Abstract
Dipotassium chlorazepate (DPC) was administered to ten patients (five males and five females), aged 18–37 years (mean 27.4), as a once daily dose of 50 mg until a steady state was reached. Plasma concentrations of the main metabolite N-desmethyldiazepam (DMD) were monitored by a high pressure liquid chromatographic (HPLC) method during the medication period and for 5 days after withdrawal of the drug. The plasma half life (t 1/2), the elimination coefficient (Kβ), the steady state concentration \(\left( {\bar C_{ss} } \right)\), and the apparent volume of distribution (Vβ), were calculated at steady state and the mean values ±SEM were 44±5 h, 0.0184±0.0026 h-1, 1590±163 ng/ml and 1.41 ±0.17 l/kg, respectively. A moderate inter-individual variability was observed. There was no tendency towards dose dependent elimination.
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References
Post C, Lindgren S, Bertler Å, Malmgren H (1977) Pharmacokinetics of N-desmethyldiazepam in healthy volunteers after single daily doses of dipotassium chlorazepate. Psychopharmacologia 53:105–109
Tognoni G, Gomeni R, De Maio D, Alberti GG, Franciosi P, Scieghi G (1975) Pharmacokinetics of N-desmethyldiazepam in patients suffering from insomnia and treated with nortriptyline. Br J Clin Pharmacol 2:227–232
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Bertler, Å., Lindgren, S. & Malmgren, H. Pharmacokinetics of dipotassium chlorazepate in patients after repeated 50 mg oral doses. Psychopharmacology 71, 165–167 (1980). https://doi.org/10.1007/BF00434406
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DOI: https://doi.org/10.1007/BF00434406