Development of silver-containing nanocellulosics for effective water disinfection

Electrospun cellulose nanofibers and cellulose-graft-polyacrylonitrile (Cell-g-PAN) copolymer nanofibers containing silver nanoparticles (AgNPs) were synthesized for effective water disinfection. Surface morphology, AgNPs content, physical distribution of AgNPs, levels of silver leaching from the fibers in water and antimicrobial efficacy were studied. Scanning electron microscope images revealed that AgNPs in cellulose nanofibers were more evenly dispersed than in Cell-g-PAN copolymer nanofibers, but with the certainty that Cell-g-PAN copolymer nanofibers had higher AgNPs content. This was confirmed by energy dispersive X-ray analysis and atomic absorption analysis. Both cellulose nanofibers and Cell-g-PAN copolymer nanofibers containing AgNPs had excellent antimicrobial activity against Escherichia coli, Salmonella typhi, and Staphylococcus aureus, with cellulose-nAg nanofibers killing between 91 and 99 % of bacteria in a contaminated water sample and Cell-g-PAN-nAg copolymer nanofibers killed 100 %. Neither Cell-g-PAN copolymer nanofibers nor cellulose nanofibers leached silver into water.     

<Emphasis Type="Italic">Stachys lavandulifolia</Emphasis> and <Emphasis Type="Italic">Lathyrus</Emphasis> sp. Mediated for Green Synthesis of Silver Nanoparticles and Evaluation Its Antifungal Activity Against <Emphasis Type="Italic">Dothiorella sarmentorum</Emphasis>

In this study, silver nanoparticles (AgNPs) were biosynthesized using Stachys lavandulifolia and Lathyrus sp. The first sign of the reduction of silver ions to AgNPs was the change in color of S. lavandulifolia and Lathyrus sp. extracts changed into dark brown and auburn after treating with silver nitrate, respectively. The UV–Vis spectroscopy of reaction mixture (extract+silver nitrate) produced by S. lavandulifolia and Lathyrus sp. showed the strong adsorption peaks at ?440 and 420 nm, respectively. The transmission electron microscope images showed the synthesis of AgNPs using S. lavandulifolia and Lathyrus sp. with an average size of 7 and 11 nm, respectively. The result of X-ray diffraction pattern showed four diffraction peaks at 38°, 44°, 64°, and 77° for both types of biosynthesized AgNPs. Fourier transform infrared spectroscopy showed the possible role of involved proteins and polyhydroxyl functional groups in the synthesis process of AgNPs. Inductively coupled plasma analysis determined the conversion rate (percentage) of silver ions to silver nanoparticles in reaction mixtures of S. lavandulifolia and Lathyrus sp. 99.73 and 99.67 %, respectively. In addition, antifungal effect of AgNPs, synthesized by both extracts, was studied separately on mycelial growth of Dothiorella sarmentorum, in a completely randomized design on potato dextrose agar (PDA) medium. The inhibition rate of mycelial growth was strongly depended on the density of AgNPs and it strongly increased with increasing the density of AgNPs in the PDA medium. AgNPs more than 90 % of them inhibited from the mycelia growth of the fungus at the concentration of 40 µg/mL and higher.     

Biosynthesis,characterization, and antimicrobial effect of silver nanoparticles obtained using <Emphasis Type="Italic">Lavandula</Emphasis> × <Emphasis Type="Italic">intermedia</Emphasis>

The use..... of aqueous leaf extract of Lavandula × intermedia for biosynthesis of silver nanoparticles (AgNPs) is presented. The plant extract was obtained by boiling dried leaves and using the obtained filtrate for the synthesis of AgNPs. The study was conducted to investigate an ecofriendly approach to metal nanoparticle synthesis and to evaluate the antimicrobial potential of both the aqueous plant extract and resulting silver nanoparticles against different microbes using the disc diffusion method. The synthesis of silver nanoparticles was monitored using ultraviolet–visible (UV–v is) spectroscopy, which showed a localized surface plasmon resonance band at 411 nm and a shift of the band to higher wavenumber of 422 nm after 90 min of reaction. Powder X-ray diffraction analysis and transmission electron microscopy of the obtained AgNPs revealed their crystalline nature, with average size of 12.6 nm. Presence of elemental silver was further confirmed by energy-dispersive X-ray spectroscopy. Fourier-transform infrared spectroscopy confirmed presence of phytochemicals from Lavandula × intermedia leaf extract on the AgNPs. The AgNPs showed good antimicrobial activity with inhibition zone ranging from 10 to 23 mm; the largest inhibition zone (23 mm) occurred against Escherichia coli. Generally, the AgNPs displayed more antimicrobial activity against all investigated pathogens compared with Lavandula × intermedia leaf extract, and were also more active than streptomycin against Klebsiella oxytoca and E. coli at the same concentration. The silver nanoparticles showed prominent antimicrobial activity with a lowest minimum inhibitory concentration (MIC) value of 15 μg/mL against E. coli, K. oxytoca, and Candida albicans.     

An amperometric uric acid biosensor based on chitosan-carbon nanotubes electrospun nanofiber on silver nanoparticles

A novel amperometric uric acid biosensor was fabricated by immobilizing uricase on an electrospun nanocomposite of chitosan-carbon nanotubes nanofiber (Chi–CNTsNF) covering an electrodeposited layer of silver nanoparticles (AgNPs) on a gold electrode (uricase/Chi–CNTsNF/AgNPs/Au). The uric acid response was determined at an optimum applied potential of ?0.35 V vs Ag/AgCl in a flow-injection system based on the change of the reduction current for dissolved oxygen during oxidation of uric acid by the immobilized uricase. The response was directly proportional to the uric acid concentration. Under the optimum conditions, the fabricated uric acid biosensor had a very wide linear range, 1.0–400 μmol L^?1, with a very low limit of detection of 1.0 μmol L^?1 (s/n?=?3). The operational stability of the uricase/Chi–CNTsNF/AgNPs/Au biosensor (up to 205 injections) was excellent and the storage life was more than six weeks. A low Michaelis–Menten constant of 0.21 mmol L^?1 indicated that the immobilized uricase had high affinity for uric acid. The presence of potential common interfering substances, for example ascorbic acid, glucose, and lactic acid, had negligible effects on the performance of the biosensor. When used for analysis of uric acid in serum samples, the results agreed well with those obtained by use of the standard enzymatic colorimetric method (P?>?0.05).

Green fabrication of silver nanoparticles via Ipomea carnea latex extract: Antibacterial activity

A versatile green and nontoxic begin method for bio-reduction of silver nanoparticles (AgNPs) using latex extract of Ipomea carnea was reported. Different instrumental tools were applied to evaluate the formation of AgNPs, as an example UV–Visible spectroscopy (UV–Vis), Fourier transform infra-red (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HR-TEM). The absorption peak of AgNPs obtained at around 413 nm. FTIR study confirmed that the bio-capping components present in latex extract served as reducing and stabilizing agent. The findings of XRD, SEM and HR-TEM images revealed that the formation of crystalline and spherical shape nanoparticles and showed well size distribution with mean size 9.8±0.27 nm. Additionally, the green fabricated AgNPs exhibited considerable zone of inhibition for both Gram-positive and Gram–negative bacteria. The outcome implies that the synthesized AgNPs also showed similar inhibition effect as streptomycin (a common reference antibiotic).     

Green Synthesis of Silver Nanoparticles Using Arachis hypogaea (Ground Nut) Root Extract for Antibacterial and Clinical Applications

The present study focused on the green synthesis of silver nanoparticles (AgNPs) using Arachis hypogaea (ground nut) root extract for the antibacterial and clinical application. The presence of major phytochemical compounds are found to be 2H-Pyaran,2,5-diethenyltetrahydro, Didodecyl phthalate, Decanoic acid, Tetradecanoic acid, Bis(2-ethylhexyl) phthalate, Dodecanoic acid, Phosphonic acid, 2-(4-Methoxyphenyl)-5-(4-methoxynaphthyl) thiophene and Methyl 2-(N-Benzylimino)-4-chloro-3,3-dimethylbutanoate by GC–MS. Nanoparticles synthesis is confirmed by UV–Vis analysis by observing the maximum absorption spectrum at 450 nm. XRD and SEM–EDX results reveals the synthesized nanoparticles are cubic crystalline with agglomerated particles of silver oxide with biomolecules present around it. TEM images clearly shows that the biosynthesized nanoparticles are mostly spherical and irregular shaped with an average particles size of 30 nm. Highest susceptibility pattern of silver nanoparticle against Enterococcus sp. (35 ± 0.4 mm) which followed by Pseudomonas sp. (33 mm) and Staphylococcus aureus (29 mm). Green synthesized nanoparticles are coated over the commercially available clinical band aid cloth by dip coating method. Silver nanoparticle incorporated band aid cloth showed good antibacterial activity against the harmful bacteria which usually cause infection and interfere during wound healing. Our findings revealed that green nanoparticle has a good antibacterial action against harmful bacteria and showed good response for efficient clinical application.     

Sunlight-Mediated Green Synthesis of Silver Nanoparticles Using the Berries of Ribes rubrum (Red Currants): Characterisation and Evaluation of Their Antifungal and Antibacterial Activities

Plants are a treasure trove of several important phytochemicals that are endowed with therapeutic and medicinal properties. Ribes rubrum L. (red currants) are seasonal berries that are widely consumed for their nutritional value and are known for their health benefits. Red currants are a rich source of secondary metabolites such as polyphenols, tocopherols, phenolic acids, ascorbic acid, and flavonoids. In this study, sunlight-mediated synthesis of silver nanoparticles (AgNPs) was successfully accomplished within 9 min after adding the silver nitrate solution to the aqueous extract of red currant. The synthesised AgNPs were characterised with UV–Vis, transmission electron microscopy (TEM), dynamic light scattering (DLS), Fourier transform infrared spectrum (FTIR), and energy-dispersive X-ray spectrum (EDX). The efficacy of aqueous extracts of red currants and AgNPs in controlling the growth of some pathogenic fungi and bacteria was also investigated. The UV–visible (UV–Vis) spectrum displayed an absorption peak at 435 nm, which corresponded to the surface plasmon band. The strong silver signal on the EDX spectrum at 3 keV, authenticated the formation of AgNPs. The several peaks on the FTIR spectrum of the aqueous extract of red currant and the nanoparticles indicated the presence of some important functional groups such as amines, carbonyl compounds, and phenols that are vital in facilitating the process of capping and bioreduction, besides conferring stability to nanoparticles. The TEM microphotographs showed that the nanoparticles were well dispersed, roughly spherical, and the size of the nanoparticles ranged from 8 to 59 nm. The red currant silver nanoparticles were highly potent in inhibiting the growth and proliferation of some fungal and bacterial test isolates, especially Alternaria alternata, Colletotrichum musae, and Trichoderma harzianum. Based on the robust antifungal and antibacterial activity demonstrated in this study, red currant nanoparticles can be investigated as potential replacements for synthetic fungicides and antibiotics.     

Exploitation of Haloferax alexandrinus for Biogenic Synthesis of Silver Nanoparticles Antagonistic to Human and Lower Mammalian Pathogens

In the present study we report the use of cells of a Haloarchaeon for the green synthesis of silver nanoparticles. Biosynthesis of AgNPs occurred within 30 s on exposure of cells of Haloferax alexandrinus to silver nitrate in direct sunlight. Maximum AgNPs production was achieved within 4 min of exposure of silver nitrate (0.05 %) to cells (5 mg/ml), at pH 7, at ambient day temperature (26–34 °C). The AgNPs had characteristic surface plasmon resonance at 420 nm in UV–Vis spectra. Spherical and irregular crystals ranging from 2 to 60 nm in size with an average size of 18 nm were observed in TEM analysis. The FTIR spectral analysis indicated involvement of N–H, –OH, C=O, C–O functional groups present in cells of Haloferax alexandrinus MTCC 3265. The biogenic AgNPs exhibited broad spectrum antimicrobial activity against human and mammalian pathogens, in the order of Pseudomonas aeruginosa ATCC 9027 > Bordetella bronchiseptica ATCC 4617 > Bacillus subtilis ATCC 6633 > Staphylococcus aureus ATCC 6538P > Staphylococcus epidermidis ATCC 12228 > Escherichia coli ATCC 8739 > Salmonella typhimurium ATCC 14028.     

Antibacterial effect of silver nanoparticles prepared in bipolymers at moderate temperature

The purpose of this study was to investigate the antibacterial effect of silver nanoparticles in chitosan–poly(ethylene glycol) suspension. The silver nanoparticles (AgNPs) were prepared by use of an environmentally benign method from chitosan (Cts) and poly(ethylene glycol) (PEG) at moderate temperature and with stirring for different times. Silver nitrate (AgNO₃) was used as the metal precursor and Cts and PEG were used as solid support and polymeric stabilizer, respectively. The antibacterial activity of silver–chitosan–poly(ethylene glycol) nanocomposites (Ag–Cts–PEG NCs) against Staphylococcus aureus, Micrococcus luteum, Pseudomonas aeruginosa, and Escherichia coli was tested by use of the Mueller–Hinton agar disk-diffusion method. Formation of AgNPs was determined by UV–visible spectroscopy; surface plasmon absorption maxima were observed at 415–430 nm in the UV–visible spectrum. The peaks in the XRD pattern confirmed that the AgNPs had a face-centered cubic structure; peaks of contaminated crystalline phases were not observed. Transmission electron microscopy (TEM) revealed that the AgNPs synthesized were spherical. The optimum stirring time for synthesis of the smallest particle size (mean diameter 5.50 nm) was 12 h. The AgNPs in Cts–PEG were effective against all the bacteria tested. Higher antibacterial activity was observed for AgNPs with smaller size. These results suggest that AgNPs can be used as an effective inhibitor of bacteria and can be used in medical applications. These results also suggest that AgNPs were successfully synthesized in Cts–PEG suspension at moderate temperature with different stirring times.     

Green Synthesis of Silver Nanoparticles Using Acacia farnesiana (Sweet Acacia) Seed Extract Under Microwave Irradiation and Their Biological Assessment

In the present study, Acacia farnesiana (Sweet acacia) seed extract is used to reduce Ag⁺ → Ag⁰ under microwave irradiation. The formation of silver nanoparticles (AgNPs) is monitored by recording the UV–Vis absorption spectra for surface plasmon resonance (SPR) peak at ~450 nm. The absorbance of SPR increases linearly with increasing temperature of the reaction mixture. Rapid reduction of silver ions occurred to form AgNPs, 80–90 % yield in about 150 s. A marginal decrease in pH and increase in solution potential (E) of the reaction mixture during the formation of AgNPs are in agreement with the proposed mechanism. XRD pattern of the AgNPs agree with the fcc structure of Ag metal, and the calculated crystallite size is ~17 nm. FT-IR and solid-state ¹³C NMR spectra indicate the functional groups of flavonones and terpenoids (biomolecules from plant extract) which are adsorbed on AgNPs, thereby the present method led to in situ biofunctionalization/bio-capping of AgNPs. TG analysis shows the thermal decomposition of these plant residues present on AgNPs at about 250 °C. The spherical shape of the particles with a diameter (?) in the range of ~15–20 nm is evident from FE-SEM image. Elemental analysis by EDX analysis confirms the presence of Ag as the only major element. The in vitro antibacterial screening of AgNPs shows that these bio-capped AgNPs have higher inhibitory action for E. coli and S. aureus followed by B. subtilis and P. aeruginosa. In addition, AgNPs show very good antioxidant property.     

Daphne mucronata-mediated phytosynthesis of silver nanoparticles and their novel biological applications,compatibility and toxicity studies

This contribution reports the biosynthesis of silver nanoparticles (AgNPs) using aqueous leaf extracts of D. mucronata and their diverse applications. Synthesized AgNPs were characterized using diverse techniques, i.e. UV, XRD, EDS, SEM, TEM, FTIR and TGA/DTA. These techniques confirmed the authenticity of the synthesized nanoparticles. The bimodulated AgNPs revealed the highest radical scavenging potential, i.e. 86.4% relative to plant extract at 600?μg/ml. Escherichia coli was found to be the most susceptible strain to AgNPs. Growth of vancomycin-resistant Staphylococcus aureus was also inhibited. Hemolytic activity revealed negligible hemolysis, indicating the biocompatible nature of biomodulated AgNPs. Furthermore, no mutagenic properties were shown by the biogenic AgNPs. Synthesized nanoparticles possessed promising insecticidal potential and had no phytotoxic activity. No haemagglutination was observed for biogenic AgNPs.     

Potential of Kalopanax septemlobus Leaf Extract in Synthesis of Silver Nanoparticles for Selective Inhibition of Specific Bacterial Strain in Mixed Culture

Silver nanoparticles (AgNPs) were synthesised using Kalopanax septemlobus plant leaf extracts. UV-visible spectrophotometric, Fourier-transform infrared, electron dispersive X-ray spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses confirmed synthesis of AgNPs. TEM micrographs revealed presence of well-dispersed AgNPs predominantly of small size and different shapes with an average particle size of 30.8 nm. Antimicrobial susceptibility tests of AgNP treatments revealed variability in sensitivity of bacteria Bacillus cereus and Saccharophagus degradans under study. Minimum inhibitory concentration (MIC) values of the AgNPs for B. cereus and S. degradans were found to be 30 and 10 μg/mL, respectively. The mixed culture of B. cereus and S. degradans treated with AgNPs at 10 μg/mL showed increase in growth with time, suggesting survival of bacteria in liquid media. The plating of mixed culture before AgNP treatment showed presence of both bacteria, but 24-h-old mixed culture treated with AgNPs at the concentration of 10 μg/mL showed presence of B. cereus colonies. SEM micrographs revealed damage to S. degradans cells but no effect on B. cereus cells after AgNP treatment. Confocal microscopic observations of AgNP-treated mixed cultures by Nile blue A staining indicated intact polyhydroxyalkanoates producing flourescent cells of B. cereus but damage and deformities in S. degradans cells. This study suggests that AgNPs can selectively inhibit growth of S. degradans and retain B. cereus at MIC of S. degradans. This report is a case study for selective inhibition of one bacteria and growth of the other in a culture using plant-synthesized silver nanoparticles.     

Synthesis of Metallic Silver Nanoparticles by Fluconazole Drug and Gamma Rays to Inhibit the Growth of Multidrug-Resistant Microbes

Here we tailored a methodology, including green synthesis of silver nanoparticles (AgNPs) in aqueous solution using Fluconazole (Fluc.), a broad-spectrum antifungal agent under the influence of gamma rays. AgNPs were characterized by UV–Vis., FTIR, XRD, DLS, and TEM image. Antimicrobial activities of AgNPs, Fluc., and Ag⁺ were investigated against multidrug-resistant (MDR) bacteria and unicellular fungi. From our results, AgNPs production was found to be dependent on the concentration of Ag⁺, Fluc. and gamma doses. DLS with TEM image explained the size and shape of AgNPs and were found to be spherical with diameter of 11.65 nm. FTIR analysis indicates that, the hydroxyl, nitrogen and fluoride moiety in Fluc. were responsible for the reduction and binding process. AgNPs possesses antimicrobial activity against all tested microbes more than Ag⁺. It produced high efficacy against Acinetobacter baumannii (20.0 mm ZOI). AgNPs are synergistically active towards Candida albicans (17.0 mm ZOI). Investigated action mechanisms for AgNPs activity had been discussed. Thereby, owing to its unique features as cost-effective with continued-term stabilization, it can discover potential targets in biomedical applications and infectious diseases control.     

Nanocomposites based on crosslinked polyacrylic latex/silver nanoparticles for waterborne high‐performance antibacterial coatings

Functional polymer/AgNPs nanocomposites have been prepared. Silver nanoparticles (NPs) were synthesized to which polyacrylamide, PAAm, was covalently bound. PAAm was synthesized via a RAFT reaction and carried thiol and carboxylic acid end groups. Thiol was used to bind the polymer to the metal surface and carboxyl for further reactions. The AgNPs were used in a post‐crosslinking reaction with a separately synthesized poly(butyl acrylate‐co‐methyl methacrylate)/polyglycidyl methacrylate core/shell latex bearing epoxy functional groups. Dynamic mechanical analysis showed that the functional AgNPs effectively crosslinked the latex polymer, and that the final product had excellent mechanical strength. Antibacterial tests revealed that the nanocomposite films had strong antibacterial activity against all types of the bacteria and the immobilization of silver NPs by crosslinking retarded the release of silver in comparison to the uncrosslinked ones. With the presented method, it is possible to obtain ductile antibacterial nanocomposites to be used as waterborne functional coatings. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1435–1447     

Synthesis of Rumex hastatus-based silver nanoparticles induced the inhibition of human pathogenic bacterial strains

The development of antibiotic resistance in pathogenic bacterial strains has drawn attention to the quest for new natural antibacterial drugs. Therefore, in the present study, extracts of Rumex hastatus leaves were obtained in methanol and water, and R. hastatus-based silver nanoparticles (AgNPs) were synthesized. Structural and functional properties of synthesized silver nanoparticles were determined by UV–vis spectroscopy, XRD, FTIR and SEM. The synthesized AgNPs and crude extracts were tested to check their antibacterial potential against human pathogenic bacterial strains of Staphylococcus aureus, Staphylococcus haemoliticus, Bacillus cereus, Escherichia coli, Salmonella typhi and Pseudomonas aeruginosa in well diffusion and broth dilution methods. The present investigation has revealed for the first time that the broth dilution method was found more reproducible than that of the well diffusion method even at lower concentrations of AgNPs and crude extracts. UV– Vis spectroscopic analysis of AgNPs revealed a peak at 367 nm_. XRD pattern showed a face-centered cubical to the spherical structure of AgNP crystals. FTIR analysis revealed that flavonoids and terpenoids are responsible for the reduction of AgNO₃ to Ag⁺. SEM analysis determined the spherical structure and 51 nm average diameter of nanoparticles. The antibacterial activity of R. hastatus-based (AgNPs) was found to be significantly higher than aqueous plant extract and silver nitrate alone. Bacterial growth was inhibited by R. hastatus-based AgNPs in a dose-dependent manner. To our knowledge, silver nanoparticles (AgNPs) of R. hastatus were synthesized and characterized for the first time in this study and, based on the findings of current research work R. hastatus extract-based silver nanoparticles are suggested to be used as an antibacterial drug instead of synthetic drugs for the treatment of various human diseases/infections caused by the tested bacterial strains.     

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.     

Detection of silver nanoparticles in parsley by solid sampling high-resolution–continuum source atomic absorption spectrometry

In this work, we present a fast and simple approach for detection of silver nanoparticles (AgNPs) in biological material (parsley) by solid sampling high-resolution–continuum source atomic absorption spectrometry (HR-CS AAS). A novel evaluation strategy was developed in order to distinguish AgNPs from ionic silver and for sizing of AgNPs. For this purpose, atomisation delay was introduced as significant indication of AgNPs, whereas atomisation rates allow distinction of 20-, 60-, and 80-nm AgNPs. Atomisation delays were found to be higher for samples containing silver ions than for samples containing silver nanoparticles. A maximum difference in atomisation delay normalised by the sample weight of 6.27?±?0.96 s mg^?1 was obtained after optimisation of the furnace program of the AAS. For this purpose, a multivariate experimental design was used varying atomisation temperature, atomisation heating rate and pyrolysis temperature. Atomisation rates were calculated as the slope of the first inflection point of the absorbance signals and correlated with the size of the AgNPs in the biological sample. Hence, solid sampling HR-CS AAS was proved to be a promising tool for identifying and distinguishing silver nanoparticles from ionic silver directly in solid biological samples.

Silver Metallic Nanoparticles with Surface Plasmon Resonance: Synthesis and Characterizations

Silver nanoparticles were synthesized by the reduction of the silver nitrate (AgNO₃) using the latex copolymer in ethanol solution under microwave (MW) heating. The reaction parameters such as silver precursor concentration (from 0.005 to 0.1 g/l) and MW power (200–800 W) significantly affect the formation rate, shape, size and distribution of the silver nanoparticles. A significant reduction of irradiation time was observed when the MW energy is compared to conventional thermal reduction processes. The prepared silver nanoparticles show uniform and stable sizes from 5 to 11 nm, which can be stored at room temperature for approximately 12 months without any visible change. These peculiarities indicate that the latex copolymer is a good stabilizer for the silver nanoparticles. The optical properties, morphology, and crystalline structure of the silver-latex copolymer nanocomposites were characterized by the Ultraviolet–Visible spectroscopy, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The study of the TEM images at high magnifications identified the silver nanoparticles as face-centered cubic (fcc) structure with spherical and hexagonal shapes.     

Biosynthesis of Bixa orellana seed extract mediated silver nanoparticles with moderate antioxidant,antibacterial and antiproliferative activity

Biosynthesis of metallic silver nanoparticles (AgNPs) has gained much interest and offers an attractive alternate to physical and chemical approaches. In recent year several safe, easy, cost-effective, reproducible, and environmentally friendly synthesis approaches for silver nanoparticles have been developed. In this research work, a simple, cheap, and unexplored method was applied on green synthesis of AgNPs using secondary metabolites extracted from Bixa orellana seeds. The seeds are rich of flavonoids and phenolic compounds which presumably responsible for the fast reduction and stabilization of silver ion into silver nanoparticles. The biosynthesis process is very likely to be able to reduce silver ions under simple physiological conditions. The surface plasmon resonance (SPR) that was appeared at 420 nm in UV–vis spectrum, had confirmed the formation of AgNPs. Moreover, the functional groups in secondary metabolite that act as reducing, capping and stabilizing agents for silver nanoparticles, are identified by Fourier transform infrared (FTIR) spectra. An X-ray diffraction analysis generated four peaks for Bixa orellana seed extract mediated AgNPs positioned at 2θ angles of 38.1°, 44.2°, 64.6°, and 77.5° corresponding to crystal planes (1 1 1), (2 0 0), (2 2 0), and (3 1 1). Field emission scanning electron microscope (FESEM) and transmission electron microscopy (TEM) images confirmed the formation of nanosized silver particles. The z-average of the synthesized particles measured by dynamic light scattering (DLS) was found to be 92.9 nm. AgNPs synthesized exhibited remarkable antioxidant activity, antibacterial and antiproliferative activity against human breast (MCF-7) cell line. On the basis of our results, we conclude that biologically synthesized AgNPs exhibited favorable characteristics and have the potential to be used in biomedical fields.     

Green Synthesis of Silver Nanoparticles Using Euphorbia wallichii Leaf Extract: Its Antibacterial Action against Citrus Canker Causal Agent and Antioxidant Potential

Biologically synthesized silver nanoparticles are emerging as attractive alternatives to chemical pesticides due to the ease of their synthesis, safety and antimicrobial activities in lower possible concentrations. In the present study, we have synthesized silver nanoparticles (AgNPs) using the aqueous extract of the medicinal plant Euphorbia wallichii and tested them against the plant pathogenic bacterium Xanthomonas axonopodis, the causative agent of citrus canker, via an in vitro experiment. The synthesized silver nanoparticles were characterized by techniques such as UV-Vis spectroscopy, Fourier transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction analysis and transmission electron microscopy. Moreover, the plant species were investigated for phenolics, flavonoids and antioxidant activity. The antioxidant potential of the extract was determined against a DPPH radical. The extract was also evaluated for phenolic compounds using the HPLC technique. The results confirmed the synthesis of centered cubic, spherical-shaped and crystalline nanoparticles by employing standard characterization techniques. A qualitative and quantitative phytochemical analysis revealed the presence of phenolics (41.52 mg GAE/g), flavonoids (14.2 mg QE/g) and other metabolites of medicinal importance. Different concentrations (1000 µg/mL to 15.62 µg/mL—2 fold dilutions) of AgNPs and plant extract (PE) alone, and both in combination (AgNPs-PE), exhibited a differential inhibition of X. axanopodis in a high throughput antibacterial assay. Overall, AgNPs-PE was superior in terms of displaying significant antibacterial activity, followed by AgNPs alone. An appreciable antioxidant potential was recorded as well. The observed antibacterial and antioxidant potential may be attributed to eight phenolic compounds identified in the extract. The Euphorbia wallichii leaf-extract-induced synthesized AgNPs exhibited strong antibacterial activity against X. axanopodis, which could be exploited as effective alternative preparations against citrus canker in planta in a controlled environment. In addition, as a good source of phenolic compounds, the plant could be further exploited for potent antioxidants.