# Evaluation of liposome-encapsulated Centella asiatica ethanolic extract for enhanced in vitro and in vivo wound healing

**Authors:** Piriya Chonsut, Weeratian Tawanwongsri, Jomkarn Naphatthalung, Julalak Chokpaisarn, Rawiwan Charoensup, Panupong Puttarak, Siau Hui Mah, Atitaya Roumwong, Lavanya Goodla, Auemphon Mordmuang

PMC · DOI: 10.3389/fmedt.2026.1740835 · Frontiers in Medical Technology · 2026-01-23

## TL;DR

This study shows that encapsulating Centella asiatica extract in liposomes improves wound healing in both lab and animal models.

## Contribution

The novel contribution is demonstrating enhanced wound-healing efficacy of liposome-encapsulated Centella asiatica extract compared to non-encapsulated forms.

## Key findings

- LEC reduced inflammation by lowering TNF-α and IL-1β in macrophages.
- LEC improved fibroblast viability and migration in vitro.
- Topical LEC accelerated wound closure in rats to 99.9% by Day 12.

## Abstract

Encapsulating herbal extracts with wound-healing properties in liposomes may enhance their stability and delivery performance. This study evaluated the biological efficacy of a liposome-encapsulated ethanolic extract of Centella asiatica (LEC) using in vitro and in vivo wound-healing models.

The ethanolic extract was incorporated into liposomes using the thin-film hydration method. Anti-inflammatory activity was assessed in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. Cell viability and migration were evaluated in normal human dermal fibroblasts (NHDFs). In vivo wound-healing efficacy was examined using a rat excision wound model with daily topical application of LEC.

LEC significantly reduced TNF-α and IL-1β production in a dose-dependent manner and enhanced fibroblast viability and migratory capacity compared with the crude extract and vitamin E controls. In vivo, topical LEC markedly accelerated wound contraction, achieving 99.9 ± 0.1% closure by Day 12, which was significantly greater than the normal saline-treated control (p < 0.05) and higher than the blank liposome group, while demonstrating comparable efficacy to vitamin E. Histological analysis revealed enhanced re-epithelialization, increased collagen deposition, and reduced inflammatory cell infiltration in LEC-treated wounds.

These findings indicate that liposomal encapsulation enhances the bioactivity of C. asiatica extract during the inflammatory and proliferative phases of wound repair, supporting further development of LEC as a topical wound-healing formulation.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL1B (interleukin 1 beta)
- **Chemicals:** vitamin E (PubChem CID 14985)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** vitamin E (MESH:D014810), LPS (MESH:D008070), C. asiatica extract (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12876173/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12876173/full.md

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Source: https://tomesphere.com/paper/PMC12876173