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The authors report Myxobacteria virescens (M. virescens) mediated synthesis of silver nanoparticles (AgNPs) and its efficacy against Staphylococcus aureus (ATCC‐33591), Salmonella typhi (ATCC‐51812), Escherichia coli (E. coli) (ATCC‐14948), Klebsiella pneumoniae (MTCC‐4030) and Pseudomonas aeruginosa (MTCC‐4673). The organism exhibiting resistance to various antibiotics showed remarkable sensitivity, when used in combination of antibiotics and AgNPs. Antimicrobial property of AgNPs is playing a significant role in medicine and food storage. In this study, they have used M. virescens for the synthesis of AgNPs, which were characterised by using UV‐Vis spectrophotometer, nano‐particles tracking and analysis, zeta potential, Fourier transform infrared spectroscopy, X‐ray diffraction and transmission electron microscopy. Synthesised AgNPs were impregnated into paper by three different methods, i.e. glass rod method (without binder), glass rod method (with binder) and direct synthesis of AgNPs on paper. Nanoparticles synthesis on paper showed the significant antimicrobial activity against Staphylococcus aureus (ATCC‐33591), Salmonella typhi (ATCC‐51812), E. coli (ATCC‐14948), Klebsiella pneumoniae (MTCC‐4030) and Pseudomonas aeruginosa (MTCC‐4673). Paper impregnated with AgNPs was used for wrapping of fruits (apples) which increases their shelf life up to 15 days. This study demonstrates a new method for wrapping of fruits, which increases the shelf life of apples. [ABSTRACT FROM AUTHOR]

This paper details the selective optical, fluorescent and electrochemical detection of Zn2+ among various divalent metal ions in aqueous solution by the green synthesized silver nanoparticles (AgNP) using the fresh extract of Myristica fragrans (MF) with the aid of microwave energy. The synthesized silver nanoparticles stabilized with MF were analysed using UV-vis., Fourier-transform infrared (FT-IR), X-ray diffraction (XRD), and transmission electron microscopy (TEM) techniques. Due to the effective complexation between silver nanoparticles and metal ions, absorbance of AgNP-MF diminished with increasing concentration of Zn2+. This is visually identified through the color changes. Fluorescent sensing studies involved the changes in fluorescent intensity of AgNP-MF in the presence of Zn2+. Electrochemical sensing of Zn2+ was carried through cyclic and differential pulse voltammetric techniques using AgNP-MF modified platinum electrode (AgNP-MF􀀀 Pt). The developed electrochemical sensor showed a limit of detection (LOD) of 0.6148 μM and its good sensing ability was checked for the detection of Zn2+ in environmental water samples. Recoveries of Zn2+ in the various real water samples were obtained in the range from 100.2% to 100.6%. The multifunctional utility of the AgNP-MF as a catalyst towards the reduction of two environmentally toxic contaminants such as o/p-nitroanilines through NaBH4 was also evaluated. The complete degradations were achieved within few minutes and the reactions followed pseudo first order kinetics. The effect of catalytic dosage on the rate of reduction reactions was also studied. [ABSTRACT FROM AUTHOR]

Anisotropic nanoparticles are a potential foundation for emerging materials engineering having anomalous properties often to an extraordinary degree‐enabling widespread new applications. In the bottom‐up approach, isotropic nanoparticles are formed by self‐assembly following the basic packing rule but lack directional interaction. On the other hand, anisotropic nanoparticles involve complex programmability having directional interaction and thus become of utmost interest in science and technology. In this paper, the anisotropic plasmonic effects in silver (Ag) nanoparticles under microwave‐induced plasma‐in‐liquid‐assisted decomposition of saccharides and di‐saccharides following the green chemistry process are investigated. The effect of microwave power, irradiation time, and relative chemical composition has been investigated in detail using extinction spectroscopy and Mie theory. The relationship between extinction curve shape parameter (S) and Mie theory has been established. The extinction spectroscopy and transmission electron microscopy (TEM) study confirm the existence of anisotropic plasmonic effects in Ag nanoparticles following two‐generation growth mechanisms having an average particle size of 2 and 32 nm. This technique offers rapid (20–40 sec) bulk production and is cost/energy effective than the conventional synthesis route. [ABSTRACT FROM AUTHOR]

Purpose: Noble metal nanoparticles have found several medical applications in the areas of radiation detection; x-ray contrast agents and cancer radiation therapy. Based on computational methods, many papers have reported the nanoparticle effect on the dose deposition in the surrounding medium. Here the authors report experimental results on how silver and gold nanoparticles affect the dose deposition in alanine dosimeters containing several concentrations of silver and gold nanoparticles, for five different beam energies, using electron spin resonance spectroscopy (ESR). Methods: The authors produced alanine dosimeters containing several mass percentage of silver and gold nanoparticles. Nanoparticle sizes were measured by dynamic light scattering and by transmission electron microscopy. The authors determined the dose enhancement factor (DEF) theoretically, using a widely accepted method, and experimentally, using ESR spectroscopy. Results: The DEF is governed by nanoparticle concentration, size, and position in the alanine matrix. Samples containing gold nanoparticles afford a DEF higher than 1.0, because gold nanoparticle size is homogeneous for all gold concentrations utilized. For samples containing silver particles, the silver mass percentage governs the nanoparticles size, which, in turns, modifies nanoparticle position in the alanine dosimeters. In this sense, DEF decreases for dosimeters containing large and segregated particles. The influence of nanoparticle size-position is more noticeable for dosimeters irradiated with higher beam energies, and dosimeters containing large and segregated particles become less sensitive than pure alanine (DEF < 1). Conclusions: ESR dosimetry gives the DEF in a medium containing metal nanoparticles, although particle concentration, size, and position are closely related in the system. Because this is also the case as in many real systems of materials containing inorganic nanoparticles, ESR is a valuable tool for investigating DEF. Moreover, these results alert to the importance of controlling the sizeposition of nanoparticles to enhance DEF. [ABSTRACT FROM AUTHOR]

Silver nanoparticles (AgNPs) have been undeniable for its antimicrobial activity while its antitumour potential is still limited. Therefore, the present study focused on determining cytotoxic effects of AgNPs on Michigan cancer foundation‐7 (MCF‐7) breast cancer cells and its corresponding mechanism of cell death. Herein, the authors developed a bio‐reduction method for AgNPs synthesis using actinomycetes isolated from marine soil sample. The isolated strain was identified by 16s ribotyping method and it was found to be Streptomyces atrovirens. Furthermore, the synthesised AgNPs were characterised by various bio‐analytical techniques such as ultraviolet–visible spectrophotometer, atomic force microscopy, transmission electron microscopy, Fourier transform infra‐red spectroscopy, and X‐ray diffraction. Moreover, the results of 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assay reveals 44.51 µg of AgNPs to have profound inhibition of cancer cell growth; furthermore, the inhibition of MCF‐7 breast cancer cell line was found to be dose dependent on treatment with AgNPs. Acridine orange and ethidium bromide double staining methods were performed for cell morphological analysis. The present results showed that biosynthesised AgNPs might be emerging alternative biomaterials for human breast cancer therapy. [ABSTRACT FROM AUTHOR]

Microbial mediated biological synthesis of metallic nanoparticles was carried out ecofriendly in the present study. Silver nanoparticles (AgNPs) were extracellularly biosynthesised from Streptomyces griseorubens AU2 and extensively characterised by ultraviolet–visible (UV–vis) and Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy, scanning electron microscopy and X‐ray diffraction analysis. Elemental analysis of nanoparticles was also carried out using energy dispersive X‐ray spectroscopy. The biosynthesised AgNPs showed the characteristic absorption spectra in UV–vis at 422 nm which confirmed the presence of metallic AgNPs. According to the further characterisation analysis, the biosynthesised AgNPs were found to be spherical and crystalline particles with 5–20 nm average size. Antioxidant properties of the biosynthesised AgNPs were determined by 2,2‐diphenyl‐1‐picrylhydrazyl free radical scavenging assay and was found to increase in a dose‐dependent matter. The identification of the strain was determined by molecular characterisation method using 16s rDNA sequencing. The present study is the first report on the microbial biosynthesis of AgNPs using S. griseorubens isolated from soil and provides that the active biological components found in the cell‐free culture supernatant of S. griseorubens AU2 enable the synthesis of AgNPs. [ABSTRACT FROM AUTHOR]

Metal nanoparticles have generated great interest due to their excellent optical and chemical properties. The widely used chemical method for synthesising nanoparticles involves capping agents for colloidal stability. However, there are scarce reports on the application of metal nanoparticles synthesised without using capping agents. Hence, there is a need to develop pristine nanoparticles devoid of capping that can be used for translational research. Here, the authors developed a facile and rapid method for synthesising bare metal nanoparticles (platinum/silver/gold) that are chemically reactive and stable for a month upon storage. They synthesised bare metal nanoparticles of sub‐15 nm and characterised using standard techniques (UV–VIS‐NIR/DLS/zeta//TEM/XRD). They assessed the safety of the synthesised nanoparticles on the liver carcinoma cell line (HepG2). Bare gold and platinum nanoparticles were non‐toxic in comparison to bare silver nanoparticles. Bare metal nanoparticles were also checked for metal detection wherein antimony, mercury and chromium were detected using bare gold and silver nanoparticles. The spectroscopic shifts of the nanoparticles when bound to metals resulted in blue and red shifting of the plasmon band, indicating the sensing of metals. These results show that bare metal nanoparticles have the potential to emerge as a promising candidate for biomedical and sensing applications. [ABSTRACT FROM AUTHOR]

This work narrates the synthesis of poly (acrylic acid) hydrogel microparticles (PAAHMPs), fabrication of silver nanoparticles (AgNPs) inside the structure of the prepared PAAHMPs and catalytic applications of PAAHMPs fabricated with AgNPs (PAAHMPs/AgNPs). The PAAHMPs were prepared by inverse suspension polymerization technique while fabrication of AgNPs was carried out by chemical reduction method using sodium borohydride (NaBH4) as reducing agent. The identification of functional groups in bare PAAHMPs and in the PAAHMPs/AgNPs composite system was carried out by the Fourier transform infrared spectroscopy. The size and morphology of the prepared hydrogel and its composite was studied by scanning electron microscopy and transmission electron microscopy. X‐ray diffraction and thermal gravimetric analyzer was also used to characterize the bare PAAHMPs and PAAHMPs/AgNPs composite. The prepared PAAHMPs/AgNPs composite was used as catalyst for the reduction of nitro aromatic pollutants and an industrial dye, that is, 4‐Nitrophenol (4‐NP), 2‐Nitrophenol (2‐NP) and methyl orange. No loss in catalytic activity was noted in seven consecutive cycles of recycling process while only 37.5% loss in catalytic activity was observed upon storing the catalyst for 90 days. [ABSTRACT FROM AUTHOR]

In this examination, we researched the advantages of DNA fragmentation and metallic nanoparticles well‐appointed with biomolecules. A novel interpretation of DNA damage by Silver Nano‐Clusters (AgNCs) which were developed by the utilization of green synthesis method was demonstrated. The green synthesis of AgNCs was accomplished by utilizing the leaf extract of Salacia mulbarica (SM). The preparation of SM‐AgNCs was developed by estimating surface plasmon resonance peak around 449 nm by using a UV–Visible spectrophotometer. The effect of phytochemicals in SM leaf extract on the development of stable SM‐AgNCs was confirmed by FTIR spectroscopy. The size of the fabricated SM‐AgNCs was estimated by dynamic light scattering and zeta‐sizer analysis and the morphology of the SM‐AgNCs was examined by transmission electron microscopy. The presence of clusters of Ag particles in the prepared SM‐AgNCs was recognized by energy dispersion X‐ray analysis. The results show that saponins, phytosterols, and phenolic compounds present in plant extract may play a great part in developing the SM‐AgNCs in their specialized particles. The succeeded SM‐AgNCs shows incredible anti‐bacterial action towards Escherichia coli and Bacillus subtilis. In‐light of the antibacterial study, these SM‐AgNCs were analyzed with calf thymus‐DNA and found significant damage to the strand of thymus‐DNA. [ABSTRACT FROM AUTHOR]

Metallic nanoparticles can be synthesised in living plants, which provide a friendly approach. In this work, the authors aimed to study the synthesis of silver nanoparticles (AgNPs) in Arabidopsis and the two‐dimensional (2D) distribution of Ag and other elements (Ca, P, S, Mg, and CI) in the Arabidopsis plant tissues. The concentrations of Ag in the plant tissues were determined by inductively coupled plasma‐atomic emission spectrometer, showing that the majority of Ag was retained in the roots. Transmission electron micrographs showed the morphology of AgNPs and the location in plant cells. The distributions of Cl and Ag were consistent in plant tissues by 2D proton‐induced X‐ray emission. In conclusion, this is the first report of the AgNP synthesis in Arabidopsis living plants and its 2D distribution of important elements, which provide a new clue for further research. [ABSTRACT FROM AUTHOR]

Silver nanoparticles (AgNPs) are toxic to various microbes, but the mechanism of action is not fully understood. The present report explores Azadirachta indica leaf extract as a reducing agent for the rapid biosynthesis of AgNPs. The effects of AgNPs on the growth, glutathione‐S‐transferase (GST) activity, and total protein concentration in Staphylococcus aureus were investigated, as was its antibacterial activity against seven other bacterial strains. Nanoparticle synthesis was confirmed by the UV‐Vis spectrum and colour change of the solution. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential analysis, and infrared spectroscopy were used to characterise the synthesised nanoparticles. The UV‐Visible spectrograph showed an absorbance peak at 420 nm. DLS analysis showed an average AgNP size of 159 nm and a Polydispersity Index of 0.373. SEM analysis showed spherical particle shapes, while TEM established an average AgNP size of 7.5 nm. The element analysis profile showed small peaks for calcium, potassium, zinc, chlorine, with the presence of oxygen and silver. AgNPs markedly affected the growth curves and GST activity in treated bacteria, and produced moderate antibacterial activity. Thus AgNPs synthesised from A. indica leaves can interrupt the growth curve and total protein concentration in bacterial cells. [ABSTRACT FROM AUTHOR]

In this work, an Fe3 O4 /HZSM‐5 nanocomposite was synthesised in the presence of Juglans regia L. leaf extract. Then, silver nanoparticles (Ag NPs) were immobilised on the surface of prepared magnetically recoverable HZSM‐5 using selected extract for reduction of Ag+ ions to Ag NPs and their stabilisation on the surface of the nanocomposite. The reduction of Ag+ ions occurs at room temperature within a few minutes. Characterisation of the prepared catalysts has been carried out using fourier transform infrared (FT‐IR), X‐ray diffraction, field‐emission scanning electron microscopy (FESEM), energy‐dispersive spectroscopy, Brunauer–Emmett–Teller method, and a vibrating sample magnetometer. According to the FESEM images of the nanocomposites, the average size of the Ag NPs on the Fe3 O4 /HZSM‐5 surface was >70 nm. The Ag/Fe3 O4 /HZSM‐5 nanocomposite was a highly active catalyst for the reduction of methyl orange and 4‐nitrophenol in aqueous medium. The utilisation of recycled catalyst for three times in the reduction process does not decrease its activity. [ABSTRACT FROM AUTHOR]

The silver nanoparticles (AgNPs) with their unique chemical and physical properties are proving as a new therapeutical agent. In the present study, the AgNPs synthesised from an aqueous extract of a macrofungus, Earliella scabrosa, were characterised by field emission scanning electron microscopy (FESEM), energy dispersive X‐ray analysis (EDX), high‐resolution transmission electron microscopy, X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and further evaluate for its in vitro antibacterial and wound healing efficacy. The mycosynthesised AgNPs exhibited the surface plasmon resonance peak at 410 nm with good stability over a period of a month. The FESEM and EDX analyses revealed the spherical‐shaped AgNPs of an average size of 20 nm and the presence of elemental Ag, respectively. The XRD pattern showed the crystalline nature of AgNPs. The FTIR spectra confirmed the conversion of Ag+ ions to AgNPs due to reduction by biomolecules of macrofungus extract. The mycosynthesised AgNPs showed effective antibacterial activity against two Gram‐positive bacteria, namely Bacillus subtilis and Staphylococcus aureus, and two Gram‐negative bacteria Escherichia coli and Pseudomonas aeruginosa. The pathogens were highly sensitive to AgNPs, whereas less sensitive to AgNO3. The mycosynthesised AgNPs showed significant wound healing potential with 68.58% of wound closure. [ABSTRACT FROM AUTHOR]

In this study, the endogenous lipid signalling molecules, N ‐myristoylethanolamine, were explored as a capping agent to synthesise stable silver nanoparticles (AgNPs) and Ag sulphide NPs (Ag2 S NPs). Sulphidation of the AgNPs abolishes the surface plasmon resonance (SPR) maximum of AgNPs at 415 nm with concomitant changes in the SPR, indicating the formation of Ag2 S NPs. Transmission electron microscopy revealed that the AgNPs and Ag2 S NPs are spherical in shape with a size of 5–30 and 8–30 nm, respectively. AgNPs and Ag2 S NPs exhibit antimicrobial activity against Gram‐positive and Gram‐negative bacteria. The minimum inhibitory concentrations (MIC) of 25 and 50 μM for AgNPs and Ag2 S NPs, respectively, were determined from resazurin microtitre plate assay. At or above MIC, both AgNPs and Ag2 S NPs decrease the cell viability through the mechanism of membrane damage and generation of excess reactive oxygen species. [ABSTRACT FROM AUTHOR]

In this study, the authors synthesised silver nanoparticles (AgNPs) using autoclave as a simple, unique and eco‐friendly approach. The effect of Zingiber officinale extract was evaluated as a reducing and stabiliser agent. According to transmission electron microscopy results, the AgNPs were in the spherical shape with a particle size of ∼17 nm. The biomedical properties of AgNPs as antibacterial agents and free radical scavenging activity were estimated. Synthesised AgNPs showed significant 1,1‐diphenyl‐2‐picryl‐hydrazyl free radical scavenging. Strong bactericidal activity was shown by the AgNPs on Gram‐positive and Gram‐negative bacteria. A maximum inhibition zone of ∼14 mm was obtained for epidermidis at a concentration of 60 μg/ml for sample fabricated at 24 h. The AgNPs also showed a significant cytotoxic effect against MCF‐7 breast cancer cell lines with an half maximal inhibitory concentration value of 62 μg/ml in 24 h by the MTT assay. It could be concluded that Z. officinale extract can be used effectively in the production of potential antioxidant and antimicrobial AgNPs for commercial application. [ABSTRACT FROM AUTHOR]

Silver nanoparticles (AgNPs) have been biosynthesised through the extracts of Ribes khorassanicum fruits, which served as the reducing agents and capping agents. Biosynthesised AgNPs have been found to be ultraviolet–visible (UV–vis) absorption spectra since they have displayed one surface plasmon resonance peak at 438 nm, attesting the formation of spherical NPs. These particles have been characterised by UV–vis, field‐emission scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, and transmission electron microscopy analysis. The formation of AgNPs at 1.0 mM concentration of AgNO3 has resulted in NPs that contained mean diameters in a range of 20–40 nm. The green‐synthesised AgNPs have demonstrated high antibacterial effect against pathogenic bacteria (i.e. Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa). Biosynthesising metal NPs through plant extracts can serve as the facile and eco‐friendly alternative for chemical and/or physical methods that are utilised for large‐scale nanometal fabrication in various medical and industrial applications. [ABSTRACT FROM AUTHOR]

Recently the use of medicinal plants potential in the production of nanoparticles has received serious attention. Here, the main component of Camellia sinensis L. (green tea) extract was detected by spectroscopy and the optimal conditions were determined for their performance in green synthesis of silver nanoparticles at room temperature. Epigallocatechin gallate was identified as the dominant component in the extract as determined by spectroscopy, and it was established that its oxidation was a function of the solution pH. Transmission electron microscopy, dynamic light scattering, and visible absorption spectroscopy (UV‐Vis) confirmed the reduction in silver ions to silver nanoparticles (Ag NPs). Controlling over Ag NPs shape and narrow size distribution was achieved with 10 ml green tea leaf extract solution and in different reaction pH. Spherical colloidal Ag NPs with well‐defined hydrodynamic diameters (with average hydrodynamic size of 27.9–50.2 nm) were produced. Silver nitrate concentrations used in this study were lower than that of reported in similar works, and synthesis efficiency was also higher. Nanoparticles were perfectly spherical and their uniformity, compared to similar studies, was much higher. These NPs showed higher degree of stability and were aqueously stable for >10 months in dark glasses at 4°C. [ABSTRACT FROM AUTHOR]

This work explores the rapid synthesis of silver nanoparticles (AgNPs) from Musa paradisiaca (M. paradisiaca) bract extract. The bio‐reduction of Ag+ ion was recorded using ultraviolet–visible spectroscopy by a surface plasmon resonance extinction peak with an absorbance at 420 nm. The phytoconstituents responsible for the reduction of AgNPs was probed using Fourier transform infrared spectroscopy. The X‐ray diffraction pattern confirmed the formation of crystalline AgNPs that were analogous to selected area electron diffraction patterns. Morphological studies showed that the obtained AgNPs were monodispersed with an average size of 15 nm. The biologically synthesised AgNPs showed higher obstruction against tested phytopathogens. The synthesised AgNPs exhibited higher inhibitory zone against fungal pathogen Alternaria alternata and bacterial pathogen Pseudomonas syringae. Free radical scavenging potential of AgNPs was investigated using 1,1‐diphenyl‐2‐picryl hydroxyl and 2,2‐azinobis (3‐ethylbenzothiazoline)‐6‐sulphonic acid assays which revealed that the synthesised AgNPs act as a potent radical scavenger. The catalytic efficiency of the synthesised AgNPs was investigated for azo dyes, methyl orange (MO), methylene blue (MB) and reduction of o‐nitrophenol to o‐aminophenol. The results portrayed that AgNPs act as an effective nanocatalyst to degrade MO to hydrazine derivatives, MB to leucomethylene blue, and o‐nitro phenol to o‐amino phenol [ABSTRACT FROM AUTHOR]

Multiple drug resistance and treatment of contaminated water has become a serious issue in past years. Silver nanoparticles (AgNPs), being bactericidal, non‐toxic, cheap and environment friendly behaviour, have drawn attention to overcome these problems. This study has been designed to synthesise AgNPs from Pseudomonas aeruginosa. AgNPs formation was confirmed by colour change and UV–vis spectroscopy. Furthermore, Fourier transform infrared spectroscopy peaks demonstrated the presence of capped proteins as reducing and stabilising agent. Transmission electron microscopy micrograph revealed spherical shape AgNPs with the size ranging between 10 and 20 nm. Antibacterial activity of AgNPs was evaluated against the most prevalent waterborne pathogens enterohaemorrhagic Escherichia coli and Salmonellae typhimurium. Moreover, the antibacterial activity of AgNPs was tested for the treatment of contaminated water which showed attenuation in bacterial load within 8 h as demonstrated by growth kinetics data. Furthermore, AgNPs did not exhibit haemolytic effects on human red blood cells (RBCs) even at 100 mg L−1 concentration of AgNPs. The results herein suggest that AgNPs synthesised by P. aeruginosa under optimised conditions exhibit microbicidal property against waterborne pathogens and having no toxic effect on human RBCs. These AgNPs could be employed for treatment of contaminated water after process optimisation. [ABSTRACT FROM AUTHOR]

Green synthesis of nanoparticles is considered an efficient method when compared with chemical and physical methods because of its bulk production, eco‐friendliness and low cost norms. The present study reports, for the first time, green synthesis of silver nanoparticles (AgNPs) at room temperature using Solanum viarum fruit extract. The visual appearance of brownish colour with an absorption band at 450 nm, as detected by ultraviolet‐visible spectrophotometer analysis, confirmed the formation of AgNPs. X‐ray diffraction confirmed the AgNPs to be crystalline with a face‐centred lattice. The transmission electron microscopy‐energy dispersive X‐ray spectroscopy image showed the AgNPs are poly‐dispersed and are mostly spherical and oval in shape with particle size ranging from 2 to 40 nm. Furthermore, Fourier transform‐infrared spectra of the synthesised AgNPs confirmed the presence of phytoconstituents as a capping agent. The antimicrobial activity study showed that the AgNPs exhibited high microbial activity against Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus susp. aureus, Aspergillus niger, and Candida albicans. The highest antimicrobial activity of AgNPs synthesised by S. viarum fruit extract was observed in P. aeruginosa, S. aureus susp. aureus and C. albicans with zone of inhibition, 26.67 mm. [ABSTRACT FROM AUTHOR]

The authors have investigated beneficial effects of 1 mM of silver nanoparticles (AgNPs) on agriculturally important plant Pennisetum glaucum (Bajara). The extracellular AgNPs were synthesised using Bacillus subtilis spizizenni and characterised using ultraviolet–visible absorption spectroscopy, Fourier transform infrared spectroscopy (FT‐IR) and transmission electron microscopy (TEM). Optical absorption spectrum showed characteristic peak of AgNPs at 423 nm. FT‐IR analysis of AgNPs showed peak at 3435 cm−1, which indicates the presence of N–H group (primary, secondary amines and amides) on the surface of AgNPs. TEM studies indicate that synthesised AgNPs have average size of ∼2 nm. Energy dispersive X‐ray spectroscopy showed strong signal of Ag at 3 keV. Treatment of 1 mM AgNPs to the bajara seeds was found to be sufficient for excellent germination of seeds within 3 days. There was also significant increase in radicle and plumule length as compared with control bajara seeds according to statistical analysis by one‐way analysis of variance, followed by Tukey's test. The percentage of AgNPs detected in root samples was 0.003% (by inductively coupled plasma atomic emission spectroscopy), which is negligible. There is still need to study the bioavailability and the type of interaction of AgNPs with plants, necessary for application in agriculture. [ABSTRACT FROM AUTHOR]

Green synthesis of nanoparticles has fuelled the use of biomaterials to synthesise a variety of metallic nanoparticles. The current study investigates the use of xylanases of Aspergillus niger L3 (NEA) and Trichoderma longibrachiatum L2 (TEA) to synthesise silver nanoparticles (AgNPs). Characterisation of AgNPs was carried out using UV–Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy, while their effectiveness as antimicrobial, antioxidant, catalytic, anticoagulant, and thrombolytic agents were determined. The colloidal AgNPs was brownish with surface plasmon resonance at 402.5 and 410 nm for NEA‐AgNPs and TEA‐AgNPs, respectively; while FTIR indicated that protein molecules were responsible for the capping and stabilisation of the nanoparticles. The spherical nanoparticles had size of 15.21–77.49 nm. The nanoparticles significantly inhibited the growth of tested bacteria (63.20–88.10%) and fungi (82.20–86.10%), and also scavenged DPPH (37.48–79.42%) and hydrogen peroxide (20.50–96.50%). In addition, the AgNPs degraded malachite green (78.97%) and methylene blue (25.30%). Furthermore, the AgNPs displayed excellent anticoagulant and thrombolytic activities using human blood. This study has demonstrated the potential of xylanases to synthesise AgNPs which is to the best of our knowledge the first record of such. The present study underscores the relevance of xylanases in nanobiotechnology. [ABSTRACT FROM AUTHOR]

The present work is emphasised on the bio‐fabrication of silver and gold nanoparticles in a single step by a microwave‐assisted method using the leaf extract of Synedrella nodiflora as both reducing and stabilising agent. The synthesised nanoparticles are highly stable and show surface plasmon resonance peak at 413 and 535 nm, respectively, for silver and gold nanoparticles in UV–Vis spectrum. The functional group responsible for the reduction of metal ions were obtained from Fourier transform infrared spectroscopy. The crystalline nature of nanoparticles with face‐centred cubic geometry was confirmed by the X‐ray diffraction and selected area electron diffraction patterns. The morphology and sizes of the silver and gold nanoparticles were obtained from transmission electron microscopy images. The nanoparticles exhibit effective antimicrobial activities against various pathogenic strains. These antimicrobial properties were analysed by employing agar well diffusion method. The nanoparticles show significant antioxidant properties, and it was determined using 2, 2‐diphenyl‐1‐picrylhydrazyl assay. The nanoparticles also show potent catalytic activity in the degradation of anthropogenic pollutant dyes Congo red and eosin Y by excess NaBH4. Thus, the current study demonstrates the potential use of S. nodiflora as a reducing and stabilising agent for the synthesis of silver and gold nanoparticles and their relevance in the field of biomedicine and catalysis. [ABSTRACT FROM AUTHOR]

Here, extracellular synthesis of silver nanoparticles (AgNPs) was carried out by Planococcus plakortidis strain BGCC‐51 isolated from dye industry effluent soil. The microbes were isolated, screened, and characterised by molecular analysis (accession number KX776160). The optimisation of synthesis of AgNPs to determine the optimum substrate level (1–5 mM), pH (5–9), and temperature (25–55°C) were further carried out. P. plakortidis strain BGCC‐51 gave best yield of AgNPs at substrate concentration 5 mM, pH 8, and at 35°C. Synthesised AgNPs were characterised by scanning electron microscope and high‐resolution transmission electron microscope. The size of synthesised AgNPs was in the range of 20–40 nm having spherical morphology. The AgNPs were found to show antimicrobial activity against bacteria such as Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), and Staphylococcus aureus (ATCC 29213). [ABSTRACT FROM AUTHOR]

The metal nanoparticles, due to interesting features such as electrical, optical, chemical and magnetic properties, have been investigated repeatedly. Also, the mentioned nanoparticles have specific uses in terms of their antibacterial activity. The biosynthesis method is more appropriate than the chemical method for producing the nanoparticles because it does not need any special facilities; it is also economically affordable. In the current study, the silver nanoparticles (AgNPs) were obtained by using a very simple and low‐cost method via Glaucium corniculatum (L.) Curtis plant extract. The characteristics of the AgNPs were investigated using techniques including: X‐ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy. The SEM and TEM images showed that the nanoparticles had a spherical shape, and the mean diameter of them was 53.7 and 45 nm, respectively. The results of the disc diffusion test used for measuring the anti‐bacterial activity of the synthesised nanoparticles indicated that the formed nanoparticles possessed a suitable anti‐bacterial activity. [ABSTRACT FROM AUTHOR]

In this study, the leaf extract of an important medicinal plant Crescentia cujete L. (CC) was employed as a green reducing agent to synthesise highly‐stable C. cujete silver nanoparticles (CCAgNPs). The reduction of Ag+ to Ag0 nanoparticles was initially observed by a colour change which generates an intense surface plasmon resonance peak at 417 nm using a UV‐Vis spectrophotometer. Various optimisation factors such as temperature, pH, time and the stoichiometric proportion of the reaction mixture were performed, which influence the size, dispersity and synthesis rate of CCAgNPs. In addition, surface chemistry of synthesised CCAgNPs through Fourier transform infrared spectroscopy reveals the reducing/stabilising agent present in the aqueous extract of C. cujete and synthesised CCAgNPs. Transmission electron microscopy analysis features the spherical shape of CCAgNPs with an average size of 39.74 nm. Furthermore, an X‐ray diffraction study confirms that the synthesised CCAgNPs were face‐centred cubic crystalline in nature. The CCAgNPs display tremendous bactericidal activity against human pathogens Bacillus subtilis, Staphylococcus epidermidis, Rhodococcus rhodochrous, Salmonella typhi, Mycobacterium smegmatis, Shigella flexneri and Vibrio cholerae via penetrating into the bacterial cell membrane and causing failure of an internal chain reaction. [ABSTRACT FROM AUTHOR]

Silver nanoparticles (SNPs) were synthesised by using the Arial part extract of Dorema ammoniacum D. and characterised by employing UV–visible spectroscopy, Fourier transform infrared spectroscopy and X‐ray diffraction techniques. Transmission electron microscopy and field emission scanning electron microscopy were applied to investigate the morphological structure of the bio‐synthesised SNPs. The antimicrobial activity of SNPs was studied against Gram positive (Bacillus cereus and Staphylococcus aureus) and Gram‐negative (Escherichia coli and Salmonella typhimurium) bacteria by employing the disk diffusion agar process. An extremely antimicrobial effect was observed for SNPs. Utilising D. ammoniacum D. as a mediator for the synthesis of SNPs helped to save time and cost. [ABSTRACT FROM AUTHOR]

Green synthesis of silver nanoparticles (AgNPs) using Shivlingi (Bryonia laciniosa) seed extract was carried out. Characterisation of synthesised nanoparticles was accomplished through the optical absorption and photoluminescence spectrum, X‐ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. The XRD analysis further confirmed the size of nanoparticles ∼15 nm. TEM images revealed homogeneous spherical ∼10 nm Bryonia extract capped AgNPs. The biological studies indicated that both Bryonia seed extract and the nanoparticles lack anti‐microbial activity; however, the nanoparticles had better cytotoxicity and total antioxidant activity. The Lethal concentration (LC)50 value of water extract and the nanoparticles were found to be 1091 and 592 μg/ml, respectively. The lower LC50 of nanoparticles indicates that it is more cytotoxic than the crude extract. The results indicate that the Bryonia seed is safe to be used as a medicine and the formation of their nanoparticle has further enriched the chemical reactivity, energy absorption and biological mobility. [ABSTRACT FROM AUTHOR]

The use of silver nanoparticles (AgNPs) in consumer products such as textiles leads to their discharge into wastewater and consequently to a transfer of the AgNPs to soil ecosystems via biosolids used as fertilizer. In urban wastewater systems (e.g., sewer, wastewater treatment plant [WWTP], anaerobic digesters) AgNPs are efficiently converted into sparingly soluble silver sulfides (Ag2S), mitigating the toxicity of the AgNPs. However, long-term studies on the bioavailability and effects of sulfidized AgNPs on soil microorganisms are lacking. Thus we investigated the bioavailability and long-term effects of AgNPs (spiked in a laboratory WWTP) on soil microorganisms. Before mixing the biosolids into soil, the sludges were either anaerobically digested or directly dewatered. The effects on the ammonium oxidation process were investigated over 140 d. Transmission electron microscopy (TEM) suggested an almost complete sulfidation of the AgNPs analyzed in all biosolid samples and in soil, with Ag2S predominantly detected in long-term incubation experiments. However, despite the sulfidation of the AgNPs, soil ammonium oxidation was significantly inhibited, and the degree of inhibition was independent of the sludge treatment. The results revealed that AgNPs sulfidized under environmentally relevant conditions were still bioavailable to soil microorganisms. Consequently, Ag2S may exhibit toxic effects over the long term rather than the short term. Environ Toxicol Chem 2017;36:3305-3313. © 2017 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals, Inc. on behalf of SETAC. [ABSTRACT FROM AUTHOR]

Fusarium wilt of tomato (Lycopersicon esculentum) caused by Fusarium oxysporum f. sp. lycopersici is one of the most important diseases that affect this crop worldwide. This study aimed to biosynthesise nanosilver (AgNPs) using Chaetomium globosum, to evaluate its in vitro antifungal activity against pathogenic F. oxysporum and in vivo control of tomato seedlings wilt in the greenhouse. AgNPs was tested for its in vitro antifungal potential against F. oxysporum using poisoned food technique on three different growth media, agar well diffusion assay, inhibition of colony formation (CFU), and tested for its potency to control seedlings wilt upon its use at different concentrations (50, 100 and 500 mg/l) and for different incubation periods (0, 1, 2 and 4 h). Results indicated that C. globosum succeeded to biosynthesise AgNPs with maximum UV/vis absorbance around 420–450 nm, spherical in shape with particle size of 11–14 nm according to Transmittance electron microscope and displayed high purity recorded through X‐ray diffraction (XRD). In vitro studies revealed high antifungal activity of AgNPs against F. oxysporum noticed especially at a concentration of 500 mg/l and after incubation period for 4 h. The CFU of F. oxysporum on potato dextrose agar (PDA) medium decreased significantly on increasing the concentration and time of incubation with AgNPs. In the greenhouse, AgNPs caused appreciable enhancement in the growth parameters of tomato seedlings such as; root, shoot fresh weight, and height of seedlings in soil infested with F. oxysporum compared with the control. In addition, AgNPs reduced the severity of wilt disease by 90% observed through decreasing the number of wilted seedlings especially after placing their roots in 500 mg/l of AgNPs suspension for 4 h prior to soil infestation with the pathogen. This study recorded for the first time that C. globosum has the ability to synthesise AgNPs which showed significant in vivo antifungal potential observed through control of Fusarium wilt of tomato seedlings, in addition to enhancing their growth parameters in the greenhouse. [ABSTRACT FROM AUTHOR]

An environmentally friendly and rapid procedure was developed to synthesise silver nanoparticles (Ag‐NPs) by Chamaemelum nobile extract and to evaluate its in vivo anti‐inflammatory and antioxidant activities. The ultraviolet–visible absorption spectrum of the synthesised Ag‐NPs showed an absorbance peak at 422. The average size of spherical nanoparticles was 24 nm as revealed by transmission electron microscopy. Fourier transform infra‐red spectroscopy analysis supported the presence of biological active compounds involved in the reduction of Ag ion and X‐ray diffraction confirmed the crystalline structure of the metallic Ag. The anti‐inflammatory and antioxidant activity of the Ag‐NPs was investigated against carrageenan‐induced paw oedema in mice. The levels of malondialdehyde (MDA) and antioxidant enzymes superoxide dismutase, catalase, glutathione peroxidase and inflammatory cytokines tumour necrosis factor (TNF‐α), interferon gamma and interleukin (IL)‐6, IL‐1β were assessed in this respect. The results demonstrated that anti‐inflammatory activity of the Ag‐NPs might be due to the ability of the nanoparticles to reduce IL‐1β, IL‐6 and TNF‐α. Moreover, reduction of antioxidant enzymes along with an increase in MDA level shows that the anti‐inflammatory activity of the synthesised Ag‐NPs by C. nobile is attributed to its ameliorating effect on the oxidative damage. [ABSTRACT FROM AUTHOR]

The biosynthesis of nanoparticles (NPs) from plant extracts is important in nanotechnology because the employed methods are environmentally friendly and cost‐effective. In this study, silver NPs (AgNPs) were synthesised using Chinese tea (Oolong tea) extract. The effects of the relative content of the employed silver nitrate, the reaction temperature, the incubation time, and the tea‐to‐water ratio on the formation of the AgNPs were examined. The synthesised AgNPs were also analysed by UV–vis spectroscopy, dynamic light scattering, transmission electron microscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, and thermo‐gravimetric analysis. The NPs were observed to be highly crystalline, approximately spherical, and 10–50 nm in diameter. They were also tested for their use in preserving the postharvest quality of cherry tomatoes, with good results obtained. The tea AgNP treatment was specifically found to reduce the weight loss of the tomatoes, as well as changes in their total soluble solids, vitamin C, and titratable acid contents. The findings of this study indicate that postharvest tea AgNP treatment affords a clean, safe, high‐quality, and environmentally friendly method for extending the shelf life of fruits. [ABSTRACT FROM AUTHOR]

Biological synthesis of nanomaterials is a growing innovative approach and it was broadly utilised in the field of nanotechnology and nanomedicine. This study illustrates that biosynthesis of silver nanoparticles (AgNPs) using fucoidan extracted from seaweed Padina tetrastromatica. The functional groups of extracted fucoidan were characterised by Fourier transform infrared spectroscopy (FTIR) and used to NPs synthesis. Synthesised AgNPs were characterised by ultraviolet–visible spectra, scanning electron microscope, energy dispersive X‐ray, transmission electron microscope, selected area electron diffraction and FTIR. In this study, their main focus is enhancement antibacterial activity of AgNPs coated antibiotics against antibiotic resistant bacteria. Among the microorganisms, Serratia nematodiphila was resistant to novobiocin and penicillin, but it was sensitive to AgNPs impregnated antibiotic discs. The zone of inhibition was 12 and 15 mm. The synergistic effect of combined antibiotics and AgNPs resulted in increased fold area which was greater than the sum of their separate effects. It reveals that AgNPs are highly sought in the medicinal field due to their broad spectrum of antibacterial activity and relatively cheaper. This enhanced synergistic effect potentially superior to control the growth of bacteria and it is the budding process for the development of new remedial agents for severe diseases. [ABSTRACT FROM AUTHOR]

Silver nanoparticles (AgNPs) were synthesised from aqueous Ag nitrate through a simple, competent and eco‐friendly method using the leaf extract of Ipomoea eriocarpa as reducing as well as capping agent. Ultraviolet–visible absorption spectroscopy was used to confirm the formation of AgNPs which displayed the substantiation of surface plasmon bands at 425 nm. The NPs were also characterised using Fourier transformer infrared spectroscopy, X‐ray diffraction method, transmission electron microscope and zeta potential. The characterisation study confirmed the formation of AgNPs, their spherical shape and average diameter of 12.85 ± 8.65 nm. Zeta potential value of −20.5 mV suggested that the AgNPs are stable in the suspension. The aqueous extract and the AgNPs were further screened for in vivo anti‐inflammatory activity using carrageenan‐induced paw edema in male Wistar rats. The study demonstrated that the AgNPs (1 ml kg−1) had a significant (p < 0.05) anti‐edemic effect and inhibition was observed from the first hour (21.31 ± 1.34) until the sixth hour (52.67 ± 1.41), when the inhibitory effect was greatest and superior to the aqueous extract and the standard, diclofenac. [ABSTRACT FROM AUTHOR]

A biological method for synthesising silver nanoparticles (AgNPs) was developed using the callus extracts from Artemisia annua L. under sunlight at 25,000 lx. The AgNPs were characterised using transmission electron microscopy, atomic force microscope, X‐ray diffraction and Fourier transform infrared spectroscopy. The AgNPs were mostly spherical with the size of 2.1 to 45.2 nm (average 10.9 nm). Pulse treatments of AgNPs at 125, 250 and 500 mg/l for 1 h extended vase life of cut carnation (Dianthus caryophyllus cv. Green Land) flowers. Four dominant bacteria strains Arthrobacter arilaitensis, Kocuria sp., Staphylococcus equorum and Microbacterium oxydans were isolated from the stem‐ends of cut D. caryophyllus flowers. AgNP pulse inhibited significantly bacterial growth in vase solution and cut stem ends during all of the vase period. The bacteria related blockage in the stem‐ends was significantly alleviated by AgNP pulse because of its higher antibacterial efficacy against the dominant bacteria. In addition, ethylene release of cut carnation flowers was inhibited in response to AgNP pulse. This is the first time that the biologically synthesised AgNPs could be applied as a promising preservative agent for cut carnation flowers. [ABSTRACT FROM AUTHOR]

Retinoblastoma is the most common intraocular malignancy basically occurs among children below five. Certain ocular treatments such as surgery, radiation therapy and chemotherapy are more likely to cause side effects. Here, a rapid method of synthesising silver nanoparticles (AgNPs) from the brown seaweed Turbinaria ornata and its cytotoxic efficacy against the retinoblastoma Y79 cell lines was studied. The AgNPs synthesis was determined by Ultraviolet–visible spectroscopy and was further characterised by X‐ray diffraction, High‐resolution transmission electron microscopy, zeta potential, Energy‐dispersive X‐ray spectroscopy, thermogravimetric analysis, Fourier transform infrared spectrum and inductively coupled plasma‐mass spectroscopy techniques. The synthesised AgNPs were found to be very stable and finely dispersed. The total phenolic content of the synthesised AgNPs was estimated at 43±2.52 mg/g gallic acid equivalent and the nanoparticles exhibited good scavenging activity analysed by 2, 2′‐azinobis‐(3‐ethylbenzothiazoline‐6‐sulphonic acid) assay. Moreover, cytotoxicity of synthesised AgNPs against in vitro retinoblastoma Y79 cell lines showed a dose‐dependent response with an inhibitory concentration (IC50) of 10.5 µg/mL. These results suggest that AgNPs could be a promising anticancer agent with enhanced activity in ocular treatment. [ABSTRACT FROM AUTHOR]

In recent years, biosynthesis and the utilisation of silver nanoparticles (AgNPs) has become an interesting subject. In this study, the authors investigated the biosynthesis of AgNPs using Trifolium resupinatum (Persian clover) seed exudates. The characterisation of AgNPs were analysed using ultraviolet–visible spectroscopy, X‐ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier transform infra‐red spectroscopy. Also, antifungal efficacy of biogenic AgNPs against two important plant‐pathogenic fungi (Rhizoctonia solani and Neofusicoccum Parvum) in vitro condition was evaluated. The XRD analysis showed that the AgNPs are crystalline in nature and have face‐centred cubic geometry. TEM images revealed the spherical shape of the AgNPs with an average size of 17 nm. The synthesised AgNPs were formed at room temperature and kept stable for 4 months. The maximum distributions of the synthesised AgNPs were seen to range in size from 5 to 10 nm. The highest inhibition effect was observed against R. solani at 40 ppm concentration of AgNPs (94.1%) followed by N. parvum (84%). The results showed that the antifungal activity of AgNPs was dependent on the amounts of AgNPs. In conclusion, the AgNPs obtained from T. resupinatum seed exudate exhibit good antifungal activity against the pathogenic fungi R. solani and N. Parvum. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

The authors report extracellular mycosynthesis of silver nanoparticles (AgNPs) by Phoma capsulatum, Phoma putaminum and Phoma citri. The AgNPs thus synthesised were characterised by UV–visible spectrophotometer, Fourier transform infrared spectroscopy, Nanosight LM20 and transmission electron microscopy, which confirmed the synthesis of mostly spherical and polydisperse nanoparticles capped with proteins. The size of AgNPs was found in the range of 10–80, 5–80 and 5–90 nm with an average size of 31.85, 25.43 and 23.29 nm by P. capsulatum, P. putaminum and P. citri, respectively. Further, potential antimicrobial activity was reported against Aspergillus niger, Candida albicans, Salmonella choleraesuis, Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli. The lowest minimal inhibitory concentration (MIC) (0.85 µg/ml) was reported for AgNPs synthesised from P. citri against S. choleraesuis. However, AgNPs synthesised from P. capsulatum showed the highest MIC (10.62 µg/ml) against S. choleraesuis, P. aeruginosa and E. coli (clinical isolate). The same MIC values (10.62 µg/ml) were also reported against P. aeruginosa and both clinical and standard isolates of E. coli for AgNPs synthesised from P. citri. It was also observed that all the silver nanoparticles showed remarkable antifungal and antibacterial activity against these tested pathogens as compared with the commercially available antifungal and antibacterial agents. [ABSTRACT FROM AUTHOR]

This study focuses on the green synthesis of noble metal nanoparticles (silver (Ag) and platinum (Pt)) and how the size and shape of the nanoparticles produced can be controlled through changes in the initial pH value of the precursor solution. The nanoparticles were characterised by ultra‐violet‐visible spectroscopy, transmission electron microscopy and X‐ray diffraction. This simple and environmentally friendly method allows the synthesis of diverse nanostructures in the absence of a surfactant or polymer to direct nanoparticle growth, and without externally adding seed crystallites. The antibacterial effects of Ag nanoparticles and catalytic properties of Pt nanoparticles were explored for future promising biotechnological approaches in different fields. [ABSTRACT FROM AUTHOR]

The authors report the biological synthesis of silver nanoparticles (NPs) by Phoma gardeniae (ITCC 4554). The detection of silver NP formation was done by visual observation, and UV–vis spectrophotometer analysis. Further, these mycogenic silver NPs were characterised by Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and nanoparticle tracking and analysis system. The TEM analysis revealed the formation of spherical and polydispersed NPs within the range of 10–30 nm. FTIR analysis confirmed the presence of proteins as capping agents. They also evaluated the antimicrobial activity of silver NPs against Candida albicans, Salmonella choleraesuis, Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli. They found remarkable inhibition of Escherichia coli followed by Staphylococcus aureus, Candida albicans, Salmonella choleraesuis and Pseudomonas aeruginosa as compared with antibiotics. The main aim of the present study was to synthesise mycogenic silver NPs by P. gardeniae and to evaluate their antimicrobial activity in order to find their potential against human pathogenic microbes. [ABSTRACT FROM AUTHOR]

Extracellular and intracellular biosynthesis of silver nanoparticles (AgNPs) by Euglena gracilis (EG) strain and Euglena intermedia (EI) strain are reported in this study. The obtained nanoparticles showed an absorption peak approximates 420 nm in the UV–visible spectrum, corresponding to the plasmon resonance of AgNPs. According to the result of inductively coupled plasma‐atomic emission spectrometer, the intakes of silver ions by EI and EG are roughly equal. The transmission electron microscope (TEM) analysis of the successful in vivo and in vitro synthesised AgNPs indicated the sizes, ranging from 6 to 24 nm and 15 to 60 nm in diameter, respectively, and a spherical‐shaped polydispersal of the particles. The successful formation of AgNPs has been confirmed by energy dispersive X‐ray analysis connected to the TEM. The Fourier transform infrared spectroscopy measurements reveal the presence of bioactive functional groups such as amines are found to be the capping and stabilising agents of nanoparticles. To our knowledge, this is the first report where two kinds of Euglena microalga were used as the potential source for in vivo and in vitro biosynthesis of AgNPs. [ABSTRACT FROM AUTHOR]

By applying a recently developed crystal engineering rationale, four C3 symmetric tris(pyridylamide) ligands namely 1,3,5-tris(nicotinamidomethyl)-2,4,6-triethylbenzene, 1,3,5-tris(isonicotinamidomethyl)-2,4,6-triethylbenzene, 1,3,5- tris(nicotinamidomethyl)-2,4,6-trimethylbenzene, and 1,3,5- tris(isonicotinamidomethyl)-2,4,6-trimethylbenzene, which contain potential hydrogen-bonding sites, were designed and synthesized for generating AgI coordination polymers and coordination-polymer-based gels. The coordination polymers thus obtained were characterized by single-crystal X-ray diffraction. The silver metallogels were characterized by transmission electron microscopy (TEM) and dynamic rheology. Upon exposure to visible light, these silver metallogels produced silver nanoparticles (AgNPs), which were characterized by TEM, powder X-ray diffraction, energy dispersive X-ray and X-ray photoelectron spectroscopy. These NPs were found to be effectively catalyzed the reduction of 4-nitrophenolate to 4-aminophenolate without the use of any exogenous reducing agent [ABSTRACT FROM AUTHOR]

ABSTRACT The use of silver nanoparticles in food, food contact materials, dietary supplements and cosmetics has increased significantly owing to their antibacterial and antifungal properties. As a consequence, the need for validated rapid screening methods to assess their toxicity is necessary to ensure consumer safety. This study evaluated two widely used in vitro cell culture models, human liver HepG2 cells and human colon Caco2 cells, as tools for assessing the potential cytotoxicity of food- and cosmetic-related nanoparticles. The two cell culture models were utilized to compare the potential cytotoxicity of 20-nm silver. The average size of the silver nanoparticle determined by our transmission electron microscopy (TEM) analysis was 20.4 nm. The dynamic light scattering (DLS) analysis showed no large agglomeration of the silver nanoparticles. The concentration of the 20-nm silver solution determined by our inductively coupled plasma-mass spectrometry (ICP-MS) analysis was 0.962 mg ml-1. Our ICP-MS and TEM analysis demonstrated the uptake of 20-nm silver by both HepG2 and Caco2 cells. Cytotoxicity, determined by the Alamar Blue reduction assay, was evaluated in the nanosilver concentration range of 0.1 to 20 µg ml-1. Significant concentration-dependent cytotoxicity of the nanosilver in HepG2 cells was observed in the concentration range of 1 to 20 µg ml-1 and at a higher concentration range of 10 to 20 µg ml-1 in Caco2 cells compared with the vehicle control. A concentration-dependent decrease in dsDNA content was observed in both cell types exposed to nanosilver but not controls, suggesting an increase in DNA damage. The DNA damage was observed in the concentration range of 1 to 20 µg ml-1. Nanosilver-exposed HepG2 and Caco2 cells showed no cellular oxidative stress, determined by the dichlorofluorescein assay, compared with the vehicle control in the concentration range used in this study. A concentration-dependent decrease in mitochondria membrane potential in both nanosilver exposed cell types suggested increased mitochondria injury compared with the vehicle control. The mitochondrial injury in HepG2 cells was significant in the concentration range of 1 to 20 µg ml-1, but in Caco2 cells it was significant at a higher concentration range of 10 to 20 µg ml-1. These results indicated that HepG2 cells were more sensitive to nanosilver exposure than Caco2 cells. It is generally believed that cellular oxidative stress induces cytotoxicity of nanoparticles. However, in this study we did not detect any nanosilver-induced oxidative stress in either cell type at the concentration range used in this study. Our results suggest that cellular oxidative stress did not play a major role in the observed cytotoxicity of nanosilver in HepG2 and Caco2 cells and that a different mechanism of nanosilver-induced mitochondrial injury leads to the cytotoxicity. The HepG2 and Caco2 cells used this study appear to be targets for silver nanoparticles. The results of this study suggest that the differences in the mechanisms of toxicity induced by nanosilver may be largely as a consequence of the type of cells used. This differential rather than universal response of different cell types exposed to nanoparticles may play an important role in the mechanism of their toxicity. In summary, the results of this study indicate that the widely used in vitro models, HepG2 and Caco2 cells in culture, are excellent systems for screening cytotoxicity of silver nanoparticles. These long established cell culture models and simple assays used in this study can provide useful toxicity and mechanistic information that can help to better inform safety assessments of food- and cosmetic-related silver nanoparticles. Published 2014. This article is a U.S. Government work and is in the public domain in the USA. [ABSTRACT FROM AUTHOR]

Lawsonia inermis mediated synthesis of silver nanoparticles (Ag‐NPs) and its efficacy against Candida albicans, Microsporum canis, Propioniabacterium acne and Trichophyton mentagrophytes is reported. A two‐step mechanism has been proposed for bioreduction and formation of an intermediate complex leading to the synthesis of capped nanoparticles was developed. In addition, antimicrobial gel for M. canis and T. mentagrophytes was also formulated. Ag‐NPs were synthesized by challenging the leaft extract of L. inermis with 1 mM AgNO3. The Ag‐NPs were characterized by Ultraviolet‐Visible (UV–Vis) spectrophotometer and Fourier transform infrared spectroscopy (FTIR). Transmission electron microscopy (TEM), nanoparticle tracking and analysis sytem (NTA) and zeta potential was measured to detect the size of Ag‐NPs. The antimicrobial activity of Ag‐NPs was evaluated by disc diffusion method against the test organisms. Thus these Ag‐NPs may prove as a better candidate drug due to their biogenic nature. Moreover, Ag‐NPs may be an answer to the drug‐resistant microorganisms. [ABSTRACT FROM AUTHOR]

In this study, facile and ecofriendly methods have been developed for the biosynthesis of silver nanoparticles from silver nitrate using the seed extract of Strychnos potatorum, a natural phytocoagulant. The effect of room temperature stirring, water bath heating and autoclaving on nanoparticle synthesis was studied. The water soluble compounds in the extract serve as reducing and stabilising agents. Analytical techniques such as UV–visible spectroscopy, transmission electron microscopy (TEM) and X‐ray diffraction were used to characterise the synthesised nanoparticles. By tuning the reaction conditions, size controlled spherical nanoparticles of around 14.1 ± 4.8 nm were generated. The face centred cubic crystalline structure of the nanoparticles is confirmed from the observed peaks corresponding to (111), (200), (220) and (311) planes in the XRD pattern, concentric rings with intermittent bright dots in selected‐area electron diffraction patterns and clear lattice fringes in high‐resolution TEM images. With Fourier transform infrared spectroscopy and Raman spectroscopy, a probable mechanism involved in the reduction and stabilisation of nanoparticles has been investigated. As the silver nanoparticles are encapsulated with functional groups, they can be easily integrated for various biomedical applications. [ABSTRACT FROM AUTHOR]

This study presents a special, economically valuable, unprecedented eco-friendly green process for the synthesis of silver nanoparticles. The silver nanoparticles were obtained from a waste material with oil palm biosolid extract as the reducing agent. The use of the oil palm biosolid extract for the nanoparticle synthesis offers the benefit of amenability for large-scale production. An aqueous solution of silver (Ag) ions was treated with the oil palm biosolid extract for the formation of Ag nanoparticles. The nanometallic dispersion was characterized by surface plasmon absorbance measuring 428 nm. Transmission electron microscopy showed the formation of silver nanoparticles in the range of 5-50 nm. Scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) and X-ray diffraction analysis of the freeze-dried powder confirmed the formation of metallic silver nanoparticles. Moreover, Fourier Transform Infrared Spectroscopy provided evidence of phenolics or proteins as the biomolecules that were likely responsible for the reduction and capping agent, which helps to increase the stability of the synthesized silver nanoparticles. In addition, we have optimized the production with various parameters. © 2010 American Institute of Chemical Engineers Biotechnol. Prog., 2011 [ABSTRACT FROM AUTHOR]

Typical laser-dependent methods such as nanoparticle tracking analysis (NTA) and dynamic light scattering (DLS) are not able to detect nanoparticles in an optically opaque medium due to scattering or absorption of light. Here, the electrochemical technique of 'nano-impacts' was used to detect nanoparticles in solution in the presence of high levels of alumina particulates causing a milky white suspension. Using the 'nano-impacts' method, silver nanoparticles were successfully detected and sized in the model opaque medium. The results obtained compared well with those using transmission electron microscopy (TEM), an ex situ method for nanoparticle size determination. The ability to use the 'nano-impacts' method in media unmeasurable to competitor techniques confers a significant advantage on the electrochemical approach. [ABSTRACT FROM AUTHOR]