Evidence map›Paper›PMID 41938055›Full record

ArticleFrontiers in bioengineering and biotechnology2026

Integrated metabolomic, nanoformulation, and network pharmacology approach reveals multifunctional bioactivities of an

Mervat S Mohamed, Amnah Obidan, Hajer Alfarteesh, Seham O Alsulami, Rehab Almassabi, Noor Alqurashi, Salma Saddeek, Raneen Salem Alsariei, Ayat G Ali

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 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
–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

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.

Mervat S MohamedDepartment of Chemistry, Biochemistry Specialty, Faculty of Science, Cairo University, Giza, Egypt.
Amnah ObidanDepartment of Biochemistry, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.
Hajer AlfarteeshBiology Department, King Khalid University, Abha, Saudi Arabia.
Seham O AlsulamiDepartment of Biochemistry, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.
Rehab AlmassabiDepartment of Biochemistry, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.
Noor AlqurashiDepartment of Biochemistry, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia.
Salma SaddeekDepartment of Chemistry, Faculty of Sciences, Universty of Hafr Al Batin, Hafr Al Batin, Saudi Arabia.
Raneen Salem AlsarieiUniversity of Tabuk, Tabuk, Saudi Arabia.
Ayat G AliDepartment of Biochemistry, El Sahel Teaching Hospital, GOTHI, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Although Ocimum sanctum (Holy Basil) exhibits broad pharmacological potential, its therapeutic application is constrained by poor solubility, instability, and limited bioavailability. Previous nanoemulsion studies have not integrated comprehensive metabolomic profiling with mechanistic and multi-bioactivity validation. This study developed and characterized an O. sanctum nanoemulsion to overcome these barriers and enhance biological activity. Methods: The ethanolic extract was profiled by GC-MS and LC-QTOF-MS/MS, identifying diverse phytochemicals. The optimized oil-in-water nanoemulsion (NE) was prepared using high-energy emulsification followed by high-pressure homogenization and ultrasonication. Physicochemical characterization included droplet size, polydispersity index (PDI), zeta potential, entrapment efficiency, and release profile. Biological activities were evaluated through cytotoxicity assays against Caco-2, HepG2, MDA-MB-231, and A549 cancer cell lines, antibacterial screening, antioxidant testing, and anti-inflammatory validation in LPS-stimulated RAW 264.7 macrophages. Network pharmacology analysis was performed to predict potential anti-inflammatory targets associated with the identified metabolites. Results: The optimized NE displayed nanoscale spherical droplets (51-73 nm), narrow polydispersity (PDI = 0.264), high negative zeta potential (-42.1 mV), and strong entrapment efficiency (96.2 ± 3.1%). A biphasic release profile reached ∼60% over eight days. The NE showed potent cytotoxicity against Caco-2, HepG2, MDA-MB-231, and A549 cells (IC Conclusion: Collectively, this metabolomics-guided O. sanctum nanoemulsion represents a promising plant-derived nanosystem. This preliminary study demonstrates its potential anticancer, antibacterial, antioxidant, and anti-inflammatory activities in vitro. However, further detailed investigations, including more extensive in vitro studies as well as in vivo evaluations, are required to better elucidate its mechanisms, safety, and potential biological applications.

Indexed as

antibacterialanticanceranti-inflammatorymetabolomicsnanoemulsionnetwork pharmacologyOcimum sanctum

Identifiers

PMID41938055
PMCPMC13047145

What Socratic holds

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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 Socratic graph.