4.7 Article

Oligonuclear polypyridylruthenium(II) complexes: selectivity between bacteria and eukaryotic cells

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 71, Issue 6, Pages 1547-1555

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkw026

Keywords

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Funding

  1. Pathfinder Grant from UniQuest (James Cook University)
  2. UNSW Canberra

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Objectives: The objectives of this study were to: (i) determine the in vitro activities of a series of di-, tri- and tetra-nuclear ruthenium complexes (Rubb(n), Rubb(n)-tri and Rubb(n)-tetra) against a range of Gram-positive and-negative bacteria and compare the antimicrobial activities with the corresponding toxicities against eukaryotic cells; and (ii) compare MIC values with achievable in vivo serum concentrations for the Least toxic ruthenium complex. Methods: The in vitro activities were determined by MIC assays and time-kill curve experiments, while the toxicities of the ruthenium complexes were determined using the Alamar blue cytotoxicity assay. A preliminary pharmacokinetic study was undertaken to determine the Rubb(12) serum concentration in mice as a function of time after administration. Results: Rubb(12), Rubb(12)-tri and Rubb(12)-tetra are highly active, with MIC values of 1-2 mg/L (0.5-1.5 mu M) for a range of Gram-positive strains, but showed variable activities against a panel of Gram-negative bacteria. Time-kill experiments indicated that Rubb12, Rubb(12)-tri and Rubb(12)-tetra are bactericidal and kill bacteria within 3-8 h. The di-, tri- and tetra nuclear complexes were similar to 50 times more toxic to Gram-positive bacteria and 25 times more toxic to Gram-negative strains, classified as susceptible, than to Liver and kidney cells. Preliminary pharmacokinetic experiments established that serum concentrations higher than MIC values can be obtained for Rubb(12) with an administered dose of 32 mg/kg. Conclusions: The ruthenium complexes, particularly Rubb(12), have potential as new antimicrobial agents. The structure of the dinuclear ruthenium complex can be readily further modified in order to increase the selectivity for bacteria over eukaryotic cells.

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