Quercetin-derived red emission carbon dots: A multifunctional theranostic nano-agent against Alzheimer's ß-amyloid fibrillogenesis.

Multifunctional agents with therapeutic and diagnostic capabilities are imperative to the prevention of Alzheimer's disease (AD), which is considered due to abnormal aggregation and deposition of ß-amyloid protein (Aß) as well as oxidative stress. Herein, quercetin (Que)- and p-phenylenediamine (p-PD)-derived red emission carbon dots (CDs) synthesized via a one-step hydrothermal method were designed as a novel theranostic nano-agent for the multi-target treatment of AD. R-CD-75 with an optimized composition exhibited significant inhibition of Aß aggregation and rapid depolymerization of mature Aß fibrils (<4 h) at micromolar concentrations (2 and 5 µg/mL, respectively). Moreover, R-CD-75 potently scavenged reactive oxygen species and showed turned-on red fluorescence imaging of Aß plaques both in vitro and in vivo. In vitro assays proved that R-CD-75 significantly mitigated the Aß-induced cytotoxicity and enhanced the cultured cell viability from 74.9 % to 98.0 %, while in vivo studies demonstrated that R-CD-75 prolonged the lifespan of AD nematodes by over 50 % (from 13 to 20 d). Compared to the precursors Que and p-PD, R-CD-75 inherited some of their structures and functional groups, such as aromatic structures, phenolic hydroxyl and amino groups, which were considered to interact with Aß species through hydrogen bonding, electrostatic interactions, hydrophobic interactions, and π-π stacking, thus contributing to its effectiveness in its theranostic functions. This research has opened a new avenue to the development of potent theranostic agents by designing novel carbon dots.

Shaping Sulfur Precursors to Low Dimensional (0D, 1D and 2D) Sulfur Nanomaterials: Synthesis, Characterization, Mechanism, Functionalization, and Applications.

Low-dimensional sulfur nanomaterials featuring with 0D sulfur nanoparticles (SNPs), sulfur nanodots (SNDs) and sulfur quantum dots (SQDs), 1D sulfur nanorods (SNRs), and 2D sulfur nanosheets (SNSs) have emerged as an environmentally friendly, biocompatible class of metal-free nanomaterials, sparking extensive interest in a wide range application. In this review, various synthetic methods, precise characterization, creative formation mechanism, delicate functionalization, and versatile applications of low dimensional sulfur nanomaterials over the last decades are systematically summarized. Initially, it is striven to summarize the progress of low dimensional sulfur nanomaterials from versatile precursors by using different synthetic approaches and various characterization. Then, a multi-faceted proposed formation mechanism with emphasis on how these different precursors produce corresponding SNPs, SNDs, SQDs, SNRs, and SNSs is highlighted. Besides, it is essential to fine-tune the surface functional groups of low dimensional sulfur nanomaterials to form new complex nanomaterials. Finally, these sulfur nanomaterials are being investigated in bio-sensing, bio-imaging, lithium-sulfur batteries, antibacterial activities, plant growth along with future perspective and challenges in emerging fields. The purpose of this review is to tailor low dimensional nanomaterials through accurately selecting precursors or synthetic approach and provide a foundation for the formation of versatile sulfur nanostructure.

Investigation on Dynamic Changes in the Morphology and Fluorescence Properties of Sulfur Quantum Dots.

Sulfur quantum dots (SQDs), an emerging metal-free quantum dot, which has received intense research interest owing to their unique optical property, good solubility, excellent biocompatibility, and facile synthetic approach. Herein, using sodium hypochlorite as the etching agent, we investigate how it functions and transforms sulfur powder to SQDs and affects the dynamics, photoluminescence, and size changes of SQDs by controlling the reaction time. Precise control of reaction time allows SQDs to be tuned between green and blue (from 515 to 420 nm) with size distribution ranging from 2.0 to 20 nm as well as the occurrence of a distinctive irregular rodlike structure. Surface functional groups and element analysis reveal that the core size and surface oxidizing sulfur species both contribute to the versatile PL properties. Morevoer, we propose a tentative formation mechanism that relies on the oxidizing sulfur surface state and quantum size effect, offering a theoretical and experimental foundation for investigation of we propose a tentative formation mechanism that relies on the oxidizing sulfur surface state and quantum size effect, offering a theoretical and experimental foundation for investigation of the formation and modulation of SQDs.

Manipulating time-dependent size distribution of sulfur quantum dots and their fluorescence sensing for ascorbic acid.

Unlike the previous commonly used strong alkaline solvent sodium hydroxide, we employ an eco-friendly solvent, ethanol, as a solvent for the preparation of ultra-small-sized sulfur quantum dots (SQDs). Ethanol can disperse bulk sulfur and allow sufficient transfer of large-sized sulfur to smaller-sized SQDs through a one-pot synthesis approach. The SQDs obtained from ethanol as the solvent displays superior photoluminescence properties to those in water and sodium hydroxide. By delicately controlling the reaction conditions, including the amount of bulk sulfur, the reaction time, and the proportion of sulfur to oxidizing reagent, highly blue emissive SQDs with a photoluminescence quantum yield (PLQY) of 7.04% with ultra-high stability for several months can be successfully prepared. Furthermore, we found out that the SQDs display a dynamic photoluminescence properties and varied particle sizes as the reaction time increases, which is possibly realized via the etching-aggregation process. Morevoer, the fluorescence of SQDs-72 can be effectively quenched by CoOOH nanosheets and recovered upon addition of ascorbic acid (AA) by consuming CoOOH nanosheets through the redox reaction, leading to fluorescence recovery. Therefore, a fluorescence "off-on" nanosensor for the detection of AA with a limit of detection (LOD) of 0.85 µM was constructed.

One-step synthesis of nitrogen-doped multi-emission carbon dots and their fluorescent sensing in HClO and cellular imaging.

Tunable multicolor carbon dots (CDs) with a quantum yield reach up to 35% were generated directly from rhodamine and urea via one-step hydrothermal approach and purified through silica gel column chromatography. Transmission electron microscopy images reveal that the as-prepared CDs possess a small size distribution below 10 nm with bright blue, green, and yellow color emission, designated as b-CDs, g-CDs, and y-CDs, respectively. The in-depth investigations reveal that the multicolor emission CDs with different fraction displays fluorescence emission wavelength ranges from 398 nm (b-CDs), 525 nm (g-CDs), to 553 nm (y-CDs) which could be well modulated by controlling the amount of heteroatom nitrogen especially amino nitrogen onto their surface structures. Further experiments verify the important role of nitrogen content by using rhodamine solely or substituting urea with sulfur containing compounds as precursors to produce corresponding CDs since the performance is lower than that of urea incorporation. Theoretical calculation results also reveal that the increasing amount of amino nitrogen into their surface structures of b-CDs, g-CDs to y-CDs is responsible for reduced band gaps energy, which result in the redshifted wavelength. Benefiting from the excellent photoluminescence properties, wide pH variation range, high photo stability, and low toxicity, these CDs were employed for HClO sensing at 553 nm within the range 5 to 140 µM with a limit of detection (LOD) of 0.27 ± 0.025 µM (n = 3) and multicolor cellular imaging in HeLa cells. Tunable multicolor carbon dots (CDs) were generated directly from rhodamine and urea via one-step hydrothermal approach and purified through silica gel column chromatography. The as-prepared CDs exhibit bright blue, green, and yellow color emission which could be well modulated by controlling the increasing incorporation of heteroatom nitrogen especially amino nitrogen into their surface structures. These CDs were employed for HClO sensing and demonstrated to multicolor cellular imaging in HeLa cells.

Bionanosensor based on N-doped graphene quantum dots coupled with CoOOH nanosheets and their application for in vivo analysis of ascorbic acid.

Herein, we employ 3D nitrogen-doped porous graphene frameworks (NPG) as raw material to prepare emissive nitrogen doped graphene quantum dots (r-NGQDs) via chemical oxidation method. The as-prepared fluorescent r-NGQDs was integrated with CoOOH nanosheets to construct a sensing platform for in vivo ascorbic acid (AA) analysis. Initially, the fluorescence emission intensity of r-NGQDs was quenched by CoOOH nanosheets based on the inner filter effect (IFE). Then the quenched intensity of r-NGQDs and CoOOH nanosheets system was enlightened by addition of AA, since AA could consume CoOOH nanosheets through redox reaction, leading to the release of r-NGQDs and fluorescence restoration. Moreover, the restored fluorescence intensity of r-NGQDs is highly dependent on the concentration of AA which endows them as a quantitative analysis of AA with a limit of detection (LOD) reach up to1.85 µM (n = 3) in aqueous solution. Finally, the as constructed bionanosensor was further employed for in vivo analysis of AA in living rat brain microdialysate with basal value up to 9.4 ± 1.4 µM (n = 3).