Abstract
Objective: The present study was an attempt to systemically deliver the most desirable schizophrenia drug, ziprasidone hydrochloride (ZRS) via the intranasal route using nanostructured lipid carrier (NLC) approach. Methods: The desired ZRS loaded NLCs were developed using central composite statistical design and the developed formulation was monitored for improving ZRS bioavailability and their brain targeting efficacy. Results: Pharmacokinetic studies revealed a 10 fold increase (ZRS blood-brain ratio) for NLCs administered through nasal route (in comparison to intravenous route). Similarly, the concentration of ZRS (in the brain) delivered via nasal route exhibits 4 fold increment at all-time points. Conclusion: Therefore, the obtained results suggest a potential nose to brain transport of loaded ZRS by effective bypassing of the Blood-Brain Barrier (BBB).
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CITATION STYLE
Sivadasu, P., Gowda, D. V., Siddaramaiah, H., & Hemalatha, S. (2020). Ziprasidone hydrochloride loaded nanostructured lipid carriers (Nlcs) for intranasal delivery: Optimization and in vivo studies. International Journal of Applied Pharmaceutics, 12(1), 31–41. https://doi.org/10.22159/ijap.2020v12i1.35683
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