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Updated: Jan 31, 2026

Chinese Herbal Retention Enema for the Treatment of Ulcerative Colitis
Published on: May 16, 2025
Synergistic Regulation of Ferroptosis via an Oral Solid Lipid Nanocomplex-Embedded Inulin Gel for Targeted Ulcerative
Luolan Ouyang1, Jia Ke1, Shanshan Xiang1
1College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, P. R. China.
A novel oral therapy targets ferroptosis, a cell death pathway implicated in ulcerative colitis (UC). This synergistic approach using a colon-targeted gel system shows promise for managing UC by reducing inflammation and restoring gut health.
Area of Science:
- Gastroenterology
- Nanomedicine
- Cell Biology
Background:
- Ulcerative colitis (UC) is a chronic inflammatory colon disorder with limited treatment options.
- Ferroptosis, a type of programmed cell death, plays a significant role in UC development.
- Targeting ferroptosis presents a potential therapeutic strategy for UC.
Purpose of the Study:
- To develop an oral, colon-targeted therapy for UC based on synergistic ferroptosis regulation.
- To investigate the therapeutic efficacy of a solid lipid nanocomplex-embedded inulin gel (SLN/Que&OA@Gel) for UC.
Main Methods:
- Encapsulation of oleic acid (OA) and quercetin (Que) in solid lipid nanoparticles (SLNs) for enhanced bioavailability.
- Embedding SLNs in an inulin gel matrix for colon targeting and sustained release.
- In vivo evaluation of the SLN/Que&OA@Gel system in a UC model.
Main Results:
- The SLN/Que&OA@Gel system effectively delivered OA and Que to the colon.
- OA modulated lipid composition to reduce ferroptosis, while Que scavenged reactive oxygen species (ROS).
- In vivo studies showed alleviation of intestinal damage, restoration of barrier integrity, and reduced inflammation in UC models.
Conclusions:
- The developed SLN/Que&OA@Gel system offers a synergistic approach to regulate ferroptosis and remodel the microenvironment.
- This strategy presents a promising therapeutic avenue for managing ulcerative colitis.
- Colon-targeted delivery and dual drug action enhance therapeutic outcomes for UC.
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