Novel antibacterial hybrid materials based on polyvinyl alcohol and mercaptopropyltriethoxysilane with embedded silver nanoparticles (PVA/AgNps/MPTES)

Hybrid materials based on polyvinyl alcohol (PVA) and mercaptopropyltriethoxysilane (MPTES) with embedded silver nanoparticles (AgNps) have been synthesized via a sol–gel method. Silver nanoparticles were obtained via thermal reduction in the presence of PVA as a stabilizer and reducing agent. The formation of silver nanoparticles within the PVA/MPTES matrix was proven by FTIR, XRD, and TEM analysis. The antibacterial activity of PVA/AgNps/MPTES materials was determined against strains belonging to Gram-positive and Gram-negative bacteria by disk diffusion and growth curve methods. The hybrid materials showed high antibacterial activity, which depends on the concentration of the silver nanoparticles.     

Surface-anisotropic polystyrene spheres by electroless deposition

Surfaces of sulfate-terminated polystyrene microspheres are anisotropically modified with silver nanoparticles covering 20-50% of the sphere surface using electroless deposition. A PDMS templating method is employed. Silver nanoparticles are found to deposit uniformly onto the exposed sphere surfaces. The deposition is diffusion-controlled and the nanoparticles adhere strongly to the polystyrene particles despite extensive exposure to ultrasonication. Silver content is confirmed by EDAX analysis. The final silver coverage is controlled via the PDMS pre-curing conditions.     

室温离子液体中银纳米微粒的制备与结构表征

利用化学还原方法在室温离子液体1-甲基-3-丁基咪唑四氟硼酸盐中制备了金属银纳米微粒,采用X射线衍射,透射电子显微镜,傅立叶红外光谱和热分析对所制备的样品进行了结构表征.结果表明,所制备的银纳米微粒具有立方相结构,粒径约为20 nm.离子液体不但作为反应的溶剂而且作为修饰剂修饰在银纳米微粒的表面,从而有效地阻止了银纳米微粒的团聚.     

Effect of filler incorporation route on the properties of polysulfone–silver nanocomposite membranes of different porosities

Flat sheet porous polysulfone–silver nanocomposite membranes were synthesized by the wet phase inversion process. The effects of casting mixture composition and nanoparticle incorporation route on the morphological and separation properties of prepared membranes were studied by comparing nanocomposites of different preparations with silver-free controls. Silver nanoparticles were either synthesized ex situ and then added to the casting solution as an organosol or produced in the casting solution via in situ reduction of ionic silver by the polymer solvent. Nanocomposite membranes of three types differing in skin porosity and macrovoid structure were prepared. The structure and properties of nanocomposites were interpreted in terms of the coupling between the processes of nanoparticle formation and gelling of the polymer-rich phase during phase inversion. Larger nanoparticles preferentially located in the skin layer were observed in composites prepared via the ex situ method while in situ reduction of silver led to formation of smaller nanoparticles homogeneously distributed along the membrane cross-section. In some cases, incorporation of nanoscale silver formed ex situ resulted in macrovoid widening and an order of magnitude decrease in hydraulic resistance accompanied by only a moderate decrease in rejection. The accessibility of the silver nanoparticles embedded in the membrane was quantitatively assessed by the degree of the growth inhibition of a membrane biofilm due to the ionic silver released by the nanocomposites and was found to depend on the method of silver incorporation.     

Silver-colloid-nucleated cytochrome c superstructures encapsulated in silica nanoarchitectures

We recently discovered that self-organized superstructures of the heme protein cytochrome c (cyt. c) are nucleated in buffer by gold nanoparticles. The protein molecules within the superstructure survive both silica sol-gel encapsulation and drying from supercritical carbon dioxide to form air-filled biocomposite aerogels that exhibit gas-phase binding activity for nitric oxide. In this investigation, we report that viable proteins are present in biocomposite aerogels when the nucleating metal nanoparticle is silver rather than gold. Silver colloids were synthesized via reduction of an aqueous solution of Ag+ using either citrate or borohydride reductants. As determined by transmission electron microscopy and UV-visible absorption spectroscopy, the silver nanoparticles vary in size and shape depending on the synthetic route, which affects the fraction of cyt. c that survives the processing necessary to form a biocomposite aerogel. Silver colloids synthesized via the citrate preparation are polydisperse, with sizes ranging from 1 to 100 nm, and lead to low cyt. c viability in the dried bioaerogels (approximately 15%). Protein superstructures nucleated at approximately 10-nm Ag colloids prepared via the borohydride route, including citrate stabilization of the borohydride-reduced metal, retain significant protein viability within the bioaerogels (approximately 45%).     

Photochemical Synthesis of Anisotropic Silver Nanoparticles in Aqueous Solutions in the Presence of Sodium Citrate

The rapid one-step photochemical synthesis of anisotropic silver nanoparticles (ANPs) is reported. Silver ANPs were prepared from silver nitrate by a citrate route in aqueous solutions at room temperature under exposure to unfiltered light of a DRK 120 high-pressure mercury lamp. The silver ANPs form through one-electron reduction of the silver cation in its chelate complex with the production of sodium citrate photolysis. In the course of synthesis, small charged silver clusters and nanoparticles are formed first, which are then stabilized by citrate ions. Key factors that influence the synthesis of silver ANPs and their further transformation have been determined.     

Colloidal silver nanoparticles stabilized by a water-soluble triosmium cluster

Silver nanoparticles stabilized by the water soluble triosmium cluster Os₃(μ-H)(CO)₁₀S(CH₂)₁₀COO]Na were prepared by both photochemical and chemical reduction of silver nitrate. The silver nanoparticles were characterized by UV-Vis spectroscopy and high resolution TEM. The particles obtained by chemical reduction showed remarkable stability.     

导电高分子PEDOT/PSS保护银纳米颗粒的制备与表征

利用导电高分子聚(3,4-二氧乙基噻吩)/聚(对苯乙烯磺酸)(PEDOT/PSS)作保护剂,制备了银纳米颗粒,用UV-Vis和TEM对其进行了表征.结果表明,选择合适量的PEDOT/PSS保护剂可以得到大小分布较窄银纳米颗粒.     

Stabilization of Silver Nanoparticles by Polyelectrolytes and Poly(ethylene glycol)

Silver nanoparticles of 23 nm size were formed by chemical reduction of silver nitrate in excess of aqueous sodium borohydride. To examine the aggregation behavior in NaCl solutions, they were coated with poly(diallyldimethylammonium chloride), poly(allylamine hydrochloride) and poly(ethylene glycol) by layer‐by‐layer assembly. Silver nanoparticles coated with PDADMAC of both high and low molecular weight revealed the lowest stability independent of salt concentration. Silver nanoparticles coated with PAH and PEG are stable in 0.1 or 0.01 M NaCl, whereas addition of 0.5 M NaCl destroys the colloidal solution. The destruction of silver agglomerates and the increase of monodispersity in the case of PEG coated silver nanoparticles were observed after heating at 90 °C. In contrast, uncoated silver nanoparticles readily agglomerate and precipitate even after heating at 65 °C.

     

Preparation of polyimide/BaTiO3/Ag nanocomposite films via in situ technique and study of their dielectric behavior

Triphase polyimide nanocomposite films were fabricated using barium titanate （BaTiO3） with high dielectric constant and silver （Ag） with high conductivity as fillers. In situ method was utilized to obtain the homogeneous dispersion of nanoparticles. The in situ polymerization of polyimide precursor-poly（amic acid） was performed in the presence of BaTiO3 particles. Silver compound 1,1,1-trifluoro-2,4-pentadionato silver（I） was added into the BaTiO3 containing poly（amic acid） solution to achieve silver nanoparticles via in situ self metallization technique. The thermally induced reduction converted silver （I） to metallic silver with concomitant imidization of poly（amic acid） to polyimide. Both BaTiO3 and silver nanoparticles were uniformly dispersed in the polyimide substrate. The dependence of dielectric behavior on the BaTiO3 and Ag contents was studied. The incorporation of small amount of silver nanoparticles greatly increased dielectric constant of composite films.     

Synthesis of silver nanoparticles for remote opening of polyelectrolyte microcapsules

Silver nanoparticles of 10, 18, and 23 nm were synthesized in aqueous medium by chemical reduction of silver nitrate in excess of sodium borohydride. Modification of polyelectrolyte shells with synthesized silver nanoparticles was performed using the layer-by-layer approach. Remote opening of the polyelectrolyte/silver capsules was performed with a CW Nd:YAG FD laser with an average incident power output up to 70 mW. Capsules with a mixture of 10 and 18 nm silver nanoparticles in its polyelectrolyte shell were ruptured after less than 7 s of laser irradiation, while microcapsules with 23 nm silver nanoparticles in the shell were broken after 11 s of laser treatment and 10 nm silver nanoparticles were broken after 26 s.     

溶剂热法制备银纳米晶

以聚乙烯吡咯烷酮(PVP)作为表面活性剂,利用乙二醇溶剂热法成功制备了银纳米颗粒;利用场发射扫描电子显微镜(FE-SEM)、透射电子显微镜(TEM)、X射线衍射(XRD)分析了样品的形貌和晶体结构,并考察了溶剂组成等因素对银纳米颗粒形貌的影响.研究结果表明所得银纳米晶粒径均一,直径约为90nm;增大PVP的加入量会降低产物的粒径,溶剂中水的引入会影响银纳米晶的形貌.     

Preparation of silver nanoparticles with controlled particle size

Silver colloids show different colors due to light absorption and scattering in the visible region based on plasmon resonance. The resonance wavelength depends on particle size and shape. Here we report chemical reduction methods for preparation of silver nanoparticles exhibiting multicolor in aqueous solutions. Depending on chemical conditions the obtained nanoparticles are different regarding size and morphology.In order to investigate the relationship between size, stability and color of silver colloids we obtained silver nanoparticles in aqueous solutions using different reducing agents. The effect of polyvinyl pyrrolidone (PVP) and polyvinyl alcohol (PVA) on stabilization of obtained silver colloids was investigated. We have also studied the effect of silver precursor and its concentration on the formation of stable silver colloids.UV-VIS spectrum for silver colloids contains a strong plasmon band near 410 nm, which confirms silver ions reduction to Ag° in the aqueous phase. The formation of metal silver was also confirmed by powder X-ray diffraction (XRD) analysis. The diameter size of silver nanoparticles was in the range from 5 nm to 100 nm     

Reduction and aggregation of silver ions in <Emphasis Type="Italic">tert</Emphasis>-butanol

Silver ions undergo reduction reactions induced by radiolytically produced products of tert-butanol, a commonly used solvent and scavenger for hydroxyl radicals. Radiolytic reduction of silver ions and the subsequent formation of their clusters are compared with the corresponding processes in aqueous solution. The surface plasmon UV-Vis absorption band of silver nanocrystallites obtained by bombardment of tert-butanol solutions of silver salts with electron pulses showed an absorption maximum at 400 nm. Formation of different sizes of silver nanoparticles was found to be dependent on the dose rate. The nanocrystallites were found to have an average size of 20 nm.     

Nucleation and growth of silver nanoparticles monitored by titration microcalorimetry

The nucleation and the growth of silver nanoparticles were studied by spectrophotometry and transmission electron microscopy, with simultaneous recording of the concomitant enthalpy changes. Silver nanoparticles were stabilized by sodium citrate and reduction was brought about by the addition of hydroquinone in aqueous medium. It was established that nucleation is an exothermic process and heat effects are basically determined by the ratio of silver ions to hydroquinone. The process of nanoparticle formation was divided to three phases: the nucleation phase is exothermic, the growth phase is endothermic and further addition of the reducing agent results in the aggregation of silver nanoparticles, which produces a second exothermic heat effect.     

Bactericidal Effect of Poly(Acrylamide/Itaconic Acid)–Silver Nanoparticles Synthesized by Gamma Irradiation Against Pseudomonas Aeruginosa

Antimicrobial activity of silver nanoparticles is gaining importance due its broad spectrum of targets in cell compared to conventional antimicrobial agents. In this context, silver nanoparticles were synthesized by gamma irradiation-induced reduction method of acrylamide and itaconic acid with irradiation dose up to 70 kGy. Silver nanoparticles were examined by Fourier-transform infrared, scanning electron microscopic images (SEM), and ultraviolet–visible spectrophotometer. The particle size was determined by X-ray diffraction, transmission electron microscopy (TEM), and dynamic light scattering. The antibacterial effect was studied by disk diffusion method against some bacterial pathogenic strains. Silver nanoparticles showed promising activity against Pseudomonas aeruginosa and slightly active against Escherichia coli, methicillin-resistant Staphylococcus aureus, and Klebsiella pneumonia. The bactericidal effect of silver nanoparticles was tested against P. aeruginosa. The killing rate of P. aeruginosa was found to be 90 % of viability at (100 μl/ml) of silver nanoparticles. Exposure of P. aeruginosa cells to silver nanoparticles caused fast loss of 260 nm absorbing materials and release of potassium ions. The TEM and SEM observation showed that silver nanoparticles may destroy the structure of bacterial cell membrane in order to enter the bacterial cell resulting in the leakage of the cytoplasmic component and the eventual death.     

On the Chemical Processes Accompanying Silver Reduction from Solutions of Its Salts in Organic Media

Silver reduction from its nitrate has been studied in the media of DGEBA-based and aliphatic epoxy resins. It has been found that, under the experimental conditions that were employed, silver ions can be reduced without chemical interaction with the medium only due to photochemical processes. The reduction rate is determined by the rate of dissolution of the initial silver salt in an organic medium and the possibility of the formation of solvates by the system components. Refractometry has been proposed for use in monitoring the kinetics of silver nitrate dissolution in epoxy resins and the formation of silver nanoparticles. Stable dispersions of silver nanoparticles in epoxy resins have been obtained.     

Biosynthesis of silver nanoparticle using flowers of Calotropis gigantea (L.) W.T. Aiton and activity against pathogenic bacteria

Silver nanoparticles (AgNPs) from silver nitrate solution are carried out using the flower extract of Calotropis gigantea. Silver nanoparticles were characterized by UV–vis spectrophotometer, X-Ray diffractometer (XRD). Reduction of silver ions in the aqueous solution of silver during the reaction was observed by UV–vis spectroscopy. Crystalline nature of synthesized silver nanoparticles was studied by XRD pattern, refraction peak using the Scherrer’s equation. Antibacterial activity of the silver nanoparticles was performed by disc diffusion method against Bacillus subtilis, Pseudomonas putida and Escherichia coli. The antibacterial activity of synthesized silver nanoparticles by flower extract of C. gigantea was found against B. subtilis (10 mm). Synthesised AgNPs has the efficient antibacterial activity against Gram positive bacteria.     

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.     

Phyto-Functionalized Silver Nanoparticles Derived from Conifer Bark Extracts and Evaluation of Their Antimicrobial and Cytogenotoxic Effects

Silver nanoparticles synthesized using plant extracts as reducing and capping agents showed various biological activities. In the present study, colloidal silver nanoparticle solutions were produced from the aqueous extracts of Picea abies and Pinus nigra bark. The phenolic profile of bark extracts was analyzed by liquid chromatography coupled to mass spectrometry. The synthesis of silver nanoparticles was monitored using UV-Vis spectroscopy by measuring the Surface Plasmon Resonance band. Silver nanoparticles were characterized by attenuated total reflection Fourier transform infrared spectroscopy, Raman spectroscopy, dynamic light scattering, scanning electron microscopy, energy dispersive X-ray and transmission electron microscopy analyses. The antimicrobial and cytogenotoxic effects of silver nanoparticles were evaluated by disk diffusion and Allium cepa assays, respectively. Picea abies and Pinus nigra bark extract derived silver nanoparticles were spherical (mean hydrodynamic diameters of 78.48 and 77.66 nm, respectively) and well dispersed, having a narrow particle size distribution (polydispersity index values of 0.334 and 0.224, respectively) and good stability (zeta potential values of −10.8 and −14.6 mV, respectively). Silver nanoparticles showed stronger antibacterial, antifungal, and antimitotic effects than the bark extracts used for their synthesis. Silver nanoparticles obtained in the present study are promising candidates for the development of novel formulations with various therapeutic applications.