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Selective photoreduction of CO2 to multicarbon products, is an important but challenging task, due to high CO2 activation barriers and insufficient catalytic sites for C−C coupling. Herein, a defect engineering strategy for incorporating copper sites into the connected nodes of defective metal–organic framework UiO‐66‐NH2 for selective overall photo‐reduction of CO2 into acetone. The Cu2+ site in well‐modified CuN2O2 units served as a trapping site to capture electrons via efficient electron‐hole separation, forming the active Cu+ site for CO2 reduction. Two NH2 groups in CuN2O2 unit adsorb CO2 and cooperated with copper ion to functionalize as a triple atom catalytic site, each interacting with one CO2 molecule to strengthen the binding of *CO intermediate to the catalytic site. The deoxygenated *CO attached to the Cu site interacted with *CH3 fixed at one amino group to form the key intermediate CO*‐CH3, which interacted with the third reduction intermediate on another amino group to produce acetone. Our photocatalyst realizes efficient overall CO2 reduction to C3 product acetone CH3COCH3 with an evolution rate of 70.9 μmol gcat−1 h−1 and a selectivity up to 97 % without any adducts, offering a promising avenue for designing triple‐atomic sites to producing C3 product from photosynthesis with water. [ABSTRACT FROM AUTHOR]

A copper‐dependent self‐cleaving DNA (DNAzyme or deoyxyribozyme) previously isolated by in vitro selection has been analyzed by a combination of Molecular Dynamics (MD) simulations and advanced Electron Paramagnetic Resonance (Electron Spin Resonance) EPR/ESR spectroscopy, providing insights on the structural and mechanistic features of the cleavage reaction. The modeled 46‐nucleotide deoxyribozyme in MD simulations forms duplex and triplex sub‐structures that flank a highly conserved catalytic core. The DNA self‐cleaving construct can also form a bimolecular complex that has a distinct substrate and enzyme domains. The highly dynamic structure combined with an oxidative site‐specific cleavage of the substrate are two key‐aspects to elucidate. By combining EPR/ESR spectroscopy with selectively isotopically labeled nucleotides it has been possible to overcome the major drawback related to the "metal‐soup" scenario, also known as "super‐stoichiometric" ratios of cofactors versus substrate, conventionally required for the DNA cleavage reaction within those nucleic acids‐based enzymes. The focus on the endogenous paramagnetic center (Cu2+) here described paves the way for analysis on mixtures where several different cofactors are involved. Furthermore, the insertion of cleavage reaction within more complex architectures is now a realistic perspective towards the applicability of EPR/ESR spectroscopic studies. [ABSTRACT FROM AUTHOR]

In this work, the ion-exchange technique in molten salts was investigated to introduce copper ions in a bioactive and ferrimagnetic devitrified glass. This approach aimed to develop a magnetic and bioactive material for oncologic bone implants, able to join the ability to promote bone bonding to hyperthermic therapy while simultaneously lowering the risk of developing post-surgery infections. The ion-exchange approach was developed in order to overcome experimental critical issues related to the influence of copper introduction as a starting reagent, during the material synthesis, on magnetite nucleation. The magnetic devitrified glass was prepared by melt and quenching route, followed by ion exchange in a mixture of molten sodium and copper nitrates, in three different Na/Cu molar ratios (20, 200, 2000). The obtained samples were analysed in terms of morphology, composition, ability to release heat, bioactivity and antibacterial properties. The results revealed that copper ion-exchange involved both sodium and calcium ions and the precipitation of few amounts of copper oxide aggregates occurred. The crystalline nature of the starting material and its ability to reach the temperature needed for hyperthermia, under exposition to an alternating magnetic field, were not affected. A bacteriostatic effect was obtained by samples with the highest copper amount and the copper doping did not affect the bioactivity of the glass ceramic. [ABSTRACT FROM AUTHOR]

Biodegradable stents have paved the way to treat coronary artery disease. However, rapid reendothelialization is required to solve the problems of mismatched degradation rates, localized inflammation, and insufficient biocompatibility. Herein, a novel passivated protein‐adsorption coating is synthesized by coordination chelation, oxidation, cross‐linking, polymerization, and deposition of dopamine, (‐)‐epigallocatechin gallate (EGCG), and copper ions (Cu2+) using two‐electron oxidation. This coating exhibits hierarchical functionality, that is, at the macroscale, its superhydrophilicity conveys antifouling ability; whereas at the microscale, the active groups (quinone‐, amino‐, hydroxyphenyl groups and aromatic ring) facilitate protein adsorption. Antifouling ability prevents acute thrombosis and inflammation and maintains initial microenvironment stability post‐implantation. The active groups facilitate gradual endothelial cells (ECs) adhesion. Meanwhile, the decomposition of nitric oxide (NO) donors to release NO is catalyzed by Cu2+, and EGCG alleviates or prevents oxidative stress damage, inflammatory responses, thrombosis formation, and excessive smooth muscle cells proliferation in the stent microenvironment. This provides favorable conditions for the rapid and healthy growth of ECs. This study proposes a novel strategy for rapid neointima formation comprising healthy ECs on the surfaces of biodegradable stents by depositing a passivated protein‐adsorption coating (polydopamine/EGCG/Cu), opening new possibilities for the efficient treatment of coronary artery disease. [ABSTRACT FROM AUTHOR]

Hydrogels, versatile materials used in various applications such as medicine, possess properties crucial for their specific applications, significantly influenced by their preparation methods. This study synthesized 18 different types of hydrogels using sodium alginate (SA) and two molecular weights of polyvinyl alcohol (PVA). Crosslinking agents such as aqueous solutions of calcium (Ca2+) and copper (Cu2+) ions and solutions of these ions in boric acid were utilized. The hydrogels were subjected to compression strength tests and drying kinetics analysis. Additionally, six hydrogel variants containing larger PVA particles underwent Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) post-drying. Some samples were lyophilized, and their surface morphology was examined using scanning electron microscopy (SEM). The results indicate that the choice of crosslinking method significantly impacts the physicochemical properties of the hydrogels. Crosslinking in solutions with higher concentrations of crosslinking ions enhanced mechanical properties and thermal stability. Conversely, using copper ions instead of calcium resulted in slower drying kinetics and reduced thermal stability. Notably, employing boric acid as a crosslinking agent for hydrogels containing heavier PVA molecules led to considerable improvements in mechanical properties and thermal stability. [ABSTRACT FROM AUTHOR]

In this paper, two experimental procedures are reported, namely electro-deposition in the ultrathin liquid layer and chemical micro-etching. Firstly, a large area quasi-two-dimensional periodic membrane with adjustable density is deposited on a Si substrate driven by half-sinusoidal voltage, which is composed of raised ridges and a membrane between the ridges. The smaller the voltage frequency is, the larger the ridge distance is. The height of a raised ridge changes synchronously with the amplitude. The grain density distribution of membrane and raised ridge is uneven; the two structures change alternately, which is closely related to the change of growth voltage and copper ion concentration during deposition. The structural characteristics of membrane provide favorable conditions for micro-etching; stable etching speed and microscope real-time monitoring are the keys to achieve accurate etching. In the chemical micro-etching process, the membrane between ridges is removed, retaining the raised ridges, thus a large scale ordered micro-nano wires array with lateral growth was obtained. This method is simple and controllable, can be applied to a variety of substrates, and is the best choice for designing and preparing new functional materials. This experiment provides a basis for the extension of this method. [ABSTRACT FROM AUTHOR]

Oncolytic viral therapy (OVT) is a novel anti-tumor immunotherapy approach, specifically replicating within tumor cells. Currently, oncolytic viruses are mainly administered by intratumoral injection. However, achieving good results for distant metastatic tumors is challenging. In this study, a multifunctional oncolytic adenovirus, OA@CuMnCs, was developed using bimetallic ions copper and manganese. These metal cations form a biomineralized coating on the virus's surface, reducing immune clearance. It is known that viruses upregulate the expression of PD-L1. Copper ions in OA@CuMnCs can decrease the PD-L1 expression of tumor cells, thereby promoting immune cell-related factor release. This process involves antigen presentation and the combination of immature dendritic cells, transforming them into mature dendritic cells. It changes "cold" tumors into "hot" tumors, further inducing immunogenic cell death. While oncolytic virus replication requires oxygen, manganese ions in OA@CuMnCs can react with endogenous hydrogen peroxide. This reaction produces oxygen, enhancing the virus's replication ability and the tumor lysis effect. Thus, this multifunctionally coated OA@CuMnCs demonstrates potent amplification in immunotherapy efficacy, and shows great potential for further clinical OVT. Oncolytic virus therapy (OVs) is a new anti-tumor immunotherapy method that can specifically replicate in tumor cells. Although the oncolytic virus can achieve a therapeutic effect on some non-metastatic tumors through direct intratumoral injection, there are still three major defects in the treatment of metastatic tumors: immune response, hypoxia effect, and administration route. Various studies have shown that the immune response in vivo can be overcome by modifying or wrapping the surface protein of the oncolytic virus. In this paper, a multifunctional coating of copper and manganese was prepared by combining the advantages of copper and manganese ions. The coating has a simple preparation method and mild conditions, and can effectively enhance tumor immunotherapy. [Display omitted] [ABSTRACT FROM AUTHOR]

L‐3,4‐dihydroxyphenylalanine (levodopa or L–DOPA) a precursor of neurotransmitter dopamine, has been universally prescribed as a gold standard for treatment of Parkinson's Disease (PD). However, direct administration of L–DOPA has risky adverse effects which makes it challenging in the treatment of PD. Hence developing simple detection platform for sensing of L–DOPA is significant. In this work, we have developed cysteine stabilized copper nanocluster quenched with Fe2+ (Fe2+@cys@CuNC) and used as both fluorescent and colorimetric probe for detection of L–DOPA. L–DOPA attributed a fluorescence quenching effect on developed probe. Fe2+@cys@CuNC detected L–DOPA within a linear range from 0.06 mM to 1.31 mM with a low limit of detection (LoD) of 6.57 nM. The probe also exhibited high selectivity for L–DOPA over other biomolecules and neurotransmitters. Furthermore, the capability of this probe was validated by sensing L–DOPA from human serum with excellent recovery rates of 85.75 % to 115.07 %. A low‐cost paper strip‐based portable detection platform was also developed for visual detection of L–DOPA. [ABSTRACT FROM AUTHOR]

Keratin, prized for its environmentally friendly nature, unique chemical composition, and binding ability, has emerged as a promising adsorbent for untreated industrial wastewater. In this study, we developed a composite derived from hydrolyzed keratin and diallylamine. We assessed the adsorption performance of this composite against metal wastewater at varying temperatures, processing time, and pH values. The keratin-derived composites exhibited an exceptional efficiency in removing copper ions, with an adsorption capacity of 337.9 mg g-1. Furthermore, keratin composites post copper ion adsorption demonstrated inhibitory activity against bacterial growth, suggesting their potential for reuse as an antibacterial material. In conclusion, this study offers an effective method for repurposing keratin waste. The developed keratin-derived sorbents exhibit the potential in wastewater treatment. Our study provides a dual functional method with potential contribution to sustainable and eco-friendly industry practice. [ABSTRACT FROM AUTHOR]

Copper ions (Cu2+) play an essential role in various cellular functions, including respiration, nerve conduction, tissue maturation, oxidative stress defense, and iron metabolism. Covalent organic frameworks (COFs) are a class of porous crystalline materials with directed structural designability and high stability due to the combination of different monomers through covalent bonds. In this study, we synthesized a porphyrin-tetrathiazole COF (TT-COF(Zn)) with Zn-porphyrin and tetrathiafulvalene (TTF) as monomers and used it as a photoactive material. The strong light absorption of metalloporphyrin and the electron-rich properties of supplied TTF contribute to its photoelectrochemical performance. Additionally, the sulfur (S) in the TTF can coordinate with Cu2+. Based on these properties, we constructed a highly sensitive photoelectrochemical sensor for detecting Cu2+. The sensor exhibited a linear range from 0.5 nM to 500 nM (R2 = 0.9983) and a detection limit of 0.15 nM for Cu2+. Notably, the sensor performed well when detecting Cu2+ in water samples. [ABSTRACT FROM AUTHOR]

BACKGROUND: Resistance to the inflammatory response is an important part of promoting the repair of damaged tissue and improving the local inflammatory response caused by medical bio-implant materials has been a key issue to be addressed in recent years. OBJECTIVE: To summarize the anti-inflammatory effects of common metal ions and related molecular mechanisms to provide some theoretical references for improving the early inflammatory response of hosts caused by bio-implant materials. METHODS: A computer search of the relevant literature in PubMed, Web of Science, CNKI and WanFang databases was conducted using “metal ions, magnesium ion, zinc ion, silver ion, copper ion, inflammation, anti-inflammatory effects, oxidative stress, immunoregulation, signaling pathways” as Chinese and English search terms. Preliminary screening was conducted by reading the titles and abstracts. Finally, 80 papers were included for result analysis and summary. RESULTS AND CONCLUSION: (1) Metal ions such as magnesium, zinc, silver and copper have a good anti-inflammatory effect. The strength of this antiinflammatory effect is strongly correlated with the dose and duration of action. In the future, consideration can be given to controlling the release rate of ions and adjusting the appropriate therapeutic concentration to achieve the best anti-inflammatory effect. (2) Magnesium ions and zinc ions exhibit excellent antiinflammatory activity, with magnesium ions often being beneficial in anti-inflammatory therapy in the form of compounds such as magnesium sulfate and zinc ions regulating the body’s inflammatory response with zinc feed as the main source of zinc supplementation. (3) Silver and copper ions have some antiinflammatory effects, but are still predominant for their excellent antibacterial activity, mainly in the form of nanoparticles and bio-coatings. (4) Magnesium and zinc metal ions can be combined with natural extracts to form complexes to exert anti-inflammatory effects, and this method has the advantage of being inexpensive and widely available and is a sustainable and green approach, which is worthy of clinical promotion. (5) Metal ions such as magnesium, zinc, silver and copper exert anti-inflammatory effects by reducing host oxidative stress damage, modulating immune cells and inhibiting inflammatory signaling pathways such as nuclear factor-κB, Toll-like receptor, STAT3 and NOD. (6) The molecular mechanism related to the anti-inflammation of metal ions is a complex network, which is not the effect of a single pathway, but should be a combination of multiple signaling pathways. There are still many potential mechanisms that have not yet been explored, and more systematic elucidation of the interconnections between various signaling pathways is needed in the future. [ABSTRACT FROM AUTHOR]

The production of Nisin, an FDA-approved food preservative, was attempted by Lactococcus lactis subsp. lactis ATCC® 11454 using the underutilized milk industry effluent, acid-whey, as a substrate. Nisin production was further improved by studying the effect of supplementation of nutrients and non-nutritional parameters. The addition of yeast extract (6% w/v) as nitrogen source and sucrose (4% w/v) as carbon source were found to be suitable nutrients for the maximum nisin production. The changes in the medium pH due to lactic acid accumulation during batch fermentation and its influence on the production of nisin were analyzed in the optimized whey medium (OWM). The production characteristics in OWM were further compared with the nisin production in MRS media. The influence of nisin as an inducer for its own production was also studied and found that the addition of nisin at 0.22 mg/ml promote the nisin production. The analysis of consumption of various metal ions present in the OWM during the nisin production was also analyzed, and found that the copper ions are the most consumed ion. The highest nisin yield of 2.6 × 105 AU/mL was obtained with OWM. [ABSTRACT FROM AUTHOR]

The effects of heavy metals such as Hg(II) and Pb(II) on the human body are profound. Moreover, they pose significant concerns due to industrial development. Thus, the rapid and stable detection of heavy metal ions and related chemicals has emerged as an urgent issue. The application of Differential Pulse Stripping Voltammetry (DPSV) facilitated accurate and rapid detection of Hg2+ utilizing MOF materials and ZIF‐8 as detection agents. Pure ZIF‐8 served as the substrate material. Copper or nickel ions were individually introduced into the substrate material. This process resulted in the formation of bimetallic MOF materials. These materials were designated as CuZn and NiZn, respectively. Transition metal‐doped materials were used to modify the glassy carbon electrode (GCE), resulting in a substantial enhancement in the detection performance of Hg2+. The CuZn/GCE configuration demonstrated the most significant enhancement. When compared to a GCE modified with pure ZIF‐8, both sensitivity and the detection limit for free Hg2+ in the environment experienced increases of 450% and 64%, respectively. Stability and repeatability tests were conducted on the CuZn‐modified GCE. Results indicated that the electrode proved to be very stable and showed strong selectivity in the presence of interfering ions. The sensor modified with CuZn shows promising potential for monitoring trace Hg2+ levels. [ABSTRACT FROM AUTHOR]

Resistance of polymer composite materials to biodamage is one of the pressing problems of our time. Incorporation of Cu2O (I) in the composition of a polymer composite based on the ED-20 epoxy resin increases its biocidal properties. Under conditions of mineral and organic contamination, the area of the samples affected by micromycetes was found to decrease with increasing concentration of dispersed particles in the composite. The affected area of the samples filled with the particles encapsulated in polylactide was 1.5 times smaller than that of the composites filled with non-encapsulated particles. Copper oxide had a toxic effect on the Aspergillus niger strain dominant on the surface of the samples, causing a decrease in the average radial growth rate on the Czapek–Dox agar medium and in the biomass weight concentration during the growth of micromycetes in a liquid medium compared to the variant without Cu2O. [ABSTRACT FROM AUTHOR]

Disulfiram (DSF) degrades to diethyldithiocarbamate (DTC) in vivo and coordinates with copper ions to form CuET, which has higher antitumor activity. In this study, DSF@CuMSN-PDA nanoparticles were prepared using mesoporous silica with copper ions, DSF as a carrier, and polydopamine (PDA) as a gate system. The nanoparticles selectively released CuET into tumor tissue by taking advantage of the tumor microenvironment, where PDA could be degraded. The release ratio reached 79.17% at pH 5.0, indicating pH-responsive drug release from the nanoparticles. The PDA-gated system provided the nanoparticles with unique photothermal conversion performance and significantly improved antitumor efficiency. In vivo, antitumor experiments showed that the designed DSF@CuMSN-PDA nanoparticles combined with near-infrared light (808 nm, 1 W/cm2) irradiation effectively inhibited tumor growth in HCT116 cells by harnessing the combined potential of chemotherapy and photothermal therapy; a synergistic effect was achieved. Taken together, these results suggest that the designed DSF@CuMSN-PDA construct can be employed as a promising candidate for combined chemo-photothermal therapy. [ABSTRACT FROM AUTHOR]

A sensitive and simple method for detecting Cu2+ in the water source was proposed by using surface-enhanced Raman scattering spectroscopy (SERS) based on the Ag@SiO2/Au core–shell composite. The Ag@SiO2 SERS tag was synthesized by a simple approach, in which Ag nanoparticles were first embedded with Raman reporter PATP and next coated with a SiO2 shell. The Ag@SiO2 nanoparticles had strong stability even in a high-concentration salty solution, and there were no changes to their properties and appearance within one month. The Ag@SiO2/Au composite was fabricated through a controllable self-assemble process. L-cysteine was decorated on the surface of a functionalized Ag@SiO2/Au composite, as the amino and carboxyl groups of it can form coordinate covalent bond with Cu2+, which shows that the Ag@SiO2/Au composite labelled with L-cysteine has excellent performance for the detection of Cu2+ in aqueous media. In this study, the SERS detection of Cu2+ was carried out using Ag@SiO2 nanoparticles, and the limit of detection (LOD) as low as 0.1 mg/L was achieved. [ABSTRACT FROM AUTHOR]

Adsorbents based on agricultural biomass have been subjected to several investigations in recent years owing to their low cost and promising adsorption capabilities. This paper aimed to demonstrate the efficiency of date pits activated with phosphoric acid as common activating agent that increases the porosity and surface area of date pits. This results in a greater number of binding sites for the heavy metals to attach to improving the bio-adsorbent's effectiveness. To get rid of heavy metals such as zinc and copper ions from industrial wastewater using a fixed bed with a continuous flow configuration, the derived adsorbent was tested under a variety of operating conditions, including a flow rate of 4-12mL/min, an initial metal ion concentration of 30-60mg/L, and temperatures ranging from 20 to 50°C, which were chosen based on industrial conditions and available data. The results revealed that the removal efficiency of heavy metals increased with an increase in the initial metal ion concentration, but conversely, it decreased with an increase in flow rate and temperature. Also, the results indicated that with the optimum conditions of 15cm static bed height, 60mg/L initial metal concentration, 8mL/min flow rate, and 25°C temperature, determining the ideal conditions results in the efficient removal of pollutants in less time and the treatment of larger quantities. Mathematical modeling of the fixed bed column was achieved using the kinetic models of Adams Thomas, Yoon-Nelson, Bohar, and Modified Dose-Response, in this regard, the Thomas model is the closest to the experimental values, it is supposed that the adsorption mechanism was a Langmuir type adsorption followed by a pseudo-second-order chemical sorption. The Yoon-Nelson approach was employed on experimental data to predict breakthrough curves through nonlinear regression. This made it easier to determine the crucial characteristic column parameters for process design. According to thermodynamic studies, heavy metals spontaneously and exothermally adsorb activated carbon in date pits. Firstly, spontaneous adsorption indicates efficient processes that occur favorably without external energy input, offering cost-effective solutions for various applications. Secondly, the exothermic nature of adsorption suggests that lower temperatures may be sufficient, reducing energy consumption and preserving the stability of sensitive materials. Additionally, the process's exothermicity facilitates desorption at higher temperatures, enhancing the efficiency of regeneration processes. This study has shown that BDP can successfully remove heavy metals from aqueous solutions. Understanding these characteristics is crucial for optimizing applications, reducing costs, and improving overall efficiency in industrial and environmental contexts. [ABSTRACT FROM AUTHOR]

This study presents two modified polymers for Cu2+ ion removal from aqueous media. Shredded maize stalk (MC) and a strong-base anionic resin (SAX) were modified with indigo carmine (IC) in order to obtain two different complexing polymers, i.e., IC-MC and SAX-IC. Initially, the complex reaction between IC and Cu2+ in the solution was studied. Additionally, the complex formation Cu2+-IC in liquid solutions was evaluated at different pH ranges of 1.5, 4.0, 6.0, 8.0, and 10.0, respectively. For Cu2+ ions, adsorption onto the IC-MC and IC-SAX batch experiments were conducted. The contact time for evaluating the optimum adsorption for Cu2+ ions on the complexing materials was established at 1 h. Efficient Cu2+ ion adsorption on the IC-MC and SAX-IC at pH = 10 was achieved. The adsorption of Cu2+ ions depends on the quantity of IC retained on MC and SAX. At 2.63 mg IC/g MC(S4) and 22 mg IC/g SAX(SR2), a high amount of Cu2+ ion adsorption was reported. The highest adsorption capacity (Qe) of IC-MC was obtained at 0.73 mg/g, and for IC-SAX, it was attained at 10.8 mg/g. Reusability experiments were performed using the HCl (0.5 M) solution. High regeneration and reusability studies of IC-MC and IC-SAX were confirmed, suggesting that they can be used many times to remove Cu2+ ions from aqueous matrices. Therefore, the development of complexing materials could be suitable for Cu2+ ion removal from wastewater. [ABSTRACT FROM AUTHOR]

In this study, we explored the formation of CuO nanoparticles, NiO nanoflakes, and CuO-NiO nanocomposites using saponin extract and a microwave-assisted hydrothermal method. Five green synthetic samples were prepared using aqueous saponin extract and a microwave-assisted hydrothermal procedure at 200 °C for 30 min. The samples were pristine copper oxide (100C), 75% copper oxide–25% nickel oxide (75C25N), 50% copper oxide–50% nickel oxide (50C50N), 25% copper oxide–75% nickel oxide (25C75N), and pristine nickel oxide (100N). The samples were characterized using FT-IR, XRD, XPS, SEM, and TEM. The XRD results showed that copper oxide and nickel oxide formed monoclinic and cubic phases, respectively. The morphology of the samples was useful and consisted of copper oxide nanoparticles and nickel oxide nanoflakes. XPS confirmed the +2 oxidation state of both the copper and nickel ions. Moreover, the optical bandgaps of copper oxide and nickel oxide were determined to be in the range of 1.29–1.6 eV and 3.36–3.63 eV, respectively, and the magnetic property studies showed that the synthesized samples exhibited ferromagnetic and superparamagnetic properties. In addition, the catalytic activity was tested against para-nitrophenol, demonstrating that the catalyst efficiency gradually improved in the presence of CuO. The highest rate constants were obtained for the 100C and 75C25N samples, with catalytic efficiencies of 98.7% and 78.2%, respectively, after 45 min. [ABSTRACT FROM AUTHOR]

Bacterial laccase has grown significantly crucial on a large scale because they have high catalytic activity and stability. This is the first study in which the laccase gene was amplified from Bhargavaea beijingensis, ligated to the pENTR-TOPO vector, and transformed into Escherichia coli. The novel laccase was purified by Ni–NTA sepharose affinity chromatography. Purified laccase showed optimum pH and temperature of 8.0 and 50 °C, respectively. The novel B. beijingensis laccase exhibited stable activity at a broad range of pH and temperature. The kinetic parameters Km of 0.23 mM and Vmax of 54.6 μmol/min/mg of protein were noted for recombinant laccase toward guaiacol. Laccase activity was significantly influenced by metal ions such as copper, magnesium, and arsenate. The efficacy of laccase in dye decolorization was investigated using various dyes, and a nearly complete decolorization of congo red was recorded. This study confirmed that laccase from B. beijingensis can be produced in the active and stable form to degrade lignin and decolorize dyes. [ABSTRACT FROM AUTHOR]

[Display omitted] • An efficient CuHCF/C electrode was prepared for Cu2+ removal by CDI. • CuHCF/C achieved high Cu2+ adsorption capacity of 134.47 mg g−1 at low applied voltage of 0.8 V. • CuHCF/C manifested excellent Cu2+ selectivity in multi-ion coexisting solution. • The mechanism of removing Cu2+ by Faradaic pseudocapacitance was explained. The efficient capture of copper ions (Cu2+) in wastewater has dual significance in pollution control and resource recovery. Prussian blue analog (PBA)-based pseudocapacitive materials with open frameworks and abundant metal sites have attracted considerable attention as capacitive deionization (CDI) electrodes for copper removal. In this study, the efficiency of copper hexacyanoferrate (CuHCF) as CDI electrode for Cu2+ treating was evaluated for the first time upon the successful synthesis of copper hexacyanoferrate/carbon sheet combination (CuHCF/C) by introducing carbon sheet as conductive substrate. CuHCF/C exhibited significant pseudocapacitance and high specific capacitance (52.92 F g−1) through the intercalation, deintercalation, and coupling of Cu+/Cu2+ and Fe2+/Fe3+ redox pairs. At 0.8 an applied voltage and CuSO 4 feed liquid concentration of 100 mg L−1, the salt adsorption capacity was 134.47 mg g−1 higher than those of most reported electrodes. Moreover, CuHCF/C demonstrated excellent Cu2+ selectivity in multi-ion coexisting solutions and in actual wastewater experiments. Density functional theory (DFT) calculations were employed to elucidate the mechanism. This study not only reveals the essence of Cu2+ deionization by PBAs pseudocapacitance with promising potential applications but also provides a new strategy for selecting efficient CDI electrodes for Cu2+ removal. [ABSTRACT FROM AUTHOR]

[Display omitted] Chronic wounds, particularly those caused by diabetes, pose a significant challenge for clinical treatment due to their prolonged healing process and associated complications, which can lead to increased morbidity. A biocompatible hydrogel with strong antibacterial properties and the ability to promote angiogenesis can be directly absorbed in the wound site for healing. A series of self-healing, antibacterial bolaamphiphilic supramolecular self-assembling hydrogels (HLQMes/Cu) were developed based on metal–ligand coordination between various concentrations of Cu2+ solution and the head group of l -histidine methyl ester in HLQMes. This is the first report on the application of bola-molecular supramolecular hydrogels for the treatment of chronic wounds. The bola-molecular hydrogels reduced the toxicity of copper ions by coordination, and the HLQMes/Cu hydrogel, with 1.3 mg/mL Cu2+ (HLQMes/Cu1.3), demonstrated good biocompatibility and antibacterial properties and effectively enhanced wound healing in a diabetic wound model with full-thickness injuries. Immunohistochemical analysis revealed that the HLQMes/Cu1.3 hydrogel enhanced epithelial formation and collagen deposition in wounds. Immunofluorescence studies confirmed that the HLQMes/Cu1.3 hydrogel attenuated the expression of proinflammatory factor (IL-6) and promoted angiogenesis by upregulating α-SMA and CD31. These findings demonstrate the potential of this bolaamphiphilic supramolecular self-assembling hydrogel as a promising candidate for diabetic wound treatment. [ABSTRACT FROM AUTHOR]

Lysyl oxidase‐like 2 (LOXL2) is a Cu2+‐dependent amine oxidase that catalyzes the oxidative deamination of lysine residues of elastin and collagen to generate aldehyde groups. In the active state of LOXL2, its conserved catalytic domain has a lysine tyrosylquinone (LTQ) cofactor and a copper ion. LTQ is post‐translationally derived from Lys653 and Tyr689 of LOXL2. In this study, well‐tempered metadynamics simulations are used to investigate the conformation modulation from the inactive state to active state and obtain the free energy landscape. Interestingly, the simulations show that LTQ precursor residues cannot get close in Zn2+−bound LOXL2, whereas the copper ion binding triggers a conformation change to form an optional structure for LTQ biosynthesis. It is found that a prominent loop, consisting of residues 654–658, hinders the formation of LTQ in Zn2+−LOXL2 by preventing Lys653 from moving into active site of LOXL2, whereas this loop is relatively flexible in Cu2+−LOXL2. After the formation of LTQ, it needs to be activated by adjusting its position to be exposed to the solvent, thus allowing it to react with its substrate proteins. The results indicate that this process involves an intermediate state and that the activation of LTQ overcomes an energy barrier of 5.9 kcal mol−1. [ABSTRACT FROM AUTHOR]

Copper-based nanomaterials have been employed as therapeutic agents for cancer therapy and diagnosis. Nevertheless, persistent challenges, such as cellular toxicity, non-uniform sizes, and low photothermal efficiency, often constrain their applications. In this study, we present Cu2+-loaded silica nanoparticles fabricated through the chelation of Cu2+ ions by silanol groups. The integration of Cu2+ ions into uniformly sized silica nanoparticles imparts a photothermal therapy effect. Additionally, the amine functionalization of the silica coating facilitates the chemical conjugation of tumor-specific fluorescence probes. These probes are strategically designed to remain in an 'off' state through the Förster resonance energy transfer mechanism until exposed to cysteine enzymes in cancer cells, inducing the recovery of their fluorescence. Consequently, our Cu2+-loaded silica nanoparticles demonstrate an efficient photothermal therapy effect and selectively enable cancer imaging. [ABSTRACT FROM AUTHOR]

In this work, sodium alginate/sodium humate @ Polyacrylamide (SA/SH@PAM) hydrogel beads were prepared using sodium alginate as encapsulant, sodium humate as filler, and polyacrylamide wrapped on the outer layer. Removal and recycling performance toward batch and column adsorption of Cu (II) was investigated. The results indicated that SA/SH@PAM had good removal behavior in the pH range of 3.0–6.0, with an optimal pH of 5.0. The maximum adsorption capacity of SA/SH@PAM beads could reach ~ 134.65 mg/g, which was 2.0 and 1.6 times higher than that of sodium alginate beads (SA) and sodium alginate/sodium humate beads (SA/SH), respectively. Pseudo-second-order kinetic model could fit experimental data better, indicating the chemisorption of Cu (II) on SA/SH@PAM surface. Isotherm and thermodynamics studies suggested that heterogeneous multilayer adsorption occurred on the surface of SA/SH@PAM and Cu (II) adsorption was a spontaneous and endothermic process. Thomas model was fitted better than Adams-Bohart model with breakthrough curves in a fixed-bed column system, signifying that internal and external diffusion was not the main factor limiting the adsorption efficiency of SA/SH@PAM. Characterization analysis (FT-IR, SEM, XPS, etc.) indicated ion exchange and the interaction of multiple functional groups (-COOH, -CO–NH-, etc.) with Cu (II) were the main adsorption mechanisms. Besides, SA/SH@PAM demonstrated good regeneration and anti-interference ability of co-existing ions. Overall, SA/SH@PAM is a potential adsorbent for Cu (II) removal from wastewater. [ABSTRACT FROM AUTHOR]

The detection of copper ions and hydrogen sulfide with high sensitivity and selectivity has become a research priority as they play a crucial role in physiopathological processes both in the human body and in the environment. Herein, a fluorescent chemosensor named FGP1 (FITC-Ahx-Ser-Ser-His-Thr-Glu-Phe-NH2) was developed using novel peptides. This chemosensor solely recognizes Cu2+ without any disruption by other metal ions that may compete. The binding of FGP1–Cu leads to the quenching of the FGP1 probe fluorescence with great sensitivity and rapid response time, resulting in a noticeable change of color observable to the naked eye. The association constant of FGP1–Cu is 7.34 × 105 M−1, and thus when S2− is added to the FGP1–Cu complexes, Cu2+ is removed and fluorescence is restored, resulting in an "off–on" process. The fluorescence titration measurements' detection limits, computed utilizing the 3σ/k equation, were 38.2 nM (Cu2+) and 37.9 nM (S2−). These values are considerably lower than the safe levels designated by the US EPA. Furthermore, on account of its favorable water solubility, high biocompatibility and low toxicity, the FGP1 probe proved effective in tracking Cu2+ and S2− in HeLa living cells using the fluorescence imaging technique. [ABSTRACT FROM AUTHOR]

Carl Wilhelm Scheele's notorious toxic pigment, commonly referred to as "Scheele's green" often resulted in a mixture of products with unknown chemical composition. Positive identification of the pigment has been limited to Raman spectroscopy and indirect analysis using FTIR and XRD methods. Despite these techniques, reported occurrences of the pigment in heritage samples are scarce, suggesting that Scheele's green is rarely reported due to challenges in its characterisation rather than infrequent use. Regarding the degradation of Cu-As green pigments, common assumptions suggest dissociation in acidic pH conditions, generating mobile arsenic and copper ions, followed by oxidation to As(V), which can co-precipitate with Fe, Al, and Ca ions. This study reproduces the fabrication of Scheele's green using historical recipes, focusing on maintaining the pH of the arsenite solution at 9.3. The research explores its relationship with Emerald green, the challenges associated with their identification, and addresses common misconceptions about the degradation of such pigments. Maintaining the pH at 9.3 proved influential in obtaining a crystalline product with an intense Raman signal, aligning with the widely accepted spectra of Scheele's green. However, Raman spectra from amorphous Cu-As samples consistently exhibited broad bands at 288 and 845 cm−1, prompting a proposed modification for a dual representation of the pigment: the "common" form with broad bands and the "uncommon" or crystalline form as reported in the literature. Demonstrating that the crystalline form shares nearly identical Raman and FTIR spectra implies an identical chemical composition to Trippkeite. Evidence presented highlights that Cu-As based pigments contain free copper, arsenite and arsenate ions prone to migration, challenging commonly described degradation pathways. The hypothesis presented here, that Emerald green synthesis may inadvertently yield small amounts of Scheele's green urges caution in pigment identification using Raman spectroscopy. Additionally, the study reveals, for the first time, the occurrence of Scheele's green in a book, with particles exhibiting a spherulite form, challenging identification of Emerald green solely based on morphology. [ABSTRACT FROM AUTHOR]

Azacitidine, a DNA methylation inhibitor, is employed for the treatment of acute myeloid leukemia (AML). However, drug resistance remains a major challenge for effective azacitidine chemotherapy, though several studies have attempted to uncover the mechanisms of azacitidine resistance. With the aim to identify the mechanisms underlying acquired azacitidine resistance in cancer cell lines, we developed a computational strategy that can identify differentially regulated gene networks between drug-sensitive and -resistant cell lines by extending the existing method, differentially coexpressed gene sets (DiffCoEx). The technique specifically focuses on cell line-specific gene network analysis. We applied our method to gene networks specific to azacitidine sensitivity and identified differentially regulated gene networks between azacitidine-sensitive and -resistant cell lines. The molecular interplay between the metallothionein gene family, C19orf33, ELF3, GRB7, IL18, NRN1, and RBM47 were identified as differentially regulated gene network in drug resistant cell lines. The biological mechanisms associated with azacitidine and AML for the markers in the identified networks were verified through the literature. Our results suggest that controlling the identified genes (e.g., the metallothionein gene family) and "cellular response"-related pathways ("cellular response to zinc ion", "cellular response to copper ion", and "cellular response to cadmium ion", where the enriched functional-related genes are MT2A, MT1F, MT1G, and MT1E) may provide crucial clues to address azacitidine resistance in patients with AML. We expect that our strategy will be a useful tool to uncover patient-specific molecular interplay that provides crucial clues for precision medicine in not only gastric cancer but also complex diseases. [ABSTRACT FROM AUTHOR]

To endow lyocell fabric with flame retardant and antibacterial properties, tri (2-hydroxyethyl) isocyanurate was utilized to synthesize a phosphorus and nitrogen-containing flame retardant (ATHEIC), which was then used to prepare flame retardant lyocell fabric (FR-lyocell). The antibacterial properties of FR-lyocell were achieved by adsorbing copper ions on the fabric surface followed by reducing to copper nanoparticles. The lyocell fabric treated with 30 wt% ATHEIC solution possessed an LOI value of 35.8%, which remained 31.9% even after 20 laundering cycles. The char residue at 800 °C of FR-lyocell under nitrogen and air atmosphere was 48.6 wt% and 27.3 wt%, respectively, indicating excellent char forming performance. Antibacterial tests showed that the modified lyocell fabric had a bacteriostatic zone width of 5.3 mm and 4.6 mm against E. coli and S. aureus, respectively. This work provides a new approach to fabricate multifunctional lyocell fabric with flame retardant and antibacterial properties. [ABSTRACT FROM AUTHOR]

The present study demonstrates an eco-friendly and cost-effective synthesis of calcium terephthalate metal–organic frameworks (Ca-MOF). The Ca-MOF were composed of metal ions (Ca2+) and organic ligands (terephthalic acid; TPA); the former was obtained from egg shells, and the latter was obtained from processing waste plastic bottles. Detailed characterization using standard techniques confirmed the synthesis of Ca-MOF with an average particle size of 461.9 ± 15 nm. The synthesized Ca-MOF was screened for its ability to remove multiple metal ions from an aqueous solution. Based on the maximum sorption capacity, Pb2+, Cd2+, and Cu2+ ions were selected for individual parametric batch studies. The obtained results were interpreted using standard isotherms and kinetic models. The maximum sorption capacity (qm) obtained from the Langmuir model was found to be 644.07 ± 47, 391.4 ± 26, and 260.5 ± 14 mg g−1 for Pb2+, Cd2+, and Cu2+, respectively. Moreover, Ca-MOF also showed an excellent ability to remove all three metal ions simultaneously from a mixed solution. The metal nodes and bonded TPA from Ca-MOF were dissociated by the acid dissolution method, which protonated and isolated TPA for reuse. Further, the crystal structure of Ca-MOF was prepared and docked with protein targets of selected pathogenic water-borne microbes, which showed its disinfection potential. Overall, multiple metal sorption capability, regeneration studies, and broad-spectrum antimicrobial activity confirmed the versatility of synthesized Ca-MOF for industrial wastewater treatment. [ABSTRACT FROM AUTHOR]

To solve the problem of the presence of heavy metals in water causing water pollution, the biodegradable film based on zein/polyvinyl alcohol (PVA) with the incorporation of nano‐hydroxyapatite (nHAP) was fabricated through an electrospinning technique. The copper ion was taken as the representative of heavy metal ions in this study. The result showed that the incorporated nHAP nanoparticles were dispersed within the zein/PVA matrix, and strong hydrogen bonding interactions were formed between the filler and matrix, improving the hydrophobicity of the nanofibrous films and maintaining thermal stability. The adsorption mechanism was analyzed by fitting the adsorption process with pseudo‐first‐order model and pseudo‐second‐order model. Based on the ion exchange effect, electrostatic interaction, and complexation, the adsorption capacities of nanofibrous films for Cu(II) were significantly increased after adding nHAP. When the nHAP content was 20 wt.%, the Cu(II) adsorption capacity reached up to 23.86 mg/g, and the adsorption efficiency was 13.94% higher than that of neat zein/PVA nanofibers. This work suggests the potential of the electrospun zein/PVA/nHAP nanofibrous films as desirable eco‐friendly materials in metal removal applications. [ABSTRACT FROM AUTHOR]

Copper ions (Cu2+), as a crucial trace element, play a vital role in living organisms. Thus, the detection of Cu2+ is of great significance for disease prevention and diagnosis. Nanochannel devices with an excellent nanoconfinement effect show great potential in recognizing and detecting Cu2+ ions. However, these devices often require complicated modification and treatment, which not only damages the membrane structure, but also induces nonspecific, low-sensitivity and non-repeatable detection. Herein, a 2D MXene–carboxymethyl chitosan (MXene/CMC) freestanding membrane with ordered lamellar channels was developed by a super-assembly strategy. The introduction of CMC provides abundant space charges, improving the nanoconfinement effect of the nanochannel. Importantly, the CMC can chelate with Cu2+ ions, endowing the MXene/CMC with the ability to detect Cu2+. The formation of CMC–Cu2+ complexes decreases the space charges, leading to a discernible variation in the current signal. Therefore, MXene/CMC can achieve highly sensitive and stable Cu2+ detection based on the characteristics of nanochannel composition. The linear response range for Cu2+ detection is 10−9 to 10−5 M with a low detection limit of 0.095 nM. Notably, MXene/CMC was successfully applied for Cu2+ detection in real water and fetal bovine serum samples. This work provides a simple, highly sensitive and stable detection platform based on the properties of the nanochannel composition. [ABSTRACT FROM AUTHOR]

The contamination of aquatic environments by heavy metals can have detrimental effects on fish, impacting their growth and overall health, including the regulation of antioxidant genes. An investigation was carried out to assess the distribution and habitat of Gymnocypris eckloni in the Yellow River basin. Simultaneously, heavy metal concentrations in its habitat and in selected locations within the upper Yellow River were measured. In an effort to explore the potential roles of specific genes in antioxidant responses, G. eckloni was exposed to low concentrations of copper (Cu2+) and lead (Pb2+) for varying durations (12, 24, and 48 hours). The mRNA levels of GeCu/Zn-SOD, GeMn-SOD, GeHsp90, and GeMT were quantified in the gills, kidneys, and liver through qRT-PCR. The findings suggest that the habitat of G. eckloni is generally safe; however, occasional exceedances of safety standards could pose a potential threat to its growth. Importantly, the expression of GeCu/Zn-SOD, GeMn-SOD, GeHsp90, and GeMT exhibited responses to the low concentrations of copper-induced and lead-induced stress. Notably, GeCu/Zn-SOD, GeMn-SOD, and GeMT demonstrated heightened sensitivity to lead compared to copper. Furthermore, the expression of these genes displayed tissue-specific responses under identical metal stress conditions. These results indicate that GeCu/Zn-SOD, GeMn-SOD, GeHsp90, and GeMT genes have the potential to serve as early, sensitive biomarkers for the detection of metal toxicity induced by Cu2+ and Pb2+. This study also provides valuable insights into the functioning of antioxidant genes under oxidative stress in fish. [ABSTRACT FROM AUTHOR]

In this research, we present a novel design protocol for the in-situ synthesis of MgAl layered double hydroxide-copper metal–organic frameworks (LDH-MOFs) nanocomposite based on the electrocoagulation process and chemical method. The overall goal in this project is the primary synthesis of para-phthalic acid (PTA) intercalated MgAl-LDH with Cu (II) ions to produce the paddle-wheel like Cu-(PTA) MOFs nanocrystals on/in the MgAl-LDH structure. The physicochemical properties of final product; Cu-(PTA) MOFs/MgAl-LDH, were characterized by the surface analysis and chemical identification methods (SEM, EDX, TEM, XRD, BET, FTIR, CHN, DLS, etc.). The Cu-(PTA) MOFs/MgAl-LDH nanocomposite was used to modification of the carbon paste electrode (CPE); Cu-(PTA) MOFs/MgAl-LDH/CPE. The electrochemical performance of Cu-(PTA) MOFs/MgAl-LDH/CPE was demonstrated through the utilization of electrochemical methods. The results show a stable redox behavior of the Cu (III)/Cu (II) at the surface of Cu-(PTA) MOFs/MgAl-LDH/CPE in alkaline medium (aqueous 0.1 M NaOH electrolyte). Then, the Cu-(PTA) MOFs/MgAl-LDH/CPE was used as a new electrocatalyst toward the oxidation of formaldehyde (FA). Electrochemical data show that the Cu-(PTA) MOFs/MgAl-LDH/CPE exhibits superior electrocatalytic performance on the oxidation of FA. Also the diffusion coefficient, exchange current density (J°) and mean value of catalytic rate constant (Kcat) were found to be 1.18 × 10–6 cm2 s−1, 23 mA cm-2 and 0.4537 × 104 cm3 mol−1 s−1, respectively. In general, it can be said the Cu-(PTA) MOFs/MgAl-LDHs is promising candidate for applications in direct formaldehyde fuel cells. [ABSTRACT FROM AUTHOR]

Separating copper and cobalt ions is crucial due to the industry's strategic reliance on both these elements. When the extraction process is able to significantly increase the separation factor, it becomes favorable to separate two ions. However, the presence of Cu(II) ions together with Co(II) hinders the achievement of optimum efficiency when using commonly available extractants. This study conducted the separation of the two elements using both batch and continuous methods in a pilot plant pulsed column equipped with a disc and doughnut structure. The initial step involved optimizing the key variables to maximize the separation factor using the central composite design procedure. The optimization of Cyanex272, Cyphos IL 101 concentrations, and the pH value of the aqueous phase were all adjusted to 0.024 M, 0.046 M, and 7.3, correspondingly. In the following step, the hydrodynamic characteristics and extraction performance were examined in the pulsed column of the pilot plant. The findings indicated that the presence of Cyphos IL 101 resulted in an increased separation factor and efficiency within the column. As a result, the ionic liquid enhances performance without encountering any operational issues. This additive is considered an environmentally friendly solvent and does not cause any negative impacts. Consequently, it is suggested for utilization in continuous industrial processes. [ABSTRACT FROM AUTHOR]

A novel copper (II) probe based on pyridinium salt was designed and synthesized, and the structure was confirmed by NMR and high-resolution mass spectrometry (HRMS). The probe exhibits strong orange fluorescent emission, and shows high selectivity for copper (II) over other cations. It may qualitatively identify copper ions from many metal cations without the use of any instruments. The fluorescent intensity at 572 nm decreases linearly with copper (II) concentration in the range of 0–10 µM. A remarkable detection limit (0.045 µM) can be achieved. [ABSTRACT FROM AUTHOR]

Functional cell treatment for critical limb ischemia is limited by cell viability loss and dysfunction resulting from a harmful ischemic microenvironment. Metal-polyphenol networks have emerged as novel cell delivery vehicles for protecting cells from the detrimental ischemic microenvironment and prolonging the survival rate of cells in the ischemic microenvironment. M2 macrophages are closely related to tissue repair, and they secrete anti-inflammatory factors that contribute to lesion repair. However, these cells are easily metabolized in the body with low efficiency. Herein, M2 macrophages were decorated with a metal‒polyphenol network that contains copper ions and epigallocatechin gallate (Cu-EGCG@M2) to increase cell survival and therapeutic potential. Cu-EGCG@M2 synergistically promoted angiogenesis through the inherent angiogenesis effect of M2 macrophages and copper ions. We found that Cu-EGCG@M2 increased in vitro viability and strengthened the in vivo therapeutic effect on the ischemic hindlimbs of mice, which promoted the recovery of blood and muscle regeneration, resulting in superior limb salvage. These therapeutic effects were ascribed to the increased survival rate and therapeutic period of M2 macrophages, as well as the ameliorated microenvironment at the ischemic site. Additionally, Cu-EGCG exhibited antioxidant, anti-inflammatory, and proangiogenic effects. Our findings provide a feasible option for cell-based treatment of CLI. [Display omitted] • Cu-EGCG modify the M2 type macrophage, which was the first successfully attempted in critical limb ischemia. • Improved the microenvironment by the antioxidant activity of EGCG and anti-inflammation activity of M2 type macrophage. • Cu-EGCG network ameliorated cell survival and strengthen the therapeutic effect. [ABSTRACT FROM AUTHOR]

The high toxicity of arsenic (As) can cause irreversible harm to the environment and human health. In this study, the chlorin e6 (Ce6), which emits fluorescence in the infrared region, was introduced as the luminescence center, and the addition of copper ion (Cu2+) and As(V) provoked a regular change in fluorescence at 652 nm, whereas that of As(III) was 665 nm, which was used to optionally detect Cu2+, arsenic (As(III), and As(V)). The limit of detection (LOD) values were 0.212 μM, 0.089 ppm, and 1.375 ppb for Cu2+, As(III), and As(V), respectively. The developed method can be used to determine Cu2+ and arsenic in water and soil with good sensitivity and selectivity. The 1:1 stoichiometry of Ce6 with Cu2+ was obtained from the Job plot that was developed from UV–visible spectra. The binding constants for Cu2+ and As(V) were established to be 1.248 × 105 M−1 and 2.35 × 1012 M−2, respectively, using B–H (Benesi–Hildebrand) plots. Fluorescence lifetimes, B–H plots, FT–IR, and 1H-NMR were used to postulate the mechanism of Cu2+ fluorescence quenching and As(V) fluorescence restoration and the interactions of the two ions with the Ce6 molecule. [ABSTRACT FROM AUTHOR]

A new copper(II) complex with 2-amino-6-methylpyrimidin-4-(1H)-one, [Cu(C5H7N3O)4](NO3)2·H2O (Cupyrim), has been synthesized and studied by X-ray diffraction, elemental analysis and FT-IR spectroscopy. The Cu(II) is four-coordinate in a square planar geometry by four nitrogen atoms of the four organic ligands. Hirshfeld Surface Analysis was conducted to understand crystalline packing. Overall, the structure is maintained by metal coordination as well as strong and weak (C,N)–H···O hydrogen bonds and C–H...π interactions. The IR spectrum primary peaks have been assigned to the vibration modes of the ligand functional groups. An investigation of the inhibitory properties of Cupyrim toward "Cyclin-dependent Kinase 2" (CdK2) and "inducible nitric oxide synthase" (iNOS) proteins was aided by molecular docking research. According to molecular docking, Cupyrim exhibits promising inhibitory efficacy against Parkinson's, schizophrenia, and Alzheimer's disorders. The temperature dependence of the real and imaginary part of the dielectric permittivity was analyzed with the Cole-Cole formalism as well as DSC diagrams from 45-147 °C. [ABSTRACT FROM AUTHOR]

Selective retrograde transport from endosomes back to the trans-Golgi network (TGN) is important for maintaining protein homeostasis, recycling receptors, and returning molecules that were transported to the wrong compartments. Two important transmembrane proteins directed to this pathway are the Cation-Independent Mannose-6-phosphate receptor (CI-MPR) and the ATP7B copper transporter. Among CI-MPR functions is the delivery of acid hydrolases to lysosomes, while ATP7B facilitates the transport of cytosolic copper ions into organelles or the extracellular space. Precise subcellular localization of CI-MPR and ATP7B is essential for the proper functioning of these proteins. This study shows that both CIMPR and ATP7B interact with a variant of the clathrin adaptor 1 (AP-1) complex that contains a specific isoform of the γ-adaptin subunit called γ2. Through synchronized anterograde trafficking and cell-surface uptake assays, we demonstrated that AP-1γ2 is dispensable for ATP7B and CI-MPR exit from the TGN while being critically required for ATP7B and CI-MPR retrieval from endosomes to the TGN. Moreover, AP-1γ2 depletion leads to the retention of endocytosed CI-MPR in endosomes enriched in retromer complex subunits. These data underscore the importance of AP-1γ2 as a key component in the sorting and trafficking machinery of CI-MPR and ATP7B, highlighting its essential role in the transport of proteins from endosomes. [ABSTRACT FROM AUTHOR]

This study investigated the suitability of moss peat and compost as adsorbents for removing copper ions from aqueous systems. Kinetic experiments were conducted at pH 4, 20 °C, and an initial copper ion concentration of 20 mM. Under these experimental conditions, moss peat and compost had a maximum adsorption capacity of 45.8 and 41.9 mg/g, respectively. The kinetic data was assessed using several models, and the data fitted well with the pseudo-second-order model for both adsorbents. Moreover, the analysis of the isotherm data showed that the Langmuir model could fit the data, suggesting that copper ions are chemically adsorbed onto moss peat and compost. The pH value of 4.5 was the most effective for the adsorption of copper ions onto moss peat and compost. At this pH value, the maximum adsorption capacities were 60.0 mg/g for moss peat and 56.9 mg/g for compost. The characterization of moss peat and compost before and after the interaction with copper ions indicated that surface precipitation was the dominant mechanism by which copper ions were removed from aqueous systems. Copper precipitation on the surface of moss peat was higher than that on the surface of compost, and it was found to be 7.7 wt% and 3.8 wt%, respectively. Overall, these findings highlight the potential of using moss peat and compost as effective adsorbents for copper ions in highly contaminated water, particularly industrial and mining effluent.

Abstract Background The development of the plant in vitro techniques has brought about the variation identified in regenerants known as somaclonal or tissue culture-induced variation (TCIV). S-adenosyl-L-methionine (SAM), glutathione (GSH), low methylated pectins (LMP), and Cu(II) ions may be implicated in green plant regeneration efficiency (GPRE) and TCIV, according to studies in barley (Hordeum vulgare L.) and partially in triticale (× Triticosecale spp. Wittmack ex A. Camus 1927). Using structural equation models (SEM), these metabolites have been connected to the metabolic pathways (Krebs and Yang cycles, glycolysis, transsulfuration), but not for triticale. Using metabolomic and (epi)genetic data, the study sought to develop a triticale regeneration efficiency statistical model. The culture’s induction medium was supplemented with various quantities of Cu(II) and Ag(I) ions for regeneration. The period of plant regeneration has also changed. The donor plant, anther-derived regenerants, and metAFLP were utilized to analyze TCIV concerning DNA in symmetric (CG, CHG) and asymmetric (CHH) sequence contexts. Attenuated Total Reflectance–Fourier Transfer Infrared (ATR-FTIR) spectroscopy was used to gather the metabolomic information on LMP, SAM, and GSH. To frame the data, a structural equation model was employed. Results According to metAFLP analysis, the average sequence change in the CHH context was 8.65%, and 0.58% was de novo methylation. Absorbances of FTIR spectra in regions specific for LMP, SAM, and GSH were used as variables values introduced to the SEM model. The average number of green regenerants per 100 plated anthers was 2.55. Conclusions The amounts of pectin demethylation, SAM, de novo methylation, and GSH are connected in the model to explain GPRE. By altering the concentration of Cu(II) ions in the medium, which influences the amount of pectin, triticale’s GPRE can be increased.

A novel, bis-salophen schiff base ligand anchored magnetic Fe3O4@SiO2 nanoparticles was prepared and applied for removal of Cu(II) from aqueous solutions. The obtained Fe3O4@SiO2/Schiff base MNPs was characterized by fourier transform infrared (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray analysis (EDX) and vibration sample magnetometry (VSM). Then, the adsorption activity for copper ions was studied by nonmagnetic, in terms of effect of adsorbent dosage on the adsorption and kinetics behavior. Furthermore, the adsorption and regeneration experiment showed there was about 5% loss in the adsorption capacity of the prepared Fe3O4@SiO2/Schiff base MNPs for copper ions after 6 times reuse. Finally, our results suggested that the Fe3O4@SiO2/Schiff base composites have a great potential to be employed for treatment of wastewater containing Cu(II).

Introduction. Copper ions (Cu2+) are structural elements of proteins such as cytochrome с oxidase (Complex IV), an enzyme that catalyzes the final step of electron transfer to oxygen during oxidative phosphorylation in the mitochondria. With Cu2+ homeostasis being of utmost importance, its disturbances in the central nervous system are involved in the mechanisms of many neurodegenerative and other brain disorders. This study aimed to assess the effects of non-toxic copper ion levels on death of cerebellar granule neurons associated with lipopolysaccharide (LPS; in vitro inflammation model) or azide sodium (NaN3; cytochrome с oxidase inhibitor). Materials and methods. LPS (10 μg/mL) or NaN3 (250 μM) was added on day 7 to 8 to the culture medium with rat cerebellar cells for 24 hours in vitro. Nitrite concentrations were measured in the culture medium by Griess assay; absorbance was recorded with a spectrophotometer at 540 nm, and morphologically intact cells were counted as survived neurons. Results. Added to the culture medium, LPS or NaN3 reduced neuron survival to 15 ± 2% or 20 ± 3% vs. control, respectively. Cu2+ (0.5 to 5.0 μM) increased neuron survival in a dose-dependent manner to 78 ± 4% with toxic levels of LPS and to 86 ± 6% with NaN3 with 5 μM Cu2+. The concentration of nitrites in the control culture medium was 2.0 ± 0.2 μM. Added to the cell cultures, LPS increased the concentration of nitrites to 8.5 ± 0.5 μM. Cu2+ 5 μM did not show any significant effects on nitrite accumulation in the culture medium. Conclusions. We showed that copper ions can exert protective effects on neurons against LPS-induced or NaN3-induced toxicity. This protection is likely to be associated rather with Cu2+ interaction with Complex IV of the electron transfer chain in the mitochondria than with inhibition of NO production. Effects of Cu2+ on apoptosis pathway proteins also cannot be ruled out.

Copper is a crucial catalyst in the synthesis of graphdiyne (GDY). However, as catalysts, the final fate of the copper ions has hardly been concerned, which are usually treated as impurities. Here, it is observed that after simple washing with water and ethanol, GDY still contains a certain amount of copper ions, and demonstrated that the copper ions are adsorbed at the atomic layers of GDY. Furthermore, we transformed in situ the copper ions into ultrathin Cu nanocrystals, and the obtained Cu/GDY hybrids can be generally converted into a series of metal/GDY hybrid materials, such as Ag/GDY, Au/GDY, Pt/GDY, Pd/GDY, and Rh/GDY. The Cu/GDY hybrids exhibit extraordinary surface enhanced Raman scattering effect and can be applied in pollutant efficient enrichment and detection. [ABSTRACT FROM AUTHOR]

Potassium magnesium phosphate cement (MKPC) can be used in the fields of solidification of heavy metal ions in hazardous waste. Scholars have demonstrated that MKPC has a good curing effect on Cu2+. However, Cu2+ can lead to a significant decrease in the mechanical properties of solidified matrix, resulting in a decrease in compressive strength and even fragility. In view of the existing problems in the current research, a method of MgKPO 4 ·6H 2 O strengthening MKPC solidifying Cu2+ is proposed to solve the problem of significant mechanical property loss of solidified matrix in the later stage, while also ensuring excellent solidifying effect. The evolution process and morphology of MKPC products after solidifying Cu2+ are studied. In addition, the long-term solidifying effect of MKPC is also tested. The results shows that MKPC with MgKPO 4 ·6H 2 O has a relatively stable 180d solidifying effect on Cu2+, with a leaching concentration of 7.64 mg/L, which meet the standard requirements. The products of MKPC solidified Cu2+ include Mg.95 Cu.05 O and Cu 3 (PO 4) 2. The process of strengthening and solidifying Cu2+ by MKPC with MgKPO 4 ·6H 2 O includes adsorption, chemical bond and physical encapsulation. MgKPO 4 ·6H 2 O provides an auxiliary alkaline environment for the solidification of Cu2+ and has adsorption properties, improving the immobilization effect of Cu2+ and achieving long-term immobilization stability. This study provides a new idea for the solidification of other waste containing divalent heavy metal ions using MKPC with MgKPO 4 ·6H 2 O. [ABSTRACT FROM AUTHOR]

The use of copper as an antimicrobial agent has a long history and has gained renewed interest in the context of the COVID-19 pandemic. In this study, the authors investigated the antimicrobial properties of an alloy composed of copper with a small percentage of silver (Cu-0.03% wt.Ag). The alloy was tested against various pathogens, including Escherichia coli, Staphylococcus aureus, Candida albicans, Pseudomonas aeruginosa, and the H1N1 virus, using contact exposure tests. Results showed that the alloy was capable of inactivating these pathogens in two hours or less, indicating its strong antimicrobial activity. Electrochemical measurements were also performed, revealing that the small addition of silver to copper promoted a higher resistance to corrosion and shifted the formation of copper ions to higher potentials. This shift led to a slow but continuous release of Cu2+ ions, which have high biocidal activity. These findings show that the addition of small amounts of silver to copper can enhance its biocidal properties and improve its effectiveness as an antimicrobial material. [ABSTRACT FROM AUTHOR]

Copper metal ions (Cu2+) are widely used in various industries, and their salts are used as supplementary components in agriculture and medicine. As this metal ion is associated with various health issues, it is necessary to detect and monitor it in environmental and biological samples. In the present report, we synthesized a naphthoquinoline-dione-based probe 1 containing three ester groups to investigate its ability to detect metal ions in an aqueous solution. Among various metal ions, probe 1 showed a vivid color change from yellow to colorless in the presence of Cu2+, as observed by the naked eye. The ratiometric method using the absorbance ratio (A413/A476) resulted in a limit of detection (LOD) of 1 µM for Cu2+. In addition, the intense yellow-green fluorescence was quenched upon the addition of Cu2+, resulting in a calculated LOD of 5 nM. Thus, probe 1 has the potential for dual response toward Cu2+ detection through color change and fluorescence quenching. 1H-NMR investigation and density functional theory (DFT) calculations indicate 1:1 binding of the metal ion to the small cavity of the probe comprising four functional groups: the carbonyl group of the amide (O), the amino group (N), and two t-butyl ester groups (O). When adsorbed onto various solid surfaces, such as cotton, silica, and filter paper, the probe showed effective detection of Cu2+ via fluorescence quenching. Probe 1 was also useful for Cu2+ sensing in environmental samples (sea and drain water) and biological samples (live HeLa cells). [ABSTRACT FROM AUTHOR]

In recent years, there has been a challenging interest in developing low-cost biopolymeric materials for wastewater treatment. In the present work, new adsorbents, based on different types of chitosan (commercial, commercial chitin-derived chitosan and chitosan synthesized from shrimp shell waste) and inorganic–organic composites have been evaluated for copper ions removal. The efficacy of the synthesis of chitosan-based composite beads has been determined by studying various characteristics using several techniques, including FTIR spectroscopy, X-ray diffraction, porosimetry (N2 adsorption), and scanning electron microscopy (SEM). Adsorption kinetics was performed using different adsorption models to determine the adsorption behavior of the materials in the aqueous media. For all composite beads, regardless of the type of chitosan used, good capacity to remove copper ions from simulated waters was observed (up to 17 mg/g), which proves that the new materials hold potential for heavy metal retention. However, the adsorption efficiency was influenced by the type of chitosan used. Thus, for the series where commercial chitosan (CC) was used, the removal efficiency was approximately 29%; for the series with chitosan obtained from commercial chitin (SC), the removal efficiency was approximately 34%; for the series with chitosan enriched with CaCO3 (SH), the removal efficiency was approximately 52%. [ABSTRACT FROM AUTHOR]