Surface Plasmon Resonance Band Research Articles

Phyto-mediated synthesis of Ag, ZnO, and Ag/ZnO nanoparticles from leave extract of Solanum macrocarpon: Evaluation of their antioxidant and anticancer activities

Silver, zinc oxide, and silver/zinc oxide nanocomposites were prepared from the facile green process using Solanum macrocarpon leave extract. Ag and ZnO nanoparticles (NPs) were composited with the aim of enhancing the synergy for improved antioxidant and anticancer activities. In the synthesis process, the formation of Ag NPs was initially observed by a colour change and was confirmed by the appearance of surface plasmon resonance (SPR) bands. Based on the crystallographic analysis of the diffraction patterns, the phyto-capped silver NPs possessed a crystalline character, featuring a lattice structure of face-centered cubic (FCC) and an estimated crystallite size of around 7.2 nm. The formation of a hexagonal crystal structure of spherical morphology was confirmed for the ZnO, while the Ag/ZnO composite showed additional planes due to the silver nanoparticles in the cubic phase. The scavenging activities of 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radicals and their anticancer potency on normal HEK and cancerous HELA cells were examined in comparison to standard drugs. They demonstrated remarkable IC50 values that were better than the control drugs. This study provides helpful insight into the synergy between Ag and ZnO nanoparticles for the possible development of new anticancer and antioxidant agents.

A Step Forward for the Treatment of Localized Prostate Cancer Using Gold Nanoparticles Combined with Laser Irradiation.

Prostate cancer (PCA) is the second most common cancer diagnosis in men and the fifth leading cause of death worldwide. The conventional treatments available are beneficial to only a few patients and, in those, some present adverse side effects that eventually affect the quality of life of most patients. Thus, there is an urgent need for effective, less invasive and targeted specific treatments for PCA. Photothermal therapy (PTT) is a minimally invasive therapy that provides a localized effect for tumour cell ablation by activating photothermal agents (PTA) that mediate the conversion of the light beam's energy into heat at the site. As tumours are unable to easily dissipate heat, they become more susceptible to temperature increases. In the PTT field, gold nanoparticles (AuNPs) have been attracting interest as PTA. The aim of this study was to formulate AuNPs capable of remaining retained in the tumour and subsequently generating heat at the tumour site. AuNPs were synthesized and characterized in terms of size, polydispersity index (PdI), zeta potential (ZP), morphology and the surface plasmon resonance (SPR). The safety of AuNPs and their efficacy were assessed using in vitro models. A preliminary in vivo safety assessment of AuNPs with a mean size lower than 200 nm was confirmed. The morphology was spherical-like and the SPR band showed good absorbance at the laser wavelength. Without laser, AuNPs proved to be safe both in vitro (>70% viability) and in vivo. In addition, with laser irradiation, they proved to be relatively effective in PCA cells. Overall, the formulation appears to be promising for use in PTT.

Green synthesis of CdS/flaxseed mucilage nanocomposite films using gamma irradiation for packaging applications

Abstract The most common ways to produce nanoparticles are through chemical and physical processes, which can be expensive and environmentally hazardous. Using plant extracts (green synthesis) as reducing and capping agents is a simple, cost-effective, and environmentally friendly method of lowering the usage of dangerous chemicals in the synthesis of metal nanoparticles. This study covers the environmentally friendly synthesis of cadmium sulphide nanoparticles (CdS NPs) using a blend of flaxseed extracts (FM), polyvinyl alcohol (PVA), and chitosan (Cs). The composites are then exposed to gamma irradiation at doses of 20 kGy and 40 kGy. UV–VIS absorption spectroscopy, SEM, HRTEM, EDX, and FTIR were used to analyse the produced nanocomposite films. UV–Vis absorption spectra showed considerable surface Plasmon resonance (SPR) bands at 396–440 nm, indicating that CdS NPs had been successfully synthesized. A progressive red shift in wavelength was noted, along with the broadening of the absorption band as the irradiation dose increased. Transmission electron microscopy pictures revealed that the generated CdS nanostructures were dispersed as spherical nanoparticles with remarkable structural homogeneity. Tensile strength and elongation measurements of the films revealed that the inclusion of CdS NPs improved their mechanical properties. The addition of CdS NPs to the current blends limits biodegradation in soil. Thermal gravimetric analysis findings showed that CdS NPs included in FM/PVA films had improved thermal stability. The antimicrobial activities of the tested films were performed against Staphylococcus aureus, Escherichia coli, and Candida albicans. The results revealed that all of the films exhibited more antibacterial activity against S. aureus than the two others, with the highest activity observed in nanocomposites with a high concentration of CdS.

Influence the diphenhydramine hydrochloride–sodium carboxymethyl cellulose complex for nanoaggregate formation

This study aimed to create nanoaggregates that improve the synergistic interaction between the opposing charges in drug-polyelectrolyte complexes. In this study, sodium carboxymethyl cellulose (NaCMC) polyelectrolytes and diphenhydramine hydrochloride (DPC) drug molecules were used to form the nanoaggregate. The aggregation behaviour of NaCMC-DPC complexes was determined by using conductivity methods. The critical micelle concentrations (CMC) of NaCMC were reduced from 0.737 to 0.337 g/l in the aqueous and 29.18 mg/l in the DPC. The modified Corrin and Harkins (CH) and Frahm's approaches evaluated the binding efficiency of the NaCMC-DPC interaction. NaCMC-DPC complexes were examined by transmission electron microscopy (TEM) and dynamic light scattering (DLS) techniques to conform to the formation of bilayer vesicles. Furthermore, we prepared the silver nanoparticles by using NaCMC-DPC complex mixtures. We demonstrated how NaCMC-DPC mixtures might influence the self-assembly of silver nanochain designs that differed from open "end-to-end" networks. The results indicated that the assembly of silver nanochains was regulated by a variation of electrostatic interactions inside the NaCMC-DPC components, which organized themselves around anisotropic nanochains surfaces. Among the optical properties altered by the linear assembly, the longitudinal surface plasmon resonance band at 624 nm has an enhanced redshift.

Pharmacological Effect of In Vitro Antioxidant Property and Green Synthesis of Silver Nanoparticles (AgNPs) Utilizing Murraya koenigii Antibacterial Application

ABSTRACT Background: Nonessential heavy metals pose a significant threat to human health due to their toxicity. Mercury, in particular, is identified as a hazardous metal. The study aims to detect mercury using colorimetric analysis with Murraya koenigii, emphasizing the eco-friendliness of the method. Aims and Objectives: The primary objective is to detect mercury using a colorimetric analysis method employing Murraya koenigii. Additionally, the study aims to investigate the eco-friendliness of this detection method. Materials and Methods: Colorimetric analysis was conducted using Murraya koenigii to detect mercury. Ultraviolet-visible (UV-vis) spectroscopy was employed to detect the formation of silver nanoparticles (AgNPs), with a characteristic surface plasmon resonance (SPR) band observed. X-ray diffraction (XRD) data analysis was performed to determine the crystalline nature and size of AgNPs. Scanning electron microscopy (SEM) was utilized to visualize the morphology of AgNPs. Fourier transform infrared (FTIR) spectroscopy was employed to identify functional groups involved in reducing silver ions. Antibacterial properties of synthesized AgNPs were tested against various microorganisms, including Escherichia coli, Staphylococcus aureus, Streptococcus mutans, and Enterococcus faecalis. Results: Mercury was successfully detected using colorimetric analysis with Murraya koenigii. Formation of AgNPs was confirmed by UV-vis spectroscopy, with a characteristic SPR band at 418 nm. AgNPs were found to be crystalline with an average size of 5.20 nm, as determined by XRD analysis. SEM images revealed spherical and polycrystalline AgNPs. FTIR spectra indicated the involvement of the -OH group of compounds in the extract in reducing silver ions. Synthesized AgNPs exhibited antibacterial properties against various microorganisms. Conclusion: A sustainable and eco-friendly method for synthesizing AgNPs using Murraya koenigii extract was successfully developed. This method not only detected mercury but also demonstrated antibacterial properties against various microorganisms. The study underscores the health implications of nonessential heavy metals, emphasizing the importance of eco-friendly detection and mitigation methods.

Synthesize Iron Oxide and Zinc Oxide Nanoparticles Using Plant Extracts

Recently, a plant-mediated approach to synthesizing nanoparticles via unconventional, eco-friendly technique-based techniques involving natural materials was developed. In this work, the microwave method has been used, where Hibiscus rosa sinensis flower extract and Myristica Fragrans have been used as reducers and stabilizers to synthesize iron oxide nanoparticles (α-Fe2O3) and zinc oxide nanoparticles (ZnO), respectively. The melting point and ultraviolet-visible spectrometer (UV-Vis) have been utilized to investigated and characterized the synthesized iron oxide and Zinc oxide nanoparticles. The results showed that the melting point of Fe2O3-NPs and ZnO-NPs were above ~300 °C, which indicated the melting of nanoparticle. Nanoparticles exhibit a significant in melting point as their size goes below ≈10 nm. in addition, the UV-Vis absorption spectra of the synthesized iron oxide NPS show peak surface plasmon resonance (SPR) band around 320 nm and Zinc oxide NPS shown peak surface plasmon resonance (SPR) band around 370 nm. The microwave method has been successfully used in this study, which has advantages over the other methods.

Biogenic silver nanoparticles of Moringa oleifera leaf extract: Characterization and photocatalytic application

Abstract The current study proposed a novel simple and environmentally friendly approach for producing silver nanoparticles (AgNPs) using an extract of Moringa oleifera leaves (MOL) and optimizing the different experimental factors required for the formation and stability of AgNPs. The formation of nanoparticles was confirmed by a color change from yellow to reddish-brown with a surface plasmon resonance band at 412 nm. The morphology, size, and elemental composition of AgNPs were investigated by zeta potential dynamic light scattering, field emission scanning electron microscopy, energy dispersive X-ray, X-ray diffraction, and transmission electron microscopy analysis, which showed crystalline and spherical AgNPs. The identification of functional groups was supported by Fourier-transform infrared spectroscopy. The photocatalytic activities of AgNPs were assessed in the degradation of organic Malachite green (MG) dye in the aqueous solution. Two kinetic adsorption models, the pseudo-first-order model and the pseudo-second-order model, and three isotherm models, the Langmuir, Freundlich, and Temkin, were used to mathematically characterize the MG degradation process. The pseudo-second-order kinetics and the Freundlich isotherm model were found to be in good agreement with the experimental data. As a result of their synergistic interaction with the MOL extract solution, the photocatalytic activity of AgNPs increases and they can successfully adapt to the photodegradation of organic dyes in industrial effluents.

Insights into the role of ionic surfactants on the morphology of gold and gold@silver nanoparticles

Cyanidin-3, 5-di-O-glycoside (anthocyanin) was extracted from the red rose flower petals in an aqueous media. Anthocyanin was used as reductant to the preparation of gold nanoparticles with cationic and anionic surfactants. UV–visible absorption spectroscope, transmission electron microscope, scanning electron microscope, and energy dispersive X-ray spectroscope were employed to determine absorption bands of anthocyanin, surface Plasmon resonance (SPR) band, and morphology of the gold and gold@silver nanoparticles. Anthocyanin exhibited two absorption peaks at 284 and 518 nm, and one shoulder at 328 nm in the UV–visible spectrum. The intensity of these peaks decreases with time after the addition of HAuCl4. The color and the position of SPR band of gold nanoparticles depend on the concentration of gold salt with and without cetyltrimethylammonium bromide (CTAB), and sodium dodecyl sulfate (SDS). The anionic and cationic head groups of SDS and CTAB micelles have significant impact of the morphology of gold nanoparticles. Seedless co-reduction method was used for the synthesis of gold@silver nanoparticles. TEM images clearly indicate the formation of bimetallic gold@silver core-shell nanoparticles. The antioxidant power of AuNPs and gold@silver nanoparticles were tested in terms of the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging activity as a function of different concentrations of nanoparticles.

“Enhancing Fruit Preservation: Fungal Growth Inhibition with Grape Seed‐Mediated Ag@AgCl Nanoparticles through Desirability‐Based Optimization”

AbstractBiological processes were used to create Ag@AgCl nanoparticles in an eco‐friendly manner. Grape seed extracts were used to create Ag@AgCl nanoparticles for this study. The antifungal activity of nanoparticles was tested using fruit‐rotting fungi. UV‐Vis spectrophotometry was used to analyze the nanoparticles to determine the extent of surface plasmon resonance (SPR) band formation. The phytochemicals employed in nanoparticle synthesis were studied using Fourier transform infrared spectroscopy (FT‐IR). X‐ray diffraction (XRD) studies revealed that the Ag@AgCl nanoparticles were crystalline. Field‐emission scanning electron microscopy (FE‐SEM) was used to determine the morphological structure of the nanoparticles. FE‐SEM images determined the average particle size of Ag@AgCl. Energy‐dispersive X‐ray spectroscopy (EDAX was used to examine the elemental composition. Transmission electron microscopy (TEM) and atomic force microscopy (AFM) were employed. Fungi that cause fruit deterioration have been isolated from bananas and papaya fruits. The Ag@AgCl nanoparticles were evaluated for fungal activity against Rhizopus stolonifer, Alternaria species, Aspergillus niger, Aspergillus fumigatus, and Fusarium oxosporum. An agar‐well diffusion study indicated that these nanoparticles had good antifungal sensitivity against fungal infections. However, this study was adequate to allow the inhibitory activity to proceed to the optimization phase, where we dealt with RSM‐based desirability function prediction. The results also demonstrate that the model performs well, implying that it can provide an accurate estimate of output. usingthe impact,the desirability of each factorzoneson

Green synthesis of silver and iron nano composites using aqueous extract of zanthoxylum armatum seeds and their application for removal of acid black 234 dye.

Green nanotechnology has gained attraction in recent years due to the growing awareness of the environmental and health risks associated with traditional methods of nanomaterial synthesis. In the present study, nanocomposite (NCs) of silver and Iron were prepared using Zanthoxylum Armatum seeds aqueous extract which acts as a reducing, stabilizing, and capping agent. The synthesized NCs were characterized using UV/Vis Spectroscopy, powder X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), and EDX. The UV/Vis spectroscopy analysis of the NCs revealed the presence of a surface plasmonic resonance band occurring at 420nm. Examination of the NCs through SEM demonstrated that they exhibited a nearly spherical morphology, with an average particle diameter measuring 54.8nm. The crystalline nature of these NCs was verified through X-ray diffraction (XRD), and the calculation of crystallite size using the Scherrer-Debye equation yielded a value of 12.6nm. The adsorption ability of newly synthesized nanocomposites was investigated against Acid Black 234 Dye. The results showed that a 0.5g of NCs dose at pH 4 removed 99.3% of 10mg/L of Acid Black 234 Dye within 60min. Based on the findings of this research, it can be inferred that the that Ag-Fe NCs synthesized from Zanthoxylum Armatum seeds aqueous extract hold significant potential for addressing environmental pollution caused by Acid Black 234 Dye. The NCs were used as adsorbent for the removal of Acid Black 234 dye from the wastewater sample and showed 98% removal of dye from the commercial sample within 60min. In this context, the research highlights that the environmentally friendly synthesis of Ag-Fe nanocrystals (Ag-Fe NCs) using Zanthoxylum Armatum as a mediator offers an efficient and cost-effective solution for mitigating environmental pollution.

Silver nanoparticles enhanced luminescence of dysprosium ions doped silica sol-gel

Silver (Ag) nanoparticles/dysprosium (Dy3+) ions co-doped in silica Xerogel having the composition of 5Ag-5Dy-90SiO2 (mol%) have been prepared using the sol-gel method. Spectral diagnosis of Ag NPs in both collide solutions and silica Xerogels shows a typical surface plasmon resonance (SPR) band centered around 431 nm and 426 nm, respectively. The nanoscale and polycrystalline structure of AgNPs was revealed through FE-SEM and XRD. Fourier transform infrared spectroscopy (FTIR) analysis illustrates the distribution of these ions (Ag, Dy3+) in the porous structures of silica Xerogels, in which this spectrum did not display bands arising from the bonding of such ions with the silica structure. The absorption and photoluminescence (PL) spectra, as a function of Dy3+ concentrations, have been recorded at room temperature. Prominent emission bands of Dy3+ ions have been observed for 4F9/2 → 6H13/2: 575 nm and 4F9/2 → 6H15/2: 482 nm at 350 nm excitation. The PL of the Dy3+ doped and AgNPs/Dy3+ co-doped silica xerogel clearly showed that silver NPs improve the (PL) intensity of the Dy3+ions spectra, and this is due to the strong local electric field induced by SPR of silver NPs in order to energy transfer from the silver NPs to Dy3+ ions. The emission cross-section (σem.) and the radiative lifetime (τrad) of the transtion4F9/2 → 6H13/2 have been determined for doped and co-doped samples. The white light emission has been investigated and observed through the Commission International deI’Eclairage (CIE) chromaticity diagram, where the colour coordinates are in the white range for all co-doped samples.

Formulation of silver nanoparticles using Duabanga grandiflora leaf extract and evaluation of their versatile therapeutic applications.

The current research focused on the green synthesis of silver nanoparticles (AgNPs) using Duabanga grandiflora leaf extract. The green synthesis of AgNPs was confirmed by the surface plasmon resonance band at 453nm in a UV-Visible analysis. The formulated AgNPs had a diameter of around 99.72nm with a spherical shape. Fourier transform infrared (FTIR) spectrum revealed the bio-reducing potential of phytochemicals present in D. grandiflora, which fundamentally influenced the synthesis of AgNPs. Zeta potential, dynamic light scattering (DLS), scanning electron microscopic (SEM), energy-dispersive X-ray spectroscopic (EDX), X-ray diffraction (XRD), and transmission electron microscopic (TEM) analyses were executed to reveal the physicochemical attributes of the AgNPs. The AgNPs were further investigated for their antioxidant, antidiabetic, anticancer, and antibacterial potential. The DPPH free radical assay revealed the potential radical scavenging capacity (IC50 = 76.73μg/ml) of green synthesized AgNPs. α-Amylase inhibitory assay displayed significant inhibitory potential (IC50 = 162.11μg/ml) of this starch-breaking enzyme by AgNPs, revealing the antidiabetic potential of AgNPs. AgNPs exhibited potential cytotoxic activity (IC50 = 244.57µg/ml) against malignant human kidney cells. In addition, AgNPs showed outstanding antibacterial activity against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacterial strains. Interestingly, AgNPs showed cytotoxic and antimicrobial activities at much higher concentrations than radical scavenging and α-amylase inhibitory concentrations. Thus, our finding elaborated the scope of green synthesized AgNPs for diverse therapeutic applications (dose-dependent) for further clinical translation.

In Vitro Antioxidant Activity of Green-Synthesized Zinc Oxide (ZnO) Nanoparticles Utilizing Extracts From Allium sativum.

The primary objective of this study was to develop an environmentally friendly and efficient method for synthesizing zinc oxide (ZnO) nanoparticles (NPs), utilizing extracts from Allium sativum (garlic) plants, characterizing the synthesized ZnO NPs using various analytical techniques, and assessing their antibacterial and antioxidant properties. The synthesis process involved utilizing extracts from garlic plants to create ZnO NPs. The NPs were subjected to comprehensive characterization through UV-visible (UV-vis) spectroscopy, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray diffraction (XRD). Antibacterial properties were assessed against different microbial strains. In vitro antioxidant properties were evaluated through 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS) assays. Bioactive compounds in the synthesized NPs were also identified. Analysis of the UV-visspectrum confirmed the synthesis of ZnO NPs with an approximate size of 280 nm, as indicated by the absorption peak in the surface plasmon resonance band. FTIR spectroscopy revealed the presence of functional groups such as hydroxyl and carboxyl groups. SEM analysis determined the dimensions of the NPs to be around 11 nm. XRD patterns exhibited distinct Bragg reflections, confirming specific crystallographic planes. In vitro antioxidant assays demonstrated a reduction in absorbance at 517 nm and 734 nm, indicating antioxidant activity. Antibacterial testing revealed inhibition zones against Escherichia coli, Staphylococcus aureus, Streptococcus mutans,and Enterococcus faecalis. The study successfully synthesized ZnO NPs using an eco-friendly method with garlic plant extracts. Characterization techniques confirmed the structural and chemical properties of the NPs. The synthesized NPsexhibited antioxidant and antibacterial activities, showcasing their potential for various applications. The identification of bioactive compounds further contributes to the understanding of the biological properties of the synthesized NPs.

Biosynthesis of gold nanoparticles mediated by medicinal phytometabolites: An effective tool against Plasmodium falciparum and human breast cancer cells

Gold nanoparticles (AuNPs) were synthesized using leaf extracts obtained from the medicinal plants Abutilon theophrasti Medik., Origanum majorana L., Euphorbia hirta L., and Senna auriculata (L.) Roxb. The in vitro antiplasmodial and anticancer activities of AuNPs were assessed against blood-stage malaria parasites and human breast cancer cells, respectively. AuNPs were examined using UV-VIS spectroscopy, HRTEM, DLS, zeta potential, XRD, and FTIR. All the AuNPs exhibited the surface plasmon resonance (SPR) band around 530 nm, which supports the formation of gold particles. The FTIR indicated possible bioactive molecules as constituents of the AuNPs formed. The fluorescence based SYBR Green I assay was utilized to investigate the anti-plasmodial action of AuNPs on the erythrocytic phases of 3D7 (chloroquine drug-sensitive) and INDO (chloroquine drug-resistant) strains of Plasmodium falciparum. The anti-plasmodial IC50 values of the synthesized A. theophrasti AuNPs (N1), O. majorana AuNPs (N2), E. hirta AuNPs (N3), and S. auriculata AuNPs (N4) were 76, 60, 32, and 20 against Pf3D7, and >100, 48, 72, and 36 μg/mL against PfINDO, respectively. N4 showed the highest activity against both P. falciparum strains and also exhibited a high CC50 (480 μg/mL) against human embryonic kidney (HEK293) cells, which leads to a great selectivity index of 24. The in vitro anticancer potential of AuNPs (N1, N2, N3, and N4) was assessed using MCF-7 cells, and the IC50 values were 8.25, 20.25, 20.40, and 24.49 μg/mL, respectively. The present study demonstrated that AuNPs derived from plant extracts may be useful therapeutic agents for treating human breast cancer and malaria.

Selective Colorimetric Detection of Pb(II) Ions by Using Green Synthesized Gold Nanoparticles with Orange Peel Extract

Gold nanoparticles (AuNPs) were prepared by using a green approach that employed orange (citrus sinensis) peel water extract (OPE) as a reducing agent. In this case, the organic compounds present in orange peel were able to reduce Au(III) to Au(0) and, at the same time, to act as a capping agent, functionalizing the surface of the AuNPs, stabilizing them in a water solution. This “green” approach valorizes orange peel waste as a resourceful material and makes the synthetic process of AuNPs more environmentally sustainable, safe, and economically feasible than the traditional methods. The obtained gold nanoparticles (AuNPs@OPE) were characterized by FT–IR, DLS, SEM analysis, and UV–Vis spectroscopy; the latter showed a characteristic surface plasmon resonance (SPR) band at 530 nm, typical of spherical gold nanoparticles. The AuNPs@OPE were then tested as colorimetric sensors for heavy metals in water, showing an affinity and selectivity toward Pb2+. In fact, in the presence of Pb2+, the added cation favors the aggregation process, and, in this case, nanoparticles form clusters due to the interactions between Pb2+ and the carboxyl/hydroxyl groups on the surface of the AuNPs@OPE, increasing the size of the nanostructure. This process is accompanied by a change in color of the AuNPs@OPE from pink to violet, with a formation of a second, new SPR band, at a higher wavelength, relative to the aggregate formation. The colorimetric assay was tested at different times with the addition of Pb2+ ions showing different LOD values of 13.31 µM and 0.05 µM after 15 min and 90 min, respectively. The proposed colorimetric assay was also tested for analyzing Pb2+ in drinking water samples demonstrating the reliability to use AuNPs@OPE with real samples.

In Situ Preparation of Dehydrodieugenol-Loaded Silver Nanoparticles and their Antischistosomal Activity.

Schistosomiasis is a major neglected disease that imposes a substantial worldwide health burden, affecting approximately 250 million people globally. As praziquantel is the only available drug to treat schistosomiasis, there is a critical need to identify new anthelmintic compounds, particularly from natural sources. To enhance the activity of different natural products, one potential avenue involves its combination with silver nanoparticles (AgNP). Based on this approach, a one-step green method for the in situ preparation of dehydrodieugenol (DHDG) by oxidation coupling reaction using silver and natural eugenol is presented. AgNP formation was confirmed by UV-Vis spectroscopy due to the appearance of the surface plasmon resonance (SPR) band at 430 nm which is characteristic of silver nanoparticles. The nanoparticles were spherical with sizes in the range of 40 to 50 nm. Bioassays demonstrated that the silver nanoparticles loaded with DHDG exhibited significant anthelmintic activity against Schistosoma mansoni adult worms without toxicity to mammalian cells and an in vivo animal model (Caenorhabditis elegans), contributing to the development of new prototypes based on natural products for the treatment of schistosomiasis.

Experimental and Theoretical Studies on Ag Nanoparticles with Enhanced Plasmonic Response, Formed Within Al2O3 Thin Films Deposited by Magnetron Sputtering

AbstractReactive magnetron sputtering was employed to prepare nanocomposite thin films of Ag/Al2O3, on a glass substrate. The films are characterized by the formation of Ag nanoparticles embedded in the Al2O3 matrix, after thermal treatment at 600 °C, which are responsible for the appearance of an outstanding pronounced and narrow localized surface plasmon resonance (LSPR) band. Electron microscopy analysis also revealed the presence of larger Ag fractal aggregates at the film’s surface, responsible for a broad band absorption. Noteworthily, the LSPR band maximum remains at the same position (about 412 nm) for Ag concentrations ranging from 23 to 34 at.%, despite some discernible alterations in both LSPR band intensity and width. An optimized thin film is characterized by full transparency in non-resonant wavelengths due to suppression of Ag aggregates at the film’s surface, while maintaining the LSPR behavior. To better explain the plasmonic behavior of the Ag/Al2O3 films, discrete dipole approximation was used to determine the extinction, scattering, and absorption efficiencies of Ag spheres surrounded by an Al2O3 cap layer. This allowed to ascertain some nanostructural features of the films, pointing to the formation of Ag nanoparticles with average sizes in the order of 40 nm.

Green Synthesis of Zinc Oxide Nanoparticles Using Clove Oil Extract (Syzygium aromaticum) and Evaluate their Antibacterial Activity against MRSA

There is a crucial need for the development of effective antimicrobial agents due to the rising incidence of hospital-acquired bacterial infections caused by multidrug-resistant microbes, leading to significant mortality and morbidity worldwide. Therefore, the current study aimed to synthesize zinc oxide nanoparticles (SaZnONPs) using clove extract through an environmentally friendly technique and to investigate their antibacterial activity against MRSA (Staphylococcus aureus). Clove extract acts as both a capping and reducing agent in the formation of ZnO-NPs. The formation of SaZnONPs was confirmed using various analytical techniques. Initially, clove extract was incubated with a zinc nitrate solution, and the subsequent change in color of the solution indicated the reduction of zinc nitrate ions to ZnO nanoparticles. UV-visible spectroscopy revealed a surface plasmon resonance band of SaZnONPs at 329.26 nm. Additionally, SEM imaging indicated that the nanoparticles had an average size of 41 nm and exhibited a spherical shape. The antibacterial activity of SaZnONPs was evaluated against MRSA using agar well diffusion and minimum inhibitory concentration assays. The phytochemicals present in clove extract facilitated the synthesis of stable ZnO-NPs, demonstrating promising antibacterial properties.

Insights into the impact of surfactants on the kinetics of selenium nanoparticles formation via lemon juice-assisted methodology, followed by their antibacterial and antioxidant assessment

Selenium nanoparticles (Se NPs) fabrication utilizing active species of natural lemon juice represents a promising pathway in the biosynthesis of nanoparticles. The reduction of Se4+ to Se(0) could be attributed to the presence of natural lemon juice, which was considered a supplier of vitamin C, polyphenolic compounds, flavonoids, and sugars. The synthesized spherical Se NPs exhibited a characteristic surface plasmon resonance band (SPR) at λ = 320 nm. The values of the rate constant for the reduction of Se (IV) to Se (0) by lemon juice were estimated to be kobs = 0.0011 s−1 for a Se concentration of 0.75 mmol.dm−3 and a lemon content of 0.001 mol.dm−3 at room temperature. Various conditions have been studied on the kinetics of Se NPs formation, such as the doses of SeO2 and lemon juice, and the presence of cationic and/or anionic surfactants like cetyltrimethyl ammonium bromide (CTABr) and sodium dodecyl sulfate (SDS), respectively. The synthesized Se particles were characterized by physicochemical techniques such as FT-IR, XRD, TEM, DLS, and zeta potential to investigate their main functional groups, crystallinity, chemical composition, particle size, and surface morphology. Moreover, the antioxidant power of Se NPs was tested in terms of their DPPH free radical scavenging activity. Finally, the antibacterial activity of the studied nanoparticles was confirmed against gram-positive and gram-negative bacteria (Staphylococcus aureus and Pseudomonas aeruginosa, respectively). In short, this study introduced the impact of surfactants on the formation of biocompatible Se NPs as an active antibacterial and antioxidant.

Photocatalytically active Ag-doped TiO2 coatings developed by plasma electrolytic oxidation in the presence of colloidal Ag nanoparticles

The plasma electrolytic oxidation process of Ti foil in the presence of a colloidal solution of Ag nanoparticles was used for the synthesis of exceptionally photocatalytically active Ag-doped TiO2 coatings. UV–Vis absorption spectroscopy was applied to follow the changes in the surface plasmon resonance band of the Ag nanoparticles as a function of the Ag:PO43− ratio in a phosphate-based electrolyte solution. Transmission electron microscopy revealed the size of the Ag nanoparticles in the range of 3–12 nm. The XRD patterns of the Ag-doped TiO2 coatings confirmed the crystalline anatase TiO2 phase regardless of the dopant concentration and without metallic Ag or crystalline Ag oxide forms. The typical porous morphology of the Ag–TiO2 coatings was observed by scanning electron microscopy. A significantly improved photocatalytic activity of the Ag–TiO2 coatings in the degradation process of the insecticide lindane (gamma isomer of benzene hexachloride) and test molecule methyl orange compared to pure TiO2 was determined using the GC technique. The degradation efficiency of Ag-doped TiO2 coatings is higher for lindane than for methyl orange.