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.     

Functional Fe3O4/TiO2 core/shell magnetic nanoparticles as photokilling agents for pathogenic bacteria

A photokilling approach for pathogenic bacteria is demonstrated using a new type of magnetic nanoprobe as the photokilling agent. In addition to their magnetic property, the nanoprobes have other features including a photocatalytic property and the capacity to target bacteria. The nanoprobes comprise iron oxide/titania (Fe(3)O(4)@TiO(2)) core/shell magnetic nanoparticles. As dopamine molecules can self-assemble onto the surface of the titania substrate, dopamine is used as the linker to immobilize succinic anhydride onto the surfaces of the Fe(3)O(4)@TiO(2) nanoparticles. This is followed by the immobilization of IgG via amide bonding. We demonstrate that the IgG-Fe(3)O(4)@TiO(2) magnetic nanoparticles not only have the capacity to target several pathogenic bacteria, but they also can effectively inhibit the cell growth of the bacteria targeted by the nanoparticles under irradiation of a low-power UV lamp within a short period. Staphylococcus saprophyticus, Streptococcus pyogenes, and antibiotic-resistant bacterial strains, such as multiantibiotic-resistant S. pyogenes and methicillin-resistant Staphylococcus aureus (MRSA), are used to demonstrate the feasibility of this approach.     

Self-supported silver nanoparticles containing bacterial cellulose membranes

Hydrated bacterial cellulose (BC) membranes obtained from cultures of Acetobacter xylinum were used in the preparation of silver nanoparticles containing cellulose membranes. In situ preparation of Ag nanoparticles was achieved from the hydrolytic decomposition of silver triethanolamine (TEA) complexes. Scanning electron microscopy (SEM) images and X-ray diffraction (XRD) patterns both lead to the observation of spherical metallic silver particles with mean diameter of 8 nm well adsorbed onto the BC fibriles.     

Direct stamping of silver nanoparticles toward residue-free thick electrode

Direct stamping of functional materials has been developed for cost-effective and process-effective manufacturing of nano/micro patterns. However, there remain several challenging issues like the perfect removal of the residual layer and realization of high aspect ratio. We have demonstrated facile fabrication of flexible strain sensors that have microscale thick interdigitated capacitors with no residual layer by a simple direct stamping with silver nanoparticles (AgNPs). Polyurethane (PU) prepolymer was utilized as an adhesive layer to transfer AgNPs more efficiently during the separation step of the flexible stamp from directly stamped AgNPs. Scanning electron microscopy images and energy dispersive x-ray spectroscopy analysis revealed residue-free transfer of microscale thick interdigitated electrodes onto two different flexible substrates (elastomeric and brittle) for the application to highly sensitive strain sensors.     

Direct stamping of silver nanoparticles toward residue-free thick electrode

Abstract

Direct stamping of functional materials has been developed for cost-effective and process-effective manufacturing of nano/micro patterns. However, there remain several challenging issues like the perfect removal of the residual layer and realization of high aspect ratio. We have demonstrated facile fabrication of flexible strain sensors that have microscale thick interdigitated capacitors with no residual layer by a simple direct stamping with silver nanoparticles (AgNPs). Polyurethane (PU) prepolymer was utilized as an adhesive layer to transfer AgNPs more efficiently during the separation step of the flexible stamp from directly stamped AgNPs. Scanning electron microscopy images and energy dispersive x-ray spectroscopy analysis revealed residue-free transfer of microscale thick interdigitated electrodes onto two different flexible substrates (elastomeric and brittle) for the application to highly sensitive strain sensors.     

Direct nucleation of silver nanoparticles on graphene sheet

Silver (Ag) nanoparticles were synthesized on the surface of graphene sheet by the simultaneous reduction of Ag+ and graphene oxide (GO) in the presence of simple reducing agent, hydrazine hydrate (N2H4 x H2O). Both the Ag+ and GO were reduced and Ag+ was nucleated onto graphene. GO flakes were prepared by conventional chemical exfoliation method and in the presence of strong acidic medium of potassium chlorate. Silver nanoparticles were prepared using 0.01 M AgNO3 solution. The reduced GO sheet decorated with Ag is referred as G-Ag sample. G-Ag was characterized by FTIR (Fourier transform infrared) spectroscopy using GO as standard. An explicit alkene peak appeared around 1625 cm(-1) was observed in G-Ag sample. Besides, the characteristic carbonyl and hydroxyl peaks shows well reduction of GO. The FTIR therefore confirms the direct interaction of Ag into Graphene. SEM (scanning electron microscopy) and TEM (transmission electron microscopy) analysis were performed for morphological probing. The average size of Ag nanoparticles was confirmed by around 5-10 nm by the high-resolution TEM (HRTEM). The Ag quantum dots incorporated nanocomposite material could become prominent candidate for diverse applications including photovoltaic, catalysis, and biosensors etc.     

Biosynthesis and structural characterization of silver nanoparticles from bacterial isolates

This study aimed to develop a green process for biosynthesis of silver nanomaterials by some Egyptian bacterial isolates. This target was achieved by screening an in-house culture collection consists of 300 bacterial isolates for silver nanoparticle formation. Through screening process, it was observed that strains belonging to Escherichia coli (S30, S78), Bacillus megaterium (S52), Acinetobacter sp. (S7) and Stenotrophomonas maltophilia (S54) were potential candidates for synthesis of silver nanoparticles. The extracellular production of silver nanoparticles by positive isolates was investigated by UV-Vis spectroscopy, X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results demonstrated that UV-visible spectrum of the aqueous medium containing silver ion showed a peak at 420 nm corresponding to the plasmon absorbance of silver nanoparticles. Scanning electron microscopy micrograph showed formation of silver nanoparticles in the range of 15-50 nm. XRD-spectrum of the silver nanoparticles exhibited 2θ values corresponding to the silver nanocrystal that produce in hexagonal and cubic crystal configurations with different plane of orientation. In addition, the signals of the silver atoms were observed by EDS-spectrum analysis that confirms the presence of silver nanoparticles (AgNPs) in all positive bacterial isolates.     

Polyelectrolyte assisted silver nanoparticles synthesis and thin film formation

Silver nanoparticles were prepared by the reduction of silver salts with sodium borohydride and capped with a copolymer of styrene sulfonate and maleic monomers. The synthesized nanoparticles were then deposited on a glass substrate using the layer-by-layer deposition technique in alternance with polycationic poly(diallyl-dimethylammonium chloride) PDADMAC. The synthesis of the silver nanoparticles as well as the layer-by-layer deposition with PDADMAC was easily monitored by UV–Vis spectroscopy due to the strong plasmon absorbance at 400 nm of the silver nanoparticles. Our study shows that increasing the concentration ration between the co-polyelectrolyte and silver nitrate has a negative effect on the size distribution of the resulting silver nanoparticles. For the layer-by-layer assembly, the PSS-co-Maleic was found to be a good capping agent since it allows later the formation of uniform thin films when deposited with PDADMAC. A linear increase in absorbance as a function of the number of deposited layers was observed.     

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.     

Preparation of silica–silver heterogeneous nanocomposite particles by one-pot preparation strategy using polyol process: Size-controlled immobilization of silver nanoparticles

The size-controlled immobilization of silver nanoparticles onto the silica surface was carried out through one-pot process involving polyol process for the first time. Thiol groups were employed as a chemical protocol to make a binding bridge between silver nanoparticle and silica surface. The size of immobilized silver nanoparticles was controlled by reaction temperature and time at two different concentrations of silver nitrate: 1000 and 10,000 ppm. This one-pot process involving polyol process can simplify the conventional complex reaction process to control the size of immobilized metal nanoparticles. Also, this research can contribute to the immobilization of the other metals onto the inorganic supports and to the control of the size of immobilized metal particles.     

Impact of Zr/Ti ratio in the PZT on the photoreduction of silver nanoparticles

Silver nanoparticle deposition from an aqueous solution of silver nitrate onto the surface of PZT thin films of stoichiometric compositions PbZr_0.3Ti_0.7O₃ and PbZr_0.52Ti_0.48O₃ has been investigated. The impact of Zr/Ti ratio on the photochemical properties of PZT is shown by the preferential growth of silver nanoparticles onto the surface. Photoreduction of silver occurs on both c⁺ and c⁻ domains on PbZr_0.52Ti_0.48O₃ whereas it occurs only on c⁺ domains on a PbZr_0.3Ti_0.7O₃ surface. The difference in deposition pattern is attributed to difference in magnitude of spontaneous polarization, effective hole concentration and band gap of the two samples which impacts shape and width of space charge layer in the two samples resulting in a change in band bending at the surface.     

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.     

Functional finishing of cotton fabrics using silver nanoparticles

We have reported a novel in situ synthesis protocol for silver nanoparticles onto cotton fabrics. Here, cotton fabric immersed in silver nitrate solution is autoclaved at 15 psi, 121 degrees C for 15 min. At this temperature and pressure, the aldehyde terminal of starch (residual size material on cotton fabric) reduced the silver nitrate to silver metal and simultaneously stabilized the nanoparticles on fabric itself. The UV-visible absorption spectrum of both cotton fabrics and bath solution showed a typical absorption peak at 420 nm corresponding to the surface plasmon resonance of silver nanoparticles. With the help of transmission electron micrographs, the average size of the dislodged silver nanoparticles in water is calculated to be 20.9 +/- 13.7 nm. This silver nanoparticles impregnated cotton fabrics showed excellent antibacterial activity against Staphylococcus aureus and bacteriostasis activity against Klebsiella pneumoniae. Also, silver nanoparticles impregnated fabrics expressed significant UV-protection capability in comparison with the untreated fabrics.     

Formation process of silver nanoparticles in DTAB/SDBS/PVP aqueous solution

Silver nanoparticles were prepared from the nitrate silver solution in dodecyl trimethyl ammonium bromide (DTAB)/sodium dodecylbenzenesulfonate (SDBS)/polyvinyl pyrrolidone (PVP) complex solution with hydrazine as the reductant. Scanning electron microscopy (SEM), X-ray diffraction (XRD) and UV–Vis spectroscopic analysis were conducted to investigate the role of anionic–cationic surfactants on the growth process of silver particles. The results showed that, before the formation of spherical silver nanoparticles, the cube and then tetrakaidecahedrons of AgBr were initially formed. It is concluded that the selective interaction of bow-like electric double-layer structure of anionic–cationic surfactants with certain crystallographic planes of crystals dominated the morphology evolvement of the reaction products. In addition; the PVP coverage finally encouraged the formation of well-dispersed spherical silver nanoparticles.     

Microwave assisted polymer stabilized synthesis of silver nanoparticles and its application in the degradation of environmental pollutants

Graft copolymers of polyacrylamide (PAM) and dextran (Dx) are synthesized by grafting PAM chains onto a Dx backbone (Dx-g-PAM) with ceric ion induced solution polymerization technique. Partial hydrolysis of Dx-g-PAM is carried out with sodium hydroxide solution to obtain HDx-g-PAM. To synthesize silver nanoparticles dispersed copolymer nano-composite (Ag-HDx-g-PAM), reduction of silver ions with HDx-g-PAM is carried out using microwave heating. The environmentally benign and biodegradable copolymer, HDx-g-PAM acts as both stabilizer and reducing agent. The copolymer nano-composite, Ag-HDx-g-PAM is characterized by FT-IR, transmission electron microscopy, scanning electron microscopy and optical spectroscopy. Further, the catalytic activity of Ag-HDx-g-PAM nano-composite towards the reduction of environmental pollutants like phenosafranine dye and aromatic nitro compounds are studied.     

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.     

Multi-walled carbon nanotube/silver nanoparticles used for thermal transportation

A green method was applied to prepare composites of multi-walled carbon nanotubes (MWNTs) decorated with silver nanoparticles (Ag-NPs). MWNTs were functionalized using ball milling technology in the presence of ammonium bicarbonate, and the traditional method of silver mirror was used to decorate MWNTs to obtain Ag/MWNT composite. The obtained Ag/MWNT composites were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transmission infrared spectroscopy, and Brunauer–Emmet–Teller (BET) surface area analysis. SEM characterization showed that Ag-NPs distributed uniformly on the walls of MWNTs. The content and size of Ag-NPs could be controlled by adjusting the redox time. XRD patterns demonstrated that the Ag-NPs are composed of pure Ag and crystallized well. BET analysis indicated that the specific surface areas of Ag/MWNT decrease with increasing the content of Ag-NPs, and this result is similar to that of the literature. The measurement results of the thermal property showed that the thermal conductivity of the nanofluid containing Ag/MWNT composites was higher than that of nanofluid containing pristine or functionalized MWNTs.     

Preparation and characterization of dendritic silver nanoparticles

Dendritic silver nanoparticles have been prepared by a soft solution technique from the aqueous solution of silver nitrate and poly (vinyl pyrrolidone) (PVP) in the presence of ethanol used as a reducing agent. The resultant silver nanoparticles were characterized by using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), energy dispersive analyses of X-ray (EDX), and UV-Visible absorption spectroscopy. It was found that the well-defined dendritic silver nanoparticles which had the length 0.5–1 m and the width of 100–200 nm.     

Green synthesis and characteristic of core-shell structure silver/starch nanoparticles

An eco-friendly method was put forward to synthesize Ag nanoparticles (Ag NPs) by using biodegradable starch as a stabilizing agent. The silver ion from AgNO₃ was reduced by glucose in soluble starch solution. Morphological observation and characterization of Ag NPs were performed by using high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD) and UV–vis absorption spectroscopy. HRTEM showed that Ag NPs were covered by starch layer to form spherical core-shell Ag/starch NPs with diameter ranging from 5 to 20 nm. XRD pattern confirmed the presence of Ag NPs with face-centered cubic (fcc) structure. All these results indicated that starch played an important role in stabilizing Ag NPs.     

Green synthesis of silver nanoparticles using tannins

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