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POWDER TECHNOLOGY · 2019 · IF 3.413

Flotation separation of smithsonite from calcite using 2-phosphonobutane-1,2,4-tricarboxylic acid as a depressant

Cheng Liu,Wencai Zhang,Shaoxian Song,Hongqiang Li,Yong Liu

The effect of depressant 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTCA) on the flotation separation of smithsonite from calcite was studied by micro-flotation and electro-kinetic tests. The micro-flotation results showed that good floatability of both smithsonite and calcite were achieved in the presence of sodium oleate. The depressant PBTCA selectively depressed calcite without interfering the floatability of smithsonite. The mixed minerals flotation results showed that efficiency separation of smithsonite from calcite was achieved using PBTCA as the depressant. Zeta potential measurements indicated that NaOl was able to adsorb on the PBTCA pre-treated smithsonite surface, but failed to adsorb on the PBTCA pre-treated calcite surface.

✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Hollow RuV-Co(OH)2 arrays for efficiently electrocatalytic H2 production assisted by glucose oxidation

Ying Wu,Min Li,Wenhui Fang,Yutao Cao,Shixian Xin,Hong Zhao

Electrochemical water splitting is a promising method for hydrogen production but is restricted by sluggish oxygen evolution reaction (OER), so we propose to replace OER with the thermodynamically preferred glucose oxidation reaction (GOR) to reduce the supply voltage. Herein, hollow RuV-Co(OH) 2 arrays have been fabricated by the hydrothermal method of sacrificing ZIF-67 to codope vanadium (V) and ruthenium (Ru). Electrochemical studies show that RuV-Co(OH) 2 has excellent hydrogen evolution reaction (HER) activity with a low overpotential of 77 mV at the current density of 10 mA cm −2 (η 10  = 77 mV) and good GOR activity. Density functional theory (DFT) calculations indicate that V and Ru tune the electronic structure of RuV-Co(OH) 2 , greatly increasing the density of the active sites. Moreover, RuV-Co(OH) 2 assembled glucose-assisted hydrogen evolution cell exhibits a battery voltage of 1.42 V for a current density of 10 mA cm −2 , a significant reduction of 240 mV compared to overall water splitting along with higher-value glucose oxidation products. Furthermore, RuV-Co(OH) 2 exhibits outstanding stability. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) analysis demonstrate that RuV-Co(OH) 2 has superior mechanical stability. This work opens up a new approach to designing novel bifunctional electrocatalysts for energy-saving H 2 production and valuable coproductions.

✓ 已验证 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Ultra-stable seawater oxidation at 1.5 A cm−2 enabled by heptafluorotantalate intercalated NiFe layered double hydroxide

Hong Tang,Zixiao Li,Xun He,Hefeng Wang,Meng Yue,Yujie Yuan,Qiuying Dai,Xiaolan Tang,Shengjun Sun,Dongdong Zheng,Yongsong Luo,Mohamed S. Hamdy,Fatma A. Ibrahim,Tingshuai Li,Xuping Sun,Bo Tang

Seawater electrolysis is a facile, economical, and ecologically friendly approach for large-scale hydrogen production. However, the presence of chloride ions (Cl − ) in seawater can cause severe anode corrosion, which hinders its further application. Herein, a heptafluorotantalate (TaF 7 2− ) intercalated NiFe layered double hydroxide on Ni foam (TF-NiFe LDH/NF) is proposed for efficient and durable alkaline seawater oxidation (ASO). Such TF-NiFe LDH/NF requires an overpotential of only 375 mV to achieve a current density ( j ) of 1 A cm −2 and maintains stable operation for 1000 h at a j of 1.5 A cm −2 . In situ Raman characterization and stability tests indicate that TaF 7 2− can not only facilitate the dynamic reconstruction process of the catalyst but also effectively repels Cl − at ampere-level j . This study highlights a novel anion (TaF 7 2− ) intercalation strategy, providing new insights into the design of efficient and stable electrocatalysts, thus offering a new approach to enhance corrosion resistance for ASO.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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CHEMBIOCHEM · 2024 · IF 2.6

Super-resolution imaging reveals the mechanism of endosomal acidification inhibitors against SARS-CoV-2 infection

Chunyu Yan,Wei Zhou,Yan Zhang,Xuelian Zhou,Qinglong Qiao,Lu Miao,Zhaochao Xu

In this study, super-resolution structured illumination microscope (SIM) was used to analyze molecular mechanism of endocytic acidification inhibitors in the SARS-CoV-2 pandemic, such as Chloroquine (CQ), Hydroxychloroquine (HCQ) and Bafilomycin A1 (BafA1). We fluorescently labeled the SARS-CoV-2 RBD and its receptor ACE2 protein with small molecule dyes. Utilizing SIM imaging, the real-time impact of inhibitors (BafA1, CQ, HCQ, Dynasore) on the RBD-ACE2 endocytotic process was dynamically tracked in living cells. Initially, the protein activity of RBD and ACE2 was ensured after being labeled. And then our findings revealed that these inhibitors could inhibit the internalization and degradation of RBD-ACE2 to varying degrees. Among them, 100 nM BafA1 exhibited the most satisfactory endocytotic inhibition (~63.9%) and protein degradation inhibition (~97.7%). And it could inhibit the fusion between endocytic vesicles in the living cells. Additionally, Dynasore, a widely recognized dynein inhibitor, also demonstrated cell acidification inhibition effects. Together, these inhibitors collectively hinder SARS-CoV-2 infection by inhibiting both the viral internalization and RNA release. The comprehensive evaluation of pharmacological mechanisms through super-resolution fluorescence imaging has laid a crucial theoretical foundation for the development of potential drugs to treat COVID-19.

✓ 已验证 DOI PubMed 高影响因子
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ChemMedChem · 2025 · IF 3.4

Discovery of Safe COX-2 Inhibitors: Achieving Reduced Colitis Side Effects through Balanced COX Inhibition

Xinlin Zhu,Qin Li,Junhui Wu,Zhiran Ju

Graphical In recent years, the development of COX-2 inhibitors has shifted from a focus on highly selective inhibition to emphasizes more moderate selectivity. This study presents a potent balanced COX-2 inhibitor, compound 21d, which effectively alleviates histological damage and provides protection against DSS-induced colitis. The severe adverse effects associated with imbalanced cyclooxygenase-2 (COX-2) inhibition continue to pose significant challenges in the development of contemporary anti-inflammatory drugs. In recent years, the approach to COX-2 inhibitor drug development has shifted from a focus on highly selective inhibition of COX-2 to a strategy that emphasizes more moderate selectivity. The amino acid sequence and structural similarities between inducible COX-2 and constitutive cyclooxygenase-1 (COX-1) isoforms present both substantial opportunities and challenges for the design of next generation of balanced COX-2 inhibitors. As part of our ongoing research into the discovering novel and safer COX-2 inhibitors, we reported herein a highly potent and balanced COX-2 inhibitor 21 d (IC 50 value=1.35 μM, selectivity profile (IC 50 (COX-1)/IC 50 (COX-2)=22.34)). In vivo assays demonstrated that 21 d significantly alleviated histological damage and provided robust protection against dextran sulfate sodium (DSS)-induced acute colitis.

✓ 已验证 DOI PubMed 高影响因子
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ENVIRONMENTAL SCIENCE & TECHNOLOGY · 2019 · IF 7.149

Bis(2-ethylhexyl)-2,3,4,5-tetrabromophthalate Affects Lipid Metabolism in Zebrafish Larvae via DNA Methylation Modification

Wei Guo,Jian Han,Shengmin Wu,Xiongjie Shi,Qiangwei Wang,Bingsheng Zhou

Bis(2-ethylhexyl)-2,3,4,5-tetrabromophthalate (TBPH) is a ubiquitous environmental contaminant, but its toxicity is not fully understood. Accordingly, we investigated the effects of TBPH and its metabolite, mono-(2-ethyhexyl)tetrabromophthalate (TBMEHP), on lipid metabolism using a zebrafish model. The molecular docking study revealed that TBPH and TBMEHP bind to zebrafish peroxisome proliferator-activated receptor γ (PPARγ), with binding energies similar to rosiglitazone, a PPARγ agonist. Zebrafish embryos 0.75 hpf were exposed to TBPH (0.2–2000 nM) or TBMEHP (0.2–2000 nM) until 72 hpf, and their effects on PPARγ-mediated lipid metabolism were evaluated. Significant regional DNA demethylation of the PPARγ promoter was observed in the larvae at 72 hpf. Demethylation of the PPARγ promoter accompanied by upregulation of tet1 and tet2 transcription caused upregulation of PPARγ transcription and certain downstream genes involved in lipid lipolysis, transport, and metabolism. The triglyceride and total cholesterol concentrations in the larvae were significantly reduced following exposure to TBPH or TBMEHP. Furthermore, significant increases in the whole ATP content and locomotor activity in the 120 hpf larvae were observed. The overall results suggest that both TBPH and TBMEHP affect methylation of the PPARγ promoter, subsequently influencing larvae lipid metabolism via the PPARγ signaling pathway and disrupting energy homeostasis.

CAS / MDL: 122320-73-4 22978-25-2
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Journal of Materials Chemistry A · 2025 · IF 9.5

Heterostructure design of Mn–Ni(OH)2@1T-MoS2 for enhanced aqueous asymmetric electrochemical capacitors

Qingyun Liu,Yi Wang,Tianzhao Hu,Shaorui Chen,Yaozu Wang,Hui Zhao,Wu Zhang,Zhigang Yuan,Yulian Wang,Zhenhua Sun,Feng Li

Achieving high energy density in aqueous asymmetric electrochemical capacitors hinges on the development of electrode materials that combine exceptional capacitance with superior conductivity. Despite its high theoretical capacitance, Ni(OH)2 is limited by low intrinsic conductivity, significantly limiting its performance. In this study, a Mn–Ni(OH)2@1T-MoS2 heterostructure was synthesized through a facile growth method, achieving significant electrochemical performance boost. The lattice matching at the heterointerface induces a controlled lattice expansion in Mn–Ni(OH)2, while the interfacial interactions promote electron transfer from Mn–Ni(OH)2 to 1T-MoS2. These synergistic effects enhance conductivity and active site utilization, addressing the core challenges of pristine Ni(OH)2. As a result, the heterostructure exhibits a high specific capacity of 244.2 mA h g−1 at 1 A g−1 and a rate capability of 51.4% at 12 A g−1. Moreover, the assembled asymmetric electrochemical capacitor delivers an energy density of 61.67 W h kg−1 at 600 W kg−1 and maintains 72.7% capacity retention after 10 000 cycles at 5 A g−1. This work not only highlights the critical role of heterointerfaces in enhanced electrochemical performance but also provides a robust strategy for designing high-performance energy storage systems.

✓ 已验证 产品关联 DOI 高影响因子
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FASEB JOURNAL · 2025 ·Vol. 39 ·期 11 ·e70691 · IF 4.2

Insulin‐Like Growth Factor 2 Reverses Synaptic and Cognitive Deficits in Fetal Growth Restriction Mice

Jianfeng Dong,Wen Chen,Shujuan Chang,Nana Liu,Wei Zhu,Li Ma,Jing Qiao,Yuhang Wang,Zhiyong Mao,Jiuhong Kang

Infants born with fetal growth restriction (FGR) are at increased risk of cognitive impairment in later life, yet the underlying mechanisms remain poorly understood, hampering clinical treatment development. Utilizing a FGR mouse model induced by prenatal dexamethasone overexposure, we observed impaired hippocampal dendritic maturation, synaptic plasticity, and hippocampal‐dependent learning and memory in FGR mice. FGR induces DNA hypomethylation in the hippocampal H19/Igf2 imprinted control region, resulting in reduced expression of Igf2, a key metabolic modulator previously implicated in FGR‐related placental and fetal growth. Using a neuron‐specific knockout mouse model, we validated the necessity of Igf2 for dendritic maturation and synaptic plasticity. Importantly, overexpression of Igf2 in the hippocampus of FGR mice improved synaptic plasticity and enhanced learning and memory abilities. Furthermore, running exercise ameliorated DNA hypomethylation driving Igf2 expression levels and counteracted synaptic and cognitive deficits in FGR mice through hippocampal Igf2. These findings unveil a molecular mechanism linking exercise‐induced epigenetic changes in the imprinting gene Igf2 to enhanced synaptic plasticity, ultimately leading to improved cognition in FGR offspring. Our results identify Igf2 as a potential mediator bridging metabolic dysfunction and cognitive impairments in FGR offspring and also propose that exercise represents a promising nondrug intervention for FGR‐related cognitive disorders. Fetal growth restriction (FGR) induces hippocampal DNA hypomethylation and loss of Igf2, contributing to impaired synaptic plasticity and cognitive deficits in offspring. Exercise restores Igf2 levels and rescues these impairments, suggesting a potential therapeutic strategy for FGR‐related cognitive dysfunction.

CAS / MDL: 75-85-4
✓ 已验证 产品关联 DOI PubMed 高影响因子
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ACS Applied Materials & Interfaces · 2025 · IF 8.2

Synergistic Cu2O@Ni(OH)2 Core–Shell Electrocatalyst for High-Efficiency Nitrate Reduction to Ammonia

Zunjie Zhang,Bingcheng Ge,Mengran Liu,Tianfang Yang,Shuaitong Wang,Yang Liu,Yingjie Yang,Shuyan Gao

The electrocatalytic reduction reaction of nitrate (NO3RR) is anticipated to convert nitrogen-containing pollutants into valuable ammonia products. Copper-based catalysts have received great attention because of their good performance in the NO3RR due to the strong binding energy with *NO3 intermediates. However, the poor H2O dissociation ability of Cu is unable to provide H• in time for the hydrogenation reaction of NOx, thus hindering the electroreduction of the NO3–. Herein, we designed a shell–core nanocube electrocatalyst Cu2O@Ni(OH)2-x (x represents the molar ratio of Ni/Cu) using the liquid phase reduction combined with the etching and precipitation method for electrocatalytic NO3RR. Due to the synergistic effect between the strong nitrate activation ability of Cu and the excellent H2O dissociation ability of Ni(OH)2, Cu2O@Ni(OH)2-3.3% shows an impressive ammonia yield rate (557.9 μmol h–1 cm–2) and Faradaic efficiency (97.4%) at −0.35 V vs. RHE. Operando Raman and Auger electron spectroscopy observe the reduction of Cu2O to Cu during the NO3RR process. Density functional theory calculations combined with electron paramagnetic resonance analysis reveals that Ni(OH)2 can lower the activation energy barrier of H2O dissociation, thereby promoting the generation of H• and accelerating the hydrogenation of *NO during the NO3RR. This research provides an efficient Cu-based catalyst for reducing NO3– and may motivate the development of effective ammonia electrocatalysts for further experimentation.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY · 2020 · IF 4.872

Effects of maternal T-2 toxin exposure on the hepatic glycolipid metabolism in young mice

Ruifen Kang,Aneela Perveen,Chunmei Li

T-2 toxin is a kind of group A trichothecenes mycotoxins , frequently detected in various foods and feeds, having high toxic effects on both humans and animals. The present study aims to investigate the toxic effects of T-2 toxin exposure to ICR mice during pregnancy and lactation on liver glycolipid metabolism of young mice. The pregnant mice were given 0, 0.005 and 0.05 mg of T-2 toxin/kg bw daily through oral gavage from late gestation (GD 14) to the lactation (LD 21). Liver and serum samples of the young mice were collected on postnatal day 21 (PND 21), PND 28 and PND 56. The results showed that T-2 toxin increased the contents of triglycerides (TG), total cholesterol (T-CHO) and glucose in serum of young mice on PND 21 and PND 28. In addition, obvious lipid droplets of liver in T-2 toxin treatment groups were observed, especially in 0.05 mg group of PND 21and PND 28. Compared with the control group, T-2 treatment also increased the expressions of genes associated with liver glycolipid metabolism, such as PEPCK , Glut2 , Fas , Acox1 , Hmgcr , PPARα , Srebp1 and CD36 . These results demonstrated T-2 toxin exposure to pregnant mice could cause liver glycolipid metabolism disruption in the young mice and the toxic effects weakened on PND 56.

✓ 已验证 DOI PubMed 高影响因子
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ANALYTICAL CHEMISTRY · 2022 · IF 8.008

Smartphone-Based Electrochemical Immunoassay for Point-of-Care Detection of SARS-CoV-2 Nucleocapsid Protein

Ruijin Zeng,Minghao Qiu,Qing Wan,Zhisheng Huang,Xiaolong Liu,Dianping Tang,Dietmar Knopp

Large-scale, rapid, and inexpensive serological diagnoses of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) are of great interest in reducing virus transmission at the population level; however, their development is greatly plagued by the lack of available point-of-care methods, leading to low detection efficiency. Herein, an ultrasensitive smartphone-based electrochemical immunoassay is reported for rapid (less than 5 min), low-cost, easy-to-implement detection of the SARS-CoV-2 nucleocapsid protein (SARS-CoV-2 N protein). Specifically, the electrochemical immunoassay was fabricated on a screen-printed carbon electrode coated with electrodeposited gold nanoparticles, followed by incubation of anti-N antibody (Ab) and bovine serum albumin as the working electrode. Accompanied by the antigen–antibody reaction between the SARS-CoV-2 N protein and the Ab, the electron transfer between the electroactive species [Fe(CN)6]3–/4– and the electrode surface is disturbed, resulting in reduced square-wave voltammetry currents at 0.075 V versus the Ag/AgCl reference electrode. The proposed immunoassay provided a good linear range with SARS-CoV-2 N protein concentrations within the scope of 0.01–1000 ng/mL (R2 = 0.9992) and the limit of detection down to 2.6 pg/mL. Moreover, the detection data are wirelessly transmitted to the interface of the smartphone, and the corresponding SARS-CoV-2 N protein concentration value is calculated and displayed. Therefore, the proposed portable detection mode offers great potential for self-differential diagnosis of residents, which will greatly facilitate the effective control and large-scale screening of virus transmission in resource-limited areas.

✓ 已验证 DOI PubMed 高影响因子
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POLYMER TESTING · 2021 · IF 4.282

Antifouling poly(N-(2-hydroxyethyl)acrylamide)/sodium alginate double network hydrogels with eminent mechanical properties

Jing Zhang,Pai Peng,Lingdong Chen,Liping Zhao,Jie Feng

In recent years, hydrogels with antifouling properties and good biocompatibility have attracted great attention in bio-devices, but most of them are lack of eminent mechanical properties that limit their practical application greatly. In this work, a newly hybrid ion-covalent cross-linked double network (DN) hydrogels with excellent antifouling as well as mechanical properties were prepared by a simple one-pot method based on sodium alginate and a kind of antifouling material, N -hydroxyethyl acrylamide (HEAA). The DN hydrogel have excellent mechanical properties, including high tensile strength (1.32 MPa), high elastic modulus (0.31 MPa) and preeminent fatigue resistance. Besides, the DN hydrogel have good antifouling properties suggested by protein adsorption and cell adhesion experiments. In addition, they also exhibit highly in vitro compatibility. These properties make the DN hydrogels suitable for application in different fields, such as tissue scaffolds, implantable devices and so on.

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