Common Metal Ions Research Articles

Detection of Silver and Mercury Ions Using Naphthalimide-Based Fluorescent Probe.

A multifunctional fluorescent probe P based on a naphthalimide derivative for the detection of Ag+ and Hg2+ through a dual-signal was designed and characterized. P exhibited a large Stokes shift (107 nm), high selectivity, good sensitivity, and fast response time. By adjusting the testing medium and the order of reagent addition, multifunctional detection with P was achieved. The addition of Ag+ or Hg2+ to P solution in either ethanol or an ethanol-water mixture resulted in a significant quenching of fluorescence emission at 537 nm and caused a decrease in the absorbance at 440 nm accompanied by the appearance of a new absorption peak at around 340 nm, and there was an obvious color change from yellow to colorless. In contrast, the addition of other common metal ions and anions did not produce substantial spectral or color changes. The detection limit of probe P for Ag+ and Hg2+ was calculated to be 0.33 μM. The sensing mechanism was proposed and validated through MS and 1H NMR spectrometry methods. Additionally, P demonstrated the capability to recognize Ag+ and Hg2+ in living cells with satisfactory results.

Novel amino-functionalized MOF-based sensor for zinc ion detection in water and blood serum samples

Aquatic systems with low zinc levels can experience a significant decrease in carbon dioxide uptake and limited growth of phytoplankton species. In this study, we describe the use of a new fluorescent sensor based on NH2-MIL-53(Al), and modified with glutaraldehyde and sulfadoxine, for selectively detecting zinc ions in water and blood serum samples. Characterization of the synthesized material was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) surface area analysis, X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM), confirming successful functionalization and preservation of the MOF structure. The sensor’s performance for Zn2+ detection was evaluated by spectrofluorometry, demonstrating a significant fluorescence enhancement upon Zn2+ binding due to the interaction between Zn2+ ions and the sulfonamide groups. With a detection limit as low as 3.14 × 10–2 ppm, the sensor demonstrates high selectivity for Zn2+ over other common metal ions. The sensor’s response is rapid, stable, and reproducible, making it suitable for practical applications. Real sample analysis was conducted in tap water and blood serum samples, with the results compared to those obtained using ICP-OES and a colorimetric test with 5-bromo-PAPS. The comparison confirmed the high accuracy and reliability of the fluorescent sensor in detecting Zn2+ ions in complex matrices. NH2-MIL-53(Al) modified with glutaraldehyde and sulfadoxine shows potential as a selective fluorescent sensor for Zn2+ detection, making it a valuable tool for monitoring the environment and biology.

Microstructural Evaluation and Linkage to the Engineering Properties of Metal-Ion-Contaminated Clay.

The rapid progress of urbanization and industrialization has led to the accumulation of large amounts of metal ions in the environment. These metal ions are adsorbed onto the negatively charged surfaces of clay particles, altering the total surface charge, double-layer thickness, and chemical bonds between the particles, which in turn affects the interactions between them. This causes changes in the microstructure, such as particle rearrangement and pore morphology adjustments, ultimately altering the mechanical behavior of the soil and reducing its stability. This study explores the effects of four common metal ions, including monovalent alkali metal ions (Na+, K+) and divalent heavy metal ions (Pb2+, Zn2+), with a focus on how ion valence and concentration impact the soil's microstructure and mechanical properties. Microstructural tests show that metal ion incorporation reduces particle size, increases clay content, and transforms the structure from layered to honeycomb-like. Small pores decrease while large pores dominate, reducing the specific surface area and pore volume, while the average pore size increases. Although cation exchange capacity decreases, cation adsorption density per unit surface area increases. Monovalent ions primarily disperse the soil structure, while divalent ions induce coagulation. Macro-mechanical tests reveal that metal ion contamination reduces porosity under loading, with compressibility rises as the ion concentration increases. Soils contaminated with alkali metal ions shows higher compression coefficients at all loads, while heavy metal ions cause higher compression under lower loads. Shear strength, the internal friction angle, and cohesion in metal-ion-contaminated clay decrease compared to uncontaminated field-state clay, with greater declines at higher ion concentrations. The Micropore Morphology Index and hydro-pore structural parameter effectively characterize both micro- and macrostructural properties, establishing a quantitative relationship between HPSP and the engineering properties of metal-ion-contaminated clay.

Restricted Intramolecular Rotation: A Dual Fluorescence Response to Hg2+ Quenching and Ag+ Enhancement in Live Rhizoctonia Solani Cells.

A novel imidazo[1,2-a]pyridine derivative probe (R) was designed, synthesized, and characterized via various characterization techniques, such as ESI-MS, 1H NMR, 13C NMR, and Dept-135 NMR. The data obtained from single-crystal XRD reveal that probe R has a coplanar configuration and is part of the monoclinic crystal system, designated the P2(1)/n space group. The fluorescence of (R) is further enhanced by silver (I) ions. On the other hand, Hg2+ significantly quenches the fluorescence of probe R. The presence of other common metal ions does not influence the fluorescence of probe R in the CH3CN: H2O (1:1) mixture, as they neither increase nor quench it. From the fluorescence enhancement data, the low detection limit (LOD) for Ag + ions was determined to be 1.24 × 10- 8 M, whereas the quenching caused by Hg2+ resulted in an LOD of 5.69 × 10- 9 M. The complex of probe R with Ag+/Hg2+ exhibited a 1:1 stoichiometry, as confirmed by mass spectrometry and a Job plot. Single-crystal XRD analysis of R and its complex with Hg2+ revealed a loss of coplanarity, which confirmed their nonfluorescent behavior. We present a promising application of probe R in visualizing living Rhizoctonia oryzae cells exposed to silver (I) and mercury (II) ions.

Agro-waste based biomass residues valorization for effective adsorption of heavy metal.

In this experiment four agro-waste based biomass residues (soybean stover-SSb, buckwheat stover-BWb, Artemisia vulgaris- AVb and Chromolaena odorata-COb) was valorized into low cost amendment called biochar followed by compositional characterization for their application in heavy metal removal. Investigation was carried out on the removal of the most common heavy metal ions including arsenic, cadmium, lead, nickel, zinc, and copper through adsorption on four types of biomass valorised biochar. According to preliminary testing, all the biochar was effective to eliminate a mixture of six heavy metals from the aqueous phase, with the removal of arsenic being the most removed and nickel being the least. In comparison to no biochar treatment, the average removal rate of heavy metal from aqueous solution using four distinct types of biochar was 45.75-62.42% (Cd), 43.64-56.33% (Pb), 41.85-59.73% (Ni), 42.87-60.28% (Zn), 45.64-59.51% (Cu), and 49.02-60.53% (As). The percent decrease of cadmium heavy metal adsorption with increase in maximum contaminant level (MCL) from 1- to fivefold was 20.0 (SSb), 20.7 (COb), 21.6 (BWb), and 22.9 (AVb). The results of the dosage study indicated that As adsorption was the most beneficial on all four types of biochar, whereas Ni adsorption was the least effective. With increase in application rate of biochar the heavy metals adsorption (%) was also increased. Four different agro-waste valorized biochar were used to treat the wastewater, and the physical and chemical changes that occurred both before and after the biochar treatment were noted. There was a drop in the wastewater CODT, CODD, TSS, ammonia, TKN, TP and pH values of 79.7-103.5%, 57.7-81.5, 52.3-68.4%, 1.23-2.23%, 14.1-20.6%, and 1.23-3.03%, respectively. Furthermore, after being passed through a biochar, the wastewater's Zn, Pb, Cd, As, Cr and Cu levels decreased by 3.26-6.15%, 0.06-0.34%, 0.01-0.08%, 2.37-3.65%, 3.95-5.53%, and 2.24-3.34%, respectively at 2.5 and 5.0g/litre of wastewater. Thus, in order to comply with regulations for the disposal of wastewater effluent, the process of valorizing biomass into biochar offered enormous potential for the removal of heavy metals in addition to wastewater treatment.

Polypod Carboxylic Acid-Rare Earth Complex with High Cyclic Stability for Nitrobenzene Compound Detection.

The 5',5''-bis(4-carboxyphenyl)-[1,1':3',1'':3'',1'''-quaterphenyl]-4,4'''-dicarboxylic (H4L1) ligand has a large conjugated rigid planar structure and good absorption of ultraviolet radiation, which can provide effective "antenna effect". However, rare earth complexes using H4L1 as the sole ligand have not been reported. In this paper, rare earth Eu was combined with H4L1 ligand to produce organic rare earth composite L1-Eu by solvothermal synthesis method. It was found through fluorescence spectroscopy that the emission of L1-Eu complex has a linear response to nitrobenzene compounds. The L1-Eu composite material has a low detection limit for nitrobenzene compounds, with detection limits of 0.910, 8.401, 24.510, and 8.171 µM for nitrobenzene, o-nitrophenol, m-nitrophenol, and p-nitrophenol, respectively. Further more the L1-Eu complex can sensitively respond to nitrobenzene compounds while resisting interference from common metal ions and organic solvents. In particular, L1-Eu composite material has good stability and recyclability. Therefore, L1-Eu composite material can serve as a fluorescent probe for specific detection of nitrobenzene compounds. We believe that the L1-Eu complex provides a new method for fluorescence detection of nitrobenzene compounds.

Synergistic on engineering layered N-doped carbon/MXene heterostructure: A potential scaffold for simultaneous electrochemical detection of Cu2+ and Hg2+ ions

The presence of heavy metal ions (HMIs) like Cu2+ and Hg2+ in natural water and foods is a major health and environmental concern. Thus advanced electrochemical sensors are required to monitor these ions. Herein, we introduce a nitrogen-rich carbon-MXene composite (layered N-doped carbon/MXene) as an electrochemical sensor suitable for the simultaneous detection of Cu2+ and Hg2+. Synthesizing 2D/2D heterostructure interfaces using controlled thermal decomposition conditions with the incorporation of quaternary nitrogen from choline chloride and the formation of hydrogen bonds of urea within the MXene (Ti3C2Tx) provided active surfaces area that is suitable for the detection of Cu2+ and Hg2+. The intermediate structure of layered N-doped carbon/MXene, had a nitrogen content of ∼6 %, maximized sensitivity for Cu2+ and Hg2+. The layered N-doped carbon/MXene composite exhibited excellent electrochemical sensing for Cu2+ and Hg2+ in 0.1 M acetate buffer at low sensing potentials. The limits of detection (LODs) of layered N-doped carbon/MXene were 0.019 and 0.056 µM with a sensitivity of 114.54 and 64.317 µA µM−1 cm−2 for Cu2+ and Hg2+, respectively. Furthermore, the layered N-doped carbon/MXene heterostructure exhibited high selectivity for Cu2+ and Hg2+ in the presence of potentially interfering common metal ions. This study introduces a promising advanced material for rapid Cu2+ and Hg2+ detection in food and environmental applications.

Thiophene appended schiff base probe for selective ‘turn-on’ response for copper (ii) ion and their applications in live cell imaging Thiophene appended schiff base probe for selective ‘turn-on’ response for copper (ii) ion and their applications in live cell imaging

In this research, we have synthesized a thiophene Schiff base from 5-phenyl thiophene-2-carboxaldehyde and 2-thiophene carboxylic acid hydrazide and characterized by using FT-IR NMR, HRMS and SC-XRD analysis techniques. The probe exhibited a selective turn-on fluorescence response for Cu2+ over 20 other common metal ions in a CH3CN (9:1, v/v) solution. The Job’s plot represents a 1:1 binding complexation mode and further DFT study was carried out to aid in understanding the geometric structure and interaction of the ligand and Cu2+. The detection limit (LOD) and limit of quantification (LOQ) were found to be 20 nM and 69 nM respectively. Furthermore, the probe’s sensing ability was tested in HeLa cells and their fluorescence imaging also supported the effective turn-on response towards Cu2+ ion.

A Multi-Functional Nanoadjuvant Coupling Manganese with Toll-Like 9 Agonist Stimulates Potent Innate and Adaptive Anti-Tumor Immunity.

The effectiveness of Toll-like 9 agonists (CpG) as an adjuvant for tumor immunotherapy is restricted due to their insufficient ability to activate anti-tumor immunity. To address that, the common nutrient metal ions are explored (Mn2+, Cu2+, Ca2+, Mg2+, Zn2+, Fe3+, and Al3+), identifying Mn2+ as a key enhancer of CpG to mediate immune activation by augmenting the STING-NF-κB pathway. Mn2+ and CpG are then self-assembled with epigallocatechin gallate (EGCG) into a nanoadjuvant MPN/CpG. Local delivery of MPN/CpG effectively inhibits tumor growth in a B16 melanoma-bearing mouse model, reshaping the tumor microenvironment (TME) by repolarizing M2-type tumor-associated macrophages (TAMs) to an M1-type and boosting intra-tumoral infiltration of CD8+/CD4+ T lymphocytes and DCs. Furthermore, compared to free CpG, MPN/CpG exhibits heightened accumulation in lymph nodes, enhancing CpG uptake and DC activation, consequently inducing significant antigen-specific cytotoxic CD8+ T cell immune response and humoral immunity. In a prophylactic tumor-bearing mouse model, MPN/CpG vaccination with OVA antigen significantly delays B16-OVA melanoma growth and extends mouse survival. These findings underscore the potential of MPN/CpG as a multifunctional adjuvant platform to drive powerful innate and adaptive immunity and regulate TME against tumors.

Bacterial Cellulose Incorporating Multicolor Fluorescent Probes for Visual Acidity Detection in Paper-Based Cultural Relics.

Paper-based cultural relics often undergo acidification and deterioration during long-term preservation. Accurate detection of paper acidity is of great significance to assess aging status and extend the preservation lifetime of paper-based cultural relics. Rapid identification of the acidification degree and acid distribution across multiple regions of paper is essential. Inspired by fluorescent sensing technology, pH-sensitive cadmium telluride (CdTe) quantum dots (QDs) and rhodamine B (RB) fluorescent probes are synthesized and incorporated onto the nanofibers of a bacterial cellulose (BC) membrane to enable visual acidity detection of paper. Due to the complementary pH detection range of CdTe QDs and RB probes, the composite BC membrane exhibits a clear pH response across an acidic to neutral range (pH 3.0-7.5). Notably, the contrasting fluorescent colors of the two probes within the BC membrane allow for easy visualization of paper pH and acidity distribution with the naked eyes. A distinct color transition from red to green was observed on the fluorescent BC membrane when it is applied to a model paper with a gradient pH distribution. The feasibility of this method was verified by using the flat-headed pH electrode method. Additionally, common metal ions in most paper fillers, inks, pigments, as well as some sugars and amino acids showed minimal interference with the pH response of the composite BC membrane, highlighting its potential and broad applicability for visual acidity detection in paper-based cultural relics.

A Novel Manganese Ion Delivery Carrier Promotes Immune Cell Proliferation and Enhances Innate Immune Responses.

Manganese is a transition metal that is an essential trace element for human health. Manganese ions (Mn2+), which serve as one of the most common transition metal ions, play vital roles in enhancing innate immune responses. However, immune agonists based on Mn2+ are poorly utilized in clinical trials due to poor chemodynamics and adverse events. In this work, we designed a novel delivery carrier for loading manganese ions by constructing hFn-MT3(Mn2+) protein nanoparticles (termed as NPs(Mn2+)), which contained human ferritin heavy chain (hFn) and metallothionein-3 (MT3), induced by isopropyl β-d-thiogalactoside (IPTG) and manganese ions in the prokaryotic expression system. The NPs(Mn2+) protein nanoparticles could not only stimulate immune cell proliferation but also activate innate immune responses via the cGAS-STING-IRF3 signaling pathway. Collectively, our results unveil a candidate strategy for delivering metal ions beyond Mn2+ and may broaden metal ion clinical use in the field of immunotherapies.

Rhodamine 6G-PAH probes for heavy metal: Fluorescence detection, bioimaging, and solid-phase sensing application

Four rhodamine 6G-PAH probes with pyrene (R6G-Pyr), anthracene (R6G-Ant), acenaphthene (R6G-Acp) or phenanthrene (R6G-PA) as fluorophore were designed and synthesized for Hg(II) detection. Probe R6G-PA, which had the lowest detection limit of 0.84 nmol/L, displayed the best fluorescence performance as compared to the other three probes. This type of probe had good anti-interference properties against most common metal ions except Cu(II). Metal Cu(II) had a certain quenching effect on the fluorescence generated by Hg(II), with a minimum detection limit of 0.31 nmol/L (for R6G-Acp), indicating its potential practicability for Cu(II) detection. The structure-fluorescence relationship was discussed based on density functional theory (DFT) calculations, and R6G-PA + Hg(II), which had the minimum dihedral angle between polycyclic aromatic rings and rhodamine spiro ring, produced the strongest π-π accumulation and provided the brightest fluorescence. Probe R6G-PA was successfully employed for fluorescence detection of Hg(II) in biological samples. Its solid-phase sensor PS@R6G-PA was developed by immobilizing R6G-PA on PS microspheres for the determination of Hg(II) in water and food samples, with excellent reproducibility and fluorescence “on/off” response. The relative error of the spiked recovery rate was less than 10 %.

Tb3+-functionalized covalent organic framework for simultaneous detection and removal of Hg2+

Hg2+ is a common heavy metal ion contaminant in the environment, as well as one of the most hazardous metal ions on the earth, posing a serious threat to the ecosystem and human health. As a result, it is vital to develop materials that can detect or remove Hg2+. In this work, we fabricated a Tb3+-functionalized covalent organic framework (Tb@COF) platform capable of both detecting and removing Hg2+ for the fluorescence enhancement of Tb3+ and the presence of thiol groups in COF. Tb@COF exhibited good selectivity and sensitivity during the detection of Hg2+, with a linear range of 0.2–50 μmol/L(R2 = 0.9985) and a limit of detection (LOD) of 0.076 μmol/L. We employed Tb@COF to detect Hg2+ in lake water with excellent results, and we developed a smartphone-assisted Tb@COF-based agar slice detection platform that could identify Hg2+ both visually and quantitatively. We discussed the sensing mechanism of Tb@COF for Hg2+. Furthermore, we found that Tb@COF displayed good removal efficiency of Hg2+. The adsorption of Hg2+ by Tb@COF followed the pseudo-second-order kinetic model and Langmuir adsorption isotherm model. Our research provided a novel method for simultaneously detecting and eliminating Hg2+ from the environment.

Colorimetric pH-sensing of artificial gastric fluid using naphthalimide-based CH acids

In this study, we introduce novel colorimetric pH-sensing probes based on naphthalimide malonate derivatives. These probes were synthesized by reacting 4-bromo-1,8-naphthalimide with various malonates, including malononitrile, ethyl cyanoacetate, and diethyl malonate. Each derivative exhibited distinct pH-sensing characteristics due to their differing CH acidities. The malononitrile-based probe, NPI-N2, demonstrated pronounced chromogenic pH-signaling behavior, transitioning from colorless to red-violet, accompanied by a decrease in fluorescence intensity. Notably, NPI-N2 retained its pH-sensing capability in the presence of common metal ions, anions, and pepsin, a key component of gastric fluid. The pKa of NPI-N2 was determined to be 3.08 through pH-dependent absorbance curve fitting. To modulate the pH-sensing range, ester-nitrile (NPI-EN) and diethyl ester (NPI-E2) subunits were incorporated into the naphthalimide framework, resulting in increased pKa values of 6.73 and 10.76, respectively. The pH-signaling mechanism of NPI-N2 was elucidated by 1H and 13C NMR spectroscopy, revealing deprotonation of the malononitrile moiety and subsequent resonance extension through the naphthalimide structure. To facilitate practical pH determination, NPI-N2 was integrated into a paper-based test strip, enabling convenient and reliable pH measurement of artificial gastric fluid.

An Overview of Optical Sensing of Copper and its Removal by Different Techniques

: The identification of heavy metals by sensing technologies is a crucial area of study since these metals are present in the environment and are hazardous. The in-depth analyses of the probes' structures and sensing capabilities improve our understanding of how to design and develop probes for the same metal in the future. The third most common metal ion and trace element, copper (Cu2+), is essential to all living things and is involved in several activities. However, different diseases are caused by excess or deficiency of Cu2+ ions, depending on what the cell requires. For all of these reasons, optical sensors have concentrated on quick, highly sensitive, and selective real-time detection of Cu2+ ions. Fluorescence in the refractive index-adsorption from the interactions between light and matter can be measured using optical sensors. Furthermore, due to their strong advantages which include real-time detection, simplicity and naked eye recognition, low cost, high specificity against analytes, quick reaction, and the requirement for less complex equipment during analysis they have attracted a lot of attention in recent years. In this review, we covered many fluoro and chemosensors for the detection of copper, along with their sensing parameters in various mediums and thorough structural analyses. This review also covers the extraction of copper from the aqueous medium. The use of membrane processes, adsorption, and electrocoagulation is examined, and the difficulties associated with their application have been presented.

A voltammetrically potentionmetric pH sensor based on multiply hydroxylated porphyrin

AbstractUsing voltammetry to readout potentiometrically the solution acidity requires easy pH tunability of the probe's redox properties. In this work, tri‐hydroxyphenyl porphyrin (POH3) was synthesized as the electrochemically active probe to develop a voltammetrically potentiometric sensor (VPS) with a pH‐sensitive response. By comparing POH3 with control di‐ and mono‐hydroxyphenyl porphyrins (POH2 and POH1), we found that protonation of the pyrrole macrocycle, electron communication of the para‐hydroxyl groups with the pyrrole nitrogens during structure tautomerization, and the presence of multiple ionizable hydroxyl groups are the critical factors to report reversibly the pH‐sensitive VPS response at the appropriate potential range. Common metal ions have negligible effects on the sensor performance. In comparison to the conventional potentiometric sensor (CPS), our VPS strategy benefits from the advantage that the electrode modification is not required. Thus, the complex phase boundary models necessary for CPS are unnecessarily involved in explaining the potential response.

A colorimetric Ag+ chemosensor based on a cyclometalated ruthenium complex with deprotonated 2-phenylbenzimidazole

A cyclometalated ruthenium complex (1) using 2-phenylbenzimidazole as a C,N-ligand was developed as a colorimetric chemosensor to detect Ag+ ions. Upon the addition of Ag+ ions, the absorption spectra of complex 1 demonstrated no change in CH3CN solution. However, an excellent solution color change from dark-green to purple and absorption spectral change with a blue-shift of 27 nm (from 612 to 585 nm) were clearly observed after Ag+ ions were added to the solution of 1 with 2-fold of fluoride (denoted as 1 + F−). When Ag+ ions were replaced by other common metal ions, the solution color changed from green to red. Therefore, the solution of 1 + F− can be used to distinguish Ag+ from the other common metal ions. The absorption intensity at 612 nm exhibited a good linear correlation for the detection of Ag+ ion from 0 to 4 µM with a detection limit of 0.34 µM. According to the absorption and 1HNMR spectral changes of complex 1, the reaction mechanism is proposed to be as a coordination between silver ion and the deprotonated nitrogen in imidazole. However, the interactions of other metal ions with 1 + F− are related to a proton transfer process.

An efficient voltammetric sensing platform for trace determination of Norfloxacin based on nanoplate-like α-zirconium phosphate/carboxylated multiwalled carbon nanotube nanocomposites

Norfloxacin (NOR) residues pose a potential threat to our health and ecosystem, so it is highly urgent to develop a simple but accurate method for NOR determination. Therefore, an efficient voltammetric sensing platform was constructed for trace detection of NOR based on nanoplate-like α-zirconium phosphate/carboxylated multiwalled carbon nanotubes (α-ZrP/CMWCNT). The physiochemical characteristics of α-ZrP/CMWCNT were scrutinized using various microscopic, spectroscopic, and electrochemical means. In order to pursuit higher voltammetric responses, detection conditions of NOR such as accumulation potential, accumulation time and buffer pH, were explored comprehensibly. The α-ZrP/CMWCNT enlarged the electrochemically active surface area and lowered the charge transfer resistance. Owing to the synergistic interactions between nanoplate-like α-ZrP NPs and CMWCNTs, the α-ZrP/CMWCNT boosted the voltammetric response signals and reduced the over-potential of NOR. Consequently, the α-ZrP/CMWCNT demonstrated remarkably catalytic activity for NOR electrooxidation, with two broad linear detection ranges (0.01–0.1 μM; 0.1–10.0 μM) and a low detection limit (2.8 nM). The α-ZrP/CMWCNT modified glassy carbon electrode (GCE) exhibited strong anti-interfering ability even in excess of other antibiotics and common metal ions, and maintained robust response peaks up to two weeks. The α-ZrP/CMWCNT/GCE realized accurate determination of NOR from complicated matrices at trace levels with good recoveries (99.00–104.40 %).

Synthesis of a dual-response signal sensor and naked-eye recognition of hypochlorite in real water samples

An innovative dual-modal colorimetric and fluorometric probe MDXM is synthesized based on the dihydro-1H-xanthene motif via Knoevenagel reaction. The incorporation of a malononitrile group into the dihydro-1H-xanthene motif via a double bond results in an extensive macroconjugated π-system, which endows MDXM with a pronounced molar absorptivity and effectively quenches the intramolecular charge transfer (ICT) effect. Upon exposure to hypochlorite, the C = C bond in MDXM undergoes cleavage, resulting in the formation of an aldehyde group. This process restores the ICT effect and manifests as a clear fluorescent ''turn-on'' signal at 530 nm, with a remarkably linear response across the ClO− concentration range of 0–60 μM. The probe achieves a notably low detection limit of 7.14 nM, reflecting its exceptional sensitivity. In the presence of 15 common metal ions and oxidizing agents, MDXM can specifically identify hypochlorite with excellent anti-interference ability. The response mechanism of MDXM to hypochlorite was confirmed through Nuclear Magnetic Resonance (NMR) spectroscopy and computational Density Functional Theory (DFT) calculations. The practical applicability of MDXM is underscored by its successful implementation in analyzing hypochlorite in 5 varied real water samples. This showcases MDXM's promise for environmental and analytical chemistry, providing a robust tool for hypochlorite detection in diverse settings.

Coordination-Driven Nanomedicine Mitigates One-Lung Ventilation-Induced Lung Injury via Radicals Scavenging and Cell Pyroptosis Inhibition.

One-lung ventilation (OLV) during thoracic surgery often leads to post-operative complications, yet effective pharmacological interventions are lacking. This study reports a baicalin-based metal-coordination nanomedicine with disulfiram (DSF) co-loading to address one-lung ventilation-induced lung injury and reperfusion injury (OLV-LIRI). Baicalin, known for its robust antioxidant properties, suffers from poor water solubility and stability. Leveraging nanotechnology, baicalin's coordination is systematically explored with seven common metal ions, designing iron/copper-mediated binary coordination nanoparticles to overcome these limitations. The self-assembled nanoparticles, primarily formed through metal coordination and π-π stacking forces, encapsulated DSF, ensuring high colloidal stability in diverse physiological matrices. Upon a single-dose administration via endotracheal intubation, the nanoparticles efficiently accumulate in lung tissues and swiftly penetrate the pulmonary mucosa. Intracellularly, baicalin exhibits free radical scavenging activity to suppress inflammation. Concurrently, the release of Cu2+ and DSF enables the in situ generation of CuET, a potent inhibitor of cell pyroptosis. Harnessing these multifaceted mechanisms, the nanoparticles alleviate lung injury symptoms without notable toxic side effects, suggesting a promising preventive strategy for OLV-LIRI.