Augmented glycerosomes as a promising approach against fungal ear infection: Optimization and microbiological, ex vivo and in vivo assessments

In the current study, voriconazole (VCZ) augmented glycerosomes were optimized for topical otomycosis management according to a 23 factorial design, employing a thin film hydration method. By optimizing Glycerol volume, limonene: VCZ ratio and Span® 60: soybean phosphatidyl choline (PC) ratio, glyce...

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Main Authors: Sadek Ahmed (Author), Heba Attia (Author), Osama Saher (Author), Abdurrahman M. Fahmy (Author)
Format: Book
Published: Elsevier, 2024-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Sadek Ahmed  |e author 
700 1 0 |a Heba Attia  |e author 
700 1 0 |a Osama Saher  |e author 
700 1 0 |a Abdurrahman M. Fahmy  |e author 
245 0 0 |a Augmented glycerosomes as a promising approach against fungal ear infection: Optimization and microbiological, ex vivo and in vivo assessments 
260 |b Elsevier,   |c 2024-12-01T00:00:00Z. 
500 |a 2590-1567 
500 |a 10.1016/j.ijpx.2024.100295 
520 |a In the current study, voriconazole (VCZ) augmented glycerosomes were optimized for topical otomycosis management according to a 23 factorial design, employing a thin film hydration method. By optimizing Glycerol volume, limonene: VCZ ratio and Span® 60: soybean phosphatidyl choline (PC) ratio, glycerosomes with maximum percentage entrapment efficiency (%EE) and zeta potential (ZP) and minimum vesicle size (VS) and polydispersity index (PDI) were to be obtained. An optimal augmented glycerosomal formula (OAG) that contained 10 mg VCZ, 150 mg PC, and 3 mL glycerol, comprising 2.5: and 0.92:1 ratios of the latter two independent variables, was proposed via numerical optimization. OAG exhibited high %EE and ZP values and acceptable low values for VS and PDI (84.3 ± 2.0 %, −38.8 ± 1.8 mV, 191.0 ± 1.1 nm, and 0.192 ± 0.01, respectively). Extensive in vitro testing of OAG revealed the entrapment of VCZ within OAG, biphasic in vitro release profile, stability for up to 3 months at 2-8 °C and spherical morphology of OAG with VS like that obtained via zetasizer. OAG demonstrated higher permeated amounts of VCZ and flux values than VCZ suspension, leading to an enhancement ratio of 2.56 in the ex vivo permeation study. The deeper penetration ability of OAG demonstrated by Confocal Laser Scanning Microscopy and its superior in vitro antifungal activity confirmed the validity of the ex vivo study. Also, the histopathological study confirmed the safety of OAG for topical use, suggesting that VCZ OAG was a promising topical antimycotic formula. 
546 |a EN 
690 |a Voriconazole 
690 |a Otomycosis 
690 |a Factorial design 
690 |a Transmission electron microscopy 
690 |a Augmented glycerosomes 
690 |a Minimal fungicidal concentration 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n International Journal of Pharmaceutics: X, Vol 8, Iss , Pp 100295- (2024) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2590156724000677 
787 0 |n https://doaj.org/toc/2590-1567 
856 4 1 |u https://doaj.org/article/ab3c98dd03a847c2a9ec2b9c3abb1ce5  |z Connect to this object online.