Abstract
This study aims to formulate a nanosystem of ofloxacin (OFLOX) for nose-to-brain delivery to enhance brain accumulation and improve management of bacterial meningitis. OFLOX loaded transfersomal nanovesicles (OFLOX-TNVs) were prepared by a thin film hydration technique. A Box-Behnken design was employed to investigate the influence of Lipid concentration, Edge Activator concentration, and Cholesterol amount on particle size, entrapment efficiency, and intranasal permeation. Lipid concentration of 5% w/v and edge activator concentration of 14.6% w/w without cholesterol produced 271.5 nm particles entrapping 79.3% of the total drug added. Percentage of OFLOX released from the optimized nanovesicles was 75.39%, and 78.7% of the drug permeated after 24 h. Histopathological investigation displayed that the optimal formula in an in situ gel is tolerable. Pharmacokinetic study showed that the brain blood ratios of OFLOX from intravenous solution, intranasal solution, and intranasal OFLOX-TNVs in an in situ gel were 0.305, 0.579, and 1.858 respectively at 30 min. It is concluded that nanotransfersomes loaded with OFLOX could be a promising colloidal drug delivery system for effective brain targeting and treatment of bacterial meningitis. However, preclinical and clinical investigations are essential to evaluate its efficacy in humans.