The increase in bacterial resistance to one or several antibiotics has become a global health problem. Recently, nanomaterials have become a tool against multidrug-resistant bacteria. The metal and metal oxide nanoparticles are one of the most studied nanomaterials against multidrug-resistant bacteria. Several in vitro studies report that metal nanoparticles have antimicrobial properties against a broad spectrum of bacterial species. However, until recently, the bacterial resistance mechanisms to the bactericidal action of the nanoparticles had not been investigated. Some of the recently reported resistance mechanisms include electrostatic repulsion, ion efflux pumps, expression of extracellular matrices, and the adaptation of biofilms and mutations. The objective of this review is to summarize the recent findings regarding the mechanisms used by bacteria to counteract the antimicrobial effects of nanoparticles.
High-throughput screening was employed to evaluate bactericidal activities of hybrid Ag-TiO₂ nanoparticles comprising variations in TiO₂ crystalline phase, Ag content, and synthesis method. Hybrid Ag-TiO₂ nanoparticles were prepared by either wet-impregnation or UV photo deposition onto both Degussa P25 and DuPont R902 TiO₂ nanoparticles. The presence of Ag was confirmed by ICP, TEM, and XRD analysis. The size of Ag nanoparticles formed on anatase/rutile P25 TiO₂ nanoparticles was smaller than those formed on pure rutile R902. When activated by UV light, all hybrid Ag-TiO₂ nanoparticles exhibited stronger bactericidal activity than UV alone, Ag/UV, or UV/TiO₂. For experiments conducted in the dark, bactericidal activity of Ag-TiO₂ nanoparticles was greater than either bare TiO₂ (inert) or pure Ag nanoparticles, suggesting that the hybrid materials produced a synergistic antibacterial effect unrelated to photoactivity. Moreover, less Ag(+) dissolved from Ag-TiO₂ nanoparticles than from Ag nanoparticles, indicating the antibacterial activities of Ag-TiO₂ was not only caused by releasing of toxic metal ions. It is clear that nanotechnology can produce more effective bactericides; however, the challenge remains to identify practical ways to take advantage of these exciting new material properties.
In recent years, the use and research in nanomaterials have increased considerably. In dentistry, nanomaterials have been investigated in all their specialties like dental prosthesis, implantology, dental operative, periodontics, and endodontics. The nanomaterials are investigated in the areas of dentistry due to their application in the improvement of the physical and chemical properties of conventional materials, as well as the use of the antimicrobial activity of nanomaterials such as silver nanoparticles. Recently, silver nanoparticles (AgNPs) have been studied for their use as an endodontic irrigator due to their high antimicrobial activity. But little is known about the possible mechanisms of the adaptation to AgNPs by endodontic bacteria. These mechanisms may be intrinsic (such as efflux pumps, downregulation of porins, and chromosomal resistance genes) or extrinsic (such as point and adaptive mutations and plasmids with resistance genes) adaptation systems. In addition to this, it has been reported that coselection or coregulation of metal resistance mechanisms, as in the case of nanoparticles, is accompanied by increased resistance to various antibiotics. For these reasons, the objective of this article is to do a review of the literature on the possible mechanisms used by endodontic bacteria to generate resistance to silver nanoparticles and the possible side effects of these mechanisms.
Silver nanoparticles with a narrow size distribution were synthesized over the surface of two different commercial TiO(2) particles using a simple aqueous reduction method. The reducing agent used was NaBH(4); different molar ratios TiO(2):Ag were also used. The nanocomposites thus prepared were characterized using transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), x-ray photoelectron spectroscopy (XPS), x-ray diffraction (XRD), dynamic light scattering (DLS) and UV-visible (UV-vis) absorption spectroscopy; the antibacterial activity was assessed using the standard microdilution method, determining the minimum inhibitory concentration (MIC) according to the National Committee for Clinical Laboratory Standards. From the microscopy studies (TEM and STEM) we observed that the silver nanoparticles are homogeneously distributed over the surface of TiO(2) particles and that the TiO(2):Ag molar ratio plays an important role. We used three different TiO(2)Ag molar ratios and the size of the silver nanoparticles is 10, 20 and 80 nm, respectively. It was found that the antibacterial activity of the nanocomposites increases considerably comparing with separated silver nanoparticles and TiO(2) particles.
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