# Advanced therapeutic strategy for managing surgical site infections with natural nanoemulsion-antimicrobial combination

**Authors:** Fatma Alshehri, Nada K. Alharbi, AbdelNaser Zaid, Amira H. Eltrawy, Shereen Fawzy, Attia M. Gabr, Sawsan A. Zaitone, Majid Alhomrani, Abdulhakeem S. Alamri, Rasha A. Mosbah, Rana Elshimy, Abdallah Tageldein Mansour, Mahmoud M. Bendary

PMC · DOI: 10.3389/fphar.2025.1617184 · Frontiers in Pharmacology · 2025-07-02

## TL;DR

This study explores a natural nanoemulsion combined with antibiotics to treat surgical site infections caused by drug-resistant bacteria, showing improved healing and bacterial clearance.

## Contribution

The study introduces a chitosan-based nanoemulsion that enhances antibiotic efficacy against multidrug-resistant surgical site infection pathogens.

## Key findings

- Chitosan nanoemulsion significantly improved amikacin's effectiveness against resistant bacterial strains.
- Combination therapy reduced bacterial loads in both Gram-negative and Gram-positive infections.
- In vivo studies showed near-complete bacterial clearance and improved wound healing by day 12.

## Abstract

Surgical site infections (SSIs) are a significant cause of morbidity and mortality, often complicated by multidrug-resistant (MDR) pathogens and biofilm formation. This study evaluates the potential of a natural nanoemulsion containing chitosan, lavender, and curcumin, in combination with antimicrobial drugs, for treating SSIs.

A comprehensive approach combining phenotypic and genotypic analyses, along with in vitro and in vivo studies, was used to assess the efficacy and safety of the combination therapy.

The most common SSI pathogens identified were Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii, with 50% exhibiting MDR, biofilm formation, and multiple virulence factors. Chitosan nanoemulsion showed the lowest minimum inhibitory concentration (MIC) (300–500 μg/mL), although it exceeded the cytotoxicity safety threshold (200 μg/mL). However, it significantly enhanced the antimicrobial activity of amikacin, resensitizing resistant strains at safe concentrations. The combination therapy of amikacin and chitosan nanoemulsion demonstrated superior efficacy in reducing bacterial loads in both Gram-negative and Gram-positive infections. In vivo studies showed near-complete bacterial clearance by day 12. Histopathological analysis revealed enhanced wound healing, reduced inflammation, and restored tissue function. The combination of amikacin and chitosan nanoemulsion presents a promising therapeutic strategy for managing SSIs caused by MDR pathogens, improving bacterial eradication and wound healing.

This study highlights chitosan nanoemulsion as an adjuvant therapy to combat antimicrobial resistance, enhance antibiotic efficacy, and improve SSI treatment outcomes. Further clinical studies are needed to optimize its use in patient care.

## Linked entities

- **Chemicals:** chitosan (PubChem CID 129662530), curcumin (PubChem CID 969516), amikacin (PubChem CID 37768)
- **Species:** Staphylococcus aureus (taxon 1280), Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573), Pseudomonas aeruginosa (taxon 287), Acinetobacter baumannii (taxon 470)

## Full-text entities

- **Diseases:** SSIs (MESH:D013530), infections (MESH:D007239), cytotoxicity (MESH:D064420), inflammation (MESH:D007249)
- **Chemicals:** curcumin (MESH:D003474), Chitosan (MESH:D048271), amikacin (MESH:D000583)
- **Species:** Acinetobacter baumannii (species) [taxon 470], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Staphylococcus aureus (species) [taxon 1280], Klebsiella pneumoniae (species) [taxon 573], Pseudomonas aeruginosa (species) [taxon 287]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12263955/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12263955/full.md

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Source: https://tomesphere.com/paper/PMC12263955