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[Pharmacokinetics of ciprofloxacin in young healthy volunteers].

D Liang, Y Qin, Ning Xu, H Zhang, Jian Li

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Abstract

Pharmacokinetic studies on ciprofloxacin were carried out in 6 young healthy volunteers. Serum and urine levels of ciprofloxacin were measured by reversed-phase high performance liquid chromatography. The drug obeyed one-compartment model kinetics in serum. The mean peak serum concentration, time to peak concentration and the area under the curve were 4.17 +/- 1.05mg/L, 1.75 +/- 0.40h and 18.09 +/- 2.69mg/L.h respectively after oral administration of 500mg of ciprofloxacin tablet. The elimination half life was 2.34 +/- 0.81h and the apparent volume of distribution was 3.71 +/- 0.75L. The urinary rate of ciprofloxacin over 24h after dosing was 34.22 +/- 6.57%. These data indicate that ciprofloxacin is easily absorbed and its concentration reaches the peak level rapidly. There are high levels of drug both in serum and urine.

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What this paper is about

Pharmacokinetic studies on ciprofloxacin were carried out in 6 young healthy volunteers. Serum and urine levels of ciprofloxacin were measured by reversed-phase high performance liquid chromatography. The drug obeyed one-compartment model kinetics in serum. The mean peak serum concentration, time to peak concentration and the area under the curve were 4.17 +/- 1.05mg/L, 1.75 +/- 0.40h and 18.09 +/- 2.69mg/L.h respectively after oral administration of 500mg of ciprofloxacin tablet. The elimination half life was 2.34 +/- 0.81h and the apparent volume of distribution was 3.71 +/- 0.75L. The urinary rate of ciprofloxacin over 24h after dosing was 34.22 +/- 6.57%. These data indicate that ciprofloxacin is easily absorbed and its concentration reaches the peak level rapidly. There are high levels of drug both in serum and urine.

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Available abstract

Pharmacokinetic studies on ciprofloxacin were carried out in 6 young healthy volunteers. Serum and urine levels of ciprofloxacin were measured by reversed-phase high performance liquid chromatography. The drug obeyed one-compartment model kinetics in serum. The mean peak serum concentration, time to peak concentration and the area under the curve were 4.17 +/- 1.05mg/L, 1.75 +/- 0.40h and 18.09 +/- 2.69mg/L.h respectively after oral administration of 500mg of ciprofloxacin tablet. The elimination half life was 2.34 +/- 0.81h and the apparent volume of distribution was 3.71 +/- 0.75L. The urinary rate of ciprofloxacin over 24h after dosing was 34.22 +/- 6.57%. These data indicate that ciprofloxacin is easily absorbed and its concentration reaches the peak level rapidly. There are high levels of drug both in serum and urine.

Key concepts: Ciprofloxacin, Pharmacokinetics, Urine, Volume of distribution, Dosing, Half-life, Urinary system, Pharmacology

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[Pharmacokinetics of ciprofloxacin in young healthy volunteers]. — Research Paper | ScholarLens