Barrdesai0761

Exposure to high-doses of ionizing radiation has been reported to be associated with the risk of stroke. However, risks associated with lower dose exposures remain unclear, and there is little information available for the risk modification according to the dose-rate. There are few studies using animal models which might be able to provide complementary information on this association. In this study, the male stroke-prone spontaneously hypertensive rat (SHRSP) was used as a model animal. The rats were acutely irradiated with doses between 0 and 1.0 Gy or chronically irradiated with a cumulative dose of 0.5 or 1.0 Gy (at a dose rate of 0.05 or 0.1 Gy/day, respectively). The onset time of stroke related symptoms in SHRSP was used as an endpoint for evaluating the effects of low dose and the low dose-rate gamma-ray exposures. With respect to acute exposure, the time to the onset of stroke in the irradiated rats suggested the presence of a threshold around 0.1 Gy. For the low dose-rate chronically exposed, no significant increase in stroke symptom was observed. These findings are novel and demonstrate that the SHRSP system can be used to determine the association between the risk of stroke and radiation exposure with high sensitivity. Moreover, these studies provide important information regarding the association between the low dose and low dose-rate radiation exposure and circulatory diseases, especially stroke.The counterions of polyoxometalates (POMs) impact properties and applications of this growing class of inorganic clusters. Here, we used density functional theory (DFT) to elucidate the impact of fully hydrated alkali metal cations on the geometry, electronic structure, and chemical properties of the polyoxotungstate anion [PW12O40]3-. The calculations show that the HOMO of the free anion [PW12O40]3- is a linear combination of the 2p AOs of the bridging oxygens, and the first few LUMOs are the 5d orbitals of the tungsten atoms. The S0→ S1 electron excitation, near 3 eV, is associated with the O(2p) → W(5d) transition. selleck Anion/cation complexation leads to formation of [PW12O40]3-[M+(H2O)16]3 ion-pair complexes, where with the increase of atomic number of M, the M+(H2O)16 cluster releases several water molecules and interacts strongly with the polyoxometalate anion. For M = Li, Na and K, [PW12O40]3-[M+(H2O)16]3 is characterized as a "hydrated" ion-pair complex. However, for M = Rb and Cs, it is a "contact" ion-pair complex, where the strong anion-cation interaction makes it a better electron acceptor than the "hydrated" ion-pair complexes. Remarkably, the electronic excitations in the visible part of the absorption spectrum of these complexes are predominantly solvent-to-POM charge transfer transitions (i.e. intermolecular CT). The ratio of the number of intermolecular charge transfer transitions to the number of O(2p)-to-W(5d) valence (i.e. intramolecular) transitions increases with the increasing atomic number of the alkali metals.A fundamental challenge to multiplexing microfluidic chemotaxis assays at scale is the requirement for time-lapse imaging to continuously track migrating cells. Drug testing and drug screening applications require the ability to perform hundreds of experiments in parallel, which is not feasible for assays that require continuous imaging. To address this limitation, end-point chemotaxis assays have been developed using fluid flow to align cells in traps or sieves prior to cell migration. However, these methods require precisely controlled fluid flow to transport cells to the correct location without undesirable mechanical stress, which introduce significant set up time and design complexity. Here, we describe a microfluidic device that eliminates the need for precise flow control by using centrifugation to align cells at a common starting point. A chemoattractant gradient is then formed using passive diffusion prior to chemotaxis in an incubated environment. This approach provides a simple and scalable approach to multiplexed chemotaxis assays. Centrifugal alignment is also insensitive to cell geometry, enabling this approach to be compatible with primary cell samples that are often heterogeneous. We demonstrate the capability of this approach by assessing chemotaxis of primary neutrophils in response to an fMLP (N-formyl-met-leu-phe) gradient. Our results show that cell alignment by centrifugation offers a potential avenue to develop scalable end-point multiplexed microfluidic chemotaxis assays.In this work, a novel DNA nanostructure with a shorter assembly time and larger loading capacity was constructed using amphiphilic DNA-alkane group (Spacer C12)10 conjugates encapsulating plentiful fat-soluble fluorescent dyes into the hydrophobic core to form the DNA micelles, which could be rapidly self-disassembled via target induced hydrophilic-hydrophobic regulation to release fluorescent dyes from micelles to the organic phase, realizing the fast and sensitive detection of microRNA.MoS2-based hybrids have aroused great interest for their outstanding performance in the application fields of biochemical sensing, catalysis and energy storage. Herein, we present a facile strategy to fabricate hierarchical microtubes by cultivating a MoS2 sheet-like nanostructure on polypyrrole microtubes (designated as PPy@MoS2 microtubes) using MoO3@PPy micro-cables as self-sacrificial templates. Such a dissolution-regrowth mechanism is demonstrated for the formation of hierarchical PPy@MoS2 microtubes by studying the morphology of the intermediate products in the process of the sulfidation reaction. The PPy microtubes are able to effectively improve the electrical conductivity of the hybrid architecture and greatly alleviate the agglomeration of the MoS2 nanosheets. Notably, the sheet-like MoS2 nanostructure can load more noble metal nanoparticles (NPs) owing to MoS2 released photogenerated electrons irradiated by light. Then, metal (Ag, Au, and Pd) NPs are reduced and in situ decorated on PPy@MoS2 microtubes, thus forming ternary PPy@MoS2@Ag, Au, and Pd nanohybrids, respectively. This decoration method also expands the wide range of application fields of PPy@MoS2. As a proof of application, the ternary PPy@MoS2@Au hybrids reveal excellent enzyme-like catalytic performance. Owing to the high coverage of Au NPs as well as one dimensional hierarchical MoS2-based ternary unique structures, the resultant PPy@MoS2@Au hybrid composites exhibited synergistically enhanced peroxidase-like catalytic activity relative to MoS2, MoS2@Au, and PPy@MoS2 alone, demonstrating the remarkable prospects of MoS2-based hybrids in chemical/biological molecule sensing application.Reflective assemblies of high refractive index organic crystals are used to produce striking optical phenomena in organisms based on light reflection and scattering. link2 In aquatic animals, organic crystal-based reflectors are used both for image-formation and to increase photon capture. Here we report the characterization of a poorly-documented reflector in the eye of the shrimp L. vannamei lying 150 μm below the retina, which we term the proximal reflective layer (PR-layer). The PR-layer is made from a dense but disordered array of polycrystalline isoxanthopterin nanoparticles, similar to those recently reported in the tapetum of the same animal. link3 Each spherical nanoparticle is composed of numerous isoxanthopterin single crystal plates arranged in concentric lamellae around an aqueous core. The highly reflective plate faces of the crystals are all aligned tangentially to the particle surface with the optical axes projecting radially outwards, forming a birefringent spherulite which efficiently scatters light. The nanoparticle assemblies form a broadband reflective sheath around the screening pigments of the eye, resulting in pronounced eye-shine when the animal is viewed from a dorsal-posterior direction, rendering the eye pigments inconspicuous. We assess possible functions of the PR-layer and conclude that it likely functions as a camouflage device to conceal the dark eye pigments in an otherwise largely transparent animal.A feasible analytical method based on high performance liquid chromatography-quadrupole/electrostatic field orbitrap high-resolution mass spectrometry (HPLC-Q/orbitrap MS) has been established for the identification and characterization of anticancer constituents in ethyl acetate components from Hedyotis diffusa in our work. The mass spectrometer provided significant fragment information both in the full MS scan and data-dependent MS2 modes. Sixty-two possible compounds were analyzed and identified from the above results. Of the above 62 compounds, 12 have good separation in the positive ion mode, and 27 compounds have good separation in the anion mode. Currently, 39 have been reported in the literature related to the chemical composition of the plant, while the other 23 of the 62 compounds have not been reported. Fifteen tentatively identified compounds were given detailed descriptions. Four representative compounds from the ethyl acetate extract among the fifteen were actually isolated in good yield with sir the rapid detection of the potential anticancer compounds from Hedyotis diffusa.Correction for 'H2 as a fuel for flavin- and H2O2-dependent biocatalytic reactions' by Ammar Al-Shameri et al., Chem. Commun., 2020, DOI 10.1039/d0cc03229h.Electrostatic interactions between a quaternary pyridyl-β-diketonate and anionic charged nanosheets were observed to produce a highly emissive dispersion in a rich water solution. A greater fluorescence quantum yield of approximately 50% was obtained when a luminogenic β-diketonate, 1-(4-methoxyphenyl)-3-(3-hydroxyethyl-pyridinium bromide)-1,3-propandione (prepared by the Claisen condensation reaction and subsequent quaternization), was molecularly dispersed and enclosed by a couple of atomically flat ultrathin (approximately 1.0 nm) silicate sheets of anionic layered clay. By accommodating β-diketonate into a narrow interlamellar space (approximately 0.4 nm distance), the molecular motion was suppressed, as confirmed by a smaller non-radiative relaxation rate constant, which was obtained by time-resolved luminescence and quantum yield measurements. Because the dense packing of β-diketonate quenched the excited state, the isolation of luminogens by the co-adsorption of photochemical inert cations (tetramethylammonium and benzylammonium) was prevented by concentration quenching. A lower quantum yield was obtained by expanding the interlayer distance above 1.0 nm by co-adsorbing a photo-inactive water-soluble polymer, poly(vinylpyrrolidone). Therefore, the fixation and spatial separation of β-diketonate in the narrow interlayer space was determined to be essential for obtaining strong emission.In the modern era, the escalation of heavy metal discharges, especially from the industrial sector, is causing an enormous threat to nature. This article explores the dual sensing of heavy metals (Cr6+ and Fe3+) using a naturally formed microcline based sensor. A nano-sized microcline (M) was obtained via a facile top-down synthesis. In order to enhance the fluorescence property of the material, nitrogenous carbon-dots were loaded into the porous structure of the microcline (MCD) causing a bright blue fluorescence with remarkable stability. Detailed analysis of the composition and structure of the natural nano-sensor was carried out using X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and BET analysis. This sensor material is highly selective towards Cr6+ and Fe3+, demonstrating a "turn-off" response in aqueous Fe3+ and a radical red shift of the fluorescence maxima for aqueous Cr6+. Density functional studies suggest that photoinduced electron transfer (PET) based quenching of fluorescence is responsible for these types of fluorescence alteration mechanisms.