18 research outputs found

    Graphene Quantum Dot Oxidation Governs Noncovalent Biopolymer Adsorption

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    Graphene quantum dots (GQDs) are an allotrope of carbon with a planar surface amenable to functionalization and nanoscale dimensions that confer photoluminescence. Collectively, these properties render GQDs an advantageous platform for nanobiotechnology applications, including optical biosensing and delivery. Towards this end, noncovalent functionalization offers a route to reversibly modify and preserve the pristine GQD substrate, however, a clear paradigm has yet to be realized. Herein, we demonstrate the feasibility of noncovalent polymer adsorption to GQD surfaces, with a specific focus on single-stranded DNA (ssDNA). We study how GQD oxidation level affects the propensity for polymer adsorption by synthesizing and characterizing four types of GQD substrates ranging ~60-fold in oxidation level, then investigating noncovalent polymer association to these substrates. Adsorption of ssDNA quenches intrinsic GQD fluorescence by 31.5% for low-oxidation GQDs and enables aqueous dispersion of otherwise insoluble no-oxidation GQDs. ssDNA-GQD complexation is confirmed by atomic force microscopy, by inducing ssDNA desorption, and with molecular dynamics simulations. ssDNA is determined to adsorb strongly to no-oxidation GQDs, weakly to low-oxidation GQDs, and not at all for heavily oxidized GQDs. Finally, we reveal the generality of the adsorption platform and assess how the GQD system is tunable by modifying polymer sequence and type.https://www.nature.com/articles/s41598-020-63769-

    Antibacterial effects of carbon dots in combination with other antimicrobial reagents

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    <div><p>This study was designed to investigate the antimicrobial effects of CDots in combination with other antimicrobial reagents, including H<sub>2</sub>O<sub>2</sub>, Na<sub>2</sub>CO<sub>3</sub>, and AcOH (acetic acid). CDots were synthesized and passivated with 2,2’-(ethylenedioxy)bis(ethylamine) (EDA). The minimal inhibitory concentration (MIC) of CDots was 64 μg/mL on both Gram negative bacteria <i>E</i>.<i>coli</i> cells and Gram positive bacteria <i>Bacillus subtilis</i> cells. When CDots were combined with H<sub>2</sub>O<sub>2</sub>, antibacterial synergistic effects were observed based on the fractional inhibitory concentration (FIC) index, and further confirmed by an isobologram analysis and viable cell number counting methods. With the combination treatment of 10 μg/mL CDots with 8.82 mM H<sub>2</sub>O<sub>2</sub>, the viable <i>E</i>.<i>coli</i> cell numbers decreased 2.46 log, which was significant lower than the log reduction from 8.82 mM H<sub>2</sub>O<sub>2</sub> (1.57 log) or 10 μg/mL CDots (0.14 log) treatment alone. However, the combination of CDots with Na<sub>2</sub>CO<sub>3</sub> or AcOH did not show synergistic effects, instead, exhibiting indifference effects according to the FIC index. This study indicated that the combination of CDots with their synergistic antimicrobial reagents, such as H<sub>2</sub>O<sub>2</sub>, could reach the goal of inhibiting bacteria growth by using lower concentration of each individual chemical in the combination than using one chemical treatment alone, reduce the risks imposed on environmental health and the possibilities of the development of microbial resistances.</p></div
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