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In this paper, a high precision detection method of copper ion (C u 2 + ) concentration based on weak measurement is proposed. The ternary complex formed by C u 2 + with L-tryptophan and phenanthroline reagents has circular dichroism (CD) signal at 605 nm in visible light. The CD signal can be obtained using the intensity contrast as a pointer in the imaginary weak-value amplification scheme. The measured sensitivity and resolution are 0.3417 mrad l/mg and 0.058 mg/l, respectively, which is improved by an order of magnitude compared to the traditional CD measurement method. It is also more accurate and less costly than commonly used C u 2 + detection methods. The C u 2 + concentration detection based on the weak measurement of CD signal detection proposed in this paper not only brings technological breakthroughs in the field of heavy metal ion detection, but also is of great significance in promoting the cross-development of chemistry, biomedicine, and life sciences. [ABSTRACT FROM AUTHOR]

This study explored the production of activated carbon from agricultural waste, specifically Punica granatum peel, and its application as an eco-friendly solution for removing copper (Cu2+) ions from industrial effluents, particularly those from copper-plating industries. The Punica granatum peel was chemically activated using ortho-phosphoric acid to produce activated carbon. The activation process involved impregnation followed by thermal activation at 500 °C. The resultant activated carbon was characterized using FTIR, TGA/DTA, and adsorption tests at room temperature and pH 5, which demonstrated a Cu2+ ion retention rate exceeding 95% within the first 15 minutes. The adsorption kinetics were analyzed using pseudo-first-order and pseudo-second-order models, while the adsorption isotherms was examined using Langmuir and Freundlich models. The study demonstrated that the activated carbon derived from Punica granatum peel exhibits high adsorption efficiency for Cu2+ ions, with a maximum adsorption capacity of 19.62 mg/g. The adsorption process was best described by the pseudo-second-order kinetic model and the nonlinear Langmuir isotherm model. The newly developed activated carbon exhibits a markedly higher adsorption efficiency compared to existing activated carbons, highlighting its innovative potential for adsorbing Cu2+ ions. Consequently, its use proves to be a cost-effective and sustainable solution for treating copper-contaminated industrial effluents. In fact, this research offers a dual benefit by providing a sustainable waste management solution for agricultural residues and an effective method for treating industrial effluents. Incorporating this activated carbon in post-copper plating rinsing water treatment ensures regulatory compliance and facilitates water reuse. This approach also supports copper recovery and reuse in new plating baths, promoting cyclic material circulation within the industry. [ABSTRACT FROM AUTHOR]

Copper is an important mineral, and moderate copper is required to maintain physiological processes in nervous system including cerebral ischemia/reperfusion (I/R) injury. Over the past few decades, copper induced cell death, named cuprotosis, has attracted increasing attention. Several lines of evidence have confirmed cuprotosis exerts pivotal role in diverse of pathological processes, such as cancer, neurodegenerative diseases, and I/R injury. Therefore, an in-depth understanding of the interaction mechanism between copper-mediated cell death and I/R injury may reveal the significant alterations about cellular copper-mediated homeostasis in physiological and pathophysiological conditions, as well as therapeutic strategies deciphering copper-induced cell death in cerebral I/R injury. [ABSTRACT FROM AUTHOR]

Organic upconverters made by integrating an infrared‐sensitive photodetector with a light‐emitting diode offer a low‐cost route to visualize images taken in the infrared. However, making such devices sufficiently efficient is challenging. Here, upconversion devices are demonstrated with an efficiency of 13.9% for converting infrared photons (980 nm, 5 mW cm−2) to visible photons (575 nm). Infrared photons are detected with a photomultiplication photodetector that includes a copper thiocyanate electron‐blocking/injection layer and an infrared‐sensitive squaraine dye dispersed (3 wt−%) in a fullerene matrix. At turn‐on, the detector achieves an external quantum efficiency of 1200% (at 1020 nm, −10 V, 44 µW cm−2). Photomultiplication occurs via hole trap‐induced injection of electrons. In the upconverter, these electrons are driven into the emitter and recombine with holes under visible light emission. During operation the photodetector current increases because, presumably, rearranging mobile ions in copper thiocyanate narrows the injection barrier. Thereby, the upconverter photoconversion efficiency gradually increases to 18.7%. The performance of the present upconverter is limited by the not‐yet‐ideal charge‐blocking/injection layer, which is too thick and blocks electrons in the dark insufficiently. With thin and compact charge‐blocking layers at hand, the device concept paves the way for widespread use in sensitive infrared imaging. [ABSTRACT FROM AUTHOR]

3D fibrous membranes of undoped and Cu-doped 70S glass were developed, by solution blow spinning. The concentration of copper ions ranged from 1 to 4 % in mol. As-spun fibers were calcined/stabilized at 700 °C. The produced membranes' morphological and biological properties and the release of Ca and Cu ions were evaluated. Amorphous materials were obtained in pure and doped with 1 % Cu2+ 70S glass, while metallic copper was observed in 4 % Cu2+ doped glass. All samples have fibers with average diameter at the submicron scale, ranging from 700 to 850 nm. The amount of Cu ions influenced the degradation of the samples and the release of Cu and Ca ions in the Tris solution, the greater the amount of copper the more these ions were degraded and released in the solution. In vitro biological results, showed that adding copper favored the biomineralization process. No toxicity was observed in the MMT test for all samples. Alamar Blue method showed cell viability for fibroblasts greater than 90 % for all samples and for osteoblasts greater than 70 % for the BG-70S.2Cu sample. The developed fibrous membranes presented antimicrobial characteristics against Staphylococcus aureus and Candida albicans. [ABSTRACT FROM AUTHOR]

In this work, chitosan was cross-linked with dialdehyde chitosan to stabilize it and also provide aldehyde segments for the further functionalization with bovine serum albumin. Then, the magnetization procedure was done through the treatment of hybrid polymer with Fe3O4 nanoparticles. BSA was covalently immobilized on the magnetic CS-CSOX biopolymer through condensation of amine groups of amino acid units with the aldehyde functional groups of dialdehyde chitosan. N-terminal peptides, histidine and tryptophan residues of BSA and also the thiol side chain of cysteine and sulfur donor atom of methionine may be as proper binding sites for the copper ions coordination. The catalytic efficiency of Fe3O4@CS-BSA-Cu nanocatalyst was examined in the synthesis of 5-substituted tetrazoles and also 1,4-diaryl-1,2,3-triazoles. The prepared nanocatalyst was separated by an external magnet and reused without significant difference in its activity. [ABSTRACT FROM AUTHOR]

Recent advancements in bacterial two-component systems (TCS) have spurred research into TCS-based biosensors, notably for their signal amplification and broad input responsiveness. The CusRS system in Escherichia coli (E. coli), comprising cusS and cusR genes, is a copper-sensing module in E. coli. However, due to insufficient sensing performance, CusRS-based biosensors often cannot meet practical requirements. To address this issue, we made improvements and innovation from several aspects. CusR and CusS expression were adjusted to enhance the Cu(II) biosensor's performance. A copy-number inducible plasmid was used for signal amplification, while removing copper detox genes cueO and cusCFBA improved sensitivity and lowered detection limits. Ultimately, in the optimized biosensor of Cu26, the fold-change (I/I0) increased from 1.5-fold to 18-fold at 1 μM, rising to 100-fold after optimizing the cell culture procedure. The biosensor's high fluorescence enabled rapid, instrument-free detection and an improved analysis strategy reduced the detection limit to 0.01 μM, surpassing traditional methods. Optimizing the CusRS copper-sensing system in E.coli by adjusting CusR/CusS expression and deleting detox genes, achieving a 100-fold signal increase and a detection limit of 0.01 μM, enabling rapid, instrument-free detection. [ABSTRACT FROM AUTHOR]

Abstract\nNOVELTY STATEMENTThe synthesis of catalysts has gained specific concern due to their versatile applications in particular azo dye decolorization. In the current work, metallic nanoparticles (copper and silver) were In-situ biosynthesised using Allium sativum and Chondrilla juncea extract. The obtained Allium-copper oxide and Allium-silver oxide materials were analyzed using SEM, TEM, FT-IR, TGA-DTG, SEM, TEM, and XRD techniques. Allium peels had a rough surface, with nanoparticles equally distributed over it. The crystal structure of Allium peels was altered after the addition of CuO and AgO nanoparticles. The highest residual mass values in the prepared materials indicated that the metallic nanoparticles were, in situ, formed. The prepared materials had worse thermal stability than Allium peel powders. The azo dyes, Calmagite and Naphthol Blue Black B were tested in the catalytic power of the resulting materials. The decolorization process was affected by the dye structure, amount of H2O2, dye concentration, time of reaction, and temperature of the bath. The activation energy values for Allium-CuO were 18.44 kJ mol−1 for calmagite, and 23.28 kJ mol−1 for naphthol blue black, respectively. Nevertheless, the energy values for Allium-AgO were 50.01 kJ mol−1 for calmagite and 12.44 kJ mol−1 for Naphthol blue black. The calculated low energy values for the prepared materials suggested the high efficiency of the use of these catalysts in azo dye decolorization under the change of some main experimental conditions.Chondrilla juncea was employed as a biological extract for in-situ reduction of copper and silver ions within Allium sativum peels. The resulting Allium sativum-CuO and Allium sativum -AgO materials were used as efficient catalysts for azo dye decolorization. [ABSTRACT FROM AUTHOR]

The use of mixed microalgae offers an effective solution for the management of contamination risks in cultivation while enhancing economic viability. In this study, mixed microalgae were used for the first time for the removal of copper (Cu) and nickel (Ni) from aqueous solutions. The characteristics of the adsorbents were examined thoroughly, and the adsorption process was assessed using isotherms, kinetics, and thermodynamics. Particle size, concentration, contact time, temperature, and pH were among the variables assessed. The findings demonstrated that, at an initial concentration of 100 mg L–1 and a pH of 6, the maximum adsorption of Cu with a particle size of 1 mm (90.20%) took place in 60 min. The highest adsorption rate (78.25%) was found for Ni. Microalgae performed best over 180 min at room temperature and at pH values that promoted metal dissolution. The removal percentages of wet and dried microalgae were comparable, and the wet adsorbent was more economical. It was feasible to remove both metals at the same time. Up to three cycles of adsorbent reuse were possible, with sodium hydroxide treatment offering superior removal to hydrochloric acid. Thermodynamic analysis demonstrated that this process, which results in a disordered state, is exothermic and spontaneous. [ABSTRACT FROM AUTHOR]

This study presents the synthesis and evaluation of a magnetic chitosan-modified biochar (M-BC-CS) composite, developed from waste maize straw, for the efficient removal of copper ions (Cu2+) and methylene blue (MB) dye from aqueous solutions. The composite was characterized using advanced techniques such as SEM, BET, FTIR, XPS, and XRD, confirming its enhanced surface area, porosity, and magnetic properties. The study is aimed at investigating the optimal conditions for adsorption of Cu2+ and MB by M-BC-CS through analysis of the influence of diverse adsorbent dosages, pH levels, reaction times, and initial solution concentrations. The findings demonstrated that the equilibrium duration for the adsorption of Cu2+ and MB by M-BC-CS was 60 min, resulting in corresponding equilibrium adsorption quantities of 54.42 mg/g and 67.23 mg/g, respectively. To elucidate the adsorption mechanism, the present investigation applied the pseudo-second-order kinetic model and the Langmuir isotherm. The outcomes suggested that the adsorption process is attributable to single molecular layer chemisorption. XPS and FTIR analysis determined that ion exchange and electrostatic interactions are the predominant mechanisms responsible for the simultaneous adsorption of Cu2+ and MB, and a competitive relationship exists between these mechanisms. In addition, M-BC-CS exhibited exceptional magnetic separation performance, enabling effortless and effective separation when exposed to an external magnetic field. Furthermore, the results demonstrated that M-BC-CS has good reusability and high adsorption capacity also in real wastewater, thus emphasizing its potential as a promising adsorbent for the elimination of Cu2+ and MB from aqueous solutions. [ABSTRACT FROM AUTHOR]

In the critical domain of wastewater treatment, the development of cost-effective, durable, and recyclable adsorbents with high adsorption capacities remains a significant challenge. This study introduces a novel magnetic bimetallic Metal–Organic Framework (MOF) adsorbent, MZIF-67-Co/Cu, doped with copper ions. The MZIF-67-Co/Cu adsorbent was successfully synthesized and structurally characterized, demonstrating remarkable selectivity for removing methyl orange (MO) from water. This high selectivity is attributed to the adsorbent's high porosity and Lewis base properties at the coordinating metal ion center. The incorporation of Cu ions significantly enhances the porous architecture and increases the number of metal adsorption sites, leading to an impressive maximum MO adsorption capacity of 39.02 mg/g under optimized conditions (0.5 g/L adsorbent concentration, pH 3.0, 250 rpm agitation speed, adsorption time > 10 min). The adsorption kinetics closely follow the pseudo-second-order model, and the isotherm data fit well with the Langmuir model. The primary adsorption mechanisms involve electrostatic attraction and mesoporous interaction. This study highlights MZIF-67-Co/Cu as a highly efficient adsorbent with magnetic recovery capabilities, positioning it as a promising candidate for addressing critical issues in wastewater treatment. [ABSTRACT FROM AUTHOR]

Transition metal sulfide compounds with high theoretical specific capacity and excellent electronic conductivity that can be used as cathode materials for secondary batteries attract great research interest in the field of electrochemical energy storage. Among these materials, MnSe2 garners significant interest from researchers due to its unique three-dimensional cubic structure and inherent stability. However, according to the relevant literature, the performance and cycle life of MnSe2 are not yet satisfactory. To address this issue, we synthesize MnSe2/CNTs composites via a straightforward hydrothermal method. MnSO4·H2O, Se, and N2H4·H2O are used as reactants, and CNTs are incorporated during the stirring process. The experimental outcomes indicate that the fabricated electrode demonstrates an initial discharge specific capacity that reaches 621 mAh g−1 at a current density of 0.1 A g−1. Moreover, it exhibits excellent rate capability, delivering a discharge specific capacity of 476 mAh g−1 at 10 A g−1. The electrode is able to maintain a high discharge specific capacity of 545 mAh g−1 after cycling for 1000 times at a current density of 2 A g−1. The exceptional electrochemical performance of the MnSe2/CNTs composites can be ascribed to their three-dimensional cubic architecture and the 3D CNT network. This research aids in the progression of aqueous Cu-ion cathode materials with significant potential, offering a viable route for their advancement. [ABSTRACT FROM AUTHOR]

Copper is an important mineral, and moderate copper is required to maintain physiological processes in nervous system including cerebral ischemia/reperfusion (I/R) injury. Over the past few decades, copper induced cell death, named cuprotosis, has attracted increasing attention. Several lines of evidence have confirmed cuprotosis exerts pivotal role in diverse of pathological processes, such as cancer, neurodegenerative diseases, and I/R injury. Therefore, an in-depth understanding of the interaction mechanism between copper-mediated cell death and I/R injury may reveal the significant alterations about cellular copper-mediated homeostasis in physiological and pathophysiological conditions, as well as therapeutic strategies deciphering copper-induced cell death in cerebral I/R injury. [ABSTRACT FROM AUTHOR]

Myracrodruon urundeuva, popularly known as 'aroeira-do-sertão', a large tree, with a tall trunk. Belonging to the Anacardiaceae family, it occurs in the 'caatinga' and dry forests of Brazil, from Ceará to the states of Paraná and Mato Grosso do Sul. The present study aimed to analyse the whitening and antioxidant activities of the aqueous extract of the leaves of Myracrodruon urundeuva (AELMU). Inhibition of the tyrosinase enzyme, as well as its copper chelating capacity and antioxidant effect were evaluated. The AELMU (at 2000 µg/mL) showed excellent inhibitory action (83.76%) on tyrosinase by chelating the copper ion while kojic acid at the same concentration inhibited 97.81%. Moreover, the extract displayed important antioxidant activity (inhibited 76,46% of the 2,2-diphenyl-1-picrylhydrazyl radical - DPPH; 49,59% of thiobarbituric acid reactive substances and 51,07% of the hydroxyl radical). Thus, the extract under study is promising for use in cosmetics, given its multifactorial action. [ABSTRACT FROM AUTHOR]

Background: Traditional chemotherapeutic agents suffer from a lack of selectivity, poor targeting ability, and drug resistance. Developing tumor-specific therapies is crucial for precisely eliminating tumors while circumventing toxicity to normal tissues. Disulfiram (DSF), an FDA-approved drug for treating alcohol dependence, exhibits antitumor effect by forming complexes with copper ions (Cu(DDC)2). Here, we developed a Cu-doped polydopamine-based nanosystem (DSF@CuPDA-PEGM) to achieve in situ generation of toxic Cu(DDC)2. Results: In cancer cells with elevated H2O2 contents, CuPDA responsively degrades to release Cu ions and DSF, allowing on-site synthesis of Cu(DDC)2 with potent antitumor activity. DSF@CuPDA-PEGM exhibits excellent therapeutic efficacy against both drug-sensitive and drug-resistant cancer cells while minimizing toxicity to noncancerous cells. Moreover, DSF@CuPDA-PEGM promotes the immune response by inducing cancer cell immunogenic death, thereby augmenting anti-PD-1-based immune checkpoint blockade therapy. Conclusion: A tumor-specifically degradable Cu-doped polydopamine-based nanosystem is developed to achieve in situ synthesis of antitumor compounds, providing a promising approach to precisely eliminate tumors and heighten chemo-immunotherapy. [ABSTRACT FROM AUTHOR]

Owing to the toxicity and widespread use of copper, the pollution caused by copper ions has become a long-standing environmental and industrial challenge. In this study, a new adsorbent was developed to dispose of and remove copper ions from water. The modified chitosan–carboxymethyl starch (MCTS-CMS) polymer was characterised, and FTIR and SEM-EDS confirmed the successful graft modification of the receptor. The adsorption behaviour was investigated through various parameters, and the results showed that the optimal parameters were pH > 4.0, an adsorption time of 30 min, a reaction temperature of 293 K, and an initial concentration of 100–120 mg/L. The experimental data exhibited a good fit with pseudo-second-order models, and the Langmuir isotherm revealed that the polymer was found to be highly suitable for adsorption, with a maximum adsorption capacity of 321.16 mg/g. Thermodynamic analysis revealed that the adsorption process was exothermic and spontaneous. XRD and XPS confirmed the generation of posnjakite after the adsorption and the predominant roles of nitrogen- and sulphur-containing groups in the adsorption. Further analysis confirmed the existence of chemisorption and physical adsorption, with chemisorption mainly facilitating the Cu(II) absorption of the polymer. MCTS-CMS showed an excellent removal efficiency of 98% in acidic solutions. On the basis of these findings, the MCTS-CMS polymer demonstrates excellent performance and high selectivity in the removal of copper ions from industrial wastewater or polluted water bodies. This work recommends expanding the polymer's practical applications to contribute to water purification efforts. [ABSTRACT FROM AUTHOR]

Pyrite has natural floatability and thus readily enters valuable mineral flotation concentrates, diluting their quality and decreasing their economic value. Its separation is challenging, depending on process conditions, the presence of activating ions, and water quality, particularly in regions where seawater is used. This study examines the effect of various doses of sodium metabisulfite (SMBS) on pyrite depression in freshwater and seawater under weakly alkaline conditions and with different copper ion concentrations. Without the addition of activators or depressants, pyrite recovery is 40% in freshwater and 60% in seawater, whereas with 10 ppm of SMBS, recoveries drop to 28% and 38%, respectively. The addition of 10 ppm Cu2+ increases recovery by 10% in freshwater and by 20% in seawater. In the presence of 75 ppm of PAX, maximum recovery reached 50% in freshwater and 80% in seawater. These results suggest that cationic bridges formed by seawater ions, combined with CaOH+ activation, play a critical role in pyrite activation, even in the presence of depressants. [ABSTRACT FROM AUTHOR]

The performance of the anode varies from the impurity ions in the copper electrowinning process. This work focused on the variation of the electrochemical behavior of the Pb-0.06%Ca-1.2%Sn anode as the Fe ions (Fe3+ and/or Fe2+) existed in the electrolyte by electrochemical characterization. Copper electrodeposition experiments were conducted under a current density of 300 A/m2, with the Fe ion concentration in the electrolyte controlled within the range of 0 to 20 g/L and the Cu ion concentration maintained at 45 g/L at a temperature of 45 °C. The variation in the corrosion resistance, catalytic activity, and structural composition of the anode film layer was analyzed in-depth according to the presence of Fe ions. The results show that the structure of PbO2 on the surface of the film was changed as Fe ions doped into the anode film, and the oxygen evolution activity of the anode was also improved. However, the corrosion resistance decreased with increasing Fe3+ concentration. Furthermore, the addition of 2 g/L Fe2+ in the electrolyte containing 2 g/L Fe3+ led to an elevation in the corrosion resistance of the anode to some extent and further increased the oxygen evolution activity. [ABSTRACT FROM AUTHOR]

This study investigates the development and application of electrospun wound dressings based on polylactic acid (PLA) nanofibers, chitosan, and copper nanoparticles (CuNPs) for the treatment of purulent skin wounds. The materials were evaluated for their structural, antibacterial, and wound healing properties using an animal model. PLA/Ch-CuNPs demonstrated the most significant antibacterial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, surpassing the other tested materials. The integration of CuNPs into the nanofiber matrices not only enhanced the antimicrobial efficacy but also maintained the structural integrity and biocompatibility of the dressings. In vivo experiments using a rat model showed that PLA/Ch-CuNPs facilitated faster wound healing with reduced exudative and inflammatory responses compared to PLA alone or PLA-CuNPs. Histological and immunohistochemical assessments revealed that the combination of PLA, chitosan, and CuNPs mitigated the inflammatory processes and promoted tissue regeneration more effectively. However, this study identified potential toxicity related to copper ions, emphasizing the need for careful optimization of CuNP concentrations. These findings suggest that PLA/Ch-CuNPs could serve as a potent, cost-effective wound dressing with broad-spectrum antibacterial properties, addressing the challenge of antibiotic-resistant infections and enhancing wound healing outcomes. [ABSTRACT FROM AUTHOR]

Oxidative stress caused by pregnancy‐induced hypertension syndrome significantly affects the health of pregnant women. Hydrogen sulfide is a typical gaseous signal molecule against oxidative stress, and it is of profound significance to develop a detection method. In this study, a stimuli‐responsive hydrogel was constructed based on the coordination and bonding principle of metal ions and chitosan (CS) to realize the quantitative detection of hydrogen sulfide (H2S). The chain of CS contains a large number of amino groups and hydroxyl groups, which can form the coordination structure with Cu2+, triggering CS to form a stable hydrogel. The hydrogel can be formed within about 5 s, which has the characteristics of rapid preparation. In the presence of target H2S, the cross‐linking agent Cu2+ in the hydrogel can compete out, resulting in the collapse of the hydrogel and the release of the electrochemical probe. By detecting the concentration of the released electrochemical probe, the quantitative detection of H2S can be achieved. The prepared hydrogel has a good linear relationship with the concentration of H2S from 1 μM to 60 μm. At the same time, the hydrogel has good specificity and stability, and it can be applied to the detection of H2S in serum samples. [ABSTRACT FROM AUTHOR]

In this research copper tagged magnetic surface imprinted polymer (IIP) has been developed using 1,10-phenanthroline immobilized magnesium ferrite–starch. Maximum removal of 95% was achieved at the optimum conditions i.e., 10 min contact time, pH of 6, and IIP amount of 20 mg. According to the kinetic study copper adsorption followed pseudo-second-order model moreover, based on the isotherm study Freundlich model better described the adsorption process as the maximum adsorption capacity of 33.7 mg g−1 was achieved. Adsorbed copper ions were eluted from the adsorbent surface with an HCl solution (0.5 mol L−1) and the IIP exhibited appropriate reusability (removal of more than 92%) after four cycles of sorption and elution. The limit of detection, linear dynamic range and RSD were 0.5 and 3.0–100 µg L−1 and 3%, respectively. The copper-tagged IIP showed a selectivity factor of 8.8, 4.6, 3.3, 3.2 and 5.4 concerning Zn, Ni, Co, Mn and Cd, respectively. The developed IIP-based adsorption system was employed for copper adsorption/preconcentration from water and food samples with an efficiency more than of 95%. Results confirmed that the IIP system is an appropriate route to reduce the side effects of heavy metals in aqueous media. [ABSTRACT FROM AUTHOR]

A novel coordination CuCl2(L)2 complex was synthesized by complexation of the 2-thiophenimidazoline ligand with CuCl2.2H2O in less than 10 min. The synthesis was done using ultrasound irradiation in an ethanol solvent. The complexation was confirmed using CHN and FT-IR analysis and linked to the theoretical IR and DFT calculations. The single-crystal X-ray diffraction approach was employed to figure out the arrangement of atoms in the crystal structure of the CuCl2(L)2 complex. The copper ion is coordinated by two symmetry-related non-chelating 2-thiophenimidazoline ligands and two symmetry-related chlorine atoms. 2-Thiophenimidazoline ligands coordinate with the metal center by N-atom, whereas S-atom does not coordinate with the metal center. The X-ray results revealed a square planar coordination geometry, as evident from the respective bond angles around the Cu(II) ion. Hirshfeld surface analysis was done to learn more about intermolecular contacts. Theoretical calculations were carried out using DFT employing the B3LYP/Def2-TZVP level of theory, which showed that theoretical conclusions were reliable with experimental data. [ABSTRACT FROM AUTHOR]

In polymer materials technology, replacing synthetic stabilizers with natural antioxidants is a current and developing issue. Cloves have antimicrobial and antioxidant properties, which is why they are often used in medicine and in gastronomy. Eugenol – the main component of clove oil, is also a strong antioxidant. The aim of the study was to analyze and compare the anti-aging effects of eugenol and cloves in epoxidized natural rubber (ENR) compositions. The 2,2′-azinobis- (3-ethylbenzothiazoline-6-sulfonate (ABTS), 2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric reducing antioxidant power (FRAP) and CUPric reducing antioxidant capacity (CUPRAC) tests showed the ability of plant materials to reduce free radicals, as well as iron and copper ions. ENR compositions with additives were characterized by a longer oxidation induction time (OIT). The samples after solar aging showed better resistance to elevated temperature and solar radiation, as evidenced by aging coefficients (K) calculated on the basis of mechanical properties and carbonyl indexes of samples with eugenol and cloves. Cloves and eugenol can be successfully used as natural stabilizers in elastomeric materials. [ABSTRACT FROM AUTHOR]

The synthetic dyes have gained attention nowadays because of their adverse and toxic effects on the human health and their environment. In this study, a green polymer Ca-alginate/CuO bionanocomposite was synthesized from copper oxide nanoparticles which were applied for the remediation of Reactive Yellow 145. The bionanocomposite was prepared by using a simple and eco-friendly process, following the reduction of copper ions in the presence of Ca-alginate, followed by characterization using different analytical techniques including SEM–EDX, XRD, UV–vis and FTIR spectroscopy. Ca-alginate-based bionanocomposite was analyzed by UV–vis spectroscopy, showing a λmax at 280 nm. Ca-alginate/CuO biopolymer was applied for the remediation of RY 145, and it was investigated using batch experiments following the optimization of experimental variables such as pH 6, 80 °C temperature, 0.04 mg/L initial dye concentration, 0.06 mg/L dose of catalyst and a 0.06 mg/L H2O2 concentration. The experimental results of COD and TOC were found to be 95.3% and 92.3% for RY 145. The bionanocomposite showed stability and high efficiency for degradation of dye up to four cycles of reusability. It was concluded that the Ca-alginate-based copper oxide bionanocomposite exhibited good photocatalytic adsorption capacity for the degradation of a toxic Reactive Yellow 145 dye, with a degradation efficiency of over 90% within 80 min under optimized conditions. [ABSTRACT FROM AUTHOR]

2-Mercaptomethylbenzo[d]imidazole (2-MMBI) derivatives were designed and synthesized as tyrosinase (TYR) chelators using 2-mercaptomethylimidazole scaffolds. Seven of the ten 2-MMBI derivatives exhibited stronger inhibition of mushroom TYR activity than kojic acid. Their ability to chelate copper ions was demonstrated through experiments using the copper chelator pyrocatechol violet and assays measuring TYR activity in the presence or absence of exogenous CuSO4. The inhibition mechanisms of derivatives 1, 3, 8, and 9, which showed excellent TYR inhibitory activity, were elucidated through kinetic studies and supported by the docking simulation results. Derivatives 3, 7, 8, and 10 significantly inhibited cellular TYR activity and melanin production in B16F10 cells in a dose-dependent manner, with stronger potency than kojic acid. Furthermore, in situ, derivatives 7 and 10 showed stronger inhibitory effects on B16F10 cell TYR activity than kojic acid. Six derivatives, including 8, showed highly potent depigmentation in zebrafish larvae, outpacing kojic acid even at 200–670 times lower concentrations. Additionally, all derivatives could scavenge for reactive oxygen species without causing cytotoxicity in epidermal cells. These results suggested that 2-MMBI derivatives are promising anti-melanogenic agents. [ABSTRACT FROM AUTHOR]

We present a novel miniaturized, gear-shaped, fuel-free actuator capable of autonomously propelling itself in an aquatic environment to absorb heavy metals, such as copper ions. While hydrogel-based absorbents are promising solutions for cationic pollutant remediation, their stationary nature limits their effectiveness in areas where contaminants are unevenly distributed. To address this, we developed a bio-inspired soft actuator that mimics natural propulsion mechanisms. The Marangoni effect, driven by its inherent chemical properties, demonstrated a self-propelled motion without requiring external fuel. The proof-of-concept actuator generated a plane motion lasting up to 2 h and swept over an area approximately 400 times bigger than its size. By harnessing the chemical and optical properties of the hydrogel, we efficiently removed and quantitatively analyzed copper ions through a colorimetric method. This innovative integration of self-propelled movement and efficient copper ion absorption underscores its potential for advancing miniaturized devices in environmental remediation, paving the way for more active and efficient pollutant removal systems in challenging aquatic environments. [ABSTRACT FROM AUTHOR]

To study the antioxidant activity of polysaccharides from Dendrobium officinale, the polysaccharide was extracted and purified from Dendrobium officinale, and its preliminary structure was characterized. Free radical scavenging activity and inhibition of low density lipoprotein (LDL) in vitro oxidation of Dendrobium officinale polysaccharides were evaluated. The results showed that the total sugar content of the obtained Dendrobium officinale polysaccharide was 90.17%±3.90%, the protein content was 0.14%±0.05%, the ash content was 4.47%±1.42% and the glucuronic acid content was 2.53%±1.02%, the relative molecular weight was 23970 Da and the monosaccharides were mainly mannose and glucose in this test. Dendrobium officinale polysaccharide had certain free radical scavenging capacity. It could inhibit the production of conjugated diene in the oxidative modification system of LDL. The inhibition rate of thiobarbituric acid reactive substances (TBARS) by copper ion reached 57.46%±0.56% when the polysaccharide concentration was 3.00 mg⋅mL-1. This study could provide theoretical support for the development of drugs for diseases such as arteriosclerosis due to LDL oxidation. [ABSTRACT FROM AUTHOR]

Heavy metals existed in wastewater could bio-accumulate in aquatic organisms and bring a serious threat to human health. Many methods and adsorbents have been explored to remove heave metals from wastewater, however, developing new adsorbents with satisfied adsorptive property still needs further study. An eco-friendly aerogel adsorbent (CA-Arg) was synthesized through chemical grafting between sodium alginate and L-arginine, which showed outstanding adsorption efficiencies of Cd2+ and Cu2+ ions. The adsorption kinetics and thermodynamics were investigated, and results demonstrated that the adsorption processes were consistent with pseudo-second-order kinetics and Langmuir isotherm equation, illustrating the adsorption processes of target metals were endothermic and spontaneous. The maximum adsorption capacity of Cd2+ and Cu2+ could reach 248.11 mg·g− 1 and 237.45 mg·g− 1, respectively. In addition, the possible adsorption mechanism between the surface functional groups of CA-Arg aerogels and metal ions was explored. This biomass-based aerogel provided a promising adsorbent for the treatment of industrial heavy metals. [ABSTRACT FROM AUTHOR]

In this work, two novel pyrimidine‐cored covalent organic frameworks TpTap‐COF and TpTan‐COF were synthesized for the first time and used for the adsorption of heavy metal ions in aqueous solution. Both COFs are nanofiber clusters with preferable crystallinity and thermal stability. The impact parameters such as pH value, shaking time, initial concentration, and temperature were studied by batch adsorption experiments in the multi‐metal ions system. The adsorption of six metal ions onto COFs follows the pseudo‐second‐order kinetic model and the Freundlich isotherm model, which is a chemical adsorption process that occurs on non‐uniform surfaces. The adsorption rate is determined by both film diffusion and intraparticle diffusion. Further research on the adsorption of copper ions onto COFs indicates the formation of metal complexes between O#N#N/O#O chelating sites in the COF skeleton and Cu ions through the sharing of lone pair electrons. [ABSTRACT FROM AUTHOR]

Malachite is a common copper oxide mineral that is often enriched using the sulfidization–xanthate flotation method. Currently, the direct sulfidization method cannot yield copper concentrate products. Therefore, a new sulfidization flotation process was developed to promote the efficient recovery of malachite. In this study, Cu2+ was used as an activator to interact with the sample surface and increase its reaction sites, thereby strengthening the mineral sulfidization process and reactivity. Compared to single copper ion activation, the flotation effect of malachite significantly increased after stepwise Cu2+ activation. Zeta potential, X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectroscopy (ToF–SIMS), scanning electron microscopy and energy dispersive spectrometry (SEM–EDS), and atomic force microscopy (AFM) analysis results indicated that the adsorption of S species was significantly enhanced on the mineral surface due to the increase in active Cu sites after Cu2+ stepwise activation. Meanwhile, the proportion of active Cu–S species also increased, further improving the reaction between the sample surface and subsequent collectors. Fourier-transform infrared spectroscopy (FT-IR) and contact angle tests implied that the xanthate species were easily and stably adsorbed onto the mineral surface after Cu2+ stepwise activation, thereby improving the hydrophobicity of the mineral surface. Therefore, the copper sites on the malachite surface after Cu2+ stepwise activation promote the reactivity of the mineral surface and enhance sulfidization flotation of malachite. [ABSTRACT FROM AUTHOR]

Copper in vegetables can enter the human body, and excessive copper may cause uncomfortable symptoms; thus, it is urgent to test copper ions for safety concerns. Herein, we prepared Zn2GeO4:Mn2+,In3+ (ZGO:Mn,In) persistent luminescent nanoparticles (PLNPs) and then grafted glutathione for the determination of copper ions. ZGO:Mn,In was prepared by doping In3+ in ZGO:Mn to improve the emission at 532 nm under excitation at 258 nm. The doping amount, temperature, time, and pH were carefully optimized for a stronger emission intensity than ZGO:Mn. The fractional densities and energy band gaps were calculated by density functional theory, revealing the excitation enhancement mechanism of ZGO:Mn,In. The surface of ZGO:Mn,In was modified with carboxyl groups for linking glutathione to specially identify Cu2+ ions. The identification resulted in the aggregation-induced quenching of PLNPs' emission. Thus, the sensor exhibited good selectivity for copper ions, and the composite was successfully applied to the detection of copper ions in serum and vegetable samples. [ABSTRACT FROM AUTHOR]

The combination of cuproptosis and immune checkpoint inhibition has shown promise in treating malignant tumors. However, it remains a challenge to deliver copper ions and immune checkpoint inhibitors efficiently and simultaneously to tumors. Herein, a mitochondria‐targeted nanoscale coordination polymer particle, Cu/TI, comprising Cu(II), and a triphenylphosphonium conjugate of 5‐carboxy‐8‐hydroxyquinoline (TI), for effective cuproptosis induction and programmed cell death‐1 (PD‐L1) downregulation is reported. Upon systemic administration, Cu/TI efficiently accumulates in tumor tissues to induce immunogenic cancer cell death and reduce PD‐L1 expression. Consequently, Cu/TI promotes the intratumoral infiltration and activation of cytotoxic T lymphocytes to greatly inhibit tumor progression of colorectal carcinoma and triple‐negative breast cancer in mouse models without causing obvious side effects. [ABSTRACT FROM AUTHOR]

ABSTRACT This study highlights the synergistic interplay between a Lewis acidic copper ion and a dissociated ligand from Cu(triNHC) complexes in the synthesis of cyclic carbonates from CO2 and epoxy compounds. The reactions were found to proceed efficiently under Cu(triNHC)‐catalyzed conditions, yielding significant quantities of cyclic carbonates across various epoxy substrates encompassing amine, sulfide, and ether functionalities. Stereochemical analyses underscore a pronounced propensity for retaining the stereochemistry of epoxy compounds in the resultant carbonates. This suggests a mechanism involving double inversion of stereochemistry during the reaction, which comprises catalyst‐mediated epoxide ring opening, subsequent CO2 addition, and carbonate ring closing. These findings align with established mechanisms for CO2 fixation reactions, shedding light on the intricate pathways underlying this catalytic process. [ABSTRACT FROM AUTHOR]

Growing volumes of textile waste and heavy metal pollution of water are emerging environmental challenges. In an attempt to tackle these issues, a non-woven sorbent based on jute fibers was fabricated by recycling the textile waste from the carpet industry. The influence of contact time, concentration, pH and temperature on the sorption of lead and copper ions from aqueous solutions was studied. In order to enhance the sorption capacity of the non-woven material, in situ synthesis of polyaniline (PANI) in the presence of TiO2 nanostructures was performed. The contribution of TiO2 nanoparticles and TiO2 nanotubes to the uniformity of PANI coating and overall sorption behavior was compared. Electrokinetic measurements indicated increased swelling of modified fibers. FTIR and Raman spectroscopy revealed the formation of the emeraldine base form of PANI. FESEM confirmed the creation of the uniform nanocomposite coating over jute fibers. The modification with PANI/TiO2 nanocomposite resulted in a more than 3-fold greater sorption capacity of the material for lead ions, and a 2-fold greater absorption capacity for copper ions independently of applied TiO2 nanostructure. The participation of both TiO2 nanostructures in PANI synthesis resulted in excellent cover of jute fibers, but the form of TiO2 had a negligible effect on metal ion uptake. [ABSTRACT FROM AUTHOR]

Ca- and Cu-decorated TiO2 microparticles are titanium dioxide nanoparticles that have been decorated with calcium and copper ions. TiO2, CaO, and CuO are low-cost, non-toxic, and non-hazardous materials. The aim of the present study was the physicochemical characterization of Ca- and Cu-decorated TiO2 microparticles and the evaluation of their antimicrobial activity. Thus, Ca2+ and Cu2+ species were incorporated onto TiO2 surfaces by a two-step wet method. The obtained TiO2-CaO-CuO composites were characterized by several experimental techniques. The electronic structure and charge properties of the composites were investigated by density functional theory calculations. Furthermore, the composites were successfully tested for inhibitory effects on Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, and Candida albicans standard strains. The zeta potential data indicate that the physiological condition of investigated microbial strains was strongly affected in presence of a dispersion of 10 μg/L of composites in a saline phosphate buffer also, the recorded SEM images show a damaged microbial cell surface in the presence of composites. [ABSTRACT FROM AUTHOR]

In traditional sulfate electroforming copper without additives, the electroformed deposit often exhibits defects such as pinholes, burrs and nodules. The mechanical properties of copper electroforming deposits can be improved through an abrasive-assisted electroforming process at high current density. However, excessive dissolution of copper anodes often results in the generation of a significant amount of copper ions, which subsequently turn into copper powder by disproportionation reaction, leading to the formation of burrs on the surface of cathode. In this paper, the anode area is increased to reduce the anode current density and enhance the electric field. This can improve electric field and decrease Cu+ or copper powder in the solution. The experimental results show that the mechanical properties of the electroformed deposit with bilateral anodes are significantly improved. The electroformed copper deposit with a microhardness value of 138.4 HV, a tensile strength of 259.2 Mpa and an elongation of 13.6% can be obtained, which is increased by 8.5, 27.2 and 1.7%, respectively, compared with the one-sided placement. [ABSTRACT FROM AUTHOR]

Both copper (Cu2+/+) and iodine (I−) are essential elements in all living organisms. Increasing the intracellular concentrations of Cu or I ions may efficiently inhibit tumor growth. However, efficient delivery of Cu and I ions into tumor cells is still a challenge, as Cu chelation and iodide salts are highly water-soluble and can release in untargeted tissue. Here we report mitochondria-targeted Cu-I cluster nanoparticles using the reaction of Cu+ and I− to form stable bovine serum albumin (BSA) radiation-induced phosphors (Cu-I@BSA). These solve the stability issues of Cu+ and I− ions. Cu-I@BSA exhibit bright radioluminescence, and easily conjugate with the emission-matched photosensitizer and targeting molecule using functional groups on the surface of BSA. Investigations in vitro and in vivo demonstrate that radioluminescence under low-dose X-ray irradiation excites the conjugated photosensitizer to generate singlet oxygen, and combines with the radiosensitization mechanism of the heavy atom of iodine, resulting in efficient tumor inhibition in female mice. Furthermore, our study reveals that BSA protection causes the biodegradable Cu-I clusters to release free Cu and I ions and induce cell death by modulating mitochondrial function, damaging DNA, disrupting the tricarboxylic acid cycle, decreasing ATP generation, amplifying oxidative stress, and boosting the Bcl-2 pathway. Efficient delivery of copper and iodine ions into tumor cells is promising for boosting the antitumor effect but elusive. Here the authors report a mitochondrial-targeted copper-iodide nanoparticles for the cancer treatment in which copper and iodide ions induce cell death by modulating mitochondrial functions under low-dose Xray irradiation. [ABSTRACT FROM AUTHOR]

Lung cancer, predominantly non-small cell lung cancer (NSCLC), remains a significant global health challenge, with limited therapeutic options for patients with KRAS-mutated tumors. Herein, a copper-based metal-organic framework (Cu-MOF) was applied as a novel cuproptosis-mediated nanoplatform for lung cancer therapy. Cu-MOF would disassemble and liberate copper ions under the acidic microenvironment of lysosomes of cancer cells, initiating a cascade of cellular events. The released copper ions catalyzes the Fenton reaction, generating hydroxyl radicals that induce oxidative damage, leading to cytoskeletal disruption and activation of caspase-3, ultimately triggering apoptosis. Simultaneously, with the mediation of the key regulatory factor FDX1, we found that the copper ions binding to the mitochondrial protein DLAT could result in the loss of iron-sulfur cluster proteins and aggregation of lipoylated proteins, which culminated in proteotoxic stress-induced cuproptosis. The pronounced anti-tumor effects of Cu-MOF with apoptosis and cuproptosis were confirmed both in vitro and in vivo experiments. Such dual induction of apoptosis and cuproptosis by Cu-MOF presents a promising therapeutic strategy for NSCLC, particularly for KRAS-mutated tumors, and expands potential applications of Cu-based nanomateirals for other cancers. [ABSTRACT FROM AUTHOR]

Positive allosteric modulators (PAMs) are of great interest to compensate for the lack of NMDA receptor function in the CNS in dementia. Known PAMs increase the amplitude of whole-cell ionic currents carried by NMDA receptors, but do not affect their calcium-calmodulin dependent desensitization. We studied the possibility of modulating NMDA receptor desensitization by the recently synthesized PAM GNE-9278, which has a unique binding site on the transmembrane domain. Experiments were performed on native NMDA receptors expressed in rat cortical neurons in primary tissue culture. Using the method of "patch-clamp" recording of transmembrane currents, a comparative study of the effect on NMDA receptor desensitization of three substances potentiating NMDA receptor currents was carried out: GNE-9278 (10 µM), dithiothreitol (1 mM) and copper ions (5 µM). These substances increased the amplitude of currents evoked by 100 µM NMDA, but only GNE-9278 reduced the difference between equilibrium and peak current amplitudes by 15%. In addition, GNE-9278 doubled the time constant of the decline from peak to equilibrium state thus attenuating NMDA receptor desensitization. Because GNE-9278 did not alter the effective concentration of extracellular calcium to induce desensitization, its effect probably does not interfere with receptor-calmodulin interaction. Analysis of the shape of the currents within the kinetic model showed that GNE-9278 reduced two kinetic parameters: the channel closure rate, which determines the open state time, and the rates of receptor entry into and exit from the desensitized state, which determines the probability of the open state of the channel. Modulation of calcium-dependent NMDA receptor desensitization places GNE-9278 apart from other known PAMs, which is likely determined by the GNE-9278 binding site in the pre-M1 segment of the GluN1 subunit. [ABSTRACT FROM AUTHOR]

Legionella longbeachae is the leading cause of Legionnaires' disease (LD) in Australasia and has been linked to exposure to compost and potting soils. Adding antimicrobial metal ions such as copper (Cu2+), zinc (Zn2+), and manganese (Mn2+) to potting soils may reduce the load of L. longbeachae bacteria and infection risk. Baseline concentrations of metal ions in leachate from peat, bark dust, bagging base, and an all-purpose potting soil were: iron 0.40–0.99 µg/ml, Cu of 0.003–0.03 µg/ml, Zn 0.01–0.06 µg/ml and Mn 0.11–0.29 µg/ml. Addition of Cu2+ ions to leachate reduced L. longbeachae viability in a concentration dependent manner. A similar effect was seen in potting soil with Zn2+ and Mn2+ but 10-fold higher concentrations were needed. These metal ions have potential to reduce the load of L. longbeachae in potting soils but toxicity in plants needs to be determined. [ABSTRACT FROM AUTHOR]

Measuring the mass concentration and distribution of copper ions in copper containing sludge is a necessary step for recovering copper ions. Therefore, it is very important to study the application of high- precision X-ray fluorescence spectroscopy in the determination of Cu ions in copper containing sludge. Due to the interference caused by the overlapping wavelength of X-rays generated by other elements and copper during the measurement process, the final Cu ion measurement results are biased. Therefore, high-precision X-ray fluorescence spectroscopy was used to study the determination of Cu ions in copper containing sludge in the Shandonggou copper mine area in Zhongtiao, Shanxi, in order to solve the problem of measurement result deviation caused by interferen PHA range of 100~300, use high-precision X-ray fluorescence spectroscopy to determine the mass concentration of Cu ions in the molten sheet and correct it. The results showed that based on X-ray fluorescence spectroscopy, the range of Cu ion mass concentration in 36 sampling point samples was measured, from the lowest 8. 78 mg/kg to the highest 334. 98 mg/kg. Through the drawn Cu ion mass concentration distribution characteristic map, it was found that the Cu ion mass concentration was highest in the southeast and gradually decreased towards the northwest, indicating a wide variation in Cu ion mass concentration in copper containing sludge. [ABSTRACT FROM AUTHOR]

We studied the effect of extracellular acidosis, cysteine, glutathione, and iron ions (Fe3+) on the neurocytotoxic effect of copper ions (Cu2+) in vitro. At acidic pH of the culture medium (pH 6.8), the toxic effect of copper on cultured neurons significantly increased in comparison with that at neutral pH 7.3. In the presence of 25 μM Cu2+ in the culture medium at pH 7.3 and 6.8, the neuronal survival was 89±2 and 63±4%, respectively. In the presence of glutathione or cysteine (1 μM) in the culture medium, even 0.5 μM Cu2+ caused 100% death of cultured neurons, while the presence of Fe3+ (10-50 μM) had no effect on the toxicity of Cu2+. In general, acidosis or the presence of glutathione or cysteine increases the cytotoxicity of copper ions. [ABSTRACT FROM AUTHOR]

Copper and Mercury ions have vital role to play in biological world as their excess or deficiency can cause different type of diseases in human being as well as biological species including plants and animals. Therefore, their detection at trace level becomes very important in term of biological. The current studies embody the fabrication, structural characterization and recognition behavior of a novel rhodamine B hydrazone formed when hydrazide of rhodamine B was condensed with 5-Allyl-3-methoxy salicylaldehyde (RBMA). RBMA was found to be responsive towards the very trace level of Cu2+ and Hg2+ among other tested cations so far. The sensing procedure is based on the classical opening of the spiroatom ring of rhodamine. The limit of detection (LOD) and binding constant is 5.35 ppm, 2.06 × 104 M−1 and 5.16 ppm, 1.26 × 104 M−1 for Cu2+ and Hg2+ ions respectively. The probable mechanism correlates the specific binding of RBMA with Cu2+ and Hg2+ ions. The 1:1 stoichiometry of RBMA with Cu2+ and Hg2+ ions have been supported by HRMS, FT-IR data, Job's plot, and binding constant data. Reversibility is well exhibited by RBMA by the involvement of CO32− ions via demetallation process. The real time application is well demonstrated by the use of paper strip test. The DFT study also carried out which agrees well with the experimental findings. The results displayed the novelty of this current work towards the trace level analysis of the Cu2+ and Hg2+ of the cations which are play the crucial role in industry. [ABSTRACT FROM AUTHOR]

As an essential trace element, copper has major effects on cell metabolism. Therefore, interfering with the balance of copper metabolism in such a way that leads to copper deficiency or excess causes disease. It has been reported that copper metabolic imbalance, or cuproptosis, affects the development of cardiovascular diseases by mediating cellular oxidative stress and vascular remodeling and by interfering with mitochondrial functions. Importantly, copper chelators, copper ion carriers, small molecule inhibitors of copper chaperones, and dietary copper can alleviate cardiovascular diseases caused by copper metabolic imbalance or cuproptosis. In this review, we comprehensively considered the molecular mechanisms of copper metabolic homeostasis and cuproptosis, as well as their significance and therapeutic advances in cardiovascular diseases, aiming to provide insights on therapeutically targeting copper metabolic homeostasis and cupro-ptosis as a novel strategy for managing cardiovascular diseases. [ABSTRACT FROM AUTHOR]

Mono- and di-substituted cerium oxide catalysts, viz. Ce0.95Cu0.05O2-δ, Ce0.90Cu0.10O2-δ, Ce0.90 Cu0.05Mn0.05O2-δ, Ce0.85Cu0.10Mn0.05O2-δ, and Ce0.80Cu0.10Mn0.10O2-δ, were synthesized via a one-step urea-assisted solution combustion method. The elemental composition and textural and structural properties of the catalysts were determined by various physical, electronic, and chemical characterization techniques. Hydrogen temperature-programmed reduction showed that co-doping of copper and manganese ions into the CeO2-δ lattice improved the reducibility of copper. Powder XRD, XPS, HR-TEM, and Raman spectroscopy showed that the catalysts were a singled-phased, solid-solution metal oxide with a cerium oxide cubic fluorite (cerianite) structure, and evidence of oxygen vacancies was observed. Catalytic results in the preferential oxidation of CO in a hydrogen-rich stream showed that complete CO conversion occurred between 150 and 180 °C. Furthermore, at 150 °C, Ce0.90Cu0.05Mn0.05O2-δ, Ce0.90 Cu0.10O2-δ, and Ce0.85Cu0.10Mn0.05O2-δ catalysts were the most active, achieving complete CO conversion and CO2 selectivity of 81, 79, and 71%, respectively. The catalysts performed moderately in the presence of CO2 and water, with the Ce0.90Cu0.05Mn0.05O2-δ catalyst giving a CO conversion of 80% in CO2, which decreased to about 60% when water was added. [ABSTRACT FROM AUTHOR]

A fluorescent and colorimetric dual-mode strategy based on carbon dots (CDs) was rationally designed for sensitive determination of Cu2+. Green fluorescent CDs with high absolute quantum yield of 72.9% were synthesized by facile one-step hydrothermal treatment of triethylenetetramine and Rose Bengal. Cu2+ could trigger the oxidative and chromogenic reaction of p-phenylenediamine (PPD) to generate chromogenic PPDox, accompanied by the fluorescence quenching of the CDs. The quenching mechanism was identified as the inner filter effect between PPDox and CDs. Therefore, a colorimetric/fluorescent dual-mode detection method for Cu2+ recognition was constructed. The limits of detection for Cu2+ were 4.14 μM and 1.28 μM for colorimetric and fluorescent mode, respectively. In addition, this method had achieved satisfactory results in the detection of Cu2+ in real serum samples. [ABSTRACT FROM AUTHOR]

64Cu is gaining recognition not only for its diagnostic capabilities in nuclear medical imaging but also for its therapeutic and theranostic potential. The simultaneous βˉ and Auger emissions of 64Cu can be utilized to induce a therapeutic effect on cancerous lesions. The finding of the exceptional biodistribution characteristics of the radionuclide 64Cu, when administered as basic copper ions, has highlighted its potential therapeutic application in cancer treatment. Preclinical and clinical research on the effectiveness of [64Cu]CuCl2 as a theranostic radiopharmaceutical has commenced only in the past decade. Current clinical studies are increasingly demonstrating the high specificity and uptake of [64Cu]Cu2+ by malignant tissues during early cancer progression, indicating its potential for early cancer diagnosis across various organs. This short review aims to present the latest preclinical studies involving [64Cu]CuCl2, offering valuable insights for researchers planning new in vitro and in vivo studies to explore the theranostic potential of [64Cu]Cu2+. [ABSTRACT FROM AUTHOR]

Lenvatinib resistance (LenR) presents a significant challenge in hepatocellular carcinoma (HCC) treatment, leading to high cancer-related mortality rates globally. Unlike traditional chemotherapy resistance mechanisms, LenR in HCC is primarily driven by increased cancer cell stemness. Disulfiram, (DSF), functioning as a Cu ionophore, can coordinate with Cu2+ to overcome LenR in HCC by inhibiting cancer cell stemness and cuproptosis. However, DSF faces challenges due to its poor water solubility, while copper ions present issues related to systemic toxicity during widespread use. To address this, DSF and CuO nanoparticles (NPs) were co-encapsulated to form an oil-in-water Pickering emulsion (DSF@CuO), effectively elevating DSF and copper ion concentrations within the tumor microenvironment (TME). DSF@CuO was then combined with sodium alginate (SA) to form a DSF@CuO-SA solution, which gelatinizes in situ with Ca2+ in the TME to form a DSF@CuO Gel, enhancing Pickering emulsion stability and sustaining DSF and copper ion release. A DSF@CuO Gel exhibits enhanced stability and therapeutic efficacy compared to conventional administration methods. It effectively induces mitochondrial dysfunction and cuproptosis in LenR HCC cells by downregulating DLAT, LIAS, and CDKN2A, while upregulating FDX1. Furthermore, it suppresses cancer stemness pathways through activation of the JNK/p38 MAPK pathway and inhibition of the NF-κB and NOTCH signaling pathways. These findings suggest that DSF@CuO Gels are a promising therapeutic strategy for treating LenR HCC. In vivo and in vitro LenR HCC models demonstrated significant therapeutic efficacy. In conclusion, this novel approach underscores DSF@CuO Gel's potential to overcome LenR in HCC, offering a novel approach to address this clinical challenge. [ABSTRACT FROM AUTHOR]

The present study focuses on the synthesis and structural characterization of a novel dinuclear CuII complex, [trichloridocopper(II)]-μ-chlorido-{bis[2-hydroxy-N′-(propan-2-ylidene)benzohydrazide]copper(II)} monohydrate, [Cu2Cl4(C10H12N2O2)2]·H2O or [Cu(H2L)2(μ-Cl)CuCl3]·H2O [H2L = 2-hydroxy-N′-(propan-2-ylidene)benzohydrazide]. The complex crystallizes in the monoclinic space group P21/n with one molecule of water, which forms interactions with the ligands. The first copper ion is penta-coordinated to two benzohydrazine-derived ligands via two nitrogen and two oxygen atoms, and one bridging chloride, which is also coordinated by the second copper ion alongside three terminal chlorines in a distorted tetrahedral geometry. The arrangement around the first copper ion exhibits a distorted geometry intermediate between trigonal bipyramidal and square pyramidal. In the crystal, chains are formed via intermolecular interactions along the a-axis direction, with subsequent layers constructed through hydrogen-bonding interactions parallel to the ac plane, and through slipped π–π stacking interactions parallel to the ab plane, resulting in a three-dimensional network. The intermolecular interactions in the crystal structure were quantified and analysed using Hirshfeld surface analysis. Residual electron density from disordered methanol molecules in the void space could not be reasonably modelled, thus a solvent mask was applied. [ABSTRACT FROM AUTHOR]

The scarcity of essential minerals in the wort used for bioethanol production has long been a persistent concern in industrial processes. This scarcity can negatively impact various aspects of production, including yeast cell vitality and sugar-to-ethanol conversion. In this study, we assessed the nutritional profile of key components of the industrial bioethanol production process and identified nitrogen, phosphorus, magnesium, manganese, zinc, and copper ions deficiencies. Supplementation of fermentation assays with TMNitrofós was carried out until reaching the maximum allowed for manganese (24.5%), zinc (49.4%), and copper (8.8%). Laboratory-scale fermentation assays were conducted under varying conditions of soluble solids in the wort (20, 24, and 26°Brix). These experiments aimed to assess the primary productivity parameters in response to the application of TMNitrofós. Results showed that fermentations using wort with 24 and 26°Brix supplemented with TMNitrofós led to 7% higher fermentative efficiency compared to the control group. The supplemented fermentations demonstrated higher levels of cellular vitality (76.6%) compared to the control group (55.3%). Considering a scale-up in the bioethanol production process with TMNitrofós supplementation, an increase of 266 m3 of ethanol per month was achieved compared to the control group, resulting in cost savings of R$ 586,879.20. [ABSTRACT FROM AUTHOR]