Cerium vanadate/modified bentonite (CeVO4/mbt) nanocomposite with different composition percentages was synthesized through a simple one-step hydrothermal method at 180 ℃, and then its photocatalytic activity was evaluated by decolorizing methylene blue (MB) in an aqueous solution under light exposure. In order to increase the surface area as an important parameter in photocatalytic processes, bentonite was modified by ball mill method. The structural and optical properties of the synthesized composites were determined by XRD, FT-IR, DRS, FESEM, EDS, and BET measurements. XRD and EDS results confirmed the successful synthesis of pure CeVO4. FESEM images and EDS mapping showed a proper distribution of rice-like CeVO4 nanoparticles on bentonite. The removal efficiency of MB with only 0.1 g of CeVO4/mbt nanocomposite in 15 min was about 99%, which is significant compared to neat bentonite and pure CeVO4 with efficiency of 30% and 57%. The mentioned nanocomposite followed the first-order kinetics, had a reaction rate constant equal to 0.1483 min-1, and showed acceptable stability in five consecutive cycles.

This article reports a simple hydrothermal method for synthesizing nickel disulfide (NiS2) on the surface of fluorine-doped tin oxide (FTO) glass, followed by the deposition of 5 nm Au nanoparticles on the electrode surface by physical vapor deposition. This process ensures the uniform distribution of Au nanoparticles on the NiS2 surface to enhance its conductivity. Finally, an Au@NiS2-FTO electrochemical biosensor is obtained for the detection of dopamine (DA). The composite material is characterized using transmission electron microscopy (TEM), UV-Vis spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The electrochemical properties of the sensor are investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and time current curves in a 0.1 M PBS solution (pH = 7.3). In the detection of DA, Au@NiS2-FTO exhibits a wide linear detection range (0.1~1000 μM), low detection limit (1 nM), and fast response time (0.1 s). After the addition of interfering substances, such as glucose, L-ascorbic acid, uric acid, CaCl2, NaCl, and KCl, the electrode potential remains relatively unchanged, demonstrating its strong anti-interference capability. It also demonstrates strong sensitivity and reproducibility. The obtained Au@NiS2-FTO provides a simple and easy-to-operate example for constructing nanometer catalysts with enzyme-like properties. These results provide a promising method utilizing Au coating to enhance the conductivity of transition metal sulfides.

BACKGROUND: Breast cancer remains a challenge for physicians. Metformin, an antidiabetic drug, show promising anticancer properties against cancers. An emerging quantum dot (QD) material improves therapeutic agents\' anticancer and imaging properties. QD are nano-sized particles with extreme application in nanotechnology captured by cells and accumulated inside cells, suggesting bioimaging and effective anticancer outcomes. In this study, a simple one-pot hydrothermal method was used to synthesize fluorescent metformin-derived carbon dots (M-CDs) and then investigated the cytotoxic effects and imaging features on two human breast cancer cell lines including, MCF-7 and MDA-MB-231 cells.
RESULTS: Results showed that M-CDs profoundly decreased the viability of both cancer cells. IC50 values showed that M-CDs were more cytotoxic than metformin either 24-48 h post-treatment. Cancer cells uptake M-CDs successfully, which causes morphological changes in cells and increased levels of intracellular ROS. The number of Oil Red O-positive cells and the expression of caspase-3 protein were increased in M-CDs treated cells. Authophagic factors including, AMPK, mTOR, and P62 were down-regulated, while p-AMPK, Becline-1, LC3 I, and LC3 II were up-regulated in M-CDs treated cells. Finally, M-CDs caused a decrease in the wound healing rate of cells.
CONCLUSIONS: For the first, M-CDs were synthesized by simple one-pot hydrothermal treatment without further purification. M-CDs inhibited both breast cancer cells through modulating autophagy signalling.

A challenge in tissue engineering and the pharmaceutical sector is the development of controlled local release of drugs that raise issues when systemic administration is applied. Strontium is an example of an effective anti-osteoporotic agent, used in treating osteoporosis due to both anti-resorptive and anabolic mechanisms of action. Designing bone scaffolds with a higher capability of promoting bone regeneration is a topical research subject. In this study, we developed composite multi-layer three-dimensional (3D) scaffolds for bone tissue engineering based on nano-hydroxyapatite (HA), Sr-containing nano-hydroxyapatite (SrHA), and poly-ε-caprolactone (PCL) through the material extrusion fabrication technique. Previously obtained HA and SrHA with various Sr content were used for the composite material. The chemical, morphological, and biocompatibility properties of the 3D-printed scaffolds obtained using HA/SrHA and PCL were investigated. The 3D composite scaffolds showed good cytocompatibility and osteogenic potential, which is specifically recommended in applications when faster mineralization is needed, such as osteoporosis treatment.

Teff (Eragrostis tef) is a staple crop and holds the biggest share of grains cultivated area in Ethiopia, consequently, a large quantity of Teff straw is produced. The Teff straw was pretreated for the first time with Chromium-based Metal-Organic Framework, MIL-101(Cr), assisted hydrothermal method at temperatures ranging from 160 to 240 °C for 1/2, 1, or 2 h time independently. With an increase of pretreatment severity, the yield of total reducing sugar (TRS) was increased until reaching maximum (185 mg g-1). The identified optimum hydrothermal pretreatment condition, (180 °C and 1 h), had a feature of higher TRS yield and lower furfural concentration. The morphological analysis showed that treated Teff straw had degraded structure, higher surface area, and distorted bundles than native Teff straws. This study insight into MOFs\' application in lignocellulose biomass processing, and optimizing the pretreatment condition of Teff straw biomass.

Background Electrochemical sensing is a versatile field that uses electrochemistry concepts to detect and measure various substances. It finds applications in clinical diagnostics and environmental monitoring. Scientists are currently working on creating reliable electrochemical sensing devices that can accurately detect ascorbic acid. Iron sulfide (FeS) has emerged as a promising material for these sensors due to its excellent electrical conductivity, catalytic activity, and stability.  Materials and methods The FeS nanoparticles were synthesized through the hydrothermal method of synthesis. The glassy carbon electrode (GCE) with a surface area of 0.071 cm2 was modified with FeS before the working electrode was mechanically polished with 1 µm, 0.3 µm, and 0.05 µm alumina pastes for mirror finishing. Then it was subjected to ultrasonication in double distilled water for a few minutes to clean the surface of GCE. The FeS suspension was prepared by dispersing 5 mg of FeS in 10 mL of ethanol during 20 minutes of ultrasonic agitation then the GCE was coated with 10 μL of the suspension by drop coating method and dried in air. Results In this study, FeS nanoparticles were synthesized by the hydrothermal method of synthesis, and it was tested for their electrochemical sensing properties by various tests. Based on the field emission-scanning electron microscope (FE-SEM) analysis, scan rate effect test, cyclic voltammetric test, X-ray diffraction (XRD), and energy-dispersive X-ray (EDX) spectroscopy analysis done and results obtained, it was seen that the synthesized FeS nanoparticles are highly pure and have a crystalline structure. FeS has an even morphology. The synthesized particles also showed highly sensitive and specific sensing toward ascorbic acid when compared to unmodified 10.1 µA electrodes with a sensing value of 12.51 μA, thereby fulfilling the aim of this study. Conclusion Based on the outcomes of the diverse tests carried out, it is evident that the sample displayed a high crystalline nature as indicated by the XRD test. Additionally, the sample exhibited a uniform morphology, exceptional stability, and remarkable sensitivity. The developed FeS-based electrochemical sensor was found to be exceptionally pure and showed excellent performance, showcasing both high sensitivity and selectivity toward ascorbic acid.

Water pollution containing dyes become increasingly serious environmental problem with the acceleration of urbanization and industrialization process. Renewable adsorbents for cationic dye wastewater treatment are becoming an obstacle because of the difficulty of desorbing the dye from the adsorbent surface after adsorption. To overcome this dilemma, herein, we report a hydrothermal method to fabricate sulfonic acid modified yeast carbon microspheres (SA/YCM). Different characterization techniques like scanning electron microscopy, FTIR spectroscopy, and X-ray diffraction have been used to test the SA/YCM. Decorated with sulfonic acid group, the modified yeast carbon microspheres possess excellent ability of adsorbing positively charged materials. The removal rate of Methyl blue (MB) by renewable adsorbent SA/YCM can reach 85.3% when the concentration is 500 mg/L. The SA/YCM regenerated by HCl showed excellent regeneration adsorption capacity (78.1%) after five cycles of adsorption-desorption regeneration experiment. Adsorption isotherm and kinetic behaviors of SA/YCM for methylene blue dyes removal were studied and fitted to different existing models. Owing to the numerous sulfonic acid groups on the surface, the SA/YCM showed prominent reusability after regeneration under acidic conditions, which could withstand repeated adsorption-desorption cycles as well as multiple practical applications.

In this study, photocatalysts with high photocatalytic activity performance are synthesized by synthesizing graphene aerogel-supported, cadmium-doped TiO2 composites by hydrothermal method for the effective degradation of organic dyes in wastewater. Here, GA-TiO2-Cd is investigated as a photocatalyst for the degradation of toxic dyes named Orange G, Acid Blue 161, and Brilliant Green in the UV part of the light spectrum. As a result of the experiments, it is observed that the effective decomposition of organic dyes is due to graphene aerogel (GA) and cadmium-doped TiO2 nanoparticles. The results show that for 20 ppm solutions of Orange G, Acid Blue 161, and Brilliant Green, dyes are removed at approximately 81.075%, 84.15%, and 95.18% in 120 min. The morphology and elemental analysis of the synthesized composites are determined using SEM-EDS, crystal structure analysis by XRD, chemical bond analysis by FTIR, optical properties by UV-Vis-NIR spectrophotometry, and thermal resistance by TGA analysis.

UNASSIGNED: Yeast cell walls are a sustainable biomass source containing carbon and other elements like phosphorus. Converting cell walls into valuable nanomaterials like carbon quantum dots (CQDs) is of interest.
UNASSIGNED: Cell walls from Saccharomyces cerevisiae were hydrothermally treated in 0.5 M H2SO4 to produce CQDs. Multiple analytical techniques were utilized to confirm phosphorus-doping (P-CQDs), characterize the fluorescence properties, determine quantum yield, and evaluate the sensing, antimicrobial, photocatalytic, and antioxidant capacities.
UNASSIGNED: A successful synthesis of P-CQDs was achieved with strong blue fluorescence under UV excitation, 19 % quantum yield, and excellent stability. The P-CQDs showed sensitive fluorescence quenching in response to ferric ions with a 201 nM detection limit. Antibacterial effects against Escherichia coli and Staphylococcus aureus were demonstrated. P-CQDs also exhibited dye degradation under sunlight and antioxidant activity. So, the prepared P-CQDs displayed promising multifunctional capabilities for metal ion detection, disinfection, and environmental remediation. Further research is required to fully realize and implement the multifunctional potential of P-CQDs in real-world applications.

The photocatalytic activity of titanium dioxide (TiO2) nanoparticles toward hydrogen generation can be significantly improved via the loading of various metals e.g., Ru, Co, Ni as co-catalysts. The metal co-catalysts are loaded into TiO2 nanoparticles via different deposition methods; incipient wet impregnation (Imp), hydrothermal (HT), or photocatalytic deposition (PCD). Among all of the tested materials, 0.1 wt% Ru-TiO2 (Imp) provided the highest initial hydrogen catalytic rate of 23.9 mmol h-1 g-1, compared to 10.82 and 16.55 mmol h-1 g-1 for 0.3 wt% Ni-TiO2 (Imp) and 0.3 wt% Co-TiO2 (Imp), respectively. The loading procedures, co-catalyst metals type, and their loading play a significant role in elevating the photocatalytic activity of pristine TiO2 semiconductors toward hydrogen generation. Redox transition metals e.g., Co and Ni exhibit comparable photocatalytic performance to expensive elements such as Ru.