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INTRODUCTION: Triple-negative breast cancer (TNBC) is the primary cause of breast cancer-induced death in women. Literature has confirmed the benefits of Salidroside (Sal) in treating TNBC. However, the study about potential therapeutic targets and mechanisms of Sal-anchored TNBC remains limited. OBJECTIVE: This study was designed to explore the main targets and potential mechanisms of Sal against TNBC. METHODS: Network pharmacology, bioinformatics, and machine learning algorithm strategies were integrated to examine the role, potential targets, and mechanisms of the Sal act in TNBC. MDA-MB-231 cells and tumor-bearing nude mice were chosen for in vitro and in vivo experimentation. Cell viability and cytotoxicity were determined using CCK-8, LDH test, and Calcein-AM/PI staining. Antioxidant defense, lipid peroxidation, and iron metabolism were explored using glutathione, glutathione peroxidase, malondialdehyde (MDA), C11-BODIPY 581/591 probe, and FerroOrange dye. Glutathione peroxidase 4 (GPX4) or stearoyl-CoA desaturase 1 (SCD1) overexpression or nuclear receptor co-activator 4 (NCOA4) deficiency was performed to demonstrate the mechanism of Sal on TNBC. RESULTS: The prediction results confirmed that 22 ferroptosis-related genes were identified in Sal and TNBC, revealing that the potential mechanism of the Sal act on TNBC was linked with ferroptosis. Besides, these genes were mainly involved in the mTOR, PI3K/AKT, and autophagy signaling pathway by functional enrichment analysis. The in vitro validation results confirmed that Sal inhibited TNBC cell proliferation by modulating ferroptosis via elevation of intracellular Fe2+ and lipid peroxidation. Mechanistically, Sal sensitized TNBC cells to ferroptosis by inhibiting the PI3K/AKT/mTOR axis, thereby suppressing SCD1-mediated lipogenesis of monounsaturated fatty acids to induce lipid peroxidation, additionally facilitating NCOA4-mediated ferritinophagy to increase intracellular Fe2+ content. The GPX4 or SCD1 overexpression or NCOA4 deficiency results further supported our mechanistic studies. In vivo experimentation confirmed that Sal is vital for slowing down tumor growth by inducing ferroptosis. CONCLUSIONS: Overall, this study elucidates TNBC pathogenesis closely linked to ferroptosis and identifies potential biomarkers in TNBC. Meanwhile, the study elucidates that Sal sensitizes TNBC to ferroptosis by SCD1-mediated lipogenesis and NCOA4-mediated ferritinophagy, regulated by PI3K/AKT/mTOR signaling pathways. Our findings provide a theoretical basis for applying Sal to treat TNBC.
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BACKGROUND: Researchers have not studied the integrity, orderly correlation, and dynamic openness of complex organisms and explored the laws of systems from a global perspective. In the context of reductionism, antidepressant development formerly focused on advanced technology and molecular details, clear targets and mechanisms, but the clinical results were often unsatisfactory. PURPOSE: MDD represents an aggregate of different and highly diverse disease subtypes. The co-occurrence of stress-induced nonrandom multimorbidity is widespread, whereas only a fraction of the potential clusters are well known, such as the MDD-FGID cluster. Mapping these clusters, and determining which are nonrandom, is vital for discovering new mechanisms, developing treatments, and reconfiguring services to better meet patient needs. STUDY DESIGN: Acute stress 15-minute forced swimming (AFS) or CUMS protocols can induce the nonrandom MDD-FGID cluster. Multiple biological processes of rats with depression-like behaviours and gastrointestinal dysmobility will be captured under conditions of stress, and the Fructus Aurantii-Rhizoma Chuanxiong (ZQCX) decoction will be utilized to dock the MDD-FGID cluster. METHODS/RESULTS: Here, Rhizoma Chuanxiong, one of the seven components of Chaihu-shugan-San, elicited the best antidepressant effect on CUMS rats, followed by Fructus Aurantii. ZQCX reversed AFS-induced depression-like behaviours and gastrointestinal dysmobility by regulating the glutamatergic system, AMPAR/BDNF/mTOR/synapsin I pathway, ghrelin signalling and gastrointestinal nitric oxide synthase. Based on the bioethnopharmacological analysis strategy, the determined meranzin hydrate (MH) and senkyunolide I (SI) by UPLC-PDA, simultaneously absorbed by the jejunum and hippocampus of rats, have been considered major absorbed bioactive compounds acting on behalf of ZQCX. Cotreatment with MH and SI at an equivalent dose in ZQCX synergistically replicated over 50.33 % efficacy of the parent formula in terms of antidepressant and prokinetic actions by modulating neuroinflammation and ghrelin signalling. CONCLUSION: Brain-centric mind shifts require the integration of multiple central and peripheral systems and the elucidation of the underlying neurobiological mechanisms that ultimately contribute to novel therapeutic options. Ghrelin signalling and the immune system may partially underlie multimorbidity vulnerability, and ZQCX anchors stress-induced MDD-FGID clusters by docking them. Combining the results of micro details with the laws of the macro world may be more effective in finding treatments for MDD.
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Medicamentos Herbarios Chinos , Ratas Sprague-Dawley , Estrés Psicológico , Animales , Medicamentos Herbarios Chinos/farmacología , Estrés Psicológico/tratamiento farmacológico , Masculino , Ratas , Antidepresivos/farmacología , Modelos Animales de Enfermedad , Enfermedades Gastrointestinales/tratamiento farmacológico , Depresión/tratamiento farmacológico , Trastorno Depresivo Mayor/tratamiento farmacológico , Motilidad Gastrointestinal/efectos de los fármacos , Sistemas Neurosecretores/efectos de los fármacos , Conducta Animal/efectos de los fármacos , Citrus/química , Factor Neurotrófico Derivado del Encéfalo/metabolismoRESUMEN
To investigate the gut microbiota distribution and its functions in children with avoidant/restrictive food intake disorder (ARFID). A total of 135 children were enrolled in the study, including 102 children with ARFID and 33 healthy children. Fecal samples were analyzed to explore differences in gut microbiota composition and diversity and functional differences between the ARFID and healthy control (HC) groups via 16S rDNA and metagenomic sequencing. The gut microbiota composition and diversity in children with ARFID were different from those in heathy children, but there is no difference in the composition and diversity of gut microbiota between children at the age of 3-6 and 7-12 with ARFID. At the phylum level, the most abundant microbes in the two groups identified by 16S rDNA and metagenomic sequencing were the same. At the genus level, the abundance of Bacteroides was higher in the ARFID group (P > 0.05); however, different from the result of 16SrDNA sequencing, metagenomic sequencing showed that the abundance of Bacteroides in the ARFID group was significantly higher than that in the HC group (P = 0.041). At the species level, Escherichia coli, Streptococcus thermophilus and Lachnospira eligens were the most abundant taxa in the ARFID group, and Prevotella copri, Bifidobacterium pseudocatenulatum, and Ruminococcus gnavus were the top three microbial taxa in the HC group; there were no statistically significant differences between the abundance of these microbial taxa in the two groups. LefSe analysis indicated a greater abundance of the order Enterobacterales and its corresponding family Enterobacteriaceae, the family Bacteroidaceae and corresponding genus Bacteroides, the species Bacteroides vulgatus in ARFID group, while the abundance of the phylum Actinobacteriota and its corresponding class Actinobacteria , the order Bifidobacteriales and corresponding family Bifidobacteriaceae, the genus Bifidobacterium were enriched in the HC group. There were no statistically significant differences in the Chao1, Shannon and Simpson indices between the Y1 and Y2 groups (P = 0.1, P = 0.06, P = 0.06). At the phylum level, Bacillota, Bacteroidota, Proteobacteria and Actinobacteriota were the most abundant taxa in both groups, but there were no statistically significant differences among the abundance of these bacteria (P = 0.958, P = 0.456, P = 0.473, P = 0.065). At the genus level, Faecalibacterium was more abundant in the Y2 group than in the Y1 group, and the difference was statistically significant (P = 0.037). The KEGG annotation results showed no significant difference in gut microbiota function between children with ARFID and healthy children; however, GT26 was significantly enriched in children with ARFID based on the CAZy database. The most abundant antibiotic resistance genes in the ARFID group were the vanT, tetQ, adeF, ermF genes, and the abundance of macrolide resistance genes in the ARFID group was significantly higher than that in the HC group (P = 0.041). Compared with healthy children, children with ARFID have a different distribution of the gut microbiota and functional genes. This indicates that the gut microbiome might play an important role in the pathogenesis of ARFID.Clinical trial registration: ChiCTR2300074759.
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Actinobacteria , Trastorno de la Ingesta Alimentaria Evitativa/Restrictiva , Microbiota , Humanos , Niño , Antibacterianos , Farmacorresistencia Bacteriana , Macrólidos , Bacterias/genética , Actinobacteria/genética , Ingestión de Alimentos , ARN Ribosómico 16S/genéticaRESUMEN
With the rapid development of industrialization and agriculture, a series of critical imminent environmental problems and water pollution have caught wide attention from the public and society. Piezoelectric catalysis technology with piezoelectric materials is a green and environmental method that can efficiently improve the separation of electron-hole pairs, then generating the active substances such as OH, H2O2 and O2-, which can degrade water pollutants. Therefore, we firstly surveyed the piezoelectric catalysis in piezoelectric materials and systematically concluded and emphasized the relationship between piezoelectric materials and the piezoelectric catalytic mechanism, the goal to elucidate the effect of polarization on piezoelectric catalytic performance and enhance piezoelectric catalytic performance. Subsequently, the applications of piezoelectric materials in water treatment and environmental pollutant remediation were discussed including degradation of organic pollutants, removal of heavy mental ions, radionuclides, bacteria disinfection and water splitting for H2 generation. Finally, the development prospects and future outlooks of piezoelectric catalysis were presented in detail.
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On high-speed roads, there are certain blind areas within the radar coverage, especially when the blind zone is in curved road sections; because the radar does not have the measurement point information in multiple frames, it is easy to have a large deviation between the real trajectory and the filtered trajectory. In this paper, we propose a track prediction method combined with a high-precision map to solve the problem of scattered tracks when the targets are in the blind area. First, the lane centerline is fitted to the upstream and downstream lane edges obtained from the high-precision map in certain steps, and the off-north angle at each fitted point is obtained. Secondly, the normal trajectory is predicted according to the conventional method; for the extrapolated trajectory, the northerly angle of the lane centerline at the current position of the trajectory is obtained, the current coordinate system is converted from the north-east-up (ENU) coordinate system to the vehicle coordinate system, and the lateral velocity of the target is set to zero in the vehicle coordinate system to reduce the error caused by the lateral velocity drag of the target. Finally, the normal trajectory is updated and corrected, and the normal and extrapolated trajectories are managed and reported. The experimental results show that the accuracy and convergence effect of the proposed methods are much better than the traditional methods.
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Algoritmos , RadarRESUMEN
Retraction of 'Sequestration and speciation of Eu(III) on gamma alumina: role of temperature and contact order' by Yawen Cai et al., Environ. Sci.: Processes Impacts, 2015, 17, 1904-1914, https://doi.org/10.1039/C5EM00412H.
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In this work, a CdS/BiVO4 step-scheme (S-scheme) heterojunction with self-photothermally enhanced photocatalytic effect was synthesized and applied for efficient U(VI) photoextraction. Characterizations such as transient absorption spectroscopy and Tafel test together confirmed the formation of S-scheme heterojunctions, which allows CdS/BiVO4 to avoid photocorrosion while retaining the strong reducing capacity of CdS and the oxidizing capacity of BiVO4. Experimental results such as radical quenching experiments and electron spin resonance show that U(VI) is rapidly oxidized by photoholes/â¢OH to insoluble UO2(OH)2 after being reduced to U(IV) by photoelectrons/â¢O2 -, which precisely avoids the depletion of electron sacrificial agents. The rapid recombination of electron-hole pairs triggered by the S-scheme heterojunction is found to release large amounts of heat and accelerate the photocatalysis. This work offers a new enhanced strategy for photocatalytic uranium extraction and presents a direction for the design and development of new photocatalysts.
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With the fast development of industry, large amounts of organic and inorganic pollutants are inevitably released into the natural environment, which results in the pollution of the environment and are thereby dangerous to human health. The efficient elimination of these pollutants is crucial to environment protection and human health. The high sorption capacity of carbon-based materials and high photocatalytic ability of carbon-based composites result in the application of carbon-based materials in environmental pollution cleanup. In this review article, we summarized recent studies on the synthesis of carbon-based materials, and their application in the sorption of organic and inorganic pollutants, the photocatalytic degradation of organic pollutants, and the in situ photocatalytic reduction-solidification of heavy metal ions. The sorption method is useful to remove pollutants from aqueous solutions. The sorption-photocatalytic degradation of organic pollutants is applicable, especially at low concentrations, whereas the catalytic reduction of metal ions is the best method for the in situ immobilization of high valent metal ions under complicated conditions. The interaction mechanism is discussed using advanced spectroscopy analysis and theoretical calculations, and at the end the challenges in the future are described.
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With the fast development of industry and nuclear energy, large amounts of different radionuclides are inevitably released into the environment. The efficient solidification or elimination of radionuclides is thereby crucial to environmental pollution and human health because of the radioactive hazardous of long-lived radionuclides. The properties of negatively or positively charged radionuclides are quite different, which informs the difficulty of simultaneous elimination of the radionuclides. Herein, we summarized recent works about the selective sorption or catalytic reduction of target radionuclides using different kinds of nanomaterials, such as carbon-based nanomaterials, metal-organic frameworks, and covalent organic frameworks, and their interaction mechanisms are discussed in detail on the basis of batch sorption results, spectroscopy analysis and computational calculations. The sorption-photocatalytic/electrocatalytic reduction of radionuclides from high valent to low valent is an efficient strategy for in situ solidification/immobilization of radionuclides. The special functional groups for the high complexation of target radionuclides and the controlled structures of nanomaterials can selectively bind radionuclides from complicated systems. The challenges and future perspective are finally described, summarized, and discussed.
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Background: Shenlingbaizhu powder (SLBZP), one of the classic Earth-cultivating and gold-generating prescriptions of traditional Chinese medicine, is widely used to treat various diseases. However, the pharmacological mechanisms of SLBZP on bronchial asthma (BA) and allergic colitis (AC) remain to be elucidated. Methods: Network pharmacology and molecular docking technology were used to explore the potential mechanism of SLBZP in treating BA and AC with the simultaneous treatment of different diseases. The potential active compounds of SLBZP and their corresponding targets were obtained from BATMAN-TCM, ETCM, SymMap TCM@TAIWAN, and TCMSP databases. BA and AC disease targets were collected through DisGeNET, TTD, GeneCards, PharmGKB, OMIM, NCBI, The Human Phenotype Ontology, and DrugBank databases. Common targets for drugs and diseases were screened by using the bioinformatics and evolutionary genomics platform. The analyses and visualizations of Gene Ontology (GO) function and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment of common targets were carried out by R software. The key targets were screened by using the plug-in "cytoHubba" of Cytoscape software, and the "active compound-key target" network was constructed. Molecular docking analysis was performed using AutoDock software. The miRTarBase database was used to predict microRNAs (miRNAs) targeting key targets, and the key target-miRNA network was constructed. Result: Through screening, 246 active compounds and 281 corresponding targets were obtained. Common targets were mainly enriched in 2933 biological processes and 182 signal pathways to play the role of treating BA and AC. There were 131 active compounds related to key targets. The results of molecular docking showed that the important active compounds in SLBZP had good binding ability with the key targets. The key target-miRNA network showed that 94 miRNAs were predicted. Conclusion: SLBZP has played the role of treating different diseases with the same treatment on BA and AC through the characteristics of multicompound, multitarget, and multipathway of traditional Chinese medicine, which provides a theoretical basis for explaining the mechanism and clinical application of SLBZP treating different diseases with the same treatment in BA and AC.
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Backgrounds: Psoriasis and atopic dermatitis are two common chronic inflammatory skin diseases that enormously deteriorate the psycho-physical and socio-economic condition of the patients. Although differential immune responses have been found to operate in the pathomechanisms of atopic dermatitis and psoriasis, the epidermal keratinocytes are the major targets in both diseases, and sometimes, they show similar clinical presentations. The skin barrier, itching, and inflammation are current and future treatment targets for both of them, but the relevant shared mechanisms of the two diseases are far from understood. Methods: The differential analyses of GSE14905 (psoriasis) and GSE32924 (atopic dermatitis) deposited in GEO database were conducted and obtained their differential expressed genes. Moreover, PPI, functional modules, GO, and KEGG enrichment analyses were used for the further analysis. The mouse models of psoriasis and atopic dermatitis were established, and then, RT-qPCR and Western blotting assay were performed to check the abundant changes of hub genes. Results: There are 732 differentially expressed genes in psoriasis versus nonlesional skin samples. Besides, 611 differentially expressed genes were identified in atopic dermatitis versus nonlesional skin data sets. Based on these differentially expressed genes, we predicted their joint and individual protein-protein interaction networks and functional modules in both psoriasis and atopic dermatitis. Through the PPI network of genes, we calculated the hub nodes and do the GO and KEGG enrichment analysis of overlapped genes of psoriasis and atopic dermatitis, which suggested there were some terms like "positive regulation of interleukin-12 production," "centromeric region," and "TNF signaling pathway." Conclusion: We constructed the predicted PPI networks and functional modules related to psoriasis and atopic dermatitis and distinguished the key candidate target genes CXCL8, STAT1, and MMP9 in the diagnosis and therapy of similar pathogenesis.
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Dermatitis Atópica , Psoriasis , Animales , Dermatitis Atópica/metabolismo , Perfilación de la Expresión Génica , Humanos , Ratones , Mapas de Interacción de Proteínas/genética , Psoriasis/metabolismo , Piel/patologíaRESUMEN
Depression is a common and serious mental disorder. Data on its pathogenesis remain unclear and the options of drug treatments are limited. Here, we explored the role of pyroptosis, a novel pro-inflammatory programmed cell death process, in depression as well as the anti-depression effects and mechanisms of salidroside (Sal), a bioactive extract from Rhodiola rosea L. We established a corticosterone (CORT)-induced or lipopolysaccharide (LPS)-induced mice in vivo, and CORT, or nigericin (NLRP3 agonist)-induced PC12 cells in vitro. Our findings demonstrated that Sal profoundly mediated CORT or LPS-induced depressive behavior and improved synaptic plasticity by upregulating the expression of brain-derived neurotrophic factor (BDNF) gene. The data showed upregulation of proteins associated with NLRP3-mediated pyroptosis, including NLRP3, cleaved Caspase-1, IL-1ß, IL-18, and cleaved GSDMD. The molecular docking simulation predicted that Sal would interact with P2X7 of the P2X7/NF-κB/NLRP3 signaling pathway. In addition, our findings showed that the NLRP3-mediated pyroptosis was regulated by P2X7/NF-κB/NLRP3 signaling pathway. Interestingly, Sal was shown to ameliorate depression via suppression of the P2X7/NF-κB/NLRP3 mediated pyroptosis, and rescued nigericin-induced pyroptosis in the PC12 cells. Besides, knock down of the NLRP3 gene by siRNA markedly increased the inhibitory effects of Sal on pyroptosis and proinflammatory responses. Taken together, our findings demonstrated that pyroptosis plays a crucial role in depression, and Sal ameliorates depression by suppressing the P2X7/NF-κB/NLRP3-mediated pyroptosis. Thus, our study provides new insights into the potential treatment options for depression.
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The selective elimination of long-lived radioactive actinides from complicated solutions is crucial for pollution management of the environment. Knowledge about the species, structures and interaction mechanism of actinides at solid-water interfaces is helpful to understand and to evaluate physicochemical behavior in the natural environment. In this review, we summarize recent works about the sorption and interaction mechanism of actinides (using U, Np, Pu, Cm and Am as representative actinides) on natural clay minerals and man-made nanomaterials. The species and microstructures of actinides on solid particles were investigated by advanced spectroscopy techniques and computational theoretical calculations. The reduction and solidification of actinides on solid particles is the most effective way to immobilize actinides in the natural environment. The contents of this review may be helpful in evaluating the migration of actinides in near-field nuclear waste repositories and the mobilization properties of radionuclides in the environment.
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The efficient decontamination of pertechnetate (99TcO4-) is an essential task for managing radioactive 99Tc in nuclear wastes. Perrhenate, (ReO4-), as a nonradioactive analog, exhibits almost identical physicochemical properties as 99TcO4-. Herein, a novel magnetic amine-functionalized MIL-101(Cr) (NH2-MIL-101(Cr)@Fe3O4) was prepared and used to efficiently remove ReO4- from solution for the facile magnetic separation. A series of environmental parameters were considered to investigate the adsorption performance of NH2-MIL-101(Cr)@Fe3O4. Experimental results suggested that NH2-MIL-101(Cr)@Fe3O4 has reached a satisfied adsorption capacity (~401 mg/g) and a very fast adsorption kinetics at pH 7.0. The selectivity for ReO4- was maintained even in the presence of interfering anions with relatively high concentrations. ReO4- were mainly captured by N-donor sites of the surface-decorated amine via complexation and were trapped in the cavities of modified MIL-101(Cr). NH2-MIL-101(Cr)@Fe3O4 exhibits satisfactory adsorption performance for ReO4- and can be conveniently separated from wastewaters after adsorption.
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Amyloid ß-protein (Aß) is reported to activate NLRP3 inflammasomes and drive pyroptosis, which is subsequently involved in the pathogenesis of neurodegenerative diseases, such as Alzheimer's disease (AD). To date, the pathogenesis of AD is unfortunately insufficiently elucidated. Therefore, this study was conducted to explore whether Salidroside (Sal) treatment could benefit AD by improving pyroptosis. Firstly, two animal models of AD, induced, respectively, by Aß1-42 and D-galactose (D-gal)/AlCl3, have been created to assist our appreciation of AD pathophysiology. We then confirmed that pyroptosis is related to the pathogenesis of AD, and Sal can slow the progression of AD by inhibiting pyroptosis. Subsequently, we established the D-gal and Nigericin-induced PC12 cells injury model in vitro to verify Sal blocks pyroptosis mainly by targeting the NLRP3 inflammasome. For in vivo studies, we observed that Aß accumulation, Tau hyperphosphorylation, neurons of hippocampal damage, and cognitive dysfunction in AD mice, caused by bilateral injection of Aß1-42 into the hippocampus and treatments with D-gal combine AlCl3. Besides, accumulated Aß promotes NLRP3 inflammasome activation, which leads to the activation and release of a pro-inflammatory cytokine, interleukin-1 beta (IL-1ß). Notably, both Aß accumulation and hyperphosphorylation of Tau decreased and inhibited pyroptosis by downregulating the expression of IL-1ß and IL-18, which can be attributed to the treatment of Sal. We further found that Sal can reverse the increased protein expression of TLR4, MyD88, NF-κB, P-NF-κB, NLRP3, ASC, cleaved Caspase-1, cleaved GSDMD, IL-1ß, and IL-18 in vitro. The underlying mechanism may be through inhibiting TLR4/NF-κB/NLRP3/Caspase-1 signaling pathway. Our study highlights the importance of NLRP3 inflammasome-mediated pyroptosis in AD, and how the administration of pharmacological doses of Sal can inhibit NLRP3 inflammasome-mediated pyroptosis and ameliorate AD. Thus, we conclude that NLRP3 inflammasome-mediated pyroptosis plays a significant role in AD and Sal could be a therapeutic drug for AD.
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Adsorbents with the combination of magnetic separation and removal performance are expected for reducing the adverse impact of nuclear pollution. In this study, the core-shell Fe3O4@polydopamine (Fe3O4@PDA) was successfully synthesized and used for removal of uranium (U(VI)) ion from aqueous solution. The abundant N-containing groups derived from PDA exist as the chelate sites for U(VI) and contribute greatly for U(VI) removal. Experimental results show that Fe3O4@PDA (56.39 mg g-1) exhibits greater sorption capacity for U(VI) removal compared with the pure Fe3O4 (9.17 mg g-1). The sorption isotherm can be well fitted with Freundlich model and the sorption process is endothermic and spontaneous. The removal of U(VI) can be explained by the complexation of U(VI) with -NH-, -NH2 and C-O in the surface of Fe3O4@PDA by X-ray photoelectron spectroscopy (XPS) analysis.
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Uranio , Adsorción , Indoles , Polímeros , Uranio/análisisRESUMEN
Elimination of U(VI) from polluted solutions is important for human health and environmental safety. In this work, a relatively low-cost 3D flower-like phosphate-functionalized layered double hydroxides (phos-LDH) was fabricated by a one-pot hydrothermal method. The prepared phos-LDH inherited the structure of 3D flower-like layered double hydroxides (LDH), and had a higher specific surface area (â¼203.4 m2â g-1) than that of LDH. The kinetic process indicated that U(VI) adsorption onto phos-LDH achieved equilibrium within 15 min and obeyed general order model. The adsorption isotherms of phos-LDH illustrated that the U(VI) adsorption obeyed Langmuir model, the adsorption capability of phos-LDH can reach 923.1 mgâ g-1 at 298 K. The U(VI) adsorption was a spontaneous and endothermic process according to the thermodynamic data. There was the electrostatic attraction between U(VI) and phos-LDH at pH = 5.0. FTIR and XPS analyses educed that the hydroxyl and phosphate groups played a very useful role for the complexation between U(VI) and phos-LDH. In addition, the excellent selective adsorption capability for U(VI) in competitive cation and anion solutions further confirmed the practical application of phos-LDH in real wastewater treatment.
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In the original publication Fig. 10b was erroneously plotted due to the authors' carelessness and unintentional misoperation.
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This study investigated the modification of moso bamboo biochar with polyethyleneimine (PEI) for the efficient enrichment of U(VI) in aqueous solution. The alkali/acid treated biochars with amine groups (PEI-alkali-biochar or PEI-acid-biochar) were characterized by SEM, BET, TGA, FTIR and XPS. The effects of contact time, U(VI) concentration, pH and ionic strength on U(VI) adsorption by PEI-alkali/acid-biochar were studied. U(VI) adsorption process on PEI-alkali/acid-biochar obeys pseudo-second-order model. Intraparticle diffusion model was used to investigate the controlled factors of the adsorption process. The fitting of Langmuir model gives the maximum adsorption capacities of 212.7 mg/g for PEI-alkali-biochar and 185.6 mg/g for PEI-acid-biochar, which are almost 9-10 times higher than that of pristine biochar (20.1 mg/g). The thermodynamic parameters illustrate that U(VI) adsorption on PEI-alkali/acid-biochar is an exothermic and spontaneous process. The FTIR and XPS analyses imply that U(VI) adsorption by PEI-alkali/acid-biochar is mainly controlled by complexation between U(VI) and amine groups. PEI-alkali/acid-biochar could be considered as a low-cost and outstanding material for U(VI) removal from radionuclide wastewater in practical application.