Evidence map›Paper›PMID 41073906›Full record

ArticleBMC microbiology2025

Multifunctional nanostructured lipid carriers encapsulating Bacillus megaterium supernatant and magnetic nanoparticles for combating methicillin-resistant Staphylococcus aureus and cancer cells.

Mohamed A Fareid, Gamal M El-Sherbiny, Mohamed H Sharaf, Asmaa M Hegazy, Rosilah Ab Aziz, Ahmed A Askar, Fatma A Hamada

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Mohamed A FareidClinical Laboratory Science Department, Applied Medical Science College, University of Ha'il, Hail, 2440, Saudi Arabia. m.alekhtaby@uoh.edu.sa.
Gamal M El-SherbinyBotany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, 11884, Egypt. gamalelsherbiny1970@azhar.edu.eg.ORCID 0000-0003-3968-0536
Mohamed H SharafBotany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, 11884, Egypt.
Asmaa M HegazyClinical Laboratory Science Department, Applied Medical Science College, University of Ha'il, Hail, 2440, Saudi Arabia.
Rosilah Ab AzizFirst Year of Health and Medical Colleges, Basic Sciences Department, University of Ha'il, Hail, 2440, Saudi Arabia.
Ahmed A AskarBotany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, 11884, Egypt.
Fatma A HamadaFirst Year of Health and Medical Colleges, Basic Sciences Department, University of Ha'il, Hail, 2440, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanostructured lipid carriers (NLCs), liposomes, and microemulsions represent significant advancements in drug delivery systems. This study aimed to synthesize NLCs encapsulating Bacillus megaterium supernatant (BMS) and magnetic nanoparticles (MNPs) for potential application against MRSA and cancer cells. The NLCs were prepared using the emulsification-solvent evaporation technique and loaded with BMS and MNPs to form NLC-BMS-MNPs. Characterization of the NLC-BMS-MNPs was performed using X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), and zeta potential. The NLC-BMS-MNPs exhibited a spherical morphology with an average size of 74.45 nm, a polydispersity index (PDI) of 0.350, and a zeta potential of − 4.44 mV. NLC-BMS-MNPs demonstrated antibacterial activity, with minimum inhibitory concentrations (MICs) ranging from 7.5 to 30 µg/mL. They also significantly downregulated the expression of biofilm-associated genes fnbA, icaA, and cna, with fold changes ranging from − 1.9 to -3, -2 to 3, -4 to5.2, respectively (P < 0.0001). Furthermore, the formulation showed antioxidant activity, with IC₅₀ values of 299 µg/mL and 521 µg/mL in DPPH and ABTS assays, respectively. Additionally, NLC-BMS-MNPs exhibited selective cytotoxicity toward cancer cells. HepG2 and MCF-7 cells displayed significantly reduced viability, with IC₅₀ values of 13.74 ± 0.02 µg/mL and 19.12 ± 0.51 µg/mL, respectively, compared to normal Vero and HFB-4 cells, which showed IC₅₀ values of 36.1 ± 0.65 µg/mL and 33.45 ± 2.29 µg/mL. In conclusion, NLC-BMS-MNPs represent a promising multifunctional nanomaterial with potential applications in both antimicrobial and anticancer therapies.

Indexed as

Anti-Bacterial AgentsBacillus megateriumDrug CarriersLipidsMagnetite NanoparticlesMethicillin-Resistant Staphylococcus aureusNanostructuresAnimalsAntineoplastic AgentsBiofilmsCell Line, TumorHumansMicrobial Sensitivity TestsParticle SizeX-Ray DiffractionAnti-Bacterial AgentsAntineoplastic AgentsDrug CarriersLipidsMagnetite NanoparticlesAntibiofilmAnticancerAntioxidantBacillus megateriumGenes related to biofilmMethicillin-resistant Staphylococcus aureusNanomaterialNanostructured lipids

Identifiers

PMID41073906
PMCPMC12512938

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.