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Amiodarone kinetics after oral doses
Author(s) -
Kannan Ramaswamy,
Nademanee Koonlawee,
Hendrickson Jo Ann,
Rostami Hojat J,
Singh Bramah N
Publication year - 1982
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/clpt.1982.57
Subject(s) - amiodarone , metabolite , microgram , half life , medicine , pharmacokinetics , active metabolite , oral administration , serum concentration , chemistry , oral dose , pharmacology , endocrinology , atrial fibrillation , biochemistry , in vitro
Amiodarone serum kinetics after single oral doses and after long‐term therapy were investigated in patients with ventricular tachyarrhythmias. When amiodarone was given as a single oral dose (1400 to 1800 mg, n = 6), serum levels of amiodarone and its metabolite, measured by high‐performance liquid chromatography, correlated (r = 0.69, P < 0.01). Peak concentrations (amiodarone, 3 to 14 μg/ml; metabolite, 0.7 μg/ml) were attained in 4.9 ± 1.2 hr. Using computer fits to the data, amiodarone mean elimination rate constant and half‐life (t½e) were 0.128 ± 0.063 hr −1 and 7.2 ± 5.0 hr. In 12 patients given a mean dose of 1327 ± 338 mg/day of amiodarone for 4.1 ± 2.3 wk, mean serum amiodarone level was 3.84 ± 2.92 μg/ml (range 0.92 to 11.99); in three patients simultaneous determination of concentrations of amiodarone and its metabolite revealed that concentration of the latter was about 50% of that of the parent drug during long‐term therapy. In four patients on maintenance therapy (400 to 800 mg/day, serum level 1.08 ± 1.13 μg / ml) drug was discontinued and serum amiodarone levels were determined serially. Serum drug disappearance followed a single exponential function with an elimination rate constant of 0.030 ± 0.012 day −1 and t½e of 29 ± 19 days. Our kinetic data are consistent with the long therapeutic amiodarone t l / 2 noted in the treatment of cardiac arrhythmias. Clinical Pharmacology and Therapeutics (1982) 31, 438–444; doi: 10.1038/clpt.1982.57