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Nickel molybdate (NiMoO4) attracts superior hydrogen desorption behavior but noticeably poor for efficiently driving the hydrogen evolution reaction (HER) in alkaline media due to the sluggish water dissociation step. Herein, we successfully accelerate the water dissociation kinetics of NiMoO4 for prominent HER catalytic properties via simultaneous in situ interfacial engineering with molybdenum dioxide (MoO2) and doping with phosphorus (P). The as-synthesized P-doped NiMoO4/MoO2 heterostructure nanorods exhibit outstanding HER performance with an extraordinary low overpotential of −23 mV at a current density of 10 mA cm−2, which is highly comparable to the performance of the state-of-art Pt/C coated on nickel foam (NF) catalyst. The density functional theory (DFT) analysis reveals the enhanced performance is attributed to the formation of MoO2 during the in situ epitaxial growth that substantially reduces the energy barrier of the Volmer pathway, and the introduction of P that provides efficient hydrogen desorption of NiMoO4. This present work creates valuable insight into the utilization of interfacial and doping systems for hydrogen evolution catalysis and beyond.

The immune checkpoint blockade therapy has profoundly revolutionized the field of cancer immunotherapy. However, despite great promise for a variety of cancers, the efficacy of immune checkpoint inhibitors is still low in colorectal cancer (CRC). This is mainly due to the immunosuppressive feature of the tumor microenvironment (TME). Emerging evidence reveals that certain chemotherapeutic drugs induce immunogenic cell death (ICD), demonstrating great potential for remodeling the immunosuppressive TME. In this study, the potential of ginsenoside Rg3 (Rg3) as an ICD inducer against CRC cells was confirmed using in vitro and in vivo experimental approaches. The ICD efficacy of Rg3 could be significantly enhanced by quercetin (QTN) that elicited reactive oxygen species (ROS). To ameliorate in vivo delivery barriers associated with chemotherapeutic drugs, a folate (FA)-targeted polyethylene glycol (PEG)-modified amphiphilic cyclodextrin nanoparticle (NP) was developed for co-encapsulation of Rg3 and QTN. The resultant nanoformulation (CD-PEG-FA.Rg3.QTN) significantly prolonged blood circulation and enhanced tumor targeting in an orthotopic CRC mouse model, resulting in the conversion of immunosuppressive TME. Furthermore, the CD-PEG-FA.Rg3.QTN achieved significantly longer survival of animals in combination with Anti-PD-L1. The study provides a promising strategy for the treatment of CRC., Graphical abstract A folate-targeted PEGylated cyclodextrin-based nanoparticle was developed for co-delivery of Rg3 and QTN. The combination of the resultant co-formulation and anti-PD-L1 antibody achieved chemo-immunotherapy for colorectal cancer.Image 1

A new catalyst for both water reduction and oxidation, based on an infinite chain, {[Ni(tn)2]3 [Fe(CN)4 (μ-CN)2]2}n, is formed by the reaction of NiCl2, 1,3-propanediamine (tn) and K3 [Fe(CN)6]. {[Ni(tn)2]3 [Fe(CN)4 (μ-CN)2]2}n can electro-catalyze hydrogen evolution from a neutral aqueous buffer (pH 7.0) with a turnover frequency (TOF) of 1561 mol of hydrogen per mole of catalyst per hour (H2/mol catalyst/h) at an overpotential (OP) of 837 mV {[Ni(tn)2]3 [Fe(CN)4 (μ-CN)2]2}n also can electro-catalyze O2 production from water with a TOF of ∼45 mol O2 (mol cat)−1s−1 at an OP of 591 mV. Under blue light (λ = 469 nm), together with CdS nanorods (CdS NRs) as a photosensitizer, and ascorbic acid (H2A) as a sacrificial electron donor, {[Ni(tn)2]3 [Fe(CN)4 (μ-CN)2]2}n can photo-catalyze hydrogen generation from an aqueous buffer (pH 4.0) with a turnover number (TON) of 11,450 mol H2 per mole of catalyst (mol of H2 (mol of cat)−1) during 10 h irradiation. The average of apparent quantum yield (AQY) is as high as 40.96% during 10 h irradiation. Studies indicate that {[Ni(tn)2]3 [Fe(CN)4 (μ-CN)2]2}n exists in two forms: a cyano-bridged chain ({[Ni(tn)2]3 [Fe(CN)4 (μ-CN)2]2}n) in solid, and a salt ([Ni(tn)2]3 [Fe(CN)6]2) in aqueous media; Catalytic reaction occurs on the nickel center of [Ni(tn)2]2+, and the introduction of [Fe(CN)6]3- can improve the catalytic efficiency of [Ni(tn)2]2+ for H2 or O2 generation. We hope these findings can afford a new method for the design of catalysts for both water reduction and oxidation.

In order to obtain a lignin-based adsorbent with low cost, simple operation and no further modification, a calcium lignin adsorbent was prepared from chemical mechanical pulping (CMP) waste liquor by directly calcification from lime. The calcium lignin was characterized by BET, SEM, TEM, FT-IR and solid-state NMR analyses. The results showed that the molecular structure of the calcium lignin particles did not change when compared to sodium lignin, the formation mechanism of calcium lignin was revealed. The initial COD and lignin contents of CMP waste liquid were 54858 mg/L and 24.39 g/L, the conversion rate of lignin can reach 71.36% when was deal with lime. Thus, most of the lignin resources in the waste liquid were recovered. The middle-stage wastewater (MSWW) of pulping and papermaking was dealt with calcium lignin, the COD removal rate was up to 85.83%. The adsorption isotherms and kinetics were well fitted by the Langmuir model and pseudo-second-order kinetic model, respectively. Lime was regenerated from the used calcium lignin with high-temperature calcination, the conversion rate of calcium ions can reach 83.56%. Overall, the calcium lignin prepared by the one-step method exhibited great potential for effectively removing COD from middle-stage wastewater.

Background/purpose: Pyroptosis is a form of programmed cell death dependent on the activation of caspase-1. Porphyromonas gingivalis (P. gingivalis) is a major pathogenic bacterium in periodontitis and its lipopolysaccharide (LPS) can trigger inflammation. However, whether P. gingivalis-LPS affects epithelial connections or triggers pyroptosis in the gingival epithelium is unknown. Materials and methods: Gingival samples from human donors were collected and the expression levels of E-cadherin, nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3), caspase-1/4/5, interleukin (IL)-18, and IL-1β were examined. P. gingivalis-LPS was injected into rat gingival sulcus to establish gingivitis models, and the expression levels of E-cadherin, NLRP3, caspase-1/11, IL-18, and IL-1β were compared via immunohistochemistry. The mRNA levels of E-cadherin, caspase-1, IL-18, and IL-1β were evaluated in oral mucosa epithelial cells (OMECs) and rat gingival tissues. Results: In the present study, NLRP3 (p

The growth of Zn dendrites and self-corrosion reaction during electrochemical cycling is a long-standing issue impeding the practical application of zinc-ion batteries. Although various surface engineering strategies have shown great promise in suppressing zinc dendrites, the protective layers unavoidably hinder Zn2+ diffusion, resulting in increased internal impedance/polarization. Therefore, constructing smart interface protective layers with fast Zn2+ transfer kinetics is highly desirable but remains a key challenge. Here, an Mg-Al layered double hydroxide (LDH)-based artificial solid electrolyte interface (SEI) with Zn-ion diffusion channels is proposed. The well-aligned interlayer channels in the Mg-Al LDH skeleton is proved to efficiently engineer the distribution of Zn2+ ions and facilitate Zn2+ diffusion between the electrode/electrolyte interface, thus giving rise to stable Zn deposition. Moreover, the mechanically robust Mg-Al LDH artificial SEI acts as an interfacial layer to constrain H2O-induced corrosion and hydrogen evolution reaction. Consequently, the Mg-Al LDH artificial SEI improves the Coulombic efficiency to 99.2% for more than 2000 cycles, and an ultralong lifespan of 1400 h has been achieved at 0.5 mA cm−2. Notably, the zinc-ion capacitors by pairing the Zn@LDH anode and high-loading active carbon cathode deliver outstanding cycling stability with a high capacity retention of 93.7% up to 10000 cycles at the high areal current density of 37.5 mA cm−2, portending the feasibility of practical applications.

Purpose The application of fungicides is one of the main strategies to prevent clubroot disease. Currently, numerous studies focus on changes in the soil microbial community at different levels of clubroot disease severity. However, the effects of fungicides on the soil microbial community and causative pathogen, Plasmodiophora brassicae, while preventing clubroot disease remain unclear. Methods In this study, we evaluated the control efficacy of three fungicides (fluazinam, metalaxyl-mancozeb, and carbendazim) on clubroot disease of tumorous stem mustard in greenhouse experiment. Uninoculated and Water treatments after inoculation were performed as controls. At three (3 W) and six weeks (6 W) post-inoculation of P. brassicae, soil properties, bacterial composition (sequencing of 16S rRNA genes), and effector gene expression of the pathogen were analyzed. The correlation of these factors with disease index (DI) was explored. Results Fluazinam was the most effective in controlling clubroot disease of tumorous stem mustard with a controlled efficacy of 59.81%, and the abundance of P. brassicae in the soil decreased 21.29% after 3 weeks of treatment. Compared with other treatments, twelve out of twenty effector genes showed higher expression in fluazinam 3 W samples. Different fungicides had different effects on soil properties. EC (electrical conductivity), the main factor that positively associated with DI, was significantly lower in fluazinam treatment than the other two fungicide treatments. The application of fungicides, especially carbendazim, significantly reduced bacterial α-diversity and the composition of soil bacteria. Pseudomonas, Microbacterium, and Sphingobacterium (positively correlated with DI) were enriched in Water, metalaxyl-mancozeb, and carbendazim treatments, but were less abundant in fluazinam treatment. Among the three fungicide treatments, DI was significantly negatively correlated with Shannon and Chao 1 indices. Soil properties and the top bacterial genera that positively correlated with DI were influenced to a lesser degree in the fluazinam treatment. Conclusion Among three fungicides, fluazinam was the most effective agent with the highest control effects against clubroot disease. The strong virulence of fluazinam against P. brassicae was one of the main reasons for the prevention of clubroot disease, and in addition the alteration of rhizosphere bacterial community by fluazinam to the detriment of P. brassicae infection. Based on our results, EC could be an indicator of the severity of clubroot disease.

In the presence of KCN, the reaction of 1,10-phenanthroline (phen) with Co (ClO4)2 affords a cobalt(II) complex, [(phen)2Co(CN)2], a co-catalyst for photochemical driven CO2 reduction to CO. Under visible light (λ = 469 nm), together with [Ru(phen)3](PF6)2] as a photosensitizer and triethanolamine (TEOA) as a sacrificial electron donor, [(phen)2Co(CN)2] shows a high selectivity (95%) for the catalytic reduction of CO2 to CO with a turnover number (TON) of 1450 during 10 h irradiation. The photocatalytic mechanism for CO2 reduction by [Co(phen)2(CN)2] is afforded. I hope that these findings can afford a new chemical paradigm for the design of catalysts for CO2 reduction that is highly active and selective. Co(phen)2(CN)2, a catalyst for visible-light-driven driven CO2 reduction to CO with a high selectivity.

Based on that hydrogen energy is widely used in fuel cells, we focus our interests on the design and research of new complexes that catalyze the reaction in both directions, such as hydrogen evolution reactions (HERs) and hydrogen oxidation reactions (HORs). A highly efficient catalyst for both hydrogen evolution and oxidation, based on a nickel(II) complex, [Ni-en-P2](ClO4)2, has been designed and provided by the reaction of Ni(ClO4)2 with N,N′-bis[o-(diphenylphosphino)benzylidene]ethylenediamine (en-P2) in our group. Its structure has been determined by X-ray diffraction. [Ni-en-P2](ClO4)2 can electro-catalyze hydrogen evolution both from acetic acid and a neutral buffer (pH 7.0) with a turnover frequency (TOF) of 204 and 1327 mol of hydrogen per mole of catalyst per hour (H2/mol catalyst/h) under an overpotential (OP) of 914.6 mV and 836.6 mV, respectively. [Ni-en-P2](ClO4)2 also can electro-catalyze hydrogen oxidation with a TOF of 111.7 s−1 under an OP of 330 mV. The results can be attributed to that [NiII-en-P2](ClO4)2 has three good reversible redox waves at 1.01 (NiIII/II), −0.79 (NiII/I) and −1.38 V (NiI/0) versus Fc+/0, respectively. We hope these findings can afford a new method for the design of electrocatalysts for both H2 evolution and H2 oxidation.

Sr(Ti0·3Fe0.7)O3-δ (STF) materials with satisfactory stability and no rare-metal elements have attracted increasing research interest as oxygen electrodes of solid oxide electrochemical cells. However, STF-based electrodes are still limited by their modest catalytic activities at low temperatures. This can be improved by A-site deficiency of STF-based materials; however, data related to the influence of A-site deficiency of perovskite-oxide-based materials on sintering behavior and electrochemical performance are still lacking. Herein, porous electrodes with different Srx (Ti0·3Fe0.7)O3-δ compositions (x = 0.85–1) were prepared. The effects of A-site cation deficiency ratios and sintering temperatures on the microstructures and electrochemical performance of the as-obtained STF electrodes were investigated. Electrochemical performance was improved for A-site deficient Srx (Ti0·3Fe0.7)O3-δ. For Sr0·9(Ti0·3Fe0.7)3-δ electrode material sintered at 1050 °C, the lowest polarization resistance measured at 700 °C was ~0.14 Ω⸳cm2 but increased at higher x values. At sintering temperatures above 1050 °C, the sintering diffusion occurred, where the electrolyte diffused through the deficient electrodes to form a dense layer at the electrode/electrolyte interface. On the other hand, although the presence of such diffused dense layer did not have significant effect on the electrochemical performance of the cells, it could be prevented by using lower sintering temperatures (≤1000 °C) to avoid possible negative effects on comprehensive performance. For the electrode obtained at x = 0.9 and sintered at 1000 °C, the overall polarization resistance was recorded as 0.099 Ω⸳cm2 at 700 °C. In sum, these findings look promising for future research.

The first examples of cyclic (alkyl)(amino)carbene (CAAC) lanthanide (Ln) complexes were synthesized from the reaction of CAAC with Yb[N(SiMe3)2]2 and Eu[N(SiMe3)2]2(THF)2 (THF = tetrahydrofuran). The structures of (CAAC)Yb[N(SiMe3)2]2 (2) and (CAAC)Eu[N(SiMe3)2]2(THF) (3) were determined by X-ray diffraction analysis. Density functional theory calculations of 2 revealed the predominantly ionic bond between the Ln ion and CAAC. Complex 3 enabled catalytic hydrosilylation of aryl- and silylalkenes with primary and secondary silanes in high yields and Markovnikov selectivity.

An analysis of the correlation between polycyclic aromatic hydrocarbons (PAHs) and economic parameters demonstrates that the total population, gross domestic product, coal consumption, petroleum, temperature, and day consumption significantly affect PAH concentrations in Dianchi Lake, Yunnan province, China. An artificial neural network (ANN) model was developed to predict the trend in PAH concentrations in the sediments of Dianchi Lake over the next 10 years based on current indicators of economic development. The ANN model estimated the concentration of PAHs from 1980 to 2014. The model was evaluated using available observations for the historical trends; concentrations of PAHs in the sediments of Dianchi Lake are calculated to be at 2128.1 ng/g in 2025 and are expected to decline up to 1044.3 ng/g by 2030. These concentrations are considered relatively high because of their impacts on the health of people and aquatic organisms and the development of surrounding industries. We show the importance of the socioeconomic and climate factors in increasing the pollution levels. Our results could support the local government to formulate effective measures to reduce the pollution levels in the lake.

To investigate the structure–function correlation analysed by full-field electroretinography (ffERG) and optical coherence tomography (OCT) in typical and pericentral subtypes of retinitis pigmentosa (RP). A retrospective, cross-sectional, observational study of right eyes was conducted. The primary analysis used ffERG data to compare the RP subtypes. The subgroup analysis was used to correlate the structure, analysed by OCT, and function, determined by ffERG. Linear regressions explored the relationship between best-corrected visual acuity (BCVA) and multiple parameters. A total of 188 eyes were included. Amplitudes of responses of rod, rod-cone, cone, and 30 Hz flicker of typical type were lower than those of pericentral and other types. In the subgroup analysis, 41 and 21 eyes of the typical and pericentral types were studied, respectively. The correlation between the estimated preserved photoreceptor area and all ffERG amplitude parameters were significant in the typical type, but not in pericentral type. Old age, decreased intact ellipsoid zone length, typical type, and thin central retinal thickness were negatively correlated with BCVA. Typical type RP developed more extensive degeneration and poorer BCVA compared to others. Strong structure–function correlation was found in typical type while not in pericentral type. OCT may be a useful tool for monitoring RP status in typical type, providing useful parameters for the prediction of BCVA.

The purpose of this study was to detect the presence of retinitis pigmentosa (RP) based on color fundus photographs using a deep learning model. A total of 1670 color fundus photographs from the Taiwan inherited retinal degeneration project and National Taiwan University Hospital were acquired and preprocessed. The fundus photographs were labeled RP or normal and divided into training and validation datasets (n = 1284) and a test dataset (n = 386). Three transfer learning models based on pre-trained Inception V3, Inception Resnet V2, and Xception deep learning architectures, respectively, were developed to classify the presence of RP on fundus images. The model sensitivity, specificity, and area under the receiver operating characteristic (AUROC) curve were compared. The results from the best transfer learning model were compared with the reading results of two general ophthalmologists, one retinal specialist, and one specialist in retina and inherited retinal degenerations. A total of 935 RP and 324 normal images were used to train the models. The test dataset consisted of 193 RP and 193 normal images. Among the three transfer learning models evaluated, the Xception model had the best performance, achieving an AUROC of 96.74%. Gradient-weighted class activation mapping indicated that the contrast between the periphery and the macula on fundus photographs was an important feature in detecting RP. False-positive results were mostly obtained in cases of high myopia with highly tessellated retina, and false-negative results were mostly obtained in cases of unclear media, such as cataract, that led to a decrease in the contrast between the peripheral retina and the macula. Our model demonstrated the highest accuracy of 96.00%, which was comparable with the average results of 81.50%, of the other four ophthalmologists. Moreover, the accuracy was obtained at the same level of sensitivity (95.71%), as compared to an inherited retinal disease specialist. RP is an important disease, but its early and precise diagnosis is challenging. We developed and evaluated a transfer-learning-based model to detect RP from color fundus photographs. The results of this study validate the utility of deep learning in automating the identification of RP from fundus photographs.

Therapeutic options for Parkinson's disease (PD) are limited to a symptomatic approach, making it a global threat. Targeting aggregated alpha-synuclein (α-syn) clearance is a gold standard for ameliorating PD pathology, bringing autophagy into the limelight. Expression of autophagy related genes are under the regulation by histone modifications, however, its relevance in PD is yet to be established. Here, preformed fibrillar form (PFF) of α-syn was used to induce PD in wistar rats, which were thereafter subjected to treatment with trehalose (tre, 4g/kg, orally), a potent autophagy inducer and sodium butyrate (SB, 300 mg/kg, orally), a pan histone deacetylase inhibitor alone as well as in combination. The combination treatment significantly reduced motor deficits as evidenced after rotarod, narrow beam walk, and open field tests. Novel object location and recognition tests were performed to govern cognitive abnormality associated with advanced stage PD, which was overcome by the combination treatment. Additionally, with the combination, the level of pro-inflammatory cytokines were significantly reduced, along with elevated levels of dopamine and histone H3 acetylation. Further, mRNA analysis revealed that levels of certain autophagy related genes and proteins implicated in PD pathogenesis significantly improved after administration of both tre and SB. Immunofluorescence and H&E staining in the substantia nigra region mirrored a potential improvement after treatment with both tre and SB. Therefore, outcomes of the present study were adequate to prove that combinatorial efficacy with tre and SB may prove to be a formidable insight into ameliorating PD exacerbated by PFF α-syn as compared to its individual efficacy.

The effect of deep eutectic solvent (DES) modified silica on the properties of nature rubber (NR) composites were investigated. The DES is an environment-friendly and low-cost solvent, which was prepared by mixing choline chloride and urea in a 1:2 molar ratio. The NR composites filled with DES modified silica were prepared and the properties were tested. The interaction between the DES and silica were characterized by Fourier transform infrared spectroscopy (FTIR), the interaction between silica and silica were tested by differential scanning calorimetry (DSC). The dynamic properties, such as rolling resistance and wet skid resistance, and were tested by dynamic mechanical analysis (DMA). Morphologies of the composites were characterized by scanning electron microscopy (SEM). The results indicate that the DES can interact with silica by hydrogen bond to improve the compatibility between the rubber and silica. When the content of DES was 3 phr, the tensile strength, modulus at 300%, tear strength, and the crosslinking density of the composites was increased. At the same time, the proper content of DES can reduce the rolling resistance of the vulcanized rubber while maintaining good wet skid resistance.

Cellular senescence is linked to chronic age-related diseases including atherosclerosis, diabetes, and neurodegeneration. Compared to proliferating cells, senescent cells express distinct subsets of proteins. In this study, we used cultured human diploid fibroblasts rendered senescent through replicative exhaustion or ionizing radiation to identify proteins differentially expressed during senescence. We identified acid ceramidase (ASAH1), a lysosomal enzyme that cleaves ceramide into sphingosine and fatty acid, as being highly elevated in senescent cells. This increase in ASAH1 levels in senescent cells was associated with a rise in the levels of ASAH1 mRNA and a robust increase in ASAH1 protein stability. Furthermore, silencing ASAH1 in pre-senescent fibroblasts decreased the levels of senescence proteins p16, p21, and p53, and reduced the activity of the senescence-associated β-galactosidase. Interestingly, depletion of ASAH1 in pre-senescent cells sensitized these cells to the senolytics Dasatinib and Quercetin (D+Q). Together, our study indicates that ASAH1 promotes senescence, protects senescent cells, and confers resistance against senolytic drugs. Given that inhibiting ASAH1 sensitizes cells towards senolysis, this enzyme represents an attractive therapeutic target in interventions aimed at eliminating senescent cells.

Ferroptosis is a new type of programmed cell death characterized by intracellular iron accumulation and lipid peroxidation that leads to oxidative stress and cell death. The metabolism of iron, lipids, and amino acids and multiple signalling pathways precisely regulate the process of ferroptosis. Emerging evidence has demonstrated that ferroptosis participates in the occurrence and progression of various pathological conditions and diseases, such as infections, neurodegeneration, tissue ischaemia-reperfusion injury and immune diseases. Recent studies have also indicated that ferroptosis plays a critical role in the pathogenesis of acute lung injury, chronic obstructive pulmonary disease, pulmonary fibrosis, pulmonary infection and asthma. Herein, we summarize the latest knowledge on the regulatory mechanism of ferroptosis and its association with iron, lipid and amino acid metabolism as well as several signalling pathways. Furthermore, we review the contribution of ferroptosis to the pathogenesis of lung diseases and discuss ferroptosis as a novel therapeutic target for various lung diseases.

Active Lamb wave detection is an effective and simple monitoring method for structural health monitoring (SHM). Piezoelectric lead zirconate titanate (PZT) ceramics are most commonly used as transducers to excite and receive Lamb wave. However, due to their hardness, thickness and brittleness, PZT ceramics are severely limited in detecting damage on curved surface structures. Herein, we report that flexible PZT film sensor is an excellent candidate for receiving Lamb wave used in Lamb wave-based SHM of aircraft. An improved piezoelectric coefficient d33 (~130 pm V−1) is obtained in epitaxial PZT films grown on flexible inorganic mica substrates via van der Waals heteroepitaxy. Superior stable ferroelectricity and piezoelectricity retain in flexible PZT film after bending 104 cycles under a radius of 8 mm. As proven by experiment and simulation, flexible PZT film is demonstrated as an ultrasonic sensor with high sensitivity to be bonded on the curved aluminum plate for Lamb wave-based damage monitoring. Our work demonstrates that flexible PZT films have enormous potential for real-time light-weight and high-sensitivity receiver sensors for the SHM of aging aircraft.

The metabolic and bioactivity effects of Eurycoma longifolia (Eucalyptus longifolia) in obesity treatment were studied in mice fed with a high-fat diet using a metabolomics approach. Aqueous extracts of E. longifolia were obtained via grinding, dissolving, and freeze-drying. The hepatic steatosis effect of E. longifolia was characterized by hematoxylin and eosin histological staining. External performance of the obesity-alleviation effect was monitored by measuring body and food weight. In addition, the metabolomics analysis of the E. longifolia-mice interaction system was performed using the established platform combining liquid chromatography-tandem mass spectrometry with statistical analysis. The presence and spatial distribution patterns of differential molecules were further evaluated through desorption electrospray ionization-mass spectrometry imaging. The results showed that E. longifolia played a vital role in downregulating lipid accumulation (especially triacylglycerols) and fatty acids biosynthesis together with enhanced lipid decomposition and healing in Bagg albino mice. During such a process, E. longifolia mainly induced metabolomic alterations of amino acids, organic acids, phospholipids, and glycerolipids. Moreover, under the experimental concentrations, E. longifolia induced more fluctuations of aqueous-soluble metabolites in the plasma and lipids in the liver than in the kidneys. This study provides an advanced alternative to traditional E. longifolia-based studies for evaluating the metabolic effects and bioactivity of E. longifolia through metabolomics technology, revealing potential technological improvement and clinical application.

It is usually seen that DC flashover voltage of the water droplet on the surface of silicone rubber (SIR) composite insulator is lower than AC flashover voltage. It is necessary to study the mechanisms and influencing factors of the surface properties. In this article, experiments are performed to study the moving processes of the water droplet and the influences of its dynamic behaviours on flashover voltage under DC/AC electric field. Besides, an electrohydrodynamic coupling method is employed to establish the simulating model. Moreover, the theoretical physical model is established to reveal the mechanisms of dynamic behaviours of a droplet. It is indicated that the simulation results are in good consistency with the experimental data. The elongation behaviours of a droplet on the surface of a composite insulator can influence the homogeneity of the electric field distribution along the sample's surface. It is shown that the different dynamic behaviours and flashover performances for a single water droplet on the SIR surface are both affected by the volume of the droplet and the type of voltage applied.

Objective To explore the adipogenic effects of the small extracellular vesicles derived from the lipoma tissues (sEV-LT), and to find a new cell-free therapeutic approach for adipose tissue regeneration. Methods Adipose tissue-derived stem cells (ADSCs) and small extracellular vesicles derived from the adipose tissues (sEV-AT) were isolated from human adipose tissue, while sEV-LT were isolated from human lipomatous tissue. ADSCs were characterized by using flow cytometric analysis and adipogenic and osteogenic differentiation assays. sEV was identified by electron microscopy, nanoparticle tracking, and western blotting. ADSCs were treated with sEV-LT and sEV-AT, respectively. Fluorescence confocal microscopy was used to investigate whether sEV-LT and sEV-AT could be taken by ADSCs. The proliferation and migration abilities and adipogenic differentiation assay of ADSCs were evaluated by CCK-8 assays, scratch test, and oil red O staining test, and the expression levels of adipogenic-related genes C/EBP-δ, PPARγ2, and Adiponectin in ADSCs were assessed by real-time quantitative PCR (RT-PCR). The sEV-LT and sEV-AT transplantation tubes were implanted subcutaneously in SD rats, and the neotissues were qualitatively and histologically evaluated at 2, 4, 8, and 12 weeks after transplantation. Hematoxylin and eosin (H&E) staining was subsequently used to observe and compare the adipogenesis and angiogenesis in neotissues, while immunohistochemistry was used to examine the expression and the distribution of C/EBP-α, PPARγ, Adiponectin, and CD31 at the 4th week. Results The in vitro experiments showed that both sEV-LT and sEV-AT could be taken up by ADSCs via endocytosis. The scratch experiment and CCK-8 experiment showed that the migration area and proliferation number of ADSCs in sEV-LT group and sEV-AT group were significantly higher than those in the non-sEV group (p p p p > 0.05). In addition, no significant difference in the amount of lipid droplets and adipogenesis-related genes between the sEV-LT groups and sEV-AT was seen (p > 0.05). At 2, 4, 8, and 12 weeks, the adipocyte area and the number of capillaries in neotissues in the sEV-LT groups and sEV-AT groups were significantly increased compared with the Matrigel group (p p > 0.05). At the 4th week, neotissues in the sEV-LT groups and sEV-AT groups all showed upregulated expression of C/EBP-α, PPARγ, Adiponectin, and CD31 protein, while neotissues in the Matrigel group only showed positive expression of CD31 protein. Conclusions This study demonstrated that sEV-LT exerted promotion effects on adipose tissue regeneration by accelerating the proliferation, migration, and adipogenic differentiation of ADSCs in vitro and recruiting adipocytes and promoting angiogenesis in vivo. The sEV-LT could serve as an alternative cell-free therapeutic strategy for generating adipose tissue, thus providing a promising application prospect in tissue engineering.

Bifunctional hydrogen electrocatalysis (hydrogen-oxidation and hydrogen-evolution reactions) in alkaline solution is desirable but challenging. Among all available electrocatalysts, Ni-based materials are the only non-precious-metal-based candidates for alkaline hydrogen oxidation, but they generally suffer from low activity. Here, we demonstrate that properly alloying Ni with Mo could significantly promote its electrocatalytic performance. Ni4 Mo alloy nanoparticles are prepared from the reduction of molybdate-intercalated Ni(OH)2 nanosheets. The final product exhibits an apparent hydrogen-oxidation activity exceeding that of the Pt benchmark and a record-high mass-specific kinetic current of 79 A g-1 at an overpotential of 50 mV. A superior hydrogen-evolution performance is also measured in alkaline solution. These experimental data are rationalized by our theoretical simulations, which show that alloying Ni with Mo significantly weakens its hydrogen adsorption, improves the hydroxyl adsorption and decreases the reaction barrier for water formation.

Radical S-adenosyl-l-methionine (SAM) enzymes initiate biological radical reactions with the 5’-deoxyadenosyl radical (5’-dAdo•). A [4Fe-4S](+) cluster reductively cleaves SAM to form the Ω organometallic intermediate in which the 5’-deoxyadenosyl moiety is directly bound to the unique iron of the [4Fe-4S] cluster, with subsequent liberation of 5’-dAdo•. Here we present synthesis of the SAM analog S-adenosyl-l-ethionine (SAE) and show SAE is a mechanistically-equivalent SAM-alternative for HydG, both supporting enzymatic turnover of substrate tyrosine and forming the organometallic intermediate Ω. Photolysis of SAE bound to HydG forms an ethyl radical trapped in the active site. The ethyl radical withstands prolonged storage at 77 K and its EPR signal is only partially lost upon annealing at 100 K, making it significantly less reactive than the methyl radical formed by SAM photolysis. Upon annealing above 77K, the ethyl radical adds to the [4Fe-4S](2+) cluster, generating an ethyl-[4Fe-4S](3+) organometallic species termed Ω(E).

Developing advanced electrocatalysts to convert CO2 into liquid fuels such as ethanol is critical for utilizing intermittent renewable energy. The formation of ethanol, however, is generally less f...

Seawater oxygen evolution is one of the promising energy conversion technologies for large-scale renewable energy storage. It requires efficient catalysts to accelerate the oxygen evolution reactio...

A twin-axial pseudorotaxane is constructed using a phenylpyridine salt with diethanolamine (DA-PY) and cucurbit[8]uril (CB[8]), and it not only displays phosphorescence in aqueous solution but it can also be used for targeted cell-imaging.

Perovskite transition metal oxides with ABO3 structure are considered as potential alternative non-precious metal electrocatalysts for designing highly active and durable electrocatalysis for the oxygen evolution reaction (OER). Herein, we successfully enable LaFeO3 coated on nickel foam (denoted LFO@NF) perovskite with impressive OER activity by systematically tailoring the Fe cation sites and the introduction of oxygen vacancies. The cationic site involves dual cation modulation with Cr and Mo, which creates lattice distortions inducing strong electronic interaction, while the anionic site entails reduction via a hydrogen-treatment process, creating oxygen vacancy sites to improve the electronic conductivity of the perovskite oxide. As a result, the optimized LFO-based catalyst, specifically hydrogenated LaFe0.75Cr0.15Mo0.10O3-coated on the nickel foam (denoted H-LFCMO@NF), requires the lowest overpotential of 263 mV at 10 mA cm−2, and has superior kinetics and excellent stability, which are superior to its counterparts. Theoretical analysis also confirmed that the tailoring of the LFO@NF perovskite leads to an increase in the exposure of active sites, optimization of the adsorption energy of reaction intermediates and enhanced electronic conductivity. This work may provide a promising concept to enhance the performance of LFO-based perovskite electrocatalysts for alkaline OER and beyond.

Facilitated transport membranes, with a uniform distribution of facilitated transport carriers, are highly desirable to reduce the separation energy barrier. Nevertheless, the disordered and random assembly of membrane building materials/blocks makes it hard to obtain the controlled uniform distribution of carriers within membranes. Covalent organic frameworks (COFs), equipped with a regular structure and tailored functionality, provide a favorable platform for the uniform distribution of carriers. Herein, we report an ion-exchange strategy to achieve a uniform distribution of facilitated transport carriers within a cationic COF membrane for efficient carbon capture. With the assistance of a small amount of flexible graphene oxide (GO), the potential defects between the junctions of cationic COF nanosheets were eliminated, and ultrathin (20–60 nm), defect-free COF membranes were obtained. By synergistically intensifying the diffusion selective and facilitated transport mechanisms within membranes, the optimized COF membrane exhibits a CO2 permeance of 164.2 GPU with a CO2/CH4 selectivity of 27, both of which exceed those of pure COF membranes in most literature studies. Our findings may stimulate further research on functionalized COF membranes and other kinds of organic framework membranes with uniformly distributed carriers for molecule separation.

Bismuth vanadate (BiVO4) is one of the most fascinating building blocks for the design and assembly of highly efficient artificial photosynthesis devices for solar water splitting. Our recent report has shown that borate treated BiVO4 (B-BiVO4) results in an improved water oxidation performance. In this study, further improvement of both the photoelectrochemical (PEC) activity and stability of B-BiVO4 was successfully achieved by introducing NiFeV LDHs as an oxygen evolution catalyst and interfacial hole transporter. Benefiting from the synergistic effect of co-catalyst and borate pretreatment, the as-prepared NiFeV/B-BiVO4 exhibited a high photocurrent density of 4.6 mA cm−2 at 1.23 VRHE and an outstanding onset potential of ∼0.2 VRHE with good long-term stability. More importantly, NiFeV was found to play a pivotal role in the critically efficient suppression of charge combination on the BiVO4 surface and acceleration of charge transfer rather than a mere electrocatalyst for water oxidation.

A new type of purely organic light-harvesting phosphorescence energy transfer (PET) supramolecular assembly is constructed from 4-(4-bromophenyl)-pyridine modified β-cyclodextrin (CD-PY) as a donor, cucurbit[8]uril (CB[8]) as a mediator, rhodamine B (RhB) as an acceptor, and adamantane modified hyaluronic acid (HA-ADA) as a cancer cell targeting agent. Interestingly, the complexation of free CD-PY, which has no RTP emission in aqueous solution, with CB[8] results in the formation of CD-PY@CB[8] pseudorotaxane with an RTP emission at 510 nm. Then the addition of RhB leads to an efficient light-harvesting PET process with highly efficient energy transfer and an ultrahigh antenna effect (36.42) between CD-PY@CB[8] pseudorotaxane and RhB. Importantly, CD-PY@CB[8]@RhB assembles with HA-ADA into nanoparticles with further enhanced delayed emission at 590 nm. The nanoparticles could be successfully used for mitochondria targeted imaging in A549 cancer cells. This aqueous-state PET based on a supramolecular assembly strategy has potential application in delayed fluorescence cell imaging., A new type of purely organic light-harvesting PET supramolecular assembly is constructed with efficient energy transfer and ultrahigh antenna effect. Moreover, the assembly could be used for mitochondria targeted imaging in A549 cancer cells.

Immunoglobulin G (IgG) molecules modulate an immune response. However, site-specific N-glycosylation signatures of plasma IgG in patients with chronic kidney disease (CKD) remain unclear. This study aimed to propose a novel method to explore the N-glycosylation pattern of IgG and to compare it with reported methods. We separated human plasma IgG from 58 healthy controls (HC) and 111 patients with CKD. Purified IgG molecules were digested by trypsin. Tryptic peptides without enrichment of intact N-glycopeptides were analyzed using a combination of electron-transfer/higher-energy collisional dissociation (EThcD) and stepped collision energy/higher-energy collisional dissociation (sceHCD) mass spectrometry (EThcD-sceHCD-MS/MS). This resulted in higher spectral quality, more informative fragment ions, higher Byonic score, and nearly twice the depth of intact N-glycopeptide identification than sceHCD or EThcD alone. Site-specific N-glycosylation mapping revealed that intact N-glycopeptides were differentially expressed in HC and CKD patients; thus, it can be a diagnostic tool. This study provides a method for the determination of glycosylation patterns in CKD and a framework for understanding the role of IgG in the pathophysiology of CKD. Data are available via ProteomeXchange with identifier PXD027174.

Among all CO2 electroreduction products, methane (CH4) and ethylene (C2H4) are two typical and valuable hydrocarbon products which are formed in two different pathways: hydrogenation and dimerization reactions of the same CO intermediate. Theoretical studies show that the adsorption configurations of CO intermediate determine the reaction pathways towards CH4/C2H4. However, it is challenging to experimentally control the CO adsorption configurations at the catalyst surface, and thus the hydrocarbon selectivity is still limited. Herein, we seek to synthesize two well-defined copper nanocatalysts with controllable surface structures. The two model catalysts exhibit a high hydrocarbon selectivity toward either CH4 (83%) or C2H4 (93%) under identical reduction conditions. Scanning transmission electron microscopy and X-ray absorption spectroscopy characterizations reveal the low-coordination Cu-0 sites and local Cu-0/Cu+ sites of the two catalysts, respectively. CO-temperature programed desorption, in-situ attenuated total reflection Fourier transform infrared spectroscopy and density functional theory studies unveil that the bridge-adsorbed CO (COB) on the low-coordination Cu-0 sites is apt to be hydrogenated to CH4, whereas the bridge-adsorbed CO plus linear-adsorbed CO (COB + COL) on the local Cu-0/Cu+ sites are apt to be coupled to C2H4. Our findings pave a new way to design catalysts with controllable CO adsorption configurations for high hydrocarbon product selectivity. (C) 2020 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.

Recently, hydrogel-based flexible sensors have attracted tremendous attention for use in wearable soft electronics. However, under sub-zero temperatures, common hydrogel-based flexible devices are always out of work due to their poor stability in freezing environments. To endow hydrogel-based sensors with long-term stability and anti-freezing ability as well as multi-functional abilities, we developed a polydopamine-reduced graphene oxide (PDA-rGO)/sodium alginate (SA)/polyacrylamide (PAM) composite organohydrogel with dual crosslinking networks. The excellent conductivity of the organohydrogel is due to the well-dispersed rGO endowed by mussel-inspired chemistry and ions such as Ca2+, which give the organohydrogel strain, pressure, and temperature sensing capabilities with a high gauge factor (2.09) within a broad strain range (0–250%), short response time (200 ms), and a wide temperature detection range (−20 °C to 60 °C), respectively. Moreover, the assembled sensors can also detect multiple human motions such as finger bending, facial micro-expression, and hand gesture recognition. Especially, owing to the synergistic effects of ion transportation, water–glycerol binary solvent, and the reduced graphene oxide in the composite hydrogel, the organohydrogel achieved an unprecedented thermal sensitivity of 97.60% °C−1 at sub-zero temperatures, which is the most sensitive stretchable thermistor so far reported. Therefore, this as-prepared functional organohydrogel paves the way for potential applications in human–machine interactions and personalized multi-signal monitoring in a broad temperature range.

Chirality, a fascinating property ubiquitous in nature, plays an important role in living organisms. DNA-programmed self-assembly has been extensively applied to precisely organize metal nanoparticles and/or small molecules in a chiral fashion at the nanometer scale. These assemblies exhibit significant chiroptical activities and are potential in biological detection and imaging, information processing, optical metamaterials, etc. In this review, we conclude on the DNA-enabled chiral plasmonic systems, uniquely from the perspective of the evolution of DNA programming methodology. We start by introducing a variety of natural and artificial DNA nanostructures to illustrate the fine programmability of DNA. Then we discuss the broad library of DNA-programmed chiral plasmonic nanostructures, spanning from individual nanoparticle–molecule chiral hybrids to the hierarchical chiral arrangements of nanoparticles enabled by DNA nanostructures of different complexities, which are from the primary DNA double helix to advanced architectures. Some cutting-edge applications of DNA-programmed chiral plasmonic nanostructures will also be introduced. We conclude this review with our personal perspectives on the future challenges and opportunities in this rapidly developing field. We expect this comprehensive review will inspire future studies in chiral materials at the convergence of DNA nanotechnology and chiral plasmonics.

Human amniotic epithelial cells (hAECs) have been reported to have neuroprotective roles in Parkinson’s disease (PD) animal models. However, the molecular mechanism is not fully understood. The present study was designed to explore the possible mechanism by which hAECs ameliorate PD symptoms and the important paracrine factors produced by hAECs that attribute to the recovery of dopaminergic neurons. Thus, we performed in vivo and in vitro experiments with hAECs in PD models or lesioned dopaminergic neurons, respectively. First, hAECs were transplanted into the striatum of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced PD mice and motor deficits were significantly attenuated. Second, the grafts prevented the loss of nigral dopaminergic neurons and promoted the outgrowth of neurites and striatal axon fibers in PD mice. In addition, decreased microglial activation, inflammatory factor levels and MPTP-induced excessive reactive oxygen species (ROS) levels were also observed in hAEC-treated PD mice. In vitro, we found that the conditioned medium (CM) from hAECs promoted the survival of mesencephalic dopaminergic neurons stimulated with 1-methyl-4-phenylpyridine (MPP+) and induced neurite outgrowth. Next, analysis of hAEC-CM with an antibody array of 507 soluble target proteins revealed that the levels of many neurotrophic factors, growth factors, neuronal cell adhesion molecule (NrCAM) and anti-inflammatory factors were evidently high. In addition, antibody neutralization experiments showed that many of these factors contributed to the survival and growth of dopaminergic neurons and neurite outgrowth. More importantly, we found that the anti-inflammatory factor interleukin-1 receptor antagonist (IL-1ra) also augmented the survival of dopaminergic neurons, demonstrating for the first time an anti-oxidative and anti-inflammatory role of hAECs in PD mice, which represents a novel molecular mechanism of hAECs in the treatment of PD.

The renewable electricity-driven reduction of carbon dioxide (CO2RR) is a promising technology for carbon utilization. However, it is still a challenge to broaden the application of CO2RR. Herein, we report a Te-doped Pd nanocrystals (Te-Pd NCs) for promoting urea synthesis by coupling CO2RR with electrochemical reduction of nitrite. The electrochemical synthesis of urea has been achieved with nearly 12.2% Faraday efficiency (FE) and 88.7% N atom efficiency (NE) at -1.1 V versus reversible hydrogen electrode (vs RHE), much higher than those of pure Pd NCs (4.2% FE and 21.8% NE). Significantly, an FE of ∼10.2% and an NE of ∼82.3% for urea solution production via an optimized flow cell system have been realized, where a solution with up to 0.95 wt % of urea has been obtained. Mechanistic insights show that Te-doping not only optimizes the CO2/CO adsorption but also promotes NH3 production, fully meeting the requirements of urea synthesis.

Triboelectric nanogenerators (TENGs) with high-energy output and high flexibility and transparency are desirable for a number of applications including flexible and transparent wearable devices. Th...

In plants, 3´,5´-cyclic adenosine monophosphate (cAMP) is an important second messenger with varied functions; however, only a few adenylyl cyclases (ACs) that synthesize cAMP have been identified. Moreover, the biological roles of ACs/cAMP in response to stress remain largely unclear. In this study, we used quantitative proteomics techniques to identify a maize heat-induced putative disease-resistance RPP13-like protein 3 (ZmRPP13-LK3), which has three conserved catalytic AC centres. The AC activity of ZmRPP13-LK3 was confirmed by in vitro enzyme activity analysis, in vivo RNAi experiments, and functional complementation in the E. coli cyaA mutant. ZmRPP13-LK3 is located in the mitochondria. The results of in vitro and in vivo experiments indicated that ZmRPP13-LK3 interacts with ZmABC2, a possible cAMP exporter. Under heat stress, the concentrations of ZmRPP13-LK3 and cAMP in the ABA-deficient mutant vp5 were significantly less than those in the wild-type, and treatment with ABA and an ABA inhibitor affected ZmRPP13-LK3 expression in the wild-type. Application of 8-Br-cAMP, a cAMP analogue, increased heat-induced expression of heat-shock proteins in wild-type plants and alleviated heat-activated oxidative stress. Taken together, our results indicate that ZmRPP13-LK3, a new AC, can catalyse ATP for the production of cAMP and may be involved in ABA-regulated heat resistance.

利用间歇性可再生能源电转化二氧化碳和一氧化碳制备多碳工业原料和燃料能够完善碳循环. 然而, 二氧化碳转化为乙酸的法拉第效率难以满足大规模应用的要求. 研究发现, 调控铜的局域电子结构至正价态, 以及使用一氧化碳作为反应气均能够提高多碳产物的选择性. 因此, 我们提出杂原子调控策略, 用于调节催化剂表面活性位点的氧化态. 密度泛函理论研究表明, 掺杂氮原子调控正价态铜位点, 在热力学上有利于形成中间体*CCO, 进而生成乙酸. 我们进一步利用溶剂热法合成氮掺杂的铜催化剂, 并通过软X射线吸收谱和X射线光电子能谱证实催化剂表面存在大量正价态铜位点. 同时, 该催化剂在一氧化碳还原反应中实现了42%的乙酸法拉第效率和已知最高的乙酸偏电流密度 180 mA cm−2.

Oriented “shish-kebab” structures could be obtained by shearing to enhance the mechanical properties of polymer samples markedly. However, the effect of shear mode on mechanical properties is still uncertain. The study of stepped hoop shear field on the isotactic polypropylene (iPP) pipe was developed through applying a self-designed rotational shear system (RSS). The effect of stepped shear field on the microstructure and comprehensive properties of iPP pipe was investigated by the comparison with continuous shear. It could be found that the loosely-assembled shish-kebabs with the larger size were formed in the continuous shear pipes, but the smaller and tightly-stacked ones existed in the pipes with stepped shear. Surprisingly, due to differential morphologies under different shear modes, better comprehensive mechanical properties were obtained in the pipes with stepped shear.

The development of superabsorbent materials with high absorption capacity, selectivity, and stable performance is needed for oil recovery. Remote-controlled oil absorption is highly favorable for oil absorption in harsh environment. In this study, a novel ultralight superhydrophobic nanocomposite aerogel composed of organic cellulose nanofibrils (CNFs), inorganic silica fiber, and magnetic Fe3O4 nanoparticles was developed through a simple freeze drying and surface modification method as a magnetically driven superabsorbent material. The aerogel has a highly porous and fibrous structure that contains hierarchical micro-nano surface topography. Low surface energy carbon–fluorine chains were grafted on aerogel surface which rendered the aerogel superhydrophobic. The addition of Fe3O4 nanoparticles significantly improved the surface area, compressive property, water contact angle, and the separation efficiency of the aerogel, but reduced the absorption capacity due to the increase of bulk density. The developed nanocomposite aerogel has a high absorption capacity (weight gain of 3420–5837%), separation efficiency ~ 100%, and a water contact angle of 150°. It also demonstrated high elasticity and performance stability in repetitive use. Given its magnetic property, the CNF/silica/Fe3O4 nanocomposite aerogel is a promising candidate for selective oil removal from open water, especially for remotely controlled applications.

An efficient gold-catalyzed hydroarylation of alkynes under soft reaction conditions is developed by utilizing a bifunctional ligand. This transformation features a broad substrate scope and thus exhibits moderate to excellent efficiency.

Effective bone repair applications of titanium-based biometals must have excellent self-antibacterial properties and osteogenesis. Due to the special nano-geometric structure of titanium dioxide nanotubes (TN), the modified TN can confer various biological functions on the surface of titanium-based biometals. In this study, we used anodization, hydrothermal synthesis, and dopamine self-assembly to develop a Sm/Sr-doped TN (SSNT) array that integrated the antibacterial properties of Sm and the bone formation properties of Sr. AFM, SEM, FTIR, EDS, and XPS methods were used to characterize the SSTN, and the antibacterial and cell compatibility of the SSTN were systematically studied. Sm ions and Sr ions were slowly and stably released from the surface of dopamine and SrTiO3 crystals, respectively. Compared with TN, SSTN had a smaller roughness and significantly improved hydrophilicity. The colony count, inhibition zone and turbidity experiments demonstrated that the SSTN structure containing Sm had obvious antibacterial effect on E. coli and S. aureus. The nanotube structure containing strontium ions can promote the early differentiation and osteogenic gene expression of MC3T3-E1 cells adhered to the SSTN surface. Based on the above results, the dual doping of Sm and Sr, and the ideal hydrophilicity can not only improve the osteogenesis of titanium-based biometals, but also make such bone implant biometals have effective self-infection resistance.

Poly(l-lactic acid) (PLLA) has been the most commonly used polymer for making bioresorbable vascular scaffolds (BVS). Despite owning remarkable properties, BVS made from PLLA are facing higher rates of early thrombosis compared with permanent metallic scaffolds. To solve this issue, we modified the PLLA film surface with heparin-mimetic polysaccharide multilayers consisting of sulfated Chinese yam polysaccharide (SCYP) and chitosan (CS) through layer-by-layer (LBL) assembly. The surface chemical compositions, morphologies and growth manner of SCYP/CS multilayers were investigated using X-ray photoelectron spectroscopy, scanning electron microscopy, atomic force microscopy and UV-vis spectroscopy. The relevant hemocompatibility results showed that multilayer-modified PLLA could effectively resist protein adsorption, suppress the platelet adhesion, prolong clotting time, prevent contact and complement activation as well as reduce hemolysis rate. Moreover, the multilayer-modified PLLA exhibited non-cytotoxicity, good antibacterial ability against E. coli and S. aureus, and drug loading/sustained releasing behavior. Overall, the multifunctional PLLA film with integrated properties of hemocompatibility, non-cytotoxicity, antibacterial and drug loading/releasing behavior could be successfully achieved by deposition of SCYP/CS multilayers, which will have potential application in blood-contacting biomedical materials.

Importance The clinical implications of different morphologies of choroidal neovascularization (CNV), as evaluated by ocular coherence tomography angiography (OCTA) in neovascular age-related macular degeneration (nAMD), are lacking. Background To describe the morphology of CNV in nAMD using OCTA, and to compare the visual prognosis and other structural OCT biomarkers between different morphologic patterns. Design Retrospective cohort study. Participants One hundred and forty eyes with nAMD treated with anti-vascular endothelial growth factor (VEGF). Methods Patients were examined using OCTA prior to and at 3, 6 and 12 months after receiving anti-VEGF therapy. Main outcome measures Best-corrected visual acuity (BCVA) and morphologic retinal features. Results Organized CNV was identified in 110/140 eyes (78.6%) using OCTA. These CNV complexes could be divided into three OCTA patterns: the 'medusa' pattern (n = 41), characterized by branching vessels radiating in all directions; the 'seafan' pattern (n = 43), characterized by branching vessels radiating to one side of the lesion; and the 'tangled' pattern (n = 26), characterized by globular entwined vessels without a main trunk. At baseline, the eyes with the tangled pattern were from younger patients (P = .031) with better BCVA (P = .007). There were also fewer intraretinal cysts (P = .021), less fibrovascular pigment epithelial detachment (P = .009), and more pachychoroid (P = .007) in eyes with the tangled pattern on OCT. At 12 months post-treatment, patients with the tangled CNV pattern also showed greater visual improvement than patients with the other two patterns (P = .049). Conclusions and relevance Using OCTA, distinct morphologies of CNV in nAMD patients were identified. These different patterns might be useful predictors for the prognosis of nAMD patients after anti-VEGF therapy.