Evidence map›Paper›PMID 41673028›Full record

ArticleScientific reports2026

Bioinspired 8‑hydroxyquinoline-Fe

Ahmad Gholami, Milad Mohkam, Navid Omidifar, Seyyed Mojtaba Mousavi, Khadije Yousefi, Mohammad Hashem Hashempur, Kamran Bagheri Lankarani, Wei-Hung Chiang, Chin Wei Lai

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Ahmad Gholami *Biotechnology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Milad Mohkam *Zanjan Pharmaceutical Biotechnology Research Center, Zanjan University of Medical Sciences, Zanjan, Iran.
Navid OmidifarBiotechnology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. omidifar@gmail.com.
Seyyed Mojtaba MousaviDepartment of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan. kempo.smm@gmail.com.
Khadije YousefiHealth Policy Research Center, Institute of Health, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammad Hashem HashempurResearch Center for Traditional Medicine and History of Medicine, Department of Persian Medicine, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Kamran Bagheri LankaraniHealth Policy Research Center, Institute of Health, Shiraz University of Medical Sciences, Shiraz, Iran.
Wei-Hung ChiangBiotechnology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Chin Wei LaiNanotechnology and Catalysis Research Centre, Institute for Advanced Studies, Universiti Malaya, Level 3, Block A, 50603, Kuala Lumpur, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study presents a novel green-synthesized iron oxide nanostructure (ION) using Citrullus colocynthis extract (CCE) and functionalized with 8-hydroxyquinoline (8HQ) to enhance antibacterial, antifungal, and anticancer activities. IONs were synthesized via CCE-mediated reduction or chemical coprecipitation, coated with 8HQ, and characterized by FE-SEM, EDAX, and FT-IR. The antimicrobial efficacy was assessed against Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, and Candida albicans through CLSI-guided MIC/MBC assays, while cytotoxicity was evaluated on MCF7 and Hep-G2 cancer cells using MTT assays. Results demonstrated that CCE-ION exhibited enhanced antimicrobial activity compared to chemically synthesized ION. The MIC values for CCE-ION were 125 µg/mL for P. aeruginosa, 250 µg/mL for E. coli, 500 µg/mL for S. aureus and C. albicans, and 1000 µg/mL for E. faecalis, with corresponding MBC values of 250, 250, 500, 500, and 1000 µg/mL, respectively, indicating strong bactericidal and fungicidal properties. FE-SEM analysis confirmed spherical nanoparticles (35–40 nm) with balanced iron oxide and organic composition. The 8HQ@CCE-ION nanocomposite exhibited significant cytotoxicity, with IC50 values of ≈ 489 µg/mL against MCF-7 cells and ≈ 183 µg/mL against Hep-G2 cells (compared to ≈ > 500 µg/mL and ≈ 450 µg/mL for free CCE, respectively), achieving > 80% cell death at 250 µg/mL and highlighting enhanced cellular uptake and synergistic effects. This eco-friendly nanoplatform successfully integrates CCE’s natural bioactivity with 8HQ’s metal-chelating properties, achieving significant pathogen viability reduction at MIC doses while offering promising anticancer potential. The dual-functional approach positions 8HQ@CCE-ION as a potential therapeutic candidate for drug-resistant infections and cancer treatment.

Indexed as

Anti-Bacterial AgentsAntifungal AgentsAntineoplastic AgentsCitrullus colocynthisNanostructuresOxyquinolineCandida albicansEscherichia coliHep G2 CellsHumansMCF-7 CellsMicrobial Sensitivity TestsPlant ExtractsStaphylococcus aureusAnti-Bacterial AgentsAntifungal AgentsAntineoplastic AgentsOxyquinolinePlant Extracts8-hydroxyquinolineAntibacterial efficacyAnticancer activityCitrullus colocynthisHep-G2MCF7Medicinal plants

Identifiers

PMID41673028
PMCPMC12972304

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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.