N, N'-Olefin Functionalized Bis-Imidazolium Gold

Keratitis treatment has become more complicated due to the emergence of bacterial or fungal pathogens with enhanced antibiotic resistance. The pharmaceutical applications of N-heterocyclic carbene complexes have received remarkable attention due to their antimicrobial properties. In this paper, the...

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Veröffentlicht in:PloS one 2013-03, Vol.8 (3), p.e58346
Hauptverfasser: Samanta, Tapastaru, Roymahapatra, Gourisankar, Porto, William F, Seth, Saikat, Ghorai, Sudipta, Saha, Suman, Sengupta, Jayangshu, Franco, Octávio L, Dinda, Joydev, Mandal, Santi M
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Sprache:eng
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Zusammenfassung:Keratitis treatment has become more complicated due to the emergence of bacterial or fungal pathogens with enhanced antibiotic resistance. The pharmaceutical applications of N-heterocyclic carbene complexes have received remarkable attention due to their antimicrobial properties. In this paper, the new precursor, 3,3'-(p-phenylenedimethylene) bis{1-(2- methyl-allyl)imidazolium} bromide (1a) and its analogous PF.sub.6 salt (1b) were synthesized. Furthermore, silver(I) and gold(I) -N-heterocyclic carbene (NHC) complexes [Ag.sub.2 LBr.sub.2 /Au.sub.2 LBr.sub.2 ; 2a/3a], [(Ag.sub.2 L.sub.2 )(PF.sub.6).sub.2 /(Au.sub.2 L.sub.2 )(PF.sub.6).sub.2 ; 2b/3b] were developed from their corresponding ligands. All compounds were screened for their antimicrobial activities against multiple keratitis-associated human eye pathogens, including bacteria and fungi. Complexes 2a and 3a showed highest activity, and the effectiveness of 3a was also studied, focusing eradication of pathogen biofilm. Furthermore, the structures of 1a, 2a and 3b were determined using single crystal X-ray analysis, 2b and 3a were optimized theoretically. The mechanism of action of 3a was evaluated by scanning electron microscopy and docking experiments, suggesting that its target is the cell membrane. In summary, 3a may be helpful in developing antimicrobial therapies in patients suffering from keratitis-associated eye infections caused by multidrug-resistant pathogens.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0058346