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Updated: Apr 24, 2026

Electrophoretic Delivery of γ-aminobutyric Acid GABA into Epileptic Focus Prevents Seizures in Mice
Published on: May 16, 2019
Conversion from immediate-release to extended-release lamotrigine improves seizure control.
Patsy Ramey1, Melissa Osborn1, Bassel Abou-Khalil1
1A-0118 MCN, Department of Neurology, Vanderbilt University, A-0118 MCN, Nashville 37232, TN, USA.
Converting from immediate-release lamotrigine (LTG-IR) to extended-release lamotrigine (LTG-XR) improved seizure control and tolerability in patients with drug-resistant epilepsy. This switch offers a potential benefit for managing epilepsy symptoms and side effects.
Area of Science:
- Epilepsy and Neurology
- Pharmacology and Therapeutics
- Drug Delivery Systems
Background:
- Immediate-release lamotrigine (LTG-IR) dosing is limited by peak-dose toxicity, potentially causing adverse effects like dizziness and unsteadiness.
- Trough levels of LTG-IR may be associated with a reduced seizure threshold, impacting seizure control.
- Extended-release lamotrigine (LTG-XR) aims to reduce drug level fluctuations, potentially mitigating adverse effects and improving seizure control.
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