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Optimizing the electrode/electrolyte interface structure is the key to realizing high-voltage Li-metal batteries (LMBs). Herein, a functional electrolyte is introduced to synergetically regulate the interface layer structures on the high-voltage cathode and the Li-metal anode. Saccharin sodium (NaSH) as a multifunctional electrolyte additive is employed in fluorinated solvent-based electrolyte (FBE) for robust interphase layer construction. On the one hand, combining the results of ex-situ techniques and in-situ electrochemical dissipative quartz crystal microbalance (EQCM-D) technique, it can be seen that the solid electrolyte interface (SEI) layer constructed by NaSH-coupled fluoroethylene carbonate (FEC) on Li-metal anode significantly inhibits the growth of lithium dendrites and improves the cyclic stability of the anode. On the other hand, the experimental results also confirm that the cathode-electrolyte interface (CEI) layer induced by NaSH-coupled FEC effectively protects the active materials of LiCoO2 and improves their structural stability under high-voltage cycling, thus avoiding the material rupture. Moreover, theoretical calculation results show that the addition of NaSH alters the desolvation behavior of Li+ and enhances the transport kinetics of Li+ at the electrode/electrolyte interface. In this contribution, the LiCoO2ÇLi full cell containing FBE+NaSH results in a high capacity retention of 80% after 530 cycles with a coulombic efficiency of 99.8%.
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Mallotus apelta leaf, recorded in the quality standard of Yao Medicinal Material in Guangxi Zhuang autonomous region, is commonly used in the treatment of liver diseases. Total flavonoids of M. apelta leaf (TFM) had good anti-fibrosis activity, but the anti-fibrosis mechanism of TFM is still unclear. Nuclear magnetic resonance technology was used to study the dynamic changes of urine metabolites in CCl4 -induced liver fibrosis before and after TFM treatment. Ingenuity Path Analysis (IPA) was used to find potential target genes for TFM to improve liver fibrosis and verify the expression of target genes by real-time fluorescent quantitative PCR and Western blotting. TFM can significantly reduce serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) levels, improve liver steatosis and reduce inflammation; in urine metabolomics, a total of seven potential biomarkers were found, mainly involving two metabolic pathways; IPA analysis showed that TNF may be a potential target for TFM to improve liver fibrosis induced by CCl4 in rats. This study found that TNF may be a potential target gene for TFM treatment of liver fibrosis, and shows that the anti-fibrosis mechanism of TFM could improve liver fibrosis by regulating the tricarboxylic acid cycle and subtaurine metabolism.
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Tetracloreto de Carbono , Mallotus (Planta) , Animais , Ratos , Tetracloreto de Carbono/toxicidade , China , Cirrose Hepática/induzido quimicamente , Cirrose Hepática/tratamento farmacológico , Metabolômica , Flavonoides/farmacologia , Folhas de PlantaRESUMO
Understanding the release of pollutants from the formal e-waste dismantling site could provide the basic information and potential risk to guide the normative regulation of the process. In this study, the distribution of typical polybrominated diphenyl ethers (PBDEs) and heavy metals in a relocating site of a formal e-waste dismantling company was firstly investigated down to the saturated zone, with a maximum depth of 3.0 m. The mean concentrations of Σ13PBDEs were ranged from 2.815 to 7.178 ng/g, with a peak value of 7.178 ng/g in storage area. BDE-209 was the predominant congener of PBDEs in the soil, with the value ranged from 1.688 to 2.483 ng/g. A higher pollution of PBDEs and HMs was presented in the storage area. The risk assessment of PBDEs mostly posed a low environmental risk (RQ ≤ 0.01) and pentaBDE was found to be the most harmful driver for the potential environmental risk.
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Resíduo Eletrônico , Poluentes Ambientais , Metais Pesados , Monitoramento Ambiental , Éteres Difenil Halogenados/análise , Resíduo Eletrônico/análise , Metais Pesados/análise , ChinaRESUMO
Medium-low temperature pyrolysis is an effective method of retaining active components in sludge char. However, we found that incomplete cracking reactions resulted in residues of microplastics (MPs) remaining in the char; moreover, high levels of environmentally persistent free radicals (EPFRs) were detected in these MPs. Here, we investigated the temperature-dependent variations in the char-volatile products derived from sludge and MPs under different pyrolysis scenarios using multiple in situ probe coupling techniques and electron paramagnetic resonance spectroscopy, thereby identifying the sources of EPFRs and elucidating the corresponding formation-conversion mechanisms. The temperature was the key factor in the formation of EPFRs; in particular, in the 350-450 °C range, the abundance of EPFRs increased exponentially. Reactive EPFR readily formed in MPs with conjugated aromatic-ring structures (polyethylene terephthalate and polystyrene) at a temperature above 350 °C; EPFR concentrations were 5-17 times higher than those found in other types of polymers, and these radicals exhibited half-lives of more than 90 days. The EPFR formation mechanism could be summarized as solid-solid/solid-gas interfacial interactions between the polymers and the intermediate products from sludge pyrolysis (at 160-350 °C) and the homolytic cleavage-proton transfer occurring in the polymers themselves under the dual action of thermal induction and acid sites (at 350-450 °C). Based on the understanding of the evolution of EPFRs, temperature regulation and sludge components conditioning may be effective approaches to inhibit the formation of EPFRs in MPs, constituting reliable strategies to diminish the environmental risk associated with the byproducts of sludge pyrolysis.
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Pirólise , Esgotos , Esgotos/química , Microplásticos , Plásticos , Temperatura , Radicais Livres/química , PolímerosRESUMO
The relationship between the migration process and speciation distribution of Cr is important for the risk assessment in the underground environment. In this work, soil columns were collected from the chromate production site, with a 40-year operation, in the groundwater depression cone area of North China plain. The relationship between chromium pollution features and the geochemical properties of soil was established, and the migration risk of Cr(VI) was assessed based on the Nemerow composite index and Hydrus-1D model. The maximum total Cr concentration in the chromium slag dumping site reached 907 mg/kg, and that in the chromate production workshop was more than 200 mg/kg across the depth. The migration of Cr might be accelerated in the soil with abundant Mn (236-1461 mg/kg) but scarce organic matters (< 0.45%). The Hydrus simulation indicated that Cr(VI) would reach a cumulative flux of 300-729 mg/cm2 after 50 years.
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Água Subterrânea , Poluentes do Solo , Cromatos , Cromo/análise , Depressão , Água Subterrânea/química , Solo/química , Poluentes do Solo/análiseRESUMO
Background: Liver cancer had become the sixth most common cancer. Nitidine chloride (NC) has demonstrated promising anti-HCC properties; however, further elucidation of its mechanism of action is necessary. Methods: The anti-HCC targets of NC were identified through the utilization of multiple databases and ChIPs data analysis. The GO and KEGG analyses to determine the specific pathway affected by NC. The Huh 7 and Hep G2 cells were subjected to a 24-h treatment with NC, followed by evaluating the impact of NC on cell proliferation and cell cycle. The involvement of the p53/14-3-3 Sigma/CDK1 axis in HCC cells was confirmed by qPCR and WB analysis of the corresponding genes and proteins. Results: The GO and KEGG analysis showed the targets were related to cell cycle and p53 signaling pathways. In vitro experiments showed that NC significantly inhibited the proliferation of HCC cells and induced G2/M phase arrest. In addition, qPCR and WB experiments showed that the expression of p53 in HCC cells increased after NC intervention, while the expression of 14-3-3 Sigma and CDK1 decreased. Conclusion: NC can inhibit the proliferation of HCC cells and induce G2/M cell cycle arrest, potentially by regulating the p53/14-3-3 Sigma/CDK1 axis.
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Background and Purpose: Nitidine chloride (NC) is a botanical drug renowned for its potent anti-inflammatory, antimalarial, and hepatocellular carcinoma-inhibiting properties; however, its limited solubility poses challenges to its development and application. To address this issue, we have devised a colon-targeted delivery system (NC-CS/PT-NPs) aimed at modulating the dysbiosis of the gut microbiota by augmenting the interaction between NC and the intestinal microbiota, thereby exerting an effect against nonalcoholic fatty liver disease. Methods: The NC-CS/PT-NPs were synthesized using the ion gel method. Subsequently, the particle size distribution, morphology, drug loading efficiency, and release behavior of the NC-CS/PT-NPs were characterized. Furthermore, the impact of NC-CS/PT-NPs on non-alcoholic fatty liver disease (NAFLD) induced by a high-fat diet (HFD) in mice was investigated through serum biochemical analysis, ELISA, and histochemical staining. Additionally, the influence of NC-CS/PT-NPs on intestinal microbiota was analyzed using 16S rDNA gene sequencing. Results: The nanoparticles prepared in this study have an average particle size of (255.9±5.10) nm, with an encapsulation rate of (72.83±2.13) % and a drug loading of (4.65±0.44) %. In vitro release experiments demonstrated that the cumulative release rate in the stomach and small intestine was lower than 22.0%, while it reached 66.75% in the colon. In vivo experiments conducted on HFD-induced NAFLD mice showed that treatment with NC-CS/PT-NPs inhibited weight gain, decreased serum aspartate aminotransferase (AST), Alanine aminotransferase (ALT) and lipid levels, improved liver and intestinal inflammation, and altered the diversity of gut microbiota in mice. Conclusion: This study provides new evidence for the treatment of NAFLD through the regulation of gut microbiota using active ingredients from traditional Chinese medicine.
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Benzofenantridinas , Microbioma Gastrointestinal , Hepatopatia Gordurosa não Alcoólica , Camundongos , Animais , Hepatopatia Gordurosa não Alcoólica/tratamento farmacológico , Fígado , Intestino Delgado , Dieta Hiperlipídica , Camundongos Endogâmicos C57BLRESUMO
Plastics in landfills undergo a unique micronization process due to multi-factor and light-avoided conditions, but their aging process in such a typical environment remains unexplored. This study investigated the aging behavior of polyethylene plastics, representative of landfills, under simulated dynamic mechanical forces and high temperature-two prevalent environmental factors in landfills. The study explored the individual and combined contributions of these factors to the aging process. Results indicated that high temperature played a primary role in aging plastics by depolymerization and degradation through ·OH production, while mechanical forces contributed mainly to surface structure breakdown. The combined effect leads to more serious surface damage, creating holes, cracks, and scratches that provide access for free radical reactions to plastic bulk, thereby accelerating the aging and micronization process. The resulting microplastics were found to be 14.25 ± 0.53 µg L-1. Aged plastics exhibit a rapid aging rate of depolymerization and oxidation compared to virgin plastics due to their weak properties, suggesting a higher potential risk of microplastic generation. This study fills a knowledge gap regarding the aging behavior of plastics under complex and light-avoided landfill conditions, emphasizing the need for increased attention to the evolution process of microplastics from aged plastic waste in landfills.
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Eliminação de Resíduos , Poluentes Químicos da Água , Eliminação de Resíduos/métodos , Plásticos/química , Microplásticos , Instalações de Eliminação de ResíduosRESUMO
Landfills are the main plastic sinks and microplastics (MPs) sources in the anthropogenic terrestrial system. Understanding the dynamic process of generating MPs is a prerequisite to reducing their potential risk, which remains unexplored because of the complex stabilization process of landfills. In this study, we investigated the evolution process of MPs generated in a partitioned landfill, with well-recorded disposal ages of over 30 years. Considering the initial plastic proportions in fresh landfilled waste, the occurrence of MPs increased exponentially with the disposal age. A booming generation of MPs occurred from 71.3 ± 17.7 items/(g plastic) to 653.1 ± 191.5 items/(g plastic). The generation rates of MPs varied greatly depending on the individual polymer types, with polyethylene (PE) having the highest generation rate of 28.4 items/(g plastic) per year at 31 years, compared to that of polypropylene (PP) and polystyrene (PS) at 15.0 and 9.6 items/(g plastic) per year, respectively. The variation in the carbonyl index indicated that environmental oxidation might facilitate the fragmentation of plastic waste. The relative abundance of plastic-degrading microbes increased more than three times in the plastisphere after 30 years of landfilling, indicating that the potential biodegradation might be a nonnegligible driver for plastic fragmentation after long-term natural acclimatization. This study revealed the dynamic evolution process of MPs in landfills and predicted the booming stage, which might provide an important guideline for reducing the leakage risk of MPs during the reclamation of old landfills or dumping sites.
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Microplásticos , Poluentes Químicos da Água , Monitoramento Ambiental , Plásticos , Polietileno , Polipropilenos , Poliestirenos , Instalações de Eliminação de Resíduos , Poluentes Químicos da Água/análiseRESUMO
OBJECTIVE: To study the plasma protein binding rate of Tetramethylpyrazine Phosphate. METHODS: The ultrafiltration was employed to determine the plasma protein binding rate of Tetramethylpyrazine Phosphate. The plasma concentrations of Tetramethylpyrazine Phosphate were measured by RP-HPLC. RESULTS: The plasma protein binding rate of Tetramethylpyrazine Phosphate with HSA, human plasma and rat plasma were (64.64 +/- 0.68)%, (65.85 +/- 7.35)% and (73.65 +/- 2.35)%, respectively. CONCLUSION: The binding rate of Tetramethylpyrazine Phosphate with plasma protein is middling strength.
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Proteínas Sanguíneas/metabolismo , Fosfatos/metabolismo , Pirazinas/metabolismo , Ultrafiltração/métodos , Vasodilatadores/metabolismo , Animais , Apiaceae/química , Cromatografia Líquida de Alta Pressão , Humanos , Ligação Proteica , Ratos , Ratos Sprague-Dawley , Sensibilidade e EspecificidadeRESUMO
ETHNOPHARMACOLOGICAL RELEVANCE: The Mallotus apelta (Lour.) Muell.Arg. is a well-known traditional Chinese medicine (TCM) used for anti-inflammatory, hemostasis and chronic hepatitis. AIM: The purpose of this study was to explore the antifibrotic effect of total flavonoids of Mallotus apelta leaf (TFM) and its potential mechanism. METHODS: Hepatic fibrosis was induced by carbon tetrachloride (CCl4) in rats. The CCl4-induced rats received intragastric administration of colchicine (0.2 mg/kg per day), TFM (25, 50, 100 mg/kg per day) and the equal vehicle was given to normal rats. Pathological evaluation in hepatic tissue were examined by hematoxylin and eosin (HE) staining. And the levels of serum biochemical parameters were detected by automatic biochemical analysis. Meanwhile, the collagen deposition in liver was observed by staining with Masson's trichrome. Collagenic parameters and inflammatory factors were measured by enzyme-linked immunosorbent assay (ELISA) kits. Additionally, corresponding assay kit was used to estimate the antioxidant enzyme and lipid peroxidation. In order to explore the potential mechanism of anti-fibrotic effects in TFM, the expressions of liver fibrosis related gene and protein were analyzed by real-time quantitative reverse transcription polymerase chain reaction (RT-PCR) and Western blot. RESULTS: The CCl4-induced hepatic fibrosis were inhibited dose-dependently in rats by TFM. The results showed that the key hallmarks of liver injury including aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), albumin (ALB) and total protein (TP) in the serum were reversed in CCl4-induced hepatic fibrosis rats which were treated by TFM. Furthermore, TFM significantly alleviates collagen accumulation and reduces the contents of hydroxyproline (Hyp), Type III precollagen (PC-III), collagen I (Col I), hyaluronic acid (HA) and laminin (LN). RT-PCR and Western blot results showed that TFM markedly inhibits liver fibrosis hallmark factor α-smooth muscle actin (α-SMA) expressions in CCl4-induced hepatic fibrosis rats. Moreover, TFM alleviated the oxidative stress and lipid peroxidation in rats induced by CCl4. TFM also attenuated the pro-inflammatory cytokines including interleukin-1ß (IL-1ß), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) via inhibiting nuclear factor-κB (NF-κB) activation. Meanwhile, transforming growth factor-ß1 (TGF-ß1)/Smad signaling pathway was inhibited by TFM treatment. CONCLUSIONS: TFM can alleviate CCl4-induced hepatic fibrosis in rats, which potential mechanism may be due to its ability of reducing ECM accumulation, improving antioxidant and regulating TGF-ß1/Smad signaling pathways and NF-κB-dependent inflammatory response.