Surface Plasmon Resonance Band Research Articles

Plant-assisted green preparation of silver nanoparticles using leaf extract of Dalbergia sissoo and their antioxidant, antibacterial and catalytic applications.

Plant-mediated preparation of silver nanoparticles (AgNPs) is thought to be a more economical and environmentally benign process in comparison to physical and chemical synthesis methods. In the present study, the aqueous leaf extract of Dalbergia sissoo was prepared and utilized to reduce silver ion (Ag+) during the green synthesis of silver nanoparticles (DL-AgNPs). The formation of DL-AgNPs was verified using UV-Vis spectra, exhibiting the surface plasmon resonance (SPR) band at around 450nm. FT-IR analysis revealed the kinds of phytochemicals that serve as reducing and capping agents while DL-AgNPs are being synthesized. Analysis of scanning electron microscope (SEM) and high-resolution transmission electron microscopy (HR-TEM) images verified the development of spherical and oval-shaped DL-AgNPs, with sizes ranging from 10 to 25nm. The stability and particle size distribution of synthesized DL-AgNPs were ensured by zeta potential and DLS (dynamic light scattering) investigations. Additionally, X-ray diffraction (XRD) analysis confirmed the crystalline nature of DL-AgNPs. In antioxidant experiments, DL-AgNPs demonstrated significant scavenging capacities of DPPH and ABTS radicals with EC50 values of 51.32 and 33.32μg/mL, respectively. The antibacterial activity of DL-AgNPs was shown to be significant against harmful bacteria, with a maximum zone of inhibition (21.5 ± 0.86mm) against Staphylococcus aureus. Furthermore, DL-AgNPs exhibited effective catalytic activity to degrade environment-polluting dyes (methylene blue, methyl orange, and Congo red) and toxic chemicals (p-nitrophenol). The results of all these studies suggested that DL-AgNPs made from the leaf extract of Dalbergia sissoo have merit for application in the environmental and biomedical fields.

Insights on the effect of process conditions on the optical properties of silver ion exchanged soda-lime silicate glass

The effects of ion exchange time and temperature on the optical properties and plasmonic response of silver ion exchanged soda-lime silicate glass were investigated using scanning electron microscopy (SEM) in energy dispersive spectrometry (EDS) configuration, m-lines spectroscopy, photoluminescence (PL) spectroscopy, and UV–visible absorption spectroscopy. SEM analyses in EDS mode provided profiles of silver oxide molar concentration. These profiles were directly correlated to the silver diffusion coefficient using an adjustment procedure. The effective indices of ion exchanged glasses measured by the standard prism coupling technique (m-lines) allowed access to refractive index distributions in ion exchange regions. These ion-exchanged glasses underwent evaluation to determine their potential suitability for use in multimode planar systems. The PL results acquired after ion exchange demonstrated that the creation of Ag0 atoms from Ag+ ions was responsible for the decline and quenching of PL intensity at ion exchange times and temperatures increase. Silver nanoparticles were generated in the samples subjected to ion exchange at 480 °C without the need for post-exchange treatments. The emergence of the surface plasmon resonance band around 427 nm in the optical absorption spectra confirmed the formation of Ag nanoparticles in annealed glasses. Estimates of the UV–visible absorption spectra indicated an average size of silver nanoparticles ranging from 1.8 to 2.4 nm.

Ag nanocubes-decorated ammonium hydroxide-treated carbon nitride to improve photocatalytic H2O2 production and fuel cell performance

A novel photocatalyst is designed by surface modification and cocatalyst loading of graphitic carbon nitride (g-C3N4) with ammonium hydroxide and silver nanocubes (AgNCs), respectively. The synergistic effect of the modification in the intralayer of g-C3N4 and surface plasmon resonance (SPR) bands of AgNCs significantly enhances the migration and separation efficiency of photo-induced charge carriers. A nickel mesh coated with photocatalyst and the carbon paper loaded with pristine g–C3N4–mixed iron phthalocyanine (FeIIPc) used as the photoanode and cathode, respectively, are constructed for the self-powered photoelectrochemical cell, which exhibits the maximum power density of 0.74 mW cm−2. The AHCN/AgNCs-based cell reveals approximately a 3.1-times enhancement in maximum power density compared with the pristine g–C3N4–based cell. In addition, the photocatalytically generated H2O2 (chemical energy) can be stored in water, and then used as fuel by the connection of two electrodes in the dark. After the fuel cell is operated for 12 h, the specific capacitance retention rate still maintains as high as 57.2 %, which is the greatest retention rate in comparison with the previously reported H2O2 fuel cell systems. Our work offers a feasible opinion on how to improve the visible light utilization of semiconductors by tuning the intralayer properties and loading plasmonic metal.

Development of PVA/sodium alginate incorporated with histidine capped silver nanoparticles for food packaging application

AbstractPackaging is a growing field of interest, and the use of nanotechnology is accelerating its expansion. The study reports the fabrication of poly(vinyl alcohol) (PVA) blended sodium alginate (SA) and incorporated with different ratios of histidine‐capped silver (H‐AgNPs) nanoparticle films. Fabrication of PVA/SA/H‐AgNPs films was confirmed with the surface plasmon resonance (SPR) band denoted AgNPs presence between 400 and 420 nm measured by UV–Vis absorption spectroscopy. The characteristics of the polymeric biocomposite films were significantly altered by different ratios of AgNPs. The interaction of PVA/SA and PVA/SA with AgNPs was analyzed by using FT‐IR analysis. The degree of crystallinity was increased upon increasing the concentration of H‐AgNPs as confirmed by XRD measurements. The homogeneity of dispersion and surface morphology of samples were studied by FESEM. The addition of H‐AgNPs in the polymeric film increased the surface roughness of the polymeric film confirmed by AFM analysis. The contact angle of the PVA/SA blend matrix was observed to be 46.97°, and with the incorporation of AgNPs ranging from 3%, 5%, and 7% to the blend matrix, the contact angle of the nanocomposite films in increasing hydrophobic order was 60.53°, 83.57°, and 96.20°, respectively. The incorporation of AgNPs also demonstrates that the PVA/SA blend matrix has desirable thermal stability. The improved qualities were due to H bonding between PVA, SA, and H‐AgNPs, in which molecules contact strongly with one another. Furthermore, the PVA/SA/H‐AgNPs showed significant antibacterial activity against both Gram‐positive (G+) strains (Staphylococcus aureus) and Gram‐negative (G−) strains (Escherichia coli) bacterial infections. The findings of this research indicate that the PVA/SA/H‐AgNPs fabricated composite films considerable for applications in food packaging.

Antibacterial properties of synthesized Melaleuca cajuputi-leaf gold nanoparticles

Biosynthesized gold nanoparticles (AuNPs) were successfully synthesized by using Melaleuca cajuputi leaf extract, and their prospective antibacterial efficacy was assessed against Vibrio parahaemolyticus. TEM analysis revealed biosynthesized M. cajuputi gold nanoparticles (MC-AuNPs) were spherical in shape with a surface plasmon resonance (SPR) band observed at 535 nm and particle sizes ranging from 10–50 nm. The MC-AuNPs showed good antibacterial properties against V. parahaemolyticus with MIC and MBC values of 0.0075 g/mL.

Evaluation of PVC@Silver Nanocomposite as Sensor for Low Limit Detection of Cadmium Ion By Surface Plasmon Resonance Based Method

AbstractThis study explores the development of a PVC@Silver nanocomposite for enhanced detection of cadmium ions in water samples. Various characterization techniques confirmed the successful incorporation of silver nanoparticles into the polyvinyl chloride (PVC) matrix across different concentrations (1–4%). X-ray diffraction revealed the face-centered cubic crystalline structure of the silver nanoparticles, with the intensities of the (111), (200), (220), and (311) peaks increasing with higher Ag concentrations. The average crystallite sizes ranged from 26.1 nm (3% Ag) to 30.0 nm (2% Ag). Dynamic light scattering showed nanoparticle sizes of 24–43 nm, while zeta potential values of -24 to -40 mV indicated reasonable colloidal stability. Brunauer–Emmett–Teller (BET) surface area analysis demonstrated a decreasing surface area from 30.09 m2/g (1% Ag) to 25.27 m2/g (3% Ag), attributed to pore filling by silver nanostructures. Significantly, the PVC@Silver nanocomposite facilitated sensitive detection of Cd(II) ions using surface plasmon resonance (SPR), exhibiting an SPR angle shift of 26.30° with intensity values ranging from 10.80 (4% Ag) to 12.19 (3% Ag). UV–vis spectra revealed a prominent surface plasmon resonance band at 420–430 nm, indicating the presence of silver nanoparticles. The optical band gap varied from 4.51eV (1% Ag) to 4.12eV (4% Ag).

Weak plasmonic photocatalysis in unsupported colloidal gold nanorods

Metal-semiconductor plasmonic nanosystems have the ability to extract photocarriers generated on colloidal gold nanoparticles efficiently through the Schottky junction. This process leads to effective visible light photocatalysis. However, due to the short lifespan of plasmon carriers, plasmonic loss occurs before extraction by the semiconductor and transfer to the adsorbent. We aim to investigate the direct transfer of plasmonic energy to adsorbed organic pollutants in visible light photocatalysis using unsupported colloidal gold nanorods (Au NRs). Our decision to use gold nanorods is based on their exceptional ability to harness a greater amount of visible light through their longitudinal surface plasmon resonance (LSPR) at 765 nm and transverse surface plasmon resonance (TSPR) band at 521 nm. Additionally, we conducted experiments to evaluate the photocatalytic capabilities under specific wavelengths, such as blue (405 nm), green (532 nm), and red (660 nm) lasers, to gain a better understanding of the -d-sp interband transition and the role of surface plasmon in photocatalysis. Surprisingly, unsupported Au NRs showed only weak plasmonic photocatalysis under all these excitations. With the help of supporting characterization tools, we observed that without semiconductor support, the photoexcited carriers over Au nanorods are not well separated, resulting in reduced photocatalysis.

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.

Antibacterial and cytotoxicity activity of green synthesized silver nanoparticles using aqueous extract of naartjie (Citrus unshiu) fruit peels

The application of plant extracts in the green synthesis of silver nanoparticles (AgNPs) has attracted significant attention owing to their eco-friendliness and cost-effective features. However, nanoparticles synthesized from plant materials may also display unique physicochemical properties. This study described an improved synthesis process for silver nanoparticles (AgNPs) from the peel of the Citrus unshiu fruit, an agricultural waste product. In addition to evaluating the produced AgNPs' physico-chemical characteristics, the research also examines their antibacterial and cytotoxic/anticancer capabilities. The color change from yellow to dark brown was observed immediately when 20 ml of Citrus unshiu fruit peel extract was added to 0.5 g of silver nitrate. A surface plasmon resonance band at 424 nm revealed by ultra-violet spectroscopy was used as additional confirmation that AgNP had formed. The scanning electron microscope (SEM), and the transmission electron microscope (TEM), revealed spherical-shaped NPs with a mean size of 23 nm. Furthermore, X-ray diffraction (XRD) confirmed the high crystallinity of the obtained NPs while Fourier transform infrared spectroscopy (FTIR) confirmed the bioreducing capacity of the Citrus unshiu fruit peel extract. The minimum inhibitory concentration (MIC) (31.25 μg/mL) of AgNPs significantly revealed a strong dose-dependent antibacterial effect on Staphylococcus aureus and Bacillus cereus. In contrast, their impact on gram-negative bacteria, such as Escherichia coli and Salmonella typhimurium, displayed an MIC of 250 μg/mL. The assessment of cytotoxicity on human embryonic kidney cells (HEK293) and lung cancer cells (A549) through a 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide assay revealed no detectable cytotoxic effects. The IC50 values were determined as 37.73 ± 0.34 μg/mL for HEK293 and 56.37 ± 0.73 μg/mL for A549, indicating the absence of significant adverse impacts on these cell lines. The anticancer drug doxorubicin was used as a reference standard, and had an IC50 value of 1.22 ± 0.09 and 0.76 ± 0.12 μg/mL against HEK293 and A549 cells, respectively. The results show that AgNPs synthesized from Citrus unshiu fruit peel could serve as antibacterial agents that may in the future be optimized for us in for example nanofiltration systems.

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.