Green synthesis of gold nanoparticles using Parsley leaves extract and their applications as an alternative catalytic,antioxidant, anticancer,and antibacterial agents

For the first time in this study, gold nanoparticles (AuNPs) were biosynthesized by the eco-friendly and cost-effective procedure using Presley leaf (Petroselinum crispum) extract then used as antioxidant, anticancer, antibacterial and photocatalytic agents. Different four-volume of the extract 2.5 mL, 5 mL, 10 mL, and 20 ML named AuNPs(A), AuNPs(B), AuNPs(C) and AuNPs(D) were used to module the size and shape of AuNPs. The prepared NPs were characterized by various techniques including UV–Vis absorption spectroscopy, Transmission Electron Microscopy (TEM), dynamic light scattering (EDX), and X-ray diffractometric (XRD). TEM imaging confirmed the formation of spherical, semi-rod aggregates, and flower-shaped NPs. The reduction and stabilization effect of the plant extract to fabricate AuNPs were explained by FTIR analysis. The four AuNPs provided high antioxidant ability, while AuNPs(D) was the best one. The NPs showed an emerging antimicrobial activity against two gram-negative microbes and not effective against the gram-positive microbes. The photocatalytic capacity for degradation of methylene blue dye was achieved after only one minute (the four samples have an equal effect). The AuNPs(D) provide the best anticancer activity on the human cancerous colorectal cell line using MTT assay rather than the other three AuNPs. The results spotlight for using Presley as a common cheap plant for bio-fabricating AuNPs who possess huge multifunctional applications.     

Green synthesis of silver nanoparticles using Nervalia zeylanica leaf extract and evaluation of their antioxidant,catalytic, and antimicrobial potentials

ABSTRACT

Here we report a simple, one-pot, inexpensive, and eco-friendly method for the synthesis of silver nanoparticles. The leaf extract of a medicinal plant Nervalia zeylanica was used as reducing and stabilizing agent for the synthesis of nanoparticles by microwave-assisted strategy. The nanoparticles show characteristic surface plasmon peak at 468?nm in UV–vis absorption spectrum. The involvement of phytochemicals in the reduction and stabilization of nanoparticles was confirmed by FTIR analysis. Using X-ray diffraction analysis, the crystalline nature of the nanoparticles was demonstrated. Transmission electron microscopic analysis shows that the nanoparticles were in spherical shape with average particle size of 34.2?nm. The antioxidant studies were performed by the 1,1-diphenyl-2-picryl hydrazyl method. The nanoparticles show excellent scavenging activities than the leaf extract. The IC₅₀ values of silver nanoparticles and the leaf extract, respectively, were 15.20 and 92.83?µg?mL^?1. The catalytic activities of synthesized nanoparticles were examined by using them in the reduction of organic dyes. The nanoparticles show excellent catalytic activities and follow pseudo-first-order kinetics. The antimicrobial activities of nanoparticles were analyzed by an agar well diffusion method against six microbial strains and found that the nanoparticles were highly toxic against all the tested microbial strains.     

Green synthesis and characterization of hexagonal shaped MgO nanoparticles using insulin plant (Costus pictus D. Don) leave extract and its antimicrobial as well as anticancer activity

Green synthesis is an ecofriendly novel technology and attractive research area for the production of metal oxide nanoparticles in bio-medical and chemical applications. The green perspective includes solvents, reductants or stabilizing agents obtained from a natural resource as they are non-toxic and ecofriendly. In this study, a sustainable green synthetic strategy to synthesize magnesium oxide nanoparticles by employing Costus pictus D. Don plant leaf extract as a reducing agent. The successful formation of magnesium oxide nanoparticles was confirmed by comprehensive characterization techniques. The presence of biomolecules and metal oxides were confirmed by Fourier transform Infrared (FT-IR) spectral data analysis. The X-ray diffraction (XRD) revealed the formation of pure cubic MgO crystalline nanoparticles. The surface morphology of MgO particles observed by Scanning electron microscope (SEM) showed the hexagonal-shaped MgO crystallites. The average size of biosynthesized MgO nanoparticles was measured to be around 50?nm by Transmission Electron Microscopy (TEM). The mechanism for the formation of MgO nanoparticles was suggested in this study. The biosynthesized magnesium oxide particles showed good antimicrobial and exhibited maximum inhibition rate for MgO nanoparticles at 200?µg showing efficient anticancer activity.     

Green synthesis of silver oxide nanoparticles using Panicum miliaceum grains extract for biological applications

In this report, the silver oxide nanoparticles were green synthesized using Panicum miliaceum grains extract and were proposed for the first time. GC–MS analysis explicated 2-Acetylbenzoic acid was the active phytocompound with 97.07% of presence in aqueous grains extract. The synthesized silver oxide nanoparticles were analyzed by several analytical techniques such as UV–visible, XRD, FT-IR, HR-TEM, TG, XPS, EDX and mapping analyses. The results of various analytical techniques confirmed the silver oxide nanoparticles formation. The formed nanoparticles were in 10–25 nm size. The effectual bioactive properties of nanoparticles were revealed through antioxidant, anti-diabetic, anti-inflammatory, larvicidal and insecticidal activities. The high mortality of larvae and insect was observed at 48 h in 100 ppm and 72 h in 100 μg/Kg concentration, respectively. The antibacterial activity explained the bactericidal property of nanoparticles on S. aureus and S. typhi at 150 μg/mL concentration. The effective drug activity of nanoparticles was observed from 98.10 % of toxicity against A549 lung cancer cells at 100 μg/mL concentration. The growth of Vigna unguiculata was efficiently increased by lower concentration (60 ppm) of nanoparticles. According to results, the green synthesized nanoparticles can be applied in pharmaceutical and agricultural sectors as biocompatible, non-toxic and cost-effective material.     

Green synthesis of zinc oxide nanoparticles using tomato (Lycopersicon esculentum) extract and its photovoltaic application

With an increasing awareness of green and clean energy, zinc oxide-based solar cells were found to be suitable candidates for cost-effective and environmentally friendly energy conversion devices. In this paper, we have reported the green synthesis of zinc oxide nanoparticles (ZnONPs) by thermal method and under microwave irradiation using the aqueous extract of tomatoes as non-toxic and ecofriendly reducing material. The synthesised ZnONPs were characterised by UV–visible spectroscopy (UV–vis), infra-red spectroscopy, particle size analyser, scanning electron microscopy (SEM), atomic force microscopy (AFM) and X-ray diffraction study (XRD). A series of ZnO nanocomposites with titanium dioxide nanoparticles (TiO₂) and graphene oxide (GO) were prepared for photovoltaic application. Structural and morphological studies of these nanocomposites were carried out using UV–vis, SEM, XRD and AFM. The current–voltage measurements of the nanocomposites demonstrated enhanced power conversion efficiency of 6.18% in case of ZnO/GO/ TiO₂ nanocomposite.     

Rapid biologically one-step synthesis of stable bioactive silver nanoparticles using Osage orange (Maclura pomifera) leaf extract and their antimicrobial activities

Synthesis of nanoparticles by using natural products as reducing and stabilizing agents have been widely used in various fields especially medicine, primarily because of its lower cost, simplicity, and less toxic byproducts. In the present work, silver nanoparticles (Ag NPs) were rapidly synthesized from silver nitrate in a green one-step synthesis by the aqueous extracts of Osage orange (Maclura pomifera) leaf as a reducing and stabilizing agent simultaneously. The effects of pH, extract quantity, and silver salt concentration were investigated to determine the optimum conditions of green synthesis of Ag NPs. The synthesized Ag NPs were characterized by different techniques including UV–Visible (UV–Vis) absorption spectroscopy, X-ray diffraction (XRD), Fourier transform Infrared (FT-IR) Spectroscopy, and Transmission Electron Microscopy (TEM). The Ag NPs showed surface plasmon resonance centered at 415?nm. The XRD pattern and TEM analysis revealed spherical, stable, and uniform Ag NPs with the average particle size of about 12?nm. The FT-IR spectroscopy showed that mainly hydroxyl functional groups, as both the reducing and stabilizing agent are responsible for silver nanoparticles synthesis. The antimicrobial activity of the synthesized Ag NPs showed a significant microbicidal effect on all clinical isolates especially, Gram-negative bacteria and fungi. These results suggest that such stable and uniform Ag NPs can be synthesized rapidly and simply for clinical as well as pharmaceutical applications.     

Phytochemicals-mediated green synthesis of gold nanoparticles using Pterocarpus santalinus L. (Red Sanders) bark extract and their antimicrobial properties

In the present study, phytochemicals-mediated rapid, stable and eco-friendly synthesis of gold nanoparticles (GNPs) using Pterocarpus santalinus L. (Red Sanders) bark extract is reported. The powerful characteristics of different phytochemicals present in P. santalinus L. bark prompted us to determine their efficacy in the bio-reduction of gold chloride trihydrate to the corresponding GNPs. The biosynthesis of GNPs was investigated at the physiological condition (pH?=?7.4). The synthesized GNPs were characterized by UV–visible spectroscopy by measuring the peak in the range of 400–700?nm. The GNPs synthesized at physiological conditions revealed surface plasmon resonance (SPR) at 545?nm. The crystalline nature of GNPs was confirmed by using x-ray diffraction (XRD), and the functional groups adhered on the surface of the GNPs were analyzed by Fourier Transform Infrared spectroscopy (FTIR). Transmission Electron Microscopy (TEM) analysis showed spherical GNPs in the size range of 13–26?nm. The synthesized GNPs exhibited antibacterial activity against Gram-positive and Gram-negative bacterial strains.     

Green synthesis of metal nanoparticles loaded ultrasonic‐assisted Spirulina platensis using algal extract and their antimicrobial activity

The synthesis of metal nanoparticles (NPs) loaded on the ultrasonic‐assisted Spirulina platensis (MNPs/UASP) was investigated using the green synthesis method. The S. platensis algal extract was taken as a reducing agent. The formations of metal NPs were characterised using UV–visible spectroscopy, Fourier transform infrared spectroscopy and scanning electron microscopy. The antimicrobial activity of different metal NPs demonstrated various inhibitory activities against one gram‐positive bacteria (Staphylocicus aureus), four gram‐negative bacteria (Klebsiella pneumonia, Proteus vulgaris, Pseudomonas aeruginosa and Escherichia coli) and one fungus (Aspergillus niger). Both CrNPs/UASP and ZnNPs/UASP show good antimicrobial activity when compared with other MNPs/UASP against microorganisms. This MNPs/UASP is effective in preventing and treating the microbial infection and water pollution in the environment.Inspec keywords: antibacterial activity, nanoparticles, nanomedicine, ultraviolet spectra, visible spectra, microorganisms, Fourier transform infrared spectraOther keywords: metal nanoparticles loaded ultrasonic‐assisted Spirulina platensis, algal extract, antimicrobial activity, green synthesis method, UV–visible spectroscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, gram‐positive bacteria, Staphylocicus aureus, Klebsiella pneumonia, Proteus vulgaris, Pseudomonas aeruginosa, Escherichia coli, Aspergillus niger, fungus, microorganisms, microbial infection, water pollution     

Green synthesis of silver nanoparticles using Cyathea nilgirensis Holttum and their cytotoxic and phytotoxic potentials

The present study aimed at synthesizing silver nanoparticles (AgNPs) from the aqueous extract of C. nilgirensis and their biopotential using cytotoxicity and phytotoxicity. On mixing the aqueous extract with 1?mM AgNO₃ solution, the color changes from pale yellow to yellowish brown color. The absorption spectra of yellowish brown nanoparticle showed a plasmon absorption band with a maximum of 3.806 and 1.028 abs in 311 and 440?nm, respectively. The Fourier transform infrared spectroscopy (FTIR) spectra confirmed that phenolic compounds have stronger ability to bind with metal, indicating that phenolics could possibly form metal nanoparticles to prevent agglomeration and thereby stabilize the medium. The size of AgNP is found to be in the 45.0–74.0?nm range. The Energy-dispersive X-ray (EDX) spectra analysis revealed the presence of a strong Ag peak. The results indicated that C. nilgirensis aqueous extract was found efficient for the synthesis of AgNPs.     

Eco-friendly green synthesis of silver nanoparticles and their potential applications as antioxidant and anticancer agents

Abstract

Eco-friendly green synthesis of nanoparticles using medicinal plants gained immense importance due to its potential therapeutic uses. In the current study, silver nanoparticles (AgNPs) were synthesized using water extract of Jurinea dolomiaea leaf and root at room temperature. MTT assay was used to study anticancer potential of AgNPs against cervical cancer cell line (HeLa), breast cancer cell lines (MCF-7), and mouse embryonic fibroblast (NIH-3 T3) cell line for toxicity evaluation. The antioxidant potential was evaluated using stable DPPH radicals. In addition, the apoptotic nuclear changes prompted by AgNPs in more susceptible HeLa cells were observed using fluorescence microscope through DAPI and PI staining. Physiochemical properties of biosynthesized AgNPs were characterized using various techniques. AgNPs were formed in very short time and UV–vis spectra showed characteristic absorption peak of AgNPs. SEM and TEM showed spherical shape of AgNPs and XRD revealed their crystalline nature. EDX analysis revealed high percentage of silver in green synthesized AgNPs. FTIR analysis indicated involvement of secondary metabolites in fabrication of AgNPs. In vitro cytotoxic and antioxidant study revealed that herb and biosynthesized AgNPs exhibited significant dose-dependent and time-dependent anticancer and antioxidant potential. Furthermore, study on normal cell line and microscopic analysis of apoptosis revealed that AgNPs exhibited good safety profile as compared to cisplatin and induces significant apoptosis effect. Based on the current findings, it is strongly believe that use of J. dolomiaea offers large scale production of biocompatible AgNPs that can be used as alternative anticancer agents against cancer cell lines tested.     

Green synthesis of silver nanoparticles using Mentha pulegium and investigation of their antibacterial,antifungal and anticancer activity

A simple and eco‐friendly method for efficient synthesis of stable colloidal silver nanoparticles (AgNPs) using Mentha pulegium extracts is described. A series of reactions was conducted using different types and concentrations of plant extract as well as metal ions to optimize the reaction conditions. AgNPs were characterized by using UV–vis spectroscopy, transmission electron microscopy, atomic force microscopy, dynamic light scattering, zetasizer, energy‐dispersive X‐ray spectroscopy (EDAX) and Fourier transform infrared spectroscopy (FTIR). At the optimized conditions, plate shaped AgNPs with zeta potential value of ‐15.7 and plasmon absorption maximum at 450 nm were obtained using high concentration of aqueous extract. Efficient adsorption of organic compounds on the nanoparticles was confirmed by FTIR and EDAX. The biogenic AgNPs displayed promising antibacterial activity on Escherichia coli, Staphylococcus aureus, and Streptococcus pyogenes. The highest antibacterial activity of 25 µg mL‐1 was obtained for all the strains using aqueous extract synthesized AgNPs. The aqueous extract synthesised AgNPs also showed considerable antifungal activity against fluconazole resistant Candida albicans. The cytotoxicity assay revealed considerable anticancer activity of AgNPs on HeLa and MCF‐7 cancer cells. Overall results indicated high potential of M. pulegium extract to synthesis high quality AgNPs for biomedical applications.Inspec keywords: silver, nanoparticles, nanofabrication, botany, antibacterial activity, biomedical materials, nanomedicine, ultraviolet spectra, visible spectra, transmission electron microscopy, atomic force microscopy, X‐ray chemical analysis, Fourier transform infrared spectra, electrokinetic effects, microorganisms, cellular biophysics, cancerOther keywords: antibacterial activity, antifungal activity, anticancer activity, stable colloidal silver nanoparticle, Mentha pulegium, plant extract, UV‐visible spectroscopy, transmission electron microscopy, atomic force microscopy, DLS, zetasizer, energy‐dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy, methanolic extract, aqueous extract, plate‐shaped silver nanoparticle, zeta potential, plasmon absorption maximum, organic compounds adsorption, biogenic silver nanoparticle, Escherichia coli, Staphylococcus aureus, Streptococcus pyogenes, fluconazole‐resistant Candida albicans, MTT assay, HeLa cancer cell, MCF‐7 cancer cell, Ag     

Green synthesis of lanthanum oxide nanoparticles using Moringa oleifera leaves extract and its biological activities

Phytosynthesis is a reliable way to produce metal nanoparticles without affecting the environment. Plant extracts act as reducing agent and favors nanoparticle synthesis. Recently, potential drugs were developed in nanotechnology platforms by the green synthesis approach. In this study, the leaves extract of ‘Moringa Oleifera’ (M. oleifera) used as a reducing agent for the synthesis of Lanthanum oxide nanoparticles (La₂O₃ NPs). The X-ray diffraction (XRD) confirmed the formation of body-centered cubic structure of La₂O₃ NPs. The optical behavior of La₂O₃ NPs was analyzed by UV–Vis spectrum. The bandgap energy of the La₂O₃ NPs was found to be 4.31 eV using Tauc’s plot. The morphology and purity of La₂O₃ NPs was analyzed by using Field Emission Scanning Electron Microscope (FESEM) and Energy Dispersive X-ray (EDX) spectrum. High Resolution Transmission Electron Microscope (HR-TEM) analysis reveals the morphology, lattice spacing, and selected area electron diffraction (SAED) pattern of the La₂O₃ NPs. The XPS analysis of the La₂O₃ NPs reveals the binding energy of La (3d_5/2 and 3d_3/2) and O 1s at 835.5, 852.3, and 536 eV respectively. The total antioxidant activity (TOA) of La₂O₃ NPs was found to be 75.32% at 500 µg/mL with the standard drug of vitamin C. The anti-inflammatory activity of the La₂O₃NPs was found to be 94.15% at 500 µg/mL using the bovine serum albumin denaturation (BSA) technique. The inhibitory activity of La₂O₃ NPs against α-amylase was found to be 79.99% at 500 µg/mL. In summary, the pure, highly stable and good biocompatible, greener approach based M. oleifera assisted La₂O₃ was synthesized for radical scavenging, α-amylase and BSA denaturation inhibition activities which can play a key role in the future biomedical and nano-biotechnological applications.     

Green synthesis of zinc oxide nanoparticles by aloe barbadensis miller leaf extract: Structure and optical properties

Biological methods for nanoparticle synthesis using microorganisms, enzymes, and plants or plant extracts have been suggested as possible ecofriendly alternatives to chemical and physical methods. In this paper, we report on the synthesis of nanostructured zinc oxide particles by both chemical and biological method. Highly stable and spherical zinc oxide nanoparticles are produced by using zinc nitrate and Aloe vera leaf extract. Greater than 95% conversion to nanoparticles has been achieved with aloe leaf broth concentration greater than 25%. Structural, morphological and optical properties of the synthesized nanoparticles have been characterized by using UV-Vis spectrophotometer, FTIR, Photoluminescence, SEM, TEM and XRD analysis. SEM and TEM analysis shows that the zinc oxide nanoparticles prepared were poly dispersed and the average size ranged from 25 to 40 nm. The particles obtained have been found to be predominantly spherical and the particle size could be controlled by varying the concentrations of leaf broth solution.     

Green synthesis of copper oxide nanoparticles using aqueous extract of Convolvulus percicus L. as reusable catalysts in cross‐ coupling reactions and their antibacterial activity

CuO nanoparticles (NPs) were prepared by Convolvulus percicus leaves extract as a reducing and stabilising agent. The green synthesised copper oxide NPs was characterised by transmission electron microscope, energy dispersive X‐Ray spectroscopy, X‐ray diffraction, Fourier transform infrared and ultraviolet‐visible analysis. The activities of the CuO NPs as catalyst were tested in the formation of C‐N and C‐O bonds. The N ‐arylated and O ‐arylated products of amides, N‐H heterocycles and phenols were obtained in excellent yields. Furthermore, the separation and recovery of copper oxide NPs was very simple, effective and economical. The recovered catalyst can be reused several times without significant loss of its catalytic activity. Moreover, the antibacterial activity of these NPs was tested against two human pathogenic microbes and showed significant antimicrobial activity against these pathogenic bacteria.Inspec keywords: copper compounds, nanoparticles, nanomedicine, antibacterial activity, biomedical materials, nanofabrication, microorganisms, catalysts, transmission electron microscopy, X‐ray chemical analysis, X‐ray diffraction, Fourier transform spectra, infrared spectra, ultraviolet spectra, visible spectra, catalysisOther keywords: green synthesis, copper oxide nanoparticles, Convolvulus percicus L. aqueous extract, reusable catalysts, cross‐coupling reactions, antibacterial activity, reducing agent, stabilising agent, transmission electron microscope, energy dispersive X‐ray spectroscopy, X‐ray diffraction, Fourier transform infrared spectra, ultraviolet‐visible spectra, C‐N bonds, C‐O bonds, N‐arylated products, O‐arylated products, amides, N‐H heterocycles, phenols, catalytic activity, human pathogenic microbes, antimicrobial activity, CuO     

Green synthesis of zinc oxide nanoparticles using aqueous extract of <Emphasis Type="BoldItalic">Garcinia mangostana</Emphasis> fruit pericarp and their photocatalytic activity

We reported a facile, green and eco-friendly approach for the synthesis of zinc oxide nanoparticles (ZnO NPs) using aqueous extract of Garcinia mangostana (G. mangostana) fruit pericarp as reducing agent as well as capping agent. Biosynthesized ZnO NPs were characterized by various analytical tools using X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy and UV–Vis spectroscopy. The results showed that ZnO NPs synthesized by aqueous extract of G. mangostana fruit pericarp with high purity, mostly spherical in shape with an average size of 21 nm. The photocatalytic activity of biosynthesized ZnO NPs was evaluated by carrying out the degradation of malachite green dye under solar irradiation. The extent of MG dye degradation was monitored spectrophotometrically by measuring absorbance at its characteristics \(\lambda _{\max }\) value of 615 nm. Degradation products were detected using liquid chromatography–mass spectrophotometry technique. The biosynthesized ZnO NPs showed an excellent photocatalyst performance due to the small size and high purity.     

Hydrothermal synthesis of tin-doped indium oxide nanoparticles using pamoic acid as an organic additive and their photoluminescence properties

We report a facile hydrothermal method using the disodium salt of pamoic acid (Na₂PA) as an organic additive, In(NO₃)₃·xH₂O as an indium precursor, and SnCl₂·2H₂O as a tin precursor for preparation of ITO nanoparticles (NPs) at low temperature (200 °C). After drying at 110 °C, the as hydrothermally synthesized materials were found to be monodisperse spherical NPs with diameters in the range of ca. 30–40 nm as an intermediate NP product, as confirmed by field emission scanning electron microscopy, transmission electron microscopy and XRD analysis. The XRD analysis confirmed the presence of InOOH in the intermediate NPs. For comparison, the formation of the intermediate NPs under the same reaction conditions was also examined using two analogs of PA instead of Na₂PA, i.e., 3-hydroxy-2-naphthalene carboxylic acid (3H2NA) or 2-naphthol (2NP). These additives yielded spherical NPs but with different sizes and different homogeneities compared to the NPs formed using Na₂PA. In terms of size and homogeneity of the intermediate NPs, the additives followed the order Na₂PA > 2NP > 3H2NA. However, in photoluminescence (PL) studies, the intermediate prepared using 3H2NA showed the highest intensity followed by the intermediates formed using Na₂PA and 2NP. After calcination at 420 °C, only the NPs obtained with Na₂PA were converted to ITONPs; the other NPs remained in the InOOH form. These results correlated with the corresponding TGA analysis. Interestingly, the ITONPs prepared using Na₂PA did not change their morphology during calcination at 420 °C. The morphology of the ITONPs prepared using Na₂PA was found to be comparable in terms of homogeneity and shape to that of a commercially available ITO nanopowder. However, the ITONPs prepared using Na₂PA showed superior PL intensities compared to the commercial ITONPs.     

Green synthesis of copper oxide nanoparticles and its effective applications in Biginelli reaction,BTB photodegradation and antibacterial activity

Metal/metal oxide nanoparticles have gained much attention in the field of organic catalysis and photocatalysis reactions for development of greener methodology. In the present work, copper oxide nanoparticles (CuO NPs) were synthesized by a greener route using Cordia sebestena (C. sebestena) flower aqueous extract. The nanoparticles were evaluated for their catalytic efficiency. The green synthesized CuO NPs were characterized using various analytical studies. A UV–Visible spectrum with peak at 267?nm and the peaks in their FT-IR spectrum at 431 and 542?cm^?1 showed reduction by the plant metabolites. FESEM-EDX analysis of CuO NPs shows an agglomerated spherical shape with signatures of Cu and O and XRD reveals characteristic crystallinity. TEM and DLS analyses showed particle size between 20 and 35?nm and TEM-SAED pattern ensured crystallinity. A Zeta potential of ?26?mV demonstrates moderate stability. The CuO NPs acted as a catalyst in the Biginelli reaction to produce 3,4-dihydropyrimidinones rapidly and at high yield. The NPs also degraded bromothymol blue (BTB) by photocatalysis with hydrogen peroxide. 100% dye removal efficiency was achieved by 3?h exposure of BTB to natural sunlight inferring it as economy, ecofriendly and effective catalyst. This finding illustrates that the NPs could be used in photolysis to remove water pollutants. Moreover, the biological significance of green synthesized CuO NPs was assessed by antibacterial activity against selected pathogenic bacterial organisms.     

Green synthesis of silver nanoparticles using aqueous solution of Ficus benghalensis leaf extract and characterization of their antibacterial activity

The present study reports an environmentally friendly and rapid method for synthesis of silver nanoparticles. Although several articles have been reported for the synthesis of silver nanoparticles from plant extract, here we have developed a green synthetic method for silver nanoparticles using Ficus benghalensis leaf extract which acts as a reducing and capping agent. It was observed that use of Ficus benghalensis leaf extract makes a fast and convenient method for the synthesis of silver nanoparticles and can reduce silver ions into silver nanoparticles within 5 min of reaction time without using any harsh conditions. Silver nanoparticles so prepared were characterized by using UV-visible spectroscopy, transmission electron microscope-energy dispersive spectra (TEM-EDS) and X-ray diffraction (XRD). Further, these nanoparticles show effective antibacterial activity toward E.coli MTCC1302 due to high surface to volume ratio.     

Evaluation of ‘green’ synthesis and biological activity of gold nanoparticles using Tragopogon dubius leaf extract as an antibacterial agent

Currently, the use of ‘green’ synthesised nanoparticles with environmentally friendly properties is considered a novel therapeutic approach in medicine. Here, the authors evaluated gold nanoparticles (AuNPs) conjugated with Tragopogon dubius leaf extract and their antibacterial activity in vitro and in vivo. Colour changes from yellow to dark brown and a peak at 560 nm on ultraviolet–visible spectroscopy confirmed the formation of nanoparticles. Additionally, transmission electron microscopy, X‐ray diffraction, and Fourier transform infrared spectroscopy analyses were performed to determine particle sizes and functional groups involved in gold reduction. Moreover, using standard micro‐dilution and disc‐diffusion assays against Klebsiella pneumoniae, Bacillus cereus, Escherichia coli, and Staphylococcus aureus, the antimicrobial properties of synthesised AuNPs were investigated. To confirm antibacterial activity, synthesised AuNPs were applied in a rat model on burn wounds infected with S. aureus, and the nanoparticles were as effective as tetracycline in bacterial reduction and wound healing. In conclusion, the synthesis of AuNPs with aqueous T. dubius extract was rapid, simple, and inexpensive, and the synthesised nanoparticles had significant antibacterial activity in vitro and in vivo.Inspec keywords: transmission electron microscopy, wounds, nanoparticles, ultraviolet spectra, reduction (chemical), particle size, nanofabrication, gold, X‐ray diffraction, antibacterial activity, microorganisms, visible spectra, nanomedicine, biomedical materials, Fourier transform infrared spectraOther keywords: biological activity, gold nanoparticles, antibacterial agent, therapeutic approach, colour changes, ultraviolet–visible spectroscopy, transmission electron microscopy, gold reduction, antimicrobial properties, Fourier transform infrared spectroscopy analyses, disc‐diffusion assay, green synthesis, Tragopogon dubius leaf, in vitro antibacterial activity, in vivo antibacterial activity, X‐ray diffraction, particle sizes, functional groups, standard microdilution assay, burn wounds, S. aureus, tetracycline, bacterial reduction, wound healing, wavelength 560.0 nm     

Green synthesis of Cordia myxa incubated ZnO,Fe2O3, and Co3O4 nanoparticle: Characterization,and their response as biological and photocatalytic agent

The imperative necessity for new therapy and catalysts has risen significantly due to infectious agents that are multi-resistant and organic toxins draining into our ecosystem. To address these problems, highly biocompatible Cordia myxa incubated I-ZnO, I-Co₃O₄, and I-Fe₂O₃ NPs were prepared and characterized by using a variety of techniques, including ultraviolet–visible spectroscopy (UV–vis), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR). The XRD diffraction pattern confirmed that I-ZnO hexagonal, while I-Co₃O₄ and I-Fe₂O₃ cubic structure. UV–vis spectra show the energy bandgap for I-ZnO, I-Fe₂O₃, and I-Co₃O₄ 3.35 eV, 2.32 eV, and 2.44 eV, respectively. TEM analyses show the patterns of the morphology of I-ZnO as flower-shaped, I-Fe₂O₃ as rectangular, I-Co₃O₄ looks like prism crystals. EDX mapping confirmed the elemental presence of Zn, Fe, Co in the samples. The antibacterial study show that the I-NPs have bigger zone of inhibition (ZOI) than pristine NPs. The highest percentage for E-coli strain obtained in this trend (I- Fe₂O₃)_81%>(I-ZnO)_76%>(I-Co₃O₄)_63%. Photocatalytic activity results revealed that the MB dye degraded after 80 min and efficiencies of I-(Fe₂O₃)_{98.38 %}>I-ZnO_98.12%>(I-Co₃O₄)_93.93%. Furthermore, the green synthesis strategy certifies a new pathway for minimizing infections, oxidative stress, and degradation of key pollutants from the environment.