Simultaneous Imaging of Endogenous Survivin mRNA and On‐Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher

The design of multifunctional drug delivery systems capable of simultaneous target detection, imaging, and therapeutics in live mammalian cells is critical for biomedical research. In this study, by using mesoporous silica nanoparticles (MSNs) chemically modified with a small‐molecule dark quencher, followed by sequential drug encapsulation, MSN capping with a dye‐labeled antisense oligonucleotide, and bioorthogonal surface modification with cell‐penetrating poly(disulfide)s, the authors have successfully developed the first mesoporous silica nanoquencher (qMSN), characterized by high drug‐loading and endocytosis‐independent cell uptake, which is able to quantitatively image endogenous survivin mRNA and release the loaded drug in a manner that depends on the survivin expression level in tumor cells. The authors further show that this novel drug delivery system may be used to minimize potential cytotoxicity encountered by many existing small‐molecule drugs in cancer therapy.     

Rational Design and Synthesis of Extremely Efficient Macroporous CoSe2–CNT Composite Microspheres for Hydrogen Evolution Reaction

Uniquely structured CoSe₂–carbon nanotube (CNT) composite microspheres with optimized morphology for the hydrogen‐evolution reaction (HER) are prepared by spray pyrolysis and subsequent selenization. The ultrafine CoSe₂ nanocrystals uniformly decorate the entire macroporous CNT backbone in CoSe₂–CNT composite microspheres. The macroporous CNT backbone strongly improves the electrocatalytic activity of CoSe₂ by improving the electrical conductivity and minimizing the growth of CoSe₂ nanocrystals during the synthesis process. In addition, the macroporous structure resulting from the CNT backbone improves the electrocatalytic activity of the CoSe₂–CNT microspheres by increasing the removal rate of generated H₂ and minimizing the polarization of the electrode during HER. The CoSe₂–CNT composite microspheres demonstrate excellent catalytic activity for HER in an acidic medium (10 mA cm^?2 at an overpotential of ≈174 mV). The bare CoSe₂ powders exhibit moderate HER activity, with an overpotential of 226 mV at 10 mA cm^?2. The Tafel slopes for the CoSe₂–CNT composite and bare CoSe₂ powders are 37.8 and 58.9 mV dec^?1, respectively. The CoSe₂–CNT composite microspheres have a slightly larger Tafel slope than that of commercial carbon‐supported platinum nanoparticles, which is 30.2 mV dec^–1.     

Carbon Nanodot‐Sensitized Modulation of Alzheimer's β‐Amyloid Self‐Assembly,Disassembly, and Toxicity

The self‐assembly of amyloidogenic peptides into β‐sheet‐rich aggregates is a general feature of many neurodegenerative diseases, including Alzheimer's disease, which signifies the need for the effective attenuation of amyloid aggregation toward alleviating amyloid‐associated neurotoxicity. This study reports that photoluminescent carbon nanodots (CDs) can effectively suppress Alzheimer's β‐amyloid (Aβ) self‐assembly and function as a β‐sheet breaker disintegrating preformed Aβ aggregates. This study synthesizes CDs using ammonium citrate through one‐pot hydrothermal treatment and passivates their surface with branched polyethylenimine (bPEI). The bPEI‐coated CDs (bPEI@CDs) exhibit hydrophilic and cationic surface characteristics, which interact with the negatively charged residues of Aβ peptides, suppressing the aggregation of Aβ peptides. Under light illumination, bPEI@CDs display a more pronounced effect on Aβ aggregation and on the dissociation of β‐sheet‐rich assemblies through the generation of reactive oxygen species from photoactivated bPEI@CDs. The light‐triggered attenuation effect of Aβ aggregation using a series of experiments, including photochemical and microscopic analysis, is verified. Furthermore, the cell viability test confirms the ability of photoactivated bPEI@CDs for the suppression of Aβ‐mediated cytotoxicity, indicating bPEI@CDs' potency as an effective anti‐Aβ neurotoxin agent.     

Synthesis of Co/SiO2 hybrid nanocatalyst via twisted Co3Si2O5(OH)4 nanosheets for high-temperature Fischer-Tropsch reaction

A cobalt-silica hybrid nanocatalyst bearing small cobalt particles of diameter ～5 nm was prepared through a hydrothermal reaction and hydrogen reduction.The resulting material showed very high CO conversion (＞82％) and high hydrocarbon productivity (～1.0 gHc·g-1cat,·h-11) with high activity (～8.5 x 10-5 molco·g-1Co·S-1) in the Fischer-Tropsch synthesis reaction.     

Numerical simulation of 2D granular flow entrainment using DEM

To understand the entrainment process in granular flow, numerical experiments have been conducted using a Discrete Element Method model. A flow channel of 8 m long with \(15^\circ \) slope is setup with monitoring points located in an erodible bed. Particles, ranging from 3 to 4 mm in diameters, are used in the simulations. In the simulations, translational, rotational and average velocities, total volume, shear stresses are calculated in the measurement circles. The sizes of the measurement circles have been varied to see their effects on the results. It is found the minimum size of the measurement circles should include 20–30 particles. An new analytical model has been developed to calculate entrainment in granular flow. Results of the numerical experiment are compared with analytical model. Shear stresses at the interface between flowing particles in motion and the immobile particles in the channel bed, change of depth of erosion and entrainment rate are used to verify the analytical model. It is found that the calculated shear stresses in the PFC model agree well with the shear stresses calculated using Mohr–Coulomb frictional relationship in the analytical model. The calculated depth of erosion using the new analytical model is also compared with that from dynamic and static entrainment model. The results indicates that the analytical model is able to capture the mechanism of erosion and it can be used in granular flow analysis.     

Rational design and synthesis of hierarchically structured SnO<Subscript>2</Subscript> microspheres assembled from hollow porous nanoplates as superior anode materials for lithium-ion batteries

Herein, hierarchically structured SnO₂ microspheres are designed and synthesized as an efficient anode material for lithium-ion batteries using hollow SnO₂ nanoplates. Three-dimensionally ordered macroporous (3-DOM) SnO _x -C microspheres synthesized by spray pyrolysis are transformed into hierarchically structured SnO₂ microspheres by a two-step post-treatment process. Sulfidation produces hierarchically structured SnS-SnS₂-C microspheres comprising tin sulfide nanoplate and carbon building blocks. A subsequent oxidation process produces SnO₂ microspheres from hollow SnO₂ nanoplate building blocks, which are formed by Kirkendall diffusion. The discharge capacity of the hierarchically structured SnO₂ microspheres at a current density of 5 A·g^?1 for the 600^th cycle is 404 mA·h·g^?1. The hierarchically structured SnO₂ microspheres have reversible discharge capacities of 609 and 158 mA·h·g^?1 at current densities of 0.5 and 30 A·g^?1, respectively. The ultrafine nanosheets contain empty voids that allow excellent lithium-ion storage performance, even at high current densities.

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