A Self‐Complementary, Self‐Assembling Microsphere System: Application for Intravenous Delivery of the Antiepileptic and Neuroprotectant Compound Felbamate

• Published in: Journal of pharmaceutical sciences 2000-07, Vol.89 (7), p.867-875
• Main Authors: Lian, Huiling, Steiner, Solomon S., Sofia, R.Duane, Woodhead, Jose H., Wolf, Harold H., White, H.Steve, Shen, Gregory S., Rhodes, Christopher A., McCabe, R.Tyler
• Format: Article
• Language: English
• Subjects: Animals; Anticonvulsants - administration & dosage; Anticonvulsants. Antiepileptics. Antiparkinson agents; antiepileptic; Biological and medical sciences; Chromatography, High Pressure Liquid; Drug Carriers; drug delivery; Electroshock; Felbamate; Fumarates - chemistry; General pharmacology; Injections, Intravenous; Male; Medical sciences; Mice; Microscopy, Electron, Scanning; microsphere; Microspheres; Neuropharmacology; neuroprotection; Neuroprotective agent; Neuroprotective Agents - administration & dosage; Particle Size; Pharmaceutical technology. Pharmaceutical industry; Pharmacology. Drug treatments; Phenylcarbamates; Piperazines - chemistry; Propylene Glycols - administration & dosage; Surface Properties
• ISSN: 0022-3549; 1520-6017
• DOI: 10.1002/1520-6017(200007)89:7<867::AID-JPS3>3.0.CO;2-S

Felbamate (FBM) is a novel antiepileptic drug (AED) and neuroprotectant (NP) compound that interacts with strychnine‐insensitive (SI) glycine receptors in brain (IC50 = 374 μM). FBM concentrations required to interact with SI glycine receptors are consistent with brain levels following oral and intraperitoneal administration of AED and NP doses. Because of the solubility limits of FBM, an intravenous (iv) form has not been developed. Nevertheless, an iv form could be important for the treatment of disorders such as status epilepticus and neuronal damage due to hypoxic/ischemic events. Substituted diketopiperazines precipitate in acid to form microspherical particles of uniform size (∼2 μm). The microsphere system entraps drugs on precipitation and dissolves near physiological pH to release the drug cargo. Therefore, microspheres were used to produce an iv formulation of FBM. Mice were administered the FBM/microsphere (20–60 mg/kg FBM) and tested for protection against tonic extension seizures using maximal electroshock. The FBM/microsphere was effective in a time‐ and dose‐dependent manner following iv administration. The median effective dose (ED50) for protection against MES seizures at 30 min was 27.2 mg/kg [95% confidence interval (CI) = 20.8–33.4, slope = 6.5]. The ED50 for minimal motor impairment at 30 min was 167 mg/kg (95% CI = 155–177, slope = 28.1). Thus, the feasibility of encapsulating FBM or similar aqueous insoluble compounds in a microsphere system with delivery by the iv route for treatment of epilepsy and various central nervous system disorders has been clearly demonstrated. Studies were performed in accordance with the Guide for the Care and Use of Laboratory Animals. © Wiley‐Liss Inc. and the American Pharmaceutical Association J Pharm Sci 89:867–875, 2000