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Development and in vitro evaluation of buccoadhesive tablets using a new model substrate for bioadhesion measures:
1Dipartimento di Chimica e Tecnologie Farmaceutiche e Alimentari, Università di Genova, Italy.
Drug Development and Industrial Pharmacy
|March 11, 1999
Summary
Mucoadhesive tablets using gelatin with cellulose derivatives were developed for oral drug delivery. Bioadhesion varied with substrate, and drug release followed an erosion-diffusion mechanism.
Area of Science:
- Pharmaceutical Sciences
- Materials Science
Background:
- Mucoadhesive drug delivery systems enhance oral drug absorption and prolong residence time.
- Gelatin and cellulose derivatives (HPC, HPMC, NaCMC) are common polymers for mucoadhesive tablet formulation.
Purpose of the Study:
- To formulate and characterize mucoadhesive tablets using gelatin combined with different cellulose derivatives.
- To evaluate the in vitro bioadhesive properties and drug release mechanisms of these formulations.
Main Methods:
- Mucoadhesive tablets were prepared by direct compression using gelatin/HPC, gelatin/HPMC, and gelatin/NaCMC blends.
- In vitro bioadhesion was assessed using a tensile tester with polypropylene and eggshell membranes.
- Drug release kinetics were studied for metronidazole and benzydamine.
Main Results:
- Bioadhesive properties were significantly influenced by the substrate used for evaluation (polypropylene vs. biological membrane).
- Eggshell membrane provided more reliable bioadhesion data compared to polypropylene.
- All formulations exhibited an anomalous (non-Fickian) erosion-diffusion release mechanism.
Conclusions:
- Gelatin-based mucoadhesive tablets with HPC, HPMC, and NaCMC are feasible for oral drug delivery.
- The choice of substrate is critical for accurate in vitro bioadhesion assessment.
- The observed erosion-diffusion release mechanism is characteristic of swellable mucoadhesive systems.