# Therapeutic Effects of PSL-Loaded PLGA-PEG-PLGA NPs in Allergic Contact Dermatitis Model Mice

**Authors:** Ryo Fujisawa, Ryuse Sakurai, Takeshi Oshizaka, Kenji Mori, Akiyoshi Saitoh, Issei Takeuchi, Kenji Sugibayashi

PMC · DOI: 10.3390/molecules30153292 · Molecules · 2025-08-06

## TL;DR

This study evaluates a new nanoparticle drug delivery system for treating allergic contact dermatitis in mice.

## Contribution

A novel PLGA-PEG-PLGA triblock copolymer nanoparticle is proposed as an improved carrier for prednisolone in treating allergic contact dermatitis.

## Key findings

- PSL-loaded PLGA-PEG-PLGA NPs significantly reduced TNF-α and IL-4 levels in a mouse model of allergic contact dermatitis.
- The nanoparticle formulation was as effective as a PSL ointment at a 40 times lower steroid dose.
- The results suggest PLGA-PEG-PLGA NPs may be more effective than traditional PLGA-based drug delivery systems for ACD treatment.

## Abstract

This study focused on the poly(DL-lactide-co-glycolide)-block-poly(ethylene glycol)-block-poly(DL-lactide-co-glycolide) (PLGA-PEG-PLGA) triblock copolymer, which was recently reported as a novel material for polymeric nanoparticles to replace poly(DL-lactide-co-glycolide) (PLGA) as a drug carrier for prednisolone (PSL), and aimed to evaluate the efficacy of PSL-loaded PLGA-PEG-PLGA nanoparticles (NPs) against allergic contact dermatitis (ACD). PSL-loaded PLGA-PEG-PLGA NPs were prepared using the nanoprecipitation method, and their particle size distribution and mean particle size were measured using dynamic light scattering. 1-Fluoro-2,4-dinitrobenzene (DNFB) was used to create a mouse model of contact hypersensitivity (CHS). PSL-loaded PLGA-PEG-PLGA NPs were administered before sensitization with DNFB, and the therapeutic effect was evaluated by quantifying intracutaneous TNF-α and IL-4 levels suing ELISA. When PSL-loaded PLGA-PEG-PLGA NPs were administered before sensitization, TNF-α expression and IL-4 statements were significantly lower in the PSL-loaded PLGA-PEG-PLGA NP group than in the non-treated group. No significant difference was observed between the PSL-loaded PLGA-PEG-PLGA NP and PSL-loaded ointment groups, even though the steroid dose was 40 times lower than in the PSL-containing ointment. These results suggest that PSL-loaded PLGA-PEG-PLGA NPs may have a better effect in the treatment of ACD than PSL-loaded PLGA NPs.

## Linked entities

- **Chemicals:** prednisolone (PubChem CID 5755), 1-Fluoro-2,4-dinitrobenzene (PubChem CID 6264), IL-4 (PubChem CID 171905173)
- **Diseases:** allergic contact dermatitis (MONDO:0006525)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** ACD (MESH:D017449), CHS (MESH:D003877)
- **Chemicals:** PSL (MESH:D011239), steroid (MESH:D013256), PLGA (MESH:D000077182), 1-Fluoro-2,4-dinitrobenzene (MESH:D004139), poly(ethylene glycol (MESH:D011092), PLGA-PEG-PLGA (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12348954/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12348954/full.md

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Source: https://tomesphere.com/paper/PMC12348954