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For various chronic wounds, bacterial infection is one of the important reasons that hinder their healing. Ion‐crosslinked antibacterial hydrogel dressings based on Ag+, Cu2+ and Zn2+, have made progress in clinical application. However, the toxicity of released metal ions cannot be ignored. Therefore, how to ensure the antibacterial performance of hydrogel dressing while reducing the amount of metal ions is a major challenge for the fabrication of metal ion based antibacterial hydrogel. In this study, a general method is proposed to design cationic ion‐crosslinked hydrogel based on thiourea groups. Taking the hydrogel formed by mixing thiourea modified hyaluronic acid (H‐ANCSN) with Ag+ (HA‐NCSN/Ag+ hydrogel) as an example, the characteristics and application potential of this kind of hydrogel are thoroughly explored. Due to the strong cationic chelation characteristics of thiourea groups, HA‐NCSN/Ag+ hydrogel can gel at low Ag+ concentration and achieve long‐term slow release of Ag+ at stable concentration to balance the antibacterial and biocompatible properties. Moreover, this dynamic thiourea‐Ag+ crosslinking also endowed the hydrogel with the property of "gelation and encapsulation first, injection to cover wound when necessary". Then, the mangiferin self‐assembled nanoparticles are loaded into HA‐NCSN/Ag+ hydrogel as the radical oxygen species scavenger. [ABSTRACT FROM AUTHOR]

The drug‐resistant bacterial‐infected skin wound is still a severe healthcare problem. Uncontrolled bacterial infection, abundant reactive oxygen species (ROS) content, and prolonged inflammatory response are detrimental to wound healing. Moreover, excessive vessel growth can result in unsatisfactory scar formation. Herein, a three‐step regenerative strategy based on a bilayered gelatin/acryloyl β‐cyclodextrin (BGACD) hydrogel containing physical host–guest complexations and chemical crosslinks is proposed. The hydrogel is loaded with humic acids (HAs) and astragaloside IV (AS) in the lower layer and verteporfin (Vt) in the upper layer. Different gelatin/acryloyl β‐cyclodextrin ratios endow the lower and upper layers of the hydrogel with different degradation rates. Under light irradiation, the combination of HAs‐induced photothermal therapy (PTT) and verteporfin‐induced photodynamic therapy effectively inhibits MRSA growth. The HAs and astragaloside IV are released from the lower layer to scavenge ROS and promote M2 macrophage polarization and angiogenesis during the inflammation and early proliferation phases, while verteporfin releases from the upper layer suppress excessive vessel growth during the late proliferation and remodeling phases. The HAs‐AS@Vt@BGACD hydrogel successfully achieves rapid and scarless wound healing in an MRSA‐infected wound model in rats. Therefore, the HAs‐AS@Vt@BGACD hydrogel shows promising potential for the treatment of drug‐resistant bacteria‐infected skin wound healing. [ABSTRACT FROM AUTHOR]

Despite the immense potential of immune checkpoint blockade (ICB) therapy in tumor treatment, its widespread clinical application is currently limited by unsatisfactory curative effect and off‐target adverse effect. Herein, an injectable sericin (SS)/silk fibroin (SF) recombinant hydrogel, termed SF‐SS‐SMC hydrogel, is developed to enable local delivery of anti‐CD47 antibody (α CD47). The hydrogel displays self‐reinforcement in high H2O2 concentration of tumor microenvironment (TME), as the SS/Fe2+ supramolecular nanocomplex (SS‐SMC) inside the hydrogel converts H2O2 to reactive oxygen species (ROS), further triggering additional crosslinking among the SF polymers. Therefore, the SF‐SS‐SMC hydrogel has an in vivo retention time longer than 21 days and acts as a reservoir for the long‐term sustained release of α CD47. More importantly, the SF‐SS‐SMC hydrogel itself efficiently regulates the remodeling of a protumor immunosuppressive TME to an antitumoral TME through switching of tumor‐associated macrophages from an anti‐inflammatory M2 phenotype to a proinflammatory M1 phenotype without additional drugs. Based on the combined effect of sustained α CD47 release and TME reprogramming, the SF‐SS‐SMC hydrogel has satisfactory immunotherapeutic effects in the treatment of local, abscopal, remitting, and metastatic tumors. Further advantages, including low cost of production, simple fabrication, and ease of use, make it promising for commercial mass production. [ABSTRACT FROM AUTHOR]

Graphitic carbon nitride decorated with appropriate co‐catalysts has attracted widespread attention owing to its excellent photocatalytic H2 evolution activity. Herein, monodisperse Pt nanoparticles are synthesized by a facile method and anchored on graphitic carbon nitride (PCN) via self‐assembly route. Among the different Pt content, the 3 % Pt‐loaded PCN (Pt/PCN3) hybrid reveals highest photocatalytic activity for water splitting with the H2 evolution rate of 2.02 mmol g−1 h−1, about 4 times higher than that of Pt‐PCN by traditional photo‐deposition way. This work provides a new strategy for constructing high‐performance Pt‐based co‐catalysts on PCN to boost its photocatalytic activity. [ABSTRACT FROM AUTHOR]

Early studies have shown that autophagy and TPPII are associated with HBV infection. In this study, adenovirus vector containing TPPII was constructed to immunize HBV transgenic mice in vivo to explore the potential mechanism of autophagy and HBV infection. Our goal is to provide new ideas for immunotherapy of hepatitis B. First, adenovirus vector containing TPPII was constructed. Then, we used adenovirus to immunize HBV transgenic mice and ATG5 knockout HBV transgenic mice. The autophagy of CD8+ T cells was detected by transmission electron microscopy and immunofluorescence electron microscopy, Western blot was used to detect the expression of autophagy LC3 and BECN1, CTL reaction, HBV DNA and HBsAg in serum, HBsAg and HBcAg in liver tissues by immunohistochemistry, to further examine the possible mechanisms involved in autophagy. Adv‐HBcAg‐TPPII promotes autophagy of CD8+ T lymphocyte, activates CTL response, inhibits HBV DNA replication and HBsAg expression, and PI3K/ Akt /m TOR signalling pathway may be involved in autophagy. This study demonstrates that autophagy of CD8+ T cells was induced by Adv‐HBcAg‐TPPII and the molecular mechanism may be related to the PI3K/ Akt /m TOR signalling pathway, providing a possible theoretical basis for immunotherapy of hepatitis B. [ABSTRACT FROM AUTHOR]

Palladium (Pd)‐based materials have attracted increasing attentions as a kind of novel candidate catalysts for many electrocatalytic reactions to replace classic platinum (Pt) catalysts, especially in the fuel cell‐related electrocatalysis. However, the requirement of high activity and stability toward further practical applications makes the development of Pd‐based catalysts cease to advance. Combining alloying and structure‐controlled strategies has well addressed this challenge by optimizing the adsorption/desorption behaviors toward reaction intermediates. Herein, the recent advances of rational structural designs in terms of tuning the dimensionalities of Pd‐based nanoalloys are overviewed. To further enhance the intrinsic electrocatalytic activity, several advanced strategies, including intermetallics, doping, defects, surface, and interface engineering, are presented to engineer the electronic and/or physical properties of Pd‐based electrocatalysts. Using typical electrocatalytic reactions as probes, the significance of structural regulation of Pd‐based nanocrystals on the enhanced electrocatalysis is demonstrated. Finally, several possible trends and challenges for future advanced research directions are presented. It is anticipated that the rational structural regulation can make promising Pd‐based catalysts touch the ceiling of electrocatalytic activity and stability. [ABSTRACT FROM AUTHOR]

Flexible conductive materials and flexible electronic devices are driving the development of the next generation of cutting‐edge wearable electronics. However, the existing hydrogel‐based flexible conductive materials have limited tensile capacity, low toughness, and poor anti‐fatigue performance, resulting in narrow sensing area and insufficient durability. In this paper, a conductive nanocomposite hydrogel with high ductility, toughness, and fatigue resistance is prepared by combining silver coated copper (Ag@Cu) nanoparticles with gelatin followed by one‐step immersion in sodium sulfate (Na2SO4) solution. The salting‐out of gelatin in Na2SO4 solution greatly improve the mechanical properties of this gelatin‐based hydrogel. The uniform distribution of Ag@Cu nanoparticles inside the whole hydrogel endow the composite hydrogel with excellent electrical conductivity (1.35 S m−1). In addition, it displayed high and stable tensile strain sensitivity over a wide strain range (gauge factor = 2.08). Therefore, the Ag@Cu‐Gel hydrogel is sensitive and stable enough to be successfully utilized as flexible wearable sensor for detecting human motion signals in real time, such as bending of human joints, swallowing, and throat vocalization. Furthermore, this hydrogel is also suitable for application as electronic skin for bionic robots. The above results demonstrate the promising application of Ag@Cu‐Gel hydrogel for wearable electronics. [ABSTRACT FROM AUTHOR]

Ultrathin nanosheet catalysts deliver great potential in catalyzing the oxygen reduction reaction (ORR), but encounter the ceiling of the surface atomic utilizations, thus presenting a challenge associated with further boosting catalytic activity. Herein, a kind of PdPtCu ultrathin nanorings with increased numbers of electrocatalytically active sites is reported, with the purpose of breaking the activity ceiling of conventional catalysts. The as‐made PdPtCu nanorings possess abundant high‐index facets at the edge of both the exterior and interior surfaces. An ultrahigh electrochemical active surface area of 92.2 m2 g–1PGM is achieved on this novel catalyst, much higher than that of the commercial Pt/C catalyst. The optimized Pd39Pt33Cu28/C shows a great enhanced ORR activity with a specific activity of 2.39 mA cm–2 and a mass activity of 1.97 A mg–1PGM at 0.9 V (versus RHE), as well as superior durability within 30 000 cycles. Density function theory calculations reveal that the high‐index facets and alloying Cu atoms can optimize the oxygen adsorption energy, explaining the enhanced ORR activity. Overcoming a key technical barrier in sub‐nanometer electrocatalysts, this work successfully introduces the hollow structures into the ultrathin nanosheets, heralding the exciting prospects of high‐performance ORR catalysts in fuel cells. [ABSTRACT FROM AUTHOR]

Core/shell nanocatalysts are a class of promising materials, which achieve the enhanced catalytic activities through the synergy between ligand effect and strain effect. However, it has been challenging to disentangle the contributions from the two effects, which hinders the rational design of superior core/shell nanocatalysts. Herein, we report precise synthesis of PdCu/Ir core/shell nanocrystals, which can significantly boost oxygen evolution reaction (OER) via the exclusive strain effect. The heteroepitaxial coating of four Ir atomic layers onto PdCu nanoparticle gives a relatively thick Ir shell eliminating the ligand effect, but creates a compressive strain of ca. 3.60%. The strained PdCu/Ir catalysts can deliver a low OER overpotential and a high mass activity. Density functional theory (DFT) calculations reveal that the compressive strain in Ir shell downshifts the d‐band center and weakens the binding of the intermediates, causing the enhanced OER activity. The compressive strain also boosts hydrogen evolution reaction (HER) activity and the strained nanocrystals can be served as excellent catalysts for both anode and cathode in overall water‐splitting electrocatalysis. [ABSTRACT FROM AUTHOR]

Controllable synthesis and rational design of ordered nanostructures are crucial for their renewable energy applications. In this work, a mesoporous CoP/Fe2P doped with 5 % Ce by a simple nanocasting method is designed as a superior electrocatalyst for the oxygen evolution reaction (OER). The well‐designed composite delivers an efficient electrocatalytic activity with a low overpotential of 250 mV at 10 mA cm−2 and excellent long‐term stability with no degradation after 10 h of electrochemical OER test, superior to that of the state‐of‐the‐art RuO2 electrocatalyst in alkaline electrolyte. A comprehensive analysis demonstrates that the outstanding OER performance is due to the desirable combination of the highly exposed active centers in the Ce‐doped bimetallic phosphides, efficient mass transfer, and effective electron conduction owing to the hierarchically mesoporous hybridization. Furthermore, the synergistic effect between Ce and CoP/Fe2P accelerates the migration rate of electrons/ions and increases the electrochemical active area. This excellent OER performance observed by Ce doping of CoP/Fe2P makes them possible candidates toward OER in alkaline electrolytes. [ABSTRACT FROM AUTHOR]

The design of robust and highly efficient heterogeneous catalyst for ammonia borane (AB) hydrolysis is of great importance to realize its application in energy storage. Herein, bimetallic ultrafine PtPd nanoparticles (NPs), supported on NH2‐functionalized and N‐doped reduced grapheme oxide (NH2‐N‐rGO), were prepared by a simple and effective method under mild condition. The introduction of the −NH2−N group on rGO is the critical issue for the formation of the ultrafine and well‐dispersed bimetallic PtPd NPs (1.9 nm) with relatively large surface area and enough active sites. These catalysts have excellent catalytic activities in the hydrolytic dehydrogenation of AB and their activity was composition dependent. Among these catalysts, the Pt0.5Pd0.5/NH2‐N‐rGO composite catalysts exhibit the highest catalytic activity with an initial turnover frequency of 699.6 mol(hydrogen)•mol(catalyst)−1•min−1 for the hydrolytic dehydrogenation of AB. This work offers a new way for the design and preparation of the bimetallic ultrafine nanocatalysts with excellent catalytic activities for AB hydrolysis. [ABSTRACT FROM AUTHOR]

Developing noble‐metal‐free, earth‐abundant, highly active, and stable electrocatalysts with high efficiency for both hydrogen and oxygen evolution reactions is of great importance for the development of overall water‐splitting devices, but still remains a challenging issue. Herein, a 3D heterostructured NiC/MoC/NiMoO4 electrocatalyst was prepared through a facile synthetic procedure. The electrocatalyst shows a superior catalytic activity and stability toward the hydrogen and oxygen evolution reactions. The optimized NiC/MoC/NiMoO4 catalyst presents low overpotentials of 68 and 280 mV to reach a current density of 10 mA cm−2 in 1.0 m KOH for the hydrogen and oxygen evolution reactions, respectively. Assembled as an electrolyzer for overall water splitting, such a heterostructure shows quite a low cell voltage of 1.52 V at 10 mA cm−2 and remarkable stability for more than 20 h. This work provides a facile but efficient approach for the design and preparation of highly efficient bifunctional and self‐supported heterostructured electrocatalysts that can serve as promising candidates in electrochemical energy storage and conversion. Non‐precious potential: Developing noble‐metal‐free, earth‐abundant, highly active, and stable electrocatalysts with high efficiency for both hydrogen and oxygen evolution reactions in the same electrolyte is of great importance for the development of overall water‐splitting devices. Heterostructured NiC/MoC/NiMoO4 electrocatalysts have been synthesized through a facile method and the influence of anions with same morphology on water splitting has also been studied. [ABSTRACT FROM AUTHOR]

Background and Purpose: Myocardial infarction (MI) is one of the leading causes of death in China and often results in the development of heart failure. In this work, we tested the therapeutic role of Interleukin-19 (IL-19) in mice with MI and investigated the underlying molecular mechanism.Experimental Approach: Mice were subjected to MI by ligation of left anterior descending coronary artery (LAD) and treated with IL-19 (10ng g-1 ; i.p.).Key Results: Protein expression of IL-19 and its receptor in myocardium were upregulated 24 hrs post-MI in male mice. IL-19 treatment decreased infarct and apoptosis in myocardium, accompanied by enhanced haem oxygenase-1 (HO-1) activities and reduced malondialdehyde (MDA) formation. Pretreatment with IL-19 upregulated HO-1 expression in cultured neonatal mouse ventricular myocytes and attenuated oxygen-glucose deprivation (OGD)-induced injuries in vitro. Furthermore, IL-19 preserved cardiac function and improved survival of mice with MI. IL-19 reduced inflammatory infiltrates and suppressed formation of TNF-α, IL-1β, and IL-6. More importantly, IL-19 inhibited polarization toward proinflammatory M1 macrophages and stimulated M2 macrophage polarization in myocardium of mice with MI. IL-19 enhanced protein levels of vascular endothelial growth factor (VEGF) and promoted angiogenesis in myocardium of mice with MI. In addition, IL-19 treatment increased DNA-binding of the transcription factor STAT3 in myocardium of mice with MI.Conclusions and Implications: Treatment with exogenous IL-19 attenuated acute ischemic injury and improved survival of mice with MI. The mechanisms underlying these effects involved induction of HO-1, M2 macrophage polarization, angiogenesis, and STAT3 activation. [ABSTRACT FROM AUTHOR]

We report a general chemical approach to synthesize strongly ferromagnetic rare‐earth metal (REM) based SmCo and SmFeN nanoparticles (NPs) with ultra‐large coercivity. The synthesis started with the preparation of hexagonal CoO+Sm2O3 (denoted as SmCo‐O) multipods via decomposition of Sm(acac)3 and Co(acac)3 in oleylamine. These multipods were further reduced with Ca at 850 °C to form SmCo5 NPs with sizes tunable from 50 to 200 nm. The 200 nm SmCo5 NPs were dispersed in ethanol, and magnetically aligned in polyethylene glycol (PEG) matrix, yielding a PEG‐SmCo5 NP composite with the room temperature coercivity (Hc) of 49.2 kOe, the largest Hc among all ferromagnetic NPs ever reported, and saturated magnetic moment (Ms) of 88.7 emu g−1, the highest value reported for SmCo5 NPs. The method was extended to synthesize other ferromagnetic NPs of Sm2Co17, and, for the first time, of Sm2Fe17N3 NPs with Hc over 15 kOe and Ms reaching 127.9 emu g−1. These REM based NPs are important magnetic building blocks for fabrication of high‐performance permanent magnets, flexible magnets, and printable magnetic inks for energy and sensing applications. A new chemical process is developed to prepare strongly ferromagnetic SmCo5 nanoparticles (NPs) via controlled reduction of SmCo‐O multipods. The 200 nm SmCo5 NPs embedded in polyethylene glycol are aligned magnetically and show the room temperature coercivity of 49.2 kOe. The synthetic method has also been extended to prepare ferromagnetic Sm2Co17 and Sm2Fe17N3 NPs. [ABSTRACT FROM AUTHOR]

A facile approach to bimetallic phosphides, Co-Fe-P, by a high-temperature (300 °C) reaction between Co-Fe-O nanoparticles and trioctylphosphine is presented. The growth of Co-Fe-P from the Co-Fe-O is anisotropic. As a result, Co-Fe-P nanorods (from the polyhedral Co-Fe-O nanoparticles) and sea-urchin-like Co-Fe-P (from the cubic Co-Fe-O nanoparticles) are synthesized with both the nanorod and the sea-urchin-arm dimensions controlled by Co/Fe ratios. The Co-Fe-P structure, especially the sea-urchin-like (Co0.54Fe0.46)2P, shows enhanced catalysis for the oxygen evolution reaction in KOH with its catalytic efficiency surpassing the commercial Ir catalyst. Our synthesis is simple and may be readily extended to the preparation of other multimetallic phosphides for important catalysis and energy storage applications. [ABSTRACT FROM AUTHOR]

Mesoporous materials have recently gained much attention owing to their large surface area, narrow pore size distribution, and superior pore structure. These materials have been demonstrated as excellent solid supports for immobilization of a variety of proteins and enzymes for their potential applications as biocatalysts in the chemical and pharmaceutical industries. However, the lack of efficient and reproducible methods for immobilization has limited the activity and recyclability of these biocatalysts. Furthermore, the biocatalysts are usually not robust owing to their rapid denaturation in bulk solvents. To solve these problems, we designed a novel hybrid material system, mesoporous silica immobilized with NiO nanoparticles (SBA-NiO), wherein enzyme immobilization is directed to specific sites on the pore surface of the material. This yielded the biocatalytic species with higher activity than free enzyme in solution. These biocatalytic species are recyclable with minimal loss of activity after several cycles, demonstrating an advantage over free enzymes. [ABSTRACT FROM AUTHOR]

AdipoRon is an orally active adiponectin receptor agonist. The aim of this study was to characterize the metabolites of AdipoRon in rat and human liver microsomes using ultra‐high performance liquid chromatography combined with Q‐Exactive Orbitrap tandem mass spectrometry (UPLC‐Q‐Exactive‐Orbitrap‐MS) together with data processing techniques including extracted ion chromatograms and a mass defect filter. AdipoRon (10 μm) was incubated with liver microsomes in the presence of NADPH and this resulted in a total of 11 metabolites being detected. The identities of these metabolites were characterized by comparing their accurate masses and fragment ions as well as their retention times with those of AdipoRon using MetWorks software. Metabolites M1–M3, M6, and M8–M11 were identified for the first time. Metabolite M4, the major metabolite both in rat and human liver microsomes, was further confirmed using the reference standard. Our results revealed that the metabolic pathways of AdipoRon in liver microsomes were N‐dealkylation (M2), hydroxylation (M, M5–M9), carbonyl reduction (M4) and the formation of amide (M10 and M11). Our results provide valuable information about the in vitro metabolism of AdipoRon, which would be helpful for us to understand the mechanism of the elimination of AdipoRon and, in turn, its effectiveness and toxicity. [ABSTRACT FROM AUTHOR]