The aim of this study was to assess the pharmacokinetic profile of pancopride after repeated oral dose administration of 20mg pancopride in tablet form once a day for 5 d in 12 healthy male volunteers. Plasma levels were measured by HPLC using a solid phase extraction method and automated injection.
Pharmacokinetics of rosoxacin in human volunteers
โ Scribed by G. B. Park; J. Saneski; T. Weng; J. Edelson
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 214 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
โฆ Synopsis
Reversed-phase liquid chromatography was used to determine plasma rosoxacin concentrations in normal, healthy males, each of whom received one 300 mg capsule of rosoxacin. The plasma data for each subject were described by an open one-compartment body model with first-order absorption, and the pharmacokinetic parameters were determined. The mean ( k S E ) apparent first-order terminal elimination rate constant was 0.203 f 0.015 hr-' ( N = 16), the mean apparent volume of distribution was 0.644 f 0.050 litedkg, and the mean apparent plasma clearance was 2.08 f 0.15 ml/min/kg.
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