Background: Voriconazole has been given a more potent antifungal action in-vitro and is the most commonly used drug for the treatment of onychomycosis. In this voriconazole-loaded nanoemulgel for the management of onychomycosis was developed and evaluated. This development preparation mainly delivers poorly aqueous soluble drugs across the nail. Different types of components, such as o/w nanoemulsions, were mildly stirred using the aqueous titration technique before being homogenized under high pressure to minimize the particle size. DOE software is used to develop various batches for the selection of optimized batches. Nanoemulsion containing was prepared by using, olive as oil, Tween 80, and PEG 400 as used as a surfactant and co-surfactant respectively. The gelling agent is Carbopol 934. Thioglycolic acid is used as a nail penetration enhancer. The optimized batch was evaluated for physical appearance, pH, viscosity, stress stability study, vesicle size, particle size, drug release, drug content, and stability study.
Result: Drug polymer compatibility study show that drug and excipient are compatible with each other, The formulation was found to be clear and pH is a 5.2 it is suitable for nail pH.
A nanoemulgel study of in vitro drug release revealed improved drug release, i.e. that is 68% in 8th hrs. Thus more than 90% of drug release will happen in 24th hrs. which shows good controlled release. Zone of inhibition of optimized batch was found to be 9.8mm.
Conclusion: Voriconazole-loaded nanoemulsion was created in the current study by utilizing olive oil, Tween 80, and PEG 400. As a result of the drug's antifungal effectiveness against C. albicans, the F16 may be able to alleviate onychomycosis symptoms more quickly than with traditional treatment. Thus, nanoemulgel is a formulation for the topical treatment of onychomycosis that is safe and effective.