Pharmacokinetics of oxiracetam following intravenous and oral administration in healthy volunteers Authors
Received: 30 January 1984 DOI:
Cite this article as: Perucca, E., Albrici, A., Gatti, G. et al. European Journal of Drug Metabolism and Pharmacokinetics (1984) 9: 267. doi:10.1007/BF03189650 Summary
The kinetics of oxiracetam after single intravenous and oral doses (2000 mg) were investigated in four healthy volunteers. Following intravenous administration, the decline in serum levels showed a prolonged, rapid phase followed by a delayed terminal phase. Mean residence times ranged from 3.9 to 6.5 h. Volumes of distribution ranged from 0.9 to 1.81 · kg
−1, whereas clearance values ranged from 100 to 119 ml·.h −1· kg -1 More than 90% of the intravenous dose was recovered unchanged in the urine within 48 h. Oral administration resulted in peak levels within 1–2 h; thereafter, the decline in serum levels showed a pattern similar to that observed after the intravenous dose — almost 50% of the oral dose was excreted in the urine within 6 h. The absolute availability of oral oxiracetam was 75 ± 7%. Key-words Pharmacokinetics oxiracetam bioavailability References
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