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Targeting pathophysiological changes using biomaterials-based drug delivery systems: A key to managing inflammatory
Sahar Mohajeri1, Saeed Moayedi1, Shabnam Mohajeri2
1Department of Pharmaceutical Biomaterials, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
New biomaterials-based drug delivery systems offer promising treatments for inflammatory bowel disease (IBD). Targeting specific gastrointestinal changes in IBD patients can improve therapeutic efficacy.
Area of Science:
- Biomaterials Science
- Gastroenterology
- Drug Delivery Systems
Background:
- Inflammatory bowel disease (IBD) affects millions globally, with current treatments often inadequately managing symptoms and impacting quality of life.
- The need for novel therapeutic strategies for IBD is critical due to treatment limitations.
Purpose of the Study:
- To explore the potential of biomaterials-based drug delivery systems for improved inflammatory bowel disease (IBD) management.
- To discuss how targeting specific pathophysiological changes in the IBD gastrointestinal tract can inform the design of advanced drug delivery systems.
Main Methods:
- Review and discussion of biomaterials properties (biocompatibility, sustained release).
- Analysis of pathophysiological alterations in the inflamed colon of IBD patients (pH, surface charge, reactive oxygen species, biomolecules).
- Conceptual framework for designing targeted biomaterial-based systems.
Main Results:
- Biomaterials offer unique advantages for drug delivery in IBD due to their properties.
- Understanding IBD-specific gastrointestinal changes is key for rational design of drug delivery systems.
- Targeting these changes can enhance therapeutic outcomes.
Conclusions:
- Biomaterials-based drug delivery systems represent a promising avenue for developing more effective IBD treatments.
- Tailoring delivery systems to the unique pathophysiological environment of the inflamed colon is crucial for efficient IBD management.
- This approach provides a roadmap for future research in IBD therapeutics.
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