# Nanostructured Dual-Delivery System with Antioxidant and Synergistic Approach for Targeted Dermal Treatment

**Authors:** Lucia Dzurická, Julie Hoová, Barbora Dribňáková, Petra Skoumalová, Paola Rappelli, Ivana Márová

PMC · DOI: 10.3390/ijms26199485 · 2025-09-28

## TL;DR

A new nanofiber-based wound dressing combines antioxidants and antibiotics to fight infection and promote healing.

## Contribution

A novel dual-delivery system using PHB-nanofibers and liposomes for targeted release of bioactive agents is first reported.

## Key findings

- The system showed synergistic antimicrobial effects against multiple bacteria with FIC indices of 0.09–0.73.
- The highest antimicrobial increase (~73.56%) was observed against Staphylococcus epidermidis.
- The dressing retained bioactive properties and supported wound re-epithelisation despite slight immune response stimulation.

## Abstract

Biocompatible nanofibrous dressings integrating bioactive compounds with antioxidative and antimicrobial properties offer a promising solution for effective wound healing. In the presented study, we developed a novel dual-delivery system by combining forcespun nanofibres with poly(3-hydroxybutyrate) (PHB)-liposomes to enhance bioavailability and enable targeted release of bioactive agents (eugenol, thymol, curcumin, ampicillin, streptomycin, gentamicin). These agents exhibited notable antioxidant activity (2.27–2.33 mmol TE/g) and synergistic or partially synergistic antimicrobial effects against E. coli, M. luteus, S. epidermidis, and P. aeruginosa ( Fractional Inhibitory Concentration index 0.09–0.73). The most potent combinations, particularly thymol, eugenol, and ampicillin, were encapsulated in the nanofibre–liposomal matrix. The successful preparation of a new combined delivery system was confirmed by structural analysis using Electron and Fluorescence Microscopy. The dual-composite materials retained the antimicrobial properties of the individual compounds upon release, with the highest increases of ~73.56% against S. epidermidis. Cell viability and in vitro immunology assays using the human keratinocyte cell line (HaCaT) showed a slight decrease in viability and immune response stimulation, while not impairing wound re-epithelisation. These findings highlight the potential of firstly reported novel carrier utilising both PHB-nanofibres and PHB-liposomes, exhibiting simultaneous antioxidant and antimicrobial activity as promising candidates for the treatment of infected wounds under oxidative stress.

## Linked entities

- **Chemicals:** eugenol (PubChem CID 3314), thymol (PubChem CID 6989), curcumin (PubChem CID 969516), ampicillin (PubChem CID 6249), streptomycin (PubChem CID 5297), gentamicin (PubChem CID 3467), PHB (PubChem CID 135)
- **Species:** Escherichia coli (taxon 562), Micrococcus luteus (taxon 1270), Staphylococcus epidermidis (taxon 1282), Pseudomonas aeruginosa (taxon 287)

## Full-text entities

- **Diseases:** infected (MESH:D007239)
- **Chemicals:** streptomycin (MESH:D013307), curcumin (MESH:D003474), gentamicin (MESH:D005839), ampicillin (MESH:D000667), PHB (MESH:C003182), eugenol (MESH:D005054), thymol (MESH:D013943)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12525100/full.md

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Source: https://tomesphere.com/paper/PMC12525100