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A novel class of nanomaterials as subunit nano vaccines has shown great potential for delivering antigens to the target in a safe and effective manner. Herein, functionalized superparamagnetic iron oxide nanoparticle (SPION) surfaces with conjugated a malaria protein (vaccine) and carboxyl groups have a comparatively high capacity to bind protein. SPIONs were synthesized using the chemical coprecipitation process, then coated with either 3-aminopropyltriethoxysilane or with PEG plus APTS and characterized using DSL-zeta potential, VSM, TG and SEM. Furthermore, SDS-PAGE was used to measure the amount of protein specifically attached to particles. The idea behind this project is that by gradually and continuously releasing the antigen, it could trigger and sustain a strong immune response over an extended period. The results showed that functionalized SPIONs conjugated to the PyMSP119 antigen might be exploited for the antigen's controlled release and could be applied to various types of antigens in the future. The current study results demonstrated the effectiveness of SPIONS-based antigen vaccination systems for eliciting antibody responses that may be suitable for a variety of illnesses not just malaria. [ABSTRACT FROM AUTHOR]

To synthesize silver nanoparticles suspended in deionized water, Elettaria cardamomum (Car) seed extract and Car@Ag nanoparticles were prepared in three steps. The first used a hot aqueous extract of Elettaria cardamomum seed, and then, the second used pulsed laser ablation technique (PLAL) by Nd:YAG laser (λ = 1064 nm wavelength) at laser energy of 400 mJ, and the number of pulses was 500 pulses and third step for the synthesis of creating a non-conjugated Elettaria cardamomum extract. Ultraviolet visible (UV–Vis) spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared (FTIR) were used to investigate the optical, structural, and morphological characterizations of synthesized Car@AgNPs. The nanoparticles were spherical in shape, and a size distribution exhibited a mean size of 21 nm, according to the TEM findings. AgNPs and Car@AgNPs have free radical scavenging activity in the DPPH assay. Additionally, Car@AgNPs were examined in vitro for zones of inhibition against pathogenic bacteria like Escherichia coli and Staphylococcus aureus. The inhibition rate of Escherichia coli was higher than that observed in Staphylococcus aureus. Finally, Car@AgNPs demonstrated a potential cytotoxicity agent breast cancer (MCF-7) cell line that was evaluated by MTT assay. [ABSTRACT FROM AUTHOR]

This contribution presents the biosynthesis, physiochemical properties, toxicity and photocatalytic activity of biogenic CeO2 NPs using, for the first time, marine oyster extract as an effective and rich source of bioreducing and capping/stabilizing agents in a one-pot recipe. CeO2 NPs formation was initially confirmed through the color change from light green to pale yellow and subsequently, their corresponding absorption peak was spectroscopically determined at 310 nm with an optical band-gap of 4.67 eV using the DR-UV technique. Further, XRD and Raman analyses indicated that nanoceria possessed face-centered cubic arrangements without any impurities, having an average crystallite size of 10 nm. TEM and SEM results revealed that biogenic CeO2 NPs was approximately spherical in shape with a median particle size of 15 ± 1 nm. The presence of various bioorganic substances on the surface of nanoparticles was deduced by FTIR and TGA results. It is found that marine-based nanoceria shows no cytotoxic effect on the normal cell, thus indicating their enhanced biocompatibility and biosafety to living organisms. Environmentally, due to energy band gap, visible light-activated CeO2 nanocatalyst revealed superior photocatalytic performance on degradation of methylene blue pollutant with removal rate of 99%. Owing to the simplicity, cost-effectiveness, and environmentally friendly nature, this novel marine biosynthetic route paves the way for prospective applications of nanoparticles in various areas. [ABSTRACT FROM AUTHOR]

Waste-water pollution by radioactive elements such as uranium has emerged as a major issue that might seriously harm human health. Graphene oxide, graphene oxide nanoribbons, and sodium alginate nanocomposite aerogels (GO/GONRs/SA) were combined to create a novel nanocomposite using a modified Hummer's process and freeze-drying as an efficient adsorbent. Batch studies were conducted to determine the adsorption of uranium (VI) by aerogel. Aerogels composed of (GO/GONRs/SA) were used as an effective adsorbent for the removal of U (VI) from aqueous solution. Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to describe the structure, morphologies, and characteristics of (GO/GONRs/SA) aerogels. The initial concentration of uranium (VI) and other environmental factors on U (VI) adsorption were investigated, period of contact, pH, and temperature. A pseudo-second-order kinetic model can be employed to characterize the kinetics of U (VI) adsorption onto aerogels. The Langmuir model could be applied to understand the adsorption isotherm, and the maximum adsorption capacity was 929.16 mg/g. The adsorption reaction is endothermic and occurs spontaneously. [ABSTRACT FROM AUTHOR]

In this work, gold nanoparticles (NPs) have been synthesized using second harmonic generation ND-YAG laser ablation in ethanol employing 532 nm and 1.064 nm wavelengths. Field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), atomic force microscopy (AFM), photoluminescence (PL) spectroscopy, and UV–Vis absorption were employed to examine the structural, chemical, and optical properties of Au NPs. XRD results showed that all synthesized Au nanoparticles are crystalline in nature. The optical band gap upon ablation using the higher wavelength (1064 nm) was about 4.02 eV. The value of the optical band gap increases to reach a value of 4.22 eV at the shorter wavelength (532 nm). The FESEM results reveal the formation of smaller nanorod size at second harmonic generation (SHG) wavelength was found to be about 30 nm at wavelength 532 nm and 44 nm at 1064 nm. After that, finite element analysis is used to simulate the photonic crystal fiber (PCF) as biosensors, depending on the surface plasmon resonance (SPR) phenomenon using the COMSOL multiphasic program. The hollow core photonic crystal fiber (HC-PCF) HC-800 was thus overfilled with water. The confinement loss (CL) of the fundamental mode for the proposed PCF with and without the gold nanoparticles was calculated; we observe without gold NPs the CL at the water and colon tissue about 1.08E + 03 and 5.46E + 02 dB/m, while at use the deposited PCF with gold NPs, the results ensured the decrease more than in the confinement loss at the water and colon tissue about 1.01E + 03 and 3.16E + 02 dB/m with a clear shift toward higher wavelengths, also when calculating the sensitivity, to increase HC-PCF biosensor performance by using wavelength interrogation and amplitude measurements; it found the bio-liquid (colon tissue) has the best electric field using the gold nanowire (NW) layer in the biosensor equal to 68.8 V/m by comparison when without using the gold NW layer which leads to high sensitivity. [ABSTRACT FROM AUTHOR]

Combining viruses and nanoparticles may be a way to successfully treat cancer and minimize adverse effects. The current work aimed to evaluate the efficacy of a specific combination of gold nanoparticles (GNPs) and Newcastle disease virus (NDV) to enhance the antitumor effect of breast cancer in both in vitro and in vivo models. Two human breast cancer cell lines (MCF-7 and AMJ-13) and a normal epithelial cell line (HBL-100) were used and treated with NDV and/or GNPs. The MTT assay was used to study the anticancer potentials of NDV and GNP. The colony formation assay and apoptosis markers were used to confirm the killing mechanisms of NDV and GNP against breast cancer cell lines. p53 and caspase-9 expression tested by the qRT-PCR technique. Our results showed that combination therapy had a significant killing effect against breast cancer cells. The findings demonstrated that NDV and GNPs induced apoptosis in cancer cells by activating caspase-9, the p53 protein, and other proteins related to apoptosis, which holds promise as a combination therapy for breast cancer. [ABSTRACT FROM AUTHOR]

Under conventional and silica-supported Muffle furnace methods, water-soluble substituted trimeric triaryl pyridinium cations with various inorganic counter anions are synthesized. The solvent-free synthesis method is superior to the conventional method in terms of non-toxicity, quicker reaction times, ease of workup, and higher yields. Trimeric substituted pyridinium salts acted as excellent catalytic responses for the preparation of Gem-bisamide derivatives compared with available literature. To evaluate the molecular docking, benzyl/4-nitrobenzyl substituted triaryl pyridinium salt compounds with VEGFR-2 kinase were used with H-bonds, π–π stacking, salt bridges, and hydrophobic contacts. The results showed that the VEGFR-2 kinase protein had the most potent inhibitory activity. Intriguingly, the compound [NBTAPy]PF6- had a strongly binds to VEGFR-2 kinase and controlled its activity in cancer treatment and prevention. [ABSTRACT FROM AUTHOR]

This study investigated for the first time a simple bio-synthesis approach for the synthesis of copper oxide nanoparticles (CuO NPs) using Annona muricata L (A. muricata) plant extract to test their anti-cancer effects. The presence of CuONPs was confirmed by UV–visible spectroscopy, Scanning electron microscope (SEM), and Transmission electron microscope (TEM). The antiproliferative properties of the synthesized nanoparticles were evaluated against (AMJ-13), (MCF-7) breast cancer cell lines, and the human breast epithelial cell line (HBL-100) as healthy cells. This study indicates that CuONPs reduced cell proliferation for AMJ-13 and MCF-7. HBL-100 cells were not significantly inhibited for several concentration levels or test periods. The outcomes suggest that the prepared copper oxide nanoparticles acted against the growth of specific cell lines observed in breast cancer. It was observed that cancer cells had minor colony creation after 24 h sustained CuONPs exposure using (IC50) concentration for AMJ-13 was (17.04 µg mL−1). While for MCF-7 cells was (18.92 µg mL−1). It indicates the uptake of CuONPs by cancer cells, triggering apoptosis. Moreover, treatment with CuONPs enhanced Lactate dehydrogenase (LDH) production, probably caused by cell membrane damage, creating leaks comprising cellular substances like lactate dehydrogenase. Hence, research results suggested that the synthesized CuONPs precipitated anti-proliferative effects by triggering cell death through apoptosis. [ABSTRACT FROM AUTHOR]

Silver Oxide nanoparticles (AgONPs) have been revealed to have many applications, including antibacterial behavior. However, the conventional methods for synthesizing AgO NPs often use toxic chemicals that may be detrimental to human health and environmental factors. The crystalline structure and size of obtained AgO NPs were confirmed by Powder X-ray diffraction analysis with 35–70 nm. Functional groups have been identified in Fourier transform infrared spectroscopy. The result of Energy Dispersive X-ray Spectroscopy confirmed the presence of the elements in the synthesized AgO NPs. The energy band gap is determined using UV–visible spectroscopy. Morphological examination of prepared AgO NPs, comprising spherical and rod-like structures, was performed using a Transmission, and scanning electron microscope. The antibacterial activity was evaluated using Gram-negative (Klebsiella pneumonia, Escherichia coli) and Gram-positive (Staphylococcus aureus, Bacillus cereus) bacteria from Agar Well Diffusion Method. The results show that the green synthesis of AgO NPs have better antibacterial activity. The inhibition zone diameter were observedfor all microorganisms. The green synthesis of AgO NPs from herbal plant leaf extracts is a promising method for developing safe and effective antibacterial agents. [ABSTRACT FROM AUTHOR]

In this contribution, we report the screening of different parameters contributing to the electrodeposition of Cu2O nanostructures as an electrode material to provide an overall understanding of the effect of the entire method conditions. We varied different parameters (pH, potential, and deposition time) during the electrodeposition of cuprous oxide (Cu2O) thin films on ITO glass substrate and integrated different methods: X-ray diffraction (XRD), UV-vis absorption (UV-Vis), scanning electron microscope (SEM), cyclic voltammetry (CV), and chronoamperometry (CA) to deeply examine the as-synthesized materials and interrogate their efficiency towards the conversion of light to current (photo-current). From the chronoamperometry experiments, all the curves of current transients exhibit a typical response of a progressive 3D nucleation growth. Highly crystalline Cu2O structures of nano-cubes can be seen in the XRD and SEM results at high pH (12.5) and at potentials -0.5 and -0.6 V Vs. SCE during 60 min of deposition time. UV-Vis results showed high optical absorption in the region of 300-500 nm. The photocurrent measurements of Cu2O coupled with Cu-doped ZnO suggested that the synthesized Cu2O proved to be the best candidate as a solar cell. [ABSTRACT FROM AUTHOR]

With the demand for better chronic wound care, the clinical problem of managing wound infections has already reached a critical level. Therefore, the development of novel antibiotic-free wound dressings is essential for wound care. The proteolytic enzyme bromelain, silver nanoparticles (AgNPs), and bromelain loaded on silver nanoparticles (Br-AgNPs) were assessed for their impact on wound healing in the albino mice. The formulated nanoparticles were characterized using different techniques, i.e., ultraviolet (UV), Fourier transform infrared (FTIR), and X-ray diffraction (XRD) analysis. The antibacterial and fungal activities of the formulated nanoparticles were also investigated. After 5 days of treatment, the wound healing progression and wound size reduction rate were monitored. In addition, serum and skin tissue samples were collected to assess the changes in inflammation levels and observe the histological changes. The results indicated a spherical shape and regular distribution of the synthesized gold nanoparticles, with an average particle size of 41.33–61.30 nm, where the size was about 39.84 and 82.91 nm after loading bromelain. The Br-AgNPs were the most active antimicrobial agents against Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Candida albicans, as compared to the other samples and positive controls. The fibronectin and collagen III levels were significantly increased in the animal groups treated with bromelain and Br-AgNPs (7132.52 ± 324.67 and 7006.00 ± 565.19 pg/ml, respectively), compared to the negative control group. Moreover, wound closure was significantly enhanced in the Br-AgNP-treated animals compared to the other treated and control groups. The histopathological analysis supported the wound healing potential of the Br-AgNPs through their ability to induce dense fibrous connective tissue in the wound area, which was rich in irregular bundles of collagen fibers and interspersed with numerous fibroblasts. The present findings could provide valuable insight into how Br-AgNPs can accelerate wound healing, reduce recovery time, and provide an antimicrobial barrier for wounds. [ABSTRACT FROM AUTHOR]

In the present work, raw materials, namely zinc acetate dihydrate, iron nitrate nonahydrate, and solvent 2-methoxyethanol, were utilized to synthesize zinc ferrite nanoparticles by sol–gel method. The synthesized material was annealed at different temperatures of 500 °C, 600 °C, and 700 °C to study its effect on morphological, optical, and magnetic properties. Formation of single phase spinel cubic structure with intense peak orientation along (311) direction was confirmed by powder X-ray diffraction pattern. FESEM and EDX spectra of the annealed samples confirmed the surface morphology and elemental composition. UV–visible spectral analysis was used to examine the optical properties of the samples. VSM at room temperature revealed the ferromagnetic behavior of zinc ferrite nanoparticles. All the prepared samples at different annealing temperatures showed good antibacterial properties against different bacterial strains. [ABSTRACT FROM AUTHOR]