Evidence map›Paper›PMID 40787908›Full record

ArticleNanomedicine (London, England)2025

Rombus-shaped α-Fe₂O₃ nanoparticles for antibacterial and anticancer applications.

Sakshi Bajhal, Nishakavya Saravanan, Anandhakumar Sundaramurthy

Abstract read
In one paragraph

Article in Nanomedicine (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sakshi BajhalDepartment of Biotechnology, Faculty of Science and Humanities, SRM Institute of Science and Technology, Chengalpattu, India.
Nishakavya SaravananDepartment of Physics and Nanotechnology, SRM Institute of Science and Technology, Chengalpattu, India.
Anandhakumar SundaramurthyBiomaterials Research Laboratory (BMRL), Department of Chemical Engineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Chengalpattu, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing incidence of bacterial infections in cancer patients, combined with the growing limitations of conventional antibiotics such as poor site-specific targeting and antibiotic resistance, necessitates the development of advanced therapeutic strategies. METHODOLOGY: Rhombus-shaped α-Fe₂O₃ nanoparticles (NPs) were synthesized via hydrothermal route and characterized for their structural, optical, and morphological properties. Lymecycline was encapsulated into NPs, and its pH-dependent release was assessed. Antibacterial activity was evaluated using the well diffusion and minimum inhibitory concentration assay, while anticancer potential was examined using AlamarBlue and cytotoxicity assays against THP-1 cells. Biocompatibility was assessed using normal L-929 fibroblast cells.

resultsThe synthesized Fe₂O₃ NPs measured ~80 to 150 nm in length and ~50 nm in width. Lymecycline-loaded NPs demonstrated pH-responsive release, with 60% drug release at pH 5.5 and 43% at pH 7.4. They exhibited enhanced cytotoxicity (72%) against THP-1 cancer cells, while showing good biocompatibility with L-929 normal cells. Additionally, strong antibacterial activity was observed against

conclusionsLymecycline-loaded α-Fe₂O₃ NPs exhibited pH-responsive drug release, selective cytotoxicity toward THP-1 cancer cells, strong antibacterial efficacy, and good biocompatibility with normal cells. These findings highlight their dual functionality and potential as a promising nanoplatform for future anticancer and antimicrobial therapies.

Indexed as

Anti-Bacterial AgentsAntineoplastic AgentsFerric CompoundsNanoparticlesAnimalsCell LineCell Line, TumorCell SurvivalDrug LiberationEscherichia coliHumansHydrogen-Ion ConcentrationMiceMicrobial Sensitivity TestsNeoplasmsStaphylococcus aureusAnti-Bacterial AgentsAntineoplastic AgentsFerric Compoundsferric oxideantibacterial activityanticancer activitylipid peroxidationlymecyclinepH dependent-drug release and encapsulationα-Fe2O3 NPs

Identifiers

PMID40787908
PMCPMC12490402

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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.