Synthesis and Characterization of Silver Nanoparticles from Psidium Guajava Leaf Extract

Green route for the synthesis of nanoparticles has become more acceptable than the other chemical as well as biological route. In the present study, silver nanoparticle is synthesized using ethanolic extract of Psidium guajava leaves. Further the synthesized silver nanoparticles were characterized by UV-Visible Spec, FT-IR, X-Ray Diffraction FESEM and E-DAX. The results of FT-IR provided evidence of the involvement of phytochemicals present in the leaf extract in the reduction of silver nitrate to silver nanoparticles. XRD confirmed the crystalline structure as well as shape of the synthesized nanoparticle as face-centred cubic. E-DAX profiling helped in determining the presence of elemental silver. The size of the nanoparticle procured by SEM analysis was found to be approximately 30-50 nm in size. Thus, the findings of this study showed that the plant assisted method for silver nanoparticle synthesis is more effective and further application level studies can shed lights on their use in healing of various human ailments.

Preparation and characterization of silver orthophosphate photocatalytic coating on glass substrate

The photocatalytic activity of silver orthophosphate Ag3PO4 has been studied and shown to have a high photo-oxidation capability. However, there is few reported example of a simple method to prepare Ag3PO4 coatings on various substrates. In this study a novel and simple method to immobilize Ag3PO4 on the surface of glass substrates has been developed. A silver phosphate paste based on a polyelectrolyte solution was applied to a smooth glass surface. The resulting dried material was calcined to obtain a coating that remained on the glass substrate. The coating layer was characterized by X-ray diffraction and energy dispersive X-ray spectrometry, and the optical band gap of the material was determined. The results indicated that an Ag3PO4 coating responsive to visible light was successfully prepared. The coating, under visible light irradiation, has the ability to decompose methylene blue. Although the coating contained some elemental silver, this did not adversely affect the optical band gap or the photocatalytic ability.

Syzygium cumini Mediated Green Synthesis of Silver Nanoparticles for Reduction of 4-Nitrophenol and Assessment of its Antibacterial Activity

The biosynthesis of silver nanoparticles (AgNPs) has become more significant in the recent years owing to its applications in catalysis, imaging, drug delivery, nano-device fabrication and in medicine. We propose the synthesis of silver nanoparticles from the plant extract of Syzygium cumini and evaluation of its antibacterial and chemocatalytic potential. Synthesis of AgNPs carried out by using aqueous silver nitrate. The UV–Vis absorption spectrum of the synthesized AgNPs showed a broad absorption peak at 470 nm. TEM analysis shows the morphology of AgNPs as a hexagonal matrix with average particle size is about 50 nm. XRD analysis displays the crystalline structure of AgNPs. The presence of elemental silver was confirmed with EDX analysis. FTIR analysis shows that amide groups present in proteins are dominant reducing agents and play an important role in the bioreduction of Ag+ ions to Ag0. The bioreduced AgNPs demonstrated significant catalytic properties in a reduction reaction of 4-nitrophenol to 4-aminophenol using NaBH4 in an aqueous condition. The biosynthesized AgNPs have potent antibacterial activity against common clinical pathogens. Considering the remarkable antibacterial activity against common pathogenic microorganisms, AgNPs can be used in the pharmaceutical industries.

Preparation of Antimicrobial Fibres from the EVOH/EPC Blend Containing Silver Nanoparticles

The article presents a new fabrication method for bioactive fibres with a microporous structure of ethylene–vinyl alcohol copolymers (EVOH)/ethylene−propylene copolymer (EPC) blends. The experimental work carried out resulted in obtaining EVOH/EPC polymer blends fibres with the addition of glycerol and sodium stearate. Different concentrations of glycerol (38%, 32%) and sodium stearate (2%, 8%) were used to prepare the fibres. The purpose of using different concentrations of stearate and glycerol was to evaluate the effect of additives on the structure and properties of the fibres. A significant influence of the additives used on the morphological structure of the fibres was found. The resulting fibres were modified with an AgNO3 solution and reduced to silver nanoparticles (AgNPs), to give the fibres bioactive properties. The fibres obtained with the addition of 8% stearate have a more developed surface, which may influence the amount of adsorbed silver particles inside the fibre. However, the durability of depositing silver particles after multiple washes has not been tested. Three types of microorganisms were selected to assess the microbiological activity of the obtained fibres, i.e., Gram-positive Staphylococcus aureus and Gram-negative Pseudomonas aeruginosa and Escherichia coli. The fibres have antibacterial activity against gram positive and negative bacteria. The largest inhibition zones were obtained for gram-positive bacteria Staphylococcus aureus, ranging from 3 to 10 mm depending on the concentration of AgNPs. The morphology of the blends fibres was characterized by scanning electron microscopy (SEM) and optical microscopy (OM). The occurrence of elemental silver was analysed by energy dispersive spectroscopy (EDS) analysis. The changes of the polymer structure chemistry are studied by Fourier transform infrared spectroscopy (FTIR).

Synthesis of Silver Nanoparticles of Corn Silk Agrowaste and Their Bioactivities

Present study was intended to synthesize silver nanoparticles (AgNPs) using corn silk aqueous extract (CSAE) and evaluate for antimicrobial and antiurolithiatic potential. The aqueous decoction of corn silk offered light yellow CSAE. Treatment of AgNO3 with CSAE offered AgNPs with absorbance 430 nm. Optimization study established 5 mM silver nitrate, 2.5:7.5 extract to AgNO3 ratio, pH 8, and 24 h time as parametric requirement for synthesis of AgNPs using CSAE. Stability study supported the AgNPs stability based on retention of SPR signal between 428 to 450 nm. The synthesis of AgNPs was confirmed on broad and shifted FTIR bands; XRD signals at 2θ values of 32.27º, 40.72º, 46.20º, 65.69º, 69.31º and 76.49º indexed to 111, 200, 220 and 311 planes, respectively; particle size range from 22.05-36.69 nm in FESEM; and elemental silver content of 62.17% as per EDX spectrum. The synthesized AgNPs exhibited high antibacterial and antiurolithiatic potential. Present study recommends that synthesis of AgNPs using CSAE is a facile and eco-friendly method

Silver-coated magnetic nanocomposites induce growth inhibition and protein changes in foodborne bacteria

Cytotoxicity concerns of nanoparticles on animal or human bodies have led to the design of iron oxide core nanocomposites, coated with elemental silver to allow their magnetic removal from bio-mixtures. Although the antimicrobial effect of silver is well-described, the effects of nanoparticles derived from silver on microorganisms remain unfolded. Here, we characterized a customized magnetic silver nanocomposite (Ag-MNP) and evaluated its effects on bacterial growth and protein changes. The Ag-MNP displayed both longitudinal and round shapes under High-Resolution Transmission Electron Microscopy imaging, while the Energy Dispersive X-ray Spectroscopy and X-ray diffraction analysis confirmed the presence of Ag, Fe3O4 (Magnetite) and FeO2 (Goethite). Optical density, bioluminescence imaging, and Colony Forming Unit assessments revealed that the presence of Ag-MNP induced strong dose-dependent bacteria (Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium and S. Anatum) growth inhibition. The TEM imaging showed penetration and infiltration of bacteria by Ag-MNP, leading to membrane degeneration and vacuole formation. The presence of Ag-MNP led to fifteen up-regulated and nine down-regulated proteins (P < 0.05) that are involved in cell membrane synthesis, inhibition of protein synthesis, interference with DNA synthesis, and energy metabolism inhibition. This study provides insights to develop alternative antimicrobials to treat foodborne pathogens with antibiotic resistance avoidance.

Elemental Silver Nanoparticles: Biosynthesis and Bio Applications

The data on the specifics of synthesis of elemental silver nanoparticles (Ag-NP) having various geometric shapes (pseudo spherical, prismatic, cubic, trigonal-pyramidal, etc.), obtained by using various biological methods, and their use in biology and medicine have been systematized and generalized. The review covers mainly publications published in the current 21st century. Bibliography: 262 references.

Biosynthesis of Silver Nanoparticles Mediated by Extracellular Pigment from Talaromyces purpurogenus and Their Biomedical Applications

In recent years, green syntheses have been researched comprehensively to develop inexpensive and eco-friendly approaches for the generation of nanoparticles. In this context, plant and microbial sources are being examined to discover potential reducing agents. This study aims to utilize an extracellular pigment produced by Talaromyces purpurogenus as a prospective reducing agent to synthesize silver nanoparticles (AgNPs). Biosynthesized AgNPs were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS), electron probe micro analyser (EPMA), and zeta potential. The pigment functional groups involved in the generation of AgNPs were investigated using Fourier transform infrared spectroscopy. TEM images showed that the generated nanoparticles were spherical, hexagonal, rod-shaped, and triangular-shaped with a particle size distribution from 4 to 41 nm and exhibited a surface plasmon resonance at around 410 nm. DLS and zeta potential studies revealed that the particles were polydispersed and stable (−24.8 mV). EPMA confirmed the presence of elemental silver in the samples. Biosynthesized AgNPs exhibited minimum inhibitory concentrations of 32 and 4 μg/mL against E. coli and S. epidermidis, respectively. Further, cytotoxicity of the AgNPs was investigated against human cervical cancer (HeLa), human liver cancer (HepG2), and human embryonic kidney (HEK-293) cell lines using 5-fluorouracil as a positive control. A significant activity was recorded against HepG2 cell line with a half-maximal inhibitory concentration of 11.1 μg/mL.

Medicago polymorpha-mediated antibacterial silver nanoparticles in the reduction of methyl orange

The aim of the presented work was to assess the potential of Medicago polymorpha extract to synthesize silver nanoparticles (AgNPs) as a green method. It was a simple one-step synthesis approach and the product obtained was characterized by UV-visible spectroscopy, Fourier transform infrared (FTIR), powder X-ray diffraction, thermogravimetric analysis, and field-emission scanning electron microscopy (FE-SEM). At room temperature, the optimum time for the completion of the reaction (i.e. the formation colloidal solution) was just 5 min. FE-SEM images showed that AgNPs were predominantly in spheres, whereas FTIR spectrum analysis inferred that gallic acid present in the extract initially reduced silver ions to elemental silver. The carboxylic and hydroxyl groups of biomolecules present in the extract stabilized AgNPs by passivating the surface to prevent aggregation, resulting in uniform distribution. The antibacterial activity of synthesized AgNPs showed effective inhibitory effects against waterborne pathogens, including Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), at a minimum inhibitory concentration of 10 μg/ml. Membrane permeability and respiration studies were also performed to assess the surface role of the synthesized AgNPs. The prepared AgNPs exhibited excellent antioxidant activity and catalytic reduction of methyl orange with a rate constant of 6.8×10−3 s−1.