Biosynthesis of Silver Nanoparticles by Streptomyces griseorubens isolated from Soil and Their Antioxidant Activity

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.Inspec keywords: silver, microorganisms, nanoparticles, nanofabrication, DNA, molecular biophysics, ultraviolet spectra, visible spectra, scanning electron microscopy, Fourier transform infrared spectra, transmission electron microscopy, X‐ray diffraction, X‐ray chemical analysis, absorption coefficients, cellular biophysicsOther keywords: silver nanoparticles, Streptomyces griseorubens AU2, soil, antioxidant activity, microbial mediated biological synthesis, ultraviolet‐visible spectroscopy, Fourier transform infrared spectroscopy, UV‐vis spectroscopy, high‐resolution transmission electron microscopy, scanning electron microscopy, X‐ray diffraction, elemental analysis, energy dispersive X‐ray spectroscopy, absorption spectra, spherical particles, crystalline particles, 2,2‐diphenyl‐1‐picrylhydrazyl free radical scavenging assay, strain identification, molecular characterisation method, rDNA sequencing, active biological components, cell‐free culture supernatant, wavelength 422 nm, size 5 nm to 20 nm, Ag     

Green synthesis of silver nanoparticle by cauliflower extract: characterisation and antibacterial activity against storage

Green synthesis of silver nanoparticles (AgNPs) was accomplished using different volumes of cauliflower extract and 0.001 M silver nitrate solution at 80°C for 15 min. A brownish‐red solution of AgNPs formed was tested by ultraviolet–visible absorption spectroscopy, Fourier‐transform infrared (FTIR), scanning electron microscopy (SEM), and X‐ray diffraction (XRD). Surface plasmon resonance of AgNPs appeared at 416 nm. Also, the kinetic of AgNPs formation was studied and follows a sigmoidal pattern. Storing time was studied for the freshly prepared AgNPs after 60 days. FTIR analysis shows the adsorption of active components on AgNPs surface, and these components are responsible for reduction besides working as a stabiliser like a capping agent, also FTIR analysis of AgNPs after storage showed no change in peaks location. The SEM exhibited a globular shape of AgNPs, and the particle size ranged from 25 to 100 nm, while the XRD particle size calculation was 25 nm with cubic phase lattice. The antibacterial activity was tested against Gram‐positive and ‐negative bacteria showed an inhibition zone of 16–27 mm and the antibacterial activity tested for the same bacteria after storage for about 10 months showed an inhibition zone of 6–10 mm.Inspec keywords: microorganisms, reduction (chemical), nanofabrication, surface plasmon resonance, silver, transmission electron microscopy, nanoparticles, particle size, visible spectra, ultraviolet spectra, adsorption, antibacterial activity, scanning electron microscopy, X‐ray diffraction, Fourier transform infrared spectra, nanomedicineOther keywords: antibacterial activity, green synthesis, silver nanoparticle, brownish‐red solution, surface plasmon resonance, FTIR analysis, active components, silver nitrate solution, ultraviolet‐visible absorption spectroscopy, AgNP surface, cauliflower extract, Fourier‐transform infrared spectroscopy, scanning electron microscopy, SEM, X‐ray diffraction, XRD, sigmoidal pattern, storing time, adsorption, stabiliser, capping agent, globular shape, particle size, cubic phase lattice, Gram‐positive bacteria, Gram‐negative bacteria, inhibition zone, reduction, time 60.0 d, temperature 80.0 degC, time 15.0 min, wavelength 416.0 nm, Ag     

Biofabrication of silver nanoparticles using bacteria from mangrove swamp

The last decade has observed a rapid advancement in utilising biological system towards bioremediation of metal ions in the form of respective metal nanostructures or microstructures. The process may also be adopted for respective metal nanoparticle biofabrication. Among different biological methods, bacteria‐mediated method is gaining great attention for nanoparticle fabrication due to their eco‐friendly and cost‐effective process. In the present study, silver nanoparticle (AgNP) was synthesised via continuous biofabrication using Aeromonas veronii, isolated from swamp wetland of Sunderban, West Bengal, India. The biofabricated AgNP was further purified to remove non‐conjugated biomolecules using size exclusion chromatography, and the purified AgNPs were characterised using UV–visible spectroscopy, X‐ray diffraction, field emission scanning electron microscopy and transmission electron microscopy (TEM). Additionally, the presence of proteins as capping and stabilising agents was confirmed by the amide‐I and amide‐II peaks in the spectra obtained using attenuated total reflection Fourier transform infrared spectroscopy. The size of biofabricated AgNP was 10–20 nm, as observed using TEM. Additionally, biofabricated AgNP shows significant antibacterial potential against E. coli and S. aureus. Hence, biofabricated AgNP using Aeromonas veronii, which found resistant to a significant concentration of Ag ion, showed enhanced antimicrobial activity compared to commercially available AgNP.Inspec keywords: silver, nanoparticles, microorganisms, nanofabrication, purification, chromatography, ultraviolet spectra, visible spectra, X‐ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, proteins, molecular biophysics, biochemistry, molecular configurations, attenuated total reflection, Fourier transform infrared spectra, particle size, antibacterial activity, biomedical materials, nanomedicineOther keywords: capping agents, stabilising agents, amide‐I peaks, amide‐II peaks, attenuated total reflection Fourier transform infrared spectroscopy, antibacterial potential, E. coli, S. aureus, Aeromonas veronii, antimicrobial activity, size 10 nm to 20 nm, Ag, proteins, TEM, transmission electron microscopy, field emission scanning electron microscopy, X‐ray diffraction, UV‐visible spectroscopy, size exclusion chromatography, nonconjugated biomolecules, purification, swamp wetland, Aeromonas veronii, cost‐effective process, eco‐friendly, bacteria‐mediated method, biological methods, metal nanoparticle biofabrication, microstructures, metal nanostructures, metal ions, bioremediation, biological system, mangrove swamp, bacteria, silver nanoparticles     

Green synthesis,characterisation and biological evaluation of plant‐based silver nanoparticles using Quercus semecarpifolia Smith aqueous leaf extract

The development of reliable and green methods for the fabrication of metallic nanoparticles (NPs) has many advantages in the field of nanotechnology. In this direction, the present work describes an eco‐friendly and cost‐effective protocol for the production of silver NPs (AgNPs) using an aqueous extract of Quercus semecarpifolia leaves. Different techniques were carried out for the characterisation of the synthesised AgNPs. The ultraviolet–visible spectroscopic analysis showed the highest absorbance peak at 430 nm. The particle size and structure were confirmed by scanning electron microscopy as well as transmission electron microscopy (TEM) analysis. From TEM imaging, it was revealed that the formed particles were spherical with an average size of 20–50 nm. The crystalline nature of the NPs was determined by X‐ray powder diffraction patterns. Thermogravimetry and differential thermal analysis were also evaluated by a temperature increment from 100 to 1000°C. Bio‐inspired synthesis of AgNPs was performed for their pharmacological evaluation in relation to the activities of the crude methanolic, n ‐hexane, chloroform, ethyl acetate, and aqueous extracts. Good cytotoxic activity was exhibited by the green‐synthesised AgNPs (77%). Furthermore, the AgNPs were found to exhibit significant antioxidant activity at 300 μg/ml (82%). The AgNPs also exhibited good phytotoxic potential (75%).Inspec keywords: scanning electron microscopy, toxicology, visible spectra, particle size, nanofabrication, nanomedicine, transmission electron microscopy, silver, ultraviolet spectra, differential thermal analysis, nanoparticles, X‐ray diffraction, botany, biochemistry, cellular biophysicsOther keywords: green synthesis, biological evaluation, plant‐based silver nanoparticles, reliable methods, metallic nanoparticles, eco‐friendly cost‐effective protocol, silver NPs, ultraviolet–visible spectroscopic analysis, highest absorbance peak, particle size, structure, transmission electron microscopy analysis, TEM imaging, crystalline nature, X‐ray powder diffraction patterns, differential thermal analysis, pharmacological evaluation, aqueous extracts, good cytotoxic activity, significant antioxidant activity, AgNPs exhibited good phytotoxic potential, bio‐inspired synthesis, Quercus semecarpifolia Smith aqueous leaf extract, scanning electron microscopy, thermogravimetry, crude methanolic, n‐hexane, chloroform, ethyl acetate, phytotoxic potential, haemagglutination activity, size 20.0 nm to 50.0 nm, wavelength 430.0 nm, temperature 100 degC to 1000 degC, Ag     

Green synthesis,characterisation and biological evaluation of AgNPs using Agave americana,Mentha spicata and Mangifera indica aqueous leaves extract

The current study was performed to synthesize stable, eco‐friendly and bio‐compatible silver nano‐particles (AgNPs) of Agave americana, Mentha spicata and Mangifera indica leaves and to screen them for biological activities. The ultraviolet‐visible spectroscopic analysis revealed that λ‐max for AgNPs range from 350–500 nm. All AgNPs possessed polycrystalline structure as notified as intense graphical peaks in complete spectrum of 20 values ranging from 10–80° in X‐ray diffraction measurements and supported by scanning electron microscopy data. The size of the nano‐particles was confirmed by transmission electron microscopy (30–150 nm). Mass loss at variable temperatures was evaluated by simultaneous thermogravimetric and differential thermal analysis revealed reduction in mass and activity of compounds was notified by temperature increase from 200 to 800 °C, thus concluding it as thermally sensitive compounds. A. americana AgNPs showed significant (96%) activity against Methicillin resistant Staphylococcus aureus, Escherichia coli (95%) and Fusarium oxysporum (89%). Good antioxidant activity was shown by M. spicata AgNPs at 300 µl (79%). M. indica AgNPs showed significant phytotoxic activity (88%) at highest concentration. No haemagglutination reaction was observed for the test samples. The above results revealed that AgNPs synthesized from selected plant species possesses significant antimicrobial and phytotoxic effect.Inspec keywords: silver, nanoparticles, nanofabrication, X‐ray diffraction, transmission electron microscopy, scanning electron microscopy, differential thermal analysis, microorganisms, antibacterial activity, nanomedicine, particle size, toxicologyOther keywords: green synthesis, biological evaluation, Agave americana aqueous leave extract, Mentha spicata aqueous leave extract, Mangifera indica aqueous leave extract, stable ecofriendly biocompatible silver nanoparticles, ultraviolet‐visible spectroscopy, polycrystalline structure, X‐ray diffraction, scanning electron microscopy, nanoparticle size, transmission electron microscopy, thermogravimetric analysis, differential thermal analysis, mass loss, thermally sensitive compounds, Methicillin resistant Staphylococcus aureus, Escherichia coli, Fusarium oxysporum, antioxidant activity, phytotoxic activity, plant species, antimicrobial effect, temperature 200 degC to 800 degC, Ag     

Antibacterial and dye degradation potential of zero‐valent silver nanoparticles synthesised using the leaf extract of Spondias dulcis

The present study reports a simple and low cost synthesis of zero‐valent silver nanoparticles (ZVSNPs) from silver nitrate using the leaf extract of Spondias dulcis. The ZVSNPs showed a unique peak at 420 nm in UV–vis spectrum. The SEM image portrayed cuboidal shaped particles. The EDX spectrum designated the elemental silver peak at 3 keV. In XRD, a sharp peak at 32.47° denoted the existence of (1 0 1) lattice plane and the average crystallite size was calculated as 48.61 nm. The lattice parameter was determined as 0.39 nm. The FTIR spectra of the leaf extract and ZVSNPs showed shifts in the specific functional group bands which ascertained the involvement of phytoconstituents in the formation and capping of nanoparticles. The average hydrodynamic size was measured as 59.66 nm by DLS method. A low PDI, 0.187 witnessed the monodispersity. A negative zeta potential value of −15.7 mV indicated the negative surface charges of the nanoparticles. The bactericidal action of ZVSNPs was demonstrated against two pathogens S.typhimurium and E.coli during which a dosage dependent zone of inhibition results was observed. Additionally, the catalytic potential of ZVSNPs was examined for the degradation of methylene blue dye in which an accelerated degradation of the dye was observed.Inspec keywords: antibacterial activity, crystallites, electrokinetic effects, scanning electron microscopy, nanoparticles, particle size, ultraviolet spectra, X‐ray chemical analysis, microorganisms, light scattering, nanofabrication, materials preparation, X‐ray diffraction, visible spectra, silver, dyes, Fourier transform infrared spectraOther keywords: wavelength 420.0 nm, Ag, voltage ‐15.7 mV, size 59.66 nm, size 0.39 nm, size 48.61 nm, electron volt energy 3.0 keV, Fourier transform infrared spectra, methylene blue dye, bactericidal action, dynamic light scattering, lattice parameter, Escherichia coli, Salmonella typhimurium, Spondias dulcis, negative zeta potential, polydispersity index, crystallite size, leaf extract, X‐ray diffraction, energy dispersive X‐ray spectrum, cuboidal‐shaped particles, scanning electron microscopy image, ultraviolet–visible spectrum, silver nitrate, zero‐valent silver nanoparticles     

Biosynthesised AgCl NPs using Bacillus sp. 1/11 and evaluation of their cytotoxic activity and antibacterial and antibiofilm effects on multi‐drug resistant bacteria

Silver nanoparticles (AgNPs) have attracted the attention of researchers due to their properties. Biological synthesis of AgNPs is eco‐friendly and cost‐effective preferred to physical and chemical methods, which utilize environmentally harmful agents and large amounts of energy. Microorganisms have been explored as potential biofactories to synthesize AgNPs. Bacterial NP synthesis is affected by Ag salt concentration, pH, temperature and bacterial species. In this study, Bacillus spp., isolated from soil, were screened for AgNP synthesis at pH 12 with 5 mM Ag nitrate (AgNO₃) final concentration at room temperature. The isolate with fastest color change and the best ultraviolet‐visible spectrum in width and height were chosen as premier one. AgNO₃ and citrate salts were compared in terms of their influence on NP synthesis. Spherical Ag chloride (AgCl) NPs with a size range of 35–40 nm were synthesized in 1.5 mM Ag citrate solution. Fourier transform infrared analysis demonstrated that protein and carbohydrates were capping agents for NPs. In this study, antimicrobial and antitumor properties of the AgNP were investigated. The resulting AgCl NPs had bacteriostatic activity against four standard spp. And multi‐drug resistant strain of Pseudomonas aeruginosa. These NPs are also cytotoxic to cancer cell lines MCF‐7, U87MG and T293.Inspec keywords: silver compounds, nanoparticles, nanomedicine, nanofabrication, particle size, biomedical materials, microorganisms, ultraviolet spectra, visible spectra, Fourier transform infrared spectra, proteins, macromolecules, antibacterial activity, tumours, cancer, cellular biophysics, toxicologyOther keywords: citrate salts, spherical Ag chloride, particle size, Ag citrate solution, Fourier transform infrared analysis, protein, carbohydrates, capping agents, antitumour properties, bacteriostatic activity, Pseudomonas aeruginosa, multidrug resistant strain, cancer cell lines MCF‐7,U87MG, size 35 nm to 40 nm, temperature 293 K to 298 K, AgCl, ultraviolet‐visible spectrum, colour change, room temperature, Ag nitrate final concentration, soil, bacterial species, temperature effect, pH, Ag salt concentration, biofactories, microorganisms, environmentally harmful agents, chemical methods, physical methods, antibacterial properties, electrical properties, mechanical properties, silver nanoparticles, multidrug resistant bacteria, antibiofilm effects, antibacterial effects, cytotoxic activity, Bacillus sp. 1/11, biosynthesised AgCl NPs     

Optimisation of nitrate reductase enzyme activity to synthesise silver nanoparticles

Today, the synthesis of silver nanoparticles (Ag NPs) is very common since it has many applications in different areas. The synthesis of these nanoparticles is done by means of physical, chemical, or biological methods. However, due to its inexpensive and environmentally friendly features, the biological method is more preferable. In the present study, using nitrate reductase enzyme available in the Escherichia coli (E. coli) bacterium, the biosynthesis of Ag NPs was investigated. In addition, the activity of the nitrate reductase enzyme was optimised by changing its cultural conditions, and the effects of silver nitrate (AgNO₃) concentration and enzyme amount on nanoparticles synthesis were studied. Finally, the produced nanoparticles were studied using ultraviolet –visible (UV–Vis) spectrophotometer, dynamic light scattering technique, and transmission electron microscopy. UV–Visible spectrophotometric study showed the characteristic peak for Ag NPs at wavelength 405–420 nm for 1 mM metal precursor solution (AgNO₃) with 1, 5, 10, and 20 cc supernatant and 435 nm for 0.01M AgNO₃ with 20 cc supernatant. In this study, it was found that there is a direct relationship between the AgNO₃ concentration and the size of produced Ag NPs.Inspec keywords: enzymes, molecular biophysics, silver, nanoparticles, nanofabrication, microorganisms, cellular biophysics, silver compounds, ultraviolet spectra, visible spectra, light scattering, transmission electron microscopyOther keywords: nitrate reductase enzyme activity, optimisation, silver nanoparticle synthesis, Escherichia coli bacterium, E. coli bacterium, biosynthesis, ultraviolet‐visible spectrophotometer, UV‐vis spectrophotometer, dynamic light scattering technique, transmission electron microscopy, supernatant, metal precursor solution, AgNO₃ ‐Ag     

Green synthesis of silver nanoparticles using Zea mays and exploration of its biological applications

The biosynthesis of silver nanoparticles (AgNPs) has been proved to be a cost effective and environmental friendly approach toward chemical and physical methods. In the present study, biosynthesis of AgNPs was carried out using aqueous extract of Zea mays (Zm) husk. The initial colour change from golden yellow to orange was observed between 410 and 450 nm which confirmed the synthesis of AgNPs. Also, dynamic light scattering‐particle size analysis confirmed the average size to be 113 nm and zeta potential value of −28 kV. The morphology of synthesised Zm AgNPs displayed flower‐shaped structure, X‐ray diffraction pattern revealed the strongest peaks at 2θ = 38.6° and 64° which proved that the nanoparticle has the face centred crystalline structure. The Fourier transform infrared spectroscopy results showed strong absorption bands at 1394.53, 2980.02 and 2980.02 cm⁻¹ due to the presence of alkynes, carboxylic acids, alcoholic and phenolic groups. The maximum zone of inhibition was observed against Salmonella typhi (22 mm) and Candida albicans (18 mm). The synthesised nanoparticles exhibited more free radical scavenging activity than the aqueous plant extract. This is the first report on the synthesis of AgNP from Zm husk, delivers the efficient and stable Zm AgNPs through simple feasible approach toward green biotechnology.Inspec keywords: silver, nanoparticles, nanofabrication, light scattering, particle size, X‐ray diffraction, crystal structure, Fourier transform infrared spectra, absorption coefficients, free radicalsOther keywords: green synthesis, silver nanoparticles, biosynthesis, environmental friendly approach, aqueous extract, Zea mays husk, colour change, golden yellow, dynamic light scattering‐particle size analysis, average size, zeta potential value, flower‐shaped structure, X‐ray diffraction pattern, face centred crystalline structure, Fourier transform infrared spectroscopy, absorption bands, alkynes, carboxylic acids, alcoholic groups, phenolic groups, Salmonella typhi, Candida albicans, free radical scavenging activity, aqueous plant extraction, green biotechnology, size 113 nm, wavelength 410 nm to 450 nm     

Eco‐friendly synthesis of silver nanoparticles and its larvicidal property against fourth instar larvae of Aedes aegypti

In this study, larvicidal activity of silver nanoparticles (AgNPs) synthesised using apple extract against fourth instar larvae of Aedes aegypti was determined. As a result, the AgNPs showed moderate larvicidal effects against Ae. aegypti larvae (LC₅₀  = 15.76 ppm and LC₉₀  = 27.7 ppm). In addition, comparison of larvicidal activity performance of AgNPs at high concentration prepared using two different methods showed that Ae. aegypti larvae was fully eliminated within the duration of 2.5 h. From X‐ray diffraction, the AgNP crystallites were found to exhibit face centred cubic structure. The average size of these AgNPs as estimated by particle size distribution was in the range of 50–120 nm. The absorption maxima of the synthesised Ag showed characteristic Ag surface plasmon resonance peak. This green synthesis provides an economic, eco‐friendly and clean synthesis route to Ag.Inspec keywords: silver, nanofabrication, X‐ray diffraction, zoology, particle size, nanoparticles, biomedical materials, nanomedicineOther keywords: time 2.5 h, size 50 nm to 120 nm, silver nanoparticle, larvicidal property, instar larvae, Aedes aegypti, larvicidal effect, larvicidal activity performance, X‐ray diffraction, nanoparticle particle size distribution, absorption maxima, silver surface plasmon resonance peak     

Removal of toxic contaminants from water by sustainable green synthesised non‐toxic silver nanoparticles

The study describes the synthesis of silver nanoparticles using 21 different plant extracts having medicinal properties. Molecular ultraviolet‐visible spectroscopy shows that the λ _max of nanoparticles synthesised by different plant extracts varied and ranged between 400 and 468 nm. The ultraviolet results revealed that although synthesis of nanoparticles occurred by all plant extracts successfully, their size varies, this was further confirmed by differential light scattering. The synthesised nanoparticles were investigated for their antimicrobial properties. The most promising silver nanoparticles Ocimum sanctum and Artemisia annua assisted were further characterised using transmission electron microscopy and energy dispersive X‐ray spectroscopy (EDX). EDX data confirms that synthesised nanoparticles are highly pure. Further these two plant assisted nanoparticles were studied for chemocatalytic and adsorptive properties. The silver nanoparticles from Ocimum sanctum can catalyse the reduction of 4‐nitrophenol (63%) within 20 min in the presence of NaBH₄, whereas Artemisia annua assisted silver nanoparticles did not show significant chemocatalytic activity. Both the promising nanoparticles can efficiently adsorb textile dyes from aqueous solutions. These synthesised nanoparticles were also exploited to remove microbial and other contaminants from Yamuna River water. The nanoparticles show excellent antimicrobial properties and can be reused repeatedly.Inspec keywords: antibacterial activity, nanofabrication, silver, dyes, light scattering, visible spectra, microorganisms, X‐ray diffraction, transmission electron microscopy, X‐ray chemical analysis, catalysis, nanoparticles, ultraviolet spectra, adsorption, reduction (chemical)Other keywords: sustainable green synthesised nontoxic silver nanoparticles, silver nitrate, molecular ultraviolet–visible spectroscopy, plant assisted nanoparticles, plant extracts, Ocimum sanctum, Artemisia annua, E. coli, C. albicans, plasmon absorbance, differential light scattering, energy dispersive X‐ray spectroscopy, 4‐nitrophenol, chemocatalytic activity, Yamuna River water, antimicrobial properties, time 20.0 min, time 5.0 min to 240.0 hour, size 1.0 nm to 5.0 nm, size 5.0 nm to 20.0 nm, wavelength 400.0 nm to 468.0 nm, NaBH₄ , Ag     

Synthesis of gold and silver nanoparticles using Mukia maderaspatna plant extract and its anticancer activity

The present investigation reveals the in vitro cytotoxic effect of the biosynthesised metal nanoparticles on the MCF 7 breast cancer cell lines. The gold and silver nanoparticles were synthesised through an environmentally admissible route using the Mukia Maderaspatna plant extract. Initially, the biomolecules present in the plant extract were analysed using phytochemical analysis. Further, these biomolecules reduce the metal ion solution resulting from the formation of metal nanoparticles. The reaction parameters were optimised to control the size of nanoparticles which were confirmed by UV visible spectroscopy. Various instrumental techniques such as Fourier transform‐infrared spectroscopy, high resolution transmission electron microscopy, energy dispersive X‐ray and scanning electron microscopy were employed to characterise the synthesised gold and silver nanoparticles. The synthesised gold and silver nanoparticles were found to be 20–50 nm and were of different shapes including spherical, triangle and hexagonal. MTT and dual staining assays were carried out with different concentrations (1, 10, 25, 50 and 100 µg/ml) of gold and silver nanoparticles. The results show that the nanoparticles exhibited significant cytotoxic effects with IC 50 value of 44.8 µg/g for gold nanoparticles and 51.3 µg/g for silver nanoparticles. The observations in this study show that this can be developed as a promising nanomaterial in pharmaceutical and healthcare sector.Inspec keywords: gold, silver, nanoparticles, nanofabrication, nanomedicine, biomedical materials, cancer, cellular biophysics, ultraviolet spectra, visible spectra, Fourier transform infrared spectra, transmission electron microscopy, X‐ray chemical analysis, scanning electron microscopyOther keywords: gold nanoparticle synthesis, silver nanoparticle synthesis, Mukia maderaspatna plant extract, anticancer activity, MCF 7 breast cancer cell line, biomolecule, phytochemical analysis, size 20 nm to 50 nm, healt hcare sector, pharmaceutical sector, nanomaterial, dual staining assay, MTT assay, scanning electron microscopy, energy dispersive X‐ray spectrocopy, high resolution transmission electron microscopy, Fourier transform‐infrared spectroscopy, instrumental technique, ultraviolet‐visible spectroscopy, metal nanoparticle formation, metal ion solution     

Fabrication and characterisation of silver nanoparticles using bract extract of Musa paradisiaca for its synergistic combating effect on phytopathogens,free radical scavenging activity,and catalytic efficiency

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 phenolInspec keywords: catalysis, dyes, electron diffraction, nanofabrication, silver, catalysts, surface plasmon resonance, reduction (chemical), free radicals, nanoparticles, transmission electron microscopy, nanobiotechnology, X‐ray diffraction, microorganisms, organic compounds, Fourier transform spectra, nanomedicine, visible spectra, antibacterial activity, infrared spectra, ultraviolet spectraOther keywords: silver nanoparticles, musa paradisiaca, synergistic combating effect, free radical scavenging activity, catalytic efficiency, M. paradisiaca, bio‐reduction, ultraviolet–visible spectroscopy, surface plasmon resonance extinction peak, Fourier transform infrared spectroscopy, X‐ray diffraction pattern, selected area electron diffraction patterns, radical scavenging potential, potent radical scavenger, size 420.0 nm, size 15.0 nm, Ag⁺      

Synthesis and characterisation of silver nanoparticles using leaf extract of Artemisia afra and their in vitro antimicrobial and antioxidant activities

In this study, the conversion of silver ions into ∼30.74 nm sized silver nanoparticles (AgNPs) was achieved in 30 min at a reaction temperature of 80–90°C in aqueous leaf extract of Artemisia afra. The synthesised AgNPs showed surface plasmon resonance in the range of 423–438 nm. Spherical and face‐centred cubic nanoparticles were confirmed by transmission electron microscope (TEM) and X‐ray diffraction (XRD) analysis, respectively. Fourier transform infra‐red (FTIR) results indicated that the obtained nanoparticles were stabilised and capped through the carbonyl and carboxylate ion groups possibly from flavonoids, terpenoids, phenolics and esters content of the extracts. In addition, the AgNPs were assessed for their biological potentials against some microbes and, also, their free radical scavenging ability was established. The AgNPs exhibited interesting antimicrobial and antioxidant properties better than the aqueous extract of A. afra. Inspec keywords: silver, transmission electron microscopy, ultraviolet spectra, visible spectra, surface plasmon resonance, antibacterial activity, X‐ray diffraction, microorganisms, nanoparticles, nanofabrication, Fourier transform infrared spectraOther keywords: silver nanoparticles, reaction temperature, surface plasmon resonance, face‐centred cubic nanoparticles, antioxidant properties, silver ion conversion, aqueous leaf extract, carboxylate ion group, antimicrobial properties, Artemisia afra, spherical nanoparticles, TEM, XRD, FTIR spectra, Ag, temperature 80 degC to 90 degC, time 30.0 min, free radical scavenging, esters, phenolics, terpenoids, flavonoids, carbonyl ion group     

Biosynthesis of silver nanoparticles using Azadirachta indica leaves: characterisation and impact on Staphylococcus aureus growth and glutathione‐S‐transferase activity

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.Inspec keywords: ultraviolet spectra, microorganisms, nanomedicine, visible spectra, nanoparticles, electrokinetic effects, antibacterial activity, scanning electron microscopy, infrared spectra, transmission electron microscopy, light scattering, nanofabrication, particle size, silver, enzymes, biochemistry, molecular biophysics, cellular biophysicsOther keywords: silver nanoparticles, glutathione‐S‐transferase activity, green leaves, rapid biosynthesis, total protein concentration, nanoparticle synthesis, colour change, zeta potential analysis, UV‐Visible spectrograph, DLS analysis, SEM analysis, element analysis profile, growth curve, GST activity, bacterial strains, antibacterial activity, staphylococcus aureus growth, microbes, Azadirachta azadirachta indica leaf, reducing agent, scanning electron microscopy, transmission electron microscopy, dynamic light scattering, infrared spectroscopy, absorbance peak, polydispersity index, spherical particle shapes, TEM, bacterial cells, Ag     

Process optimisation for green synthesis of zero‐valent iron nanoparticles using Mentha piperita

The potential of Mentha piperita in the iron nanoparticles (FeNPs) production was evaluated for the first time. The influences of the variables such as incubation time, temperature, and volume ratio of the extract to metal ions on the nanoparticle size were investigated using central composite design. The appearance of SPR bands at 284 nm in UV–Vis spectra of the mixtures verified the nanoparticle formation. Incubating the aqueous extract and metal precursor with 1.5 volume ratio at 50°C for 30 min leads to the formation of the smallest nanoparticles with the narrowest size distribution. At the optimal condition, the nanoparticles were found to be within the range of 35–50 nm. Experimental measurements of the average nanoparticle size were fitted well to the polynomial model satisfactory with R ² of 0.9078. Among all model terms, the linear term of temperature, the quadratic terms of temperature, and mixing volume ratio have the significant effects on the nanoparticle average size. FeNPs produced at the optimal condition were characterised by transmission electron microscopy, thermogravimetry analysis (TGA), and Fourier‐transform infrared spectroscopy. The observed weight loss in the TGA curve confirms the encapsulation of FeNPs by the biomolecules of the extract which were dissociated by heat.Inspec keywords: thermal analysis, iron, X‐ray chemical analysis, particle size, nanoparticles, X‐ray diffraction, scanning electron microscopy, transmission electron microscopy, nanofabrication, ultraviolet spectra, mixtures, Fourier transform infrared spectraOther keywords: incubation time, metal ions, central composite design, SPR bands, UV–Vis spectra, nanoparticle formation, metal precursor, narrowest size distribution, optimal condition, average nanoparticle size, particle size, mixing volume ratio, green synthesis, zero‐valent iron nanoparticles, mentha piperita, transmission electron microscopy, thermogravimetry analysis, Fourier‐transform infrared spectroscopy, TGA curve, biomolecules, temperature 50.0 degC, time 30.0 min, size 35.0 nm to 50.0 nm, Fe     

Biosynthesis of eco‐friendly and recyclable Pd/LDHs catalyst using the withered leaves extract for Suzuki coupling reaction

The hydrotalcite‐supported palladium (Pd) catalyst is prepared with a green and environmentally friendly route, introducing the extract of withered leaves as a dispersant and reducing agent (Pd/LDHs‐B). Compared with the as‐prepared catalyst (Pd/LDHs‐P with the average diameter of 4.3 nm) using a chemical synthesis method with polyvinylpyrrolidone as a dispersant and ascorbic acid (Vc) as a reductant, the results indicate that the size of Pd nanoparticles in Pd/LDHs‐B is smaller (ca. 3.6 nm). The Pd‐LHDs‐B (0.5 mmol‰) exhibits higher activity (98.66%) than Pd/LDHs‐P (98.19%) in the Suzuki reaction of 4‐bromotoluene and phenylboronic acid at 60°C for 30 min. Also, the reusability of Pd/LDHs‐B is confirmed by recycling tests without a significant decrease in activity.Inspec keywords: nanoparticles, reduction (chemical), chemical engineering, catalysts, X‐ray diffraction, recycling, catalysis, organic compounds, palladium, particle sizeOther keywords: Suzuki reaction, reducing agent, hydrotalcite‐supported palladium catalyst biosynthesis process, environmentally friendly material, withered leaves extract, dispersant agent, chemical synthesis method, polyvinylpyrrolidone, ascorbic acid, nanoparticle size, 4‐bromotoluene, phenylboronic acid, recycling test, temperature 60.0 degC, size 4.3 nm, size 3.6 nm, time 30.0 min, Pd     

Multifaceted activities of plant gum synthesised platinum nanoparticles: catalytic,peroxidase, PCR enhancing and antioxidant activities

A single pot, green method for platinum nanoparticles (Pt NP) production was devised with gum ghatti (Anogeissus latifolia). Analytical tools: ultraviolet–visible (UV‐vis), dynamic light scattering, zeta potential, transmission electron microscope, X‐ray diffraction (XRD), and Fourier transform infrared spectroscopy were employed. Wide continuous UV‐vis absorption and black solution colouration proved Pt NP formation. Face‐centred cubic crystalline structure of NP was evidenced from XRD. NPs formed were nearly spherical with a mean particle size of 3 nm. NP demonstrated a myriad of properties including catalytic, peroxidase, polymerase chain reaction (PCR) enhancing and antioxidant activities. Catalytic action of NP was probed via NaBH₄ reduction of arsenazo‐III dye. NP displayed considerable peroxidase activity via catalysis of 3, 3′, 5, 5′‐tetramethylbenzidine oxidation by H₂ O₂. NP showed exceptional stability towards varying pH (3–11), temperature (25–100°C), salt concentration (0–100 mM) and storage time duration (0–12 months). In comparison with horse radish peroxidase, its applicability as an artificial peroxidase is advantageous. NP caused a two‐fold enhancement in PCR yield at 0.4 nM. Also showed significant 1′, 1′ diphenyl picryl‐hydrazyle scavenging (80.1%) at 15 µg/mL. Author envisages that the biogenic Pt NP can be used in a range of biological and environmental applications.Inspec keywords: nanofabrication, ultraviolet spectra, catalysis, molecular biophysics, enzymes, dyes, platinum, electrokinetic effects, transmission electron microscopy, particle size, X‐ray diffraction, visible spectra, pH, nanomedicine, nanoparticles, biochemistry, light scattering, scanning electron microscopy, Fourier transform infrared spectra, reduction (chemical), oxidationOther keywords: antioxidant activities, catalytic action, salt concentration, artificial peroxidase, two‐fold enhancement, PCR yield, multifaceted activities, plant gum synthesised platinum nanoparticles, gum ghatti, anogeissus latifolia, analytical characterisation tools, dynamic light scattering, zeta potential, X‐ray diffraction, XRD, black solution colouration, Pt NP formation, face‐centred cubic crystalline structure, peroxidase activity, ultraviolet‐visible spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, particle size, catalytic activity, PCR enhancing activity, single pot green method, wide continuous UV‐visible absorption, polymerase chain reaction enhancing activity, arsenazo‐III, azo dye decolourisation, 3, 3′, 5, 5′‐tetramethylbenzidine oxidation, pH, environmental conditions, 1′,1′ diphenyl picryl‐hydrazyle scavenging, time 0.0 month to 12.0 month, temperature 25.0 degC to 100.0 degC, Pt     

Role of catalytic protein and stabilising agents in the transformation of Ag ions to nanoparticles by Pseudomonas aeruginosa

Biological routes of synthesising metal nanoparticles (NPs) using microbes have been gaining much attention due to their low toxicity and eco‐friendly nature. Pseudomonas aeruginosa JP2 isolated from metal contaminated soil was evaluated towards extracellular synthesis of silver NPs (AgNPs). Cell‐free extract (24 h) of the bacterial isolate was reacted with AgNO₃ for 24 h in order to fabricate AgNPs. Preliminary observations were recorded in terms of colour change of the reaction mixture from yellow to greyish black. UV‐visible spectroscopy of the reaction mixture has shown a progressive increase in optical densities that correspond to peaks near 430 nm, depicting reduction of ionic silver (Ag⁺) to atomic silver (Ag⁰) thereby synthesising NPs. X‐ray diffraction spectra exhibited the 2θ values to be 38.4577° confirming the crystalline and spherical nature of NPs [9.6 − 26.7 (Ave. = 17.2 nm)]. Transmission electron microscopy finally confirmed the size of the particles varying from 5 to 60 nm. Moreover, rhamnolipids and proteins were identified as stabilising molecules for the AgNPs through Fourier transform‐infrared spectroscopy. Characterisation of bacterial crude and purified protein fractions confirmed the involvement of nitrate reductase (molecular weight 66 kDa and specific activity = 3.8 U/mg) in the Synthesis of AgNPs.Inspec keywords: microorganisms, silver, nanoparticles, enzymes, molecular biophysics, ultraviolet spectra, visible spectra, X‐ray diffraction, transmission electron microscopy, Fourier transform infrared spectra, catalysis, biochemistry, nanobiotechnologyOther keywords: catalytic protein, stabilising agents, Pseudomonas aeruginosa, metal nanoparticles, UV–visible spectroscopy, optical densities, ionic silver, atomic silver, X‐ray diffraction spectra, transmission electron microscopy, nitrate reductase, rhamnolipids, Fourier transform‐infrared spectroscopy, Ag     

Green synthesis of silver nanoparticles using flower extract of Malva sylvestris and investigation of their antibacterial activity

High‐quality colloidal silver nanoparticles (AgNP) were synthesised via a green approach by using hydroalcoholic extracts of Malva sylvestris. Silver nitrate was used as a substrate ion while the plant extract successfully played the role of reducing and stabilising agents. The synthesised nanoparticles were carefully characterised by using transmission electron microscopy, atomic‐force microscopy, energy dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy and UV–vis spectroscopy. The maximum absorption wavelengths of the colloidal solutions synthesised using 70 and 96% ethanol and 100% methanol, as extraction solvents, were 430, 485 and 504 nm, respectively. Interestingly, the size distribution of nanoparticles depended on the used solvent. The best particle size distribution belonged to the nanoparticles synthesised by 70% ethanol extract, which was 20–40 nm. The antibacterial activity of the synthesised nanoparticles was studied on Escherichia coli, Staphylococcus aureus and Streptococcus pyogenes using disk diffusion, minimum inhibitory concentrations and minimum bactericidal concentrations assays. The best antibacterial activity obtained for the AgNPs produced by using 96% ethanolic extract.Inspec keywords: silver, nanoparticles, nanofabrication, antibacterial activity, colloids, particle size, transmission electron microscopy, atomic force microscopy, X‐ray chemical analysis, Fourier transform spectra, infrared spectra, ultraviolet spectra, visible spectra, microorganisms, nanomedicine, biomedical materialsOther keywords: Green synthesis, flower extract, Malva sylvestris, antibacterial activity, high‐quality colloidal silver nanoparticles, hydroalcoholic extracts, plant extract, reducing agents, stabilising agents, transmission electron microscopy, atomic‐force microscopy, energy dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy, UV– vis spectroscopy, colloidal solutions, particle size distribution, Escherichia coli, Staphylococcus aureus, Streptococcus pyogenes, disk diffusion, minimum inhibitory concentrations, minimum bactericidal concentrations assays, ethanolic extract, size 430 nm, size 485 nm, size 504 nm, size 20 nm to 40 nm, Ag