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     

Evaluation of antimicrobial activity of synthesised silver nanoparticles using Thymus kotschyanus aqueous extract

Development of a green chemistry process for the synthesis of silver nanoparticles (AgNPs) has become a focus of interest. Characteristics of AgNPs were determined using techniques, such as ultraviolet–visible spectroscopy (UV–vis), Fourier transform infrared (FTIR) analysis, scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy and X‐ray diffraction (XRD). The synthesised AgNPs using Thymus kotschyanus had the most growth inhibition against gram‐positive bacteria such as Staphylococcus aureus and Bacillus subtilise, while the growth inhibition of AgNPs at 1000–500 µg/ml occurred against Klebsiella pneumonia and at 1000–250 µg/ml of AgNPs was observed against E. coli. The UV–vis absorption spectra confirmed the formation of the AgNPs with the characteristic peak at 415 nm and SEM micrograph acknowledged spherical particles in a nanosize range. FTIR measured the possible biomolecules that are responsible for stabilisation of AgNPs. XRD analysis exhibited the crystalline nature of AgNPs and showed face‐centred cubic structure. The synthesised AgNPs revealed significant antibacterial activity against gram‐positive bacteria.Inspec keywords: visible spectra, microorganisms, ultraviolet spectra, biomedical materials, nanofabrication, nanoparticles, X‐ray diffraction, scanning electron microscopy, molecular biophysics, X‐ray chemical analysis, nanomedicine, silver, antibacterial activity, Fourier transform infrared spectraOther keywords: green chemistry process, ultraviolet–visible spectroscopy, gram‐positive bacteria, silver nanoparticles, Thymus kotschyanus aqueous extract, UV–vis spectroscopy, Fourier transform infrared spectroscopy, FTIR analysis, scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, SEM micrograph, X‐ray diffraction, XRD, Staphylococcus aureus, Bacillus subtilise, Klebsiella pneumonia, E. coli, UV–vis absorption spectra, face‐centred cubic structure, antibacterial activity, antimicrobial activity, wavelength 415.0 nm, Ag     

Role of Ribes khorassanicum in the biosynthesis of AgNPs and their antibacterial properties

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.Inspec keywords: X‐ray diffraction, X‐ray chemical analysis, nanofabrication, surface plasmon resonance, nanoparticles, antibacterial activity, microorganisms, scanning electron microscopy, silver, nanomedicine, visible spectra, ultraviolet spectra, transmission electron microscopy, Fourier transform infrared spectra, field emission scanning electron microscopy, biomedical materialsOther keywords: antibacterial properties, silver nanoparticles, reducing agents, capping agents, surface plasmon resonance peak, spherical NPs, field‐emission scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, X‐ray diffraction, transmission electron microscopy analysis, plant extracts, ultraviolet‐visible absorption spectra, Fourier transform infrared spectroscopy, antibacterial effect, Ribes khorassanicum fruits, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, surface plasmon resonance, AgNO₃ , Ag     

Facile phyto‐mediated synthesis of silver nanoparticles using Chinese winter jujube (Ziziphus jujuba Mill. cv. Dongzao) extract and their antibacterial/catalytic properties

The aqueous extract of Chinese winter jujube (Ziziphus jujuba Mill. cv. Dongzao) was used as reducing and capping agents for the synthesis of silver nanoparticles (AgNPs) for the first time. The resulting AgNPs were characterised by UV/Visible (UV–Vis) spectroscopy, atomic force microscope, transmission electron microscopy, selected area electron diffraction, X‐ray diffraction, scanning electron microscopy, energy‐dispersive X‐ray and Fourier transform infrared spectroscopy (FTIR). The colloidal solution of AgNPs gave a maximum UV–Vis absorbance at 446 nm. The synthesised nanoparticles were almost in the spherical shapes with an average size of 11.5 ± 4. 8 nm. FTIR spectra were applied to identify the functional groups which were possibly responsible for the conversion of metal ions into nanoparticles. The results showed that the prepared AgNPs were coated with the biomolecules in the extract. The biosynthesised AgNPs showed a remarkable catalytic activity at room temperature, and they also showed good antibacterial properties against Escherichia coli and Staphylococcus aureus.Inspec keywords: silver, nanoparticles, nanofabrication, antibacterial activity, biomedical materials, nanobiotechnology, scanning electron microscopy, X‐ray diffraction, transmission electron microscopy, ultraviolet spectra, visible spectra, X‐ray chemical analysis, Fourier transform infrared spectra, catalysisOther keywords: wavelength 446 nm, temperature 293 K to 298 K, Ag, Escherichia coli, Staphylococcus aureus, biomolecules, catalytic activity, metal ions, colloidal solution, FTIR spectra, UV‐vis absorbance, TEM, SEM, XRD, Fourier transform infrared spectroscopy, energy‐dispersive X‐ray spectroscopy, scanning electron microscopy, X‐ray diffraction, selected area electron diffraction, transmission electron microscopy, atomic force microscopy, UV‐visible spectroscopy, catalytic properties, antibacterial properties, Chinese winter jujube extract, silver nanoparticles, facile phyto‐mediated synthesis     

Biosynthesis of Selenium Nanoparticles using yeast Nematospora coryli and examination of their anti‐candida and anti‐oxidant activities

Selenium (Se) is a rare and essential element for the human body and other living organisms because of its role in the structure of several proteins and having anti‐oxidant properties to reduce oxidative stress at cells. Some microorganisms can absorb Se oxyanions and convert them into zero‐valent Se (Se0) in the nanoscale dimensions, which can be used for producing Se nanoparticles (SeNPs). In the present study, SeNPs were intracellularly biosynthesised by yeast Nematospora coryli, which is an inexpensive method and does not involve using materials hazardous for human and environment. The produced NPs were refined by a two‐phase system and then characterised and identified by ultraviolet–visible, X‐ray diffraction, X‐ray fluorescence, transmission electron microscope, and Fourier transform infrared spectroscopy analyses. The structural analysis of biosynthesised SeNPs showed spherical‐shaped NPs with size ranging from 50 to 250 nm. Also, extracted NPs were applied to explore their anti‐candida and anti‐oxidant activities. The results of this investigation confirm the biological properties of Se.Inspec keywords: X‐ray diffraction, microorganisms, oxidation, transmission electron microscopy, reduction (chemical), nanomedicine, biomedical materials, visible spectra, nanoparticles, proteins, nanofabrication, selenium, ultraviolet spectra, particle size, Fourier transform infrared spectra, antibacterial activityOther keywords: proteins, oxidative stress, Se oxyanions, yeast, biosynthesised SeNPs, anti‐oxidant activities, human body, living organisms, Se nanoparticles, Nematospora coryli, anti‐candida activities, biosynthesis, ultraviolet–visible analysis, X‐ray diffraction, X‐ray fluorescence, transmission electron microscope, Fourier transform infrared spectroscopy, structural analysis, size 50.0 nm to 250.0 nm, Se     

Phyto‐mediated synthesis,biological and catalytic activity studies of gold nanoparticles

In the present study, a phyto‐mediated synthesis of gold nanoparticles (AuNPs) using an isoflavone, Dalspinosin (5,7‐dihydroxy‐6,3′,4′‐trimethoxy isoflavone) isolated from the alcoholic extract of roots of Dalbergia coromandeliana is reported. It is observed that Dalspinosin itself acts both as a reducing and a capping agent in the synthesis of the nanoparticles (NPs). An ultraviolet–visible (UV–Vis) spectral study showed a surface plasmon resonance band at 526 nm confirming the formation of AuNPs. The NPs formed were characterised by UV–Vis spectroscopy, Fourier transform‐infrared spectroscopy, X‐ray diffraction (XRD), high‐resolution transmission electron microscopy (HR‐TEM) with energy‐dispersive x‐ray spectroscopy (EDX) and dynamic light scattering. HR‐TEM analysis showed the synthesised AuNPs were spherical in shape with a size of 7.5 nm. The AuNPs were found to be stable for seven months when tested by in vitro methods showed good antioxidant and anti‐inflammatory activities. They also showed moderate anti‐microbial activities when tested against Gram positive (Staphylococcus aureus and Streptococcus sp), Gram negative bacterial strains (Klebsiella pneumonia and Klebsiella terrigena) and fungal strain (Candida glabrata). The biosynthesised AuNPs showed significant catalytic activity in the reduction of methylene blue with NaBH₄ to leucomethylene blue.Inspec keywords: biomedical materials, catalysis, Fourier transform infrared spectra, gold, light scattering, microorganisms, nanomedicine, nanoparticles, spectrochemical analysis, surface plasmon resonance, transmission electron microscopy, ultraviolet spectra, visible spectra, X‐ray chemical analysis, X‐ray diffractionOther keywords: phyto‐mediated synthesis, biological activity studies, catalytic activity studies, dalspinosin (5,7‐dihydroxy‐6,3′,4′‐trimethoxy isoflavone), alcoholic extract, roots, Dalbergia coromandeliana, ultraviolet‐visible spectral study, surface plasmon resonance band, UV‐Vis spectroscopy, Fourier transform‐infrared spectroscopy, X‐ray diffraction, high‐resolution transmission electron microscopy, EDX analysis, dynamic light scattering, HR‐TEM analysis, antioxidant activities, antiinflammatory activities, antimicrobial activities, Gram positive bacterial strains, Staphylococcus aureus, Streptococcus sp, Gram negative bacterial strains, wavelength 526 nm, size 7.5 nm, time 7 month, Au     

Sunlight induced biosynthesis of silver nanoparticle from the bark extract of Amentotaxus assamica D.K. Ferguson and its antibacterial activity against Escherichia coli and Staphylococcus aureus

Green synthesis of nanoparticles has gained importance due to its eco‐friendly, low toxicity and cost effective nature. This study deals with the biosynthesis of silver nanoparticles (AgNPs) from the bark extract of Amentotaxus assamica. The AgNPs have been synthesised by reducing the silver ions into stable AgNPs using the bark extract of Amentotaxus assamica under the influence of sunlight irradiation. The characterisation of the biosynthesised AgNPs was carried out by UV–vis spectroscopy, X‐ray diffraction analysis (XRD), Fourier transform infrared spectroscopy, scanning electron microscopy (SEM) and energy dispersive X‐ray analysis. The UV–vis spectrum showed a broad peak at 472 nm. Also, the XRD confirmed the crystalline structure of the AgNPs. Moreover, the SEM analysis revealed that the biosynthesised AgNPs were spherical in shape. Also, dynamic light scattering techniques were used to evaluate the size distribution profile of the biosynthesised AgNPs. Furthermore, the biosynthesised AgNPs showed a prominent inhibitory effect against both Escherichia coli (MTCC 111) and Staphylococcus aureus (MTCC 97). Thus the biosynthesis of AgNPs from the bark extract of Amentotaxus assamica is found to eco‐friendly way of producing AgNPs compared to chemical method.Inspec keywords: X‐ray chemical analysis, microorganisms, transmission electron microscopy, nanoparticles, toxicology, scanning electron microscopy, ultraviolet spectra, particle size, Fourier transform spectra, X‐ray diffraction, antibacterial activity, visible spectra, infrared spectra, nanomedicine, silverOther keywords: stable AgNP, biosynthesised AgNP, SEM analysis, sunlight irradiation, silver ions, silver nanoparticle, amentotaxus assamica, biosynthesis, escherichia coli     

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     

Biosynthesis of reusable and recyclable CuO@Magnetite@Hen Bone NCs and its antioxidant and antibacterial activities: a highly stable magnetically nanocatalyst for excellent reduction of organic dyes and adsorption of polycyclic aromatic hydrocarbons

For the first time, through a fast, eco‐friendly and economic method, the aqueous extract of the leaf of Euphorbia corollate was used to the green synthesis of the highly stable CuO@Magnetite@Hen Bone nanocomposites (NCs) as a potent antioxidant and antibacterial agent against Pseudomonas aureus, Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae pathogenic bacteria. The biosynthesised NCs were identified using the scanning electron microscopy (SEM), energy dispersive X‐ray spectroscopy, elemental mapping, X‐ray diffraction (XRD), Fourier transforms infrared spectroscopy and UV–vis analytical techniques. Also, the radical scavenging activity using (2,2‐diphenyl‐1‐picrylhydrazyl) method was used to evaluate the antioxidant activity of the NCs. The stability of nanocatalyst was monitored using the XRD and SEM analyses after 30 days from its synthesis. Furthermore, its excellent catalytic activity, recycling stability, and high substrate applicability were demonstrated to the adsorption of the polycyclic aromatic hydrocarbons of the light crude oil from Shiwashok oil fields and destruction of methylene blue and methyl orange as harmful organic dyes at ambient temperature using UV–vis spectroscopy. Moreover, the green CuO@Magnetite@Hen Bone NCs were recovered and reused several times without considerable loss of its catalytic activity.Inspec keywords: nanobiotechnology, X‐ray diffraction, infrared spectra, catalysis, crude oil, Fourier transform spectra, ultraviolet spectra, scanning electron microscopy, dyes, catalysts, photochemistry, iron compounds, X‐ray chemical analysis, antibacterial activity, adsorption, visible spectra, microorganisms, organic compounds, reduction (chemical), nanomedicine, toxicology, recycling, chemical industryOther keywords: antioxidant activity, XRD, SEM analyses, recycling stability, polycyclic aromatic hydrocarbons, harmful organic dyes, UV–vis spectroscopy, green CuO@Magnetite@Hen Bone NCs, reusable CuO@Magnetite@Hen Bone NCs, recyclable CuO@Magnetite@Hen Bone NCs, antioxidant activities, antibacterial activities, highly stable magnetically nanocatalyst, eco‐friendly method, economic method, euphorbia corollate, green synthesis, CuO@Magnetite@Hen Bone nanocomposites, antibacterial agent, pseudomonas aureus, staphylococcus aureus, escherichia coli, klebsiella pneumoniae pathogenic bacteria, biosynthesised NCs, X‐ray spectroscopy, X‐ray diffraction, radical scavenging activity, antioxidant agent, 2,2‐diphenyl‐1‐picrylhydrazyl, catalytic activity, organic dye reduction, light crude oil, CuO     

Biosynthesised silver nanoparticles using aqueous leaf extract of Tagetes patula L. and evaluation of their antifungal activity against phytopathogenic fungi

In the recent decades, nanotechnology is gaining tremendous impetus due to its capability of modulating metals into their nanosize, which drastically changes the chemical, physical, biological and optical properties of metals. In this study, silver nanoparticles (AgNPs) synthesis using aqueous leaf extracts of Tagetes patula L. which act as reducing agent as well as capping agent is reported. Synthesis of AgNPs was observed at different parameters like temperature, concentration of silver nitrate, leaf extract concentration and time of reduction. The AgNPs were characterized using UV‐vis spectroscopy, scanning electron microscope with energy dispersive spectroscopy, transmission electron microscopy with selected area electron diffraction, X‐ray diffraction, Fourier transform infrared and dynamic light scattering analysis. These analyses revealed the size of nanoparticles ranging from 15 to 30 nm as well revealed their spherical shape and cubic and hexagonal lattice structure. The lower zeta potential (−14.2mV) and the FTIR spectra indicate that the synthesized AgNPs are remarkably stable for a long period due to the capped biomolecules on the surface of nanoparticles. Furthermore, these AgNPs were found to be highly toxic against phytopathogenic fungi Colletotrichum chlorophyti by both in vitro and in vivo and might be a safer alternative to chemical fungicides.Inspec keywords: silver, nanoparticles, nanofabrication, nanobiotechnology, ultraviolet spectra, visible spectra, scanning electron microscopy, X‐ray chemical analysis, electron diffraction, X‐ray diffraction, Fourier transform infrared spectra, crystal structure, electrokinetic effects, antibacterial activityOther keywords: biosynthesised silver nanoparticles, aqueous leaf extract, Tagetes patula L, antifungal activity, phytopathogenic fungi, nanotechnology, UV–vis spectroscopy, scanning electron microscope, energy dispersive spectroscopy, transmission electron microscopy, selected area electron diffraction, X‐ray diffraction, Fourier transform infrared spectra, dynamic light scattering analysis, hexagonal lattice structure, zeta potential, phytopathogenic fungi Colletotrichum chlorophyti, cubic lattice structure, size 15 nm to 30 nm, Ag     

Postprandial anti‐hyperglycemic activity of marine Streptomyces coelicoflavus SRBVIT13 mediated gold nanoparticles in streptozotocin induced diabetic male albino Wister rats

The present study focuses on the biosynthesis of gold nanoparticles (AuNPs) using Streptomyces coelicoflavus (S. coelicoflavus) SRBVIT13 isolated from marine salt pan soils collected from Ongole, Andhra Pradesh, India. The biosynthesised AuNPs are characterised by UV–visible spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy and energy‐dispersive X‐ray analysis. Transmission electron microscopy study suggests that the biosynthesised AuNPs are spherical in shape within a size range of 12–20 nm (mean diameter as 14 nm). The anti‐type II diabetes activity of AuNPs is carried out by testing it in vitro α ‐glucosidase and α ‐amylase enzyme inhibition activity and in vivo postprandial anti‐hyperglycemic activity in sucrose and glucose‐loaded streptozotocin induced diabetic albino Wister rats. AuNPs has shown a significant inhibitory activity of 84.70 and 87.82% with IC₅₀ values of 67.65 and 65.59 μg/mL to α ‐glucosidase and α ‐amylase enzymes, while the diabetic rats have shown significant reduction in the post postprandial blood glucose level by 57.80 and 88.09%, respectively compared with control group after AuNPs treatment at the concentration of 300 and 600 mg/kg body weight. Hence, this biosynthesised AuNPs might be useful in combating type II diabetes mellitus for the betterment of human life.Inspec keywords: gold, nanoparticles, ultraviolet spectra, visible spectra, X‐ray diffraction, Fourier transform infrared spectra, transmission electron microscopy, X‐ray chemical analysis, diseases, enzymes, nanomedicine, biochemistry, spectrochemical analysisOther keywords: gold nanoparticles, Streptomyces coelicoflavus SRBVIT13, biosynthesis, UV–visible spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, high‐resolution transmission electron microscopy, energy‐dispersive X‐ray analysis, antitype II diabetes activity, in vitro enzyme inhibition activity, in vivo postprandial antihyperglycemic activity, streptozotocin induced diabetic albino Wister rats, type II diabetes mellitus, Au     

Preparation of silver iodide nanoparticles using laser ablation in liquid for antibacterial applications

In this study, the authors reported the first synthesis process of silver iodide (AgI) nanoparticles (NPs) by pulsed laser ablation of the AgI target in deionised distilled water. The optical and structural properties of AgI NPs were investigated by using UV–vis absorption, X‐ray diffraction, scanning electron microscope (SEM), energy dispersive X‐ray, Fourier transform infrared spectroscopy, and transmission electron microscope (TEM). The optical data showed the presence of plasmon peak at 434 nm and the optical bandgap was found to be 2.6 eV at room temperature. SEM results confirm the agglomeration and aggregation of synthesised AgI NPs. TEM investigation showed that AgI NPs have a spherical shape and the average particle size was around 20 nm. The particle size distribution was the Gaussian type. The results showed that the synthesised AgI NPs have antibacterial activities against both bacterial strains and the activities were more potent against gram‐negative bacteria.Inspec keywords: antibacterial activity, nanoparticles, X‐ray chemical analysis, particle size, transmission electron microscopy, X‐ray diffraction, nanofabrication, scanning electron microscopy, visible spectra, ultraviolet spectra, silver compounds, pulsed laser deposition, Fourier transform infrared spectra, optical constants, energy gap, aggregationOther keywords: synthesis process, pulsed laser ablation, AgI target, deionised distilled water, optical properties, structural properties, UV–vis absorption, X‐ray diffraction, transmission electron microscope, optical data, optical bandgap, antibacterial activities, silver iodide nanoparticles, energy dispersive X‐ray analysis, SEM, wavelength 434.0 nm, temperature 293 K to 298 K, AgI     

Biomimetic production,characterisation, in vitro cytotoxic and anticancer assessment of aqueous extract‐mediated AgNPs of Teucrium stocksianum Boiss

Owing to the numerous biological applications, cost effectiveness and low cytotoxicity of the biomimetic nanoparticles (NPs), the authors optimised the production of silver NPs (AgNPs) using aqueous extract of Teucrium stocksianum Boiss. The NPs were characterised by ultraviolet‐visible (UV‐vis) spectroscopy, X‐ray diffraction (XRD), scanning electron microscopy (SEM), dynamic light scattering (DLS) and Fourier transform‐infrared spectroscopy (FTIR). The UV‐vis spectroscopy revealed a surface plasmon resonance (410‐440 nm) at an incubation temperature of 90°C when 1 mM Ag nitrate combined to 5 mg/ml extract concentration in the ratio of 1:10. DLS results show an average zeta size of ∼44.61 nm and zeta potential of −15.3 mV. SEM and XRD confirmed the high crystallinity and cubical symmetry with an average size below 100 nm. FTIR measurement shows the presence of various functional groups, responsible for the capping and reduction of Ag metal. The 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide cell viability assay shows that AgNPs are less cytotoxic to J774 and L929 cells as compared with enhanced anticancer activity with low IC50 concentrations (68.24 µg/ml) against Michigan Cancer Foundation‐7 (MCF‐7) cells. The ethidium bromide/acridine orange assay shows that the AgNPs kill the cell by apoptosis. Overall, the results show that AgNPs possesses potent anticancer activities.Inspec keywords: cellular biophysics, cancer, nanobiotechnology, nanomedicine, ultraviolet spectra, X‐ray diffraction, scanning electron microscopes, light scattering, patient treatmentOther keywords: anticancer assessment, in vitro cytotoxic assessment, aqueous extract‐mediated AgNPs, Teucrium stocksianum Boiss, nanoparticles, biological applications, biosynthesis, silver NPs, X‐ray diffraction, scanning electron microscopy, dynamic light scattering, Fourier transform‐infrared spectroscopy, UV‐vis spectroscopy, surface plasmon resonance, extract concentration, zeta potential, high crystallinity, FTIR measurement, amide molecules, viability assay, enhanced anticancer activity, potent anticancer activities     

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     

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     

Synthesis and characterisation of magnetite nanoparticles using gelatin and starch as capping agents

Nanoparticles of magnetite passivated with gelatin and starch were synthesised using a co‐precipitation technique. The nanoparticles were characterised using ultraviolet–visible (UV–vis), dynamic light scattering (DLS), Zeta potential, transmission electron microscope (TEM), X‐ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The UV–vis spectra showed characteristic surface plasmon resonance of magnetite nanoparticles. The DLS results showed the nanoparticles to have average hydrodynamic diameters of 138 ± 2 and 283 ± 21 nm for particles passivated with gelatin and starch, respectively. The stability in a colloidal solution was greater in nanoparticles passivated with gelatin than nanoparticles obtained with starch, as can be seen by their Zeta potential value (−31 ± 2 and −16 ± 0.5 mV, respectively). According to the TEM evaluation, the use of gelatin allowed to obtain nanoparticles with a spherical morphology and an average size of 10 ± 2 nm. However, when using starch the nanoparticles exhibited diverse morphologies with an average size of 25 ± 7 nm. The XRD results confirmed the crystalline structure of the samples, which showed crystallite sizes of 14.90 and 24.43 nm for nanoparticles passivated with gelatin and starch, respectively. FTIR analysis proved the establishment of interactions between functional groups of biopolymers and magnetite nanoparticles.Inspec keywords: crystallites, nanofabrication, ultraviolet spectra, gelatin, surface plasmon resonance, transmission electron microscopy, scanning electron microscopy, visible spectra, X‐ray diffraction, iron compounds, electrokinetic effects, particle size, colloids, nanoparticles, nanomedicine, precipitation (physical chemistry), light scattering, magnetic particles, Fourier transform infrared spectra, nanomagnetics, filled polymers, nanocompositesOther keywords: magnetite nanoparticles, gelatin, starch, characteristic surface plasmon resonance, capping agents, passivation, co‐precipitation technique, ultraviolet–visible spectra, zeta potential value, dynamic light scattering, DLS, transmission electron microscopy, TEM, X‐ray diffraction, XRD, Fourier transform infrared spectroscopy, FTIR, surface plasmon resonance, hydrodynamic diameters, colloidal solution, spherical morphology, crystalline structure, crystallite size, biopolymers, Fe₂ O₃      

Synthesis,characterisation and anti‐tumour activity of biopolymer based platinum nanoparticles and 5‐fluorouracil loaded platinum nanoparticles

A facile and green synthesis of platinum nanoparticles [gum kondagogu platinum nanoparticles (GKPtNP)] using biopolymer‐ gum kondagogu was developed. The formation of GKPtNP was confirmed by ultraviolet (UV)–visible spectroscopy, scanning electron microscopy–energy dispersive X‐ray spectroscopy, transmission electron microscopy, X‐ray diffraction, Zeta potential, Fourier transform infrared, inductively coupled plasma mass spectroscopy. The formed GKPtNP are well dispersed, homogeneous with a size of 2–4 ± 0.50 nm, having a negative zeta potential (−46.1 mV) indicating good stability. 5‐Fluorouracil (5FU) was loaded onto the synthesised GKPtNP, which leads to the development of a new combination of nanomedicine (5FU–GKPtNP). The in vitro drug release studies of 5FU–GKPtNP in pH 7.4 showed a sustained release profile over a period of 120 min. Agrobacterium tumefaciens induced in vitro potato tumour bioassay was employed for screening the anti‐tumour potentials of GKPtNP, 5FU, and 5FU–GKPtNP. The experimental results suggested a complete tumour inhibition by 5FU–GKPtNP at a lower concentration than the GKPtNP and 5FU. Furthermore, the mechanism of anti‐tumour activity was assessed by their interactions with DNA using agarose gel electrophoresis and UV‐spectroscopic analysis. The electrophoresis results revealed that the 5FU–GKPtNP totally diminishes DNA and the UV‐spectroscopic analysis showed a hyperchromic effect with red shift indicating intercalation type of binding with DNA. Over all, the present study revealed that the combined exposure of the nanoformulation resulted in the enhanced anti‐tumour effect. Inspec keywords: nanoparticles, transmission electron microscopy, biomedical materials, tumours, ultraviolet spectra, DNA, drugs, electrophoresis, polymers, platinum, pH, drug delivery systems, biochemistry, X‐ray chemical analysis, microorganisms, molecular biophysics, electrokinetic effects, X‐ray diffraction, scanning electron microscopy, cancer, nanofabrication, visible spectra, nanomedicine, Fourier transform infrared spectra, materials preparationOther keywords: 5FU–GKPtNP, 5‐fluorouracil loaded platinum nanoparticles, gum kondagogu platinum nanoparticles, antitumour activity, scanning electron microscopy‐energy dispersive X‐ray spectroscopy, biopolymer‐based platinum nanoparticles, biopolymer‐based platinum nanoparticles, ultraviolet‐visible spectroscopy, UV‐visible spectroscopy, transmission electron microscopy, X‐ray diffraction, zeta potential, Fourier transform infrared spectroscopy, inductively coupled plasma mass spectroscopy, nanomedicine, in vitro drug release studies, sustained release profile, Agrobacterium tumefaciens, in vitro potato tumour bioassay, tumour inhibition, tumour activity, agarose gel electrophoresis, UV‐spectroscopic analysis, DNA, time 120.0 min, Pt     

Catalytic degradation of methylene blue by biosynthesised copper nanoflowers using F. benghalensis leaf extract

This study reports the unprecedented, novel and eco‐friendly method for the synthesis of three‐dimensional (3D) copper nanostructure having flower like morphology using leaf extract of Ficus benghalensis. The catalytic activity of copper nanoflowers (CuNFs) was investigated against methylene blue (MB) used as a modal dye pollutant. Scanning electron micrograph evidently designated 3D appearance of nanoflowers within a size range from 250 nm to 2.5 μm. Energy‐dispersive X‐ray spectra showed the presence of copper elements in the nanoflowers. Fourier‐transform infrared spectra clearly demonstrated the presence of biomolecules which is responsible for the synthesis of CuNFs. The catalytic activity of the synthesised CuNFs was monitored by ultraviolet–visible spectroscopy. The MB was degraded by 72% in 85 min on addition of CuNFs and the rate constant (k) was found to be 0.77 × 10⁻³ s⁻¹. This method adapted for synthesis of CuNFs offers a valuable contribution in the area of nanomaterial synthesis and in water research by suggesting a sustainable and an alternative route for removal of toxic solvents and waste materials.Inspec keywords: catalysis, dyes, nanostructured materials, nanofabrication, scanning electron microscopy, X‐ray chemical analysis, copper, Fourier transform infrared spectra, visible spectra, ultraviolet spectra, molecular biophysicsOther keywords: catalytic degradation, methylene blue, biosynthesised copper nanoflowers, F. benghalensis leaf extract, three‐dimensional copper nanostructure synthesis, 3D copper nanostructure synthesis, flower like morphology, Ficus benghalensis leaf extract, modal dye pollutant, electron micrograph, 3D appearance, energy‐dispersive X‐ray spectra, copper elements, Fourier‐transform infrared spectra, biomolecules, ultraviolet‐visible spectroscopy, toxic solvent removal, waste materials, size 250 nm to 2.5 mum, Cu     

Silver nanoparticles biosynthesised using Centella asiatica leaf extract: apoptosis induction in MCF‐7 breast cancer cell line

The aim of this study was to green synthesised silver nanoparticles (AgNPs) using Centella asiatica leaf extract and investigate the cytotoxic and apoptosis‐inducing effects of these nanoparticles in MCF‐7 breast cancer cell line. The characteristics and morphology of the green synthesised AgNPs were evaluated using transmission electron microscopy, scanning electron microscopy, UV–visible spectroscopy, X‐ray diffraction, and Fourier‐transform infrared spectroscopy. The MTT assay was used to investigate the anti‐proliferative activity of biosynthesised nanoparticles in MCF‐7 cells. Apoptosis test was performed using flow cytometry and expression of caspase 3 and 9 genes. The spherical AgNPs with an average size of 19.17 nm were synthesised. The results showed that biosynthesised AgNPs exhibited cytotoxicity, anti‐cancer, apoptosis induction, and increased expression of genes encoding for caspases 3 and 9 in MCF‐7 cancer cells in a concentration‐ and time‐dependent manner. It seems that green synthesised AgNPs have potential uses for pharmaceutical industries.Inspec keywords: ultraviolet spectra, transmission electron microscopy, cellular biophysics, infrared spectra, visible spectra, nanofabrication, cancer, toxicology, nanomedicine, nanoparticles, biomedical materials, scanning electron microscopy, silver, Fourier transform spectra, X‐ray diffraction, genetics, enzymes, botany, biochemistryOther keywords: spherical AgNPs, biosynthesised AgNPs, anti‐cancer, apoptosis induction, green synthesised AgNPs, MCF‐7 breast cancer cell line, green synthesised silver nanoparticles, Ag, caspase gene expression, flow cytometry, anti‐proliferative activity, MTT assay, pharmaceutical industries, cytotoxicity, UV–visible spectroscopy, nanoparticle morphology, scanning electron microscopy, Centella asiatica leaf extract, biosynthesised nanoparticles, Fourier‐transform infrared spectroscopy, transmission electron microscopy     

Bacteriogenic synthesis of selenium nanoparticles by Escherichia coli ATCC 35218 and its structural characterisation

A biosynthetic method for the production of selenium nanoparticles under ambient temperature and pressure from sodium selenite was developed using Gram‐negative bacterial strain Escherichia coli ATCC 35218. Bacteriogenic nanoparticles were methodologically characterized employing UV‐vis, XRD, Raman spectroscopy, SEM, TEM, DLS and FTIR techniques. Generation of nanoparticles was visualized from the appearance of red colour in the selenite supplemented culture medium and broad absorption bands in the UV‐vis. Biofabricated nanoparticles were spherical, polydisperse, ranged from 100‐183 nm and the average particle size was about 155 nm. Based on selected‐area electron diffraction, XRD patterns; and Raman spectroscopy the nanospheres were found to be amorphous. IR spectrum revealed the involvement of bacterial proteins in the reduction of selenite and stabilization of nanoparticles. Used bacterial strain demonstrated efficient selenite reduction capability which was evident from 89.2% of selenium removal within 72 h at a concentration of 1 mM. Observation noted in the current study highlight the importance of bacterial reduction in selenium nanoparticle generation which can be scaled up for commercial production. Also, the bacteriogenic, amorphous nanoparticles can also be used as nutritional supplements for humans since selenium nanoparticles of 5‐200 nm are bioavailable and known to induce seleno enzymes involved in antioxidant defence.Inspec keywords: Fourier transform infrared spectra, transmission electron microscopy, scanning electron microscopy, electron diffraction, ultraviolet spectra, microorganisms, X‐ray diffraction, nanofabrication, Raman spectra, visible spectra, nanoparticles, particle size, seleniumOther keywords: bacteriogenic synthesis, selenium nanoparticles, Escherichia coli ATCC 35218, structural characterisation, biosynthetic method, gram negative bacterial strain, UV–visible spectroscopy, X‐ray diffraction, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy, particle size, selected area electron diffraction, bacteriological reduction, seleno enzymes, size 100 nm to 183 nm, Se