# A Nasal Spray Combining Camostat with a Natural Polysaccharide for the Prevention of Viral Infection via Nasal Mucosal Barrier Formation and Entry Inhibition

**Authors:** Yujeong Na, Byeongyong Kim, Dongjin Lee, Jongseo Choi, Sangeun Cho, Kyungmin Lee, Gwanyoung Kim, Eunyoung Cho, Jonggeun Kim, Seong Kug Eo, Sokho Kim

PMC · DOI: 10.3390/ijms27021053 · 2026-01-21

## TL;DR

This study develops a nasal spray combining camostat and xanthan gum to prevent respiratory viral infections by forming a protective barrier and inhibiting virus entry.

## Contribution

The novel dual-action nasal spray formulation offers a non-invasive method to prevent viral infection at the nasal mucosa.

## Key findings

- The combination of xanthan gum and camostat showed significantly enhanced muco-adhesiveness compared to individual components.
- The formulation inhibited viral penetration and replication in human nasal epithelial cells and an influenza-infected mouse model.
- The spray suppressed TMPRSS2 expression, a key factor in influenza virus entry, in mouse lung tissues.

## Abstract

In recent years, numerous researchers have investigated various preventive strategies against respiratory viruses that pose a threat to human health. This study aims to develop a nasal spray formulation based on the natural polysaccharide xanthan gum (XG) and camostat, and to evaluate its dual protective mechanism at the nasal mucosa, the primary entry point for respiratory viral infections. The efficacy of the formulation was assessed through physicochemical characterization, cell-based assays, and animal experiments. Initially, muco-adhesiveness was evaluated by monitoring the drying dispersion area of the test formulation over time on a Petri dish. The combination of XG and camostat exhibited a dispersion area more than ten times larger than that of each component used alone. The antiviral efficacy was demonstrated in both human nasal epithelial cells (HNEc) and an influenza-infected mouse model. The cell-based experiment demonstrated a significant inhibition of viral penetration and replication. Furthermore, suppression of transmembrane protease, serine 2 (TMPRSS2) expression, a key factor in influenza virus entry, was observed in mouse lung tissues. These findings suggest that the Camostat–Polysaccharide Dual-Action Nasal Spray (CPNS), currently under development, holds promise as a non-invasive, first-line barrier to prevent the initial infection and replication of respiratory viruses.

## Linked entities

- **Proteins:** TMPRSS2 (transmembrane serine protease 2)
- **Chemicals:** camostat (PubChem CID 2536)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** TMPRSS2 (transmembrane serine protease 2) [NCBI Gene 7113] {aka PRSS10}
- **Diseases:** influenza (MESH:D007251), Viral Infection (MESH:D014777), infected (MESH:D007239)
- **Chemicals:** Polysaccharide (MESH:D011134), Camostat (MESH:C034532), Natural (-), XG (MESH:C002563)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12841919/full.md

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Source: https://tomesphere.com/paper/PMC12841919