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The synthesis of Cyanobacteria‐mediated nanoparticles has attracted great attention due to its ecofriendly, cost‐effective and biocompatible properties. Silver nanoparticles (AgNPs) are used in different areas such as medicine, household products, disinfectants or food storage. The present study aimed the biosynthesis of AgNPs from Cyanobacterial Chroococcus sp. and their antimicrobial activities on some important pathogen bacterial species. According to the obtained data, optimal conditions for synthesis of AgNPs were extract rate 3 : 1 v/v (cell extract/AgNO3), silver salt concentration 10 mM, pH 7, temperature 60 °C and time 30 minutes. The surface plasmon resonance peak of AgNPs was observed at 420–430 nm, and AgNPs were well‐dispersed spherical with an average size of 11–13 nm in diameter by TEM. SEM‐EDX analysis revealed a strong signal of silver. With FTIR analyzes, shift in the absorption bands after the AgNPs formation was confirmed. X‐ray diffraction analysis exhibited that the AgNPs were cubic crystalline shape. Zeta potential of AgNPs showed ‐ 20 mV. The AgNPs strong showed antibacterial activity on an opportunistic bacterial pathogens of Micococcus luteus, Bacillus subtilis and Pseudomonas aeroginosa. The effective and rapid synthesis of Chroococcus‐mediated AgNPs and their strong antimicrobial effects can create an important potential for their use in biomedical and environmental applications. [ABSTRACT FROM AUTHOR]

Nanotechnology has emerged as a promising field for the development of novel antibacterial agents with reduced environmental impact. In this study, we present a novel green synthesis approach for the production of silver nanoparticles (AgNPs) using a plant-based extract. These AgNPs were subsequently characterized using various analytical techniques, including UV-Vis spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and Fourier-transform infrared spectroscopy (FTIR). UV-Vis spectroscopy confirmed the formation of AgNPs by exhibiting a characteristic surface plasmon resonance peak at around 401 and 420 nm. XRD analysis revealed the crystalline nature of the AgNPs, with distinct diffraction peaks corresponding to the face-centered cubic structure of silver. TEM analysis demonstrated that the synthesized AgNPs were predominantly spherical in shape and exhibited an average size within the nanoscale range. FTIR analysis was employed to elucidate the potential bioactive compounds present in the plant extract responsible for the reduction and stabilization of AgNPs. Furthermore, we evaluated the antibacterial activity of these synthesized AgNPs against a panel of bacterial isolates. All the bacterial isolates were sensitive to the silver nanoparticles. Staphylococcus aureus as found to be most resistant, while E. coli as found to be the most sensitive. [ABSTRACT FROM AUTHOR]

Background: Increasing prevalence of microbial resistance and side effects of currently available drugs compels the researchers to look for alternate therapies and formulations to overcome this problem. Plant based formulations have been proved to be most reliable agents in recent times. Objective: In the current study, bio fabricated herbal silver nanoparticles (HSNPs) were prepared by reducing silver nitrate (AgNO3) solution with ethyl acetate fractions (EAF) of Blumea lacera extracts. These bios conjugated HSNPs were then assessed for potential anti-inflammatory and antibacterial activities along with in vitro antioxidant effect. Methods and results: The synthesis was confirmed by absorbance peak at 441 nm due to surface plasmon resonance in UV-visible spectrophotometer. FTIR spectra of HSNPs indicated the phytochemicals having C-O bond responsible for reducing of Ag+ to Ago. Average size of HSNPs was found to be 59.21 nm which was in good agreement with TEM and SEM results. EDS analysis showed the existence of Silver, Nitrogen and Carbon in HSNPs. The antibacterial activity of HSNPs in terms of zone of inhibition (ZOI) via disc diffusion assay and against Staphylococcus aureus and Escherichia coli was found to be 25.0±1.19 mm and 18.3±2.08 mm, respectively. The minimum inhibitory concentration (MIC) of HSNPs was found to be 50 µg/ml and 60 µg/ml against S. aureus and E. coli, respectively. The antioxidant capacity of the HSNPs was insignificant as compared to EAF but the results of anti-inflammatory activity was significant (p<0.05). Conclusion: The overall result demonstrated better in-vitro pharmacological potential of HSNPs compared to neat extract/EAF. [ABSTRACT FROM AUTHOR]

[Display omitted] • Caralluma adscendens R.Brown var. bicolor was used for the phytosynthesis of nanomaterials. • Both nanoparticles exhibited greater pharmacological activities. • Prepared nanomaterials were characterized using FTIR, HR-TEM, EDX, and UV–Vis analysis. • Both nanoparticles showed higher wound-healing activity than CABL extract based on the MTT assay and fluorescence analysis. Nanomaterials employed in nanomedicine have the potential to function as both diagnostic and therapeutic tools for individuals. Over the past few decades, significant efforts have been made to synthesize a range of metal nanoparticles through the utilization of different plant extracts. Caralluma adscendens R. Brown var. bicolor leaves (CABL) extract was employed in this study as a reducing/capping agent for the synthesis of gold/silver nanoparticles (CABL@AgNPs/CABL@AuNPs) and explore their pharmacological properties. The successful synthesis of CABL@AgNPs and CABL@AuNPs was confirmed through the observation of surface plasmon resonance (SPR) at 439 and 522 nm using ultraviolet–visible spectrophotometer (UV–Vis). High resolution-transmission electron microscopy (HR-TEM) and energy dispersive X-ray (EDX) techniques were employed to evaluate the shape, size, and chemical composition of the as-synthesized CABL@AgNPs and CABL@AuNPs. Fourier-transform infrared spectroscopy (FTIR) was used to determine the biomolecules responsible for the reduction of metal ions and the stability of metal nanoparticles generated using plant extract. An evaluation was performed to assess the antibacterial and antifungal efficacy of the prepared aqueous CABL extract, CABL@AgNPs, and CABL@AuNPs through the implementation of the disc diffusion technique. The results demonstrated that CABL@AgNPs exhibited greater efficiency when compared to both CABL extract and CABL@AuNPs. The dose-dependent nature of antimicrobial activities was clearly demonstrated through the results of antioxidant and anti-inflammatory experiments. The wound healing activity of the prepared nanomaterials was evaluated using a variety of techniques, including MTT assay, fluorescence staining test, and in vitro scratch assay. The wound-healing capacity of prepared nanomaterials was evaluated using an in vitro scratch assay with Fibroblast L929 cells. The impact of nanoparticles at the IC 50 concentration range was analysed through a fluorescence staining experiment and MTT assay to determine toxicity levels. The environmentally friendly approach of current study shown that both nanoparticles have the potential to be effective therapeutic agents for treating different illnesses. [ABSTRACT FROM AUTHOR]

The measurement of total antioxidant capacity (TAC) indicating the cooperative action of all antioxidants in a complex sample is an important analytical challenge. A novel green silver nanoparticle-based antioxidant capacity (GSNP-AC) method using carob extract was designed for TAC measurement. Green synthesis of nanoparticles has various advantages such as environmentally friendliness, reliability, sustainability and fast production. In the presence of silver seeds formed with carob extract, Ag+ is reduced to spherical silver nanoparticles (SNPs) with antioxidants, resulting in enlarged particles with a symmetric surface plasmon resonance (SPR) absorption band at 434 nm. The SPR of SNPs allowed quantification of antioxidants (i.e., increase in SPR absorbance being correlated to antioxidant concentration), and the GSNP-AC method gave a linear response over a wide concentration range of antioxidants. The molar absorptivity and LOD for trolox were 11700 L mol−1 cm−1 and 0.31 µM, respectively. The proposed method was validated in terms of concentration-dependent linear response, additivity of absorbances, precision and accuracy. The results obtained with the proposed method for standard antioxidants, synthetic mixtures and real sample extracts were correlated with those of the traditional CUPRAC method. This green synthesized silver nanoparticle-based TAC method showed simple, rapid, cost-effective, and eco-friendly superiorities over similar other nanoparticle-based assays. [ABSTRACT FROM AUTHOR]

This study aimed at using a green, rapid, and efficient method for silver nanoparticles synthesis using different types of agri-waste. Ag was reduced to Ag-NPs using the banana, apple and walnut waste extracts that served as both capping and reducing agent. Silver nitrate solution (1mM) was mixed with the vegetal extract (1:9 ratio) and sonicated in a cleaning bath, at 60C. The successful bio-reduction of silver nitrate into silver nanoparticles was confirmed by UV-Vis spectroscopy, a characteristic surface plasmon resonance (SPR) band being recorded for all the samples. Concluding, agri-waste may be harnessed to phyto-fabricate eco-friendly silver nanoparticles, with multiple applications in the agri-food sector. [ABSTRACT FROM AUTHOR]

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

The synthesis of nanoparticles by utilising plant extract has revolutionised the field of nanotechnology. In the present study, AgNPs were synthesised by utilising the leaves of Moringa oleifera as reducing and stabilising agent. UV‐visible spectroscopy showed characteristic surface plasmon band in the range of 413–420 nm. Scanning electron microscopy (SEM) elucidated rectangular segments fused together. X‐ray diffraction (XRD) analysis confirmed the crystalline nature of AgNPs and presence of metallic silver ions was confirmed by energy dispersive X‐ray (EDX). The different concentrations (10, 20, 30 and 40 ppm) of AgNPs were exogenously applied on Citrus reticulata to record the disease incidence at different day intervals. The disease intensity was progressively increased in all the applied treatments with the passage of time. The 30 ppm concentration of AgNPs was found to be most suitable concentration for creating the resistance against brown spot disease. Moreover, the effects of AgNPs were also assessed for biochemical profiling in C. reticulata. The enhanced production of endogenous enzymes and non‐enzymatic components was observed in response to 30 ppm concentration of AgNPs. The present work highlighted that green synthesised AgNPs can be as used as biological control of citrus diseases and the enhanced production of secondary metabolites antioxidants. [ABSTRACT FROM AUTHOR]

Nanoparticles are being increasingly used in day‐to‐day life. Therefore, concerns have been raised regarding their interactions with the surrounding environment. This study focused on a simple green method for synthesizing silver nanoparticles (Ag‐NPs) in an autoclave at 15 psi (103 kPa) and 121°C. An aqueous solution of AgNO3 as a precursor of Ag‐NPs and gelatin (type B) reducing and/or stabilizing (capping) agent were used. The effect of various AgNO3 concentrations of certain gelatin concentration and various gelatin concentrations at constant AgNO3 concentration, and autoclaving time, was studied. UV‐Vis spectra ascribed that the presence of localized surface plasmon resonance (SPR) of the synthesized Ag‐NPs. TEM images and the selected area of electron diffraction confirmed, the formation of Ag‐NPs with a diameter of approximately 5 ±0.35 nm. Furthermore, FT‐IR revealed that a gelatin polymer matrix stabilized the synthesized Ag‐NPs. The Well diffusion assay was used to test the effect of Ag‐NPs on six clinical bacterial isolates, where Gram positive bacteria were more susceptible to Ag‐NPs than Gram negative bacteria. Therefore, Ag‐NPs capped by gelatin have remarkable potential effect as an antibacterial agent, and they not only have various medical applications but can also be used in biological, pharmaceutical and industrial fields. [ABSTRACT FROM AUTHOR]

Green synthesis of silver nanoparticles (AgNPs) has gained widespread interest as the alternative method to use natural, non-toxic substances to facilitate the formation of AgNPs. This work reported on the alternative source of reducing and stabilizing agents from tissue extract of weaver ant ( Oecophylla smaragdina ) larvae. The formation of AgNPs in the reaction containing silver nitrate, the tissue extract, and glucose at 60 °C was indicated by the surface plasmon resonance at 428 nm. Transmission electron microscopy images revealed spherical AgNPs with the average diameter of 67.4 nm. The synthesized AgNPs exhibited potent antibacterial activity against both Staphylococcus aureus and Escherichia coli with the minimum bactericidal concentrations equally at 16 μg/mL. [ABSTRACT FROM AUTHOR]

Green synthesis of metallic nanoparticles has lured the world from the chemical and physical approaches owing to its rapid, non‐hazardous and economic aspect of production mechanism. In this study, silver nanoparticles (AgNPs) were synthesised using petal extracts of Hibiscus rosa‐sinensis. The AgNPs displayed characteristic surface plasmon resonance peak at around 421 nm having a mean particle size of 76.25 ± 0.17 nm and carried a charge of −41 ± 0.2 mV. The X‐ray diffraction patterns displayed typical peaks of face centred cubic crystalline silver. The surface morphology was characterised by scanning electron microscopy and atomic force microscopy. Fourier transform infrared spectroscopy studies confirmed the surface modifications of the functional groups for the synthesis of AgNPs. Furthermore, the synthesised AgNPs displayed proficient antimicrobial activity against pathogenic strains of Vibrio cholerae, Escherichia coli, Klebsiella pneumoniae and Staphylococcus aureus. [ABSTRACT FROM AUTHOR]

The production of pure silver nanoparticles (Ag-NPs) with unique properties remains a challenge even today. In the present study, the synthesis of silver nanoparticles (Ag-NPs) from natural pullulan (PL) was carried out using a radiation-induced method. It is known that pullulan is regarded as a microbial polysaccharide, which renders it suitable to act as a reducing and stabilizing agent during the production of Ag-NPs. Pullulan-assisted synthesis under gamma irradiation was successfully developed to obtain Ag-NPs, which was characterized by UV-Vis, XRD, TEM, and Zeta potential analysis. Pullulan was used as a stabilizer and template for the growth of silver nanoparticles, while gamma radiation was modified to be selective to reduce silver ions. The formation of Ag-NPs was confirmed using UV–Vis spectra by showing a surface plasmon resonance (SPR) band in the region of 410–420 nm. As observed by TEM images, it can be said that by increasing the radiation dose, the particle size decreases, resulting in a mean diameter of Ag-NPs ranging from 40.97 to 3.98 nm. The XRD analysis confirmed that silver metal structures with a face-centered cubic (FCC) crystal were present, while TEM images showed a spherical shape with smooth edges. XRD also demonstrated that increasing the dose of gamma radiation increases the crystallinity at a high purity of Ag-NPs. As examined by zeta potential, the synthesized Ag-NP/PL was negatively charged with high stability. Ag-NP/PL was then analysed for antimicrobial activity against Staphylococcus aureus, and it was found that it had high antibacterial activity. It is found that the adoption of radiation doses results in a stable and green reduction process for silver nanoparticles. [ABSTRACT FROM AUTHOR]

In the present study, we have developed a green approach for the synthesis of silver nanoparticles (DSAgNPs) using aqueous extract of Durio zibethinus seed and determined its antibacterial, photocatalytic and cytotoxic effects. Surface plasmon resonance confirmed the formation of DSAgNPs with a maximum absorbance (λmax) of 420 nm. SEM and TEM images revealed DSAgNPs were spherical and rod shaped, with a size range of 20 nm and 75 nm. The zeta potential was found to be −15.41 mV. XRD and EDX analyses confirmed the nature and presence of Ag and AgCl. DSAgNPs showed considerable antibacterial activity, exhibited better cytotoxicity against brine shrimp, and shown better photocatalytic activity against methylene blue. Based on the present research work, it can be concluded that DSAgNPs could be used in the field of water treatment, pharmaceuticals, biomedicine, biosensor and nanotechnology in near future. [ABSTRACT FROM AUTHOR]