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Soybean, one of the major food and fodder crops, yield is significantly reduced by different abiotic and biotic stresses, and salinity is one of the major abiotic stresses. The research objective of this study was to investigate the effect of foliar application of potassium chloride and potassium sulfate fertilizers at the early growth stage of soybean under medium (6 dS/m) and high (12 dS/m) salinity stresses. The effect of fertilizer application was measured on the bases of plant growth, levels of antioxidant activities, total polyphenol, flavonoid, chlorophyll, and carotenoid contents. Potassium sulfate showed better positive effect on the antioxidant activities, polyphenol, flavonoid, carotenoid, and chlorophyll contents compared to those of potassium chloride although the contribution was not noteworthy in comparison to the fertilizer unsprayed plants. The results of this study implied that foliar applications of 2.5% potassium fertilizers could not help reduce the negative effect of salinity stress at the early stage of soybean growth. This study suggests further researches using different concentrations of fertilizers at different plant growth and development stages. [ABSTRACT FROM AUTHOR]

Peanut shell; a byproduct of an important leguminous crop, peanut; is a potential source of different functional compounds. Antioxidant activities, secondary metabolites and amino acid contents in peanut shells of six Korean cultivars were studied in the present study. Peanut shells showed remarkable antioxidant potentials with high amounts of total polyphenol (428.1–739.8 µg gallic acid equivalents/g), flavonoid (142.6–568.0 µg quercetin equivalents/g), and amino acid (5.76–34.56 mg/g) contents. 2, 2-diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS), superoxide dismutase (SOD)-like activity, and reducing power potential of the peanut shells were considerable. The results suggest that the shells of Korean peanut cultivars could be a potential source of natural antioxidants and functional compounds for various industrial uses including cosmetics. [ABSTRACT FROM AUTHOR]

Ethyl pyruvate (EP) is a simple aliphatic ester of pyruvic acid and has been shown to have protective properties, which have been attributed to its anti-inflammatory, anti-oxidative, and anti-apoptotic functions. In an effort to develop better derivatives of EP, we previously synthesized DEOPA (N,N-diethyl-2-oxopropanamide, a novel isoster of EP) which has greater neuroprotective effects than EP, probably due to its anti-inflammatory and anti-excitotoxic effects. In the present study, we synthesized 3 DEOPA derivatives, in which its diethylamino group was substituted with diisopropylamino, dipropylamino, or diisobutylamino groups. Among them, DIPOPA (N,N-diisopropyl-2-oxopropanamide) containing diisopropylamino group had a greater neuroprotective effect than DEOPA or EP when administered intravenously to a rat middle cerebral artery occlusion (MCAO) model at 9 h after MCAO. Furthermore, DIPOPA had a wider therapeutic window than DEOPA and a marked reduction of infarct volume was accompanied by greater neurological and behavioral improvements. In particular, DIPOPA exerted robust anti-inflammatory effects, as evidenced by marked suppressions of microglia activation and neutrophil infiltration in the MCAO model, in microglial cells, and in neutrophil-endothelial cocultures at lower concentration, and did so more effectively than DEOPA. In particular, DIPOPA remarkably suppressed neutrophil infiltration into brain parenchyma, and this effect was attributed to the expressional inhibitions of cell adhesion molecules in neutrophils of brain parenchyma and in circulating neutrophils via NF-κB inhibition. Together, these results indicate the robust neuroprotective effects of DIPOPA are attributable to its anti-inflammatory effects and suggest that DIPOPA offers a potential therapeutic means of ameliorating cerebral ischemic injury and other inflammation-related pathologies. [ABSTRACT FROM AUTHOR]

Abstract Pt-based catalysts are suffering from the intrinsic high cost and poor stability for practical use in fuel cells. We develop a free-standing fabric type Pt-free high-performance oxygen reduction reaction (ORR) catalyst, consisting of N, Fe-codoped carbon nanofibers and graphene (N/Fe-CG) hybrids. Electrospinning is used to synthesize the free-standing fabric catalysts. Incorporation of graphene into the nanofiber structure greatly increases the electrical conductivity and catalytic surface area. X-ray photoelectron spectroscopy (XPS) analysis provides evidence that Fe-N 4 active centers are possibly formed in the catalyst, as is confirmed by electrochemical tests also. Compared to commercial Pt/C, our N/Fe-CG exhibits a similar level of catalytic activity but superior stability and methanol tolerance in both alkaline and acidic media, making it a good candidate for an ORR electrocatalyst in energy storage/conversion and other relevant applications. Graphical abstract fx1 Highlights • N, Fe-codoped free-standing carbon fabric ORR catalyst is successfully developed • The catalyst shows excellent catalytic properties in both alkaline and acidic media • Sample with N, Fe-codoping reveals better performance than single atom doped samples • FeN 4 complex formation is confirmed by electrochemical performance and XPS analysis [ABSTRACT FROM AUTHOR]

To date, lithium-oxygen batteries (LOBs) using porous carbon materials as the air cathode have been widely studied. However, a fundamental issue of carbon electrode still remains; the carbon surface is unstable and is highly reactive in contact with Li 2 O 2 , resulting in the formation of irreversible byproducts ( e.g. , Li 2 CO 3 ). To address this issue, we investigated the use of surface protection layers for improving the cycling stability of porous carbon-based LOB cathode. We employed atomic layer deposition (ALD) for conformal coating of two types of overlayers (In 2 O 3 and TiN), i.e. , oxide and nitride thin film, on an electrospun carbon nanopaper (CNp) membrane. The LOB cell with In 2 O 3 -coated CNp exhibited much enhanced cycling performance (over 140 cycles) compared with pristine CNp and TiN-coated CNp as control samples (less than 60 cycles for both cases). To further improve cell efficiency by reducing overpotentials, the surface of In 2 O 3 -coated CNp electrode was functionalized by catalytic RuO x nanoparticles, which enables stable and complete discharging and recharging reactions below 4.2 V for an extended period of 165 cycles. Interestingly, after each discharge, nanosheet-like Li 2 O 2 growth was observed on In 2 O 3 -coated CNps, which is advantageous for enhanced cycle life. This work demonstrates that use of a free-standing, high surface area carbon membrane, that is conformally encapsulated by a highly conductive and stable oxide protection layer, is essential for enhanced Li-O 2 cell performance by preventing direct contact between underneath carbon and electrolyte. [ABSTRACT FROM AUTHOR]

With the rapid development of portable/wearable electronic devices, the demand for highly efficient and sustainable self-powered systems to support their off-grid operation has risen considerably. Recently, metal halide perovskites (MHPs) have been suggested as promising materials for energy harvesting and storage devices because of their excellent optoelectronic, ferro/piezoelectric, and ion migration properties. However, the high toxicity and poor physicochemical stability of MHPs hamper their practical application. Herein, for the first time, the potential of methylammonium tin halide (MA 2 SnX 6 ; X = Cl, Br, and I) double perovskite thin films for high-efficiency self-charging power units (SPUs) is elucidated by virtue of their high stability in air. To this end, the integration of an MA 2 SnCl 6 -based piezoelectric nanogenerator (PENG) with a lithium metal battery (LMB), which also uses an MA 2 SnCl 6 -based thin film as the cathode, is demonstrated. The MA 2 SnCl 6 -based PENG exhibited a high output power density of 7.33 μW cm−2 and an excellent mechanical durability. Furthermore, MA 2 SnCl 6 as a cathode in LMB recorded the highest specific capacity of 589.98 mAh g−1. A 1 nm-thick Al 2 O 3 coating on the MA 2 SnCl 6 surface improved the capacity retention from 16.9 % to 75.1 % for 100 cycles, indicating its stable performance. The MA 2 SnCl 6 -based LMB is charged by the MA 2 SnCl 6 -based PENG and utilized as an SPU for operating various small-scale electronics (humidity meter, calculator, and LED). This work not only demonstrates the feasibility of MHPs toward high-capacity batteries and energy harvesters but also provides insights into the general design principles of MHP-based devices. [Display omitted] • Lead-free MA 2 SnX 6 double halide perovskite as an active material for efficient energy harvester and storage device. • MA 2 SnCl 6 -based PENG exhibited a high output power density of 7.33 μW cm−2. • MA 2 SnCl 6 -based Li metal battery recorded the highest specific capacity of 589.98 mAh g−1. • Improved capacity retention of MA 2 SnCl 6 -based LMB by the Al 2 O 3 surface coating. • Realizing of self-charging power unit by combing MA 2 SnCl 6 -based Li metal battery and PENGs. [ABSTRACT FROM AUTHOR]

The configuration of reinforced composite membrane (RCM), composed of porous polytetrafluoroethylene (PTFE) as a mechanical reinforcement and perfluorosulfonic acid (PFSA) as a proton conductive polymer, has gained a large interest due to its promisingly high performance for polymer electrolyte membrane (PEM) fuel cells. However, the inaccessible polymeric nanocomposites in preparing RCMs are still faced with critical challenges associated with immiscible interactions between hydrophilic sulfonate groups in PFSA and the hydrophobic nanoporous PTFE matrix. Herein, we report a well-refined and facile fabrication strategy for producing a cross-aligned PTFE (CA-PTFE) framework. The electric-field guided electrospinning enables the creation of unique micron-scale, grid-type PTFE matrix, which is synthesized by annealing of electrospun conjugated polymers, resulting in the removal of carrier polymer and the formation of continuous fibrious structure via fusion of PTFE particles. The CA-PTFE RCM embodying uniformly impregnated PFSA in a grid-type PTFE matrix, facilitates hydration of the membranes, with minimal swelling and efficient diffusion of protons through concentrated sulfonate groups. The CA-PTFE RCM adopted cell showed outstanding fuel cell currents during both low and high humidity operation, with a current density of 1.38 A cm−2 at 0.6 V and maximum power density of 0.85 W cm−2 under RH 100% condition. Furthermore, the CA-PTFE RCM was able to achieve a long-lasting single-cell operation with a significantly low hydrogen crossover (less than 5 mA cm−2 at 0.4 V) even after 21,000 wet/dry cycles, which surpasses the standard of membrane durability for transportation application. The rational design of fibrous PTFE reinforcements opens up new engineering opportunities for the future development of high-stability PEM fuel cells. [Display omitted] • Cross-aligned PTFE (CA-PTFE) framework is synthesized via electric-field guided electrospinning and subsequent calcination. • As a reinforcement, micron-scale patterned CA-PTFE framework is beneficial for the PFSA impregnation and the proton conduction. • CA-PTFE reinforced composite membrane shows the outstanding current density and exceptional durability in PEM fuel cells. [ABSTRACT FROM AUTHOR]

The therapeutic efficacy of intranasal iNOS siRNA delivery was investigated in the postischemic rat brain after encapsulating on in gelatin nanoparticles (GNPs; diameter 188.0 ± 60.9 nm) cross-linked with 0.0667% glutaraldehyde (GA). Intranasally delivered GNPs were found in extracellular and intracellular compartments of many brain regions, including the olfactory bulb, cerebral cortex, and striatum at 1 hour after infusion and continued to be detected for days. Infarct volumes were markedly suppressed (maximal reduction to 42.1 ± 2.6%) at 2 days after 60 minutes of middle cerebral artery occlusion (MCAO) when iNOS siRNA/GNPs were delivered at 6 hours post-MCAO. In addition, this protective effect was manifested by reductions in neurological and behavioral deficits that were sustained for 2 weeks. Therapeutic potency of iNOS siRNA/GNPs was significantly greater and sustained longer than that of bare siRNA and prolonged and efficient iNOS by iNOS siRNA/GNP is responsible for the robust neuroprotective effect. [ABSTRACT FROM AUTHOR]

Formation of stable solid electrolyte interphase (SEI) layer is critical to outstanding performance of energy storage devices, because it acts as a passive layer that allows facile transport of ions but forbids electron transport between the electrolyte and electrode. Although much study has been devoted to investigate the morphology and structure of SEI layer using a myriad of analytical devices on past decades, the direct observation of SEI layer on a real time scale has remained as a formidable challenge. In addition, it has been difficult to observe both the decomposition of electrolytes and formation process of stable SEI layer at nanometer scale. Here we utilize in situ transmission electron microscopy (TEM) using graphene liquid cell (GLC) to realize the observation of stable SEI layer formation in a sequential time scale. Upon e − beam irradiation, Li salts in the electrolytes react with reduced electrolytes and form gel-like agglomerates, which are deposited on the surface of the active material as a passivation layer and later stabilized to become more uniform in overall thickness. Additionally, growth dynamics of stable SEI layer were suggested, where the deposition of decomposed electrolytes eventually result in relatively uniform SEI layer. This paper demonstrates that it is possible to observe not only the formation of non-crystalline SEI layer but also the movement of decomposed electrolytes onto the surface of active materials which account for broader understanding of SEI layer, and has the potential to detect important interfacial phenomena in electrochemical devices that were overlooked so far. [ABSTRACT FROM AUTHOR]

High mobility group box 1 (HMGB1) is an endogenous danger signal molecule. In the postischemic brain, HMGB1 is massively released during acute damaging process and triggers inflammatory processes. Moreover, it has been reported HMGB1 augments the proinflammatory effect of LPS by direct interaction. In previous studies, the authors showed intranasally delivered a HMGB1 binding heptamer peptide (HBHP; HMSKPVQ) has robust neuroprotective effects in the ischemic brain after middle cerebral artery occlusion and that it exerts an anti-inflammatory effect. In the present study, the authors investigated whether HBHP suppresses the augmentation of the proinflammatory effect of LPS by HMGB1. In primary microglial cultures, low doses of LPS (5 ng/ml) and recombinant HMGB1 (rHMGB1, 20 ng/ml) synergistically activated microglial cells, and HMGB1–LPS binding was detected. In addition, synergistic NO accumulation along with direct HMGB1–LPS binding was also observed when primary microglial cultures were treated with LPS (5 ng/ml) and HMGB1 accumulated in NMDA-conditioned medium (NCM). Co-treatment of microglial cells with HBHP and LPS or rHMGB1 (NCM), or treatment with rHMGB1 or NCM and LPS after pre-incubating rHMGB1 (or NCM) with HBHP markedly suppressed their synergistic activation. Furthermore, interactions between rHMGB1 and LPS or between HMGB1 in NCM and LPS were suppressed dose-dependently by HBHP, indicating that HBHP suppressed the synergism between HMGB1 and LPS and the underlying mechanism involved inhibition of HMGB1–LPS binding. Together these results show HBHP has anti-inflammatory effects, and that it inhibits synergism caused by the binding of HMGB1 and LPS. [ABSTRACT FROM AUTHOR]

Hydro-electric technology has gathered much attention by the virtue of water as the energy source. However, the low energy density of this technology severely limits its practical use. Here, we demonstrate a PEDOT:PSS-based transpiration-driven electrokinetic power generator (p-TEPG) that enables the utilization of a wider variety of real-world water resources for maximizing energy generation efficiencies. In addition to the conventional electrical double layer on the material surface, the p-TEPG builds an additional potential difference in the polymer matrix by the selective penetration of cations into the matrix that contains sulfonate functional groups. p-TEPG exhibits 80–250% higher energy density than carbon-based TEPG at the same resistance. Moreover, seawater produced enhanced volumetric energy/power densities (34.36 mJ cm−3 and 44.70 μW cm−3) and areal energy/power densities (410 μJ cm−2 and 0.45 μW cm−2), respectively, compared to DI water on a single p-TEPG device, which is sufficient to charge electrical energy storage systems and directly operate low-powered electronic. • p-TEPG maximizes energy harvesting efficiency by ion-permselective PEDOT:PSS. • Green water resources improve performance of p-TEPG. • p-TEPG adsorbs more cations into its polymer matrix by sulfonate groups. • p-TEPG can increases energy harvesting efficiency by using anions and cations with smaller radii. • p-TEPG can be fueled with seawater, demonstrating its potential for blue energy generating system. [ABSTRACT FROM AUTHOR]

Abstract: Gelatin microspheres (GMSs) are widely used as drug carriers owing to their excellent biocompatibilities and toxicologically safe degradation products. The drug release profile is easily tailored by controlling the cross-linking density and surface-to-volume ratio, i.e. size, of the GMS. In this study, we employed GMSs which are 25μm in diameter and cross-linked with 0.03125% glutaraldehyde, to enable rapid initial and a subsequent sustained release. Therapeutic potency of human recombinant osteopontin (rhOPN) with or without encapsulation into GMSs was investigated after administrating them to rat stroke model (Sprague–Dawley; middle cerebral artery occlusion, MCAO). The administration of rhOPN/GMS (100ng/100μg) at 1h post-MCAO reduced the mean infarct volume by 81.8% of that of the untreated MCAO control and extended the therapeutic window at least to 12h post-MCAO, demonstrating a markedly enhanced therapeutic potency for the use of OPN in the post-ischemic brain. Scanning electron microscopy micrographs revealed that GMSs maintained the three-dimensional shape for more than 5days in normal brain but were degraded rapidly in the post-ischemic brain, presumably due to high levels of gelatinase induction. After encapsulation with GMS, the duration of OPN release was markedly extended; from the period of 2days to 5days in normal brain, and from 2days to 4days in the post-ischemic brain; these encompass the critical period for recovery processes, such as vascularization, and controlling inflammation. Together, these results indicate that GMS-mediated drug delivery has huge potential when it was used in the hyperacute period in the post-ischemic brain. [Copyright &y& Elsevier]

Abstract: Three different compositions of ZnO–In2O3 composite nanofibers were prepared by electrospinning, and their gas sensing characteristics were compared to those of pure ZnO and In2O3 nanofibers. All ZnO–In2O3 composite nanofibers showed high response to trimethylamine (TMA), relatively low cross-response to C2H5OH, and negligible cross-responses to CO and H2; pure ZnO or In2O3 nanofibers did not show selective detection of TMA. The maximum responses to 5ppm TMA of the ZnO–In2O3 composite nanofibers with the compositions of [Zn]:[In]=67:33, 50:50, and 33:67 by at% were 133.9 at 300°C, 82.9 at 350°C, and 119.4 at 375°C, respectively. Considering all the sensing characteristics such as gas response, selectivity, and sensing/recovering kinetics together, the operation of the ZnO–In2O3 nanofiber sensor with the composition of [Zn]:[In]=33:67 by at% at 375°C was determined to be in optimal condition to detect TMA. The significant enhancement of gas response and selectivity by the formation of composite nanofibers is discussed in relation to the variation of particle size, the formation of hetero-interfaces between ZnO and In2O3, and the combination of two sensing materials with different catalytic properties, gas adsorption behaviors, and acid–base properties. [Copyright &y& Elsevier]

Abstract: Gas sensors are employed in many applications including detection of toxic and combustible gases, monitoring emissions from vehicles and other combustion processes, breath analysis for medical diagnosis, and quality control in the chemicals, food and cosmetics industries. Many of these applications employ miniaturized solid-state devices, whose electrical properties change in response to the introduction of chemical analytes into the surrounding gas phase. Key challenges remain as to how to optimize sensor sensitivity, selectivity, speed of response and stability. The principles of operation of such devices vary and a brief review of operating principles based on potentiometric/amperometric, chemisorptive, redox, field effect and nanobalance approaches is presented. Due to simplicity of design and ability to stand up to harsh environments, metal oxide-based chemoresistive devices are commonly selected for these purposes and are therefore the focus of this review. While many studies have been published on the operation of such devices, an understanding of the underlying physicochemical principles behind their operation have trailed behind their technological development. In this article, a detailed review is provided which serves to update progress made along these lines. The introduction of nanodimensioned materials has had a particularly striking impact on the field over the past decade. Advances in materials processing has enabled the fabrication of tailored structures and morphologies offering, at times, orders of magnitude improvements in sensitivity, while high-resolution analytical methods have enabled a much improved examination of the structure and chemistry of these materials. Selected examples, illustrating the type of nanostructured devices being fabricated and tested, are discussed. This review concludes by highlighting trends suggesting directions for future progress. [Copyright &y& Elsevier]

Abstract: High mobility group box 1 (HMGB1) is an endogenous danger signal molecule. In a previous report, we showed that HMGB1 is massively released during NMDA-induced acute damaging process in the postischemic brain and triggers inflammatory processes and induces neuronal apoptosis. We have also reported a robust neuroprotection of intranasally delivered HMGB1 siRNA in the postischemic rat brain (middle cerebral artery occlusion (MCAO), 60min). In the present study, we investigated the therapeutic efficacy of intranasally delivered HMGB1 binding heptamer peptide (HBHP; HMSKPVQ), which was selected using a phage display approach, in the same stroke animal model. A pull-down assay using biotin-labeled HBHP showed that HBHP binds directly to HMGB1, specifically to HMGB1 A box, confirming HMGB1/HBHP interaction. HBHP significantly suppressed HMGB1-mediated neuronal cell death in primary cortical cultures and HMGB1/HBHP binding was detected in NMDA-conditioned culture media. However, a heptamer peptide composed of a scrambled sequence of the seven amino acids in HBHP failed to bind HMGB1 and had no protective effect. Furthermore, HBHP (300ng) delivered intranasally at 30min before MCAO significantly suppressed infarct volume in the postischemic rat brain (maximal reduction by 41.8±5.4%) and ameliorated neurological and behavioral deficits. In contrast, scrambled heptamer peptide had no protective effect at the same dose. Together these results suggest that intranasal HBHP ameliorates neuronal damage in the ischemic brain by binding HMGB1, which might inhibit the function of HMGB1 as an endogenous danger signal molecule. [Copyright &y& Elsevier]

Noninvasive intranasal drug administration has been noted to allow direct delivery of drugs to the brain. In the present study, the therapeutic efficacy of intranasal small interfering RNA (siRNA) delivery was investigated in the postischemic rat brain. Fluorescein isothiocyanate (FITC)-labeled control siRNA was delivered intranasally in normal adult rats using e-PAM-R, a biodegradable PAMAM dendrimer, as gene carrier. Florescence-tagged siRNA was found in the cytoplasm and processes of neurons and of glial cells in many brain regions, including the hypothalamus, amygdala, cerebral cortex, and striatum, in 1 hour after infusion, and the FITC-fluorescence was continuously detected for at least 12 hours. When siRNA for high mobility group box 1 (HMGB1), which functions as an endogenous danger molecule and aggravates inflammation, was delivered intranasally, the target gene was significantly depleted in many brain regions, including the prefrontal cortex and striatum. More importantly, intranasal delivery of HMGB1 siRNA markedly suppressed infarct volume in the postischemic rat brain (maximal reduction to 42.8 ± 5.6% at 48 hours after 60 minutes middle cerebral artery occlusion (MCAO)) and this protective effect was manifested by recoveries from neurological and behavioral deficits. These results indicate that the intranasal delivery of HMGB1 siRNA offers an efficient means of gene knockdown-mediated therapy in the ischemic brain. [ABSTRACT FROM AUTHOR]