Evidence map›Paper›PMID 41786806›Full record

ArticleScientific reports2026

Synthesis, characterization of Mg doped CuFe

Mohamed Ali, Nabila Zein, M A Abdo, Gehan Adel, Basel Sitohy

Abstract read
In one paragraph

Article in Scientific reports, 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

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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.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Mohamed AliBiochemistry Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt. mohamedali_eg@zu.edu.eg.
Nabila ZeinBiochemistry Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt.
M A AbdoPhysics Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt.
Gehan AdelBiochemistry Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt.
Basel SitohyDepartment of Clinical Microbiology, Infection and Immunology, Umeå University, Umeå, 90185, Sweden. basel.sitohy@umu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferrite nanoparticles (NPs) have emerged as promising candidates for cancer therapy. In this study, Mg-doped copper ferrite NPs, MgₓCu₁₋ₓFe2O4 (x = 0.0, 0.5, and 1.0), were synthesized via a citrate–nitrate combustion method and evaluated for their anticancer potential. Structural and morphological characteristics were analyzed using powder X-ray diffraction, field-emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy. Cytotoxicity against human cancer cell lines was assessed using MTT and flow cytometry assays, along with analyses of reactive oxygen species (ROS) generation and apoptosis. Among the compositions studied, Cu0.5Mg0.5Fe2O4 demonstrated the highest cytotoxic efficacy, with IC₅₀ values of 17.2 ± 0.15 µg/mL (PC-3) and 25.04 ± 0.28 µg/mL (Caco-2). Flow cytometric analysis revealed increased total apoptosis of 42.08% and 34.95% in PC-3 and Caco-2 cells, respectively. Gene expression analysis revealed downregulation of Bcl-2 and Cyclin D and upregulation of BAX, P53, and Caspase-3, indicating ROS-mediated mitochondria-dependent apoptosis. The enhanced anticancer activity of Cu0.5Mg0.5Fe2O4 is attributed to its optimized size, surface charge, and composition, which promote cellular uptake, ROS generation, DNA damage, and interactions with cellular components. These findings highlight the potential of mixed-metal ferrite nanoparticles as effective nanomaterial-based cancer therapeutics.

Indexed as

Antineoplastic AgentsCopperFerric CompoundsFerrous CompoundsMetal NanoparticlesNanoparticlesApoptosisCaco-2 CellsCell Line, TumorHumansPC-3 CellsReactive Oxygen SpeciesAntineoplastic AgentsCopperCuFe2O4Ferric CompoundsferriteFerrous CompoundsReactive Oxygen SpeciesApoptosisCell cycle analysisCytotoxicityNanoferriteReactive oxygen species

Identifiers

PMID41786806
PMCPMC12966289

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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.