Evidence mapPaperPMID 42370018Full record

ArticleIranian journal of medical sciences2026

Surface-Engineered Selenium Nanoparticles with L-Asparagine and Tartaric Acid: Therapeutic Efficacy Against Breast Cancer and Bacterial Infections.

Abdolrazagh Marzban, Khadije Salari Nejad, Maryam Zand, Masumeh Jalalvand, Hamed Esmaeil Lashgarian

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Article in Iranian journal of medical sciences, 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Abdolrazagh MarzbanRazi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran.
Khadije Salari NejadDepartment of Medical Biotechnology, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Maryam ZandDepartment of Medical Biotechnology, Zanjan University of Medical Sciences, Zanjan, Iran.
Masumeh JalalvandDepartment of Medical Biotechnology, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Hamed Esmaeil LashgarianDepartment of Medical Genetics and Biotechnology, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Selenium nanoparticles (SeNPs), compared to other forms of selenium, have shown promising antioxidant and anticancer properties with lower toxicity. However, SeNPs precipitate and aggregate in aqueous solutions due to their high surface energy. To overcome this limitation and improve stability, solubility, and enhance biological efficacy, we functionalized them with L-asparagine/tartaric acid (Asn-Tar). This study aimed to evaluate the antimicrobial, cytotoxic, and antioxidant properties of SeNPs conjugated to Asn-Tar on MDA-MB-231 breast cancer cells. Methods: This study was conducted at Lorestan, Iran, in 2023. SeNPs were synthesized using a co-precipitation method and then coated with Asn-Tar. Structural characterization was performed using Fourier transform infrared spectroscopy (FTIR), X-ray Diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Dynamic light scattering (DLS), zeta potential analysis, and Ultraviolet-visible (UV-Vis) spectroscopy. Antioxidant activity was assessed. For biological evaluation, an Results: The synthesized Asn-Tar/SeNPs nanocomposite exhibited a spherical morphology with an average size of 460.8 nm, a negative zeta potential (-9.37±0.44 mV), and successful coating was confirmed by FTIR and XRD. The nanocomposite demonstrated dose-dependent antioxidant activity, with an IC Conclusion: The produced Asn-Tar/SeNPs nanocomposite exhibited potent antimicrobial, selective cytotoxicity, and antioxidant properties. Our findings confirm the potential of these Asn-Tar/SeNPs nanocomposites for targeted therapy of breast cancer.

Indexed as

Bacterial InfectionsBreast NeoplasmsNanoparticlesSeleniumTartratesAntineoplastic AgentsAntioxidantsFemaleHumansMDA-MB-231 CellsAntineoplastic AgentsAntioxidantsSeleniumtartaric acidTartratesAntioxidantsBreast neoplasmsNanoparticlesSelenium

Identifiers

PMID42370018
PMCPMC13309735

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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 Socratic graph.