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With the increasing demand for synthetic rubber, the purification of 1,3-butadiene (C4H6) is of great industrial significance. Herein, the successful removal of n-butene (n-C4H8) and iso-butene (iso-C4H8) from 1,3-butadiene (C4H6) was realized by synthesizing a novel TaOF52– anion-pillared ultramicroporous material TaOFFIVE-3-Ni (also referred to as ZU-96, TaOFFIVE = TaOF52–, 3 = pyrazine). Single-component adsorption isotherms show that TaOFFIVE-3-Ni can achieve the exclusion of n-C4H8 and iso-C4H8 in the low pressure region (0–30 kPa), and uptake C4H6 with a high capacity of 92.78 cm3·cm–3 (298 K and 100 kPa). The uptake ratio of C4H6/iso-C4H8 on TaOFFIVE-3-Ni was 20.83 (298 K and 100 kPa), which was the highest among the state-of-the-art adsorbents reported so far. With the rotation of anion and pyrazine ring, the pore size changes continuously, which makes smaller-size C4H6 enter the channel while larger-size n-C4H8 and iso-C4H8 are completely blocked. The excellent breakthrough performance of TaOFFIVE-3-Ni shows great potential in industrial separation of C4 olefins. The specific adsorption binding sites within ZU-96 was further revealed through the modeling calculation.

Optimization of mathematical model of flow field in slab continuous casting mold was performed by means of industrial measurement and mathematical modeling. The rod deflection method was used to quantitatively measure the velocities near the mold surface at high temperature. The measurement results were compared with the simulation results of three mathematical models at different argon gas flow rates of 6, 10 and 14 L min−1. The model 1 neglects the mold powder layer, thermal effect and solidified shell. The model 2 only considers the influence of mold powder layer. The model 3 considers the influence of mold powder layer, thermal effect and solidified shell on the flow field. In all three models, the diameter of argon bubbles obeys Rosin–Rammler distribution fitted according to the experimental data of others’ previous work. With increasing the argon gas flow rate, the velocity of liquid steel near the mold surface decreases. The model 1 seriously underestimates the shear stress of liquid steel near the mold surface, and its calculation results show higher velocity near the mold surface, lower turbulent kinetic energy and wider distribution of argon gas bubbles in the mold. The simulation results of model 2 only considering the viscous resistance of the mold powder layer to liquid steel makes the velocity near the surface lower than the measurement results obviously. The calculated velocities near the mold surface with model 3 are in best agreement with the measured results, showing the reasonable spatial distribution range of argon bubbles in the mold and the moderate turbulent kinetic energy. In the present conditions, the best argon gas flow rate is 10 L min−1 due to the moderate velocity near the mold surface, the appropriate distribution of argon gas bubbles in the mold and the smallest fluctuation amplitude on the mold surface.

Conductive metal-organic frameworks (MOFs) have a wide range of applications in supercapacitors, electrocatalysts, and fuel cells, while gas-driven conductive MOFs have not yet been synthesized so far. Herein, we report a gas-driven conductive MOF (A) constructed from calix[4]resorcinarene macrocycle and Co(II) cations, which shows the conductivity enhancement by about eight orders of magnitude through NO2 adsorption. The conductivities of MOF A before and after the adsorption of NO2 were calculated to be about 1.3 × 10-11 and 8.4 × 10-4 S/cm, respectively. MOF A realizes the conversion from an insulator to a conductor by adsorbing NO2. When NO2 is evacuated, MOF A quickly changes from a conductor back to an insulator in 42 s. In the crystal structure of NO2-adsorbed MOF (termed as A-NO2), NO2 molecule connects Co(II) and uncoordinated carboxylate groups through hydrogen-bonding interactions to form a conductive pathway, greatly reducing the electron transmission distance between each two metal clusters. In addition, NO2 molecule and H3O+ may also form a conductive pathway by hydrogen-bonding interactions. This work presents an interesting macrocycle-based MOF with a NO2-driven on/off conductivity switch, proving the possibility for designing advanced gas-driven conductive systems.

To investigate the relationship between retinal vascular parameters and cystatin C in patients with type 2 diabetes in northwestern China. This was a cross-sectional study of 1689 patients with type 2 diabetes. A validated fully automated computer program was used to extract retinal vascular parameters from the entire vascular tree. Multiple logistic regression analyses were conducted to investigate the relationship between these vascular measurements and cystatin C. For retinal vascular geometrical measurements, smaller arteriolar fractal dimension was related to high cystatin C after adjusting for multiple variables (odds ratio [OR] 0.149, 95% CI 0.042–0.532). For retinal vascular caliber measurements, narrower central and middle arteriolar calibers were related to high cystatin C after adjusting for multiple variables (central: OR 0.922, 95% CI 0.886–0.960; middle: OR 0.940, 95% CI 0.901–0.981). Wider central, middle and peripheral venular calibers were associated with high cystatin C after adjusting for multiple variables (central: OR 1.058, 95% CI 1.003–1.117; middle: OR 1.094, 95% CI 1.040–1.150; peripheral: OR 1.075, 95% CI 1.023–1.130). Multiple retinal vascular geometrical and caliber measurements are associated with cystatin C in type 2 diabetic patients. Further studies are needed to explore whether these retinal vascular changes can predict the incidence and progress of diabetic nephropathy.

Hydroliquefaction behavior of preasphaltenes, derived from direct coal liquefaction, was carried out in a 30 mL autoclave with FeS + S catalyst and tetralin at initial hydrogen of 5.0 MPa, residence time of 0–60 min and reaction temperature of 380–440°C in order to optimize the conditions of direct coal liquefaction and improve oil yield. The products distribution and kinetic parameters of preasphaltenes catalytic hydroliquefaction were investigated. A new kinetic model was established to simulate the preasphalteneshydroliquefaction catalyzed by FeS + S catalyst using lump kinetic model. It was found that preasphaltenes were hydroliquefaction into asphaltenes and char directly, and then asphaltenes were hydrocracked into oil + gas products. Regressive reactions of preasphaltenes to char and asphaltenes to preasphaltenes occurred at higher temperatures. Higher temperature and longer time were favorable for increasing the conversion of preasphaltenes and the oil + gas yield. The hydroliquefaction of preasphaltenes under 440°C and 60 min reached 79.45% with 34.7% of oil + gas yield. The hydroliquefaction conversions calculated from the model agreed well with the experimental data, and the activation energies ranged within 50–245 kJ/mol.

Background and aims 17-Beta hydroxysteroid dehydrogenase 13 (HSD17B13) is genetically associated with human nonalcoholic fatty liver disease (NAFLD). Inactivating mutations in HSD17B13 protect humans from NAFLD-associated and alcohol-associated liver injury, fibrosis, cirrhosis, and hepatocellular carcinoma, leading to clinical trials of anti-HSD17B13 therapeutic agents in humans. We aimed to study the in vivo function of HSD17B13 using a mouse model. Approach and results Single-cell RNA-sequencing and quantitative RT-PCR data revealed that hepatocytes are the main HSD17B13-expressing cells in mice and humans. We compared Hsd17b13 whole-body knockout (KO) mice and wild-type (WT) littermate controls fed regular chow (RC), a high-fat diet (HFD), a Western diet (WD), or the National Institute on Alcohol Abuse and Alcoholism model of alcohol exposure. HFD and WD induced significant weight gain, hepatic steatosis, and inflammation. However, there was no difference between genotypes with regard to body weight, liver weight, hepatic triglycerides (TG), histological inflammatory scores, expression of inflammation-related and fibrosis-related genes, and hepatic retinoid levels. Compared to WT, KO mice on the HFD had hepatic enrichment of most cholesterol esters, monoglycerides, and certain sphingolipid species. Extended feeding with the WD for 10 months led to extensive liver injury, fibrosis, and hepatocellular carcinoma, with no difference between genotypes. Under alcohol exposure, KO and WT mice showed similar hepatic TG and liver enzyme levels. Interestingly, chow-fed KO mice showed significantly higher body and liver weights compared to WT mice, while KO mice on obesogenic diets had a shift toward larger lipid droplets. Conclusions Extensive evaluation of Hsd17b13 deficiency in mice under several fatty liver-inducing dietary conditions did not reproduce the protective role of HSD17B13 loss-of-function mutants in human NAFLD. Moreover, mouse Hsd17b13 deficiency induces weight gain under RC. It is crucial to understand interspecies differences prior to leveraging HSD17B13 therapies.

On-site protein analysis is crucial for disease diagnosis in community and family medicine in which microfluidic paper-based analytical devices (μPADs) have attracted growing attention. However, the practical applications of μPADs in protein analysis for physiological samples with high complexity is still limited. Herein, we developed a three-dimensional (3D) paper-based isoelectric focusing (IEF) platform, which is composed of power supply, reservoirs, and separation channel and made by the origami and stacking method, to simultaneously separate and enrich proteins in both low-salt and high-salt samples. Under the optimized experimental conditions, standard proteins (bovine hemoglobin (BHb) and phycocyanin (Phy)) were separated within 18 min under a 36 V power supply and obtained a 10-fold enrichment using the 3D paper-based IEF platform. Then, the capability of the 3D paper-based IEF platform for direct pretreatment of high-salt samples using a 12 V battery as power supply was measured through separating three standard proteins in saline (0.9% NaCl) with separation resolution (SR) > 1.29. Through further coupling with colorimetric and lateral flow strip measurements, the 3D paper-based IEF platform was applied to directly pretreat and quantitatively analyze microalbuminuria and C-reactive proteins in clinical urine and serum samples with analytical results with relative deviations of

Low stability of photoanodes in electrolytes, especially in alkaline electrolytes, greatly limits their practical applications. Therefore, it is highly meaningful to develop a strategy to stabilize photoanodes under strongly alkaline conditions. Herein, a metal-free poly(p-phenylene pyromellitimide) film is coated onto a BiVO4 photoanode as a bifunctional catalyst layer and protective layer by in situ thermal polymerization. Structural characterization shows that the polymer film can effectively protect the BiVO4 semiconductor. Photoelectrochemical studies verify that the polymer film can improve the efficiency of the surface-reaching hole reaction and promote the separation of surface carriers. Thus, the polymer-coated photoanode shows a superior photoelectrochemical activity, which is 2.5 times higher than that of the pristine photoanode. Meanwhile, the polymer-coated photoanode also exhibits excellent stability in neutral and alkaline electrolytes. The photocurrent remains above 70% even after a six-hour reaction in a strongly alkaline electrolyte. This work provides a simple solution to stabilize semiconductor photoanodes under alkaline conditions for efficient photoelectrochemical applications.

Background & Aims: Liver fibrosis is a common consequence of chronic liver injury and is characterized by the accumulation of extracellular matrix mainly generated from activated hepatic stellate cells (HSCs). At present, the mechanisms underlying liver fibrogenesis remain obscure and effective pharmacological therapies are lacking. Neutrophil-specific microRNA-223 (miR-223) plays an important role in controlling the development of various liver diseases; however, its role in HSC activation and liver fibrosis remains unclear. Methods: Liver fibrosis was induced by chronic carbon tetrachloride (CCl4) injection of miR-223 knockout (miR-223KO) mice and littermate wild-type controls. MiR-223 was overexpressed in cultured HSCs to determine its function and targets during HSC activation and proliferation. The expression of miR-223 and pri-miR-223 was examined in primary HSCs isolated from CCl4-treated mice and in cultured HSCs. The communication between HSCs and neutrophils was studied by performing in vitro co-culture experiments. Results: Genetic deletion of miR-223 exacerbated chronic CCl4-induced liver fibrosis. Administration of miR-223 inhibited liver fibrosis by inhibiting the transcriptional coactivator with PDZ-binding motif (TAZ)-Indian hedgehog (IHH)-GLI Family Zinc Finger 2 (GLI2) pathway via the crosstalk between hepatocytes and HSCs. Overexpression of miR-223 also directly attenuated Gli2 as well as platelet-derived growth factor receptor α/β (Pdgfra/b) expression in HSCs, thereby suppressing HSC activation and proliferation. The expression of pri-miR-223 and miR-223 was downregulated during HSC activation in vitro. Expression of pri-miR-223 was also decreased in activated HSCs in vivo in fibrotic livers but mature miR-223 expression was not reduced. Finally, in co-culture experiments, activated HSCs were able to take up miR-223-enriched extracellular vesicles from neutrophils, resulting in elevation of miR-223. Conclusion: MiR-223 restricts liver fibrosis by targeting multiple genes in hepatocytes and HSCs, providing potential therapeutic targets for the treatment of liver fibrosis.

Background: Spectrin, beta, non-erythrocytic 1 (SPTBN1), an adapter protein for transforming growth factor beta (TGF-β) signaling, is recognized as a tumor suppressor in the development of hepatocellular carcinoma (HCC); however, the underlying molecular mechanisms of this tumor suppression remain obscure. Methods: The effects on expression of pro-inflammatory cytokines upon the inhibition or impairment of SPTBN1 in HCC cell lines and liver tissues of Sptbn1+/- and wild-type (WT) mice were assessed by analyses of quantitative real-time reverse-transcription polymerase chain reaction (QRT-PCR), enzyme linked immunosorbent assay (ELISA), Western blotting and gene array databases from HCC patients. We investigated the detailed molecular mechanisms underlying the inflammatory responses by immunoprecipitation-Western blotting, luciferase reporter assay, chromatin immunoprecipitation quantitative real time PCR (ChIP-qPCR), immunohistochemistry (IHC) and electrophoretic mobility shift assay (EMSA). The proportion of myeloid-derived suppressor cells in liver, spleen, bone marrow and peripheral blood samples from WT and Sptbn1+/- mice were measured by fluorescence-activated cell sorting (FACS) analysis. Further, the hepatocacinogenesis and its correlation with inflammatory microenvironment by loss of SPTBN1/SOCS1 and induction of p65 were analyzed by treating WT and Sptbn1+/- mice with 3,5-diethoxycarbonyl-1,4-dihydrocollidine (DDC). Results: Loss of SPTBN1 in HCC cells upregulated the expression of pro-inflammatory cytokines including interleukin-1α (IL-1α), IL-1β, and IL-6, and enhanced NF-κB transcriptional activation. Mechanistic analyses revealed that knockdown of SPTBN1 by siRNA downregulated the expression of suppressor of cytokine signaling 1 (SOCS1), an E3 ligase of p65, and subsequently upregulated p65 accumulation in the nucleus of HCC cells. Restoration of SOCS1 abrogated this SPTBN1 loss-associated elevation of p65 in HCC cells. In human HCC tissues, SPTBN1 gene expression was inversely correlated with gene expression of IL-1α, IL-1β and IL-6. Furthermore, a decrease in the levels of SPTBN1 gene, as well as an increase in the gene expression of IL-1β or IL-6 predicted shorter relapse free survival in HCC patients, and that HCC patients with low expression of SPTBN1 or SOCS1 protein is associated with poor survival. Heterozygous loss of SPTBN1 (Sptbn1+/- ) in mice markedly upregulated hepatic expression of IL-1α, IL-1β and IL-6, and elevated the proportion of myeloid-derived suppressor cells (MDSCs) and CD4+CD25+Foxp3+ regulatory T cells (Foxp3+Treg) cells in the liver, promoting hepatocarcinogenesis of mouse fed by DDC. Conclusions: Our findings provided evidence that loss of SPTBN1 in HCC cells increases p65 protein stability via the inhibition of SOCS1 and enhances NF-κB activation, stimulating the release of inflammatory cytokines, which are critical molecular mechanisms for the loss of SPTBN1-induced liver cancer formation. Reduced SPTBN1 and SOCS1 predict poor outcome in HCC patients.

A single-crystal BiVO4 photoanode with a surface nanostructure is prepared by a low-cost and simple etching process. As a result, the modified photoanode shows a higher photocurrent density and a lower onset potential, which is because of the larger electrochemical active surface area and abundant oxygen vacancies on the surface.

Most of the photocathode semiconductors that can be used for hydrogen production are difficult to prepare or get corroded in the electrolyte of an aqueous solution. Hence it is a huge challenge to develop stable photoelectrochemical (PEC) hydrogen evolution systems. Perovskite-type LaFeO3, as a new p-type semiconductor, is used in the PEC hydrogen evolution reaction and shows excellent stability. We synthesized a high-purity LaFeO3 nanorod array on an FTO substrate and its bandgap is 2.14 eV. Moreover, the carrier migration efficiency of a LaFeO3 photocathode is improved by doping with Li ions, and the doping effect also causes a red-shift of the optical maximum absorption edge. As a result, the photocurrent density of the Li-doped LaFeO3 photocathode is increased from −30 μA cm−2 (LaFeO3) to −50 μA cm−2 at 0.4 V (vs. RHE). Herein, the Li-doped LaFeO3 show great potential as a PEC photocathode for achieving an efficient, stable and inexpensive PEC hydrogen evolution reaction.

The hybrid lithium oxygen batteries (LOBs) have been limited by the sluggish electrochemical catalytic performance towards both oxygen reduction (ORR) and oxygen evolution reaction (OER). Previous research has utilizing the light illumination to promote the charge process in non-aqueous electrolyte. However, the organic electrolyte has been blamed for the poor electrochemical stability and volatilization during illumination. For the first time, photo-enhanced aqueous LOBs have been promoted, where the reaction mechanism of OER is familiar with photo electrochemical (PEC) water-oxidation. The α-Fe2O3 nanorods and BiVO4 nanoplates are synthesized by the hydrothermal method combined with heat treatment, showing good photo-electrocatalytic property. Herein, the α-Fe2O3 electrode exhibits a superior longtime stability than the BiVO4 nanoplates, which suffer from the severe photo-corrosion. The photo-assisted hybrid Li–O2 battery based on α-Fe2O3 electrode is realized with a discharge potential of 2.56 ​V. Compared with the traditional hybrid LOBs, the charge potential is reduced from 3.96 ​V to 3.15 ​V. This work indicates that most n-type semiconductors used in PEC water-oxidation can have positive effect on the charge process in hybrid LOBs.

Aim The aim of this study was to evaluate amino acids as glucagon receptor (GCGR)-specific biomarkers in rodents and cynomolgus monkeys in the presence of agonism of both glucagon-like peptide-1 receptor (GLP1R) and GCGR with a variety of dual agonist compounds. Materials and methods Primary hepatocytes, rodents (normal, diet-induced obese and GLP1R knockout) and cynomolgus monkeys were treated with insulin (hepatocytes only), glucagon (hepatocytes and cynomolgus monkeys), the GLP1R agonist, dulaglutide, or a variety of dual agonists with varying GCGR potencies. Results A long-acting dual agonist, Compound 2, significantly decreased amino acids in both wild-type and GLP1R knockout mice in the absence of changes in food intake, body weight, glucose or insulin, and increased expression of hepatic amino acid transporters. Dulaglutide, or a variant of Compound 2 lacking GCGR agonism, had no effect on amino acids. A third variant with ~31-fold less GCGR potency than Compound 2 significantly decreased amino acids, albeit to a significantly lesser extent than Compound 2. Dulaglutide (with saline infusion) had no effect on amino acids, but an infusion of glucagon dose-dependently decreased amino acids on the background of GLP1R engagement (dulaglutide) in cynomolgus monkeys, as did Compound 2. Conclusions These results show that amino acids are sensitive and translatable GCGR-specific biomarkers.

Bio-organic–chemical fertilizer (BCF) has great potential to enhance agricultural production, protect environment, and improve sustainability. However, current BCFs are used only in a limited scope mainly due to the low activity of beneficial bacteria. It is significant to develop new BCFs with high beneficial bacteria activity for sustainable agricultural production. In this study, a novel slow-release bio-organic–chemical fertilizer (SBCF) was prepared from activated lignite, bacillus AMCC100153 (B153) (beneficial bacteria for tomato), and slow-release fertilizer (CSF) with suitable pH and low dissolubility salt content (to protect the bacterial activity). The pH and EC of different types of SBCFs with different compositions were determined and compared with those of BCFs derived from common chemical fertilizers (BCCF). The B153 activities were measured and compared with the optimum formula of SBCF. The bacillus colonization rules of SBCF and BCCF in tomato pot soil were explored by the Real-time qPCR. SBCF had higher bacillus activity than the corresponding BCCF. Pot experiments also showed that the bacillus formed colonization rapidly on tomato roots and secreted substances to promote root growth. The HPLC analysis found that the promoting substances were auxin and zeatin. Compared with no fertilizer control (CK) and the BCCF treatments, the SBCF treatment increased tomato yields by 73.08% and 29.04%, respectively. Findings of this work suggest that SBCF with high biological activity and growth promoting effect has great potential in agriculture production system in the future.

Thermal management has been considered as a key issue for high-power electronics. Thermal interface materials (TIMs) play an extremely important role in the field of thermal management. Owing to their excellent insulation, mechanical properties and low processing costs, functional polymers have become the popular candidate for preparing TIMs. In order to develop high thermally conductive TIMs, the inorganic fillers with high thermal conductivity are generally composited with polymers. For this purpose, some key technologies are needed to improve the dispersibility of fillers to reduce interfacial thermal resistance and increase thermal conduction channels. This paper reviews recent progresses on effective methods for improving thermal conductivity, which mainly include filler functionalization and processing, filler hybridization and coating, filler orientation and network. After implementing these strategies, the interfacial interaction between fillers and polymers, the synergy effect of different fillers and the thermal conduction pathway inside the matrix can be highly improved, hence enhancing the thermal conductivity of TIMs.

Realizing the reduction of N2 to NH3 at low temperature and pressure is always the unremitting pursuit of scientists and then electrochemical nitrogen reduction reaction offers an intriguing alternative. Here, we develop a feasible way, gamma irradiation, for constructing defective structure on the surface of WO3 nanosheets, which is clearly observed at the atomic scale by high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM). The abundant oxygen vacancies ensure WO3 nanosheets with a Faradaic efficiency of 23% at −0.3 V vs. RHE. Moreover, we start from the regulation of the surface state to suppress proton availability towards hydrogen evolution reaction (HER) on the active site and thus boost the selectivity of nitrogen reduction.

A memristor1 has been proposed as an artificial synapse for emerging neuromorphic computing applications2,3. To train a neural network in memristor arrays, changes in weight values in the form of device conductance should be distinct and uniform3. An electrochemical metallization (ECM) memory4,5, typically based on silicon (Si), has demonstrated a good analogue switching capability6,7 owing to the high mobility of metal ions in the Si switching medium8. However, the large stochasticity of the ion movement results in switching variability. Here we demonstrate a Si memristor with alloyed conduction channels that shows a stable and controllable device operation, which enables the large-scale implementation of crossbar arrays. The conduction channel is formed by conventional silver (Ag) as a primary mobile metal alloyed with silicidable copper (Cu) that stabilizes switching. In an optimal alloying ratio, Cu effectively regulates the Ag movement, which contributes to a substantial improvement in the spatial/temporal switching uniformity, a stable data retention over a large conductance range and a substantially enhanced programmed symmetry in analogue conductance states. This alloyed memristor allows the fabrication of large-scale crossbar arrays that feature a high device yield and accurate analogue programming capability. Thus, our discovery of an alloyed memristor is a key step paving the way beyond von Neumann computing.

With the goal of improving the removal of anionic contaminants, copper oxide (CuO)-modified biochar (BC) nanocomposites were successfully prepared through simply ball milling CuO particles with BC. The physicochemical properties of the fabricated CuO/BC nanocomposites were systematically characterized by a series of techniques; their adsorption performances were assessed, and the main adsorption mechanism was revealed. X-ray powder diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy analyses of the nanocomposites showed the strong interaction between CuO and BC and confirmed the success of the ball-milling syntheses. Because of strong electrostatic attraction between the embedded CuO nanoparticles and reactive red (RR120), the composited adsorbents exhibited excellent RR120 removal. The 10%-CuO/BC nanocomposite achieved the best RR120 removal efficiency (46%), which is much higher than that of pristine BC (20%). In addition, the adsorption was insensitive to the change of solution initial pH (4-10). The 10%-CuO/BC also showed fast adsorption kinetics (equilibrium time < 3 h) and extremely high adsorption capacity (Langmuir maximum capacity of 1399 mg g-1) to RR120 in aqueous solutions. Findings from this study demonstrate not only the strong feasibility of ball-milling synthesis of BC-based nanocomposites but also the promising potential of the CuO/BC nanocomposites to remove aqueous anionic contaminants.

Biochar functionalized with electroactive components is gaining increasing attention owing to its versatile redox roles and tuneable structural configurations. In this review, we summarise and highlight the electrochemical properties of biochar with various theoretical, methodological, and experimental approaches, and offer new perspectives on electrochemical carbocatalysis of biochar to guide future environmental applications. Electrochemical carbocatalysis is for the first time correlated with the synergistic effects among reactive-active moieties, metal contents, defective sites, heteroatom doping, and conductive graphitic surfaces within a manoeuvrable biochar framework for environmental interactions involving biochar. It is worth noting that milder redox reactions including the formation of surface-confined reactive complexes, singlet oxygenation, and direct electron transfer can be properly introduced with specific protocols, thus minimizing undesirable carbon oxidation and enhancing reaction sustainability. Overall, this review presents future research directions on the mechanistic aspects of electroactive components on biochar to facilitate its applications in sustainable carbocatalysis and green chemistry.

A BiVO4 photoanode was combined with bioinspired Mn4O4-cubane, which has a structure and composite similar to those of the oxygen-evolving complex (Mn4CaO5) in photosystem II. The hybrid photoanode exhibited a lower onset potential and higher photocurrent than the pristine photoanode because of the faster kinetics of the reaction and reduced rate of recombination of the carriers.

Bioreducible cationic polymers have gained considerable attention in gene delivery due to their low cytotoxicity and high efficiency. In the present work, we reported a cationic polymer, poly(disulfide-l-lysine)-g-agmatine (denoted as SSL-AG), and evaluated its ability to transfer pEGFP-ZNF580 plasmid (pZNF580) into human umbilical vein endothelial cells (HUVECs). This SSL-AG polymeric carrier efficiently condensed pZNF580 into positively charged particles (

The highly efficient treatment of azo dye contaminated wastewater from the textile industry is an important but challenging problem. Herein, polydimethylsiloxane (PDMS) microparticles, incorporating multiple-walled carbon nanotubes/titanium dioxide (MWCNTs/TiO2) nanocomposites, were successfully synthesized to treat wastewater containing Rhodamine B (RhB) dyes in a synergetic approach, by combining sorption and photocatalytic degradation. The surfactant wrapping sol–gel method was applied to synthesize MWCNTs/TiO2 nanocomposites with TiO2 nanoparticles evenly distributed on the surface of the MWCNTs. The PDMS microparticles were fabricated with an oil-in-water (O/W) single emulsion template, using needle-based microfluidic devices. MWCNTs/TiO2 nanocomposites (at a weight ratio of 1%, and 2%, respectively) were mixed with the PDMS precursor as the dispersed phase, and an aqueous solution of polyvinyl alcohol (PVA) was used as the continuous phase. Highly monodispersed microparticles, with average diameters of 692.7 μm (Coefficient of Variation, CV = 0.74%) and 678.3 μm (CV = 1.04%), were formed at an applied flow rate of the dispersed and continuous phase of 30 and 200 μL min−1, respectively. The fabricated hybrid microparticles were employed for the treatment of RhB, involving a dark equilibrium for 5 hours and UV irradiation for 3 hours. The experimental conditions of applied PDMS type, mass loading amount, treatment duration, photodegradation kinetics, initial concentration of pollutants and environmental pH values were investigated in this work. The PDMS microparticles with 2 wt% MWCNTs/TiO2 nanocomposites can exhibit a removal efficiency of 85%. Remarkably, an efficiency of 70% can be retained after the microparticles have been recycled and reused for 3 cycles. The PDMS–MWCNTs/TiO2 microparticles possess a superior performance over conventional treatment approaches for dye contaminated wastewater, especially in recyclability and the prevention of secondary pollution. This work provides a feasible and eco-friendly route for developing an efficient and low-cost microfluidic method for treating complicated water environmental systems.

Although the treatment of burn wounds has made great progress, the incidence of wound infection is still the main cause of high mortality. In this study, a silk fibroin (SF) scaffold wound dressing incorporated with Gentamicin Sulfate (GS) was developed for the treatment of burn infected wounds, in which GS was used as anti-bacterial agent. GS was mixed with silk fibroin solution and then processed into GS-SF composite scaffold via electro-spinning. The results showed the scaffold exhibited uniform polyporous morphology with 80% porosity. Induced by methanol, the scaffold presented much improved mechanical properties and stability to protease XIV. More important, the scaffold presented significant growth inhibition on both Gram-positive (Staphylococcus aureus) and Gram-negative (Pseudomonas aeruginosa and Escherichia coli) bacteria.

Polymeric nano-carriers have been developed as a most capable and feasible technology platform for gene therapy. As vehicles, polymeric nano-carriers are obliged to possess high gene loading capability, low immunogenicity, safety, and the ability to transfer various genetic materials into specific sites of target cells to express therapeutic proteins or block a process of gene expression. To this end, various types of polymeric nano-carriers have been prepared to release genes in response to stimuli such as pH, redox, enzymes, light and temperature. These stimulus-responsive nano-carriers exhibit high gene transfection efficiency and low cytotoxicity. In particular, dual- and multi-stimulus-responsive polymeric nano-carriers can respond to a combination of signals. Markedly, these combined responses take place either simultaneously or in a sequential manner. These dual-stimulus-responsive polymeric nano-carriers can control gene delivery with high gene transfection both in vitro and in vivo. In this review paper, we highlight the recent exciting developments in stimulus-responsive polymeric nano-carriers for gene delivery applications.

Biochar, a low-cost porous carbonaceous adsorbent, has low adsorption capacity for anion contaminants. The objective of this study was to improve biochar's ability to adsorb phosphorus (P) through polyethyleneimine (PEI) modification to form an amine-functionalized biochar. Biochars prepared by pyrolysis of bamboo biomass, before and after PEI modification, were characterized using the Fourier transformed infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), elemental analysis, and batch sorption experiments. The effects of pH, coexisting anions, and ionic strength on P adsorption by PEI-modified biochar were also investigated. Results indicated that PEI was successfully grafted onto biochar which resulted an increase in surface amine group and in P adsorption. The peak of P adsorption occurred at pH of three and adsorption of P was decreased with increasing of ionic strength and when coexisting ions, such as HCO3-, SO42-, NO3-, and Cl-, were coexisted. The electrostatic interaction between P and surface functional groups of PEI-modified biochar served as the primary mechanism controlling the adsorption process. These results indicate that chemically functionalized biochar with amine groups can enhance P adsorption.

Per- and polyfluoroalkyl substances (PFASs) are commonly used in many consumer and industrial products. However, their resulting widespread release into aqueous environments and their potential tox...

Crops grow poorly in saline-sodic soils, and the productivity of these soils can be dramatically improved with proper amendments. Current research mainly focuses on either organic or inorganic soil amendments, whereas few studies address options of combining organic and inorganic amendments. The objective of this study was to develop new organic and inorganic soil amendments which can lower the soil pH, replace sodium, and improve soil structure. Polyhalite (PL), microporous potassium-silicon-calcium mineral fertilizer (MF), furfural residue (FR), and fulvic acid (FA) were mixed with four different ratios to produce organic and inorganic soil amendments: PLFR, PLFA, MFFR, and MFFA. And their optimum mixing ratios were determined by comparing the potassium, calcium concentrations, and pH of filtrate after dissolution. Then, a leaching experiment was conducted by packing mixtures (mass ratio of soil to amendment = 219:1, equivalent to 13 t/hm2) of the saline-sodic soil with each one of these amendments plus two contrasts, gypsum (GP), and no amendment (CK). And the remediation effect was compared by pH, EC, ESP, texture, organic recombination degree of clay, saturated hydraulic conductivity, water-stable aggregates fraction, and enzyme (urease, alkaline phosphatase, and catalase) activities of soil. After four times leaching experiment, soil treated with PLFR had lower pH and 25.86% lower exchangeable sodium than untreated soils. The water-stable small macroaggregate fractions and saturated hydraulic conductivity of the MFFR-treated soils were significantly increased by 133% and 31%, respectively. Also, the total soil and heavy fraction organic carbons of the soils treated with MFFR in addition to its alkaline phosphatase activity were all significantly higher than the other treatments. The results revealed that MFFR has more potential as a soil amendment to improve soil structure and quality and thus help in the development and use of saline-sodic lands for agriculture.

It was found that polyurea coating could improve the integrity and the corresponding durability of the structural components. However, the strengthening effect of polyurea coatings for structures built with emerging ultra-high-performance concrete (UHPC) is still unknown due to the lack of studies. Therefore, this paper investigated the effect of the polyurea coating on the lateral impact resistance of UHPC columns through a combined numerical and experimental study. A total of five specimens were fabricated, including two UHPC columns and three UHPC columns with polyurea coating. To better characterize the structural response under dynamic loading, impact cases with different drop weight impact heights and axial force ratios were employed. The results showed that the UHPC column with polyurea coating exhibited superior lateral impact resistance compared to the UHPC column. The presence of the axial force increased the lateral impact stiffness and further reduced the deflection of the specimen. In contrast, the polyurea coating improved the specimen’s ductility and mitigated the peak impact force, thereby maintaining the specimen’s integrity without sudden shear failure. A three-dimensional finite element (FE) model of polyurea-coated UHPC columns under impact loading was then established and confirmed the experimental results. With the validated FE model, an intensive parametric study was conducted to investigate the effects of polyurea thickness, axial force ratio and impact energy on the lateral impact resistance of the UHPC column. The presence of the polyurea coating could significantly improve the lateral impact resistance of the specimen, thereby preventing the shear failure of the UHPC column, and thus, the effective thickness of the polyurea layer for the UHPC column was determined to be 2–6[Formula: see text]mm. The outcome of this research demonstrates the great merits of polyurea coating in improving the ductility and integrity of the UHPC column under lateral impact loading.

Detection of biomarkers associated with body conditions provides in‐depth healthcare information and benefits to disease management, where the key challenge is to develop a minimally invasive platform with the ability to directly detect multiple biomarkers in body fluid. Dermal tattoo biosensor holds the potential to simultaneously detect multiple health‐related biomarkers in skin interstitial fluid because of the features of minimal invasion, easy operation, and equipment‐free result reading. Herein, a colorimetric dermal tattoo biosensor fabricated by a four‐area segmented microneedle patch is developed for multiplexed detection of health‐related biomarkers. The biosensor exhibits color changes in response to the change of biomarker concentration (i.e., pH, glucose, uric acid, and temperature), which can be directly read by naked eyes or captured by a camera for semi‐quantitative measurement. It is demonstrated that the colorimetric dermal tattoo biosensor can simultaneously detect multiple biomarkers in vitro, ex vivo, and in vivo, and monitor the changes of the biomarker concentration for at least 4 days, showing its great potential for long‐term health monitoring., Simultaneous detection of multiple biomarkers provides in‐depth healthcare information, where the key challenge is to develop a minimally invasive platform. To this end, a colorimetric dermal tattoo biosensor fabricated by a four‐area segmented microneedle patch is developed. The biosensor exhibits color changes in response to biomarker concentration variations, showing its great potential for health monitoring.

Objective: Kidney renal clear cell carcinoma (KIRC) is a common cancer with high morbidity and mortality in renal cancer. Thus, the transcriptome data of KIRC patients in The Cancer Genome Atlas (TCGA) database were analyzed and drug candidates for the treatment of KIRC were explored through the connectivity map (CMap) database. Methods: The transcriptome data of KIRC patients were downloaded from TCGA database, and KIRC-associated hub genes were screened out through differential analysis and protein-protein interaction (PPI) network analysis. Afterward, the CMap database was used to select drug candidates for KIRC treatment, and the drug-targeted genes were obtained through the STITCH database. A PPI network was constructed by combining drug-targeted genes with hub genes that affected the pathogenesis of KIRC to obtain final hub genes. Finally, combining hub genes and KIRC-associated hub genes, the pathways affected by drugs were explored by pathway enrichment analysis. Results: A total of 2,312 differentially expressed genes were found in patients, which were concentrated in immune cell activity, cytokine, and chemokine secretion pathways. Drug screening disclosed 5 drug candidates for KIRC treatment: fedratinib, Ly344864, geldanamycin, AS-605240, and luminespib. Based on drug-targeted genes and KIRC-associated hub genes, 16 hub genes were screened out. Pathway enrichment analysis revealed that drugs mainly affected pathways such as neuroactive ligand pathways, cell adhesion, and chemokines. Conclusion: The above results indicated that fedratinib, LY 344864, geldanamycin, AS-605240, and luminespib could be used as candidates for KIRC therapy. The findings from this study will make contributions to the treatment of KIRC in the future.

Kupffer cells (KCs), which are liver-resident macrophages, originate from the fetal yolk sac and represent one of the largest macrophage populations in the body. However, the current data on the origin of the cells that restore macrophages during liver injury and regeneration remain controversial. Here, we address the question of whether liver macrophage restoration results from circulating monocyte infiltration or local KC proliferation in regenerating livers after partial hepatectomy (PHx) and uncover the underlying mechanisms. By using several strains of genetically modified mice and performing immunohistochemical analyses, we demonstrated that local KC proliferation mainly contributed to the restoration of liver macrophages after PHx. Peak KC proliferation was impaired in Il6-knockout (KO) mice and restored after the administration of IL-6 protein, whereas KC proliferation was not affected in Il4-KO or Csf2-KO mice. The source of IL-6 was identified using hepatocyte- and myeloid-specific Il6-KO mice and the results revealed that both hepatocytes and myeloid cells contribute to IL-6 production after PHx. Moreover, peak KC proliferation was also impaired in myeloid-specific Il6 receptor-KO mice after PHx, suggesting that IL-6 signaling directly promotes KC proliferation. Studies using several inhibitors to block the IL-6 signaling pathway revealed that sirtuin 1 (SIRT1) contributed to IL-6-mediated KC proliferation in vitro. Genetic deletion of the Sirt1 gene in myeloid cells, including KCs, impaired KC proliferation after PHx. In conclusion, our data suggest that KC repopulation after PHx is mainly driven by local KC proliferation, which is dependent on IL-6 and SIRT1 activation in KCs.

The widespread usage of per- and polyfluoroalkyl substances (PFASs) has led to their ubiquitous co-existence with hydrocarbon surfactants in the subsurface environment. In this study, column experiments were conducted to investigate the effect of an anionic hydrocarbon surfactant (sodium dodecylbenzene sulfonate, SDBS, 1 and 10 mg/L) on the transport of perfluorooctanoic acid (PFOA) in two saturated natural soils under different cation type (Na+ and Ca2+) conditions. Results showed that SDBS (10 mg/L) significantly enhanced the transport of PFOA in two soils. This was likely because SDBS had a stronger adsorption affinity to the soils than PFOA, and can outcompete PFOA for the finite adsorption sites on the soil surface. The effect of SDBS on PFOA transport varied greatly in the two soils. More negatively charged soil surface and greater soil particle size likely contributed to the more noticeable transport-enhancement of PFOA resulting from the presence of SDBS. Also, the enhancement effect of SDBS (10 mg/L) with Ca2+ on PFOA transport was more significantly than that with Na+. This was possibly due to the blocking effect of SDBS to the more positively charged soil surface induced by Ca2+. Findings of this study point out the importance of anionic hydrocarbon surfactants on PFOA transport when assessing its environmental risks and implementing remediation efforts.

Alcohol consumption is associated with gut dysbiosis, increased intestinal permeability, endotoxemia, and a cascade that leads to persistent systemic inflammation, alcoholic liver disease, and other ailments. Craving for alcohol and its consequences depends, among other things, on the endocannabinoid system. We have analyzed the relative role of central vs. peripheral cannabinoid CB1 receptors (CB1R) using a “two-bottle” as well as a “drinking in the dark” paradigm in mice. The globally acting CB1R antagonist rimonabant and the non-brain penetrant CB1R antagonist JD5037 inhibited voluntary alcohol intake upon systemic but not upon intracerebroventricular administration in doses that elicited anxiogenic-like behavior and blocked CB1R-induced hypothermia and catalepsy. The peripherally restricted hybrid CB1R antagonist/iNOS inhibitor S-MRI-1867 was also effective in reducing alcohol consumption after oral gavage, while its R enantiomer (CB1R inactive/iNOS inhibitor) was not. The two MRI-1867 enantiomers were equally effective in inhibiting an alcohol-induced increase in portal blood endotoxin concentration that was caused by increased gut permeability. We conclude that (i) activation of peripheral CB1R plays a dominant role in promoting alcohol intake and (ii) the iNOS inhibitory function of MRI-1867 helps in mitigating the alcohol-induced increase in endotoxemia.

Coronavirus Disease 2019 (COVID−19) elicited by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS−CoV−2) is calling for novel targeted drugs. Since the viral entry into host cells depends on specific interactions between the receptor−binding domain (RBD) of the viral Spike protein and the membrane−bound monocarboxypeptidase angiotensin converting enzyme 2 (ACE2), the development of high affinity RBD binders to compete with human ACE2 represents a promising strategy for the design of therapeutics to prevent viral entry. Here, we report the discovery of such a binder and its improvement via a combination of computational and experimental approaches. The binder micasin, a known fungal defensin from the dermatophytic fungus Microsporum canis with antibacterial activity, can dock to the crevice formed by the receptor−binding motif (RBM) of RBD via an extensive shape complementarity interface (855.9 Å2 in area) with numerous hydrophobic and hydrogen−bonding interactions. Using microscale thermophoresis (MST) technique, we confirmed that micasin and its C−terminal γ−core derivative with multiple predicted interacting residues exhibited a low micromolar affinity to RBD. Expanding the interface area of micasin through a single point mutation to 970.5 Å2 accompanying an enhanced hydrogen bond network significantly improved its binding affinity by six−fold. Our work highlights the naturally occurring fungal defensins as an emerging resource that may be suitable for the development into antiviral agents for COVID−19.

A novel one-pot synthesis method was developed to prepare modified hydrochar by co-hydrothermal carbonization of waste distillers grains using low-cost clay minerals (attapulgite or vermiculite). The loading of the clay minerals onto hydrochar surfaces altered the structure and surface composition of the hydrochar such that the clay-modified hydrochars showed better ability to adsorb methylene blue and phosphate in aqueous solution than the pristine hydrochar. The maximum methylene blue and phosphate adsorption capacities of the modified hydrochar reached 340.3 and 96.9 mg g−1, respectively, comparable or higher than that of many commercial sorbents. Multiple mechanisms, including electrostatic attraction, ion exchange, complexation, and physical adsorption, controlled the adsorption process. These results highlight excellent potential for distillers grains-derived hydrochar-clay composites as an environmental sorbent, capable of removing a variety of contaminants from aqueous solutions.