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Colon-Targeted Hydrogel Microsphere System Encapsulating Oleic Acid-Emodin for Crohn's Disease Treatment via
Danxi Yan1, Yingqi Wei2, Xijie Ye3
1College of Pharmacy, Shenzhen Technology University, Shenzhen 518118, China.
A novel hydrogel microsphere system (HM@OAE) effectively delivers emodin to the colon for Crohn's disease (CD) treatment. This targeted approach reduces inflammation and restores intestinal integrity, offering a promising therapy for CD patients.
Area of Science:
- Biomaterials Science
- Gastroenterology
- Nanotechnology
Background:
- Crohn's disease (CD) is a chronic inflammatory condition with limited oral treatment efficacy due to poor drug targeting and bioavailability.
- Current therapies face challenges including inadequate colon retention and low drug absorption, necessitating advanced drug delivery systems.
Purpose of the Study:
- To develop a colon-targeted hydrogel microsphere (HM@OAE) system for enhanced emodin delivery in Crohn's disease therapy.
- To improve emodin's bioavailability and solubility using oleic acid (OA) encapsulation within hyaluronic acid (HA) and calcium alginate (CA) hydrogels.
Main Methods:
- Encapsulation of oleic acid-emodin (OAE) into HA/CA hydrogel microspheres (HM@OAE) for oral administration.
- Evaluation of pH-responsive, colon-specific drug release and in vitro anti-inflammatory effects (cytokine reduction, ROS scavenging, ferroptosis inhibition).
- In vivo assessment of HM@OAE efficacy in a dextran sulfate sodium-induced colitis mouse model.
Main Results:
- HM@OAE demonstrated pH-responsive release in the colon, bypassing stomach degradation.
- In vitro studies showed significant reduction in proinflammatory cytokines, reactive oxygen species, and ferroptosis.
- In vivo studies confirmed HM@OAE's therapeutic efficacy, alleviating colonic inflammation and restoring intestinal barrier function.
Conclusions:
- The HM@OAE system represents a promising colon-targeted drug delivery strategy for Crohn's disease.
- This approach enhances emodin's therapeutic potential by improving bioavailability and targeted delivery to the inflamed colon.
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