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Disintegrants combination: development and optimization of a cefadroxil fast disintegrating tablet
Najia Rahim1, Syed Baqir-Shyum Naqvi2, Rehana Bibi2
1Department of Pharmaceutics, Dow College of Pharmacy, Dow University of Health Sciences, Karachi, Sindh, Pakistan.
This study optimized cefadroxil fast disintegrating tablets (FDTs) using croscarmellose and crospovidone. Formulation F9 demonstrated superior pharmacotechnical properties and improved dissolution, suggesting enhanced bioavailability for patient compliance.
Area of Science:
- Pharmaceutical Technology
- Drug Delivery Systems
- Formulation Science
Background:
- Fast disintegrating tablets (FDTs) offer advantages for specific patient populations and improved bioavailability.
- Optimizing FDTs is crucial for enhancing patient compliance and therapeutic efficacy.
- Cefadroxil is an antibiotic that can benefit from improved dosage form design.
Purpose of the Study:
- To design and optimize cefadroxil fast disintegrating tablets (FDTs).
- To evaluate the impact of croscarmellose and crospovidone on FDT properties.
- To identify a formulation with optimal pharmacotechnical attributes and enhanced bioavailability.
Main Methods:
- Utilized central composite design with croscarmellose and crospovidone as independent variables.
- Employed Design-Expert software for optimization and response surface analysis.
- Assessed various pharmacopeial and non-pharmacopeial parameters for tablet quality.
Main Results:
- Formulations F3, F8, and F9 exhibited promising results.
- Formulation F9, containing 15mg croscarmellose and 33.075mg crospovidone, showed excellent pharmacotechnical attributes and stability.
- F9 demonstrated rapid dissolution, with 90% drug release (t90%) in over 2 minutes.
Conclusions:
- The optimized cefadroxil FDT formulation (F9) possesses favorable characteristics for pharmaceutical application.
- The study successfully identified optimal levels of disintegrants for cefadroxil FDTs.
- The developed FDTs are expected to improve cefadroxil bioavailability and patient compliance.
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