# “Salvia officinalis extract–conjugated magnetite and selenium nanocomposites showed enhanced antibacterial and anti-biofilm activity against multidrug-resistant pathogens”

**Authors:** Gamal Enan, Neveen Abou El-Wafa, Mahmoud M. El-Saber, Ali Osman, Seham Abdel-Shafi, Mahmoud Sitohy

PMC · DOI: 10.1038/s41598-026-39983-6 · Scientific Reports · 2026-03-16

## TL;DR

This study shows that combining Salvia officinalis extract with magnetite and selenium nanoparticles improves antibacterial and anti-biofilm effects against drug-resistant bacteria.

## Contribution

The novel use of Salvia officinalis extract-conjugated nanocomposites for enhanced antibacterial activity against MDR pathogens.

## Key findings

- SaO-Fe3O4NPs and SaO-SeNPs showed significantly lower MIC values than SaO extract and metal nanoparticles alone.
- The nanocomposites exhibited potent antibiofilm activity, outperforming meropenem in some cases.
- TEM and growth curve analysis confirmed the nanocomposites' ability to deform bacterial cells.

## Abstract

The increased prevalence of multidrug-resistant (MDR) pathogens and biofilm-associated infections underscores the urgent need for alternative antimicrobial strategies. In this study, MDR testing revealed lower resistance in Gram-positive bacteria (Staphylococcus pasteuri, Listeria monocytogenes, and Bacillus cereus; 69–77%) than in Gram-negative strains (Proteus mirabilis, Pseudomonas aeruginosa, and Escherichia coli; 83–92%). Magnetite nanoparticles (Fe3O4NPs) and selenium nanoparticles (SeNPs) were synthesized via a green chemical reduction using L-ascorbic acid, followed by their conjugation with Salvia officinalis (SaO) aqueous extract to enhance stability and biological activities. TEM, DLS, XRD, and FT-IR analyses confirmed the nanoscale crystalline structure of the synthesized metal nanoparticles (MNPs) and the successful integration of SaO phytoconstituents into the nanocomposites. Phytochemical characterization further revealed variable adhesion and retention of SaO bioactive compounds within the two nanocomposites. The MIC values of SaO-Fe3O4NPs (0.03–1) and SaO-SeNPs (0.03–0.5 µg/mL) were not only dramatically lower than the SaO extract (125–500 µg/mL) and MNPs (0.5–25 µg/mL), but also comparable to or even exceeded meropenem (0.25–2 µg/mL). Vigorous antibacterial activity validated by TEM, revealing extracellular and intracellular deformations, in accordance with the growth curve inhibition patterns. The nanocomposites also demonstrated potent antibiofilm activity, achieving 32.5–59.5% inhibition with SaO-Fe₃O₄NPs and 30.2–56.7% with SaO-SeNPs, surpassing meropenem, which exhibited maximum inhibition values of 32.5–47.6%.

The online version contains supplementary material available at 10.1038/s41598-026-39983-6.

## Linked entities

- **Chemicals:** L-ascorbic acid (PubChem CID 54670067), meropenem (PubChem CID 441130)
- **Species:** Staphylococcus pasteuri (taxon 45972), Listeria monocytogenes (taxon 1639), Bacillus cereus (taxon 1396), Proteus mirabilis (taxon 584), Pseudomonas aeruginosa (taxon 287), Escherichia coli (taxon 562)

## Full-text entities

- **Diseases:** CLSI (MESH:D007757), cytotoxicity (MESH:D064420), associated infections (MESH:D007239), Brain Heart Infusion (MESH:D000075662)
- **Chemicals:** acetic acid (MESH:D019342), trimethoprim (MESH:D014295), A (MESH:D001151), Iron oxide (MESH:C000499), Fe (MESH:D007501), NaOH (MESH:D012972), Carbapenems (MESH:D015780), beta-lactams (MESH:D047090), agar (MESH:D000362), caffeic acid (MESH:C040048), oxacillin (MESH:D010068), Phenolic acids (MESH:C017616), Meropenem (MESH:D000077731), Fe3+ (-), clindamycin (MESH:D002981), carboxylic acid (MESH:D002264), chloramphenicol (MESH:D002701), ferulic acid (MESH:C004999), thiol (MESH:D013438), azithromycin (MESH:D017963), ethanol (MESH:D000431), crystal violet (MESH:D005840), O (MESH:D010100), FT- (MESH:D005641), rifampin (MESH:D012293), C (MESH:D002244), L-ascorbic acid (MESH:D001205), Metal (MESH:D008670), lipopolysaccharides (MESH:D008070), polyphenols (MESH:D059808), Flavonoids (MESH:D005419), Se (MESH:D012643), quercetin (MESH:D011794), levofloxacin (MESH:D064704), formic acid (MESH:C030544), linezolid (MESH:D000069349), essential oils (MESH:D009822), gentamicin (MESH:D005839), water (MESH:D014867), chlorogenic acid (MESH:D002726), KBr (MESH:C039004), nitrofurantoin (MESH:D009582), ROS (MESH:D017382), doxycycline (MESH:D004318), Na2SeO3 (MESH:D018038), glycopeptides (MESH:D006020), apigenin (MESH:D047310), Magnetite (MESH:D052203), acetonitrile (MESH:C032159), senps (MESH:C059702), luteolin (MESH:D047311), vancomycin (MESH:D014640), fluoroquinolones (MESH:D024841), methanol (MESH:D000432)
- **Species:** Staphylococcus pasteuri (species) [taxon 45972], Listeria monocytogenes (species) [taxon 1639], Homo sapiens (human, species) [taxon 9606], Bacillus cereus (species) [taxon 1396], Salvia officinalis (garden sage, species) [taxon 38868], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas aeruginosa (species) [taxon 287], Proteus mirabilis (species) [taxon 584], Bacillus cereus ATCC 14579 (strain) [taxon 226900]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12996575/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996575/full.md

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Source: https://tomesphere.com/paper/PMC12996575