# A Charge‐Adhesive Targeted DNA Gel Bandage for the Precision Treatment of Inflammatory Bowel Disease

**Authors:** Peifen Lu, Hongxiu Yuan, Gang Wang, Tao Cheng, Lie Li, Yixi Dong, Runyu Zhao, Xuerui Zhang, Jianwei Jiao, Jin Jiao

PMC · DOI: 10.1002/advs.202509419 · Advanced Science · 2025-07-20

## TL;DR

A new DNA-based gel bandage targets inflamed gut areas to treat inflammatory bowel disease with high precision and reduced side effects.

## Contribution

A charge-adhesive DNA gel bandage is introduced for targeted IBD treatment through dual-specific localization and anti-inflammatory effects.

## Key findings

- DNAgb targets inflamed mucosa via electrostatic interactions and aptamer-mediated affinity targeting.
- DNAgb inhibits NF-κB signaling and reduces secretion of inflammatory factors.
- Transcriptome analysis reveals DNAgb's role in repressing inflammation in IBD.

## Abstract

The exacerbation and recurrence of inflammatory bowel disease (IBD) are closely related to the overactivation of the immune system and the destruction of the intestinal mucosa. Current small‐molecule and biopharmaceutical therapies for IBD are often limited by off‐target effects, low bioavailability, and poor treatment outcomes, leading to systemic side effects and severe complications. To address these challenges, DNA gel bandage (DNAgb) designed to block immune cell homing and inhibit inflammatory responses are proposed. DNAgb is a negatively charged “sticky excipient” formed by a rolling circle amplification production hydrogel and an integrin α4 aptamer (ApITGA4) ‐guided tetrahedral DNA nanostructure. This unique design enables dual‐specific localization to inflamed mucosa through electrostatic interactions and ApITGA4‐mediated affinity targeting. Our studies have demonstrated that DNAgb exhibits precise targeting, superior stability, and robust anti‐inflammatory efficacy. It effectively inhibits activation of the NF‐κB signaling pathway, decreases the secretion of inflammatory factors and reshapes the immune microenvironment. Transcriptome analysis further reveals the underlying mechanism of DNAgb in IBD therapy, highlighting its role in inflammation repression. Therefore, DNAgb provides a promising strategy for local therapeutic agents that effectively inhibit the inflammatory response and provides a new and effective choice for the treatment of IBD.

DNA gel bandage (DNAgb) is designed to precisely target the site of inflammation of IBD, by achieving dual specific localization of inflamed mucosa through electrostatic interactions and ApITGA4‐mediated affinity targeting. DNAgb effectively the activation of inflammatory pathways and reshapes the immune microenvironment. Therefore, DNAgb provides a promising strategy for local therapeutic agents that effectively inhibit the inflammatory response of IBD.

## Linked entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790]
- **Diseases:** inflammatory bowel disease (MONDO:0005265), IBD (MONDO:0005265)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, ITGA4 (integrin subunit alpha 4) [NCBI Gene 3676] {aka CD49D, IA4}
- **Diseases:** IBD (MESH:D015212), inflammation (MESH:D007249)
- **Chemicals:** ApITGA4 (-)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12520488/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12520488/full.md

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Source: https://tomesphere.com/paper/PMC12520488