2021
DOI: 10.2147/ijn.s295928
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The Effects of Luminescent CdSe Quantum Dot-Functionalized Antimicrobial Peptides Nanoparticles on Antibacterial Activity and Molecular Mechanism

Abstract: Background With the development of bacterial resistance, the range of effective antibiotics is increasingly becoming more limited. The effective use of nanoscale antimicrobial peptides (AP) in therapeutic and diagnostic methods is a strategy for new antibiotics. Methods Combining both AP and cadmium selenide (CdSe) into a composite material may result in a reagent with novel properties, such as enhanced antibacterial activity, fluorescence and favorable stability in aqu… Show more

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Cited by 21 publications
(10 citation statements)
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“…However, the exact mechanism still needs further research. One possible cause of the change in the permeability of E. coli is oxidative stress, where the adhesion of CQDs to the bacterial cell wall leads the superoxide anion and free radicals being produced that rapidly and directly interact with bacteria, destroying the cell membrane and causing leakage of the cytoplasm [ 32 , 33 ].…”
Section: Discussionmentioning
confidence: 99%
“…However, the exact mechanism still needs further research. One possible cause of the change in the permeability of E. coli is oxidative stress, where the adhesion of CQDs to the bacterial cell wall leads the superoxide anion and free radicals being produced that rapidly and directly interact with bacteria, destroying the cell membrane and causing leakage of the cytoplasm [ 32 , 33 ].…”
Section: Discussionmentioning
confidence: 99%
“…At the end of the incubation, the cells were stained in the dark for 30 min using the Live/Dead live bacteria/dead bacteria double-staining kit [SYTO9 and propidium iodide (PI), Life Technologies]. The excess staining solution was removed by washing three times with PBS at the end of staining . The samples were prepared, and the fluorescence colocalization in the images was observed.…”
Section: Methodsmentioning
confidence: 99%
“…The excess staining solution was removed by washing three times with PBS at the end of staining. 42 The samples were prepared, and the fluorescence colocalization in the images was observed.…”
Section: Establishment Of In Vitro Biofilm Model and Inhibition Asses...mentioning
confidence: 99%
“…Log-phase S. aureus cultures were inoculated (1:40) in medium containing MoS 2 -Van-FITC (100 μg/mL), MoS 2 (100 μg/mL), or Van (1 μg/mL) and incubated in a shaking incubator at 37°C for 12 h. The irradiation power density was 1.5 W/cm 2 , and the irradiation time was 300 s. Thereafter, the cells were stained with SYTO9 and propidium iodide for 30 min in the dark, washed twice with PBS, and red and green channels were examined under a fluorescence microscope. The number of non-viable bacterial cells was determined by the CytoFLEX system (Beckman Coulter, Brea, CA, USA) [ 2 , 39 ].…”
Section: Methodsmentioning
confidence: 99%
“…Bacterial infections are consistently ranked as one of the leading causes of human mortality, with infection rates, mortality rates, and hospitalization costs increasing annually [ 1 , 2 , 3 ]. The high prevalence of bacterial infections has led to the misuse of antibiotics, resulting in the emergence of superbugs as bacteria become resistant to treatment.…”
Section: Introductionmentioning
confidence: 99%