Evidence map›Paper›PMID 42859228›Full record

ArticleArchives of microbiology2026

Experimental characterization of Pleurotus tuber-regium-derived silver nanoparticles and antifungal activity against Aspergillus fumigatus, Cryptococcus neoformans, and Candida albicans.

Alya Aljuaid

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Article in Archives of microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

1 author.

Alya AljuaidDepartment of Biology, College of Science and Humanities, Shaqra University, Shaqra, 11961, Saudi Arabia. aaljuaied@su.edu.sa.ORCID https://orcid.org/0009-0006-3583-5544

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mushroom-mediated silver nanoparticles (AgNPs) offer a lower-reagent synthetic route to antifungal nanomaterials, but the contribution of Pleurotus tuber-regium sclerotial chemistry and activity across morphologically distinct opportunistic fungi remain insufficiently defined. In this experimental study, an aqueous sclerotial extract was characterized by gas chromatography-mass spectrometry (GC-MS) and used to synthesize P. tuber-regium-derived AgNPs (Pt-AgNPs). Data from three independent synthesis batches were evaluated by ultraviolet-visible spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential analysis, and energy-dispersive X-ray spectroscopy (EDX). The resulting Pt-AgNPs showed a surface-plasmon peak at 421.7 ± 2.1 nm, a TEM diameter of 24.8 ± 5.4 nm, a DLS Z-average of 68.7 ± 3.8 nm, a polydispersity index of 0.246 ± 0.021, and a zeta potential of -26.4 ± 1.9 mV. Broth microdilution was performed using Clinical and Laboratory Standards Institute M38 and M27 procedures. Modal minimum inhibitory concentrations were 8, 4, and 4 µg/mL for Aspergillus fumigatus, Cryptococcus neoformans, and Candida albicans, respectively. Across 4-128 µg/mL, Pt-AgNPs produced larger inhibition zones than crude extract for each species (formulation effects, all p < 0.001). At 2× MIC, viable counts fell by at least 3 log10 CFU/mL by 12 h for A. fumigatus and C. neoformans. These findings provide an integrated characterization and antifungal-testing dataset and warrant further experimental validation across a broader isolate panel, mechanistic investigation, and safety assessment.

Indexed as

Antifungal AgentsAspergillus fumigatusCandida albicansCryptococcus neoformansMetal NanoparticlesPleurotusSilverGas Chromatography-Mass SpectrometryMicrobial Sensitivity TestsMicroscopy, Electron, TransmissionSpectroscopy, Fourier Transform InfraredX-Ray DiffractionAntifungal AgentsSilverBroth microdilutionColloidal stabilityMyconanotechnologySclerotial extractTime–kill kinetics

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.