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Optimized Enoxolone-Loaded Microsponges for Drug Delivery: A Design of Experiments Approach
Juste Baranauskaite1, Sedef Sefer1, Augusta Zevzikoviene2
1Department of Pharmaceutical Technology, Faculty of Pharmacy, Yeditepe University, Kayisdagi Cad., Atasehir, 34755 Istanbul, Türkiye.
This study developed optimized enoxolone-loaded microsponges for enhanced drug delivery. The novel formulation showed a significantly higher release rate, suggesting potential for treating chronic periodontitis.
Area of Science:
- Pharmacology and Drug Delivery
- Materials Science
Background:
- Enoxolon possesses significant antioxidant, anti-inflammatory, anticancer, and antiviral properties.
- Novel drug delivery systems are needed to enhance enoxolon's therapeutic efficacy.
Purpose of the Study:
- To develop and optimize enoxolone-loaded microsponges using a design of experiments (DoE) approach.
- To evaluate the physicochemical properties and in vitro drug release of the optimized formulation.
Main Methods:
- Microsponges were fabricated using the quasi-emulsion technique.
- A DoE methodology was used to optimize methylcellulose, polyvinyl alcohol, and Tween 80 concentrations.
- Physicochemical characterization included yield, particle size, and entrapment efficiency.
- In vitro release studies were conducted comparing the microsponge formulation to pure enoxolon.
Main Results:
- The optimized formulation achieved a particle size of 142.8 ± 10.02 µm and an entrapment efficiency of 80.3 ± 1.99%.
- The optimized microsponge formulation exhibited a 1.29 times higher release rate compared to pure enoxolon (p ≤ 0.05).
Conclusions:
- Microsponge-based delivery systems offer a promising platform for enoxolon.
- This optimized formulation demonstrates potential for the topical treatment of chronic periodontitis.
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