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Single-dose pharmacokinetics and anticonvulsant efficacy of primidone in mice

✍ Scribed by Mr K. W. Leal; R. L. Rapport; A. J. Wilensky; P. N. Friel


Publisher
John Wiley and Sons
Year
1979
Tongue
English
Weight
374 KB
Volume
5
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The pharmacokinetics and efficacy of the anticonvulsant primidone (PRM) and its active metabolites, phenobarbital (PB) and phenylethylmalonamide (PEMA), were studied after single‐dose administration in mice. The half‐life of PB is twice that of PRM and PEMA. The plasma/brain ratios provide evidence of poor penetration of PRM into brain. The results support our findings of negligible or absent PRM concentrations in the brains of patients on primidone therapy who were undergoing surgery for intractable epilepsy.

The anticonvulsant properties of PRM, PB, and PEMA against maximal electroshock in mice were also studied with the use of the metabolic inhibitor SKF 525A. The half‐life, potency, peak anticonvulsant effect, and effective dose curves of these compounds indicate that the anticonvulsant effect of short‐term oral PRM administration in mice is from derived PB.


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