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Prepared nanoparticles were biologically (antioxidant, antimicrobial and blood cytotoxicity) characterized to screen their further utility in therapeutic strategies. Characteristics and activities of green gold nanoparticles were compared with conventional citrate stabilized gold nanoparticles. It was observed that green gold nanoparticles prepared using M. oleifera show less cytotoxicity and helps in regeneration of neuronal cells in animal model study. It establishes the fact that conjugation of different plant extract fraction for stabilization of gold nanoparticle may be responsible factor for enhancement of bioactive nature of green gold nanoparticle. In addition, the green gold nanoparticle show efficient photo-catalytic efficiency. Development of such bioactive gold nanoparticles will lead to functional materials for biomedical and therapeutic applications.The present finding illuminates the physics of the formation of interfaces of metal based hetero-structures near layer continuous limit as an approach to develop high-efficiency W/B4C multilayer (ML) optics with ML periodicity varying d = 1.86-1.23 nm at a fixed number of layer pairs N = 400. The microstructure of metal layers is tailored near the onset of grain growth to control the surface density of grains resulting in small average sizes of grains to sub-nanometers. This generates concurrently desirable atomically sharp interfaces, high optical contrast, and desirable stress properties over a large number of periods, which have evidence through the developed ML optics. We demonstrate significantly high reflectivities of ML optics measured in the energy range 10-20 keV, except for d = 1.23 nm due to quasi-continuous layers. The reflectivities at soft gamma-rays are predicted.The work demonstrates tin oxide quantum dots/graphene oxide/polypyrrole (SnO2QDs/GO/PPY) ternary composite deposited on titanium foil as a positive electrode and graphene oxide (GO)/charcoal on titanium foil as negative electrode separated by polyvinyl alcohol/potassium hydroxide (PVA/KOH) gel-electrolyte as a solid-state asymmetric supercapacitor for high energy storage applications. Here, tin oxide quantum dots (SnO2QDs) were successfully synthesized by a hydrothermal technique, and SnO2QDs/GO/PPY ternary composite was synthesized by an in situ method with pyrrole monomer, SnO2, and GO. A pH value controlled, which maintained the uniform size of SnO2QDs dispersed on PPY, through GO ternary composite was used for fabricating the asymmetric supercapacitor electrode with the configuration (SnO2QDs/GO/PPY)/GO/charcoal (85  10  5). The device achieved the highest specific capacitance of 1296 F g-1, exhibited an energy density of 29.6 W h kg-1 and the highest power density of 5310.26 W kg-1 in the operating voltage from 0 to 1.2 V. The device also possessed excellent reliability and retained the capacitance of 90% after 11 000 GCD cycles. This ternary composite is a prominent material for potential applications in next-generation energy storage and portable electronic devices.Herein we report a multifunctional high performance metal organic framework (Zn-DHNDC MOF) based chemosensor that displays an exceptional excited state intramolecular proton transfer (ESIPT) tuned fluorescence turn-on-off response for OH-, Al3+ and Fe3+ ions along with mitochondria targeted bio-imaging. Properly tuning ESIPT as well as the hydroxyl group (-OH) allows Zn-DHNDC MOF to optimize and establish chelation enhanced fluorescence (CHEF) and chelation enhanced quenching (CHEQ) based sensing mechanisms. The MOF benefits from acid-base interactions with the ions which generate a turn-on bluish green fluorescence (λ Em 492 nm) for OH-, an intense turn-on green fluorescence (λ Em 528 nm) for Al3+ and a turn-off fluorescence quenching response for Fe3+ ions. The aromatic -OH group indeed plays its part in triggering CHEF and CHEQ processes responsible for the turn-on-off events. Low limits of detection (48 nM of OH-, 95 nM for Al3+, 33 nM for Fe3+ ions), high recyclability and fast response time (8 seconds) further assist the MOF to implement an accurate quantitative sensing strategy for OH-, Al3+ and Fe3+ ions. The study further demonstrates the MOF's behaviour in cellular medium by subjecting it to live cell confocal microscopy. Along with a bio-compatible nature the MOF exhibited successful accumulation inside the mitochondria of MCF7 cancer cells, which defines it as a significant bio-marker. Therefore the present work successfully represents the multidisciplinary nature of Zn-DHNDC MOFs, primarily in sensing and biomedical studies.Amorphous cobalt-calcium phosphate composite (CCPC) films are electrochemically prepared on various electrodes by utilizing the solid phase of hydroxyapatite as a phosphate source. The CCPC film formation is surface process in which the dissolution of hydroxyapatite and the deposition of CCPC film concurrently occur on the electrode surface without the mass transfer of phosphate ions into the bulk solution. Elemental, crystallographic, and morphological analyses (EDX, ICP-AES, XPS, and XRD) indicate that the CCPC is composed of amorphous cobalt oxide with calcium and phosphate. The film exhibits durable oxygen evolution reaction (OER) catalytic properties under neutral and basic aqueous condition. Compared to using solution phase of phosphate source, our preparation method utilizing solid hydroxyapatite has advantage of preventing unnecessary chemical reaction between phosphate and other chemical species in bulk solution.Real time detection of explosive compounds in today's time is of utmost necessity due to security and severe environmental safety issues. Herein, we have synthesized a biobased conjugated molecular system from riboflavin and l-cystine utilized it for detecting picric acid in trace amount using optical sensing technique. The bioconjugate probe showed high quenching efficiency towards picric acid, which is 92.2%. In depth mechanistic study showed that ground state electrostatic interaction and inner filter effect are the factors leading to the diminishing of the probe's fluorescence intensity on addition of trace amount of the nitrophenol, picric acid. The detection limit of the conjugate is 0.37 nM which is extremely low and highly desirable for clinical applications of this system.Strong 1.5 μm emission with full width at half maximum (FWHM) of 64 nm has been obtained in 3 mol% Yb2O3 and 1 mol% Er2O3 codoped tungsten tellurite glass under the excitation of a 980 nm laser diode. Spectroscopic properties of Yb3+/Er3+ codoped tungsten tellurite glasses as a function of Yb3+ and Er3+ contents are systematically investigated by absorption spectra, emission spectra and lifetime measurement. The structure of tungsten tellurite glass is characterized by Raman spectrum. In addition, emission cross section and gain coefficient of Er3+ ions near 1.5 μm are determined and respective maximum values attain 1.06 × 10-20 cm2 and 4.07 cm-1. Moreover, gain bandwidth and figure of merit associated with gain properties in tungsten tellurite glass are calculated and compared with other reported glasses. These results indicate that Yb3+/Er3+ codoped tungsten tellurite glasses with better gain properties are promising candidates in constructing broadband optical fiber amplifiers and tunable fiber lasers in the optical telecommunication window.The significant electrochemical performance in terms of both specific energy and power delivered via hybrid energy storage devices (supercapattery) has raised their versatile worth but electrodes with flashing electrochemical conduct are still craved for better performance. In this work, binary and ternary metal phosphates based on copper, cobalt, and manganese were synthesized by a sonochemical method. Then, the compositions of copper and cobalt were optimized in ternary metal phosphates. The structural studies and morphological aspects of synthesized materials were scrutinized by X-ray diffraction and scanning electron microscopy. Furthermore, the electrochemical characterizations were performed in three- and two-cell configurations. The sample with equal compositions of copper and cobalt (50/50) demonstrates the highest specific capacity of 340 C g-1 at a current density of 0.5 A g-1 among all. This optimized composition was utilized as a positive electrode material in a supercapattery device that reveals a high specific capacity of 247 C g-1. The real device exhibits an excellent energy density of 55 W h kg-1 while delivering a power density of 800 W kg-1. Furthermore, the device was able to provide an outstanding specific power of 6400 W kg-1 while still exhibiting a specific energy of 19 W h kg-1. The stability potential of the device was tested for 2500 continuous charge and discharge cycles at 8 A g-1. Excellent capacitive retention of 90% was obtained, which expresses outstanding cyclic stability of the real device. A theoretical study was performed to investigate the capacitance and diffusion-controlled contribution in the device performance using Dunn's model. The maximum diffusion-controlled contribution of 85% was found at 3 mV s-1 scan rate. The study demonstrates the utilization of ternary metal phosphates as self-supported electrode materials for potential energy storage applications.[This corrects the article DOI 10.1039/D0RA10222A.].A novel cathodic photoelectrochemical (PEC) sensor was developed for the ultrasensitive detection of kanamycin sulfate (KAM) based on the g-C3N4 coupled zirconium-based porphyrinic metal-organic framework (PCN-222). Photocathodes made by double n-type semiconductors, which was attributed to the transfer of electrons and holes from g-C3N4 broad band to PCN-222 with narrow band gap. selleck inhibitor The photocurrent decreased when KAM was added, which was conducive to the construction of the PEC sensor. Then, the PCN-222@g-C3N4 was used as a photosensitive platform to construct a label-free strategy and ultrasensitive detection of KAM with wide linear range from 1 to 1000 nM and a low detection limit of 0.127 nM. Moreover, this sensing platform shows good selectivity, favourable reproducibility and brilliant stability. The reported sensors provided great potential for the detection of KAM in actual samples.Most research concerning pyrazine formation in the Maillard reaction is mainly focused on free amino acids (FAAs), but limited information is available on the effect of peptides and proteins. In this study, three Maillard model systems (i.e., glucose and native sunflower seed protein, hydrolyzed peptides or FAAs, respectively) were prepared, and their effect on the formation of volatiles were further compared at different heating conditions by using of headspace solid-phase microextraction equipped with gas chromatography/mass spectrometry (HS-SPME-GC/MS). It was found that pyrazines were the characteristic volatile compounds in tested Maillard models, and with increasing heating temperature and time, the varieties of pyrazine formation significantly increased. The optimum reaction condition for pyrazine formation was at 140 °C for 90 min, which was subsequently applied to all sets of Maillard models. Further analysis showed that the short chain peptides generated by hydrolyzing sunflower seed protein (SSP), especially the molecular weight ranging from 1.

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