Volume 66, Issue 8 pp. 1154-1156
Research Article

Time-dependent kinetics III: Diurnal oscillations in steady-state plasma valproic acid levels in rhesus monkeys

R. H. Levy

Corresponding Author

R. H. Levy

Department of Pharmaceutical Sciences, School of Pharmacy, and the Department of Neurological Surgery, School of Medicine, University of Washington, Seattle, WA 98195

Department of Pharmaceutical Sciences, School of Pharmacy, and the Department of Neurological Surgery, School of Medicine, University of Washington, Seattle, WA 98195Search for more papers by this author
J. S. Lockard

J. S. Lockard

Department of Pharmaceutical Sciences, School of Pharmacy, and the Department of Neurological Surgery, School of Medicine, University of Washington, Seattle, WA 98195

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I. H. Patel

I. H. Patel

Department of Pharmaceutical Sciences, School of Pharmacy, and the Department of Neurological Surgery, School of Medicine, University of Washington, Seattle, WA 98195

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W. C. Congdon

W. C. Congdon

Department of Pharmaceutical Sciences, School of Pharmacy, and the Department of Neurological Surgery, School of Medicine, University of Washington, Seattle, WA 98195

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First published: August 1977
Citations: 9

Abstract

Valproic acid was administered by constant rate intravenous infusion to catheterized chaired rhesus monkeys for 8–10 weeks under controlled environmental conditions. Steady-state plasma levels were monitored at 2-hr intervals for 26 hr (10 am–12 noon on the following day), 1 day/week for 6 weeks. Individual steady-state plasma concentration-time plots exhibited the following characteristics. During Period A (10 am–6 pm), plasma levels remained stable or decreased. During Period B (6 pm–6 am), plasma levels increased, reached a maximum, and remained markedly higher than during Period A. The maximum concentrations were 40–140% higher than the observed minimum concentrations. During Period C (6 am—noon), plasma levels tended to decline from the maximum concentrations achieved in Period B. In most cases, plasma concentrations at 10 am and 12 noon of the 2nd experimental day fell within 10% of their respective values on the previous day. The mean (±SD) periods obtained by cross-correlation analysis of individual plasma concentration-time plots were 30.7 (±3.7) and 22.8 (±3.6) hr for Animals 903 and 923, respectively. The corresponding mean (±SD) amplitudes were 27.3 (±12.6) and 17.4 (±2.3)%. A circadian rhythm in total body clearance was hypothesized, and its pharmacokinetic implications are discussed.

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