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Updated: Jan 12, 2026

Delivery of Therapeutic siRNA to the CNS Using Cationic and Anionic Liposomes
Published on: July 23, 2016
Liposomes for epilepsy treatment: Toward better brain targeting and reduced toxicity
Zainab Lafi1, Sherine Asha2, Nisreen Asha3
1Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Al-Ahliyya Amman University, Al-Salt Road, Amman, 19328, Jordan; Pharmacological and Diagnostic Research Center, Faculty of Pharmacy, Al-Ahliyya Amman University, Al-Salt Road, Amman, 19328, Jordan.
Abstract:
Epilepsy is a chronic neurological disorder marked by recurrent, unprovoked seizures that can lead to cognitive impairment, psychiatric comorbidities, and reduced quality of life. While seizure control is critical for minimizing long-term neurological harm, conventional antiseizure medications (ASMs) are often hindered by limited brain penetration, systemic toxicity, and pharmacoresistance. Liposomal drug delivery systems offer a promising approach to overcome these limitations by enhancing central nervous system targeting, improving drug solubility and stability, and reducing off-target effects. Recent advances in surface-functionalized and immunoliposomes support site-specific delivery to epileptogenic regions and neuroinflammatory targets, contributing to more precise and better-tolerated therapies. Despite encouraging progress, important challenges remain in formulation optimization, targeting specificity, and clinical translation. Continued refinement of liposomal platforms may significantly advance personalized and effective epilepsy management.
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