Solubilization of caffeic acid into the cationic micelles and biogenic synthesis of silver nanoparticles for the degradation of dye

Solubilization of caffeic acid into the aqueous solution of cationic cetyltrimethlyammonium bromide (CTAB) has been studied by using differential spectroscopic and conductivity methods. The solubility of caffeic acid increases with increasing the CTAB concentrations. The solubilization constant of caffeic acid into CTAB (K_X = 1.8 × 10⁵), standard free energy (ΔG⁰_P = ?30.0 kJ/mol), and relative solubility (S_t/S₀ = 53.5) were estimated at room temperature from UV–visible data. The critical micellar concentration (CMC) of CTAB decreases linearly with caffeic acid concentration due to the presence of hydrophobic benzene moiety. The interaction of caffeic acid with CTAB has also been discussed. The solubilized caffeic acid was used as a reducing agent for the preparation of silver nanoparticles (AgNPs). The as-prepared AgNPs were used as an activator of persulphate. The generated reactive oxygen species (OH^?) and reactive sulphur species SO₄^-?) were responsible for the degradation of xylenol orange dye in water.     

Preparation of high-capacity substrates from polycrystalline silver chloride for the selective detection of tyrosine by surface-enhanced infrared absorption (SEIRA) measurements

In this work, stacked but isolated silver nanoparticles (AgNPs) on silver chloride were prepared in order to create sensitive substrates that could be used to determine analytes in aqueous solution by performing surface-enhanced infrared absorption (SEIRA) measurements. These substrates have a high loading capacity, which improves sensitivity, thus allowing the detection of biospecies such as weak infrared absorbers (including amino acids) in aqueous solution. AgNPs were obtained by converting the surface layers of the silver chloride crystals into stacked but isolated AgNPs using reducing agents. To optimize the conditions used to prepare the SEIRA substrates, the roles of four common reducing agents—hydrazine, sodium borohydride, glucose, and formaldehyde—were explored by probing the finished substrates with para-nitrobenzoic acid (PNBA). Factors that influence the morphologies of the AgNPs were examined systemically. These factors include the pH of the reducing solution, the reaction time, and the concentration of the reducing agent. Results indicate that the concentration of the reducing agent and the pH of the solution strongly influence the AgNP morphology and hence the SEIRA signals. Under optimized conditions, the resulting substrates showed intense SEIRA spectra from PNBA, with enhancement factors of around two orders of magnitude compared to conventional transmission methods. The new substrates offer a high loading capacity and good heat tolerance, allowing the direct infrared detection of tyrosine in aqueous solution.     

Phyto-Extract-Mediated Synthesis of Silver Nanoparticles Using Aqueous Extract of Sanvitalia procumbens,and Characterization,Optimization and Photocatalytic Degradation of Azo Dyes Orange G and Direct Blue-15

Green synthesis of silver nanoparticles (AgNPs) employing an aqueous plant extract has emerged as a viable eco-friendly method. The aim of the study was to synthesize AgNPs by using plant extract of Sanvitalia procumbens (creeping zinnia) in which the phytochemicals present in plant extract act as a stabilizing and reducing agent. For the stability of the synthesized AgNPs, different parameters like AgNO₃ concentration, volume ratios of AgNO₃, temperature, pH, and contact time were studied. Further, AgNPs were characterized by UV–visible spectroscopy, FT-IR (Fourier Transform Infrared Spectroscopy), XRD (X-ray Diffraction), SEM (Scanning Electron Microscopy), and EDX (Energy Dispersive X-ray Spectrometer) analysis. FT-IR analysis showed that the plant extract contained essential functional groups like O–H stretching of carboxylic acid, N–H stretching of secondary amides, and C–N stretching of aromatic amines, and C–O indicates the vibration of alcohol, ester, and carboxylic acid that facilitated in the green synthesis of AgNPs. The crystalline nature of synthesized AgNPs was confirmed by XRD, while the elemental composition of AgNPs was detected by energy dispersive X-ray analysis (EDX). SEM studies showed the mean particle diameter of silver nanoparticles. The synthesized AgNPs were used for photocatalytic degradation of Orange G and Direct blue-15 (OG and DB-15), which were analyzed by UV-visible spectroscopy. Maximum degradation percentage of OG and DB-15 azo dyes was observed, without any significant silver leaching, thereby signifying notable photocatalytic properties of AgNPs.     

Synthesis of Silver Nanoparticles Using Ionic‐Liquid‐Based Microwave‐Assisted Extraction from Polygonum minus and Photodegradation of Methylene Blue

A green biogenic, nontoxic, high‐yielding synthetic method is introduced for the synthesis of silver nanoparticles (AgNPs) using ionic‐liquid‐based, microwave‐assisted extraction (ILMAE) from Polygonum minus . The aqueous ionic liquid (1‐butyl‐3‐methylimidazolium chloride [BMIM]Cl)‐based plant extract was used as reducing agent to reduce silver ions to AgNPs. The synthesis of AgNPs was confirmed by UV–visible spectrophotometry. Fourier transforms infrared (FTIR) spectra showed that the plant bioactive compounds capped the AgNPs. The particle size and morphology of Ag NPs were characterized by dynamic light scattering (DLS) and field emission scanning electron microscopy (FESEM), respectively. Elemental analysis was carried out by energy‐dispersive X‐ray (EDX) spectroscopy. Photodegradation studies showed that the AgNPs degraded 98% of methylene blue in 12 min.     

Green synthesis of silver nanoparticles using olive leaf extract and its antibacterial activity

The silver nanoparticles (AgNPs) synthesized using hot water olive leaf extracts (OLE) as reducing and stabilizing agent are reported and evaluated for antibacterial activity against drug resistant bacterial isolates. The effect of extract concentration, contact time, pH and temperature on the reaction rate and the shape of the Ag nanoparticles are investigated. The data revealed that the rate of formation of the nanosilver increased significantly in the basic medium with increasing temperature. The nature of AgNPs synthesized was analyzed by UV–vis spectroscopy, X-ray diffraction, scanning electron microscopy and thermal gravimetric analysis (TGA). The silver nanoparticles were with an average size of 20–25 nm and mostly spherical. The antibacterial potential of synthesized AgNPs was compared with that of aqueous OLE by well diffusion method. The AgNPs at 0.03–0.07 mg/ml concentration significantly inhibited bacterial growth against multi drug resistant Staphylococcus aureus (S. aureus), Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli). This study revealed that the aqueous olive leaf extract has no effect at the concentrations used for preparation of the Ag nanoparticles. Thus AgNPs showed broad spectrum antibacterial activity at lower concentration and may be a good alternative therapeutic approach in future.     

Inhibition and enhancement of glucose oxidase activity in a chitosan-based electrode filled with silver nanoparticles

A chitosan-based electrode filled with silver nanoparticles (AgNPs) and glucose oxidase (GOD) was used as an enzyme electrode to investigate the effect of aging process of AgNPs on the GOD activity. Freshly prepared AgNPs inhibit the GOD activity, however, the inhibitory effect decreased with the increase of aging time. After aged for a period of time, AgNPs showed enhancement effect on the GOD activity. The effect of aging was studied by the measurements of Ag⁺ ions concentration, zeta (ζ) potential and X-ray photoelectron spectroscopy (XPS). And the results indicated that the concentration of Ag⁺ ions in the silver sol decreased during the aging period (i.e. Ag⁺ ions converted to more inert silver metal Ag⁰). The effect of AgNPs on the GOD activity can be changed by controlling the aging time of AgNPs. This research provides a new and simple approach to mediate AgNPs property, which is of great value in potential application of AgNPs in biosensors and nanoscale devices.     

Green synthesis and characterization of silver nanoparticles using Juniperus communis leaf extract: Catalytic activity in real-outdoor conditions and electrochemical properties

The present study investigates the green synthesis of stable silver nanoparticles using Juniperus communis leaf aqueous extract at room temperature. Synthesized silver nanoparticles (AgNPs) were characterized with different techniques such as UV–vis spectroscopy, Fourier transforms infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), Scanning electron microscopy (SEM-EDAX) and electrochemical method. Photocatalytic and anti-bacterial activities of synthesized AgNPs are evaluated based on the obtained result showed an efficient inhibition growth for gram negative P. Aeruginosa, E. Coli, and gram positive bacteria S.aureus. The AgNPs exhibited an excellent photocatalytic activity toward the degradation of methylene blue both indoor and outdoor, under sunlight, an efficiency of 95% was achieved. As an easy and environmentally friendly process, AgNPs based on Juniperus communis leaf extract could be applied for the degradation of pollutants and wastewater treatment.     

<Emphasis Type="Italic">Areca catechu</Emphasis> Assisted Synthesis of Silver Nanoparticles and its Electrocatalytic Activity on Glucose Oxidation

In this work, a facile biogenic route for the synthesis of silver nanoparticles (AgNPs) is reported. The aqueous extract of Areca catechu (A. catechu) nuts are used as reducing source. The synthesized AgNPs characterized by UV–Visible (UV–Vis) spectroscopy, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and high resolution transmission electron microscopy (HR-TEM) with energy dispersive spectrum (EDS) analysis. The formations of AgNPs are identified from the appearance of yellow color and the surface plasmon resonance absorbance peak between 407 and 437 nm. The FT-IR results exposed that the active biomolecules of A. catechu are responsible for capping of AgNPs. The synthesized AgNPs are distorted spherical shape with 45 nm of size, identified from the HR-TEM. In application, the electrocatalytic activity of AgNPs is analyzed towards glucose oxidation using cyclic voltammetry. The results showed that A. catechu derived AgNPs act as good electrocatalyst than bare bulk silver and glassy carbon electrodes.     

Preparation and properties of silver nanocomposite fabrics with in situ-generated silver nano particles using red sanders powder extract as reducing agent

Nanocomposite cotton fabrics with in situ-generated silver nanoparticles (AgNPs) were prepared by using Pterocarpus santalinus (Red sanders) extract in water as a reducing agent. The formation of AgNPs was analyzed by scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy. The SEM analysis of nanocomposites showed the presence of spherical AgNPs with a size range of 71–90?nm. FTIR spectra showed the involvement of hydroxyl and methylene groups of cellulose matrix in reducing the silver salt into AgNPs in the presence of red sanders powder extract as reducing agent for the in situ generation of AgNPs. These nanocomposite fabrics exhibited good antibacterial activity against Gram positive and Gram negative bacteria.     

Synthesis of carrageenan coated silver nanoparticles by an easy green method and their characterization and antimicrobial activities

The aim of the present work was to synthesize carrageenan coated silver nanoparticles (CA–AgNPs) using carrageenan as reducing and stabilizing agent. For this purpose, 10 mL of 0.35% (w/v) carrageenan solution was mixed with 10 mL AgNO₃ solution at different concentrations (1, 5 and 10 mM), and the resulting mixture was stirred at 100 °C at high speed for 2 h. The formation of CA–AgNPs was proven with the surface plasmon peaks observed at approximately 420 nm. The sizes and zeta potentials of CA–AgNPs were determined by Zeta-Sizer. Negative zeta potentials of CA–AgNPs indicated that the obtained AgNPs were stable. With scanning electron microscope (SEM) and transmission electron microscope analysis, it was seen that CA–AgNPs have spherical structure. According to the energy dispersion spectrometer analysis based on SEM images, it was observed that the samples were elementally composed of carbon, oxygen, sulfur, potassium and silver. The chemical structures of CA–AgNPs were determined by Fourier transform infrared spectroscopy, and it was proved that the carbonyl and OH groups of carrageenan were involved in formation and stabilizing of AgNPs, respectively. According to thermal gravimetric analysis, it has been observed that CA–AgNPs were thermally more stable than pure carrageenan. Antibacterial activity of CA–AgNPs against gram-positive and gram-negative bacteria was investigated with agar well diffusion and liquid test. It has been observed that CA–AgNPs synthesized with 1 mM AgNO₃ did not have an antibacterial activity on Escherichia coli and Staphylococcus aureus. Inhibition zones of varying diameters were observed in the 5 mM and 10 mM S-AgNPs groups. The synthesized CA–AgNPs (5 and 10 mM) have the capacity to be used in wound dressing materials or topical agents applied to burns and wounds due to their antibacterial effects and stability.

     

Biosynthesis of silver nanoparticles using Onosma sericeum Willd. and evaluation of their catalytic properties and antibacterial and cytotoxic activity

In this study, silver nanoparticle (AgNP) synthesis was carried out using Onosma sericeum Willd. aqueous extract for the first time, with a simple, economical, and green method without the need for any other organic solvent or external reducing or stabilizing agent. A variety of AgNPs, all of different particle sizes, were synthesized by controlling the silver ion concentration, extract volume, temperature, and pH. It was determined that the optimum conditions for AgNP synthesis were 1 mM AgNO3, pH 8, 25 °C, 20 g/200 mL extract, silver nitrate, and extract ratio 5:1 (v/v). The AgNPs were defined using UV-Vis spectroscopy, field emission scanning electron microscopy (FESEM), energy dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The particle size distribution and zeta potential measurements of the AgNPs were measured using the dynamic light scattering (DLS) technique. It was determined that the AgNPs with a particle size of less than 10 nm showed a higher catalytic effect in the reduction of 2-nitrobenzenamine. It was also found that these nanoparticles had a cytotoxic effect on the MCF-7 breast cancer cell line depending on dosage and time. The resulting IC50 values were between 76.63 µg/mL and 169.77 µg/mL. Furthermore, the biosynthesized AgNPs showed effective antibacterial activity against the Acinetobacter baumannii bacteria. The results of the study showed that synthesized AgNPs can have a promising role in biomedical and nanobiotechnology applications.     

Green Synthesis of Silver Nanoparticles Using the Plant Extract of Acer oblongifolium and Study of Its Antibacterial and Antiproliferative Activity via Mathematical Approaches

In this study, the antibacterial and antifungal properties of silver nanoparticles synthesized with the aqueous plant extract of Acer oblongifolium leaves were defined using a simplistic, environmentally friendly, reliable, and cost-effective method. The aqueous plant extract of Acer oblongifolium, which served as a capping and reducing agent, was used to biosynthesize silver nanoparticles. UV visible spectroscopy, X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and scanning electron microscopy were used to analyze the biosynthesized Acer oblongifolium silver nanoparticles (AgNPs). Gram-positive bacteria (Bacillus paramycoides and Bacillus cereus) and Gram-negative bacteria (E. coli) were used to test the AgNPs’ antibacterial activity. The presence of different functional groups was determined by FTIR. The AgNPs were rod-like in shape. The nanoparticles were more toxic against Escherichia coli than both Bacillus cereus and Bacillus paramycoides. The AgNPs had IC₅₀ values of 6.22 and 9.43 and mg/mL on HeLa and MCF-7, respectively, proving their comparatively strong potency against MCF-7. This confirmed that silver nanoparticles had strong antibacterial activity and antiproliferative ability against MCF-7 and HeLa cell lines. The mathematical modeling revealed that the pure nanoparticle had a high heat-absorbing capacity compared to the mixed nanoparticle. This research demonstrated that the biosynthesized Acer oblongifolium AgNPs could be used as an antioxidant, antibacterial, and anticancer agent in the future.     

Surfactant-assisted synthesis and characterization of stable silver bromide nanoparticles in aqueous media

Colloidal dispersions of silver bromide (AgBr) in aqueous surfactant medium have been prepared using a surfactant-assisted synthesis approach with hexadecyltrimethylammonium bromide (CTAB). The surfactant acts both as source of bromide ion as well as the stabilizing agent. Upon progressive addition of silver nitrate to aqueous CTAB solution, stable AgBr dispersions were obtained. Formation of surfactant cation (CTA(+)) stabilized AgBr was confirmed by way of XRD, FTIR and NMR studies. Thermal behavior of the isolated nanoparticles was investigated by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA), where the occurrence of phase transition in the surfactant-stabilized nanoparticles was observed. Kinetics of the particle growth was investigated by dynamic light scattering measurements, which predicted the formation of surfactant bilayered structures associated with the nanoparticles of AgBr. Band gap of the nanoparticles was determined by suitably analyzing the UV-visible spectral data, which concluded that the particles behaved like insulators. Morphology of the particles, studied by TEM measurements, was found to be spherical. Finally, enthalpy of formation of surfactant-stabilized AgBr, determined calorimetrically, was found to be dependent on the concentration of the precursors.     

A completely green approach to the synthesis of dendritic silver nanostructures starting from white grape pomace as a potential nanofactory

A simple, eco-friendly, cost-effective and rapid microwave-assisted method has been developed to synthetize dendritic silver nanostructures, composed of silver nanoparticles (AgNPs), using white grape pomace aqueous extract (WGPE) as both reducing and capping agent. With this aim, WGPE and AgNO₃ (1 mM) were mixed at different ratio, and microwave irradiated at 700 W, for 40 s. To understand the role of bioactive compounds involved in the green synthesis of AgNPs, preliminary chemical characterization, FT-IR analysis and ¹H NMR metabolite profiling of WGPE were carried out. The effects of bioactive extract concentration and stability over time on AgNPs formation were also evaluated. WGPE-mediated silver nanostructures were then characterized by UV–vis, FTIR analyses, and scanning electron microscopy. Interestingly, the formation of dendritic nanostructures, originated from the self-assembly of Ag rounded nanoparticles (average diameter of 33 ± 6 nm), was observed and ascribed to the use of microwave power and the presence of organic components within the used WGPE, inducing an anisotropic crystal growth and promoting a diffusion-limited aggregation mechanism. The bio-dendritic synthetized nanostructures were also evaluated for potential applications in bio-sensing and agricultural fields. Cyclic voltammetry measurements in 0.5 M phosphate + 0.1 M KCl buffer, pH 7.4 showed that green AgNPs possess the electroactive properties typical of AgNPs produced using chemical protocol. The biological activity of synthetized AgNPs was evaluated by in-vitro antifungal activity against F. graminearum. Additionally, a phytotoxicity evaluation of synthetized green nanostructures was carried out on wheat seed germination. Results highlighted the potential of WGPE as green agent for bio-inspired nanomaterial synthesis, and of green Ag nanostructures, which can be used as antifungal agent and in biosensing applications.     

Synthesis of silver nanoparticles in chitosan, gelatin and chitosan/gelatin bionanocomposites by a chemical reducing agent and their characterization

In this research, silver nanoparticles (AgNPs) were synthesized in chitosan (Cts), Cts/gelatin and gelatin suspensions using a chemical reducing agent. Cts and gelatin were used as natural stabilizers and solid support, whereas AgNO(3) was used as the silver precursor. Sodium borohydride (NaBH(4)) was used as the reducing agent. The properties of AgNPs in Cts, Cts/gelatin and gelatin bionanocomposites (BNCs) were studied in terms of their surface plasmon resonance, crystalline structure, average diameter size, particle distributions, surface topography and functional groups. All the samples were characterized by UV-visible spectroscopy, powder X-ray diffraction, transmission electron microscopy, atomic force microscopy and Fourier transform infrared spectroscopy.     

Green Synthesis of Silver Nanoparticles Using Water Extract from Galls of <Emphasis Type="Italic">Rhus Chinensis</Emphasis> and Its Antibacterial Activity

The green synthesis of silver nanoparticles (AgNPs) has been proposed as a simple, eco-friendly and cost effective alternative to chemical and physical methods. The Rhus chinensis plant is one of the well studied medicinal plant and its galls find excellent clinical and therapeutic applications. The present study reports the use of water extract from galls of R. chinensis as a reducing agent and formation of AgNPs from silver nitrate solution by a green synthesis route. The AgNPs formation was observed visually by color change and the absorbance peak at 450 nm was observed by UV–Visible spectrophotometer. The shape, size, and morphology of synthesized AgNPs were monitored by transmission electron microscopy and field-emission scanning electron microscopy. The face centered cubic structure of AgNPs was confirmed by X-ray diffraction pattern and element composition by energy dispersive X-ray analysis. The Fourier transform infrared spectroscopy spectrum revealed that the presence of components acts as a reducing and capping agent. The antibacterial activity was performed using the agar well diffusion method. Minimum inhibitory concentration and minimum bactericidal concentration were determined by broth dilution and spread plate method respectively. Synthesized nanoparticles were spotted as triangular and hexagonal shape and the particle size was around 150 nm.     

Free‐standing Graphene/Poly(methylene blue)/AgNPs Composite Paper for Electrochemical Sensing of NADH

Highly flexible graphene/poly(methylene blue)/AgNPs composite paper was successfully prepared for amperometric biosensing of NADH. For this purpose, a dispersion including graphene oxide (GO), methylene blue (MB) and silver nanoparticles (AgNPs) was prepared and GO/MB/AgNPs paper was acquired by vacuum‐filtration of this dispersion through a suitable membrane. After peeling it off from membrane, it was transformed to rGO/MB/AgNPs paper by performing reduction with hydriodic acid. In a three‐electrode cell, which is containing 0.1 M phosphate buffer solution (pH: 9.0), rGO/MB/AgNPs paper was used as working electrode and rGO/poly(MB)/AgNPs composite paper was generated by surface‐confined electropolymerization of MB using successive cyclic voltammetry approach in a suitable potential window. Characterization of this composite paper was carried out by using scanning electron microscopy, scanning tunneling microscopy, X‐ray photoelectron spectroscopy, powder X‐ray diffraction spectroscopy, Raman spectroscopy, four‐point probe conductivity measurement and cyclic voltammetry techniques. Flexible rGO/poly(MB)/AgNPs composite paper has demonstrated high sensitivity, wide linear range and low detection limit for amperometric quantification of NADH.     

Antibacterial and Antifungal Studies of Biosynthesized Silver Nanoparticles against Plant Parasitic Nematode Meloidogyne incognita,Plant Pathogens Ralstonia solanacearum and Fusarium oxysporum

The possibility of using silver nanoparticles (AgNPs) to enhance the plants growth, crop production, and control of plant diseases is currently being researched. One of the most effective approaches for the production of AgNPs is green synthesis. Herein, we report a green and phytogenic synthesis of AgNPs by using aqueous extract of strawberry waste (solid waste after fruit juice extraction) as a novel bioresource, which is a non-hazardous and inexpensive that can act as a reducing, capping, and stabilizing agent. Successful biosynthesis of AgNPs was monitored by UV-visible spectroscopy showing a surface plasmon resonance (SPR) peak at ~415 nm. The X-ray diffraction studies confirm the face-centered cubic crystalline AgNPs. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques confirm the rectangular shape with an average size of ~55 nm. The antibacterial and antifungal efficacy and inhibitory impact of the biosynthesized AgNPs were tested against nematode, Meloidogyne incognita, plant pathogenic bacterium, Ralstonia solanacearum and fungus, Fusarium oxysporum. These results confirm that biosynthesized AgNPs can significantly control these plant pathogens.     

Synthesis of Silver Nanoparticles from Extracts of Wild Ginger (Zingiber zerumbet) with Antibacterial Activity against Selective Multidrug Resistant Oral Bacteria

Antibiotic resistance rate is rising worldwide. Silver nanoparticles (AgNPs) are potent for fighting antimicrobial resistance (AMR), independently or synergistically. The purpose of this study was to prepare AgNPs using wild ginger extracts and to evaluate the antibacterial efficacy of these AgNPs against multidrug-resistant (MDR) Staphylococcus aureus, Streptococcus mutans, and Enterococcus faecalis. AgNPs were synthesized using wild ginger extracts at room temperature through different parameters for optimization, i.e., pH and variable molar concentration. Synthesis of AgNPs was confirmed by UV/visible spectroscopy and further characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy analysis (EDXA), and Fourier-transform infrared spectroscopy (FTIR). Disc and agar well diffusion techniques were utilized to determine the in vitro antibacterial activity of plant extracts and AgNPs. The surface plasmon resonance peaks in absorption spectra for silver suspension showed the absorption maxima in the range of 400–420 nm. Functional biomolecules such as N–H, C–H, O–H, C–O, and C–O–C were present in Zingiber zerumbet (Z. zerumbet) (aqueous and organic extracts) responsible for the AgNP formation characterized by FTIR. The crystalline structure of ZZAE-AgCl-NPs and ZZEE-AgCl-NPs was displayed in the XRD analysis. SEM analysis revealed the surface morphology. The EDXA analysis also confirmed the element of silver. It was revealed that AgNPs were seemingly spherical in morphology. The biosynthesized AgNPs exhibited complete antibacterial activity against the tested MDR bacterial strains. This study indicates that AgNPs of wild ginger extracts exhibit potent antibacterial activity against MDR bacterial strains.     

Ficus carica Latex-Mediated Synthesis of Silver Nanoparticles and Its Application as a Chemophotoprotective Agent

The present work provides scientific support on the use of latex of Ficus carica to synthesize stable silver nanoparticles (AgNPs). AgNPs synthesized immediately after the addition of latex to silver nitrate solution at room temperature. Synthesized nanoparticles were of spherical shape with average size of 163.7 nm. Fourier transform infrared spectroscopy analysis revealed capping of proteins and phenolic compound on AgNPs, while X-ray diffraction analysis confirmed the fcc nature of AgNPs. Particles formed were stable for a long time (6 months). It was found that incorporation of AgNPs with 2 and 4 % concentration exhibits synergistic increase in sun protection factor of commercial sunscreen and natural extracts ranging from 01 to 12,175 % than control. Further characterization of latex and AgNPs revealed total phenolic content of 98.75 and 94.88 μg/ml. The ferric ion reduction potentials of latex and AgNPs were 79.69 and 18.79 %. Reduction potential of ascorbic acid was synergistically increased after cumulative preparation of ascorbic acid with latex and AgNPs and found to be 106.76 and 101.50 % for ascorbic acid + latex and ascorbic acid + AgNPs, respectively.