Visionary NanoBoost: Revolutionizing ocular treatment with positively charged Leciplex for enhanced Fenticonazole nitrate ocular delivery

This work outlines the formulation and characterization of Fenticonazoleloaded LeciPlex (FCN-LPX), adopting a simple blending technique for the eradication of oculomycosis. Fenticonazole nitrate (FCN) is a pleiotropic fungistatic and fungicidal agent with sparse aqueous solubility, hampering its transcorneal permeation. Three independent factors were probed using a 2 3 factorial design (2 blocks, 2 replicates), namely, X 1 : Cationic surfactant type, X 2 : Amount of cationic surfactant (mM), and X 3 : Amount of soybean phosphatidyl choline (mM). The optimized formulation exhibited remarkable entrapment efficiency (82.74 % ± 0.67 %), as verified by DSC and FT-IR analysis. TEM imaging revealed uniformly nanosized vesicles (189.95 ± 2.90 nm) with a robust positive zeta potential (41.35 ± 2.62 mV), which preserved its stability following gamma sterilization and storage. The optimum FCN-LPX demonstrated a bi-phasic release pattern (48.18 % ± 5.65 % at 4 H and 92.85 % ± 6.77 % at 24 H) and notable mucoadhesive properties, ensuring complete drug release. Safety assessments, including pH, surface tension, and refractive index measurements, along with histopathological evaluation, confirmed the formulation's safety profile. Furthermore, FCN-LPX achieved superior ex-vivo transcorneal permeation (3.3-fold) and deeper in-vivo corneal uptake (2.4-fold) compared to conventional FCN suspension. Microbiological analysis highlighted the enhanced antifungal activity of FCN-LPX, evidenced by a larger inhibition zone (11 %), significantly lower minimal inhibitory and fungicidal concentrations (8-fold), as well as improved fungal biofilm inhibition and prolonged antifungal effect. In conclusion, FCN-LPX is a propitious nanoformulation for the effective eradication of persistent oculomycosis. • FCN-LPX was prepared using a simple blending technique for oculomycosis. • 2 3 factorial design optimized surfactant and phosphatidyl choline levels. • TEM confirmed nanosized vesicles with positive zeta potential and stability. • FCN-LPX showed bi-phasic release and mucoadhesion, ensuring complete release. • FCN-LPX enhanced antifungal activity with 8-fold lower MFC and MIC values.

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Publication Details

Journal
Journal of Drug Delivery Science and Technology
Published
2025-09-02
DOI
https://doi.org/10.1016/j.jddst.2025.107477
Citations
4
Primary Topic
Ocular Infections and Treatments
Type
article
Field-Weighted Citation Impact
6.83
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article

Visionary NanoBoost: Revolutionizing ocular treatment with positively charged Leciplex for enhanced Fenticonazole nitrate ocular delivery

Michael M. Farag, Eman Abdelhakeem, Heba Attia, Asmaa Ashraf Nemr et al.
4 citations
Journal of Drug Delivery Science and Technology
Ocular Infections and Treatments
6.83
article

Visionary NanoBoost: Revolutionizing ocular treatment with positively charged Leciplex for enhanced Fenticonazole nitrate ocular delivery

Michael M. Farag, Eman Abdelhakeem, Heba Attia, Asmaa Ashraf Nemr, Doaa Hegazy
article en
4 citations

Abstract

This work outlines the formulation and characterization of Fenticonazoleloaded LeciPlex (FCN-LPX), adopting a simple blending technique for the eradication of oculomycosis. Fenticonazole nitrate (FCN) is a pleiotropic fungistatic and fungicidal agent with sparse aqueous solubility, hampering its transcorneal permeation. Three independent factors were probed using a 2 3 factorial design (2 blocks, 2 replicates), namely, X 1 : Cationic surfactant type, X 2 : Amount of cationic surfactant (mM), and X 3 : Amount of soybean phosphatidyl choline (mM). The optimized formulation exhibited remarkable entrapment efficiency (82.74 % ± 0.67 %), as verified by DSC and FT-IR analysis. TEM imaging revealed uniformly nanosized vesicles (189.95 ± 2.90 nm) with a robust positive zeta potential (41.35 ± 2.62 mV), which preserved its stability following gamma sterilization and storage. The optimum FCN-LPX demonstrated a bi-phasic release pattern (48.18 % ± 5.65 % at 4 H and 92.85 % ± 6.77 % at 24 H) and notable mucoadhesive properties, ensuring complete drug release. Safety assessments, including pH, surface tension, and refractive index measurements, along with histopathological evaluation, confirmed the formulation's safety profile. Furthermore, FCN-LPX achieved superior ex-vivo transcorneal permeation (3.3-fold) and deeper in-vivo corneal uptake (2.4-fold) compared to conventional FCN suspension. Microbiological analysis highlighted the enhanced antifungal activity of FCN-LPX, evidenced by a larger inhibition zone (11 %), significantly lower minimal inhibitory and fungicidal concentrations (8-fold), as well as improved fungal biofilm inhibition and prolonged antifungal effect. In conclusion, FCN-LPX is a propitious nanoformulation for the effective eradication of persistent oculomycosis. • FCN-LPX was prepared using a simple blending technique for oculomycosis. • 2 3 factorial design optimized surfactant and phosphatidyl choline levels. • TEM confirmed nanosized vesicles with positive zeta potential and stability. • FCN-LPX showed bi-phasic release and mucoadhesion, ensuring complete release. • FCN-LPX enhanced antifungal activity with 8-fold lower MFC and MIC values.

Journal of Drug Delivery Science and TechnologyVol. 114
Cairo University (EG)
Openalex Percentile: Top 3%
Ocular Infections and Treatments
6.83
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