Evidence map›Paper›PMID 41749177›Full record

ArticleBMC complementary medicine and therapies2026

Nano-formulated pomegranate extracts with dual cytotoxic and antimicrobial activity: molecular docking and mechanistic insights into leukemia cell targeting.

Naglaa M Hamdy, Ahmed Ismail, Hoda S Sherkawy, Ayman S Yassin, Mohamed M Amin, Hanan M El-Tantawy, Abdulrahman M Saleh, Nashwa El-Khazragy

Abstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2026. 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

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Naglaa M HamdyDepartment of Medicinal and Aromatic Plants, Desert Research Center, Cairo, Egypt.ORCID http://orcid.org/0000-0002-8328-0081
Ahmed IsmailDepartment of Pharmacognosy, Faculty of Pharmacy, Fayoum University, Fayoum, Egypt.ORCID http://orcid.org/0000-0003-0266-8760
Hoda S SherkawyDepartment of Medical Biochemistry, Faculty of Medicine, Aswan University, Aswan, Egypt.ORCID http://orcid.org/0000-0001-7508-0146
Ayman S YassinDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Al-Azhar University, Assiut, Egypt.ORCID http://orcid.org/0000-0003-4264-0981
Mohamed M AminDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Aswan University, Aswan, Egypt.ORCID http://orcid.org/0000-0002-8028-7368
Hanan M El-TantawyDepartment of Medicinal and Aromatic Plants, Desert Research Center, Cairo, Egypt.ORCID http://orcid.org/0009-0009-8219-864X
Abdulrahman M SalehDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt.ORCID http://orcid.org/0000-0002-5153-7399
Nashwa El-KhazragyDepartment of Clinical Pathology-Hematology and AinShams Medical Research Institute (MASRI), Faculty of Medicine, Ain Shams University, Cairo, 11566, Egypt. nashwaelkhazragy@med.asu.edu.eg.ORCID http://orcid.org/0000-0001-6646-4674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ethnopharmacological relevancePunica granatum (pomegranate) peel is traditionally used for its antimicrobial and health-promoting properties in several cultures. Rich in polyphenols, the peel has attracted interest for its potential applications in treating infections and cancer, particularly in integrative approaches for immunocompromised patients. MATERIALS AND

methodsPomegranate peel extracts were prepared using solvents of increasing polarity, with emphasis on the ethyl acetate fraction (PPE-EA). A nano-formulated version (n-PPE-EA) was developed using a standard nano-encapsulation technique. Cytotoxic activity was evaluated in THP-1 human leukemia cells using MTT assay, flow cytometry, and biochemical analyses. Antimicrobial activity was assessed against Streptococcus pyogenes via agar diffusion. Gene expression of BCL2, PI3K, and CDK8 was measured to elucidate mechanisms of action.

resultsAmong all tested extracts, PPE-EA showed the strongest dual activity, reducing THP-1 cell viability by over 50% at 100 µg/mL and inhibiting S. pyogenes with a 10.5 ± 1.1 mm zone. Nano-encapsulation enhanced both effects, reducing the IC₅₀ from 1.48 ± 0.03 µg/mL to 0.19 ± 0.01 µg/mL and increasing the bacterial inhibition zone to 15.6 ± 0.5 mm. n-PPE-EA induced apoptosis, cell cycle arrest, elevated catalase activity, and reduced malondialdehyde levels. It also downregulated BCL2, PI3K, and CDK8 expression.

conclusionThe nano-formulated PPE-EA demonstrated potent cytotoxic and antimicrobial activities, with enhanced efficacy attributed to improved bioavailability and modulation of apoptotic and cell cycle pathways. These findings support its potential as a multifunctional therapeutic agent in integrative cancer care.

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsLeukemiaPlant ExtractsPomegranateStreptococcus pyogenesCell SurvivalHumansMolecular Docking SimulationTHP-1 CellsAnti-Bacterial AgentsAnti-Infective AgentsPlant ExtractsAntimicrobialAntioxidantCytotoxicLeukemiaPunica granatumStreptococcus pyogenes

Identifiers

PMID41749177
PMCPMC12955060

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Registered trials

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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.