Green-Emissive Copper Nanocluster with Aggregation-Enhanced Emission for Selective Detection of Al3.

Selective detection of Al3+ is of great significance both for the benefit of human health and environmental safety considerations. In this work, a sensitive and selective fluorescence assay for Al3+ was proposed based on the green-emissive Cu nanoclusters (Cu NCs). Different from the commonly reported works, the green emissive Cu NCs showed dual emission bands at 450 and 510 nm, attributed to the reaction product between polyvinyl pyrrolidone and ascorbic acid and the Cu core, respectively. Al3+ could induce the aggregation of Cu NCs by forming covalent bonds, which results in the enhancement of photoluminescence intensity. This enhancement phenomenon is rather selective to Al3+ , which endows the detection in real samples. These results provide new insights for the fluorescence mechanisms of metal NCs, which also provided a functional luminescent material for various applications, such as chemical sensing, bioimaging and photoelectric devices.

Long-Lived Afterglow from Elemental Sulfur Powder: Synergistic Effects of Impurity and Structure.

Elemental sulfur is not traditionally considered as an afterglow material, even though it can be endowed with fluorescence properties through processing it into nanodots. Herein, we discovered that elemental sulfur powder could emit room temperature phosphorescence (RTP) with a lifetime of 3.7 ms. A long-lived (>12 s) afterglow emission at 77 K could also be observed by the naked eye. Detailed investigations suggested that such a special phenomenon was attributed to impurity-related traps coupled with conduction and valence bands. After the sulfur is processed into nanodots, the rigid environment formed by the cross-linking of the surface ligands could stabilize the excited charges from quenching. This results in the promotion of RTP intensity and lifetime to achieve an emission lifetime of 200 ms. These results confirm the unique RTP of elemental sulfur powder, and also suggest the potential of sulfur-based materials as versatile components for the development of RTP materials.

Fluorescence ratiometric assay for discriminating GSH and Cys based on the composites of UiO-66-NH2 and Cu nanoclusters.

The discriminative detection of glutathione (GSH) from cysteine (Cys) remains a challenge because of their similarity in structure and chemical properties. This study reported a strategy for selective and sensitive detection of GSH based on the GSH-promoted blue fluorescence of UiO-66-NH2 and aggregation-enhanced emission (AEE) feature of orange emissive Cu nanoclusters (NCs). A relatively weak blue fluorescence of UiO-66-NH2 was converted to strong after reacting with GSH due to the rotation-restricted emission enhancement mechanism. In addition, the GSH-activated UiO-66-NH2 was further used as a template and reducing reagent for synthesizing orange-red AEE active Cu NCs composites (UiO-66-NH2@Cu NCs). A ratiometric fluorescence response was observed after forming UiO-66-NH2@Cu NCs, helping discriminate GSH over Cys. In addition, UiO-66-NH2@Cu NCs were further utilized for the detection of GSH in clinical samples. The present findings provide an efficient strategy to discriminate GSH over Cys and open a new door for utilizing and functionalizing metal-organic frameworks (MOFs) for various applications.

Composite Films of CsPbBr3 Perovskite Nanocrystals in a Hydrophobic Fluoropolymer for Temperature Imaging in Digital Microfluidics.

A composite film material that combines CsPbBr3 perovskite nanocrystals with a Hyflon AD 60 fluoropolymer was developed and utilized for high-resolution optical temperature imaging. It exhibited bright luminescence and, most importantly, long-term stability in an aqueous medium. CsPbBr3 nanocrystal-Hyflon films immersed in aqueous solutions showed stable luminescence over at least 4 months and exhibited a fully reversible pronounced temperature sensitivity of 1.2% K-1 between 20 and 80 °C. They were incorporated into a digital microfluidic (electrowetting on dielectric) platform and were used for spatially resolved temperature measurements during droplet movements. Thermal mapping with a CsPbBr3 nanocrystal-Hyflon sensing layer in a room temperature environment (22.0 °C) revealed an increase in local temperatures of up to 40.2 °C upon voltage-driven droplet manipulations in a digital microfluidic system, corresponding to a local temperature change of up to 18.2 °C.

Comparative study on stabilizing ability of food protein, non-ionic surfactant and anionic surfactant on BCS type II drug carvedilol loaded nanosuspension: Physicochemical and pharmacokinetic investigation.

Carvedilol (CAR) in its pure state has low aqueous solubility and extremely poor bioavailability which largely limit its clinical application. The aim of the study is to improve the dissolution rate and the bioavailability of CAR via preparing nanosuspensions with different stabilizers. Antisolvent precipitation-ultrasonication technique was used here. Attempts have been made to use food protein- Whey protein isolate (WPI) as a stabilizer in CAR loaded nanosuspension and also to compare its stabilizing potential with conventional nanosuspension stabilizers such as non-ionic linear copolymer-poloxamer 188 (PLX188) and anionic surfactant-sodium dodecyl sulfate (SDS). Optimized nanosuspensions showed narrow size distribution with particle size ranging from 275 to 640nm. Amorphous state of CAR nanocrystals which also improved the solubility by 16-, 25-, 55-fold accordingly was confirmed by powder X-ray diffraction (PXRD) and differential scanning calorimetry (DSC). From scanning electron microscopy (SEM), flaky shape of PLX188 and SDS nanosuspensions could be revealed but WPI nanosuspension was sphere-shaped. Up to 70% dissolution of loaded drug was observed within 15min in phosphate buffer (pH6.8). A pharmacokinetic study in rats indicated that both Cmax and AUC0-36 values of nanosuspensions were estimated to be 2-fold higher than those of reference, suggesting a significant increase in CAR bioavailability.