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

Author:

McCann Malachy1,Santos André L. S.2,da Silva Bianca A.2,Romanos Maria Teresa V.3,Pyrrho Alexandre S.4,Devereux Michael5,Kavanagh Kevin6,Fichtner Iduna7,Kellett Andrew8

Affiliation:

1. Chemistry Department, National University of Ireland, Maynooth, Kildare, Ireland. Tel: +353 (0)1 7083767

2. Departamento de Microbiologia Geral, Instituto de Microbiologia Prof. Paulo de Góes (IMPPG), Universidade Federal do Rio de Janeiro (UFRJ), Brazil

3. Departamento de Virologia, IMPPG, UFRJ, Brazil

4. Departamento de Análises Clínicas e Toxicológicas, Faculdade de Farmácia, UFRJ, Brazil

5. The Inorganic Pharmaceutical and Biomimetic Research Centre, Focas Research Institute, Dublin Institute of Technology, Camden Row, Dublin 8, Ireland

6. Medical Mycology Unit, NICB, Department of Biology, National University of Ireland, Maynooth, Co. Kildare, Ireland

7. Max Delbrück Center for Molecular Medicine, Experimental Pharmacology, Robert-Rössle-Str. 10, 13125 Berlin, Germany

8. School of Chemical Sciences and National Institute of Cellular Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland

Abstract

Abstract1,10-Phenanthroline (phen, 5), 1,10-phenanthroline-5,6-dione (phendione, 6), [Cu(phendione)3](ClO4)2·4H2O (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.

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Toxicology

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