Notes

Esculetin brings about apoptosis inside man abdominal cancer malignancy cellular material by way of a cyclophilin D-mediated mitochondrial permeability move pore related to ROS.
This work provides an efficient strategy for designing high-performance environmental catalysts for VOCs abatement.The hybridization of enzymes and inorganics in controlled manner is challenging, however, critical for the development of chemo-enzymatic cascade catalyst with high efficiency and selectivity. Here, proteins and metal oxide clusters can be facilely co-assembled on the surface of colloid of poly(4-vinylpyridine) (P4VP) via hydrogen bonding, due to their enriched surface hydrogen bonding donors. The co-assembly method can be generally applied for preparing chemo-enzymatic catalyst within the selected database of various proteins and metal oxide clusters while the assembly units retain their structures and activities. Typically, a 2.5 nm metal oxide cluster Mo72Fe30, with peroxidase-like activity, are complexed with glucose oxidase (GOX) on P4VP for the catalysis against the oxidization of o-dianisidine (ODA) with the existence of glucose. Due to the synergistic effects of chemical and enzymatic catalysis, the co-assemblies show even higher ODA oxidation activity compared to GOX/catalase bi-enzymatic system, confirming the effectiveness of the co-assembly protocol for cascade catalysis and enabling its applications in rapid glucose detection and biomass conversion.Hierarchical porous iron and nitrogen co-doped carbon (Fe-N/C) materials have been considered as an appealing non-noble metal-based catalyst in oxygen reduction reactions (ORR). selleck chemicals However, the conductivity loss caused by the scattering of electrons on pores and defects markedly limits their catalytic activity, which attracted seldom attention in this area. Herein, a novel crystalline carbon modified hierarchical porous Fe-N/C electrocatalyst with enhanced electronic conductivity is designed and prepared via a two-step calcination-catalysis process. The resistivity of hierarchical porous Fe-N/C is decreased from 2.123 Ω cm to 0.479 Ω cm after crystalline carbon introduction. The electrocatalyst annealed at 800 °C (Fe-N/C-800) exhibits a superior activity with the half-wave potential (E1/2) of 0.89 V, which outperforms the commercial carbon-supported platinum (Pt/C) catalyst (0.85 V). The strategy of crystalline carbon modification provides a fresh approach to improve the electronic conductivity of porous carbon-based materials.Supramolecular chemistry has garnered important interest in recent years toward improving therapeutic efficacy via drug delivery approaches. Although self-assemblies have been deeply investigated, the design of novel drugs leveraging supramolecular chemistry is less known. In this contribution, we show that a Low Molecular Weight Gel (LMWG) can elicit cancer cell apoptosis. This biological effect results from the unique supramolecular properties of a bolaamphiphile-based gelator, which allow for strong interaction with the lipid membrane. This novel supramolecular-drug paradigm opens up new possibilities for therapeutic applications targeting membrane lipids.Si-doped graphene nanosheets (SiGNS) have been successfully constructed via high temperature annealing of graphene oxide and tetraethoxysilane mixture in a sealed glass ampoule. The Si atoms doped into graphene's carbon network mainly existed as C3-Si-O and C2-Si-O2 configurations. The as-prepared SiGNS exhibited excellent electrochemical detection ability to nitroaromatic compounds in 0.1 M phosphoric acid buffer solution (PBS, pH = 8.0) via an electrochemical catalytic process. Five nitroaromatic compounds, including nitrobenzene, 2-nitrotoluene, 4-nitrotoluene, 2, 4-dinitrotoluene and 2, 4, 6-trinitrotoluene, were taken as the analyte to demonstrate the electrochemical catalytic ability of SiGNS. Density functional theory (DFT) calculation was carried out to explore the electrochemical catalytic mechanism of SiGNS. A hydrogen bond mediated electrochemical catalytic mechanism was proposed. Both the excellent electrical conductivity and the rich surface hydroxyl groups enhanced the electrochemical detection ability of SiGNS to nitroaromatic compounds. Si atoms in SiGNS played a key role for the excellent electrochemical detection ability of SiGNS due to most of the surface hydroxyl groups anchored on the Si atoms.Magnesium (Mg) alloy has wide potential applications due to its unique properties, but is apt to corrosion. Recently, superhydrophobic coatings are receiving great interest for corrosion protection of metals but suffer from short lifespan. Here, we report a strategy for long-term corrosion protection of Mg alloy by designing two-layer self-healing superamphiphobic coatings based on shape memory polymers (SMP) and attapulgite. The superamphiphobic coatings are composed of a bottom SMP coating containing a corrosion inhibitor (1, 2, 3-benzotriazole, BTA) and ceresine wax microparticles and a top superamphiphobic attapulgite coating. The two-layer self-healing coatings have excellent superamphiphobicity and initial anti-corrosion performance. The Mg alloy with the coatings can withstand immersion in 3.5 wt% NaCl solution for 80 days and neutral salt spray with 5 wt% NaCl for 54 days. Furthermore, the coatings show excellent self-healing capability towards various physical damages, such as 10 scratching/self-healing cycles at the same position, hexagonal star scratching and grid scratching. Moreover, the physically damaged coatings exhibit self-healing behavior of the microstructure and superhydrophobicity, driven by the shape memory effect of the bottom SMP layer. Thus, the self-healed coatings can still withstand 60 days of 3.5 wt% NaCl solution immersion and 30 days of 5 wt% NaCl salt spray. This study paves the way for applying super anti-wetting coatings for long-term corrosion protection of metals.The achievement of superlow friction is vital for the engineering application of hydrogenated diamond-like carbon (H-DLC), but it always fails in an oxygen atmosphere. In this paper, robust superlow friction was achieved by MoS2 flakes and H-DLC composite films in a large range of atmospheres, especially in oxygen. The results showed that the composite structure could only retain the superlow friction for an short time in pure argon, nitrogen and carbon dioxide; surprisingly, oxygen was capable of remaining in the near frictionless state with a friction coefficient as low as 0.002, and the duration was prolonged significantly by the introduction of oxygen in those other gases. The stability of the transfer film that induced the near frictionless state was also studied comprehensively. The experimental results and first-principle calculations demonstrated that oxygen could bond with the molybdenum, sulfur and aluminum atoms to form bridge bonds that fixed the MoS2 transfer film on the counterface; this led to the formation of incommensurate contact between the MoS2 tribo-layer and H-DLC film, which enabled robust superlow friction. This finding supports a simple strategy to resolve the challenge of superlubric failure and opens a path for the actual application of H-DLC in oxygen-rich environments.A novel and facile strategy is developed to tune parallel manganese dioxide (MnO2) to hollow parallel hydroxyl oxidize iron (FeOOH) replicas, which can exactly keep its original morphology. The key factors leading to the morphology-preserved transformation are the low-temperature and dropwise strategy via a serial of controlled experiments. Benefiting from the characteristics of parallel and hollow structures, the FeOOH replica delivers remarkable specific capacitance of 186.8F g-1 at 0.5 A g-1. The electrochemical performances delivered by the asymmetric supercapacitor (parallel MnO2//hollow parallel FeOOH) are much superior to those where conventional activated graphene or FeOOH nanoneedles are used as negative electrode materials. This can be attributed to the advantages of parallel nanostructure and high electrochemical matching effect of positive and negative electrode materials. The energy density is recorded up to 46.8 Wh kg-1 at the power density of 0.5 kW kg-1, while it still remains 20.7 Wh kg-1 with the maximum power density of 10 kW kg-1. Furthermore, this strategy shows great universality and can be broadened to almost all MnO2 related researches to synthesize ideal negative electrode materials with high structural and electrochemical matching effect, thus further enhances the electrochemical performances of as-prepared asymmetric supercapacitor devices.
It has been recently shown that, in our organism, the secretions of Ca
, Mg
and phosphate ions lead to the precipitation of amorphous magnesium-calcium phosphate nanoparticles (AMCPs) in the small intestine, where the glycoprotein mucin is one of the most abundant proteins, being the main component of the mucus hydrogel layer covering gut epithelium. Since AMCPs precipitate in vivo in a mucin-rich environment, we aim at studying the effect of this glycoprotein on the formation and features of endogenous-like AMCPs.

AMCPs were synthesized from aqueous solution in the presence of different concentrations of mucin, and the obtained particles were characterised in terms of crystallinity, composition and morphology. Solid State NMR investigation was also performed in order to assess the interplay between mucin and AMCPs at a sub-nanometric level.

Results show that AMCPs form in the presence of mucin and the glycoprotein is efficiently incorporated in the amorphous particles. NMR indicates the existence ofeen AMCPs and mucin described in the present work might be relevant to the immune system, suggesting a novel type of scenario which could be investigated by combining physico-chemical and biomedical approaches.Epoxy resin (EP) is a polymer that is widely used in different aspects of life, but its flammability property limits its fields of applications. Most flame retardants at present cannot be applied practically in scale due to their toxicity, incompatibility in polymers, degraded mechanical property or high cost of raw materials and comprehensive preparation process. Layered double hydroxides intercalated by gluconic acid anion (GLDHs) may serve as a new approach. GLDHs with Mg/Al ratio of 3/1 and 2/1 were first coprecipitated with low-cost green reactants, MgCl2·6H2O, AlCl3·6H2O, NaOH and sodium gluconate. Their structures were confirmed by X-ray diffractions (XRD), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FTIR) and elemental analysis; their thermal properties were analyzed by thermo gravimetric analysis (TGA). Composites containing 40 wt.% GLDHs were easily manufactured with normal magnetic stirring without any filler precipitation. The combustion properties of the composites filled with 40 wt.% GLDHs2 are as follows the limit oxygen index (LOI) could rise to 29.8% from 25.2% of pristine EP; UL-94 can reach V-1 level with total burning time of only 12.1 s without dropping; compared to pristine EP, the heat release rate peak (PHRR) could drop to 30% with heavy decrease in the smoke production rate and CO production rate. Dynamic mechanical thermal analysis (DMA) tests showed that the addition of 40 wt.% GLDHs had little impact on the glass transition temperature of the composites and could slightly improve their rigidity and toughness. Tensile strength of the composites filled with 40 wt.% GLDHs2 was almost close to 88% of the tensile strength of pristine EP. Above all, GLDHs with good compatibility in polymers can serve as a promising environmental friendly and low-cost flame retardant for EP and other heterochain polymers.
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