DESIGN AND EVALUATION OF TOPICAL FORMULATION OF VORICONAZOLE USING CROSS LINKED CYCLODEXTRIN NANOSPONGES Authors: Pratap R And Lankalapalli S*
ABSTRACT
The solubility of voriconazole a triazole antifungal drug in water is very low. The molecule is
semi-polar (log D=1.8), making it difficult to solubilize with oils, surfactants, or water miscible
co-solvents. It also breaks down by a retro-aldol reaction to compounds A and C. This
instability is pronounced not only in aqueous media but also in solid state.Nanosponges are
hypercross-linked cyclodextrin polymers that have recently been produced and are assembled
into three-dimensional networks via nanostructure. Cyclodextrin undergoes a reaction with a
cross-linking agent, like diphenyl carbonate or carbonyldiimidazole, to produce these
polymers. Nanosponges based on cyclodextrin were able to complex a greater number of
molecules than natural cyclodextrins. They limit the release of the weakly soluble actives,
protect the labile groups, and improve solubility. The present study investigated whether
cyclodextrin-based nanosponges may improve voriconazole chemical stability and water
solubility. The results, indicate that the cyclodextrin nanosponges-based gel formulation of
voriconazole offers great topical administration potential due to its delayed and consistent drug
release, enhanced skin penetration, and good storage stability.
Keywords: Voriconazole, nanosponges, cyclodextrin, solubility, stability Publication date: 01/06/2024 https://ijbpas.com/pdf/2024/June/MS_IJBPAS_2024_9181.pdfDownload PDFhttps://doi.org/10.31032/IJBPAS/2024/13.6.9181