Ion Activity Research Articles

Biomolecule and Ion Releasing Mesoporous Nanoparticles: Nonconvergent Osteogenic and Osteo-immunogenic Performance.

Immune-involved cell communications have recently been introduced as key role players in the fate of mesenchymal stem cells in making bone tissue. In this study, a drug delivery system for bone (re)generation based on copper-doped mesoporous bioactive glass nanoparticles (BGNPs) was developed to codeliver copper as a biologically active ion and icariin as an anti-inflammatory agent. This design was based on temporal inflammation fluctuations from proinflammatory to anti-inflammatory during bone generation. Three in vitro models were performed with human mesenchymal stem cells (hMSCs) to verify the osteo-immunomodulatory effects of released copper ions and icariin: nonstimulated, co-conditioned with macrophage medium and co-cultured with macrophages. Both icariin and copper showed increased levels of alkaline phosphatase activation, indicating a direct osteogenic effect. Copper-doped BGNPs showed the highest increase of osteo-immunogenic properties in a mineralization assay and also induced short-term inflammation. However, the mineralization dropped in copper doped BGNPs after loading with icariin due to copper-icariin chelate formation and inhibition of the early inflammatory phase in the immune-stimulated in vitro models. In the absence of copper, the direct osteogenic properties of icariin overtook its osteo-immunogenic inhibition and increased calcification. Overall, BGNPs doped with 5 mol % copper and no icariin showed the highest bone-forming capacity.

Retraction Note: Two Mn(II)-Organic Frameworks: Selective Detection of Fe3+ Ion and Treatment Activity on Alcohol-Induced Cerebellar Atrophy by Reducing ROS Accumulation in Brain

Retraction Note: Two Mn(II)-Organic Frameworks: Selective Detection of Fe3+ Ion and Treatment Activity on Alcohol-Induced Cerebellar Atrophy by Reducing ROS Accumulation in Brain

Novel Cement-Based Materials Using Seawater, Reused Construction Waste, and Alkali Agents

This study aimed to develop marine alkali paste (MAP) produced using seawater (SW), recyclable particle material from paste specimens (RPPs), and alkali agents including NaOH (NH) and Na2O·3SiO2 (NS). The physicochemical properties and strength of the MAP were investigated with uniaxial compression tests (UCTs), an Energy-Dispersive Spectrometer (EDS), X-ray diffraction (XRD), and thermal-field emission scanning electron microscopy (SEM). The key information on the MAP preparation and experiments, including mix ratios, ages, curing, and sub-specimen locations, were recorded during the investigation. The results indicated that 8-day-old MAP prepared with NS reached a maximum compressive strength of 8.3 MPa, while 8-day-old NH-prepared specimens achieved up to 5.59 MPa. By 49 days, NS-prepared MAP had strengths between 5.46 MPa and 7.34 MPa, while the strength of NH-prepared MAP ranged from 3.59 MPa to 5.83 MPa. The key hydration products were Friedel’s salt (3CaO·Al2O3·CaCl2·10H2O, FS), xCaO·SiO2·nH2O (C-S-H), CaO·Al2O3·2SiO2·4H2O (C-A-S-H), and Na2O·Al2O3·zSiO2·2H2O (N-A-S-H). C-S-H was generated under the critical curing and working conditions in SW. C-A-S-H development contributed to C-S-H network compaction. N-A-S-H development helped in resistance to SO42− erosion, thereby cutting down ettringite (Ca6Al2(SO4)3(OH)12·26H2O) development. The active ion exchange between MAP and SW mainly involving SO42− and Cl− led to the significant formation of FS at the interface of C-A-S-H and xCaO·Al2O3·nH2O (C-A-H). Therefore, FS generation inhibited SO42− and Cl− corrosion in the MAP and rebounded the interface cracks of the hydration products. Consequently, FS contributed to the protection and development of C-S-H in the MAP, which ensured the suitability and applicability of the MAP in marine environments.

Lithium-containing 45S5 Bioglass-derived glass-ceramics have antioxidant activity and induce new bone formation in a rat preclinical model of type 1 diabetes mellitus

Diabetes mellitus (DM) has been associated with complications that affect the skeletal system, such as alterations in bone repair, osteoporosis, and an increased risk of fractures. In this context, the use of biomaterials able to promote osteogenic differentiation and, at the same time, limit the oxidative stress induced by DM offers a novel perspective to ensure the repair of diabetic bone tissue. Since lithium (Li) has been recently identified as a biologically active ion with osteogenic and antioxidant properties, the localized and controlled release of Li ions from bioactive glass-ceramic materials represents a promising therapeutic alternative for the treatment of bone lesions in DM. Thus, the aim of this study was to evaluate the potential osteogenic and antioxidant effects of glass-ceramic microparticles derived from a 45S5-type bioactive glass (Bioglass) containing (% by weight) 45% SiO2, 24.5% Na2O, 24.5% CaO, and 6% P2O5, in which Na2O was partially substituted by 5% of Li2O (45S5.5Li), in an experimental model of type 1 DM (DM1). The results obtained demonstrate, for the first time, that both 45S5 and 45S5.5Li glass-ceramic microparticles possess antioxidant activity and stimulate bone formationin vivoboth under physiological conditions and under experimental DM1 in rats. In this sense, they would have potential application as inorganic osteogenic agents in different strategies of bone tissue regenerative medicine.

Molecular Structure of the Na+,K+-ATPase α4β1 Isoform in Its Ouabain-Bound Conformation.

Na+,K+-ATPase is the active ion transport system that maintains the electrochemical gradients for Na+ and K+ across the plasma membrane of most animal cells. Na+,K+-ATPase is constituted by the association of two major subunits, a catalytic α and a glycosylated β subunit, both of which exist as different isoforms (in mammals known as α1, α2, α3, α4, β1, β2 and β3). Na+,K+-ATPase α and β isoforms assemble in different combinations to produce various isozymes with tissue specific expression and distinct biochemical properties. Na+,K+-ATPase α4β1 is only found in male germ cells of the testis and is mainly expressed in the sperm flagellum, where it plays a critical role in sperm motility and male fertility. Here, we report the molecular structure of Na+,K+-ATPase α4β1 at 2.37 Å resolution in the ouabain-bound state and in the presence of beryllium fluoride. Overall, Na+,K+-ATPase α4 structure exhibits the basic major domains of a P-Type ATPase, resembling Na+,K+-ATPase α1, but has differences specific to its distinct sequence. Dissimilarities include the site where the inhibitor ouabain binds. Molecular simulations indicate that glycosphingolipids can bind to a putative glycosphingolipid binding site, which could potentially modulate Na+,K+-ATPase α4 activity. This is the first experimental evidence for the structure of Na+,K+-ATPase α4β1. These data provide a template that will aid in better understanding the function Na+,K+-ATPase α4β1 and will be important for the design and development of compounds that can modulate Na+,K+-ATPase α4 activity for the purpose of improving male fertility or to achieve male contraception.

Real-Time Estimation of CO2 Absorption Capacity Using Ionic Conductivity of Protonated Di-Methyl-Ethanolamine (DMEA) and Electrical Conductivity in Low-Concentration DMEA Aqueous Solutions

The present study investigates the real-time estimation of CO2 absorption capacity (CAC) based on the electrical conductivity (EC) of low-concentration di-methyl-ethanolamine (DMEA) solutions (0.1–0.5 M). CO2 absorption experiments are conducted to measure the variation in CAC and EC during CO2 absorption, revealing a strong correlation between the two properties. The ionic conductivity of DMEAH+ formed during absorption is calculated to be 53.1 S·cm2/(mol·z), which is found to be larger than that of TEAH+ and MDEAH+. This can be attributed to the smaller molar mass and higher ionic mobility of DMEAH+. A significant finding is that the measured EC (ECM) of the DMEA solutions consistently demonstrates a lower value than the theoretically predicted value. This discrepancy is due to the larger ionic size of DMEAH+, which results in a reduction in the real mean ionic activity coefficient. This effect becomes more pronounced with increasing DMEA concentration. Consequently, a higher CAC is required to produce the same change in EC at higher amine concentrations. Based on these findings, an empirical equation is devised to estimate CAC from ECM in solutions of constant DMEA concentration. This equation will be employed as a practical approach for the in situ monitoring of CO2 absorption using DMEA aqueous solution.

Appraisal of Heavy Metal Risk Hazards of Eisenia fetida-Mediated Steel Slag Vermicompost on Oryza sativa L.: Insights from Agro-Scale Inspection and Machine Learning Analytics

The steel industry drives world economic growth, yet it generates heavy metal-rich steel slag, which jeopardizes the environment. The utilization of vermi-technology is essential for the sustainable transformation of toxic steel waste slag (SW) into organic amendments, although field-scale use of vermiprocessed SW remains unexplored. To bridge the gap, this study evaluated the efficacy of vermiprocessed SW as an organic supplement for rice field cultivation, focusing on heavy metal (HM) bioavailability, human health risk, and yield in comparison to raw slag and NPK fertilizer. The results indicated a considerable decrease in the bioavailable fraction of heavy metals in T4 (1:1 SW vermicompost 50% + 50% fertilizer). In treatments, T9 (100% SW) and T10 (50% SW + 50% fertilizer) (FIAM) free ion activity modeling confirmed grain absorption of HMs, and the FIAM HQ values indicated the health risk for the direct application of steel slag waste on the field. The risk factor evaluation of HMs’ presence in treatments T9 and T10 established the possible cancer risk for living beings. Similarly, machine learning models like SOBOL sensitivity analysis and artificial neural networks revealed potential threats associated with HMs on different treatments, respectively. The correlation coefficient revealed the negative effects of bioavailable HMs on various soil microbial and enzymatic properties. Moreover, the abundant yield of rice was attributed to the combination treatment (1:1 50% + NPK 50%), which paved the way for an alternative agronomic approach based on the utilization of vermicomposted steel waste slag.

Anion-induced optimization of non-aqueous zinc-air battery performance: Insights into OTF− selection

Rechargeable non-alkaline zinc-air batteries (ZABs) address the CO₂ incompatibility and instability issues of conventional alkaline batteries. However, the impact of solid discharge products like zinc oxide on discharge capacity at the air cathode remains unexplored. In this study, we investigate how anions influence ion pair solvation structures using Zinc trifluoromethanesulfonate (Zn(OTF)₂)-N, N-dimethylformamide (DMF) and Zinc acetate (Zn(Ac)₂)-DMF electrolytes, and how these structures affect the distribution of discharge product. Our finding shows that anions with lower donor numbers (DNs), like the weaker ligand OTF- (20.5), enhance the zinc ion activity and promote rapid Zn2⁺ reactions with oxygen during discharge, leading to a more than tenfold increase in discharge capacity. In contrast, acetate anions with higher DNs (43.3) form stable complexes, inhibiting zinc ion activity and causing the formation of film-like discharge products, which reduces ZAB performance. The Zn(OTF)₂-DMF electrolyte also enables a battery lifespan of over 200 h, more than fivefold compared to the acetate-based system.

Origin of the Difference in Proton Transport Direction between Inward and Outward Proton-Pumping Rhodopsins.

ConspectusActive transport is a vital and ubiquitous process in biological phenomena. Ion-pumping rhodopsins are light-driven active ion transporters that share a heptahelical transmembrane structural scaffold in which the all-trans retinal chromophore is covalently bonded through a Schiff base to a conserved lysine residue in the seventh transmembrane helix. Bacteriorhodopsin from Halobacterium salinarum was the first ion-pumping rhodopsin to be discovered and was identified as an outward proton-pumping rhodopsin. Since the discovery of bacteriorhodopsin in 1971, many more ion-pumping rhodopsins have been isolated from diverse microorganisms spanning three domains (bacteria, archaea, and eukaryotes) and giant viruses. In addition to proton-pumping rhodopsins, chloride ion- and sodium ion-pumping rhodopsins have also been discovered. Furthermore, diversity of ion-pumping rhodopsins was found in the direction of ion transport; i.e., rhodopsins that pump protons inward have recently been discovered. Very intriguingly, the inward proton-pumping rhodopsins share structural features and many conserved key residues with the outward proton-pumping rhodopsins. However, a central question remains unchanged despite the increasing variety: how and why do the ion-pumping rhodopsins undergo interlocking conformational changes that allow unidirectional ion transfer within proteins? In this regard, it is an effective strategy to compare the structures and their evolutions in the proton-pumping processes of both inward and outward proton-pumping rhodopsins because the comparison sheds light on key elements for the unidirectional proton transport. We elucidated the proton-pumping mechanism of the inward and outward proton-pumping rhodopsins by time-resolved resonance Raman spectroscopy, a powerful technique for tracking the structural evolutions of proteins at work that are otherwise inaccessible.In this Account, we primarily review our endeavors in the elucidation of the proton-pumping mechanisms and determination factors for the transport directions of inward and outward proton-pumping rhodopsins. We begin with a brief summary of previous findings on outward proton-pumping rhodopsins revealed by vibrational spectroscopy. Next, we provide insights into the mechanism of inward proton-pumping rhodopsins, schizorhodopsins, obtained in our studies. Time-resolved resonance Raman spectroscopy provided valuable information about the structures of the retinal chromophore in the unphotolyzed state and intermediates of schizorhodopsins. As we ventured further into our investigations, we succeeded in uncovering the factors determining the directions of proton release and uptake in the retinal Schiff base. While it is intriguing that the proton-pumping rhodopsins actively transport protons against a concentration gradient, it is even more curious that proteins with structural similarities transport protons in opposite directions. Solving the second mystery led to solving the first. When we considered our findings, we realized that we would probably not have been able to elucidate the mechanism if we had studied only the outward pump. Our Account concludes by outlining future opportunities and challenges in the growing research field of ion-pumping rhodopsins, with a particular emphasis on elucidating their sequence-structure-function relationships. We aim to inspire further advances toward the understanding and creation of light-driven active ion transporters.

Ion Trios: Cause of Ion Specific Interactions in Aqueous Solutions and Path to a Better pH Definition.

Many important thermodynamic calculations for aqueous systems are profoundly limited because ion specific interactions have not been understood. Here an alternative modeling paradigm with compelling advantages is presented based on fundamental insights regarding ion-ion interactions at higher electrolyte concentrations. We also show how an intense ongoing controversy regarding single ion activity coefficients (SIACs) can be resolved and how SIACs can be quantified in full thermodynamic compliance using an overlooked convention. SIAC values can in fact be determined unequivocally and compatibly from two independent types of measurement at trace concentrations. These developments promise important advances, especially in defining pH and modeling multicomponent aqueous systems.

Overcoming volumetric capacitance-rate performance tradeoff with 0D/2D conductive carbon nitride/phosphorene heterostructure for flexible supercapacitor

Few-layer black phosphorus (FL-BP) is considered a rising star 2D material for flexible supercapacitors (FSCs) due to its exceptional properties, including mechanical flexibility and high active surface area. However, the disordered deposition of FL-BP nanoflakes often leads to face-to-face restacking, which diminishes the effective active area and ion transport channels. This poses a huge challenge in simultaneously achieving high volumetric capacitance and rate capability. To address this, a 3D porous 0D/2D FL-BP/conductive carbon nitride (FL-BP/c-CN) film has been developed. The introduction of 0D c-CN nanoparticles effectively prevents the restacking of FL-BP nanoflakes and expands the nanofluidic channels, thus facilitating charge transport and ions diffusion. Additionally, the highly conductive c-CN nanoparticles embedded into the FL-BP layers significantly improve overall conductivity. As a result, the FL-BP/c-CN film-based FSC demonstrates a remarkable rate performance, retaining 70% capacitance as the scan rate increases from 10 to 100 mV/s. Moreover, the incorporation of 0D c-CN nanoparticles increases the available space for charge accumulation, yielding a volumetric capacitance of 28.5 F/cm3 at a scan rate of 10 mV/s, which is three times higher than that of a pure FL-BP film electrode (9.2 F/cm3). This work presents an innovative approach for developing high-performance FL-BP-based FSCs.

An enhanced electrokinetic system for remediation of Cu-polluted clay soils by integrating purging solutions and intermittent power

This study investigated the effectiveness and underlying mechanisms of purging solutions enhanced by intermittent power in improving electrokinetic (EK) restoration of clay soils even under high levels of heavy metals (HM). In so doing, the artificially contaminated specimens containing a wide range of copper (Cu) were prepared and then subjected to a series of EK tests with various electrolytes and electric regimes. Macro and micro scale examinations revealed that under the unenhanced EK condition (i.e., continuous current without agents), the formation of non-conducting solid phases and/or the clogged fabric in the samples with the high dosages (> 250 mg/kg) of HM could dramatically impede the metal separation from the soil. Hence, increasing the remediation time would not be very effective in facilitating the decontamination process. It was observed that the EDTA-ameliorated treatment accompanied by pentetic acid and acetic acid can mitigate the metal precipitation/encapsulation effects induced by EK actions, resulting in improved rate of HM removal. In this case; however, a high portion of these enhancers would be required to ensure the stable mobility of ions and to achieve successful recovery. Such a limitation has been shown to be overcome by incorporating pulsed power (PP) at an optimal frequency. In fact, as evidenced by SEM-EDX and XRD analyses, the integration of chemical agents with PP could simultaneously retain the solubilized Cu species in the soil mass and modify the matrix tortuosity (i.e., the establishment of well-linked pores), two features that have been found to play essential roles in providing for favorable activity of HM ions during the EK operation. The corresponding refinements in the binary system would cause an almost 8 folds increase in the removal efficiency and a shorter (up to 30 %) time of treatment compared to conventional EK.

Using physicochemical properties to predict the impact of natural dissolved organic carbon on transepithelial potential in the freshwater rainbow trout (Oncorhynchus mykiss) at neutral and acidic pH.

Dissolved organic carbon (DOC) is a complex mixture of molecules that varies in composition based on origin as well as spatial and temporal factors. DOC is an important water quality parameter as it regulates many biological processes in freshwater systems, including the physiological function of the gills in fish. These effects are often beneficial, especially at low pH where DOCs mitigate ion loss and protect active ion uptake. DOCs of different compositions and quality have varied ionoregulatory effects. The molecular variability of DOCs can be characterized using optical and chemical indices, but how these indices relate to the physiological effects exerted by DOCs is not well understood. We tested the effects of five naturally sourced DOCs, at both pH 7 and pH 4, on transepithelial potential (TEP) (a diffusion potential between the blood plasma and the external water) in rainbow trout. The five chosen DOCs have been well characterized and span large differences in physicochemical characteristics. Each of the DOCs significantly influenced TEP, although in a unique manner or magnitude which was likely due to their physicochemical characteristics. These TEP responses were also a function of pH. With the goal of determining which physicochemical indices are predictive of changes in TEP, we evaluated correlations between various indices and TEP at pH 7 and pH 4. The indices included: specific absorbance coefficient at 340nm, molecular weight index, fluorescence index, octanol-water partition coefficient, molecular charge, proton binding index, % humic acid-like, % fulvic acid-like, and % protein-like components by parallel factor analysis on fluorescence data (PARAFAC). Our results demonstrate the novel finding that there are three particularly important indices that are predictors of changes in TEP across pHs in rainbow trout: specific absorbance coefficient at 340nm, octanol-water partition coefficient; and proton binding index.

High-mass loaded redox-active lignin functionalized carbonized wood collector to construct sustainable and high-performance supercapacitors

Traditional electrode materials for supercapacitors often face issues like high toxicity, cost, and non-renewability. To address these drawbacks, biomass-based alternatives are being explored, aligning with green development trends. Herein, carbonized wood (CW) with rich pore structure and redox-active lignin are combined to fabricate an all-wood-based sustainable supercapacitor electrode material. Due to its inherent porous structure, CW provides a larger surface area for accommodating active materials ion, enabling the electrode to achieve a higher lignin loading capacity of 2.82–11.68 mg/cm2. Furthermore, the utilization of lignin as a substitute for conventional transition metal-based pseudocapacitor material functionalized CW endows the electrode with exemplary electrochemical performance while guaranteeing the comprehensive sustainability of the electrode. This synergy confers the electrode with exceptional electrical performance, yielding an areal capacitance of 960.7 mF/cm2 at a current density of 1 mA/cm2. The symmetric supercapacitors (SSC) manufactured by this composite electrode can achieve a notable areal energy density of 0.14 mWh/cm2 and a power density of 15.98 mW/cm2, while maintaining an outstanding capacitance retention rate of 81 % after 50,000 cycles at 20 mA/cm2. The manufacture of CW-lignin electrode underscores the potential of utilizing renewable biomass resources as alternatives for developing high-performance energy storage applications, thereby reducing negative environmental impacts.

Calculations of mean ionic activity coefficients of copper and manganese salts in aqueous solutions

Accurately predicting the activity coefficients of copper and manganese salts in aqueous solutions is crucial for treating industrial wastewater, and it is of practical interest to calculate the activity coefficients of heavy metals in aqueous solutions using the Equation of State because of its high flexibility and wide range of applicability. This work conducts a modeling study on the mean ionic activity coefficients of copper and manganese salts in aqueous solutions. The thermodynamic framework used in this work is an electrolyte version of the Cubic Plus Association Equation of State (e-CPA). The model's ion-water binary interaction parameters are obtained by regressing the osmotic coefficients and mean ionic activity coefficients in aqueous solutions. The modeling results indicate that the electrolyte Equation of State can satisfactorily correlate the water activity, osmotic coefficients, and mean ionic activity coefficients of copper and manganese salts in aqueous solutions over a wide range of salt concentrations. Among all the systems at 298.15 K, the biggest average relative deviation between calculated and experimental values is within 6.7 % and 2.3 % for the mean ionic activity coefficients and water activity, respectively. Furthermore, this work discusses the impact of ion pairs on the phase equilibrium of aqueous systems from a microscopic mechanism perspective and analyzes and discusses the model's adaptability. The model used in this work can accurately predict the activity coefficients of a variety of copper and manganese salts in aqueous solutions over wide concentration ranges and provides an improved interface for improving the calculation accuracy of the model under high concentration or other complex conditions.

Novel Eu3+-Doped Glasses in the MoO3-WO3-La2O3-B2O3 System: Preparation, Structure and Photoluminescent Properties.

Novel multicomponent glasses with nominal compositions of (50-x)MoO3:xWO3:25La2O3:25B2O3, x = 0, 10, 20, 30, 40, 50 mol% doped with 3 mol % Eu2O3 were prepared using a conventional melt-quenching method. Their structure, thermal behavior and luminescent properties were investigated by Raman spectroscopy, differential thermal analysis and photoluminescence spectroscopy. The optical properties of the glasses were investigated by UV-vis absorption spectroscopy and a determination of the refractive index. Physical parameters such as density, molar volume, oxygen molar volume and oxygen packing density were determined. The glasses are characterized by a high glass transition temperature. Raman analysis revealed that the glass structure is built up mainly from tetrahedral (MoO4)2- and (WO4)2- units providing Raman bands of around 317 cm-1, 341-352 cm-1, 832-820 cm-1 and 928-935 cm-1. At the same time, with the replacement of MoO3 with WO3 some fraction of WO6 octahedra are produced, the number of which increases with the increasing WO3 content. A strong red emission from the 5D0 level of Eu3+ ions was registered under near-UV (397 nm) excitation using the 7F0 → 5L6 transition of Eu3+. Photoluminescence (PL) emission gradually increases with increasing WO3 content, evidencing that WO3 is a more appropriate component than MoO3. The integrated fluorescence intensity ratio R (5D0 → 7F2/5D0 → 7F1) was calculated to estimate the degree of asymmetry around the active ion, suggesting a location of Eu3+ in non-centrosymmetric sites. All findings suggest that the investigated glasses are potential candidates for red light-emitting phosphors.

Luminescence performance, temperature sensing characteristics and Judd-Ofelt theory analysis of Y2MoO6:Er3+/Yb3+/Li+ upconversion phosphors

A series of Y2MoO6:0.01Er3+/0.09 Yb3+ upconversion phosphors doped with different concentrations of Li + ions (0.05, 0.10, 0.15, 0.20, 0.25, and 0.30 mol) were prepared by the high temperature solid phase reaction method, and their physical phase structures and upconversion luminescence were analyzed. At the excitation wavelength of 980 nm, the addition of Li+ sharply increased the upconversion luminescence intensity. With the increase of Li+ ion content, the luminescence intensity first increases and then decreases. When the doping amount reaches 0.25 mol, the luminescence intensity reaches the maximum, and the sample emits green light in the two-photon process. Y2MoO6:0.01Er3+/0.09 Yb3+/0.25Li + exhibits excellent temperature sensing properties. Its absolute sensitivity Sa reaches up to 0.012 K-1, the relative sensitivity Sr is 0.017 K-1 and the measurement error δT is less than 0.3 K at room temperature. Its temperature sensing performance is far superior to similar materials. In addition, Judd-Ofelt theory calculations revealed that in comparison with Y2MoO6:0.01Er3+/0.09 Yb3+, its Ω2 increased from 0.56 × 10−20 cm2 to 3.68 × 10−20 cm2, and the spectroscopic quality factor Ω4/Ω6 ratio reached 4.09, which is much higher than that of the other fluorescent materials. The main reason is that Li + replaces the Y3+ ion lattice site, causing lattice distortion and reducing the lattice symmetry around the active ion. The increase in asymmetry increases the possibility of spontaneous radiative transitions. It is shown that the prepared upconversion luminescent materials have potential applications in the field of solid-state lasers and optical sensing.

Research progress on iron metabolism in the occurrence and development of periodontitis

Iron metabolism refers to the process of absorption, transport, excretion and storage of iron in organisms, including the biological activities of iron ions and iron-binding proteins in cells. Clinical research and animal experiments have shown that iron metabolism is associated with the progress of periodontitis. Iron metabolism not only enhances the proliferation and toxicity of periodontal pathogens, but also activate host immune-inflammatory response mediated by macrophages, neutrophils and lymphocytes. In addition, iron metabolism is also involved in regulating cellular death sensitivity of gingival fibroblasts and osteoblasts and promoting the differentiation of osteoclasts, which plays a regulatory role in the regeneration and repair of periodontal tissue. This article reviews the research progress on the pathogenesis of periodontitis from the perspective of iron metabolism, aiming to provide new ideas for the treatment of periodontitis.

Antioxidant and Xanthine oxidase inhibitory activities of the tea (Camellia sinensis) flower

The major purpose of this study was to investigate the DPPH radical scavenging activity, hydroxyl radical scavenging activity, superoxide radical scavenging activity, reducing power, ferrous ion chelating activity, and xanthine oxidase activity for research of antioxidant and xanthine oxidase inhibitory activities using a variety of extracts of tea (Camellia sinensis) flower. Among the several extracts, when 800 μg/mL of the ethanol extract was used, the maximum DPPH radical scavenging activity was obtained, 79.2%, which was approximately 80.8% compared to L-ascorbic acid, the maximum hydroxyl radical scavenging activity, 71.3%, which was approximately 73.2% compared to BHA, and the maximum super oxide radical scavenging activity, 89.4%, which was, approximately 90.6% compared to BHT, and the maximum reducing power, 1.94 at an OD of 700 nm, which was approximately 49.2% compared to L-ascorbic acid, respectively. On the other hand, when 800 μg/mL of the hot water extract was used, the maximum activity of ferrous ion chelate was obtained, 28.6%, which was approximately 48.4% compared to EDTA and the maximum xanthine oxidase inhibitory activity, 61.4%, approximately 63.8% compared to catechin, respectively. These results indicated the application potential for industries that can produce new biomaterials that can compensate for the shortcomings of existing synthetic antioxidants and use discarded tea flower as food, pharmaceutical, and cosmetic materials.

Novel sulfonylurea fluorescence probes for antiproliferative activity, detection and imaging of fluoride ions in living cells

In this study, four novel triphenylpyrazoline 4-toluenesulfonylureas (PYSUs) were synthesized to develop potential anticancer drugs and fluorescent probes for the detection of F− ions. The compounds were synthesized via a two-step microwave-assisted method. The antiproliferative activity of the PYSUs was tested against two cancer cell lines: HepG2 and MDA-MB-231. Among the compounds, 3a exhibited strong activity against both cell lines, while 3b showed strong activity against MDA-MB-231 cells but weaker inhibition of HepG2 cells. Furthermore, compound 3b was identified as the best fluorescent probe, with an increase in emission intensity in the presence of F− ions from tetrabutylammonium fluoride (TBAF). In DMSO, the emission wavelength was found to be 518 nm (green) with an excitation wavelength of 469 nm. The limit of detection (LOD) was calculated to be 0.269 mM in the linear range of 5–10 mM. The interaction mechanism between F− ions and compound 3b was further explored via DFT/TDDFT calculations. Additionally, fluorescent imaging of TBAF-incubated MDA-MB-231 and HepG2 cells confirmed the potential of PYSUs as fluorescent sensors for F− ions in living cancer cells.