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.     

One-pot synthesis and characterization of poly(alkoxysilane)s promoted by silver colloidal nanoparticles

Si-Si/Si-O dehydrocoupling of hydrosilanes with alcohols (1:1.5 mole ratio), catalyzed by AgNO3 which converted to Ag(0) colloidal nanoparticles, gave poly(alkoxysilane)s in one-pot in moderate to high yield. The hydrosilanes include p-X-C6H4SiH3 (X = H, CH3, OCH3, F), PhCH2SiH3, and (PhSiH2)2. The alcohols include MeOH, EtOH, (i)PrOH, PhOH, and CF3(CF2)2CH2OH. The weight average molecular weight and polydispersity of the poly(alkoxysilane)s were in the range of 1,600 approximately 8,000 Dalton and 1.4 approximately 3.5. The dehydrocoupling reactions of phenylsilane with ethanol (1:3 mole ratio) in the presence of the silver nanocolloid catalyst produced only triethoxyphenylsilane as product.     

Enhanced antibacterial effect of azlocillin in conjugation with silver nanoparticles against Pseudomonas aeruginosa

In recent years, the problems associated with bacterial resistance to antibiotics caused nanodrugs to be considered as a new way for infectious diseases treatment. The main purpose of this study was to develop a new agent against Pseudomonas aeruginosa, a very difficult bacterium to treat, based on azlocillin antibiotic and silver nanoparticles (AgNPs). Azlocillin was conjugated with AgNPs by chemical methods and its antimicrobial activity was studied against P. aeruginosa using well diffusion agar method. Then, minimum inhibitory concentration and minimum bactericidal concentration of the new conjugate was specified with macro‐dilution method. The animal study showed the considerable enhanced antibacterial effect of azlocillin in conjugation with AgNPs against P. aeruginosa in comparison with azlocillin alone, AgNPs alone and azlocillin in combination with AgNPs.Inspec keywords: antibacterial activity, silver, nanoparticles, organic compounds, microorganisms, drugs, nanomedicine, biomedical materials, diseases, diffusion, nanofabricationOther keywords: Ag, macrodilution method, minimum bactericidal concentration, minimum inhibitory concentration, well diffusion agar method, P. aeruginosa, antimicrobial activity, chemical methods, azlocillin antibiotic nanoparticles, infectious diseases treatment, nanodrugs, bacterial resistance, Pseudomonas aeruginosa, silver nanoparticles, antibacterial effect     

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.     

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.     

Facile synthesis of silver nanoparticles mediated by polyacrylamide‐reduction approach to antibacterial application

The current time increase in the prevalence of antibiotic resistant ‘super‐bugs’ and the risks associated with food safety have become global issues. Therefore, further research is warranted to identify new and effective antimicrobial substances. Silver nanoparticles (Ag‐NPs) were synthesized by autoclaving technique using, different concentrations of Ag salt (AgNO₃) solution (1, 5, 10, and 25 mM). Their presence was confirmed by a surface plasmon resonance band at ∼435 nm using UV–Vis absorption spectra. The morphology of the synthesized Ag‐NPs stabilized by polyacrylamide (PAM) was examined by TEM, SAED, and EDS. TEM images revealed that the synthesized Ag‐NPs had an average diameter of 2.98±0.08 nm and SAED and EDS results confirmed the formation of Ag‐NPs. In addition, FT‐IR spectroscopy revealed that a PAM polymer matrix stabilized the Ag‐NPs. The well diffusion method, was used to test, Gram positive and Gram negative bacteria were examined. Also the minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) were studied against Ag‐NPs. The Ag‐NPs exhibited strong inhibitory activity, MIC and MBC against the tested clinical bacterial isolates. These results suggest that Ag‐NPs stabilized in PAM are highly effective against clinical bacterial isolates can be applied in medical fields.Inspec keywords: antibacterial activity, silver, nanoparticles, nanomedicine, surface plasmon resonance, X‐ray chemical analysis, transmission electron microscopy, electron diffraction, Fourier transform infrared spectroscopy, microorganisms, ultraviolet spectra, visible spectraOther keywords: Ag‐NP facile synthesis, PAM‐reduction approach, antibacterial application, antibiotic resistant super‐bugs, food safety, antimicrobial agents, antibiotics, antimicrobial substances, Ag salt solution concentration, ultraviolet‐visible absorption spectra, polyacrylamide, transmission electron microscopy, electron diffraction, energy dispersive X‐ray spectroscopy, TEM images, Fourier transform infrared spectroscopy, PAM polymer matrix, diffusion method, Gram positive bacteria, Gram negative bacteria, clinical bacterial isolates, Ag     

Green synthesis of silver nanoparticles using bovine skin gelatin and its antibacterial effect on clinical bacterial isolates

Nanoparticles are being increasingly used in day‐to‐day life. Therefore, concerns have been raised regarding their interactions with the surrounding environment. This study focused on a simple green method for synthesizing silver nanoparticles (Ag‐NPs) in an autoclave at 15 psi (103 kPa) and 121°C. An aqueous solution of AgNO₃ as a precursor of Ag‐NPs and gelatin (type B) reducing and/or stabilizing (capping) agent were used. The effect of various AgNO₃ concentrations of certain gelatin concentration and various gelatin concentrations at constant AgNO₃ concentration, and autoclaving time, was studied. UV‐Vis spectra ascribed that the presence of localized surface plasmon resonance (SPR) of the synthesized Ag‐NPs. TEM images and the selected area of electron diffraction confirmed, the formation of Ag‐NPs with a diameter of approximately 5 ±0.35 nm. Furthermore, FT‐IR revealed that a gelatin polymer matrix stabilized the synthesized Ag‐NPs. The Well diffusion assay was used to test the effect of Ag‐NPs on six clinical bacterial isolates, where Gram positive bacteria were more susceptible to Ag‐NPs than Gram negative bacteria. Therefore, Ag‐NPs capped by gelatin have remarkable potential effect as an antibacterial agent, and they not only have various medical applications but can also be used in biological, pharmaceutical and industrial fields.Inspec keywords: silver, nanoparticles, nanomedicine, antibacterial activity, microorganisms, nanofabrication, skin, gelatin, ultraviolet spectra, visible spectra, surface plasmon resonance, transmission electron microscopy, electron diffraction, Fourier transform infrared spectra, polymers, biomedical materialsOther keywords: green synthesis, silver nanoparticles, bovine skin gelatin, antibacterial effect, clinical bacterial isolates, autoclave, reducing agent, stabilising agent, ultraviolet‐visible spectra, localised surface plasmon resonance, transmissions electron microscope images, electron diffraction, Fourier transform infrared spectroscopy, gelatin polymer matrix, well diffusion assay, gram negative bacteria, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, gram positive bacteria, Bacillus megaterium, Streptococcus pyogenes, Staphylococcus aureus, temperature 121 degC, Ag     

Enhanced luminescence from lanthanide complex by silver nanoparticles

Photoluminescence of europium complex, Eu(III)DPA, where DPA is dipicolinic acid, in the presence of 5 nm-diameter Ag nanoparticles, was studied. Pronounced enhancement of Eu(III) luminescence was observed in the complex solution containing Ag nanoparticle with a concentration below 3.0 × 10¹³/ml. The dependencies of emission intensity of ⁵D₀ → ⁷F₂ and ⁵D₀ → ⁷F₁ transition on the concentration of Ag nanoparticles are quite different, the enhancement of electric dipole transition is stronger than that of magnetic dipole transition. There is no significant change in fluorescence lifetime in enhanced luminescence. The enhancement was attributed to a strong coupling between the radiation transition and surface plasmon resonance.     

Synthesis and characterization of CoFe(2)O(4) ferrite nanoparticles obtained by an electrochemical method

Uniform size cobalt ferrite nanoparticles have been synthesized in one step using an electrochemical technique. Synthesis parameters such as the current density, temperature and stirring were optimized to produce pure cobalt ferrite. The nanoparticles have been investigated by means of magnetic measurements, M?ssbauer spectroscopy, x-ray powder diffraction and transmission electron microscopy. The average size of the electrosynthesized samples was controlled by the synthesis parameters and this showed a rather narrow size distribution. The x-ray analysis shows that the CoFe(2)O(4) obtained presents a totally inverse spinel structure. The magnetic properties of the stoichiometric nanoparticles show ferromagnetic behavior at room temperature with a coercivity up to 6386?Oe and a saturation magnetization of 85?emu?g(-1).     

Synthesis and antibacterial properties of silver nanoparticles

Nanometer sized silver particles were synthesized by inert gas condensation and co-condensation techniques. Both techniques are based on the evaporation of a metal into an inert atmosphere with the subsequent cooling for the nucleation and growth of the nanoparticles. The antibacterial efficiency of the nanoparticles was investigated by introducing the particles into a media containing Escherichia coli. The antibacterial investigations were performed in solution and on petri dishes. The silver nanoparticles were found to exhibit antibacterial effects at low concentrations. The antibacterial properties were related to the total surface area of the nanoparticles. Smaller particles with a larger surface to volume ratio provided a more efficient means for antibacterial activity. The nanoparticles were found to be completely cytotoxic to E. coli for surface concentrations as low as 8 microg of Ag/cm2.     

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.     

Investigative evaluation of Cassia absus for antibacterial capacity and biomimetic synthesis of silver nanoparticles

Cassia absus is used for medicinal purposes for a long time all over the world. In this study, the authors report the antimicrobial potential of C. absus extracts obtained with different solvents. The extract(s) obtained with ethyl acetate yielded the best antibacterial effects because of a rich supply of oxalates and alkaloids in it. The same extract was also exploited for reducing Ag⁺ ions (to metallic Ag⁰) for the synthesis of nanoparticles. Electron microscopy revealed that the silver nanoparticles were ∼18–25 nm in diameter. The Fourier‐transform infrared evaluation pointed towards the fact that flavonoids present in the plant extract were acting as reductants while amino groups were the bound stabilisation agents to the synthesised nanoparticles limiting the diameter to a certain threshold and avoiding aggregation naturally. A comparative antibacterial assay of C. absus versus Ag nanoparticles showed that the nanoparticles as well as organic (ethyl acetate) extract of the plant checked the growth of selected (MDR) superbugs. However, the biosynthesised Ag nanoparticles returned better antibacterial efficacies than ethyl acetate extract.Inspec keywords: biomimetics, nanomedicine, nanoparticles, nanofabrication, reduction (chemical), microorganisms, silver, antibacterial activity, Fourier transform infrared spectra, biomedical materials, electron microscopyOther keywords: antibacterial capacity, biomimetic synthesis, silver nanoparticles, antimicrobial potential, ethyl acetate, oxalates, alkaloids, electron microscopy, Fourier‐transform infrared evaluation, antibacterial efficacies, antibacterial assay, organic extract, Cassia absus, flavonoids, Ag     

In situ synthesis of silver nanoparticles on silk fabric with PNP for antibacterial finishing

This research presents a generic strategy to fabricate antibacterial textile through in situ synthesis of silver nanoparticles on the fabric with smart polymeric molecules. Silk fabric and polyamide network polymer (PNP) were chosen for this study. PNP which has numerous amino groups and three-dimensional structure was applied to entrap silver ions into silk fabric. The pretreated silk fabrics were heated by steam method to make silver nanoparticles synthesized in situ on them without any other reductant and linker to provide silk fabric with antibacterial properties. The results indicated that the treated silk fabrics had excellent antibacterial activity and laundering durability. The quantitative bacterial tests showed the bacterial reduction rates of Staphylococcus aureus and Escherichia coli were able to reach above 99 % with not more than 0.05 mmol/L of AgNO₃. The whiteness of silk fabric only changed from 90.47 to 86.49. The antibacterial activity of the treated silk fabric was maintained at 98.86 % reduction even after being exposed to 30 consecutive home laundering conditions. In addition, the results of scanning electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy confirmed that silver nanoparticles had generated and dispersed well in Ag⁰ form on the surface of silk fibers. The understanding acquired from this work will allow one to work with the preparation of other silver nanoparticles functional textiles with excellent antibacterial activities and laundering durability through this facile, eco-friendly in situ synthesis method.     

Shape- and size-selective electrochemical synthesis of dispersed silver(I) oxide colloids

Silver(I) oxide (Ag2O) micro- and nanoparticles were electrochemically synthesized by anodizing a sacrificial silver wire in a basic aqueous sulfate solution. Ag2O particles were released from the silver electrode surface during synthesis producing a visible sol "stream". The composition of these particles was established using selected area electron diffraction, X-ray diffraction, and X-ray photoelectron spectroscopy. The shape of Ag2O crystallites could be adjusted using the potential of the silver wire generator electrode. The generation of a dispersed Ag2O sol and the observed shape selectivity are both explained by a two-step mechanism involving the anodic dissolution of silver metal, Ag0 --> Ag+(aq) + 1e-, followed by the precipitation of Ag2O particles, 2Ag+ + 2OH- --> Ag2O(s) + H2O. Within 100 mV of the voltage threshold for particle growth, cubic particles with a depression in each face ("hopper crystals") were produced. The application of more positive voltages resulted in the generation of 8-fold symmetric "flower"-shaped particles formed as a consequence of fast growth in the <111> crystallographic direction. The diameter of flower particles was adjustable from 250 nm to 1.8 microm using the growth duration at constant potential.     

Peanut skin extract mediated synthesis of gold nanoparticles,silver nanoparticles and gold–silver bionanocomposites for electrochemical Sudan IV sensing

Sustainable methods are needed for rapid and efficient detection of environmental and food pollutants. The Sudan group of dyes has been used extensively as adulterants in food and also are found to be polluting the soil and water bodies. There have been several methods for detection of Sudan dyes, but most of them are not practical enough for common use. In this study, the electrochemical detection efficiency and stability of gold nanoparticle (AuNPs), silver NPs and Au–Ag bionanocomposites, synthesised by peanut skin extract, modified glassy carbon electrode has been investigated. The synthesised nanomaterial samples were characterised, for their quality and quantity, using ultra–visible spectroscopy, inductive coupled plasma mass spectrophotometer, Fourier transform infrared spectroscopy, energy‐dispersive X‐ray spectroscopy, high‐resolution transmission electron microscope and field emission scanning electron microscope. The nanomaterial hybrid electrodes showed great efficiency and stability in the detection of Sudan IV compared with the other previous electrodes. The peak current of the Sudan IV oxidation and reduction was found to be proportional to its concentration, in the range of 10–80 µM, with a detection limit of 4 µM. The hybrid electrodes showed 90% stability in detection for 20 cycles.Inspec keywords: gold, silver, nanoparticles, nanocomposites, biomedical materials, electrochemical sensors, dyes, nanofabrication, ultraviolet spectra, visible spectra, spectrophotometry, Fourier transform infrared spectra, X‐ray chemical analysis, transmission electron microscopy, scanning electron microscopy, field emission electron microscopyOther keywords: peanut skin extract mediated synthesis, gold nanoparticles, silver nanoparticles, gold–silver bionanocomposites, electrochemical Sudan IV sensing, electrochemical detection efficiency, modified glassy carbon electrode, ultra–visible spectroscopy, inductive coupled plasma mass spectrophotometer, Fourier transform infrared spectroscopy, energy‐dispersive X‐ray spectroscopy, high‐resolution transmission electron microscope, field emission scanning electron microscope, oxidation, reduction, detection limit, Au, Ag, Au‐Ag     

Green synthesis of colloidal silver nanoparticles by sonochemical method

A facile sonochemical method was developed for preparing colloidal silver nanoparticles (Ag-NPs) in aqueous gelatin solutions. The effect of the reducing agent and Ag⁺ concentrations, ultrasonic time, and ultrasonic amplitude on the particle size has been investigated. The size of the Ag-NPs decreases with the ultrasonic amplitude and increases with ultrasonic time. Well-dispersed spherical Ag-NPs with a mean particle size of about 3.5 nm have been synthesized under ultrasonic process. The use of gelatin as an eco-friendly stabilizer provides green and economic attributes to this work. This preparation method is general and may be extended to other noble metals, such as Au, Pd and Pt, and may possibly find various additional medicinal, industrial and technological applications.     

Genotoxicity tests of poly(styrene-co-maleic anhydride)-coated silver nanoparticles in vivo and in vitro

Nanosilver is thought to hold potential for use in medical materials. The safety of newly developed poly(styrene-co-maleic anhydride)-coated silver nanoparticles (SMA-AgNPs) requires investigation. In this study, three in vitro and in vivo experiments for investigating genetic toxicity–the Ames test, a micronucleus assay, and a chromosome aberration test–were conducted. Results from the Ames testing showed SMA-AgNPs to have a negative effect, either with or without S9 metabolism. In addition, SMA-AgNPs increased the number of reticulocytes and micronuclei in reticulocytes at 48 and 72 h after treatment. Indeed, SMA-AgNPs induced significant changes in the chromosomal aberration rate in CHO-K1 (Chinese hamster ovary cell clone K1) cells. In conclusion, SMA-AgNPs did cause DNA damage in terms of chromosomal aberration and may have a potential genotoxic effect in certain applications.