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Green biosynthesis of selenium nanoparticles by which demonstrate effectiveness against human cancer cells, species and multidrug-resistant .

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RSC advances 2026 Vol.16(17) p. 15379-15391
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Ahmed ME, Al-Bayaa YJ, Aboud RS, Hassan A, Ameen F, Mohamed HS

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is a major global concern due to its multidrug resistance and persistence multidrug-resistant (MDR) pathogens pose a serious threat in hospital environments, particularly among immunocompromised patie

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APA Ahmed ME, Al-Bayaa YJ, et al. (2026). Green biosynthesis of selenium nanoparticles by which demonstrate effectiveness against human cancer cells, species and multidrug-resistant .. RSC advances, 16(17), 15379-15391. https://doi.org/10.1039/d5ra09953f
MLA Ahmed ME, et al.. "Green biosynthesis of selenium nanoparticles by which demonstrate effectiveness against human cancer cells, species and multidrug-resistant .." RSC advances, vol. 16, no. 17, 2026, pp. 15379-15391.
PMID 41868325
DOI 10.1039/d5ra09953f

Abstract

is a major global concern due to its multidrug resistance and persistence multidrug-resistant (MDR) pathogens pose a serious threat in hospital environments, particularly among immunocompromised patients. In this study, selenium nanoparticles (SeNPs) were biosynthesized using isolated from petroleum-contaminated soils in Iraq. SeNP formation was confirmed by UV-visible spectroscopy, AFM, TEM, FE-SEM, and EDX analyses, which revealed predominantly spherical, well-dispersed nanoparticles in the nanoscale range. The antimicrobial activity of SeNPs was evaluated against Gram-positive and Gram-negative bacteria, spp., and ten MDR clinical isolates. SeNPs exhibited strong antimicrobial activity, with a uniform minimum inhibitory concentration (MIC) of 16 µg mL against all MDR isolates and concentration-dependent inhibition against other bacterial and fungal pathogens, showing notable activity against . To explore potential resistance-related interactions, MexB efflux pump gene expression was analyzed in two representative MDR isolates. SeNP treatment resulted in strain-dependent modulation of MexB expression, indicating variable bacterial responses rather than consistent efflux inhibition. In addition, cytotoxicity assays demonstrated dose-dependent antiproliferative effects of SeNPs against PC3 prostate cancer cells, with lower toxicity toward normal WRL68 liver cells.