Biological synthesis of gold and silver nanoparticles mediated by the bacteria Bacillus subtilis

Biological synthesis of gold and silver nanoparticles was carried out using the bacteria Bacillus subtilis. The reduction processes of chloroaurate and silver ions by B. subtilis were found to be different. Gold nanoparticles were synthesized both intra- and extracellularly, while silver nanoparticles were exclusively formed extracellularly. The gold nanoparticles were formed after 1 day of addition of chloroaurate ions, while the silver nanoparticles were formed after 7 days. The nanoparticles were characterized by X-ray diffraction, UV-vis spectra and transmission electron spectroscopy. X-ray diffraction revealed the formation of face-centered cubic (fcc) crystalline gold nanoparticles in the supernatant, broth solution and bacterial pellet. Silver nanoparticles also exhibited diffraction peaks corresponding to fcc metallic silver. UV-vis spectra showed surface plasmon vibrations for gold and silver nanoparticles centered at 530 and 456 nm, respectively. TEM micrographs depicted the formation of gold nanoparticles intra- and extracellularly, which had an average size of 7.6 +/- 1.8 and 7.3 +/- 2.3 nm, respectively, while silver nanoparticles were exclusively formed extracellularly, with an average size of 6.1 +/- 1.6 nm. The bacterial proteins were analyzed by sodium dodecyl sulfonate-polyacrylamide electrophoresis (SDS-PAGE) before and after the addition of metal ion solutions. We believe that proteins of a molecular weight between 25 and 66 kDa could be responsible for chloroaurate ions reduction, while the formation of silver nanoparticles can be attributed to proteins of a molecular weight between 66 and 116 kDa. We also believe that the nanoparticles were stabilized by the surface-active molecules i.e., surfactin or other biomolecules released into the solution by B. subtilis.     

Green synthesis of stable silver nanoparticles by the main reduction component of green tea (Camellia sinensis L.)

Recently the use of medicinal plants potential in the production of nanoparticles has received serious attention. Here, the main component of Camellia sinensis L. (green tea) extract was detected by spectroscopy and the optimal conditions were determined for their performance in green synthesis of silver nanoparticles at room temperature. Epigallocatechin gallate was identified as the dominant component in the extract as determined by spectroscopy, and it was established that its oxidation was a function of the solution pH. Transmission electron microscopy, dynamic light scattering, and visible absorption spectroscopy (UV‐Vis) confirmed the reduction in silver ions to silver nanoparticles (Ag NPs). Controlling over Ag NPs shape and narrow size distribution was achieved with 10 ml green tea leaf extract solution and in different reaction pH. Spherical colloidal Ag NPs with well‐defined hydrodynamic diameters (with average hydrodynamic size of 27.9–50.2 nm) were produced. Silver nitrate concentrations used in this study were lower than that of reported in similar works, and synthesis efficiency was also higher. Nanoparticles were perfectly spherical and their uniformity, compared to similar studies, was much higher. These NPs showed higher degree of stability and were aqueously stable for >10 months in dark glasses at 4°C.Inspec keywords: hydrodynamics, nanoparticles, particle size, pH, visible spectra, ultraviolet spectra, reduction (chemical), transmission electron microscopy, silver, microorganisms, nanofabrication, colloids, biomedical materials, nanomedicine, drug delivery systemsOther keywords: transmission electron microscopy, dynamic light scattering, visible absorption spectroscopy, silver ions, narrow size distribution, silver nitrate concentrations, green synthesis, medicinal plants, solution pH, green tea leaf, hydrodynamic size, silver nanoparticles, Camellia sinensis L, drug delivery, reduction component, epigallocatechin gallate, UV‐visible spectra, hydrodynamic diameters, spherical colloidal Ag NPs, temperature 4.0 degC, Ag     

Facile route for preparation of silica-silver heterogeneous nanocomposite particles using alcohol reduction method

Silica-silver heterogeneous nanocomposite particles were successfully prepared by facile route including alcohol reduction method. Thiol groups were employed as a chemical protocol to make a binding between silver nanoparticle and silica surface. After the reaction for 10 min, a large number of quasi-spherical silver nanoparticles with an average size of 6.9 nm in diameter were homogeneously formed on the surface of silica particles. The immobilized silver nanoparticles grew to large ones with an average size of 10.6 nm in diameter after additional reaction for 2 h. The resulting nanocomposite particles were characterized by transmission electron microscopy (TEM), energy-dispersive X-ray (EDX), UV-vis spectrophotometer, and X-ray diffraction (XRD) analysis.     

Comparative study of antifungal effect of green and chemically synthesised silver nanoparticles in combination with carbendazim,mancozeb, and thiram

This study reports synthesis and characterisation of silver nanoparticles and their effect on antifungal efficacy of common agricultural fungicides. Silver nanoparticles were synthesised using biological and chemical reduction methods employing Elettaria cardamomum leaf extract and sodium citrate, respectively. Nanoparticles were then characterised using UV–Visible spectroscopy, X‐ray diffraction (XRD), transmission electron microscopy, and dynamic light scattering (DLS). While XRD assigned particles size of 31.86 nm for green and 41.91 nm for chemical silver nanoparticles with the help of the Debye–Scherrer formula, DLS specified monodisperse nature of both suspensions. Nanoparticles were tested individually and in combination with fungicides (carbendazim, mancozeb, and thiram) against fungal phytopathogens. Silver nanoparticles exhibited good antifungal activity and minimum inhibitory concentration (MIC) was observed in the range of 8–64 µg/ml. Also, they positively influenced the efficacy of fungicides. The mean MIC value (mean ± SD) for combination of all three fungicides with green AgNPs was 1.37 ± 0.6 µg/ml and for chemical AgNPs was 1.73 ± 1.0 µg/ml. Hence, it could be concluded that green AgNPs performed better than chemical AgNPs. Synergy was observed between green AgNPs and fungicides against Fusarium oxysporum. In conclusion, this study reports synthesis of monodisperse silver nanoparticles which serve as efficient antifungal agents and also enhance the fungicidal action of reported agricultural fungicides in combination studies.Inspec keywords: X‐ray diffraction, reduction (chemical), visible spectra, ultraviolet spectra, microorganisms, particle size, nanomedicine, nanofabrication, nanoparticles, agrochemicals, antibacterial activity, transmission electron microscopy, silver, light scattering, scanning electron microscopyOther keywords: antifungal effect, green silver nanoparticles, chemically synthesised silver nanoparticles, carbendazim, mancozeb, thiram, antifungal efficacy, common agricultural fungicides, biological reduction methods, chemical reduction methods, transmission electron microscopy, XRD assigned particles size, chemical silver nanoparticles, green AgNPs, chemical AgNPs, monodisperse silver nanoparticles, antifungal activity, agricultural fungicides, Elettaria cardamomum leaf extract, sodium citrate, UV‐visible spectroscopy, X‐ray diffraction, dynamic light scattering, size 31.86 nm, size 41.91 nm     

Green synthesis of silver nanoparticles using tannins

Colloidal silver nanoparticles were prepared by rapid green synthesis using different tannin sources as reducing agent viz. chestnut (CN), mangrove (MG) and quebracho (QB). The aqueous silver ions when exposed to CN, MG and QB tannins were reduced which resulted in formation of silver nanoparticles. The resultant silver nanoparticles were characterized using UV-Visible, X-ray diffraction (XRD), scanning electron microscopy (SEM/EDX), and transmission electron microscopy (TEM) techniques. Furthermore, the possible mechanism of nanoparticles synthesis was also derived using FT-IR analysis. Spectroscopy analysis revealed that the synthesized nanoparticles were within 30 to 75 nm in size, while XRD results showed that nanoparticles formed were crystalline with face centered cubic geometry.     

Biosynthesis of gold and silver nanoparticles using Emblica Officinalis fruit extract, their phase transfer and transmetallation in an organic solution

The design, synthesis and characterization of biologically synthesized nanomaterials have become an area of significant interest. In this paper, we report the extracellular synthesis of gold and silver nanoparticles using Emblica Officinalis (amla, Indian Gooseberry) fruit extract as the reducing agent to synthesize Ag and Au nanoparticles, their subsequent phase transfer to an organic solution and the transmetallation reaction of hydrophobized silver nanoparticles with hydrophobized chloroaurate ions. On treating aqueous silver sulfate and chloroauric acid solutions with Emblica Officinalis fruit extract, rapid reduction of the silver and chloroaurate ions is observed leading to the formation of highly stable silver and gold nanoparticles in solution. Transmission Electron Microscopy analysis of the silver and gold nanoparticles indicated that they ranged in size from 10 to 20 nm and 15 to 25 nm respectively. Ag and Au nanoparticles thus synthesized were then phase transferred into an organic solution using a cationic surfactant octadecylamine. Transmetallation reaction between hydrophobized silver nanoparticles and hydrophobized chloroaurate ions in chloroform resulted in the formation of gold nanoparticles.     

Green synthesis of silver nanoparticles and their applications as colorimetric probe for determination of Fe3+ and Hg2+ ions

Silver nanoparticles (AgNPs) were prepared by a green method using Cordia myxa leaf extract. They were characterised by UV–vis spectroscopy, Fourier transform infrared spectroscopy and their X‐ray diffraction pattern. Their sizes were determined by scanning electron micrographs, transmission electron micrographs imaging and dynamic light scattering analysis. The shapes of nanoparticles were spherical or truncated triangular and their average size was determined to be 51.6 nm. Their solution was stable at least for one month. The prepared AgNPs were used as a selective chemical sensor for determination of iron(III) (only when Cl⁻ ions were present in the medium) and mercury(II) ions with detection limits of 0.084 and 0.037 nM, respectively. It was shown that the mechanism of these detections is through oxidation of Ag atoms by Fe³⁺ and Hg²⁺ ions.Inspec keywords: visible spectra, nanoparticles, transmission electron microscopy, nanofabrication, ultraviolet spectra, chemical sensors, scanning electron microscopy, silver, X‐ray diffraction, Fourier transform infrared spectra, oxidationOther keywords: Ag, Cordia myxa leaf extract, iron(III) ions, mercury(II) ions, oxidation, scanning electron micrographs, Fourier transform infrared spectroscopy, silver nanoparticles, chemical sensor, dynamic light scattering analysis, transmission electron micrographs, X‐ray diffraction pattern, UV–vis spectroscopy, colorimetric probe, green synthesis     

The bio-inspired approach to controllable biomimetic synthesis of silver nanoparticles in organic matrix of chitosan and silver-binding peptide (NPSSLFRYLPSD)

Inspired by organic matrices in some life systems which can operate as templates for biosynthesis organic materials with uniform size and morphology, in our experiment, chitosan was combined with AG4 peptide (NPSSLFRYLPSD) to form a simple organic matrix, which was used as a template to synthesize particle size and morphology-controlling silver nanoparticles. The results of UV–vis determination and TEM observation indicated that uniform spherical silver nanoparticles with about 5 nm in size were obtained at the certain concentration of chitosan and silver ions. Hence, it is possible to control the size and morphology of silver nanoparticles at a certain extent by adjusting the concentration of chitosan and silver ions. In addition, triangle and hexagonal silver nanoparticles ranging from 20 nm to 60 nm in size appeared in different conditions. The advantage of this biomimetic synthesis of silver nanoparticles is that the process could be accomplished under mild conditions rather than stringent conditions, such as high temperature, very high pressures and a toxic environment, which usually occurs with the traditional methods for preparing metal nanoparticles.     

Biosynthesised silver nanoparticles using aqueous leaf extract of Tagetes patula L. and evaluation of their antifungal activity against phytopathogenic fungi

In the recent decades, nanotechnology is gaining tremendous impetus due to its capability of modulating metals into their nanosize, which drastically changes the chemical, physical, biological and optical properties of metals. In this study, silver nanoparticles (AgNPs) synthesis using aqueous leaf extracts of Tagetes patula L. which act as reducing agent as well as capping agent is reported. Synthesis of AgNPs was observed at different parameters like temperature, concentration of silver nitrate, leaf extract concentration and time of reduction. The AgNPs were characterized using UV‐vis spectroscopy, scanning electron microscope with energy dispersive spectroscopy, transmission electron microscopy with selected area electron diffraction, X‐ray diffraction, Fourier transform infrared and dynamic light scattering analysis. These analyses revealed the size of nanoparticles ranging from 15 to 30 nm as well revealed their spherical shape and cubic and hexagonal lattice structure. The lower zeta potential (−14.2mV) and the FTIR spectra indicate that the synthesized AgNPs are remarkably stable for a long period due to the capped biomolecules on the surface of nanoparticles. Furthermore, these AgNPs were found to be highly toxic against phytopathogenic fungi Colletotrichum chlorophyti by both in vitro and in vivo and might be a safer alternative to chemical fungicides.Inspec keywords: silver, nanoparticles, nanofabrication, nanobiotechnology, ultraviolet spectra, visible spectra, scanning electron microscopy, X‐ray chemical analysis, electron diffraction, X‐ray diffraction, Fourier transform infrared spectra, crystal structure, electrokinetic effects, antibacterial activityOther keywords: biosynthesised silver nanoparticles, aqueous leaf extract, Tagetes patula L, antifungal activity, phytopathogenic fungi, nanotechnology, UV–vis spectroscopy, scanning electron microscope, energy dispersive spectroscopy, transmission electron microscopy, selected area electron diffraction, X‐ray diffraction, Fourier transform infrared spectra, dynamic light scattering analysis, hexagonal lattice structure, zeta potential, phytopathogenic fungi Colletotrichum chlorophyti, cubic lattice structure, size 15 nm to 30 nm, Ag     

Assessment of cytotoxicity and immune compatibility of phytochemicals‐mediated biosynthesised silver nanoparticles using Cynara scolymus

The study was focused on the phytochemicals‐mediated biosynthesis of silver nanoparticles using leaf extracts and infusions from Cynara scolymus. To identify the antioxidant activity and total phenolic content, the 1,1‐diphenyl‐1‐picrylhydrazyl and Folin–Ciocalteau methods were applied, respectively. The formation and stability of the reduced silver ions were monitored by UV–vis spectrophotometer. The particle sizes of the silver nanoparticles were characterised using the dynamic light scattering technique and scanning electron microscope. The phase composition of the obtained silver nanoparticles was characterised by X‐ray diffraction. The silver nanoparticles suspension, artichoke infusion, and silver ions were separately tested towards potential cytotoxicity and pro‐inflammatory effect using mouse fibroblasts and human monocytes cell line, respectively. The total phenolic content and antioxidant activity of ethanol extract and infusion were found significantly higher as compared to aqueous extract and infusion. The UV–visible spectrophotometric analysis revealed the presence of the characteristic absorption band of the Ag nanoparticles. Moreover, it was found that with the increasing volume of plant extract, the average size of particles was increased. Biocompatibility results evidently showed that silver nanoparticles do not induce monocyte activation, however in order to avoid their cytotoxicity suspension at a concentration <2 ppm should be applied.Inspec keywords: pharmaceuticals, health and safety, renewable materials, toxicology, organic compounds, antibacterial activity, X‐ray diffraction, nanomedicine, nanoparticles, nanofabrication, suspensions, ultraviolet spectra, visible spectra, scanning electron microscopy, silver, particle sizeOther keywords: phytochemicals‐mediated biosynthesis, antioxidant activity, total phenolic content, dynamic light scattering technique, silver nanoparticles suspension, scanning electron microscopy, Cynara scolymus, 1,1 diphenyl‐1‐picrylhydrazyl method, cytotoxicity, immune compatibility, leaf extracts, UV‐vis spectrophotometry, particle size, Folin‐Ciocalteau methods, phase composition, X‐ray diffraction, artichoke infusion, pro‐inflammatory effect, mouse fibroblasts, human monocytes cell line, Ag     

Formation of silver nanoparticles in poly(perfluorosulfonic) acid membrane

The formation of silver nanoparticles by chemical reduction of Ag+-loaded Nafion-117 membrane with NaBH4 was studied using radioactivity tagged ions. The counterion-exchange method (Ag(m)+ <--> Na(s)+) was used to obtain a membrane sample with a varying proportion of Ag+ ions. The X-ray elemental mapping across the thickness of the membrane by energy-dispersive X-ray spectrometer attached to the environmental scanning electron microscope (ESEM/EDAX) indicated that Na+ and Ag+ were uniformly distributed in the membrane samples before reduction. The average size of nanoparticles formed after reduction was found to be 15 +/- 3 nm, irrespective of the concentration of silver ions present in the membrane before reduction. Energy-dispersive X-ray fluorescence (EDXRF) analyses of the membrane samples, carried out before and after reduction, indicated that the Ag concentration on the membrane surface was considerably increased after reduction. EDXRF measurements of the membrane samples, obtained from reduction carried out in a dead end cell, indicated that Ag nanoparticles were formed only on the membrane surface exposed to NaBH4 solution. Reduction carried out with NaBH4 tagged with 22Na showed that the formation of Ag nanoparticles involved exchange of Ag+ ions from ion-exchange sites in the interior of the membrane with Na+ ions, followed by reduction of Ag+ ions with BH4- ions at the surface of membrane. The study of self-diffusion of water, Na+, and Cs+ ions in the membrane loaded with Ag nanoparticles indicated that formation of Ag nanoparticles did not affect the diffusional transport properties of the membrane. The ion-exchange capacity and water uptake capacity were also not affected by the formation of Ag nanoparticles in the membrane. The spatial distribution of Ag nanoparticles across the thickness of the membrane obtained by ESEM/EDAX showed that Ag nanoparticles were confined to a few-micrometer surface layer of the membrane. Based on these observations, an attempt has been made to explain the mechanism of the formation of Ag nanoparticles in the membrane.     

Sunlight induced biosynthesis of silver nanoparticle from the bark extract of Amentotaxus assamica D.K. Ferguson and its antibacterial activity against Escherichia coli and Staphylococcus aureus

Green synthesis of nanoparticles has gained importance due to its eco‐friendly, low toxicity and cost effective nature. This study deals with the biosynthesis of silver nanoparticles (AgNPs) from the bark extract of Amentotaxus assamica. The AgNPs have been synthesised by reducing the silver ions into stable AgNPs using the bark extract of Amentotaxus assamica under the influence of sunlight irradiation. The characterisation of the biosynthesised AgNPs was carried out by UV–vis spectroscopy, X‐ray diffraction analysis (XRD), Fourier transform infrared spectroscopy, scanning electron microscopy (SEM) and energy dispersive X‐ray analysis. The UV–vis spectrum showed a broad peak at 472 nm. Also, the XRD confirmed the crystalline structure of the AgNPs. Moreover, the SEM analysis revealed that the biosynthesised AgNPs were spherical in shape. Also, dynamic light scattering techniques were used to evaluate the size distribution profile of the biosynthesised AgNPs. Furthermore, the biosynthesised AgNPs showed a prominent inhibitory effect against both Escherichia coli (MTCC 111) and Staphylococcus aureus (MTCC 97). Thus the biosynthesis of AgNPs from the bark extract of Amentotaxus assamica is found to eco‐friendly way of producing AgNPs compared to chemical method.Inspec keywords: X‐ray chemical analysis, microorganisms, transmission electron microscopy, nanoparticles, toxicology, scanning electron microscopy, ultraviolet spectra, particle size, Fourier transform spectra, X‐ray diffraction, antibacterial activity, visible spectra, infrared spectra, nanomedicine, silverOther keywords: stable AgNP, biosynthesised AgNP, SEM analysis, sunlight irradiation, silver ions, silver nanoparticle, amentotaxus assamica, biosynthesis, escherichia coli     

Preparation and thermomechanical properties of Ag-PVA nanocomposite films

Metal–polymer hybrid nanocomposites have been prepared from an aqueous solution of polyvinyl alcohol (PVA) and silver nitrate (AgNO₃). The silver nanoparticles were generated in PVA matrix by the reduction of silver ions with PVA molecule at 60–70 °C over magnetic stirrer. UV–vis analysis, X-ray diffraction studies, transmission electron microscopy, scanning electron microscopy and current–voltage analysis were used to characterize the nanocomposite films prepared. The X-ray diffraction analysis reveals that silver metal is present in face centered cubic (fcc) crystal structure. Average crystallite size of silver nanocrystal is 19 nm, which increases to 22 nm on annealing the film at 150 °C in air. This result is in good agreement with the result obtained from TEM. The UV–vis spectrum shows a single peak at 433 nm, arising from the surface plasmon absorption of silver nanocolloids. This result clearly indicates that silver nanoparticles are embedded in PVA. An improvement of mechanical properties (storage modulus) was also noticed due to a modification of PVA up to 0.5 wt% of silver content. The current–voltage (I–V) characteristic of nanocomposite films shows increase in current drawn with increasing Ag-content in the films.     

Biosynthesis of waste pistachio shell supported silver nanoparticles for the catalytic reduction processes

Silver nanoparticles (NPs) are immobilised on pistachio shell surface by Cichorium intybus L. leaves extract as an antioxidant media. The Fourier transform infrared spectra, X‐ray diffraction, field‐emission scanning electron microscopy equipped with energy‐dispersive X‐ray spectroscopy, and transmission electron microscope analyses confirmed the support of silver NPs on the pistachio shell (Ag NPs/pistachio shell). Ag NPs on the pistachio shell had a diameter basically in the 10–15 nm range. Reduction reactions of 4‐nitrophenol (4‐NP), and organic dyes at ambient condition were used in the investigation of the catalytic performance of the prepared catalyst. Through this research, the Ag NPs/pistachio shell shows a high activity and recyclability, and reusability without loss of its catalytic activity.Inspec keywords: transmission electron microscopy, nanoparticles, X‐ray diffraction, catalysis, nanofabrication, dyes, X‐ray chemical analysis, reduction (chemical), silver, catalysts, Fourier transform infrared spectra, field emission scanning electron microscopyOther keywords: waste pistachio shell, silver nanoparticles, catalytic reduction processes, pistachio shell surface, antioxidant media, infrared spectra, X‐ray diffraction, field‐emission scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, transmission electron microscope analyses, reduction reactions, catalytic performance, catalytic activity, Cichorium intybus L. leaves extract, size 10.0 nm to 15.0 nm, Ag     

Preparation of linoleic acid-capped silver nanoparticles and their antimicrobial effect

Silver nanoparticles have been prepared through the chemical reduction of silver ions by ethanol using linoleic acid as a stabilising agent. This colloidal solution shows an absorption band in the visible range with an absorption peak at 421 nm. The peaks in the X-ray diffraction (XRD) pattern matches well with the standard values of the face-centred-cubic form of metallic silver. Transmission Electron Microscope (TEM) micrograph shows a nearly uniform distribution of the particles with an average size of 8 nm. This linoleic acid-capped silver nanoparticles show antimicrobial activity against Escherichia coli and Staphylococcus aureus.     

Green synthesis,characterisation and bioactivity of plant‐mediated silver nanoparticles using Decalepis hamiltonii root extract

Consistent search of plants for green synthesis of silver nanoparticles (SNPs) is an important arena in Nanomedicine. This study focuses on synthesis of SNPs using bioreduction of silver nitrate (AgNO₃) by aqueous root extract of Decalepis hamiltonii. The biosynthesis of SNPs was monitored by UV–vis analysis at absorbance maxima 432 nm. The fluorescence emission spectra of SNPs illustrated the broad emission peak 450–483 nm at different excitation wavelengths. The surface characteristics were studied by scanning electron microscope and atomic force microscopy, showed spherical shape of SNPs and dynamic light scattering analysis confirmed the average particle size 32.5 nm and the presence of metallic silver was confirmed by energy dispersive X‐ray. Face centred cubic structure with crystal size 33.3 nm was revealed by powder X‐ray diffraction. Fourier transform infrared spectroscopy indicated the biomolecules involved in the reduction mainly polyols and phenols present in root extracts were found to be responsible for the synthesis of SNPs. The stability and charge on SNPs were revealed by zeta potential analysis. In addition, on therapeutic forum, the synthesised SNPs elicit antioxidant and antimicrobial activity against Bacillus cereus, Bacillus licheniformis, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus.Inspec keywords: silver, nanoparticles, nanomedicine, antibacterial activity, biomedical materials, nanofabrication, particle size, microorganisms, ultraviolet spectra, visible spectra, fluorescence, scanning electron microscopy, atomic force microscopy, light scattering, X‐ray diffraction, X‐ray chemical analysis, Fourier transform infrared spectra, molecular biophysics, electrokinetic effectsOther keywords: phenols, zeta potential analysis, therapeutic forum, antioxidant activity, antimicrobial activity, Bacillus cereus, Bacillus licheniformis, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Ag, polyols, biomolecules, Fourier transform infrared spectroscopy, powder X‐ray diffraction, crystal size, face centred cubic structure, energy dispersive X‐ray analysis, metallic silver, particle size, dynamic light scattering analysis, spherical shape, atomic force microscopy, scanning electron microscopy, surface characteristics, excitation wavelengths, fluorescence emission spectra, UV‐visible analysis, biosynthesis, silver nitrate bioreduction, nanomedicine, Decalepis hamiltonii aqueous root extract, bioactivity, plant‐mediated silver nanoparticles, green synthesis     

Characterization of silver nanoparticles synthesized on titanium dioxide fine particles

Silver nanoparticles with a narrow size distribution were synthesized over the surface of two different commercial TiO(2) particles using a simple aqueous reduction method. The reducing agent used was NaBH(4); different molar ratios TiO(2):Ag were also used. The nanocomposites thus prepared were characterized using transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), x-ray photoelectron spectroscopy (XPS), x-ray diffraction (XRD), dynamic light scattering (DLS) and UV-visible (UV-vis) absorption spectroscopy; the antibacterial activity was assessed using the standard microdilution method, determining the minimum inhibitory concentration (MIC) according to the National Committee for Clinical Laboratory Standards. From the microscopy studies (TEM and STEM) we observed that the silver nanoparticles are homogeneously distributed over the surface of TiO(2) particles and that the TiO(2):Ag molar ratio plays an important role. We used three different TiO(2)Ag molar ratios and the size of the silver nanoparticles is 10, 20 and 80?nm, respectively. It was found that the antibacterial activity of the nanocomposites increases considerably comparing with separated silver nanoparticles and TiO(2) particles.     

Green synthesis of silver nanoparticles using Nervalia zeylanica leaf extract and evaluation of their antioxidant,catalytic, and antimicrobial potentials

ABSTRACT

Here we report a simple, one-pot, inexpensive, and eco-friendly method for the synthesis of silver nanoparticles. The leaf extract of a medicinal plant Nervalia zeylanica was used as reducing and stabilizing agent for the synthesis of nanoparticles by microwave-assisted strategy. The nanoparticles show characteristic surface plasmon peak at 468?nm in UV–vis absorption spectrum. The involvement of phytochemicals in the reduction and stabilization of nanoparticles was confirmed by FTIR analysis. Using X-ray diffraction analysis, the crystalline nature of the nanoparticles was demonstrated. Transmission electron microscopic analysis shows that the nanoparticles were in spherical shape with average particle size of 34.2?nm. The antioxidant studies were performed by the 1,1-diphenyl-2-picryl hydrazyl method. The nanoparticles show excellent scavenging activities than the leaf extract. The IC₅₀ values of silver nanoparticles and the leaf extract, respectively, were 15.20 and 92.83?µg?mL^?1. The catalytic activities of synthesized nanoparticles were examined by using them in the reduction of organic dyes. The nanoparticles show excellent catalytic activities and follow pseudo-first-order kinetics. The antimicrobial activities of nanoparticles were analyzed by an agar well diffusion method against six microbial strains and found that the nanoparticles were highly toxic against all the tested microbial strains.     

Biological synthesis of silver nanoparticles using the fungus Aspergillus flavus

The fungus, Aspergillus flavus when challenged with silver nitrate solution accumulated silver nanoparticles on the surface of its cell wall in 72 h. These nanoparticles dislodged by ultrasonication showed an absorption peak at 420 nm in UV-visible spectrum corresponding to the plasmon resonance of silver nanoparticles. The transmission electron micrographs of dislodged nanoparticles in aqueous solution showed the production of reasonably monodisperse silver nanoparticles (average particle size: 8.92 ± 1.61 nm) by the fungus. X-ray diffraction spectrum of the nanoparticles confirmed the formation of metallic silver. The Fourier transform infrared spectroscopy confirmed the presence of protein as the stabilizing agent surrounding the silver nanoparticles. These protein-stabilized silver nanoparticles produced a characteristic emission peak at 553 nm when excited at 420 nm in photoluminescence spectrum. The use of fungus for silver nanoparticles synthesis offers the benefits of eco-friendliness and amenability for large-scale production.     

Diospyros assimilis root extract assisted biosynthesised silver nanoparticles and their evaluation of antimicrobial activity

The current research study focuses on biosynthesis of silver nanoparticles (Ag NPs) for the first time from silver acetate employing methanolic root extract of Diospyros assimilis. The UV–Vis absorption spectrum of biologically synthesised nanoparticles displayed a surface plasmon peak at 428 nm indicating the formation of Ag NPs. The influence of metal ion concentration, reaction time and amount of root extract in forming Ag NPs by microscopic and spectral analysis was thoroughly investigated. Structural analysis from transmission electron microscopy confirmed the nature of metallic silver as face‐centered cubic (FCC) crystalline with an average diameter of 17 nm, which correlates with an average crystallite size (19 nm) calculated from X‐ray diffraction analysis. Further, the work was extended for the preliminary examination of antimicrobial activity of biologically synthesised Ag NPs that displayed promising activity against all the tested pathogenic strains.Inspec keywords: antibacterial activity, nanoparticles, silver, particle size, nanofabrication, nanomedicine, biomedical materials, ultraviolet spectra, visible spectra, optical microscopy, surface plasmon resonance, transmission electron microscopy, crystallites, X‐ray diffraction, microorganismsOther keywords: Diospyros assimilis root extract assisted biosynthesised silver nanoparticles, antimicrobial activity, silver acetate, methanolic root extract, UV‐visible absorption spectrum, biologically synthesised nanoparticles, surface plasmon peak, Ag NPs formation, metal ion concentration, reaction time, microscopic analysis, spectral analysis, structural analysis, transmission electron microscopy, metallic silver, FCC crystalline phase, average crystallite size, X‐ray diffraction analysis, pathogenic strains, Ag