QUALITY BY DESIGN AND CHARACTERIZATION OF EDARAVONE SLN TO IMPROVE BRAIN DELIVERY BY NASAL ROUTE FOR THE TREATMENT OF ALZHEIMER’S DISEASE

Authors

  • CH. BHAVANI Department of Pharmaceutics, School of Pharmaceutical sciences, Vels Institute of Science, Technology and Advanced Studies (VISTAS). Pallavaram, Chennai-600117, Tamilnadu, India. Department of Pharmaceutics, CMR College of Pharmacy, Medchal, Hyderabad, Telangana-501401, India https://orcid.org/0000-0002-1539-583X
  • P. BALAJI Department of Pharmacology, School of Pharmaceutical Sciences, Vels Institute of Science, Technology and Advanced Studies (VISTAS), Pallavaram, Chennai-600117, Tamilnadu, India https://orcid.org/0000-0001-5317-1661

DOI:

https://doi.org/10.22159/ijap.2026v18i1.55684

Keywords:

Solid lipid nanoparticles, Central composite design, Alzheimer’s disease, Design of experiments, Entrapment efficiency, Edaravone

Abstract

Objective: The present study aims at formulation development of solid lipid nanoparticles of Edaravone(EDN), for nasal administration to improve the permeation through blood brain barrier for therapeutically effect on Alzheimer’s disease.

Methods: Solid lipid nanoparticles(SLN) are formulated by using the lipid core of Glyceryl monostearate and Tween80 as surfactant through emulsification, solvent evaporation technique and optimized by using 32 central composite design(CCD) secondary overlay plots. Selection of the optimized formulation based on the dependable factors like entrapment efficiency(EE), particle size, polydispersity index(PDI), zeta potential and drug release studies. The selected optimized formulation was subjected to test the behavioral changes in Wister rats.

Results: the final optimized formulation was observed as particle size of <200nm. Entrapment efficiency of 87%, zeta potential of -21.23mEV and drug release of 84%. In vivo studies with the SLN encapsulated EDN showed better memory retention when comparing with the pure drug formulation. Y-Maze test behavioral score with control group 24.5±3.39% was considerably lower with the ENP-treated group (53.5±4.41% for high dose).

Conclusion: EDN encapsulated SLN delivered through the nasal route of administration has the better therapeutical applications in nano formulation strategies.

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Published

11-11-2025

How to Cite

BHAVANI, C., & BALAJI, P. (2025). QUALITY BY DESIGN AND CHARACTERIZATION OF EDARAVONE SLN TO IMPROVE BRAIN DELIVERY BY NASAL ROUTE FOR THE TREATMENT OF ALZHEIMER’S DISEASE. International Journal of Applied Pharmaceutics, 18(1). https://doi.org/10.22159/ijap.2026v18i1.55684

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