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Advances in colonic drug delivery
1The School of Pharmacy, University of London, London, England, UK. abdul.basit@ulsop.ac.uk
Drugs
|September 16, 2005
Summary
Colonic drug delivery systems aim to treat local diseases and improve drug absorption. Universal polysaccharide systems show promise by utilizing the colon
Area of Science:
- Gastroenterology
- Pharmaceutics
- Drug Delivery Systems
Background:
- Targeting drug delivery to the colon is crucial for treating local gastrointestinal disorders like inflammatory bowel disease and colorectal cancer.
- The colon is also recognized as a significant route for systemic drug absorption.
- Current challenges include limitations in specificity, manufacturing complexity, and cost of existing and developmental colonic drug delivery systems.
Purpose of the Study:
- To review and evaluate various strategies for colonic drug targeting.
- To identify the most promising approaches for effective and practical colonic drug delivery.
- To highlight the advantages of microflora-responsive systems.
Main Methods:
- Review of existing literature on colonic drug delivery systems.
- Analysis of strategies based on gastrointestinal tract features (pH, transit time, pressure, microflora).
- Evaluation of commercialized and developmental systems, including coated systems, prodrugs, and polysaccharide-based systems.
Main Results:
- Commercialized systems like pH-dependent coatings and bacterial-activated prodrugs have limitations.
- Many developmental systems face challenges in manufacturing, cost, and site-specificity.
- Universal polysaccharide systems, leveraging the colon's abundant microflora, are identified as highly promising.
Conclusions:
- Exploiting the colon's unique microflora offers a practical and effective approach for targeted drug delivery.
- Universal polysaccharide systems represent a favorable strategy due to their practicality and reliance on colonic bacteria.
- Further development in polysaccharide-based systems could overcome current limitations in colonic drug targeting.