Sonication Technique Research Articles

Development and characterization of advanced nano-coating with CeO₂, Al₂O₃, ZnO, and TiO₂ nanoparticles fWor enhanced durability and corrosion resistance

This study introduces an innovative sol-gel nano-coating designed to address silica scaling and corrosion in hydrothermal and high-stimulation environments. By incorporating CeO₂, Al₂O₃, ZnO, and TiO₂ nanoparticles into a polymer matrix through precise sonication techniques, the coating achieves uniform dispersion and enhanced functional performance. The meticulous characterization of nanoparticle integration optimizes mechanical strength, thermal stability, and chemical resistance. Applied via a directional supplying device, the nano-coating is mechanically deposited onto the cemented walls of wells, providing robust protection against scaling and corrosion across diverse conditions, including varying temperatures and pH levels. Laboratory testing demonstrates significant reductions in silica scaling and corrosion rates, confirming the coating's efficacy in maintaining production efficiency in both hydrothermal projects and fracking operations. This paper details the synthesis process and molecular chemistry involved in nanoparticle integration, alongside the resultant structural properties of the coating. Thermogravimetric analysis (TGA) assesses thermal stability, while kinetic models such as Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) evaluate activation energy without assuming specific reaction models. The findings highlight the potential of this advanced nano-coating as a robust solution for enhancing operational longevity and efficiency in challenging industrial applications.

Development and Characterization of Advanced Nano-Coating with CeO₂, Al₂O₃, ZnO, and TiO₂ Nanoparticles for Enhanced Durability and Corrosion Resistance

This study introduces an innovative sol-gel nano-coating designed to address silica scaling and corrosion in hydrothermal and high-stimulation environments. By incorporating CeO₂, Al₂O₃, ZnO, and TiO₂ nanoparticles into a polymer matrix through precise sonication techniques, the coating achieves uniform dispersion and enhanced functional performance. The meticulous characterization of nanoparticle integration optimizes mechanical strength, thermal stability, and chemical resistance. Applied via a directional supplying device, the nano-coating is mechanically deposited onto the cemented walls of wells, providing robust protection against scaling and corrosion across diverse conditions, including varying temperatures and pH levels. Laboratory testing demonstrates significant reductions in silica scaling and corrosion rates, confirming the coating's efficacy in maintaining production efficiency in both hydrothermal projects and fracking operations. This paper details the synthesis process and molecular chemistry involved in nanoparticle integration, alongside the resultant structural properties of the coating. Thermogravimetric analysis (TGA) assesses thermal stability, while kinetic models such as Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) evaluate activation energy without assuming specific reaction models. The findings highlight the potential of this advanced nano-coating as a robust solution for enhancing operational longevity and efficiency in challenging industrial applications.

Lymphatic targeting of cilnidipine by designing and developing a nanostructured lipid carrier drug delivery system

Objective The objective of current research is to design, develop, and optimize a cilnidipine (CLN) nanostructured lipid carrier (NLC)-based drug delivery system for the effective treatment of hypertension (HT). Significance Oral administration of CLN-loaded NLC (CLN NLC) containing glyceryl monostearate (GMS) as a solid and isopropyl myristate (IPM) as a liquid lipid may show remarkable lymphatic uptake through payer patches. Methods The emulsification probe sonication technique was used followed by optimization using 32 factorial designs. Results The optimized batch showed a mean particle size of 115.4 ± 0.22 nm with encapsulation efficiency of 98.32 ± 0.23%, polydispersity index (PDI) of 0.342 ± 0.03, and zeta potential (ZP, ζ) was −60.5 ± 0.24 which indicate excellent physical stability. In vitro studies showed a controlled release of CLN NLCs. Pharmacokinetics studies determined the C max of NLCs (373.47 ± 15.1) indicates 2.3-fold enhancement compared with plain drug (160.64 ± 7.63). Pharmacodynamic studies indicated that CLN NLCs were maintaining systolic blood pressure in a controlled manner without any signs of side effects. Conclusion CLN NLCs significantly improved lymphatic delivery and proved to be effective in the treatment and management of HT. It has been proved that CLN NLCs are found to be better than any traditional CLN dosage form due to enhancement in solubility, absorption, bioavailability, intestinal permeability, avoidance of first-pass metabolism, P-glycoprotein efflux and reduction in dose-related side effects, achievement of controlled and sustained release action.

Formulation optimization of chitosan surface coated solid lipid nanoparticles of griseofulvin: A Box-Behnken design and in vivo pharmacokinetic study.

Solid lipid nanoparticles (SLNs) are becoming increasingly favored for their robust biocompatibility and their capacity to enhance drug solubility, particularly for drugs with limited water solubility. This study delves into the effectiveness of the hot melt sonication technique in fabricating SLNs with high drug loading capabilities and sustained release characteristics. Griseofulvin (GF), chosen as a representative drug due to its poor water solubility, was encapsulated into SLNs composed of stearic acid. Optimization of chitosan-coated GF-loaded SLNs (CS-GF-SLN) was conducted using a Box-Behnken design. Utilizing the desirability approach, optimal parameters were determined, including a lipid quantity of 450.593 mg, chitosan content of 268.67 mg, and sonication duration of 2.14 hours. These parameters resulted in a zeta potential of -34.8 mV and a particle size (PS) of 56.87 nm. Following optimization, the refined formulation underwent comprehensive assessment across various parameters. Notably, the drug encapsulated within SLNs exhibited sustained release over three days, as illustrated by the in-vitro drug release profile. The optimized formulation demonstrated a bioavailability enhancement by approximately 1.7 to 2.0 times compared to the conventional formulation. Furthermore, administration of drug-loaded SLNs to a macrophage cell line demonstrated no cytotoxicity, affirming their suitability as conventional drug delivery platforms for GF.

Zinc cobaltite embedded in binary metal-organic frameworks using a direct binder-free electrode fabrication approach for efficient energy storage devices and monosodium glutamate detection

There is an imperative need to develop high performance electrode for advance energy storage devices. This work represents the successful synthesis of zinc cobaltite (ZnCo2O4), nickel cobalt metal organic framework, and their composite (ZnCo2O4@NiCo-MOF). The materials are synthesized by using both hydrothermal and sonication techniques. The ZnCo2O4 offers eco-friendly and diffusion regulated properties, while NiCo-MOF provides large specific surface area and tunable pore structure. The ZnCo2O4@NiCo-MOF provide superior electrochemical performance compared to ZnCo2O4 and NiCo-MOF in a three electrode setup. The ZnCo2O4@NiCo-MOF provides a specific capacity of 984 C/g at 1.5 A/g. The ZnCo2O4@NiCo-MOF is also utilized in two electrode setup with activated carbon. The ZnCo2O4@NiCo-MOF//AC device demonstrates the energy density of 92.4 Wh/kg and a power density of 930 W/kg. Additionally, the real time application of ZnCo2O4@NiCo-MOF electrode is also tested in the detection of monosodium glutamate in food. This study highlights the importance of ZnCo2O4@NiCo-MOF electrode materials for future storage and detection devices.

Rheological, mechanical, and environmental performance of printable graphene-enhanced cementitious composites with limestone and calcined clay

As extrusion-based 3D concrete printing gains wider acceptance in construction, there is a growing imperative to incorporate supplementary cementitious materials (SCMs) into printable mixtures to address their high cement content and promote sustainability. Conventional SCMs like fly ash and slag are becoming increasingly scarce, underscoring the need for alternative solutions such as limestone and calcined clay. Additionally, the utilization of nanomaterials in printable mixtures holds potential for enhancing the mechanical properties of 3D printed structures. These properties are often compromised by interlayer interfaces and void formations during printing, resulting in lower mechanical performance compared to conventionally cast concrete. Graphene nanoplatelets (GNPs), with their high aspect ratios and exceptional mechanical characteristics, offer promising avenues for reinforcing printable cementitious composites. This study explores the rheological, mechanical, and environmental aspects of graphene-enhanced cementitious composites incorporating limestone and calcined clay. Graphene nanoplatelets (GNPs) were dispersed utilizing a surfactant-assisted sonication technique, and their dispersion characteristics were evaluated through absorbance, particle size, and zeta potential measurements. Then, the influence of varying GNP concentrations on the rheological properties of limestone-calcined clay (LC2) cementitious composites was assessed. Compressive and flexural strength tests were conducted on 3D-printed LC2 samples with different GNP ratios, alongside cast specimens for comparison. Microstructural examination of failed specimens was performed using scanning electron microscopy. Furthermore, a life cycle assessment was conducted to compare the environmental impacts of printable LC2 mixtures to conventional printable mixtures. Incorporating GNPs at a ratio of 0.05 % by weight of cement in printable LC2 mixtures enhances compressive strength by 23 %, leading to a reduction of approximately 31 % in environmental impacts compared to conventional printed mixtures.

Impact of hybrid nanoparticle reinforcements on Mechanical properties of Epoxy-Polylactic Acid (PLA) Composites

This study examines the influence of graphene nanoplatelets (GNPs) and multi-walled carbon nanotubes (MWCNTs) on the mechanical properties of SiO2-loaded epoxy-polylactic acid (PLA) composites. Epoxy and PLA were mixed to form the matrix with fillers, including SiO2, GNPs, and MWCNTs. The nanocomposites were prepared with a hybrid filler combination (SiO2/GNPs and SiO2/MWCNTs) with filler concentrations ranging from 0.1 – 0.4 wt. %. The composites were prepared using a combination of bath sonication and hand-casting techniques. They are characterized using tensile, bending impact, and fracture tests. The observed characteristics of GNP/SiO2 and MWCNTs/SiO2-loaded nanocomposites exhibited significant differences. Compared to the unmodified epoxy-PLA composite, incorporating 0.1 wt% of GNP/SiO2 filler improved tensile flexural and impact strength. Conversely, adding 0.4 wt% of MWCNTs/SiO2 filler enhances tensile, flexural, and impact strength. The dispersion mechanism of nanofillers was investigated using Scanning Electron Microscopy (SEM) on fracture surfaces obtained from tensile tests. An ANSYS workbench was used to simulate the impact of filler concentration on nanocomposites' tensile and bending strength, and a numerical analysis was performed.

Synthesis of novel imidazole-based compounds via using sonication technique: Influence of chemical reaction manipulation, antiproliferative activity through apoptosis induction, cell migration inhibition, and antioxidant properties

This study presents the synthesis and biological evaluation of a new series of imidazole-based compounds and acyl thiourea derivatives derived from aroyl isothiocyanates, exploring the effects of various reaction conditions on their synthesis. Among the synthesized compounds, four candidates 4a, 4b, 8, and 9 demonstrated significant antiproliferative activities against four cancer cell lines (HepG-2, HCT-116, MCF-7, and PC-3), with IC50 values ranging from 2.89 μM to 22.01 μM. Compounds 4b and 8 were predicted to inhibit cell migration by 67 % and 43 %, respectively, and were further evaluated for their antioxidant activity. Results showed that compound 4b exhibited the highest antioxidant activity with an IC50 of 99.96 μM. Additionally, cell cycle analysis demonstrated that derivatives 4b and 8 exerted antiproliferative effects at the G1 phase. Apoptosis assays revealed that compounds 4b and 8 induced apoptosis in 39.81 % and 44.18 % of cells, respectively, compared to the control.

Optical and Electrical Properties of Spin Coated Bilayer Graphene

Graphene is a 2D material with high transparency, high carrier mobility, and high electrical conductivity [1-4]. In this work, a thin graphene layer was coated on Si through spin coating, and dip coating technique.Graphene ink was prepared by expanding the graphite flakes through microwave irradiation followed by ultrasonic liquid phase exfoliation. 5 mg of the resulting graphene was dispersed in 1 ml of IPA through a probe sonication technique to obtain the graphene suspension/ink. To form the graphene/Si junction, pieces of 3 x 3 cm2 of n-type Si were used. In addition, same size of fused silica were used to measure the reflectance of deposited graphene. The graphene layer in the first sample was formed by spin coating 40 µl of graphene ink on the Si and the fused silica at a speed of 200 rpm for 40 s. The second sample was prepared by dip coating technique, where 13 ml of the graphene ink was added to 47 ml of IPA, followed by dipping Si and the fused silica pieces with a speed of 20 mm/min till they immersed completely and were kept for 1 min and were moved up at the same speed and dried at room temperature. This dip-coating process was repeated 10 times for each sample.The morphology of graphene-coated area was analyzed using the SEM technique. The SEM images of the spin-coated shows that the surface is fully covered with graphene flakes of different sizes stacked on each other with varied orientations, this shows the ability to obtain a continuous coating of graphene by spin coating. Also, Hall effect measurements were performed, and it showed that the conductivity of the Si substrate was 1.95x10-2 ohm-1cm-1, and it increased to 2.74 ohm-1cm-1 after adding the graphene. Finally, the reflectance of the graphene on fused silica was measured using a UV-VIS spectrophotometer, and it showed that the reflectance decreased from 8% to 4% in the range from 360 to 860 nm after adding the graphene.For dip-coated sample, the SEM image shows some voids, and empty areas linked with by graphene structure with a width of few microns, this shows that the dip-coating process needs to be optimized to get a full coverage of the surface. The electrical measurement of this sample showed that the conductivity increased to 2.66 ohm-1cm-1 after the dip coating of graphene. For the reflectance measurements, it was observed that the graphene has decreased the reflectance to 6-7% in the range from 360 to 860 nm.Finally, spin coating at higher speed, and less amount of graphene can be tested, to obtain a thinner graphene layer. For the dip coating process, higher graphene concentration in IPA, and longer immersion time will be investigated to get a better coverage.

Formic and lactic acids from the conversion of xylose with the use of modified clinoptilolite by sonication

AbstractBACKGROUNDA material of natural origin, clinoptilolite, was modified with selected metals in order to obtain a catalyst for the conversion of xylose – the main component of the hemicellulose fraction present in lignocellulosic biomass – to selected carboxylic acids.RESULTSThe starting material without modification (0‐parent), the hydrogen form (0‐hydrogen) of zeolite and zeolite after hierarchization with hydrochloric acid (0‐dealuminated) were used. Iron, copper and cobalt ions were introduced as active centers using the sonication technique. The catalytic process was carried out in a pressure autoclave for 2 h at a temperature of 220 °C. Compounds such as formic acid with a yield of 91% (0‐parent) and lactic acid with a yield of 66.1% (Fe‐hydrogen) were obtained.ConclusionThe catalytic processes carried out using xylose lead to the obtaining of a mixture of carboxylic acids: lactic acid, pyruvic acid and formic acid. An important role here is played by the presence of iron as an active site, which leads to the transformation of xylose into lactic acid by dehydration, and the presence of Lewis and Brønsted active sites. In the case of formic acid, which has never been reported in publications on a similar topic, the starting zeolite without modification contributed to its preparation. It is possible that the content of alkali metals contributed to its preparation along with the coupling of the oxidation reaction of the intermediate product, because of the presence of small amounts of iron, which are present in the natural material. © 2024 Society of Chemical Industry (SCI).

Worrying Presence of Asymptomatic Bacterial Colonisation on Implanted Orthopedic Devices.

Background Bacterial infection after hardware implantation in orthopedic and trauma surgery is devastating, resulting in increased hospital costs and stays, multiple revision surgeries, and prolonged use of antibiotics. The present study aims to determine whether a symbiotic relationship between the human organism and bacteria in hardware implantation may be present, without clinically evident infection. Materials and methods We studied explanted devices for microbiological analysis, using the sonication technique, from patients who underwent surgical removal of musculoskeletal hardware for mechanical reasons. None of the patients included in the study had clinical or biochemical signs of infection. Results Forty-nine patients were enrolled. Cultures tested positive for bacteria in 42.8% of the 49 patients (21 of 49). In 13 patients, Gram-positive bacteria were isolated, while Gram-negative bacteria were isolated from nine patients. The most frequent bacterial species found was Pseudomonas aeruginosa, with six positive cultures (28.5%). Coagulase-negative staphylococci were isolated from ten implants (47%). Conclusion A pacific coexistence between humans and bacteria is possible following the implantation of metallic devices for trauma or orthopedic ailments. It is still unclear how strong or unstable this equilibrium is.

Influences of ultrasonic treatment on the physicochemical properties and microstructure of diacylglycerol-loaded emulsion stabilized with soybean protein isolate and sodium alginate

This study examined the impacts of ultrasonic power (0, 150, 300, 450, 600, and 750 W) and ultrasonic durations (3, 6, 9, 12, and 15 min) on the physicochemical properties and microstructure of diacylglycerol (DAG)-loaded emulsions stabilized with soybean protein isolate (SPI) and sodium alginate (SA). The findings indicated that the smallest particle size, zeta potential, and contact angle for SPI-SA-DAG emulsions were respectively 5.58 μm, −49.85 mV, and 48.65°, achieved at an ultrasonic power of 450 W. The emulsification properties, loss modulus, storage modulus, and apparent viscosity of the emulsions were optimal at this power setting and at a duration of 9 min. Analytical techniques, including confocal laser scanning-, scanning electron-, and atomic force microscopy, revealed that ultrasonication significantly altered emulsion aggregation state, with the surface roughness (Rq) being minimized at 450 W. These results demonstrated that the stability of SPI-SA-DAG emulsions can be effectively enhanced by an appropriate ultrasonic treatment at 450 W for 9 min. This research provides theoretical support for the broad application of sonication techniques in the food industry.

Formulation and Characterization of Silibinin Entrapped Nano-Liquid Crystals for Activity against Aβ1-42 Neurotoxicity in In-Vivo Model.

Silibinin (SIL) Encapsulated Nanoliquid Crystalline (SIL-NLCs) particles were prepared to study neuroprotective effect against amyloid beta (Aβ1-42) neurotoxicity in Balb/c mice model. Theses NLCs were prepared through hot emulsification and probe sonication technique. The pharmacodynamics was investigatigated on Aβ1-42 intracerebroventricular (ICV) injected Balb/c mice. The particle size, zeta potential and drug loading were optimized to be 153 ± 2.5nm, -21mV, and 8.2%, respectively. Small angle X-ray (SAXS) and electron microscopy revealed to crystalline shape of SIL-NLCs. Thioflavin T (ThT) fluroscence and circular dichroism (CD) techniquewere employed to understand monomer inhibition effect of SIL-NLCs on Aβ1-4. In neurobehavioral studies, SIL-NLCs exhibited enhanced mitigation of memory impairment induced on by Aβ1-42 in T-maze and new object recognition test (NORT). Whereas biochemical and histopathological estimation of brain samples showed reduction in level of Aβ1-42 aggregate, acetylcholine esterase (ACHE) and reactive oxygen species (ROS). SIL-NLCs treated animal group showed higher protection against Aβ1-42 toxicity compared to free SIL and Donopezil (DPZ). Therefore SIL-NLCs promises great prospect in neurodegenerative diseases such as Alzheimer's disease.

Enhanced binding interaction and antibacterial inhibition for nanometal oxide particles activated with Aloe Vulgarize through one-pot ultrasonication techniques

The interaction of green zinc oxide nanoparticles (ZnO NPs) with bacterial strains are still scarcely reported. This work was conducted to study the green-one-pot-synthesized ZnO NPs from the Aloe Vulgarize (AV) leaf peel extract assisted with different sonication techniques followed by the physicochemical, biological activities and molecular docking studies. The NPs structure was analyzed using FTIR, UV–vis and EDX. The morphology, particle size and crystallinity of ZnO NPs were identified using FESEM and XRD. It was found that the formed flower-like structure with sharp edge and fine size of particulates in ZnO NPs/AV could enhance the bacterial inhibition. The minimum inhibitory concentration (MIC) for all the tested bacterial strains is at 3.125 µg/ml and the bacterial growth curve are dependent on the ZnO NPs dosage. The results of disc diffusion revealed that the ZnO NPs/AV possess better antibacterial effect with bigger ZOI due to the presence of AV active ingredient. The molecular docking between active ingredients of AV in the NPs with the protein of IFCM and 1MWU revealed that low binding energy (Ebind = -6.56 kcal/mol and −8.99 kcal/mol, respectively) attributes to the excessive hydrogen bond from AV that highly influenced their interaction with the amino acid of the selected proteins. Finally, the cytotoxicity test on the biosynthesized ZnO NPs with concentration below 20 µg/ml are found nontoxic on the HDF cell. Overall, ZnO NPs/20 % AV (probe sonication) is considered as the best synthesis option due to its efficient one-pot method, short sonication time but own the best antibacterial effect.

Cytotoxic and apoptosis-inducing properties of Staphylococcus aureus cytoplasmic extract on lung cancer cells: Insights from MTT assay and bax/bcl-2 gene expression analysis

BackgroundLung cancer ranks as the second most prevalent cancer in both men and women and stands as one of the most prevalent and lethal malignancies globally. In recent decades, the therapeutic potential of bacteria has gained recognition in pharmaceutical and therapeutic research. While bacteria have historically been associated with cancer causation, recent studies have unveiled their potential as efficacious agents for targeted cancer therapy. However, limited data exist on the characterization and impact of Staphylococcus aureus (S. aureus) extract on lung cancer cell lines. Consequently, this study aims to investigate the effect of S. aureus extract on inducing apoptosis in A549, a lung cancer cell line, and MRC-5, a lung normal cell line, by evaluating the expression levels of the bax and bcl-2 genes. MethodsInitially, cytoplasmic extract of S. aureus was prepared using the sonication technique. The protein concentration was determined via the Bradford assay, and the presence of proteins was confirmed using SDS-PAGE. A549, representing a lung cancer cell line, and MRC-5, representing a lung normal cell line, were exposed to varying concentrations of bacterial extract, and cell viability was assessed using the MTT assay. Subsequently, the expression levels of the bax and bcl-2 genes were quantified utilizing the Real-Time PCR method. ResultsCytoplasmic extract derived from S. aureus demonstrated the ability to modulate the expression levels of apoptotic genes. Relative to the control group, the bax gene exhibited a fivefold overexpression, while the expression of the bcl-2 gene decreased by more than half compared to the control. Furthermore, the results of the MTT assay indicated that the bacterial cytoplasmic extract exhibited concentration-dependent cytotoxicity on cancer cells, highlighting a significant increase in cell death with escalating concentrations. ConclusionsThis research highlights the potential of S. aureus extract for targeted lung cancer therapy by promoting cancer cell apoptosis while sparing normal cells. These findings open up exciting possibilities for innovative cancer treatments and improved patient outcomes, emphasizing the promise of S. aureus extract in the fight against lung cancer.

Lipase-Responsive Lignin Composite Nanoparticles for the Delivery of Insoluble Bioactives.

Low solubility and chemical instability are the main problems with insoluble bioactives. Lignin, with its exceptional biological properties and amphiphilicity, holds promise as a delivery system material. In this study, glycerol esters were incorporated into alkali lignin (AL) through ether and ester bonds, resulting in the successful synthesis of three hydrophobically modified alkali lignins (AL-OA, AL-OGL, and AL-SAN-OGL). Subsequently, lignin composite nanoparticles (LNPs@BC) encapsulating β-carotene were prepared using antisolvent and sonication techniques. The encapsulation rates were determined to be 37.69 ± 2.21%, 84.01 ± 5.55%, 83.82 ± 5.23%, and 83.11 ± 5.85% for LNP@BC-1, LNP@BC-2, LNP@BC-3, and LNP@BC-4, respectively, with AL, AL-OA, AL-OGL, and AL-SAN-OGL serving as the wall materials under optimized preparation conditions. The antioxidant properties and UV-absorbing capacity of the four lignins were characterized, demonstrating their efficacy in enhancing the oxygen and photostability of β-carotene. Following 6 h of UV irradiation, LNP@BC-4 exhibited a retention rate of 83.03 ± 2.85% for β-carotene, while storage under light-protected conditions at 25 °C for 7 days retained 73.33 ± 7.62% of β-carotene. Furthermore, the encapsulated β-carotene demonstrated enhanced thermal and storage stability. In vitro release experiments revealed superior stability of LNPs@BC in simulated gastric fluid (SGF), with β-carotene retention exceeding 77% in both LNP@BC-3 and LNP@BC-4. LNP@BC-4 exhibited the highest bioaccessibility in simulated intestinal fluid (SIF) at 46.96 ± 0.80%, that LNP@BC-1 only achieved 10.87 ± 0.90%. The enzymatic responsiveness of AL-OGL and AL-SAN-OGL was confirmed. Moreover, LNPs@BC exhibited no cytotoxicity toward L929 cells and demonstrated excellent hemocompatibility. In summary, this study introduces a novel enzyme-responsive modified lignin that has promising applications in the fields of food, biomedicine, and animal feed.

Effect of Sm dopant on electrocatalytic activity of AgNbO3 perovskite fabricated by sonication method for Oxygen Evaluation Reaction (OER)

Excessive reliance on fossil fuels causes a variety of difficulties and the use of efficient electrocatalysts material has exhibited significant attention for high electrocatalytic activity. Most transition metal oxide materials performance can be enhanced by the incorporation of metals for OER activity. This work presents the synthesis of samarium (Sm) doped silver niobium oxide (AgNbO3) was achieved using sonication techniques. An electrocatalyst, Sm-doped AgNbO3, has shown promising results for oxygen evolution reaction (OER) in alkaline medium with a significant increase in active sites, enhanced electrical conductivity and improved stability. The Sm-doped AgNbO3 electrocatalyst exhibits overpotential of 203 mV and Tafel slope of 35.22 mV dec−1 for OER activity at current densities of 10 mA cm−2. By utilizing, electrochemical surface area (ECSA), the Sm-doped AgNbO3 electrocatalyst exhibited higher ECSA values of 1009 cm−2 with a higher roughness factor of 2008.60. Further, observations of low charge transfer resistance value (Rct = 0.17 Ω) along with a durability of 50 h, indicate that this material is highly efficient and long-lasting as an electrocatalyst for energy conversion systems.

Wet-spinning of reduced graphene oxide composite fiber by mechanical synergistic effect with graphene scrolling method

Carbon-based fibers have attracted attention in various field owing to their exceptional properties, including high tensile strength, thermal stability, and electrical conductivity. In particular, graphene-based high-strength fibers are promising materials in aerospace, automotive, and marine sectors. Recently, the hybrid fiber, consisting of carbon nanotubes (CNTs) and graphene with enhanced toughness was reported by deflecting cracks and enabling high deformation. However, complex synthesis and structural optimization of composite fiber with two different materials make challenge for mass production. Here, we introduce a novel graphene composite fiber, consisting of reduced graphene oxide (rGO) and scrolled rGO (SrGO), showing remarkable toughness. A multidimensional-state solution with 2D rGO and 1D SrGO was obtained by using a simple sonication technique. Mass production of high-toughness composite fibers was achieved via wet-spinning, with enhanced toughness attributed to microstructure optimization by controlling the SrGO ratio. Additionally, the use of poly(vinyl alcohol) (PVA) as the matrix facilitated high deformation, resulting in a remarkable 90.7 % increase in mechanical toughness without complex composite material synthesis.

CuO/CeAlO3 nanocomposite with enhanced electrocapacitive performance for supercapacitor applications

Developing an efficient system is essential for energy storage, especially sustainable sources of energy, which have expanded significantly in the last few years. However, the fabrication of effective materials proves an aid to solve such crises of high cost and low specific capacitance. Transition and inner transition metal oxides play a significant role in energy storage as well as energy conversion systems. In this research, a novel material CuO/CeAlO3 nanocomposite is synthesized by sonication technique for supercapacitor applications. The different physical methods including X-ray diffractometer (XRD), Raman and Scanning Electron Microscopy (SEM) were employed to analyze the phase purity, structure as well as morphology of the prepared electrode. Electrochemical investigations concluded that the CuO/CeAlO3 nanocomposite exhibited specific capacitance of 1091.98 F/g, high energy density of 56.26 Wh/kg, high power density of 304.55 W/kg at 1 A/g current density as well as high cyclic stability after 5000th cycle with lower charge transfer resistance of 0.09 Ω. The electrochemical characteristics of CuO/CeAlO3 nanocomposite were improved because of the increased area of surface, large active sites and decreased resistance that resulted from the addition of CeAlO3 with CuO. This research showed the great potential of CuO/CeAlO3 nanocomposite along with inexpensive fabrication cost and could be used in next-generation energy storage systems.

Optimizing clozapine-loaded nanostructured lipid carriers through central composite design for enhance bioavailability in antipsychotic therapy

Clozapine (CLZ), a tricyclic dibenzodiazepine antipsychotic drug employed for the treatment of Schizophrenia. However, CLZ's significant first-pass effect, poor water solubility, and low oral bioavailability (27%) limit its potential for therapeutic use. The present investigation aimed to prepare CLZ-loaded nanostructured lipid carriers (NLCs) to improve its solubility, bioavailability, and therapeutic efficacy. The NLCs were prepared using an ultrasonic probe sonication technique using selected solid lipids (Gelucire 44/14), liquid lipids (Labrafil M 1944), and surfactants (Monoemul 80). A central composite design approach was adopted to optimize the NLCs. The optimized CLZ-loaded NLCs were evaluated in terms of particle size, zeta potential, surface morphology, crystallinity, drug loading, and in-vitro CLZ release studies. The optimized CLZ-loaded NLCs showed a particle size, zeta potential, and entrapment efficiency of 115.1 ± 2.48 nm, −17 mV and 96.74 ±1.82%, respectively. The morphology revealed the coarsely spherical shape of NLCs. Fourier transform infrared spectroscopy indicated the physical interaction between the CLZ and lipids rather than chemical interaction. The results of powder X-ray diffraction and differential scanning calorimetry showed the conversion of crystalline to amorphous form of CLZ and distributed molecular level in lipid matrix. In the in-vitro release study, pure CLZ showed 14±1.86% release, whereas CLZ-loaded NLC showed initial burst release (20.0±0.56%) followed by sustained release (69.0±1.03%) up to 24 hours. Collectively, results revealed that the developed novel CLZ-loaded NLCs could be a potential formulation to improve efficacy by increasing solubility and prolonging CLZ release and bioavailability with enhanced patient compliance and reduced side effects.