ArticleACS omega2025
Comparative Mechanistic Insights into Quercetin-Loaded Selenium Nanoparticles and Cisplatin in HCT116 Cells.
Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Amorphous selenium nanoparticles: synthesis strategies and multifunctional applications.RSC advances · 2026Review
- Nephroprotective Effects of Quercetin-Selenium Nanoparticles Against Glycerol-Induced AKI.International journal of molecular sciences · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Colorectal cancer (CRC) remains a leading cause of cancer-related mortality worldwide, with rising incidence, treatment resistance, and chemotherapy-induced toxicity underscoring the need for safer, more effective therapeutic strategies. Nanotechnology offers a promising approach through targeted drug delivery and enhanced therapeutic efficacy. This study investigates the anticancer potential of quercetin-loaded selenium nanoparticles (Qu-SeNPs) against HCT116 colorectal cancer cells and directly compares their effects with cisplatin (CP). To our knowledge, this is the first study to systematically compare the mechanistic actions of Qu-SeNPs and CP in CRC cells. Comprehensive physicochemical characterization using UV-vis spectroscopy, FTIR, TEM, EDX, zeta potential, and DLS confirmed successful synthesis of stable, well-dispersed Qu-SeNPs, exhibiting a characteristic peak at 410 nm. MTT assays demonstrated that Qu-SeNPs reduced HCT116 cell viability in a dose-dependent manner, with an IC
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Registered trials
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