 3 which is structurally characterized by X-ray crystallography shows the presence of an oxovanadium(IV) moiety in a six coordinate VO3N3 coordination geometry. The complexes show a d-d band within 800-850 nm in DMF. The complexes display an oxidative response near 0.7 V versus SCE for V(V)-V(IV) and a reductive response within -1.1 to -1.3 V due to V(IV)-V(III) couple in DMF-0.1 M TBAP. The complexes are avid binders to calf thymus DNA giving binding constant values of 4.2 x 10(4) to 1.2 x 10(5) M (1). The complexes do not show any "chemical nuclease" activity in dark. The dpq and dppz complexes are photocleavers of plasmid DNA in UV-A light of 365 nm via O-1(2) pathway and in near-IR light (752.5 to 799.3 nm IR optics) by HO* pathway. Complex 3 exhibits significant photocytotoxicity in visible light in HeLa cells giving IC50 value of 13 mu M, while it is less toxic in dark (IC50 = 97 mu M). (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2743 / 2751
页数:9
相关论文
共 76 条
[1]   SYNTHESIS AND CHARACTERIZATION OF SOME DIBASIC TRIDENTATE SCHIFF-BASE LIGANDS [J].
ALYEA, EC ;
MALEK, A .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1975, 53 (06) :939-944
[2]   SYNTHESIS AND STUDY OF A MIXED-LIGAND RUTHENIUM(II) COMPLEX IN ITS GROUND AND EXCITED-STATES - BIS(2,2'-BIPYRIDINE)(DIPYRIDO[3,2-A, 2',3'-C]PHENAZINE-N4N5)RUTHENIUM(II) [J].
AMOUYAL, E ;
HOMSI, A ;
CHAMBRON, JC ;
SAUVAGE, JP .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1990, (06) :1841-1845
[3]   Dirhodium(II,II) complexes: Molecular characteristics that affect in vitro activity [J].
Angeles-Boza, Alfredo M. ;
Chifotides, Helen T. ;
Aguirre, J. Dafhne ;
Chouai, Abdellatif ;
Fu, Patty K. -L. ;
Dunbar, Kim R. ;
Turro, Claudia .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (23) :6841-6847
[4]   Water soluble distyryl-boradiazaindacenes as efficient photosensitizers for photodynamic therapy [J].
Atilgan, Serdar ;
Ekmekci, Zeynep ;
Dogan, A. Lale ;
Guc, Dicle ;
Akkaya, Engin U. .
CHEMICAL COMMUNICATIONS, 2006, (42) :4398-4400
[5]   POTASSIUM MONOPERSULFATE AND A WATER-SOLUBLE MANGANESE PORPHYRIN COMPLEX, [MN(TMPYP)](OAC)5, AS AN EFFICIENT REAGENT FOR THE OXIDATIVE CLEAVAGE OF DNA [J].
BERNADOU, J ;
PRATVIEL, G ;
BENNIS, F ;
GIRARDET, M ;
MEUNIER, B .
BIOCHEMISTRY, 1989, 28 (18) :7268-7275
[6]   Metal complex-DNA interactions: from transcription inhibition to photoactivated cleavage [J].
Boerner, LJK ;
Zaleski, JM .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2005, 9 (02) :135-144
[7]  
Bonnett Alastair., 2000, ANTIRACISM
[8]   Light-induced anticancer activity of [RuCl2(DMSO)4] complexes [J].
Brindell, M ;
Kulis, E ;
Elmroth, SKC ;
Urbanska, K ;
Stochel, G .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (23) :7298-7304
[9]   Cleavage of nucleic acids by bleomycin [J].
Burger, RM .
CHEMICAL REVIEWS, 1998, 98 (03) :1153-1169
[10]   Oxidative nucleobase modifications leading to strand scission [J].
Burrows, CJ ;
Muller, JG .
CHEMICAL REVIEWS, 1998, 98 (03) :1109-1151