Scanning Electron Microscopy Methods Research Articles

Gross Anatomical, Histological, Histochemical and Scanning Electron Microscopic Examination of Glandular Stomach of Chinese Goose (Anser cygnoides)

Background: The digestive system is responsible for the intake, conversion and absorption of nutrients and the elimination of wastes from the body in order to provide the necessary energy for the continuation of vitality and functions. The aim of this study was to examine the glandular stomach of the Chinese goose (Anser cygnoides) by histological, histochemical and scanning electron microscopic methods. Methods: The glandular stomachs of 12 (6 males and 6 females) healthy adult Chinese geese (Anser cygnoides) were used in the study. The tissues taken were subjected to routine histological procedures. Result: Gross anatomically, it was seen that the Proventriculus was a fusiform or spindle-shaped organ, extending along the median plane between the esophagus and the muscular stomach. Scanning electron microscopic (SEM) observations revealed that the glandular stomach surface of Chinese goose (Anser cygnoides) contained many mucosal folds. Parallel grooves and proventricular gland openings were observed between these folds. Histologically, it was observed that the glandular stomach wall of Chinese goose (Anser cygnoides) consisted of four layers: tunica mucosa, submucosa, tunica muscularis and tunica serosa. The tunica mucosa was observed to have lamina epithelialis, lamina propria and lamina muscularis sublayers. Single layer prismatic cells secreting mucus were found in the lamina epithelialis layer. These cells showed local Alcian Blue (AB) pH:2,5 positive reaction. Lamina muscularis consisted of longitudinal smooth muscle fiber bundles. Compound, branched tubular glands were observed in the submucosal layer. Again, a regional AB positive reaction was observed in the lumen-facing parts of the tubular glands. Periodic acid Schiff (PAS) positive reaction was noted in the basal parts of the tubular glands. In Gordon-Sweet (GS) staining method, reticular threads easily distinguished in all areas where connective tissue present.

The Efficiency of Polyester-Polysulfone Membranes, Coated with Crosslinked PVA Layers, in the Water Desalination by Pervaporation

Composite polymer membranes were obtained using the so-called dry phase inversion and were used for desalination of diluted saline water solutions by pervaporation (PV) method. The tests used a two-layer backing, porous, ultrafiltration commercial membrane (PS20), which consisted of a supporting polyester layer and an active polysulfone layer. The active layer of PV membranes was obtained in an aqueous environment, in the presence of a surfactant, by cross-linking a 5 wt.% aqueous solution of polyvinyl alcohol (PVA)—using various amounts of cross-linking substances: 50 wt.% aqueous solutions of glutaraldehyde (GA) or citric acid (CA) or a 40 wt.% aqueous solution of glyoxal. An ethylene glycol oligomer (PEG 200) was also used to prepare active layers on PV membranes. Witch its help a chemically cross-linked hydrogel with PVA and cross-linking reagents (CA or GA) was formed and used as an active layer. The manufactured PV membranes (PVA/PSf/PES) were used in the desalination of water with a salinity of 35‰, which corresponds to the average salinity of oceans. The pervaporation method was used to examine the efficiency (productivity and selectivity) of the desalination process. The PV was carried at a temperature of 60 °C and a feed flow rate of 60 dm3/h while the membrane area was 0.005 m2. The following characteristic parameters of the membranes were determined: thickness, hydrophilicity (based on contact angle measurements), density, degree of swelling and cross-linking density and compared with the analogous properties of the initial PS20 backing membrane. The physical microstructure of the cross-section of the membranes was analyzed using scanning electron microscopy (SEM) method.

SYNTHESIS AND PHYSICO-CHEMICAL PROPERTIES OF A NEW COMPLEX FERRITE

The article discusses the synthesis of new complex ferrite, radiographic and electron microscopic studies. The phase of complex ferrites was synthesized by the method of high-temperature sol-gel synthesis. For the first time, the structure of CrKFe2O5 Composite ferrite was studied by X-ray phase analysis and scanning electron microscope methods, the syngony type, elementary cell parameters, radiographic and pycnometric densities, and elemental analysis were determined. A comparative analysis of the relationship between the parameters of the Crystal cell of primary substances and the parameters of the obtained complex ferrite Crystal cell was carried out. Micro-samples were taken from different parts of the crystallite obtained through a scanning electron microscope, the elemental composition of the crystals was analyzed, and the general type of layer of the complex ferrite surface was demonstrated. As a result, the fact that the compound consists of two phases, the clarity of its construction was determined by the topography and chemical composition of the compound. As a result, it was found that the newly synthesized complex ferrite corresponds to the Formula CrKFe2O5. The particle size of the compounds formed is large (between 200 μm, 20.0 μm, 5.00 μm and 2.00 μm).

Regulation of the Phase Structure in the Crystallizing Curing System PCL–DGEBA

Qualitative and quantitative aspects of the formation of various types of phase structures, sizes and compositions were considered. For the studied polycaprolactone–epoxy resin/4,4′-diaminediphenylsulfone system, a phase diagram characterized by amorphous separation with a lower critical solution temperature was constructed and its evolution was traced with increasing conversion degree of epoxy groups. A method is proposed for determining the temperature–concentration parameters that determine the type of phase structure of composite materials, based on the optical interferometry method. All types of phase structures and features of structure formation in the phase reversal region and at its boundaries have been studied using optical and scanning electron microscopy methods. The dimensions of the structural elements were determined and their correlation with the temperature and concentration regimes of the system’s curing was established. The composition of phases in cured compositions was studied using FTIR spectroscopy, DSC and scanning electron microscopy. It is shown that by varying the temperature–concentration parameters of curing reactive thermoplastic systems, it is possible to specifically regulate the type of phase structure, phase sizes and their composition, which determine the operational properties of the material.

Preparation, characterization and thermal properties of the PS+Si based polymer nanocomposites

Polymer nanocomposites based on polystyrene and polycrystalline Si nanoparticles have been successfully synthesized using the solution-casting method. The scanning electron microscope and x-ray diffraction methods show that the Si nanoparticle size in the obtained nanocomposite was up to 50 nm. The thermostability of the obtained nanocomposite was studied depending on the concentration of Si nanoparticles in the PS matrix. It was found that Si nanoparticles that are distributed homogeneously in the polymer matrix act as a thermal barrier. By adding 3% Si nanoparticles into polystyrene polymer, the thermal degradation temperature of PS increases by 20°, and the decomposition rate reduces from −42,460 mg/min to −35,099 mg/min. In addition, it was shown that Si nanoparticles do not affect the PS glass transition temperature, which explains that the porous Si does not reduce the free volume for the polymer molecules to move. The polymer macromolecules just are adsorbed on the porous silicon surface, which partially limits their mobility.

Core‐flooding experiments of various concentrations of CO2/N2 mixture in different rocks: II. Effect of rock properties on residual water

AbstractDuring CO2 storage in deep saline aquifers, the presence of residual water has an important influence on the storage efficiency and safety. In this study, natural rock cores taken from deep reservoirs in the Ordos Basin and Fukang, Xinjiang are used as research objects. Nine groups of core‐flooding experiments are performed under different CO2/N2 gas mixture ratios to study the influence of rock properties (mineral composition, permeability, porosity and pore structure) on the residual water. Furthermore, the geophysical and chemical properties of rock cores are analyzed by X‐ray diffraction, electron microscopy, field emission scanning electron microscopy and piezoelectric mercury method. The results show that residual water saturation is a quantitative power function of drainage time. The residual water saturation is positively correlated with the total amount of quartz and feldspar and increases with increasing permeability. Moreover, both the average and median pore throat radius show a strong inverse correlation with irreducible residual water saturation; as these radius increase, the residual water saturation decreases. In contrast, the porosity and maximum pore throat radius display a weaker correlation with irreducible residual water saturation. This study is of great value for engineering practices such as the site selection of CO2 storage projects in saline aquifer and improvement of CO2 storage efficiency. © 2024 Society of Chemical Industry and John Wiley & Sons, Ltd.

Tire Rubber Based Microplastic Particles Cause Adverse on Quality Parameters of Rainbow Trout Sperm Cells.

In the present study, we aimed to determine the parameters of oxidative stress markers, motility and kinematics of rainbow trout (Oncorhynchus mykiss) sperm cells exposed to different doses (0.001, 0.01, 0.1, 1.0, and 10mg/L, in vitro 4h) of tire rubber based microplastic particles (TRMP-Ps) the leachates procedure of rubber pieces. First of all, TRMP-Ps were prepared by abrasion method in accordance with the literature. Structural and morphological features of TRMP-Ps were determined by Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) methods, respectively. Energy dispersive X-ray (EDX) analysis technique was used to characterize the elemental composition of TRMP-Ps. Particle size of microplastic structures was measured hydrodynamically with dynamic light scattering analysis (DLS). After exposure, the effect of TRMP-Ps was defined by the observations of kinematics and antioxidant activities in sperm cells. Our findings showed that the straight line velocity, the curvilinear velocity, the angular path velocity, and the amplitude of lateral displacement of sperm cells decreased. Moreover, while the level of superoxide dismutase decreased dose-dependently against the toxicity of TRMP-Ps, no significant change was observed in the levels of malondialdehyde and total glutathione. The 4-h median effective concentrations (EC50) of TRMP-Ps based on mobility parameters of sperm ranged from 0.31mg/L for reduced straight line velocity of sperm cells to 0.51mg/L for reduced amplitude of lateral displacement of the spermatozoa head. Therefore, we concluded that TRMP-Ps can be a risk for the reproduction cycle of fish in aquatic environments.

Hydrogel Capacitors Based on MoS2 Nanosheets and Applications in Glucose Monitoring.

Non-invasive/minimally invasive continuous monitoring of blood glucose and blood glucose administration have a high impact on chronic disease management in diabetic patients, but the existing technology is yet to achieve the above two purposes at the same time. Therefore, this study proposes a microfluidic microneedle patch based on 3D printing technology and an integrated control system design for blood glucose measurement, and a drug delivery control circuit based on a 555 chip. The proposed method provides an improved preparation of a PVA-PEG-MoS2 nanosheet hydrogel, making use of its dielectric properties to fabricate a microcapacitor and then embedding it in a microfluidic chip. When MoS2 nanosheets react with interstitial liquid glucose (and during the calibration process), the permittivity of the hydrogel is changed, resulting in changes in the capacitance of the capacitor. By converting the capacitance change into the square-wave period change in the output of the 555 chip with the control circuit design accordingly, the minimally invasive continuous measurement of blood glucose and the controlled release of hypoglycemic drugs are realized. In this study, the cross-linking structure of MoS2 nanosheets in hydrogel was examined using infrared spectroscopy and scanning electron microscopy (SEM) methods. Moreover, the critical doping mass fraction of MoS2 nanosheets was determined to be 2% via the measurement of the dielectric constant. Meanwhile, the circuit design and the relationship between the pulse cycle and glucose concentration is validated. The results show that, compared with capacitors in series, the microcapacitors embedded in microfluidic channels can be connected in parallel to obtain better linearized blood glucose measurement results.

WO2–N co-doped 2D Carbon nanosheets as multifunctional additives for enhancing the electrochemical hydrogen storage performance of Co2B

Co2B, with its high theoretical hydrogen storage capacity, is a potential solid-state hydrogen storage material. However, its poor cycling life limits its practical application. In this work, in order to improve the cycling stability and reversibility of hydrogen absorption and desorption of Co2B, we propose to use WO2–N–C nanosheets as dopants to mix with Co2B, thereby enhancing its practical performance. Two-dimensional tungsten oxide-nitrogen-carbon (WO2–N–C) nanosheets was syntheized via a liquid-phase approach, using a tungstenate-polydopamine precursor followed by thermal treatment. Subsequently, these WO2–N–C nanosheets were compounded with cobalt boride (Co2B) particles through ball milling at various ratios of 1%, 3%, and 5%, which were confirmed by XRD (X-ray diffraction) and SEM (Scanning Electron Microscope) methods. Employing a comprehensive suite of electrochemical analyses, including corrosion potential measurements, polarization curves, step voltammetry, and electrochemical impedance spectroscopy (EIS), we found that the incorporation of WO2–N–C significantly enhances the corrosion resistance and electrochemical activity of Co2B. Furthermore, cyclic life tests revealed that the WO2–N–C-doped Co2B composites exhibit superior discharge capacities and capacity retention rates compared to pristine Co2B. Notably, the 3% WO2–N–C-doped Co2B composite demonstrated the optimal electrochemical performance, achieving a maximum discharge specific capacity of 555 mAh g−1 and maintaining 82% of its initial capacity after 50 cycles. Our findings underscore the dual role of WO2–N–C in not only augmenting the surface electrochemical activity of Co2B but also providing a protective surface layer, thereby enhancing its overall electrochemical performance.

Comparison of remineralizing efficacy of two novel preparation of arginine and theobromine on white spot lesion - an in vitro SEM analysis

ABSTRACT Purpose Evaluation of the efficacy of two novel formulations of arginine and theobromine in remineralizing artificial enamel defects using in vitro testing techniques- Microhardness and SEM Materials and methods Enamel slabs measuring 3 mm by 3 mm by 1.5 mm were created using 11 healthy premolars that were excised for orthodontic treatment. Group 1 (control, treated with merely a remineralization solution), Group 2 (0.05% arginine in 10 ml distilled water), and Group 3 (2% theobromine in 10 ml distilled water) were the three groups to which the slabs were randomly allocated (n = 7 per group). The pH cycle was run for 14 days, starting with a 72-h demineralization period and ending with 11 days of remineralization in the corresponding solutions. Prior to and during remineralization, microhardness was measured, and surface features were assessed using scanning electron microscopy (SEM). Statistical analysis, including Paired T Test, one-way ANOVA, and post hoc Tukey tests, determined that the mean values were significant at the 0.05 level. Results The control group showed a mean microhardness increase from 192.09 ± 19.30 to 208.58 ± 5.76. The arginine group increased significantly from 217.20 ± 4.24 to 304.00 ± 15.96, and the theobromine group from 214.09 ± 7.67 to 283.14 ± 10.91. Statistical analysis indicated that both arginine and theobromine groups had significantly greater microhardness improvements compared to the control (p < 0.05). SEM revealed that although arginine and theobromine enhanced enamel microhardness, surface morphology remained irregular and non-uniform. Conclusion Arginine and theobromine improve enamel microhardness and promote remineralization, but they do not create a uniform surface texture. Further research is needed to optimize their use and explore long-term effects on enamel surface uniformity.

ASSESSMENT OF USING WATER OBTAINED THROUGH EVODROP TECHNOLOGY EXPOSED TO ELECTROMAGNETIC WAVES ON CONCRETE PROPERTIES BASED ON FT-IR AND SEM ANALYSES

Various methods are applied to improve the quality of cement and concrete. Many efforts are made to enhance their quality by introducing additional compounds that can stabilize the chemical bonds between their components. Significant effects on hydrogen bonds under the influence of magnetic and electromagnetic waves have been observed. Results have been published with permanent magnetic fields for water treatment for concrete preparation with magnetic inductions B = 4000, 6000, 6000, 9000, and 9250 Gauss. Electromagnetic (e. m.) treated water has emerged as a promising approach for improving the properties of construction materials.Our investigation concerns the properties of concrete. Concrete is a composite building material mainly consisting of cement, aggregates, water, and various chemical additives. Water was activated with electromagnetic fields from solenoid, ranging from 20 to 40 kHz. The study employs Fourier Transform Infrared (FT-IR) spectroscopy analysis and the Scanning Electron Microscope (SEM) method. The experiments were performed on samples and control samples. The control samples were obtained with water before activation with EM fields. Treating the water in concrete preparation with electromagnetic fields leads to greater mixture homogeneity. SEM images substantiate this outcome. The FT-IR peaks are linked to heightened chemical reactivity from improved water parameters attributed to the treatment with the EVOdrop device.

Morphological study of remineralization of the eroded enamel lesions by tyrosine-rich amelogenin peptide

BackgroundTyrosine-rich amelogenin peptide (TRAP) is the main amelogenin digestion product in the developmental enamel matrix. It has been shown to promote remineralization of demineralized enamel in our previous study. However, direct evidence of the effect of TRAP on the morphology and nanostructure of crystal growth on an enamel surface has not been reported. This study aimed to examine the effect of TRAP on the morphology of calcium phosphate crystals grown on early enamel erosion using a pH-cycling model.MethodsEroded lesions were produced in human premolars by 30-second immersion in 37% phosphoric acid. Forty-five samples of eroded human premolar enamel blocks were selected and randomly divided into 3 groups: deionized water (DDW, negative control); 100 µg/mL TRAP, and 2 ppm sodium fluoride (NaF, positive control group). For 14 days, the specimens were exposed to a pH-cycling model. Using scanning electron microscopy (SEM) and atomic force microscopy (AFM) methods, the surface morphology, calcium-phosphorus ratio, and enamel surface roughness were examined. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) were used to assess crystal characteristics.ResultsAfter pH-cycling, compared to the two control groups, the surface of the eroded enamel of the peptide TRAP group shows a large number of new, densely arranged rod-like crystals, parallel to each other, regularly arranged, forming an ordered structure, with crystal morphology similar to that of natural enamel. The crystals are mostly hydroxyapatite (HA).ConclusionThis study demonstrates that the peptide TRAP modulates the formation of hydroxyapatite in eroded enamel and that the newly formed crystals resemble natural enamel crystals and promote the remineralization of enamel, providing a promising biomaterial for remineralization treatment of enamel lesions.

Coating of Carbon Black (CB) and Graphene Oxides (GOs) with Magnetite (Fe3O4)

Composites containing iron oxides are obtained by the co-precipitation of iron(II) and iron(III) compounds in the presence of different substrates in an alkaline environment. Newly synthesized graphene oxide (GO), reduced graphene oxide (rCO) and carbon black (CB) are used as substrates. Methods of obtaining GO–amorphous iron compound, rGO–Fe3O4, and CB–Fe3O4 composites are developed. It is determined that rGO–Fe3O4 and CB–Fe3O4 magnetic composites can be obtained at 70–75°C, while in the presence of GO, a non-magnetic composite containing an amorphous iron compound is formed under the same conditions. This composite, when heated in vacuum at 170–175°C, undergoes exfoliation, in result of which a powder composite rGO–amorphous iron compound is formed, the volume of which is 2.7 times greater than that of initial powder. Partial reduction of the formed composite takes place at 550°C and rGO–Fe3O4 is obtained. Formation of the magnetite phase is determined by XRD (X-Ray Diffraction) analysis. The structural-morphological study of the synthesized composites is carried out by the SEM (Scanning Electron Microscopy) method. Their magnetic characteristics are studied using VSM (Vibrating Sample Magnetometry) method.

Surface morphology and chemical composition analysis of titanium dental implants using SEM and EDX.

The chemical content and surface morphology of titanium implants have a greater impact on the osseointegration characteristic of dental implants. Therefore this study was done to examine the surface morphology and chemical composition of commercially available titanium dental implants. (BioLine Dental Implants Series-single piece (A) and spiral implants (B)). The chemical composition was determined by the Energy Dispersive X-ray Spectroscopy (EDX) method and the surface morphology was performed by Scanning Electron Microscopy (SEM) method. The results for chemical composition of titanium implants using EDX method revealed that titanium (Ti) constitutes the major surface components on the plain and top land area of the single piece compressive implants which is 89.71 weight% and 71.55 weight % respectively. Iron (Fe)-66.60 weight % is considered as major element along with chromium (Cr)-18.34 weight %on the plain area of spiral implants and O (19.90 weight %) and Al (12.43 weight %) on the top land area of spiral implants. The surface morphology and impact of the manufacturing process on the implant surface using SEM method revealed that the similar surface irregularities with diameter ranging from 10 µm to 20 µm on the side view of the top land area and diameter of 10 µm on the side view of plain area for both the samples. Sample A showed some amorphous structures with grainy marks on the apical view whereas Sample B showed heavy grinding and shear marks on the apical view at diameter ranging from 10 µm to 20µm.

Corrosion mechanisms of Escherichia coli and Pseudomonas fluorescens on carbon steel based on biofilm perspective

Corrosion mechanisms of Escherichia coli, Pseudomonas fluorescens and E. coli–P. fluorescens on carbon steel were researched by the corrosion weight loss, electrochemical impedance, microbial inoculation culture, biofilm three-dimensional layer scanning, environmental scanning electron microscope, infrared spectroscopy and other methods. It was found that the corrosion rate in E. coli condition was 1.37–1.48 times higher than that in P. fluorescens condition and 1.23–1.33 times higher than that in E. coli–P. fluorescens condition. Although the types of functional groups contained in the EPS secreted by E. coli and P. fluorescens were the same, the hydrogen bonding was weaker in the former, resulting in a loose biofilm structure. Meanwhile, the metabolic corrosion of E. coli itself dominated in the corrosion. On the contrary, P. fluorescens condition and E. coli–P. fluorescens condition had stronger hydrogen bonding of functional groups, so their biofilm structure was tighter. For P. fluorescens condition, the corrosion behaviour was dominated by inhibitory action of EPS in late. For E. coli–P. fluorescens condition, the corrosion behaviour was dominated by metabolic corrosion of E. coli–P. fluorescens itself in early. However, corrosion behaviour was dominated by inhibitory corrosion of EPS in middle. E. coli–P. fluorescens itself and EPS had comparable roles in late.

In-Situ Liquid-Electrochemical X-Ray and Electron Microscopy for Multi-Modal Energy Materials Characterization

In-situ liquid cell electron and x-ray microscopy have enabled dynamic studies of electrochemical reactions in energy materials and revealed relationships between the performance, structure, and chemical composition of these material systems. Such fundamental relationships are critical to improving the performance of batteries, catalysts, and other energy materials. Growing research interest in energy materials systems has accelerated the development of in-situ liquid-electrochemical microscopy techniques into mature and robust characterization workflows using novel and versatile scientific hardware.Multiple characterization techniques or in-situ processing steps are often required to fully understand the mechanisms governing the behavior of energy materials for all relevant length scales and environmental conditions. A multi-modal workflow combining in-situ liquid-electrochemical transmission electron, X-ray synchrotron and scanning electron microscopy methods is presented. The breadth of research applications is discussed, including the study of chemical dynamics and structural changes to micron-scale LixFePO4 battery particles during lithium-ion insertion/extraction, electrocatalytic behavior of β-Co(OH)2 platelet particles, and electrochemical oxidation of copper nanoparticles under reductive electrolytic conditions. New insights into these materials systems provided by these experiments will directly inform the development of predictive models for material performance and guide improvement of material design and synthesis.New scientific hardware and method development has been critical to in-situ nano-scale liquid cell microscopy and spectroscopy of electrochemical systems. Therefore, best-practice hardware and method design and development for these in-situ liquid-electrochemical microscopy experiments are also discussed. The connections between potentiostat, holder, and on-chip leads must be carefully considered with respect to different ground potentials, and the incorporation of real bulk-scale reference electrodes in this hardware has yielded quantitatively higher fidelity data with less degradation from further electrochemical cycling. Heating the sample or illuminating with light during in-situ electrochemical data collection has begun to further expand the range of environmental conditions that can be incorporated into experiments.

A Nafion/BiVO4-COOH-MWCNTs/GCE for the sensitive determination of Cd2+ and Pb2+ by DPASV

BiVO4 was hydrothermally prepared and then ultrasonically mixed with carboxylated multiwalled carbon nanotubes (COOH-MWCNTs) to yield a BiVO4-COOH-MWCNTs composite. The composite were cast-coated on a glassy carbon electrode (GCE) to yield a BiVO4-COOH-MWCNTs/GCE, and then a Nafion solution was cast-coated on the BiVO4-COOH-MWCNTs/GCE to yield a Nafion/BiVO4-COOH-MWCNTs/GCE. The related materials and electrodes were characterized by field emission scanning electron microscopy, X-ray diffractometer and electrochemical methods. Under the optimal experimental conditions, Cd2+ and Pb2+ were analyzed by differential pulse anodic stripping voltammetry on the Nafion/BiVO4-COOH-MWCNTs/GCE, giving a linear detection range (LDR) from 10.0 nM to 2.00 μM and a limit of detection (LOD, S/N = 3) of 0.5 nM for Cd2+, as well as a LDR from 10.0 nM to 1.00 μM and a LOD of 0.9 nM for Pb2+. The Nafion/BiVO4-COOH-MWCNTs/GCE exhibited good selectivity, stability and reproducibility and returned satisfactory results of determining Cd2+ and Pb2+ in seafood samples.

Improving Tamoxifen Performance in Inducing Apoptosis and Hepatoprotection by Loading on a Dual Nanomagnetic Targeting System.

Although tamoxifen (TMX) belongs to selective estrogen receptor modulators (SERMs) and selectively binds to estrogen receptors, it affects other estrogen-producing tissues due to passive diffusion and non-differentiation of normal and cancerous cells and leads to side effects. The problems expressed about tamoxifen (TMX) encouraged us to design a new drug delivery system based on magnetic nanoparticles (MNPs) to simultaneously target two receptors on cancer cells through folic acid (FA) and hyaluronic acid (HA) groups. The mediator of binding of two targeting agents to MNPs is a polymer linker, including dopamine, polyethylene glycol, and terminal amine (DPN). Zeta potential, dynamic light scattering (DLS), and Field emission scanning electron microscopy (FESEM) methods confirmed that MNPs-DPN-HA-FA has a suitable size of ~105 nm and a surface charge of -41 mV, and therefore, it can be a suitable option for carrying TMX and increasing its solubility. The cytotoxic test showed that the highest concentration of MNPs-DPN-HA-FA-TMX decreased cell viability to about 11% after 72 h of exposure compared to the control. While the protective effect of modified MNPs on normal cells was evident, unlike tamoxifen, the survival rate of liver cells, even after 180 min of treatment, was not significantly different from the control group. The protective effect of MNPs was also confirmed by examining the amount of malondialdehyde, and no significant difference was observed in the amount of lipid peroxidation caused by modified MNPs compared to the control. Flow cytometry proved that TMX loaded onto modified MNPs can induce apoptosis by targeting the overexpressed receptors on cancer cells. Real-time PCR showed that the modified MNPs activated the intrinsic and extrinsic mitochondrial pathways of apoptosis, so the Bak1/Bclx ratio for MNPs-DPN-HAFA- TMX and free TMX was 70.82 and 0.38, respectively. Also, the expression of the caspase-3 gene increased 430 times compared to the control. On the other hand, only TNF gene expression, which is responsible for metastasis in some tumors, was decreased by both free TMX and MNPs-DPN-HA-FA-TMX. Finally, molecular docking proved that MNPs-DPN-HA-FA-TMX could provide a very stable interaction with both CD44 and folate receptors, induce apoptosis in cancer cells, and reduce hepatotoxicity. All the results showed that MNPs-DPN-HA-FA-TMX can show good affinity to cancer cells using targeting agents and induce apoptosis in metastatic breast ductal carcinoma T-47D cell lines. Also, the protective effects of MNPs on hepatocytes are quite evident, and they can reduce the side effects of TMX.

Physico-chemical characterization of cupola slag: Enhancing its utility in construction

Cupola slag is a waste material of the steel and iron industries. Its composition is determined by the cupola furnace and other elements used in steel and iron manufacturing. This paper investigates the characterization behavior of various cupola slag materials. As a result, x-ray fluorescence (XRF), x-ray diffraction (XRD), thermogravimetry differential thermal analysis, and scanning electron microscopy (SEM) methods were used to characterize three cupola slag samples from distinct origins. In addition, various physical properties were used to compare different cupola slags. The specific gravity values of CS-1 (cupola slag-1 sample), CS-2 (cupola slag-2 sample), and CS-3 (cupola slag-3 sample) are 1.36, 2.5, and 2.917, respectively. The density and water absorption for CS-1, CS-2, and CS-3 are 1414.86, 1477.71, and 1796 kg/m3, and 0.37%, 0.32%, and 0.26%, respectively. Cupola slag also includes a larger percentage of lime, according to XRF data, which contributes to its improved binding characteristics. A higher calcium oxide content in CS-3 could facilitate the pozzolanic process. The presence of angular particles that aid in material binding is seen in the SEM image. Compounds with a nanostructure are then flawlessly blended into the mixture and grouped with calcium alumina silicates formed by cement hydration. The XRD pattern of cupola slag exhibits high peaks, indicating that the material is crystalline in character and can be utilized as sand. It also shows the presence of other chemical compounds, such as silica, which ranges from 30% to 45%. CS-1 and CS-2 have comparable XRD patterns. However, CS-3 has a somewhat different pattern because of the greater CaO content. Weight loss begins at higher temperatures, which shows that the material is stable at higher temperatures, according to a thermo-gravimetric study. The differential thermal analysis curve of CS-3 indicates that the material remains stable up to a temperature of 600 °C. The physical characteristics of all cupola slag samples show that cupola slag may be utilized to make sustainable building materials because of its lower specific gravity, density, and water absorption.

In vitro and in silico studies of the inclusion complexation of 8-bromobaicalein with β-cyclodextrins

Baicalein, a flavone derived from Scutellaria baicalensis Georgi, exhibits potent anti-inflammatory, antiviral, and anticancer properties. Its derivative, known as 8-bromobaicalein (BB), has been found to have strong cytotoxic effect on MCF-7 human breast cancer cells. However, its limited solubility in water has hindered its potential for wider applications. To address this issue, we investigated the use of cyclodextrins specifically βCD, 2,6-di-O-methyl-β-cyclodextrin (DMβCD), and hydroxypropyl-β-cyclodextrin (HPβCD) to improve the solubility of BB through inclusion complexation. During 250 ns molecular dynamics simulations, it was found that BB can form inclusion complexes with all βCDs. These complexes exhibit two distinct orientations: chromone group insertion (C-form) and phenyl group insertion (P-form). The formation of these complexes is primarily driven by van der Waals interactions. DMβCD has the highest number of atom contacts with BB and the lowest solvent accessibility in the hydrophobic cavity. These results coincide with the highest binding affinity from the MM/GBSA-based free energy calculation method. Experimental phase solubility diagrams revealed a 1:1 stoichiometric ratio (AL type) between BB and βCDs, in which BB/DMβCD showed the highest stability. The formation of inclusion complexes was confirmed by differential scanning calorimetry and scanning electron microscope methods. Additionally, the BB/DMβCD inclusion complex demonstrated significantly higher anticancer activity against MCF-7 human breast cancer cells compared to BB alone. These findings underscore the potential of DMβCD for formulating BB in pharmaceutical and medical applications.