ArticleCell biochemistry and function2026
Characterization, Antimicrobial, and Antiproliferative Activities of Silver Nanoparticles Biosynthesized Using Terminalia phanerophlebia Engl. & Diels.
Article in Cell biochemistry and function, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Characterization, Antimicrobial, and Antiproliferative Activities of Silver Nanoparticles Biosynthesized Using Terminalia phanerophlebia Engl. & Diels.Cell biochemistry and function · 2026Article
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4 authors.
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Abstract
The application of nanoparticles (NPs) as therapeutic strategies for treating microbial infections and cancer is gaining attention due to their physicochemical properties. In this study, we synthesized silver nanoparticles (AgNPs) from the aqueous extract of the roots and leaves of Terminalia phanerophlebia. The physicochemical properties of the synthesized AgNPs were examined using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX), transmission electron microscopy (TEM), and X-ray diffraction analysis (XRD). The AgNPs were studied for their antimicrobial and cytotoxic activities. The AgNPs synthesized from T. phanerophlebia root (R-AgNPs) and leaf (L-AgNPs) showed spherical and cubic nanoparticles with average sizes of 46 and 41 nm, respectively. The R-AgNPs and leaf L-AgNPs also demonstrated antimicrobial activities against selected bacterial isolates, including Vibrio parahemolyticus, Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Listeria monocytogenes, and multidrug-resistant Staphylococcus aureus and fungal isolates, including Candida albicans and Cryptococcus neoformans, with L-AgNPs showing the highest zone of inhibition against MRSA (29.33 mm) at 1 mg/mL. Cell viability assay showed that R-AgNPs demonstrated a better cytotoxic effect against HepG2 cells (IC50 = 40.78 µg/mL), while L-AgNPs demonstrated a better toxicity against MCF-7 cells (IC
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