Azo-linked 5-ASA-coumarin prodrug: Fluorescent tracking for colonic drug release in UC treatment
- Wenchao Wang 1, Yingjie Chen 2, Yuan Wang 3, Yijian Wang 1, Wenjing Zhang 1, Keke Dai 1, Wujun Geng 4, Sicheng Tang 5
- Wenchao Wang 1, Yingjie Chen 2, Yuan Wang 3
- 1Department of Pain, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China; Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and BrainHealth), Wenzhou Medical University, Zhejiang, China.
- 2Cixi Biomedical Research Institute, Wenzhou Medical University, Zhejiang, China; University of Chinese Academy of Sciences, Wenzhou Institute, Zhejiang, China.
- 3University of Chinese Academy of Sciences, Wenzhou Institute, Zhejiang, China; School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Zhejiang, China.
- 4Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and BrainHealth), Wenzhou Medical University, Zhejiang, China.
- 5University of Chinese Academy of Sciences, Wenzhou Institute, Zhejiang, China.
- 0Department of Pain, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China; Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision and BrainHealth), Wenzhou Medical University, Zhejiang, China.
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View abstract on PubMed
Summary
This summary is machine-generated.A new theranostic prodrug system enables simultaneous delivery and tracking of 5-aminosalicylic acid (5-ASA) for ulcerative colitis (UC) treatment. This system allows real-time monitoring of drug release and biodistribution for personalized medicine.
Area Of Science
- Pharmaceutical Sciences
- Biomedical Engineering
- Drug Delivery Systems
Background
- Theranostic prodrugs are crucial for real-time, non-invasive monitoring of drug release and biodistribution.
- Optimizing therapeutic efficacy and guiding personalized medication requires advanced drug delivery systems.
Purpose Of The Study
- To develop a colon-targeted theranostic prodrug system for simultaneous delivery and tracking of 5-aminosalicylic acid (5-ASA).
- To enable real-time monitoring of drug release and biodistribution for ulcerative colitis (UC) treatment.
Main Methods
- A theranostic prodrug (P1) was synthesized, linking 5-ASA to a fluorescent reporter (7-AMC) via an azo bond.
- P1 was encapsulated in polymeric micelles (PM) for enhanced solubility and targeted delivery to inflamed colonic tissues.
- In vitro studies assessed stability and biocompatibility; in vivo studies used a UC mouse model for efficacy and biodistribution tracking.
Main Results
- The P1-loaded PM system demonstrated stability, biocompatibility, and selective activation in the colon.
- Targeted delivery of 5-ASA to the inflamed colon was achieved, effectively reducing colitis symptoms.
- In situ activation allowed real-time, non-invasive visualization of drug release and biodistribution.
Conclusions
- The developed colon-targeted theranostic prodrug system offers a promising strategy for simultaneous 5-ASA therapy and tracking in UC.
- This approach facilitates personalized medication and improved therapeutic outcomes through real-time monitoring.
- The theranostic system provides valuable insights for optimizing drug delivery and treatment strategies.
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