# Pentamidine-Functionalized Polycaprolactone Nanofibers Produced by Solution Blow Spinning for Controlled Release in Cutaneous Leishmaniasis Treatment

**Authors:** Nerea Guembe-Michel, Paul Nguewa, Gustavo González-Gaitano

PMC · DOI: 10.3390/polym18020170 · Polymers · 2026-01-08

## TL;DR

Researchers developed a new drug delivery system using nanofibers to treat cutaneous leishmaniasis with controlled release of pentamidine.

## Contribution

A novel solution blow spinning method to fabricate pentamidine-loaded nanofibers for sustained drug release in treating leishmaniasis.

## Key findings

- PCL nanofibers showed sustained pentamidine release over time, suitable for topical treatment.
- Released pentamidine demonstrated significant leishmanicidal activity against Leishmania major.
- Gene expression analysis showed drug-induced downregulation of parasite cell division genes and upregulation of drug response genes.

## Abstract

Leishmaniasis, a widespread, neglected infectious disease with limited effective treatments and increasing drug resistance, demands innovative therapeutic approaches. In this study, we report the fabrication of pentamidine (PTM)-loaded polycaprolactone (PCL) nanofibers using solution blow spinning (SBS) as a potential topical delivery system for cutaneous leishmaniasis (CL). Homogeneous PCL fiber mats were produced using a simple SBS set-up with a commercial airbrush after optimizing several working parameters. Drug release studies demonstrated sustained PTM release profile over time, which was mechanistically modeled by utilizing the complete nanofiber diameter distribution, obtained from SEM analysis of the blow-spun material. FTIR and XRD analyses were performed to investigate the drug–polymer interactions, revealing molecularly dispersed PTM at low-proportion drug/polymers and partial crystallinity at high loadings. The released PTM exhibited significant leishmanicidal activity against Leishmania major promastigotes. Biological investigations showed that SBS-formulated PTM treatment was consistent with the downregulation of parasite genes involved in cell division and DNA replication (cycA, cyc6, pcna, top2, mcm4) and upregulation of the drug response gene (prp1). The controlled delivery of PTM within SBS-fabricated PCL nanofibers provides an effective therapeutic approach to tackle CL and, through the incorporation of additional drugs, could be extended to address a broader range of cutaneous infections.

## Linked entities

- **Genes:** CycA (Cyclin A) [NCBI Gene 39340], CYC6 (putative CYC2-like cyclin) [NCBI Gene 5072092], PCNA (proliferating cell nuclear antigen) [NCBI Gene 5111], TOP2A (DNA topoisomerase II alpha) [NCBI Gene 7153], MCM4 (minichromosome maintenance complex component 4) [NCBI Gene 4173], PRP1 (prolactin-related protein 1) [NCBI Gene 281429]
- **Chemicals:** pentamidine (PubChem CID 4735)
- **Diseases:** Leishmaniasis (MONDO:0011989), cutaneous leishmaniasis (MONDO:0005446)
- **Species:** Leishmania major (taxon 5664)

## Full-text entities

- **Diseases:** Leishmaniasis (MESH:D007896), CL (MESH:D016773), infectious disease (MESH:D003141), cutaneous infections (MESH:D007239)
- **Chemicals:** PCL (MESH:C016240), PTM (MESH:D010419)
- **Species:** Leishmania major (species) [taxon 5664]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12846011/full.md

## References

109 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846011/full.md

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Source: https://tomesphere.com/paper/PMC12846011