# ROS-triggerable dual nanocoated probiotics for inflammatory bowel disease treatment

**Authors:** Guangze Sang, Sizhen Wang, Qiwei Tai, Yunchang Zhang, Xufang Wang, Baoling Yan, Weiwei Jiang, Zhendong Chen, Linhong Sun, Jiao Zhou, Xiaoxian Wu, Zi Ye, Feng Yang, Jun Luo, Beibei Guo

PMC · DOI: 10.1080/10717544.2026.2630460 · Drug Delivery · 2026-02-14

## TL;DR

This study develops ROS-triggerable probiotics with a dual nanocoating to treat inflammatory bowel disease more effectively and safely.

## Contribution

A dual nanocoating system for probiotics that responds to ROS and improves treatment of IBD is introduced.

## Key findings

- The nano-coated probiotics showed enhanced digestive stability and targeted drug release in inflamed areas.
- The combination therapy demonstrated therapeutic effects in a mouse model of ulcerative colitis.
- The method integrates biological and drug therapies to reduce IBD recurrence and side effects.

## Abstract

Inflammatory bowel disease (IBD), an immune-mediated chronic gastrointestinal disease, is difficult to treat because its specific pathogenic mechanisms are currently unclear, and its recurrence rate is high. Probiotic therapies have been used to treat IBD; however, challenges, including poor digestive stability and unstable treatment effects, remain. Catechins are natural flavonoids with anti-inflammatory and anti-oxidant properties. In this study, we link catechins to the amino side chain of ethylene glycol chitosan through phenylboronic acid as a nano coating for probiotics, and enhance their stability under acidic conditions with sodium alginate. The resulting double-layer nano coating system is triggered by reactive oxygen species (ROS) for probiotic-small molecule combination therapy. After oral administration, the nano coating helps probiotics stabilize and pass through the harsh digestive environment, respond to the high ROS environment at the site of inflammation, and release anti-inflammatory drugs. The coating breaks down and adheres to the cell surface while releasing probiotics to regulate the intestinal microbiota environment and achieve combined therapy. The method exerts a certain therapeutic effect in a dextran sulfate sodium (DSS)-induced mouse model of ulcerative colitis. This study combines traditional targeted drug therapy concepts with biological therapies to improve IBD treatment efficacy and reduce side effects.

## Linked entities

- **Chemicals:** catechins (PubChem CID 1203), phenylboronic acid (PubChem CID 66827)
- **Diseases:** inflammatory bowel disease (MONDO:0005265), ulcerative colitis (MONDO:0005101)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** ulcerative colitis (MESH:D003093), IBD (MESH:D015212), inflammatory drugs (MESH:D000081015), inflammation (MESH:D007249), gastrointestinal disease (MESH:D005767)
- **Chemicals:** ethylene glycol chitosan (-), phenylboronic acid (MESH:C010686), Catechins (MESH:D002392), DSS (MESH:D016264), flavonoids (MESH:D005419), sodium alginate (MESH:D000464), ROS (MESH:D017382)
- **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/PMC12912239/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12912239/full.md

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Source: https://tomesphere.com/paper/PMC12912239