In vitro and in vivo studies into the biological activities of 1,10-phenanthroline, 1,10-phenanthroline-5,6-dione and its copper(II) and silver(I) complexes

被引:87
|
作者
McCann, Malachy [1 ]
Santos, Andre L. S. [2 ]
da Silva, Bianca A. [2 ]
Romanos, Maria Teresa V. [3 ]
Pyrrho, Alexandre S. [4 ]
Devereux, Michael [5 ]
Kavanagh, Kevin [6 ]
Fichtner, Iduna [7 ]
Kellett, Andrew [8 ,9 ]
机构
[1] Natl Univ Ireland, Dept Chem, Maynooth, Kildare, Ireland
[2] Univ Fed Rio de Janeiro, IMPPG, Dept Microbiol Geral, BR-21941 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, IMPPG, Dept Virol, BR-21941 Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Fac Farm, Dept Anal Clin & Toxicol, BR-21941 Rio De Janeiro, Brazil
[5] Dublin Inst Technol, Focas Res Inst, Inorgan Pharmaceut & Biomimet Res Ctr, Camden 8, Ireland
[6] Natl Univ Ireland, Dept Biol, Med Mycol Unit, NICB, Maynooth, Co Kildare, Ireland
[7] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[8] Dublin City Univ, Sch Chem Sci, Dublin 9, Ireland
[9] Dublin City Univ, Natl Inst Cellular Biotechnol, Dublin 9, Ireland
关键词
RAY CRYSTAL-STRUCTURES; ANTI-TUMOR AGENTS; LIGHT-INDUCED DNA; ESCHERICHIA-COLI; METAL-COMPLEXES; BIS(4,7-DIMETHYL-1,10-PHENANTHROLINE) SULFATOOXOVANADIUM(IV); QUANTITATIVE RELATIONSHIPS; PLATINUM(II) COMPLEXES; ANTIFUNGAL ACTIVITY; CANDIDA-ALBICANS;
D O I
10.1039/c2tx00010e
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1,10-Phenanthroline (phen, 5), 1,10-phenanthroline-5,6-dione (phendione, 6), [Cu(phendione) 3]( ClO4)(2)center dot 4H(2)O (12) and [Ag(phendione)(2)]ClO4 (13) are highly active, in vitro, against a range of normal and cancerous mammalian cells, fungal and insect cell lines, with the metal complexes offering a clear enhancement in activity. Cytoselectivity was not observed between the tumorigenic and non-tumorigenic mammalian lines. In in vivo tests, using Galleria mellonella and Swiss mice, all four compounds were well tolerated in comparison to the clinical agent, cisplatin. In addition, blood samples taken from the Swiss mice showed that the levels of the hepatic enzymes, aspartate aminotransferase (AST) and alanine aminotransferase (ALT), remained unaffected. Immunocompromised nude mice showed a much lower tolerance to 13 and, subsequently, when these mice were implanted with Hep-G2 (hepatic) and HCT-8 (colon) human-derived tumors, there was no influence on tumor growth.
引用
收藏
页码:47 / 54
页数:8
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