Search Results (2,095)

Waste textiles may contain heavy metals, which can originate from dyes, mordants, or other chemical treatments used during manufacturing. To explore the impact of heavy metals on the adsorption properties of activated carbon derived from discarded textiles through pyrolysis and to mitigate heavy metal migration, this study investigated the adsorption behavior of copper-impregnated pyrolytic carbon toward typical pollutants—methylene blue and lead—in simulated dyeing wastewater. Aqueous copper nitrate was used to impregnate the waste pure cotton textiles (WPCTs) to introduce copper species as precursors for creating additional active sites. The study systematically examined adsorption mechanisms, single and binary adsorption systems, adsorption kinetics, adsorption isotherms, adsorption thermodynamics, and the influence of pH. Key findings and conclusions are as follows: Under optimal conditions, the copper-containing biochar (Cu-BC) demonstrated maximum adsorption capacities of 36.70 ± 1.54 mg/g for Pb(II) and 104.93 ± 8.71 mg/g for methylene blue. In a binary adsorption system, when the contaminant concentration reached 80 mg/L, the adsorption capacity of Cu-BC for Pb(II) was significantly enhanced, with the adsorption amount increasing by over 26%. However, when the Pb(II) concentration reached 40 mg/L, it inhibited the adsorption of contaminants, reducing the adsorption amount by 20%. SEM, XRD, Cu LMM, FTIR and XPS result analysis proves that the adsorption mechanism of methylene blue involves π–π interactions, hydrogen bonding, electrostatic interactions, and pore filling. For Pb(II) ions, the adsorption likely occurs via electrostatic interactions, complexation with functional groups, and pore filling. This study supplements the research content on the copper adsorption mechanism supported by biochar for heavy metal adsorption research and broadens the application scope of biochar in the field of heavy metal adsorption. Full article

Simultaneously inhibiting beta-amyloid protein (Aβ) aggregation and reducing metal ion overload in the brain is a promising strategy for treating Alzheimer’s disease (AD). Aloe emodin (AE) is one of the major components of the traditional Chinese medicine rhubarb. Based on its reported pharmacological effects and its structural affinity for metal ions, this study aims to explore the potential of AE in improving AD pathology. Through the injection of Aβ or copper-Aβ complex in the bilateral hippocampus of rats, we constructed two kinds of nontransgenic animal models. Behavioral tests were used to evaluate cognitive impairment, and the effects of AE on neuronal damage and Aβ deposition were measured via Nissl staining and immunohistochemistry. Furthermore, we detected copper content in the serum and brain tissues as well as some biochemical indexes of Aβ cascade pathology in the brain tissues of model rats to explore the mechanism of action. AE treatment decreased copper accumulation and regulated Aβ metabolism in the brain of model rats, thereby improving Aβ deposition, memory impairment, hippocampal nerve cell damage, and related biochemical indicators. AE ameliorated the AD pathology of the model rats by targeting copper-induced Aβ toxicity, revealing a mechanism of action by which AE may exhibit good clinical efficacy in treating AD. Full article

Background: Triple-negative breast cancer (TNBC) remains primarily treated with chemotherapy due to the lack of effective therapeutic targets, but this approach carries significant systemic toxicity and a high risk of drug resistance. Curcumin (Cur), despite its multifaceted antitumor activity, faces limitations in clinical application due to poor water solubility and weak targeting properties. This study aims to develop a folate/mitochondria dual-targeted curcumin–copper chelate liposome (Cu-Cur DTLPs) formulation that enables copper accumulation within tumor cells and induces copper-mediated cell death, thereby providing an effective and relatively low-toxicity therapeutic strategy for triple-negative breast cancer. Methods: Curcumin–copper chelates (Cu-Cur) were first synthesized and characterized using mass spectrometry, NMR, and infrared spectroscopy. Subsequently, dual-targeted liposomes (Cu-Cur DTLPs) were prepared via the thin-film dispersion method, with systematic evaluation of particle size, zeta potential, encapsulation efficiency, and in vitro release profiles. In vitro cytotoxicity was assessed against 4T-1 and MDA-MB-231 cells using the MTT assay. In a 4T-1 tumor-bearing BALB/c mouse model, comprehensive evaluation of targeting efficiency, antitumor efficacy, and mechanisms of action was conducted via in vivo imaging, tumor volume monitoring, immunohistochemistry (detecting FDX1 and DLAT proteins), and TUNEL staining. Results: Cu-Cur DTLPs with a uniform particle size of approximately 104.4 nm were successfully synthesized. In vitro and in vivo studies demonstrated that compared to free curcumin and conventional liposomes, Cu-Cur DTLPs significantly enhanced drug accumulation in tumor tissues and exhibited effective tumor growth inhibition. Mechanistic studies confirmed that this formulation specifically accumulates copper ions within tumor cells, upregulates FDX1, promotes DLAT oligomerization, and induces mitochondrial dysfunction, thereby driving copper death. TUNEL staining ruled out apoptosis as the primary mechanism. Safety evaluation revealed no significant toxicity in major organs. Conclusions: The Cu-Cur DTLPs developed in this study effectively induce copper-mediated death in TNBC through a dual-targeted delivery system, significantly enhancing antitumor activity with favorable safety profiles. This establishes a highly promising novel nanotherapeutic strategy for TNBC treatment. Full article

Bacterial contamination remains a challenge for multiple facets of modern life. While antibiotics are a primary tool for bacterial control, their overuse has accelerated the appearance of multidrug-resistant bacteria and raises global health concerns. In swine, semen is stored at 17 °C in extenders that contain antibiotics to prevent bacterial growth. Apart from the potential consequences for the female, the proliferation of bacteria in liquid-stored semen is associated with a decline in sperm quality, ultimately reducing farrowing rates and litter sizes. With the aim of reducing the use of antibiotics while keeping bacterial growth under control, we herein investigated whether metal ions could exert an antimicrobial effect without impairing sperm quality. Separate metal ions (Ag, silver sulfadiazine; Al, aluminum chloride; Zn, zinc chloride; and Cu, and cooper chloride) were added at different concentrations (100 μM, 300 μM, 500 μM, 1 mM, and 10 mM) to seminal doses, which were stored at 17 °C for 48 h. Motility, viability, and the intracellular levels of reactive oxygen species (ROS) were tested to determine their effects on sperm quality maintenance. In addition, ions were added to bacterial strains and to extended seminal samples to assess the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). Results showed that, although silver sulfadiazine exerted an antimicrobial effect at all the concentrations tested, it also affected sperm quality negatively (p < 0.05). In contrast, aluminum chloride did not impair sperm quality but failed to inhibit bacterial growth at any of the tested concentrations (p > 0.05). Finally, 1 mM concentrations of copper and zinc chloride reduced microbial growth (p < 0.05) without affecting sperm quality. In spite of this, the inhibition of bacterial growth was not complete, thus suggesting that these two ions could contribute to reducing bacterial growth but should be combined with other strategies, such as a lower storage temperature and a decreased concentration of antibiotics. Further research is warranted to address whether copper and zinc chloride could have a synergistic effect when added together. Full article

Iron (Fe), as one of the essential micronutrients for plants, plays a pivotal role in regulating growth and development through homeostatic balance. Fe deficiency is a common agricultural stress that causes visible leaf chlorosis and impairs plant growth. In this study, Arabidopsis thaliana seedlings grown under Fe deficiency for 4 days were subjected to 6 h Fe resupply via foliar spray or root supply, followed by measurements of chlorophyll fluorescence and metal ion contents in leaves and roots. Fe deficiency significantly reduced Fe levels and the maximum quantum yield of fluorescence (Fv/Fm), while increasing copper (Cu) accumulation in roots. Zinc (Zn) and manganese (Mn) levels were also altered, depending on tissue type. Fe resupply restored Fv/Fm, increased Mn levels, and rebalanced micronutrient content. MicroRNA (miRNA) mediates adaptation to Fe deficiency via post-transcriptional regulation in plants. However, the involved regulatory networks of miRNAs under stress conditions during Fe resupply following deficiency remain poorly understood. These physiological changes prompted us to explore the underlying regulatory networks using miRNA-seq and mRNA-seq. The bioinformatics analysis identified differentially expressed miRNAs responsive to Fe stress, with the Fe-deficiency-specific cis-element IDE1 characterized in their promoter regions. By integrating miRNA-seq and mRNA-seq datasets, we constructed a regulatory network and identified 13 miRNAs harboring IDE1 motifs alongside their functional target genes. Three critical Fe homeostasis modules were proposed—miR396b-LSU2, miR401-HEMA1, and miR169b-NF-YA2—that link Fe homeostasis to chlorophyll synthesis, sulfur (S) responses, and developmental signaling. This study integrates physiological phenotyping with transcriptomic insights to provide a comprehensive view of Fe deficiency and recovery in Arabidopsis. Full article

Microplastics (MPs) have been attracting considerable interest in recent years due to their ubiquitous existence and accumulation within different systems and ecosystems. Moreover, their presence in electroplating baths involves a more serious challenge considering that the electroplating industry is progressing towards the electroplating of plastic materials. Contaminated baths can lead to surface defects, poor adhesion, corrosion, and inconsistent deposit thicknesses. Despite these issues, the interactions between pollutant MPs and heavy metal ions in electroplating environments are still underexplored. The present study aims to investigate the behavior of self-produced “Nylon PA” MPs dispersed in acid copper electroplating baths and their interactions with copper ions in solution. Scanning electron microscopy (SEM) reveals several surface defects in copper deposits caused by MPs in the bath. Additionally, cyclic voltammetry and chronoamperometry indicate significant changes in nucleation and growth mechanisms, with MPs showing suppressant-like effects on copper deposition. These results shed light on the impact of MPs on copper electrodeposition, emphasizing the urgent need for further research and mitigation strategies to address this emerging issue in the electroplating industry. Full article

Highly accurate quantitative detection of heavy metals is crucial for preventing environmental pollution and safeguarding public health. To address the demand for sensitive and specific detection of Cu²⁺ ions, we have developed carbon dots using a simple hydrothermal process. The synthesized carbon dots are highly stable in aqueous media, environmentally friendly, and exhibit strong blue photoluminescence at 440 nm when excited at 352 nm, with a quantum yield of 5.73%. Additionally, the size distribution of the carbon dots ranges from 2.0 to 20 nm, and they feature excitation-dependent emission. They retain consistent optical properties across a wide pH range and under high ionic strength. The photoluminescent probes are selectively quenched by Cu²⁺ ions, with no interference observed from other metal cations such as Ag⁺, Ca²⁺, Cr³⁺, Fe²⁺, Fe³⁺, Hg²⁺, K⁺, Mg²⁺, Sn²⁺, Pb²⁺, Sr²⁺, and Zn²⁺. The emission of carbon dots exhibits a strong linear correlation with Cu²⁺ concentration in the range of 0–14 μM via a static quenching mechanism, with a detection limit (LOD) of 4.77 μM in water. The proposed carbon dot sensor is low cost and has been successfully tested for detecting Cu²⁺ ions in general water samples collected from rivers in Taiwan. Full article

The removal of copper–cyanide complexes from cyanide gold leaching tail water poses a significant challenge, as they are difficult to eliminate and risk causing secondary pollution. This study developed a synergistic flocculation–flotation process using the bio-collector sodium cocoyl glycinate (SCG) and the coagulant polyferric sulfate (PFS) for purification. Simulated wastewater, prepared based on actual gold mine effluent, was treated under optimized conditions of reagent dosage, a solution pH of 6–10, and a flotation time of 1–5 min, achieving high removal efficiencies of 96.48% for copper and 94.68% for total cyanide. Mechanistic studies via FT-IR, Zeta potential, and XPS revealed that Fe³⁺ from PFS formed Fe-CN complexes with both free and copper-complexed cyanide. Simultaneously, copper ions coordinated with SCG to generate a hydrophobic Fe-CN-Cu-SCG ternary complex, which was subsequently removed by adsorption onto air bubbles via the hydrophobic chains of SCG. This work provides a novel, efficient, and mechanistically clear strategy for the advanced treatment of cyanide-containing tailing water with a gold content of 0.021 mg/L. Full article

Dialdehyde crosslinked poly aspartate/alginate hydrogel beads were synthesized by covalently introducing poly aspartate into the alginate network via dialdehyde-mediated crosslinking, and the resulting effects on swelling and adsorption behavior were investigated. Alginate was partially oxidized to form dialdehyde alginate and crosslinked with poly aspartic acid via Schiff base formation, followed by ionic crosslinking with calcium ions. The chemical structure and morphology of the gel beads were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. Incorporation of PAsp significantly altered the swelling behavior of alginate-based gel beads. In saline solution, PAsp-modified gel beads exhibited a swelling ratio of approximately 112 g/g, which was higher than that of calcium alginate gel beads. This behavior is suggested to be associated with changes in the alginate–calcium network structure induced by polymer modification. PAsp-modified gel beads exhibited moderate but distinct adsorption behavior depending on the adsorbate. Removal efficiencies of approximately 40–50% were observed for copper and cobalt ions, while a removal efficiency of around 50% was obtained for the cationic dye crystal violet. In contrast, adsorption of the anionic dye Congo red decreased with increasing PAsp content, indicating charge-dependent adsorption behavior. Overall, this study demonstrates that PAsp modification via dialdehyde-mediated crosslinking influences both the swelling and adsorption properties of alginate-based hydrogel beads. The results provide fundamental insight into how network modification can be used to tune the behavior of alginate-based hydrogels in aqueous environments. Full article

Metal oxide nanomaterials have emerged as transformative materials in the quest to enhance the energy density and overall performance of lithium-ion batteries (LIBs) and solid-state batteries (SSBs). Their unique properties—including their large surface areas and short ion diffusion pathways—make them ideal for next-generation energy storage technologies. In LIBs, the high surface-to-volume ratio of metal oxide nanomaterials significantly enlarges the active interfacial area and shortens the lithium-ion diffusion paths, leading to an improved high-rate performance and enhanced energy density. Transition metal oxides (TMOs) such as nickel oxide (NiO), copper oxide (CuO), and zinc oxide (ZnO) have demonstrated significant theoretical capacities, while binary systems like NiCuO offer further improvements in cycling stability and energy output. Additionally, layered lithium-based TMOs, particularly those incorporating nickel, cobalt, and manganese, have shown remarkable promise in achieving high specific capacities and long-term stability. The synergistic integration of metal oxides with carbon-based nanostructures, such as carbon nanotubes (CNTs), enhances the electrical conductivity and structural durability further, leading to a superior electrochemical performance in LIBs. In SSBs, the use of oxide-based solid electrolytes like garnet-type Li₇La₃Zr₂O₁₂ (LLZO) and sulfide-based electrolytes has facilitated the development of high-energy-density systems with excellent ionic conductivity and chemical stability. However, challenges such as high interfacial resistance at the electrode–electrolyte interface persist. Strategies like the application of lithium niobate (LiNbO₃) coatings have been employed to enhance interfacial stability and maintain electrochemical integrity. Furthermore, two-dimensional (2D) metal oxide nanomaterials, owing to their high active surface areas and rapid ion transport, have demonstrated considerable potential to boost the performance of SSBs. Despite these advancements, several challenges remain. Morphological optimization of nanomaterials, improved interface engineering to reduce the interfacial resistance, and solutions to address dendrite formation and mechanical degradation are critical to achieving the full potential of these materials. Full article

Functional properties of coastal halophytes are important for development of salt-tolerant cash crop cultures. The study of salt tolerance in coastal dune-building grass Leymus arenarius holds significant importance for its application in land reclamation, soil stabilization, and enhancing crop resilience to salinity stress. We used two accessions (LA1 and LA2) of L. arenarius to compare effects of salinity caused by NaCl and NaNO₃ on growth, ion accumulation and mineral nutrition in controlled conditions. L. arenarius plants exhibited high tolerance to sodium salts, with distinct effects on growth and development observed between chloride and nitrate treatments. While both salts negatively impacted root biomass, nitrate treatment (50–100 mmol L⁻¹) increased leaf number and biomass in LA2 plants, whereas chloride treatment decreased tiller and leaf sheath biomass. Despite individual variations, salinity treatments showed comparable effects on traits like tiller and leaf count, as well as leaf blade and sheath biomass. Salinity increased water content in leaf blades, sheaths, and roots, with LA2 plants showing the most pronounced effects. Chlorophyll a fluorescence measurements indicated a positive impact of NaNO₃ treatment on photosynthesis at intermediate salt concentrations, but a decrease at high salinity, particularly in LA2 plants. The accumulation capacity for Na⁺ in nitrate-treated plants reached 30 and 20 g kg⁻¹ in leaves and roots, respectively. In contrast, the accumulation capacity in chloride-treated plants was significantly lower, approximately 10 g kg⁻¹, in both leaves and roots. Both treatments increased nitrogen, phosphorus, and manganese concentrations in leaves and roots, with varying effects on calcium, magnesium, iron, zinc, and copper concentrations depending on the type of salt and tissue. These findings highlight the potential of L. arenarius for restoring saline and nitrogen-contaminated environments and position it as a valuable model for advancing research on salt tolerance mechanisms to improve cereal crop resilience. Full article

This study prepared carbon dots (CDs) from agricultural waste pineapple peel via an eco-friendly microwave method, optimizing their performance through copper ion and chitosan doping. Multiple characterization techniques and performance tests were employed for systematic analysis. Antioxidant assays revealed that PP-CDs have excellent concentration-dependent free radical scavenging activity: the DPPH IC₅₀ values of Pineapple Peel Carbon Dots (PP-CDs), Copper-Doped Pineapple Peel Carbon Dots (Cu-PP-CDs) and Chitosan-Doped Pineapple Peel Carbon Dots (CS-PP-CDs) are 0.79, 0.95 and 0.98 mg/mL, while their ABTS IC₅₀ values are 0.22, 0.40 and 0.26 mg/mL, respectively. Antibacterial tests showed modified CDs have enhanced activity: Cu-PP-CDs exhibit inhibition zones of 23.1 ± 0.13 mm (E. coli) and 17.3 ± 0.05 mm (S. aureus) with MICs of 2.5 and 5.0 mg/mL, while CS-PP-CDs have respective zones of 12.8 ± 0.08 mm and 16.3 ± 0.12 mm with a 5.0 mg/mL MIC for both strains. All CDs present a quasi-spherical morphology and emit yellow fluorescence under UV excitation, with PP-CDs showing the strongest intensity. This study provides technical support for high-value utilization of pineapple peel and development of multifunctional CDs, which have food field potential but face large-scale production and toxicological evaluation challenges. Full article

The objective of this research is to develop environmentally friendly, risk-free and effective adsorbent composite beads that remove Cu(II) ions from aqueous solutions using cost-effective biopolymers (Carboxymethylcellulose (CMC) and sodium alginate (AL)). The synthesized hydrogel beads (AL@CMC) were dried using two drying modes, namely air-drying and freeze-drying, and characterized using scanning electron microscopy (SEM), Fourier Transform Infrared Spectroscopy (FT-IR), and Brunauer–Emmett–Teller (BET) analysis. The study investigated factors such as pH, adsorbent dosage, reaction time, Cu(II) ions concentration, and temperature to elucidate the adsorption mechanisms involved in removing copper ions. The results indicated that the hydrogel exhibited a maximum adsorption capacity of 99.05 mg·g⁻¹, which is highly competitive compared to previous studies; the AL@CMC beads prepared in this work show a significantly higher adsorption capacity, improved stability due to the interpenetrated biopolymer network, and a clear enhancement from freeze-drying, which greatly increases porosity and active surface area. In addition, the pseudo-second-order nonlinear kinetic model best described the experimental data, implying the chemical nature of the adsorption process. Furthermore, the thermodynamic studies revealed that the adsorption process was endothermic, spontaneous, and homogenous. A Monte Carlo simulation model was utilized to ensure compatibility with the adsorption mechanism, in order to delve deeper into the intricacies of the adsorption process and gain a more comprehensive understanding of its underlying mechanisms and behavior. In conclusion, the prepared hydrogel beads proved to be an effective adsorbent for efficiently removing copper ions, making them a promising solution for addressing Cu(II) ion pollution. Full article

Copper(II) complexes have great potential as antitumor and antimicrobial agents, and their coumarin derivatives bearing histamine substituents possess versatile structural and biological properties. The present article describes the synthesis of novel copper(II)–coumarin–histamine complexes and ligands and their characterization by IR, NMR, X-ray diffraction, and elemental analysis. Their antimicrobial activity (MIC, MBC/MFC) was tested against 11 reference strains. Cytotoxicity was evaluated using the MTT assay against 15 selected cancer cell lines and normal HMEC-1 cells. It presents three new ligands and three new complexes with copper(II) ions and selected histamine-containing coumarin derivatives. The new copper(II) complexes demonstrated markedly higher anticancer activity than their corresponding ligands across all evaluated cancer cell lines. The highest anticancer activity against the Hep3B liver cancer cell line was demonstrated by the copper(II) complex (3b), which also showed the strongest inhibition of S. epidermidis ATCC 12228 and S. aureus ATCC 6538. The copper(II) ions play a crucial role in the antitumor activity of these derivatives. Despite limited antimicrobial effects, the tested complexes, particularly 3a and 3b, demonstrate promising anticancer potential, especially against the Hep3B cancer cell line. Only 3b demonstrated antimicrobial activity against S. epidermidis ATCC 12228 and S. aureus ATCC 6538. Full article

Mitochondrial oxidative phosphorylation serves as a critical driving force in the progression of ovarian cancer. Recent studies have demonstrated that copper induces mitochondrial-dependent programmed cell death by directly binding to the thioacylated components of the tricarboxylic acid (TCA) cycle. The involvement of copper in OXPHOS complex IV, a rate-limiting step in the mitochondrial respiratory chain, suggests that the role of mitochondria in mediating copper-induced cell death can be further elucidated through the study of OXPHOS complex IV. The findings of this study indicate that the cuproptosis process in ovarian cancer, induced by Elesclomol, is associated with mitochondrial complex IV, with LRPPRC identified as a crucial factor. Following Elesclomol treatment of ovarian cancer cells, there was a notable increase in mitochondrial reactive oxygen species (ROS), a significant accumulation of the copper death marker protein DLAT, and a marked decrease in the lipoic acid synthesis-related protein FDX1. Furthermore, the expression levels of copper ion transporters ATP7B and CTR1, which are involved in the assembly and translation of complex IV, as well as the core subunit MTCO1 of complex IV, the copper chaperone protein SCO1, and the interacting protein LRPPRC, were significantly diminished. Inhibition of the IV-stabilizing protein LRPPRC in the ovarian cancer cell lines A2780 and SKOV3 through RNA interference resulted in increased sensitivity to Elesclomol. Concurrently, the expression levels of FDX1, LIAS, LIPT1, SCO1, and MTCO1 decreased significantly. These findings suggest that LRPPRC plays a role in inhibiting the expression of lipoic acid and copper chaperone proteins during Elesclomol-induced copper death in ovarian cancer. This inhibition collectively diminishes the expression and activity changes in complex IV, induces mitochondrial dysfunction, and promotes cuproptosis in ovarian cancer. This study further demonstrates that inhibiting the oxidative phosphorylation complex IV can enhance copper-induced cell death in ovarian cancer. Full article