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Chitosan-poly(acrylic) acid polyionic complex: in vivo study to demonstrate prolonged gastric retention
Susana Torrado1, Pablo Prada, Paloma M de la Torre
1Department of Pharmaceutical Technology, Faculty of Pharmacy, Complutense University, 28040 Madrid, Spain. torrado2@farm.ucm.es
Biomaterials
|November 12, 2003
Summary
This study developed a chitosan-poly(acrylic) acid system for controlled amoxicillin delivery to the stomach. The novel polyionic complexes significantly prolonged gastric residence time, enhancing drug delivery potential.
Area of Science:
- Pharmaceutical Sciences
- Biomaterials Science
- Drug Delivery Systems
Background:
- Effective antibiotic delivery to the stomach is crucial for treating gastric infections.
- Chitosan and poly(acrylic) acid are biocompatible polymers with potential for drug delivery applications.
- Developing controlled-release systems can improve therapeutic efficacy and reduce dosing frequency.
Purpose of the Study:
- To develop a chitosan-poly(acrylic) acid based controlled drug release system for gastric amoxicillin delivery.
- To evaluate the gastric residence time, swelling behavior, and drug release characteristics of the developed formulations.
- To compare the gastric emptying rate of the novel system with a conventional formulation.
Main Methods:
- Preparation of polyionic complexes using amoxicillin, chitosan, and poly(acrylic) acid.
- Non-invasive determination of gastric residence time.
- Swelling studies of the polyionic complexes.
- In vitro drug release studies.
- Gastric emptying rate assessment using the [13C]octanoic acid breath test.
Main Results:
- Polyionic complexes exhibited greater swelling compared to single chitosan formulations.
- Amoxicillin diffusion was effectively controlled by polymer/drug interactions and network mesh size.
- The developed gastric retentive system significantly delayed gastric emptying (mean half-emptying time 164.32 min) compared to the reference (65.06 min).
Conclusions:
- Chitosan-poly(acrylic) acid polyionic complexes show promise as effective systems for controlled gastric drug delivery.
- The enhanced gastric residence time of these complexes can improve localized antibiotic therapy in the stomach.
- This formulation strategy offers a viable approach for targeted gastric drug delivery applications.