Optimized Enoxolone-Loaded Microsponges for Drug Delivery: A Design of Experiments Approach
Juste Baranauskaite, Sedef Sefer, Augusta Zevzikoviene, Andrejus Zevzikovas, Liudas Ivanauskas

TL;DR
This study develops optimized microsponges for enoxolone delivery, showing improved drug release for potential treatment of chronic periodontitis.
Contribution
A novel enoxolone-loaded microsponge formulation optimized via design of experiments for enhanced drug delivery.
Findings
Optimized microsponges showed a particle size of 142.8 ± 10.02 µm and entrapment efficiency of 80.3 ± 1.99%.
The optimized formulation exhibited a 1.29 times higher release rate compared to pure enoxolone (p ≤ 0.05).
Microsponge-based systems show potential for topical treatment of chronic periodontitis.
Abstract
Enoxolon is widely recognized for its pharmacological potential, exhibiting antioxidant, anti-inflammatory, anticancer, and antiviral properties. Objectives: This study aimed to develop an enhanced formulation of enoxolone-loaded microsponges as a novel drug delivery system. A design of experiments (DoE) approach was employed for the optimization process. Methods: The microsponges were produced using the quasi-emulsion technique. The selected formulation was evaluated for yield, particle size, and entrapment efficiency. Furthermore, the microsponges were incorporated into a 1% MC solution matrix, and in vitro release studies were performed to assess their drug delivery performance. Results: The optimal formulation was determined through the DoE methodology, which involved varying the concentrations of methylcellulose (MC) (0.55–1.87%, w/w), polyvinyl alcohol (PVA) (0.5–1%, w/w), and…
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Taxonomy
TopicsAdvanced Drug Delivery Systems · Drug Solubulity and Delivery Systems · Advancements in Transdermal Drug Delivery
