• Evans Parker posted an update 6 months, 1 week ago

    The endometrial receptivity and pregnancy outcome significantly improved after repeated MenSCs-sEVs transplantations. In addition, all rats in the MenSCs-sEVs group had no hematological or biochemical abnormalities. Three-dimensional fluorescence imaging suggested that MenSCs tended to migrate through the bloodstream, whereas MenSCs-sEVs had a better localized therapeutic effect. Moreover, MenSCs and MenSCs-sEVs inhibited the TGFβ1/SMAD3 pathway in the IUA endometrium, while promoting the phosphorylation of SMAD1/5/8 and ERK 1/2 and upregulating the expression of BMP7. Thus, MenSCs-sEVs safely and effectively enhanced endometrial restoration, suggesting a promising non-cellular therapy for endometrial regeneration and a key role in MenSC-mediated IUA treatment.Redox processes of oxide materials are fundamental in catalysis. These processes depend on the surface structure and stoichiometry of the oxide and are therefore expected to vary between surface facets. However, there is a lack of direct measurements of redox properties on the nanoscale for analysing the importance of such faceting effects in technical materials. Here, we address the facet-dependent redox properties of vanadium-oxide-covered anatase nanoparticles of relevance to, e.g., selective catalytic reduction of nitrogen oxides. The vanadium oxidation states at individual nanoscale facets are resolved in situ under catalytically relevant conditions by combining transmission electron microscopy imaging and electron energy loss spectroscopy. The measurements reveal that vanadium on 001 facets consistently retain higher oxidation states than on 10l facets. Insight into such structure-sensitivity of surface redox processes opens prospects of tailoring oxide nanoparticles with enhanced catalytic functionalities.Surface-engineered encapsulation is a non-genetic method to protect living organisms against harsh environmental conditions. Different cell encapsulation methods exist, yielding shells with different interfacial-interactions with encapsulated, bacterial surfaces. However, the impact of interfacial-interactions on the protection offered by different shells is unclear and can vary for bacteria with different surface composition. Probiotic bacteria require protection against gastro-intestinal fluids and antibiotics. Here, we encapsulated two probiotic strains using ZIF-8 (zeolitic imidazolate framework) biomineralization (strong-interaction by coordinate-covalent bonding), alginate gelation (intermediate-interaction by hydrogen bonding) or protamine-assisted packing of SiO2 nanoparticles yielding a yolk-shell (weak-interaction across a void between shells and bacterial surfaces). The surface of probiotic Lactobacillus acidophilus was rich in protein, yielding a hydrophilic, positively-charged surface below and alls and its application for protecting bacteria.Engineering an electrode material for boosting reaction kinetics is highly desired for the oxygen evolution reaction (OER) in the anodic half reaction, and is still a grand challenge for energy conversion technologies. By taking inspiration from the catalytic properties of transition metal phosphides (TMPs) and metal-organic frameworks (MOFs), we herein propose a general MOF-intermediated synthesis of a series of hollow CoFeM (M = Bi, Ni, Mn, Cu, Ce, and Zn) trimetallic phosphides composed of ultrathin nanosheets as advanced electrocatalysts for the OER. A dramatic improvement of electrocatalytic performance toward the OER is observed for hollow CoFeM trimetallic phosphides compared to bimetallic CoFe phosphides. Remarkably, composition-optimized CoFeBiP hollow microspheres could deliver superior electrocatalytic performance, achieving a current density of 10 mA cm-2 with an overpotential of only 273 mV. Mechanistic investigations reveal that the Bi and P doping effectively optimizes the electronic structure of Co and Fe by charge redistribution, which significantly lowers the adsorption energy of oxygen intermediates. GDC-6036 in vitro Moreover, the hollow microsphere structures composed of ultrathin nanosheets also enable them to provide rich surface active sites to boost the electrocatalytic OER.Proton transfer from Brønsted acid sites (BASs) to alcohol molecules ignites the acid-catalyzed alcohol dehydration reactions. For aqueous phase dehydration reactions in zeolites, the coexisting water molecules around BASs in the zeolite pores significantly affect the alcohol dehydration activity. In the present work, proton transfer processes among the BASs of H-BEA zeolites, the adsorbed cyclohexanol and surrounding water clusters with different sizes up to 8 water molecules were investigated using ab initio molecular dynamics (AIMD) simulations combined with the multiple-walker well-tempered metadynamics algorithm. The plausible proton locations and proton transfer processes were characterized using two/three-dimensional free energy landscapes. The strong proton affinity makes the protonated cyclohexanol stable species until a water trimer is formed. The proton either is shared between protonated cyclohexanol and the water trimer or remains with the water trimer (H7O3+). With a further increase in water concentrations, the proton prefers to remain with the water clusters.Highly effective photothermal conversion performance coupled with high resolution temperature detection in real time is urgently needed for photothermal therapy (PTT). Herein, ultra-small Cu2S nanoparticles (NPs) were designed to absorb on the surface of NaScF4 Yb3+/Er3+/Mn2+@NaScF4@SiO2 NPs to form a central-satellite system, in which the Cu2S NPs play the role of providing significant light-to-heat conversion ability and the Er3+ ions in the NaScF4 Yb3+/Er3+/Mn2+ cores act as a thermometric probe based on the fluorescence intensity ratio (FIR) technology operating in the biological windows. A wavelength of 915 nm is used instead of the conventional 980 nm excitation wavelength to eliminate the laser induced overheating effect for the bio-tissues, by which Yb3+ can also be effectively excited. The temperature resolution of the FIR-based optical thermometer is determined to be better than 0.08 K over the biophysical temperature range with a minimal value of 0.06 K at 298 K, perfectly satisfying the requirements of biomedicine.

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