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Lateral flow immunoassay (LFIA) technology serves a significant role as a simple and rapid biosensor in the detection of influenza viruses. The focus of this study is the development of a rapid and convenient screening method for influenza B virus (IBV) proteins using a fluorescence lateral flow biosensor based on Ag-doped ZnIn2S4 quantum dots (Ag: ZIS QDs) as signal reporters. These Ag: ZIS QDs-emitting orange fluorescence are loaded onto dendritic mesoporous silica nanoparticles (DMSNs) and are further coated with a layer of silica shell to form a core–shell structured composite nanomaterial (SiO2 @ Ag: ZIS QDs @ DMSNs). The orange fluorescence effectively eliminates the interference of blue background fluorescence, significantly enhancing the detection sensitivity. This technology demonstrates outstanding performance in the immediate detection of IBV, with a minimum detection limit of 1 ng/mL, compared to the traditional colloidal gold strip with a detection limit of 6 ng/mL. Furthermore, both intra-assay and inter-assay coefficients of variation (CV) are less than 9%. This method holds promise for wide application in early diagnosis, epidemiological investigation, and epidemic surveillance of IBV. [ABSTRACT FROM AUTHOR]

Limited light absorption and rapid photo-generated carriers' recombination pose significant challenges to the practical applications of photocatalysts. In this study, we employed an efficient approach by combining the slow-photon effect with Z-scheme charge transfer to enhance the photo-degradation performance of antibiotics. Specifically, we incorporated 0D ZnIn2S4 quantum dots (QDs) into a 3D hierarchical inverse opal (IO) TiO2 structure through a facile one-step process. This combination enhanced the visible light absorption and provided abundant active surfaces for efficient photo-degradation. Moreover, the ZnIn2S4 QDs formed an artificial Z-scheme system with IO-TiO2, facilitating the separation and migration of charge carriers. To achieve a better band alignment with IO-TiO2, we doped Ag into the ZnIn2S4 QDs (Ag: ZIS QDs) to adjust their energy levels. Through an investigation of the different Ag contents in the ZnIn2S4 QDs, we found that the optimal photo-degradation performance was achieved with Ag (2.0): ZIS QDs/IO-TiO2, exhibiting degradation rates 19.5 and 14.8 times higher than those of ZnIn2S4 QDs and IO-TiO2, respectively. This study provides significant insights for elevating the photocatalytic capabilities of IO-TiO2 and broadening its prospective applications. [ABSTRACT FROM AUTHOR]

Lower light absorption and faster carrier recombination are significant challenges in photocatalysis. This study introduces a novel approach to address these challenges by anchoring cadmium sulfide quantum dots (CdS QDs) on inverse opal (IO)-TiO2, which increases light absorption and promotes carriers' separation by coupling slow-photon effect with Z-scheme charge transfer. Specifically, the IO-TiO2 was created by etching a polystyrene opal template, which resulted in a periodic structure that enhances light absorption by reflecting light in the stop band. The size of CdS quantum dots (QDs) was regulated to achieve appropriate alignment of energy bands between CdS QDs and IO-TiO2, promoting carrier transfer through alterations in charge transfer modes and resulting in synergistic-amplified photocatalysis. Theoretical simulations and electrochemical investigations demonstrated the coexistence of slow-photon effects and Z-scheme transfer. The system's photodegradation performance was tested using rhodamine B as a model. This novel hierarchical structure of the Z-scheme heterojunction exhibits degradability 7.82 and 4.34 times greater than pristine CdS QDs and IO-TiO2, respectively. This study serves as a source of inspiration for enhancing the photocatalytic capabilities of IO-TiO2 and broadening its scope of potential applications. [ABSTRACT FROM AUTHOR]

New tools for single‐cell interrogation enable deeper understanding of cellular heterogeneity and associated cellular behaviors and functions. Information of RNA expression in single cell could contribute to our knowledge of the genetic regulatory circuits and molecular mechanism of disease development. Although significant progresses have been made for intracellular RNA analysis, existing methods have a trade‐off between operational complexity and practical feasibility. We address this challenge by combining the ionic current rectification property of nanopipette reactor with duplex‐specific nuclease‐assisted hybridization chain reaction for signal amplification to realize a simple and practical intracellular nanosensor with minimal invasiveness, which enables single‐cell collection and electrochemical detection of intracellular RNA with cell‐context preservation. Systematic studies on differentiation of oncogenic miR‐10b expression levels in non‐malignant breast cells, metastatic breast cancer cells as well as non‐metastatic breast cancer cells were then realized by this nanotool accompanied by assessment of different drugs effects. This work has unveiled the ability of electrochemistry to probe intracellular RNA and opened new opportunities to study the gene expression and heterogeneous complexity under physiological conditions down to single‐cell level. [ABSTRACT FROM AUTHOR]

New tools for single‐cell interrogation enable deeper understanding of cellular heterogeneity and associated cellular behaviors and functions. Information of RNA expression in single cell could contribute to our knowledge of the genetic regulatory circuits and molecular mechanism of disease development. Although significant progresses have been made for intracellular RNA analysis, existing methods have a trade‐off between operational complexity and practical feasibility. We address this challenge by combining the ionic current rectification property of nanopipette reactor with duplex‐specific nuclease‐assisted hybridization chain reaction for signal amplification to realize a simple and practical intracellular nanosensor with minimal invasiveness, which enables single‐cell collection and electrochemical detection of intracellular RNA with cell‐context preservation. Systematic studies on differentiation of oncogenic miR‐10b expression levels in non‐malignant breast cells, metastatic breast cancer cells as well as non‐metastatic breast cancer cells were then realized by this nanotool accompanied by assessment of different drugs effects. This work has unveiled the ability of electrochemistry to probe intracellular RNA and opened new opportunities to study the gene expression and heterogeneous complexity under physiological conditions down to single‐cell level. [ABSTRACT FROM AUTHOR]

This report outlines the first exploration of graphene oxide (GO) itself as a light harvesting material with an innovative in situ chemical redox and functionalization (CRF) strategy for versatile and high-throughput cathodic photoelectrochemical (PEC) bioanalysis. [ABSTRACT FROM AUTHOR]

Electrochemistry, Hybridization Chain Reaction, Nanopipette, RNA, Single Cell Analysis Keywords: Electrochemistry; Hybridization Chain Reaction; Nanopipette; RNA; Single Cell Analysis EN Electrochemistry Hybridization Chain Reaction Nanopipette RNA Single Cell Analysis 1 1 1 06/05/21 20210607 NES 210607 B Einzelzellanalyse b Eine auf einer duplexspezifischen Nuklease basierende Nanopipette wurde im Forschungsartikel auf S. 13352 von Wei-Wei Zhao, Jing-Juan Xu et al. hergestellt und zur Analyse der wirkstoffinduzierten Schwankung des miR-10b-Spiegels auf Einzelzellniveau verwendet. [Extracted from the article]

Electrochemistry, Hybridization Chain Reaction, Nanopipette, RNA, Single Cell Analysis Keywords: Electrochemistry; Hybridization Chain Reaction; Nanopipette; RNA; Single Cell Analysis EN Electrochemistry Hybridization Chain Reaction Nanopipette RNA Single Cell Analysis 1 1 1 06/05/21 20210607 NES 210607 B Single-Cell Analysis b A duplex-specific nuclease-assisted nanopipette was fabricated in the Research Article on page 13244 by Wei-Wei Zhao, Jing-Juan Xu et al. for tracking the drug-induced variation of miR-10b levels at single-cell level. [Extracted from the article]