Evidence map›Paper›PMID 41742465›Full record

ArticleBiotechnology and applied biochemistry2026

Biosynthesis and Characterization of Zinc Oxide-Doped Selenium Nanocomposite Conjugated With l-Asparaginase Against Human Hepatoma Cell Line.

G Baskar, K Keerthana, A Supriya, R Pravin, S Subashini

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Article in Biotechnology and applied biochemistry, 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

G BaskarDepartment of Biotechnology, St. Joseph's College of Engineering, Chennai, India.
K KeerthanaDepartment of Biotechnology, St. Joseph's College of Engineering, Chennai, India.
A SupriyaDepartment of Biotechnology, St. Joseph's College of Engineering, Chennai, India.
R PravinDepartment of Biotechnology, St. Joseph's College of Engineering, Chennai, India.
S SubashiniCenter for Waste Management and Renewable Energy, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Chennai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanocarriers have emerged as promising systems for improving drug-delivery efficiency and advancing diagnostic strategies in cancer treatment. l-asparaginase has well-established antitumor and anti-leukemic properties, but its therapeutic performance is often restricted due to its short biological half-life and poor instability in the unmodified form. The present study investigated the encapsulation of l-asparaginase on a green-synthesized nanocarrier to enhance its overall therapeutic efficacy. The nanocarrier was produced utilizing citrus orange peel extract, which served simultaneously as a reducing, stabilizing, and capping material during the formation of zinc oxide-doped selenium nanoparticles (ZnO-Se-NPs). This eco-friendly synthesis method not only stabilized the nanoparticles but also incorporated naturally occurring phytochemicals, including flavonoids, phenolic compounds, ascorbic acid, and carotenoids-that may contribute to additional pharmacological benefits. The synthesized l-asparaginase encapsulated ZnO-Se-NPs (ZnO-Se-Asp) nanocomposite exhibited notable anticancer activity while maintaining low cytotoxicity. The detailed characterization of the nanoparticles was carried out utilizing UV-Vis spectroscopy to confirm the presence of ZnO-Se-Asp, energy dispersive x-ray (EDX), and scanning electron microscope (SEM) for morphological and elemental analysis. The Fourier transform infrared spectroscopy (FTIR) was studied to identify the functional groups, and x-ray diffraction (XRD) was performed to study the crystallinity of synthesized ZnO-Se-Asp nanocomposite. The cytotoxic potential of synthesized ZnO-Se-Asp nanocomposite was estimated using the methyl thiazolyl tetrazolium (MTT) assay through the determined IC

Indexed as

Antineoplastic AgentsAsparaginaseCarcinoma, HepatocellularLiver NeoplasmsNanocompositesSeleniumZinc OxideCell Line, TumorCell ProliferationCell SurvivalDrug Screening Assays, AntitumorHep G2 CellsHumansAntineoplastic AgentsAsparaginaseSeleniumZinc Oxideanticancer activitycancer drugcharacterizationl‐asparaginasenanobiocomposite

Identifiers

PMID41742465
PMCPMC13446448

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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.