Ruthenium(IV) Complexes as Potential Inhibitors of Bacterial Biofilm Formation.
Agnieszka Jabłońska-WawrzyckaPatrycja RogalaGrzegorz CzerwonkaSławomir MichałkiewiczMaciej HodorowiczPaweł KowalczykPublished in: Molecules (Basel, Switzerland) (2020)
With increasing antimicrobial resistance there is an urgent need for new strategies to control harmful biofilms. In this study, we have investigated the possibility of utilizing ruthenium(IV) complexes (H3O)2(HL1)2[RuCl6]·2Cl·2EtOH (1) and [RuCl4(CH3CN)2](L32)·H2O (2) (where L1-2-hydroxymethylbenzimadazole, L32-1,4-dihydroquinoxaline-2,3-dione) as effective inhibitors for biofilms formation. The biological activities of the compounds were explored using E. coli, S. aureus, P. aeruginosa PAO1, and P. aeruginosa LES B58. The new chloride ruthenium complexes were characterized by single-crystal X-ray diffraction analysis, Hirshfeld surface analysis, FT-IR, UV-Vis, magnetic and electrochemical (CV, DPV) measurements, and solution conductivity. In the obtained complexes, the ruthenium(IV) ions possess an octahedral environment. The intermolecular classical and rare weak hydrogen bonds, and π···π stacking interactions significantly contribute to structure stabilization, leading to the formation of a supramolecular assembly. The microbiological tests have shown complex 1 exhibited a slightly higher anti-biofilm activity than that of compound 2. Interestingly, electrochemical studies have allowed us to determine the relationship between the oxidizing properties of complexes and their biological activity. Probably the mechanism of action of 1 and 2 is associated with generating a cellular response similar to oxidative stress in bacterial cells.
Keyphrases
- biofilm formation
- candida albicans
- antimicrobial resistance
- pseudomonas aeruginosa
- oxidative stress
- staphylococcus aureus
- induced apoptosis
- escherichia coli
- molecularly imprinted
- gold nanoparticles
- dna damage
- crystal structure
- squamous cell carcinoma
- cell death
- quantum dots
- lymph node metastasis
- magnetic resonance imaging
- cell cycle arrest
- mass spectrometry
- heat stress
- visible light