Effect of silver nanoparticles and silver nitrate on growth of rice under biotic stress

This study was organised to check the effect of silver nanoparticles and silver nitrate on rice growth against biotic stress. Silver nanoparticles were synthesised by using plant extract as reducing agent, followed by characterisation through UV Vis spectroscopy, XRD, EDS and SEM. Aspergillus application significantly reduced rice plant fresh mass (0.9%), dry mass (0.21%), root length (2.3%), shoot length (5.2%) and root number (1%) in comparison to control. Similarly, leaf area, leaf fresh mass, dry mass and leaf number were also reduced by 23.1, 0.02, 0.11 and 0.9%, respectively. AgNPs and AgNO₃ treatments increased the root length (16.2 & 12.8%), shoot length (21 & 20%), root number (8.1 & 6.8%), plant fresh weight (6.4 & 5%) and plant dry weight (4.6 & 3.5%) in 75mg/l treatment of AgNPs and AgNO₃ respectively. Similarly, AgNPs and AgNO₃ treatment (75 mg/l concentrations) reflected remarkable increase in leaf area (58.8 & 57.2 %), leaf number (4.3 & 3.7 %), leaf fresh weight (1.7 & 1.4 %) and leaf dry weight (0.9 & 0.8 %). Overall AgNPs showed more significant results as compared to AgNO₃. The quantity of aflatoxins ranged from 3.1 to 7.7 μg/kg against tolerable limit (4 µg/kg). Overall AgNPs and AgNO₃ treatments showed significant results and it could be considered as a strategy for aflatoxin management in rice plants.Inspec keywords: crops, scanning electron microscopy, nanoparticles, X‐ray diffraction, toxicology, agricultural pollution, agricultural safety, silver compounds, ultraviolet spectroscopyOther keywords: biotic stress, silver nanoparticles, AgNPs, silver nitrate, super kernel rice, Kala Shah Kaku research centre, UV–Vis spectroscopy, X‐ray diffraction, energy‐dispersive X‐ray spectroscopy, rice plant fresh mass, root number, leaf area, leaf fresh mass, dry mass, leaf number, root length, leaf fresh weight, leaf dry weight, examined rice plants, rice growth, aflatoxins, scanning electron microscopy, Aspergillus application, AgNO₃      

Negligible particle-specific antibacterial activity of silver nanoparticles

For nearly a decade, researchers have debated the mechanisms by which AgNPs exert toxicity to bacteria and other organisms. The most elusive question has been whether the AgNPs exert direct "particle-specific" effects beyond the known antimicrobial activity of released silver ions (Ag(+)). Here, we infer that Ag(+) is the definitive molecular toxicant. We rule out direct particle-specific biological effects by showing the lack of toxicity of AgNPs when synthesized and tested under strictly anaerobic conditions that preclude Ag(0) oxidation and Ag(+) release. Furthermore, we demonstrate that the toxicity of various AgNPs (PEG- or PVP- coated, of three different sizes each) accurately follows the dose-response pattern of E. coli exposed to Ag(+) (added as AgNO(3)). Surprisingly, E. coli survival was stimulated by relatively low (sublethal) concentration of all tested AgNPs and AgNO(3) (at 3-8 μg/L Ag(+), or 12-31% of the minimum lethal concentration (MLC)), suggesting a hormetic response that would be counterproductive to antimicrobial applications. Overall, this work suggests that AgNP morphological properties known to affect antimicrobial activity are indirect effectors that primarily influence Ag(+) release. Accordingly, antibacterial activity could be controlled (and environmental impacts could be mitigated) by modulating Ag(+) release, possibly through manipulation of oxygen availability, particle size, shape, and/or type of coating.     

Bio-mechanochemical synthesis of silver nanoparticles with antibacterial activity

By using a bio-mechanochemical approach combining mechanochemistry (ball milling) and green synthesis for the first time, silver nanoparticles (Ag NPs) with antibacterial activity were successfully synthesized. Concretely, eggshell membrane (ESM) or Origanum vulgare L. plant (ORE) and silver nitrate were used as environmentally friendly reducing agent and Ag precursor, respectively. The whole synthesis took 30?min in the former and 45?min in the latter case. The photon cross-correlation measurements have shown finer character of the product in the case of milling with Origanum. UV–Vis measurements have shown the formation of spherical NPs in both samples. TEM study has revealed that both samples are composites of nanosized silver nanoparticles homogenously dispersed within the organic matrices. It has shown that the size and size distribution of the silver nanoparticles is smaller and more uniform in the case of eggshell membrane matrix implying lower silver mobility within this matrix. The antibacterial activity was higher for the silver nanoparticles synthesized with co-milling with Origanum plant than in the case of milling with eggshell membrane.     

An optical tweezer-based study of antimicrobial activity of silver nanoparticles

Understanding and characterizing microbial activity reduction in the presence of antimicrobial agents can help in the design and manufacture of antimicrobial drugs. We demonstrate the use of an optical tweezer setup in recording the changes in bacterial activity with time, induced by the presence of foreign bodies in a bacterial suspension. This is achieved by monitoring the fluctuations of an optically trapped polystyrene bead immersed in it. Examining the changes in the fluctuation pattern of the bead with time provides an accurate characterization of the reduction in the microbial activity. Here, we report on the effect of addition of silver nanoparticles on bacterial cultures of Pseudomonas aeroginosa, Escherichia coli and Bacillus subtilis. We observe a decrease in the bacterial activity with time for the investigated bacterial samples. This method in our opinion, enables one to track changes in bacterial activity levels as a function of time of contact with the antibacterial agent with greater efficacy than traditional cell counting methods.     

Antibacterial activity of silver nanoparticles stabilized on tannin-grafted collagen fiber

Bayberry tannin (BT), a typical plant polyphenol, was grafted on collagen fiber (CF) in different mass ratios. Subsequently, the BT-grafted CF (BT-CF) was used as carrier and stabilizer to prepare BT-CF stabilized silver nanoparticles (BT-CF-AgNPs). Scanning Electron Microscopy image of BT-CF-AgNPs showed that the BT-CF-AgNPs was in ordered fibrous state. X-ray Diffraction patterns and Transmission Electron Microscopy images offered evidence that the Ag nanoparticles were well dispersed on BT-CF. Fourier Transform-Infrared Spectroscopy (FTIR) and X-ray Photoelectron Spectroscopy (XPS) investigations revealed that the Ag NPs were stabilized by the phenolic hydroxyls and quinones of BT on CF through electron donation/acception interaction. Antibacterial experiments demonstrated that BT-CF-AgNPs exhibited high antibacterial activity. When cell suspensions of Escherichia coli and Staphylococcus aureus (10⁴–10⁵ cfu/mL) were contacted with BT_0.19-CF-AgNPs (mass ratio of BT to CF = 0.19, conc. of Ag = 8 μg/mL) at 310 K under constant shaking, the number of cells went down to zero within 2 h. In addition, the minimal inhibitory concentration of BT_0.19-CF-AgNPs against Escherichia coli, Staphylococcus aureus, Penicillium glaucum and Saccharomyces cerevisiae was 2 μg/mL, 4 μg/mL, 6 μg/mL and 12 μg/mL Ag, respectively. During recycling use, the antibacterial activity of BT_0.19-CF-AgNPs against Escherichia coli can last for 5 cycles. These facts suggest that BT-CF-AgNPs can be used as a new and effective antibacterial agent.     

In-vivo and in-vitro biocompatibility evaluations of silver nanoparticles with antimicrobial activity

In this study, the biocompatibility and antimicrobial activity of silver nanoparticles (Ag NPs) were evaluated in vitro and in vivo. The cytotoxicity of Ag NPs (average diameter: 2-5 nm) against CHO-K1 cells was determined via WST-8 assay, and their genotoxicity was examined via Salmonella typhimurium reverse mutation assay (Ames test). The acute toxicity and intracutaneous reactivity of Ag NPs were evaluated using animal models of mice and rabbits, respectively. The antibacterial effects of Ag NPs on the Gram (-) bacterial strains of Escherichia coli ATCC 8739 and Pseudomonas aeruginosa ATCC 9027 and on the Gram (+) bacterial strains of Staphylococcus aureus ATCC 6538p and Bacillus subtilius ATCC 6633 were determined by measuring the minimum inhibitory concentrations. The Ag NPs were highly cytotoxic to the L-929 cells at over 2 ppm but were non-cytotoxic at lower than 1 ppm. Moreover, the Ag NPs at 1 ppm or lower did not show genotoxicity, acute toxicity and intracutaneous reactivity. It was also found that the Ag NPs exerted effective antimicrobial activities on both the Gram (-) and (+) bacterial strains within the range from 0.06 to 0.98 ppm for 50% MIC.     

Synthesis and characterization of dextran-capped silver nanoparticles with enhanced antibacterial activity

Dextran-capped silver nanoparticles were synthesized by reducing silver nitrate with NaBH4 in the presence of dextran as capping agent. The characters of silver nanoparticles were investigated using UV-Vis spectrophotometer, nano-grainsize analyzer, X-ray diffraction, and transmission electron microscopy. Results showed that the silver nanoparticles capped with dextran were in uniform shape and narrow size distribution. Moreover, compared with polyvinylpyrrolidone (PVP)-capped silver nanoparticles, the dextran-capped ones possessed better stability. Antibacterial tests of these silver nanoparticles were carried out for Escherichia coli, Staphylococcus aureus, Staphylococcus epidermidis, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Results suggested that the dextran-capped silver nanoparticles had high antibacterial activity against both Gram-positive and Gram-negative bacteria. In addition, the cytotoxicity in vitro of the dextran-capped silver nanoparticles was investigated using mouse fibrosarcoma cells (L929). The toxicity was evaluated by the changes of cell morphology and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assay. Results indicated that these silver nanoparticles had slight effect on the survival and proliferation of L-929 cells at their minimal inhibitory concentration (MIC). After modified by dextran, the physiochemical properties of the silver nanoparticles had been improved. We anticipated that these dextran-capped silver nanoparticles could be integrated into systems for biological and pharmaceutical applications.     

Design of a bioprocess to produce silver nanoparticles

The development of reliable processes for the synthesis of silver nanomaterials is an important aspect of current nanotechnology research. In this work, silver nanoparticles were produced in a bioreactor by Escherichia coli (E. coli). For this purpose, a process was designed and silver nanoparticles at a scale larger than laboratorial scale were produced by considering optimum conditions and using E. coli. This research for the first time was carried out at a scale larger than laboratory scale indicating ability to produce nanoparticles at a large scale using microorganisms. In addition, UV-vis spectroscopy, atomic absorption spectroscopy (AAS), transitional electron microscopy (TEM) and dynamic light scattering (DLS) were employed to investigate characterisation of nanoparticles.     

Synthesis of oleic acid-stabilized silver nanoparticles and analysis of their antibacterial activity

The development of new and simple green chemical methods for synthesizing colloidal solutions of functional nanoparticles is desirable for environment-friendly applications. In the present work, we report a feasible method for synthesizing colloidal solutions of silver nanoparticles (Ag NPs) based on the modified Tollens technique. The Ag NPs were stabilized by using oleic acid as a surfactant and were produced for the first time by the reduction of silver ammonium complex [Ag(NH₃)₂]⁺_(aq) by glucose with UV irradiation treatment. A stable and nearly monodisperse aqueous Ag NPs solution with average-sized particles (~ 9–10 nm) was obtained. The Ag NPs exhibited high antibacterial activity against both Gram-negative Escherichia Coli (E. coli) and Gram-positive Staphylococcus aureus bacteria. Electron microscopic images and analyses provided further insights into the interaction and bactericidal mechanism of the Ag NPs. The proposed method of synthesis is an effective way to produce highly bactericidal colloidal solutions for medical, microbiological, and industrial applications.     

Superior bactericidal activity of SDS capped silver nanoparticles: Synthesis and characterization

Silver nanoparticles were synthesized through UV photo-reduction of silver nitrate aqueous solution, containing ethanol and sodium dodecyl sulfate (SDS) using an UV digester equipped with high pressure mercury lamp of 500 W. The synthesized nanoparticles were characterized by UV–vis spectroscopy (UV–vis), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The formation of silver nanoparticles was confirmed from the appearance of surface plasmon absorption maxima at 418 nm. TEM showed the spherical nanoparticles with size in 23–67 nm (average 45 ± 10 nm). The silver nanoparticles were stable for more than 8 months. The antibacterial activity of these SDS capped silver nanoparticles was tested using Pseudomonas aeruginosa as a model strain for gram-negative bacteria. SDS capped silver nanoparticles exhibit a much higher bactericidal activity compared to silver nanoparticles capped with other capping agents. Even at a low silver nanoparticle concentration of 5 μg/ml, complete inhibition of 10⁷ colony forming units (CFU) was achieved with SDS capped silver nanoparticles. This concentration is much lower than the values reported by other authors. This enhanced bactericidal activity is attributed to much efficient transport of silver nanoparticles by SDS to the outer membrane of cell wall compared to the other capping agents and have a better interaction of nanoparticles with the cell.     

Antimicrobial sensibility of Streptococcus mutans serotypes to silver nanoparticles

Dental caries is a common infectious disease in humans all over the world and is considered a public health problem with an incidence and prevalence still high. The principal pathogen associated with the development of dental caries is Streptococcus mutans (S. mutans), a microorganism that has been widely studied. A new approach to treat dental caries is the use of silver nanoparticles (SNP) due to their antibacterial effect. It has been reported the effectiveness of SNP against S. mutans, but sensibility of S. mutans serotypes to SNP is still unknown. The aim of this study is to analyze the inhibitory effect of three different sizes of silver nanoparticles on S. mutans obtained from clinical isolates and one reference bacteria strain, determining sensibility differences between serotypes, which were determined by using PCR analysis. Silver nanoparticles with sizes around 9.3, 21.3 and 98 nm were prepared, characterized and used to find, with a microdilution method, the minimum inhibitory concentration (MIC) on S. mutans. SNP showed bactericidal effect on all strains tested with statistical differences between smaller nanoparticles and larger nanoparticles, 9.3 nm SNP showed a higher antibacterial activity than 21.3 and 98 nm SNP; however, sensibility was different among all clinical strains (p < 0.05) being serotype c the most sensible and serotype e the most resistant to the three different sizes of SNP considering the inhibitory effect better when nanoparticle size is smaller.     

Study of mechanism of enhanced antibacterial activity by green synthesis of silver nanoparticles

The extensive use of silver nanoparticles needs a synthesis process that is greener without compromising their properties. The present study describes a novel green synthesis of silver nanoparticles using Guava (Psidium guajava) leaf extract. In order to compare with the conventionally synthesized ones, we also prepared Ag-NPs by chemical reduction. Their optical and morphological characteristics were thoroughly investigated and tested for their antibacterial properties on Escherichia coli. The green synthesized silver nanoparticles showed better antibacterial properties than their chemical counterparts even though there was not much difference between their morphologies. Fourier transform infrared (FTIR) spectroscopic analysis of the used extract and as-synthesized silver nanoparticles suggests the possible reduction of Ag(+) by the water-soluble ingredients of the guava leaf like tannins, eugenol and flavonoids. The possible reaction mechanism for the reduction of Ag(+) has been proposed and discussed. The time-dependent electron micrographs and the simulation studies indicated that a physical interaction between the silver nanoparticles and the bacterial cell membrane may be responsible for this effect. Based on the findings, it seems very reasonable to believe that this greener way of synthesizing silver nanoparticles is not just an environmentally viable technique but it also opens up scope to improve their antibacterial properties.     

Evaluation of antimicrobial activity of synthesised silver nanoparticles using Thymus kotschyanus aqueous extract

Development of a green chemistry process for the synthesis of silver nanoparticles (AgNPs) has become a focus of interest. Characteristics of AgNPs were determined using techniques, such as ultraviolet–visible spectroscopy (UV–vis), Fourier transform infrared (FTIR) analysis, scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy and X‐ray diffraction (XRD). The synthesised AgNPs using Thymus kotschyanus had the most growth inhibition against gram‐positive bacteria such as Staphylococcus aureus and Bacillus subtilise, while the growth inhibition of AgNPs at 1000–500 µg/ml occurred against Klebsiella pneumonia and at 1000–250 µg/ml of AgNPs was observed against E. coli. The UV–vis absorption spectra confirmed the formation of the AgNPs with the characteristic peak at 415 nm and SEM micrograph acknowledged spherical particles in a nanosize range. FTIR measured the possible biomolecules that are responsible for stabilisation of AgNPs. XRD analysis exhibited the crystalline nature of AgNPs and showed face‐centred cubic structure. The synthesised AgNPs revealed significant antibacterial activity against gram‐positive bacteria.Inspec keywords: visible spectra, microorganisms, ultraviolet spectra, biomedical materials, nanofabrication, nanoparticles, X‐ray diffraction, scanning electron microscopy, molecular biophysics, X‐ray chemical analysis, nanomedicine, silver, antibacterial activity, Fourier transform infrared spectraOther keywords: green chemistry process, ultraviolet–visible spectroscopy, gram‐positive bacteria, silver nanoparticles, Thymus kotschyanus aqueous extract, UV–vis spectroscopy, Fourier transform infrared spectroscopy, FTIR analysis, scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, SEM micrograph, X‐ray diffraction, XRD, Staphylococcus aureus, Bacillus subtilise, Klebsiella pneumonia, E. coli, UV–vis absorption spectra, face‐centred cubic structure, antibacterial activity, antimicrobial activity, wavelength 415.0 nm, Ag     

Antibacterial activity of SiO2/hydroxypropyl cellulose hybrid materials containing silver nanoparticles

Silica hybrid materials containing tetraethyl orthosilicate (TEOS) as SiO₂ precursor, hydroxypropyl cellulose (HPC) as an organic compound with incorporation of silver were prepared, and their structure and surface morphology were examined by FTIR measurements and SEM. The quantity of organic substance was 5 wt.% and the silver concentration varied from 0.5 to 2.5 wt.%. It is suggested that the main structural units build an amorphous network of synthesized hybrids from depolymerized [SiO₄] tetrahedra giving strong bands at 1050 and 790 cm^? 1. The surface morphology changed from smooth to rough with the increasing amount of silver. The possible antibacterial behavior of the hybrid materials was also studied. The results indicate pronounced antibacterial performance against Escherichia coli and Bacillus subtilis. Highest antibacterial activity was detected against B. subtilis. The increase of silver concentration up to 2.5 wt.% Ag leads to stronger antibacterial effects with both strains.     

Polyvinyl alcohol/silver nanoparticles (PVA/AgNps) as a model for testing the biological activity of hybrid materials with included silver nanoparticles

Comparing the influence of two different stabilizers as polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP), as well as organosilanes as tetraethoxysilane (TEOS), allows determining the main role of the silver nanoparticles included in hybrid materials for the realization of their antimicrobial activity. The proposed two-step testing scheme first onto control strains and then onto clinical bacterial and fungal strains resistant to antibiotics allows full investigation of these properties.     

Polyurethane–silver fibers prepared by infiltration and reduction of silver nitrate

Silver-incorporating polyurethane fibers were prepared by infiltration of silver nitrate on electrospun polyurethane fibers and reduction with sodium borohydride. They were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and energy-dispersive X-ray system. The Ag nanoparticles prepared by reduction of silver nitrate showed nano-sized crystals of 4–10 nm in diameter. However, larger aggregated Ag particles of 50–200 nm were also found to be dispersed in the polyurethane matrix when Ag particles were formed in electrospun fibers by the infiltration–reduction process of silver nitrate. As a result, infiltration method of silver nitrate into the electrospun fibers was significantly effective to produce silver-incorporating fibers due to a high specific surface area of fibers.     

A facile synthetic route to aqueous dispersions of silver nanoparticles

Stable aqueous dispersions of silver nanoparticles have been synthesized from an organometallic precursor dissolved in an organic phase. Hydrogen gas is used to reduce the precursor to form silver nanoparticles which spontaneously transfer into an immiscible aqueous phase where they are stabilized. This route provides a simple pathway for the preparation of aqueous nanoparticle solutions and avoids production of the inorganic ions that are usually associated with aqueous methods. The effectiveness of a variety of aqueous stabilizing agents is evaluated. All products show plasmon absorption bands characteristic of silver nanoparticles and transmission electron microscopy reveals most particles to be below 40 nm in diameter.     

Photo-induced growth of DNA-capped silver nanoparticles

We report the photo-induced nucleation and growth of silver nanoparticles in aqueous solution in the presence of DNA oligomers. An organic dye (Cy5) was used as a photosensitizer to initiate the nanoparticle growth upon illumination with 647 nm light. The formation of nanoparticles and growth kinetics were observed by extinction spectroscopy, dynamic light scattering, and transmission electron microscopy. Irradiation of the precursor solutions with light at the Cy5 absorption maximum triggered the instantaneous formation of spherical particles with a metallic core ~15 nm in diameter. Remarkably, the particles feature significantly larger effective hydrodynamic diameters (35 nm) in solution, indicative of a DNA ad-layer on the nanoparticle surface. Centrifugation experiments confirmed that DNA was inseparably associated with the nanoparticles and indicated that DNA oligomers adsorb onto the nanoparticle surface during growth, playing the role of a capping agent. The introduced method is a fast and facile way to prepare DNA-capped silver nanoparticles in a single growth step.     

Fluorescence enhancement of modified silver nanoparticles

Surface enhanced fluorescence (SEF) effect of acridine orange fluorophore in the proximity of silver nanoparticles (NPs) has been investigated experimentally in the aqueous solution system. It was found that the SEF effect could be influenced by the distribution of the NPs and the separation between the fluorophore molecule and metal surface. The fluorescence enhancement was improved significantly when Ag NPs was capped with 4-Aminothiophenol (PATP) that was acted as an isolating layer between the metal surface and fluorophore molecules. The results suggest that a proper distribution of metallic NPs and proper separation between fluorophore molecule and the particle surface are important for obtaining an optimal SEF effect.     

Actinobacterial‐mediated synthesis of silver nanoparticles and their activity against pathogenic bacteria

In this study, silver nanoparticles (AgNPs) were biosynthesised by using acidophilic actinobacterial SH11 strain isolated from pine forest soil. Isolate SH11 was identified based on 16S rRNA gene sequence to Streptomyces kasugaensis M338‐M1^T and S. celluloflavus NRRL B‐2493^T (99.8% similarity, both). Biosynthesised AgNPs were analysed by UV–visible spectroscopy, which revealed specific peak at λ  = 420 nm. Transmission electron microscopy analyses showed polydispersed, spherical nanoparticles with a mean size of 13.2 nm, while Fourier transform infrared spectroscopy confirmed the presence of proteins as the capping agents over the surface of AgNPs. The zeta potential was found to be −16.6 mV, which indicated stability of AgNPs. The antibacterial activity of AgNPs from SH11 strain against gram‐positive (Staphylococcus aureus and Bacillus subtilis) and gram‐negative (Escherichia coli) bacteria was estimated using disc diffusion, minimum inhibitory concentration and live/dead analyses. The AgNPs showed the maximum antimicrobial activity against E. coli, followed by B. subtilis and S. aureus. Further, the synergistic effect of AgNPs in combination with commercial antibiotics (kanamycin, ampicillin, tetracycline) was also evaluated against bacterial isolates. The antimicrobial efficacy of antibiotics was found to be enhanced in the presence of AgNPs.Inspec keywords: antibacterial activity, silver, nanoparticles, electrokinetic effects, Fourier transform infrared spectra, microorganisms, nanofabricationOther keywords: actinobacterial mediated synthesis, silver nanoparticles, pathogenic bacteria, biosynthesis, acidophilic actinobacterial SH11 strain, pine forest soil, 16S rRNA gene sequence, Streptomyces kasugaensis M338‐M1T, S. celluloflavus NRRL B‐2493T, UV–visible spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, zeta potential, gram positive bacteria, Staphylococcus aureus, Bacillus subtilis, gram negative bacteria, Escherichia coli, disc diffusion, wavelength 420 nm, Ag