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Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis
Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis
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Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis
Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis

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Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis
Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis
Journal Article

Antifungal Activity of Selenium Nanoparticles Obtained by Plant-Mediated Synthesis

2023
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Overview
The continuous need to satisfy world food demand has led to the search for new alternatives to combat economic losses in agriculture caused by phytopathogenic fungi. These organisms cause plant diseases, reducing their productivity and decreasing fruit quality. Among the new tools being explored is nanotechnology. Nanoparticles with antimicrobial properties could be an excellent alternative to address this problem. In this work, selenium nanoparticles (SeNPs) were obtained using plant extracts of Amphipterygium glaucum leaves (SeNPs-AGL) and Calendula officinalis flowers (SeNPs-COF). Characterization of the SeNPs was performed and their ability as antifungal agents against two commercially relevant plant pathogenic fungi, Fusarium oxysporum and Colletotrichum gloeosporioides, was evaluated. Assays were performed with different concentrations of SeNPs (0, 0.25, 0.5, 1.0, and 1.7 mg/mL). It was observed that both SeNPs had antifungal activity against both plant pathogens at concentrations of 0.25 mg/mL and above. SeNPs-AGL demonstrated better antifungal activity and smaller size (around 8.0 nm) than SeNPs-COF (134.0 nm). FTIR analysis evidenced the existence of different functional groups that constitute both types of SeNPs. There are factors that have to be considered in the antimicrobial activity of SeNPs such as nanoparticle size and phytochemical composition of the plant extracts used, as these may affect their bioavailability.