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Purple corn (Zea mays L.), utilized as a natural pigment in food production and processing, has been used to treat obesity, cystitis, and urinary tract infections. However, no reports of its use for benign prostatic hyperplasia (BPH) exist. Purple corn extract (PCE) contains anthocyanins, particularly cyanidin-3-O-glucoside, which have various pharmacological characteristics. Therefore, this study sought to elucidate the ameliorative effect of PCE on BPH in dihydrotestosterone (DHT)-stimulated WPMY-1 cells and testosterone propionate (TP)-induced rats. Expression levels of the upregulated androgen receptor (AR) and its related genes in DHT-stimulated WPMY-1 cells were reduced by PCE, and proapoptotic gene expression increased by modulating the phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) signaling cascade. PCE reduced the weight of the enlarged prostate by inhibiting the androgen/AR signaling-related markers. Histological variations in the prostate epithelium caused by TP injection were restored by PCE. Thus, PCE alleviates BPH by modulating prostate cell proliferation and apoptosis.Herein, we test the hypothesis that neutral, heavy-atom stibine donors can increase the extent of spin-orbit coupling on light, 3d transition metal. To this end, we developed a novel synthetic route toward coordinating a paramagnetic 3d metal ion─cobalt(II)─with neutral stibine ligands. Such complexes have not been reported in the literature due to the weak σ donor strength of stibines and the hard-soft mismatch between a 3d metal and a 5p ligand─which herein has been overcome using alkylated Sb donors. Magnetometry of [(SbiPr2Ph)2Co(I)2] (1) reveals that the stibine complex 1 exhibits a higher magnitude D value (D = |24.96| cm-1) than the spectroscopically derived value for the corresponding phosphine complex 3 (D = -13.13 cm-1), indicative of large zero-field splitting. CASSCF/NEVPT2 calculations corroborate the experimental D values for 1 and 3, predicting D = -31.9 and -8.9 cm-1, respectively. A re-examination of magnetic parameters across the entire series [(ER3)2Co(X)2] (E = P → Sb; X = Cl → I) reveals that (i) increasingly heavy pnictogens lead to an increased X-Co-X bond angle, which is correlated with larger magnitude D values, and (ii) for a given X-Co-X bond angle, the D value is always higher in the presence of a heavy pnictogen as compared with a heavy halide. Ab initio ligand field theory calculations for 1 (stibine complex) and 3 (phosphine complex) reveal no substantial differences in spin-orbit coupling (ζ = 479.2, 480.2 cm-1) or Racah parameter (B = 947.5, 943.9 cm-1), an indicator of covalency. Thus, some "heavy atom effect" on the D value beyond geometric perturbation is operative, but its precise mechanism(s) of action remains obscure.A layered oxytelluride, Ba2ZnO2Ag2Te2, which consists of alternating stacks of ZnO2 and Ag2Te2 layers with Ba ions in between, has been synthesized via high-pressure reaction. At ambient temperature, it contains discrete [ZnO2]2- linear units similar to Ba2ZnO2Ag2Se2 (Cmca), meaning that the unusual linear coordination around zinc center is stable even when a greater tensile strain is applied by the sandwiched Ag2Te2 layers in addition to barium ions. Upon heating, this compound undergoes an order-disorder phase transition from orthorhombic (Cmca) to tetragonal (I4/mmm) system at 350 K, transforming the ZnO2 lattice in linear coordination into a lattice with disordered oxide ions, suggesting the presence of cis/trans coordination coexistence as well as correlated disorder.Transition metal dichalcogenides (TMDs) possess spin-valley locking and spin-split K/K' valleys, which have led to many fascinating physical phenomena. However, the electronic structure of TMDs also exhibits other conduction band minima with similar properties, the Q/Q' valleys. The intervalley K-Q scattering enables interesting physical phenomena, including multivalley superconductivity, but those effects are typically hindered in monolayer TMDs due to the large K-Q energy difference (ΔEKQ). To unlock elusive multivalley phenomena in monolayer TMDs, it is desirable to reduce ΔEKQ, while being able to sensitively probe the valley shifts and the multivalley scattering processes. Here, we use high pressure to tune the electronic properties of monolayer MoS2 and WSe2 and probe K-Q crossing and multivalley scattering via double-resonance Raman (DRR) scattering. In both systems, we observed a pressure-induced enhancement of the double-resonance LA and 2LA Raman bands, which can be attributed to a band gap opening and ΔEKQ decrease. First-principles calculations and photoluminescence measurements corroborate this scenario. In our analysis, we also addressed the multivalley nature of the DRR bands for WSe2. Our work establishes the DRR 2LA and LA bands as sensitive probes of strain-induced modifications to the electronic structure of TMDs. Conversely, their intensity could potentially be used to monitor the presence of compressive or tensile strain in TMDs. Furthermore, the ability to probe K-K' and K-Q scattering as a function of strain shall advance our understanding of different multivalley phenomena in TMDs such as superconductivity, valley coherence, and valley transport.Tungsten disulfide (WS2) is well known to have great potential as an electrocatalyst, but the practical application is hampered by its intrinsic inert plane and semiconductor properties. In this work, owing to a Co-based zeolite imidazole framework (ZIF-67) that effectively inhibited WS2 growth, few-layered WS2 was confined to the surface of Co, N-doped carbon polyhedron (WS2@Co9S8), with more marginal active sites and higher conductivity, which promoted efficient oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). For the first time, WS2@Co9S8 was prepared by mixing in one pot of a liquid phase and calcination, and WS2 realized uniform distribution on the polyhedron surface by electrostatic adsorption in the liquid phase. The obtained hybrid catalyst exhibited excellent OER and HER catalytic activity, and the OER potential was only 15 mV at 10 mA cm-2 higher than that of noble metal oxide (RuO2). The improvement of catalytic activity can be attributed to the enhanced exposure of sulfur edge sites by WS2, the unique synergistic effect between WS2 and Co9S8 on the metal-organic framework (MOF) surface, and the effective shortening of the diffusion path by the hollow multi-channel structure. Therefore, the robust catalyst (WS2@Co9S8) prepared by a simple and efficient synthesis method in this work will serve as a highly promising bifunctional catalyst for OER and HER.Size control of supported Pd-based intermetallic nanoparticles (i-NPs) remains a major challenge because the required high-temperature annealing for atomic diffusion and ordering easily causes metal sintering. Here, we described a pentacoordinate Al3+ site (Al3+penta) anchoring approach for the preparation of Pd-based i-NPs with controlled size, which takes advantage of the strong chemical interaction between Al3+penta sites and Pd-based i-NPs to realize size control. We synthesized six types of Pd-based i-NPs, and four of them can remain an average particle size of less then 6 nm. Furthermore, one of our prepared Pd-based i-NPs (that is, Pd3Pb) demonstrated outstanding performance in catalyzing the semihydrogenation of phenylacetylene.Intracellular pH is an important regulator of cell function, and its subtle changes may greatly affect cell activities and cause diseases. find more Reliable imaging of intracellular pH remains a huge challenge. Dual-emitting Mn2+-doped quantum dots (QDs) can be directly used as a ratiometric fluorescent probe without further modification, but they displayed low performance in terms of photoluminescence, stability, and intensity ratio regulation. Here, we report intrinsic dual-emitting CdZnSe/MnZnS QDs with high photoluminescence efficiency, good stability, and biocompatibility. The emission intensity ratio was selectively regulated by Mn2+ doping. Because of aggregation-induced quenching of QDs, the exciton emission of CdZnSe/MnZnS QDs (471 nm) was sensitive to pH, while the Mn2+-doped emission (606 nm) was passive to pH, which was probably due to little self-quenching in Mn2+-doped emission caused by weak Mn-Mn coupling interaction. Dual-emitting CdZnSe/MnZnS QDs exhibited excellent pH-responsiveness in the range of pH 4.0 to 12.0 and were used for pH imaging in live HeLa cells. When the pH value of HeLa cells changed from 5.0 to 9.0, the emission changed from red to blue. Furthermore, these dual-emitting CdZnSe/MnZnS QDs can provide a versatile platform for biosensors and biological imaging.The mainstream synthesis method for MXene is using aqueous fluorine-containing acidic solutions to eliminate the A-element layers from their MAX phases. However, this strategy is environmentally hazardous and impairs the material performance (e.g., supercapacitor and Li-S batteries) owing to the presence of -F terminations. Herein, we exploit a low-temperature "soft chemistry" approach based on photo-Fenton (P.F.) reaction for the fabrication of F-free Ti3C2 (Ff-Ti3C2) with high purity of 95%. It is confirmed that the continuous generation of highly reactive oxygen species (HO• and O2•- radicals) during the P.F. reaction weakens the metallic Ti-Al bonds in the MAX phase and promotes the formation of high concentration OH- anions, which are conducive to the sequential topochemical deintercalation of Al layers. Moreover, the strengthened charge accumulation on the Ff-Ti3C2 surface creates rich electron "reservoirs" for actuating the Li-S chemistry, which not only strengthens the host-guest interactions but also propels the kinetics of the polysulfide conversion. Taking advantage of the superior mechanical robustness, better electrolyte wettability, and improved electrocatalytic activity, the resultant Ff-Ti3C2 can be used as an ideal sulfur host and Li-S chemistry mediator for advanced flexible Li-S batteries.Most cancer-related deaths are due to metastasis or recurrence. Therefore, the ultimate goal of cancer therapy will be to treat metastatic and recurrent cancers. Combination therapy for cancer will be one of trial for effective treating metastasis and recurrence. In this study, Escherichia coli-mimetic nanomaterials are synthesized using Escherichia coli membrane proteins, adhesion proteins, and gold nanorods, which are named E. coli mimetic AuNRs (ECA), for combination therapy against cancer and its recurrence. ECA treatment with 808 nm laser irradiation eliminates CT-26 or 4T1 tumors via a photothermal effect. ECA with laser irradiation induces activation of immune cells in the tumor-draining lymph nodes. The mice cured from CT-26 or 4T1 tumor by ECA are rechallenged with those cancer in the lung metastatic form, and the results showed that ECA treatment for the first CT-26 or 4T1 tumor challenge prevents cancer infiltration to the lung in the second challenge. This preventive effect of ECA against tumor growth in the second challenge is aided by cancer antigen-specific T cell immunity. Overall, these findings show that ECA is a nanomaterial with dual functions as a photothermal therapy for treating primary cancers and as immunotherapy for preventing recurrence and metastasis.