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AAPS PharmSciTech ; 25(5): 94, 2024 May 06.
Artigo em Inglês | MEDLINE | ID: mdl-38710898

RESUMO

This study introduces and assesses the potential of a Luliconazole-loaded nanofiber (LUL-NF) patch, fabricated through electrospinning, for enhancing topical drug delivery. The primary objectives involve evaluating the nanofiber structure, characterizing physical properties, determining drug loading and release kinetics, assessing antifungal efficacy, and establishing the long-term stability of the NF patch. LUL-NF patches were fabricated via electrospinning and observed by SEM at approximately 200 nm dimensions. The comprehensive analysis included physical properties (thickness, folding endurance, swelling ratio, weight, moisture content, and drug loading) and UV analysis for drug quantification. In vitro studies explored sustained drug release kinetics, while microbiological assays evaluated antifungal efficacy against Candida albicans and Aspergillus Niger. Stability studies confirmed long-term viability. Comparative analysis with the pure drug, placebo NF patch, LUL-NF patch, and Lulifod gel was conducted using agar diffusion, revealing enhanced performance of the LUL-NF patch. SEM analysis revealed well-defined LUL-NF patches (0.80 mm thickness) with exceptional folding endurance (> 200 folds) and a favorable swelling ratio (12.66 ± 0.73%). The patches exhibited low moisture uptake (3.4 ± 0.09%) and a moisture content of 11.78 ± 0.54%. Drug loading in 1 cm2 section was 1.904 ± 0.086 mg, showing uniform distribution and sustained release kinetics in vitro. The LUL-NF patch demonstrated potent antifungal activity. Stability studies affirmed long-term stability, and comparative analysis highlighted increased inhibition compared to a pure drug, LUL-NF patch, and a commercial gel. The electrospun LUL-NF patch enhances topical drug delivery, promising extended therapy through single-release, one-time application, and innovative drug delivery strategies, supported by thorough analysis.


Assuntos
Antifúngicos , Aspergillus niger , Candida albicans , Sistemas de Liberação de Medicamentos , Liberação Controlada de Fármacos , Imidazóis , Nanofibras , Antifúngicos/administração & dosagem , Antifúngicos/farmacologia , Antifúngicos/química , Nanofibras/química , Candida albicans/efeitos dos fármacos , Aspergillus niger/efeitos dos fármacos , Sistemas de Liberação de Medicamentos/métodos , Imidazóis/química , Imidazóis/administração & dosagem , Imidazóis/farmacologia , Preparações de Ação Retardada , Testes de Sensibilidade Microbiana/métodos , Portadores de Fármacos/química , Estabilidade de Medicamentos
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