ALLYL FUNCTIONALIZED BENZIMIDAZOLIUM-DERIVED AG(I)-N-HETEROCYCLIC CARBENE COMPLEXES: ANTI-BIOFILM AND ANTIMICROBIAL PROPERTIES

Abstract

Microorganisms in the biofilm structure cause severe health problems and economic losses. Therefore, it is very important to design and screen anti-biofilm molecules that can solve the related problems. This paper is aimed to demonstrate the antimicrobial and anti-biofilm properties of allyl substituted benzimidazoliumbased Ag(I)-containing N-heterocyclic carbene (NHC) complexes. In this work, the antimicrobial and antibiofilm properties of six allyl-substituted benzimidazolium-based Ag(I)-NHC complexes, the synthesis and characterization of which had been carried out previously, were investigated. The antibacterial properties of Ag(I)-NHC complexes were tested by the broth microdilution method. The biofilm formation was detected by microtiter plate assay. All test compounds (1–6) showed strong and same activity against Escherichia coli ATCC 25922 at concentrations of 3.9 g/mL as compared to that of the reference anti-biotics (ampicillin). Test compounds exhibited the same or stronger activity than the reference drug against the Acinetobacter baumannii isolate with MedIC values of 15.6 – 31.25 g/mL in comparison to the positive control colistin. All compounds inhibited the formation of E. coli biofilms at sub-MIC concentrations by 56 – 90%. Furthermore, it was found that these compounds reduced Klebsiella pneumoniae biofilm formation by 29 – 65%, S. aureus biofilm formation by 36 – 52%, E. faecalis biofilm formation by 38 – 50%, A. baumannii biofilm formation by 51 – 60%, and Candida albicans biofilm formation by 38 – 53%. Regarding the biofilms formed, it was established that the test compounds eradicated the mature of E. coli biofilm by 43 – 63%, K. pneumoniae biofilm by 16 – 40%, S. aureus biofilm by 18 – 39%, E. faecalis biofilm by 15 – 27%, A. baumannii biofilm by 27 – 53%, and C. albicans biofilm by 18 – 41%. Compounds evaluated in our work, which is one of the few studies on benzimidazolium-derived NHCs, have the potential to become new biological agents with strong antimicrobial properties and activity against microbial biofilms. Therefore, further in vivo and in vitro studies should be conducted.