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1.
J Microbiol Methods ; 199: 106517, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-35697186

RESUMO

The present study aimed at evaluating the extracellular synthesis of silver nanoparticles by soil fungus Aspergillus melleus SSS-10 for antibacterial and cytotoxic activity. In this study, the formation of silver nanoparticles (AgNPs) was estimated by the colour change in cell free extract from pale yellow to golden yellow after 24 h of the reaction. UV-Vis study showed the absorbance maxima at 410 nm. Tauc plot analysis revealed the band gap energy as 2.34 eV. Dynamic Light Scattering (DLS) data revealed polydisperse anisotropic silver nanoparticles with average hydrodynamic diameter of 92.006 nm. Zeta potential of - 19.6 mV provided evidence of stable silver nanoparticles. X-ray diffraction (XRD) analysis revealed four prominent Bragg peaks corresponding to (111), (200), (220) and (311) planes characteristic of silver (Ag) in FCC structural configuration. Average crystallite size was found to be 87.3 nm from Scherrer equation. Scanning Electron Microscope (SEM) analysis revealed irregular morphology of silver nanoparticles. EDS analysis displayed characteristic energy peaks of silver from 2.72 keV to 3.52 keV confirming the presence of silver nanoparticles. Biosynthesized AgNPs exhibited strong cytotoxic potential on MG-63 cells. AgNPs also showed antibacterial activity against both Staphylococcus aureus and Escherichia coli. In conclusion, this study provides a platform to explore the utility of fungal mediated silver nanoparticles synthesized for various pharmaceutical and cosmeceutical applications.


Assuntos
Antineoplásicos , Nanopartículas Metálicas , Antibacterianos/química , Aspergillus , Escherichia coli , Nanopartículas Metálicas/química , Testes de Sensibilidade Microbiana , Extratos Vegetais/química , Prata/química , Prata/farmacologia , Solo
2.
RSC Adv ; 10(37): 22183-22195, 2020 Jun 08.
Artigo em Inglês | MEDLINE | ID: mdl-35516621

RESUMO

Monophasic polycrystalline powders of Y1-x R x Fe1-(4/3)y Ti y O3 (R = Sm, Gd; x = 0.05, 0.10, 0.15; y = 0.05) were successfully synthesized via a low temperature solid-state synthesis route. The X-ray diffraction and Raman spectroscopy studies indicate that all the calcined powders with R3+ (Gd3+, Sm3+) at Y3+ and Ti4+ at Fe3+ sites were crystallized in an orthorhombic phase associated with a change in lattice parameters. The Williamson-Hall method employed to calculate the strain revealed that the strain increased with the increased concentration of dopants ((Gd3+, Sm3+) at Y3+) compared to an increase in the size of crystallites, corroborating the findings of SEM. Analysis of diffuse reflectance spectra indicated a drop in bandgap from 1.93 eV to 1.86 eV and 1.96 eV to 1.91 eV for Gd, Ti co-doping and Sm, Ti co-doping respectively, demonstrating the capacity of the synthesized powders to absorb visible light. Absorbance spectra also revealed the existence of mixed states of Fe3+ and Fe4+ which was corroborated by XPS studies. The magnetic hysteresis loop analysis at room temperature illustrated that with co-doping, there is a strong enhancement in magnetization as well as coercivity, suggesting a strong transition from anti-ferromagnetic behaviour to ferromagnetic behaviour. Pertaining to the greatly improved optical and magnetic properties with the addition of (Gd3+, Sm3+) at Y3+ and Ti4+ at Fe3+ sites, these materials are anticipated to be of potential use in various applications.

3.
J Phys Condens Matter ; 32(3): 035810, 2020 Jan 16.
Artigo em Inglês | MEDLINE | ID: mdl-31557738

RESUMO

Fine powders of Y1-x Sm x FeO3 (x = 0, 0.05, 0.10, 0.15) were synthesized via citrate based sol-gel route. While the as synthesized powders were amorphous, the calcined (900 °C/8 h) powders were confirmed to be polycrystalline by x-ray powder diffraction (XRD) studies. The calcined powders were found to crystallize in an orthorhombic structure associated with the lattice parameters a = 5.59 Å, b = 7.60 Å, c = 5.28 Å. These lattice parameters increased with the increase in Sm3+ content at yttrium sites. The strain that was obtained by the Williamson-Hall method increased with the increase in dopant (Sm3+) concentration vis-à-vis a decrease in crystallite size. Diffuse reflectance spectroscopic studies suggest an increase in band gap as Sm doping level increased. Significant enhancement in magnetization associated with a decrease in coercive field accompanied by a transition from anti-ferromagnetic to soft ferromagnetic behaviour in Sm doped YFeO3 were encountered. It is hoped that these materials with the enhanced magnetic properties could be of potential use for multifarious applications.

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