Literature DB >> 10991830

Comparative pharmacokinetics of ciprofloxacin, gatifloxacin, grepafloxacin, levofloxacin, trovafloxacin, and moxifloxacin after single oral administration in healthy volunteers.

A Lubasch1, I Keller, K Borner, P Koeppe, H Lode.   

Abstract

In an open, randomized, six-period crossover study, the pharmacokinetics of ciprofloxacin, gatifloxacin, grepafloxacin, levofloxacin, moxifloxacin, and trovafloxacin were compared after a single oral dose in 12 healthy volunteers (6 men and 6 women). The volunteers received 250 mg of ciprofloxacin, 400 mg of gatifloxacin, 600 mg of grepafloxacin, 500 mg of levofloxacin, 400 mg of moxifloxacin, and 200 mg of trovafloxacin. The concentrations of the six fluoroquinolones in serum and urine were measured by a validated high-performance liquid chromatography method. Blood and urine samples were collected before and at different time points up to 48 h after medication. Levofloxacin had the highest peak concentration (C(max), in micrograms per milliliter) (6.21+/-1.34), followed by moxifloxacin (4.34+/-1.61) and gatifloxacin (3.42+/-0.74). Elimination half-lives ranged from 12.12+/-3.93 h (grepafloxacin) to 5.37+/-0.82 h (ciprofloxacin). The total areas under the curve (AUC(tot), in microgram-hours per milliliter) for levofloxacin (44.8+/-4.4), moxifloxacin (39.3+/-5.35), and gatifloxacin (30+/-3.8) were significantly higher than that for ciprofloxacin (5.75+/-1.25). Calculated from a normalized dose of 200 mg, the highest C(max)s (in micrograms per milliliter) were observed for levofloxacin (2.48 +/-0.53), followed by moxifloxacin (2.17+/-0.81) and trovafloxacin (2.09+/-0.58). The highest AUC(tot) (in microgram-hours per milliliter) for a 200-mg dose were observed for moxifloxacin (19.7+/-2.67) and trovafloxacin (19.5+/-3.1); the lowest was observed for ciprofloxacin (4.6+/-1.0). No serious adverse event was observed during the study period. The five recently developed fluoroquinolones (gatifloxacin, grepafloxacin, levofloxacin, moxifloxacin, and trovafloxacin) showed greater bioavailability, longer half-lives, and higher C(max)s than ciprofloxacin.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10991830      PMCID: PMC90121          DOI: 10.1128/AAC.44.10.2600-2603.2000

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  13 in total

1.  Oral bioavailability of trovafloxacin with and without food in healthy volunteers.

Authors:  R Teng; L C Dogolo; S A Willavize; H L Friedman; J Vincent
Journal:  J Antimicrob Chemother       Date:  1997-06       Impact factor: 5.790

2.  Absence of age and gender effects on the pharmacokinetics of a single 500-milligram oral dose of levofloxacin in healthy subjects.

Authors:  S C Chien; A T Chow; J Natarajan; R R Williams; F A Wong; M C Rogge; R K Nayak
Journal:  Antimicrob Agents Chemother       Date:  1997-07       Impact factor: 5.191

Review 3.  Pharmacokinetics of grepafloxacin.

Authors:  C Efthymiopoulos
Journal:  J Antimicrob Chemother       Date:  1997-12       Impact factor: 5.790

4.  Pharmacokinetics of ciprofloxacin in healthy volunteers after oral and intravenous administration.

Authors:  K Borner; G Höffken; H Lode; P Koeppe; C Prinzing; P Glatzel; R Wiley; P Olschewski; B Sievers; D Reinitz
Journal:  Eur J Clin Microbiol       Date:  1986-04       Impact factor: 3.267

5.  New regression function for absorption kinetics.

Authors:  P Koeppe
Journal:  Arzneimittelforschung       Date:  1988-09

6.  Determination of trovafloxacin in human body fluids by high-performance liquid chromatography.

Authors:  K Borner; H Hartwig; H Lode
Journal:  J Chromatogr A       Date:  1999-06-18       Impact factor: 4.759

7.  Pharmacokinetic profile of levofloxacin following once-daily 500-milligram oral or intravenous doses.

Authors:  S C Chien; M C Rogge; L G Gisclon; C Curtin; F Wong; J Natarajan; R R Williams; C L Fowler; W K Cheung; A T Chow
Journal:  Antimicrob Agents Chemother       Date:  1997-10       Impact factor: 5.191

8.  Pharmacokinetics and tissue penetration of the new fluoroquinolone grepafloxacin.

Authors:  J Child; J M Andrews; R Wise
Journal:  Antimicrob Agents Chemother       Date:  1995-02       Impact factor: 5.191

9.  Liquid chromatographic determination of ciprofloxacin and some metabolites in human body fluids.

Authors:  K Borner; H Lode; G Höffken; C Prinzing; P Glatzel; R Wiley
Journal:  J Clin Chem Clin Biochem       Date:  1986-05

10.  Pharmacokinetics, safety, and tolerability of ascending single doses of moxifloxacin, a new 8-methoxy quinolone, administered to healthy subjects.

Authors:  H Stass; A Dalhoff; D Kubitza; U Schühly
Journal:  Antimicrob Agents Chemother       Date:  1998-08       Impact factor: 5.191

View more
  52 in total

Review 1.  Pharmacokinetic and pharmacodynamic issues in the treatment of mycobacterial infections.

Authors:  E Nuermberger; J Grosset
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2004-03-13       Impact factor: 3.267

2.  Comparison of the effects of levofloxacin on QT/QTc interval assessed in both healthy Japanese and Caucasian subjects (pages.

Authors:  Atsushi Sugiyama; Yuji Nakamura; Satomi Nishimura; Satomi Adachi-Akahane; Yuji Kumagai; Juleen Gayed; Asif Naseem; Georg Ferber; Jorg Taubel; John Camm
Journal:  Br J Clin Pharmacol       Date:  2012-03       Impact factor: 4.335

3.  Urinary bactericidal activity of extended-release ciprofloxacin (1,000 milligrams) versus levofloxacin (500 milligrams) in healthy volunteers receiving a single oral dose.

Authors:  Florian M E Wagenlehner; Martina Kinzig-Schippers; Uwe Tischmeyer; Christine Wagenlehner; Fritz Sörgel; Kurt G Naber
Journal:  Antimicrob Agents Chemother       Date:  2006-09-18       Impact factor: 5.191

Review 4.  Comparative pharmacokinetics and pharmacodynamics of the newer fluoroquinolone antibacterials.

Authors:  A Aminimanizani; P Beringer; R Jelliffe
Journal:  Clin Pharmacokinet       Date:  2001       Impact factor: 6.447

Review 5.  Pharmacokinetic considerations for antimicrobial therapy in patients receiving renal replacement therapy.

Authors:  Federico Pea; Pierluigi Viale; Federica Pavan; Mario Furlanut
Journal:  Clin Pharmacokinet       Date:  2007       Impact factor: 6.447

Review 6.  New drugs against tuberculosis: problems, progress, and evaluation of agents in clinical development.

Authors:  Jossy van den Boogaard; Gibson S Kibiki; Elton R Kisanga; Martin J Boeree; Rob E Aarnoutse
Journal:  Antimicrob Agents Chemother       Date:  2008-12-15       Impact factor: 5.191

Review 7.  Investigational antimicrobial agents of 2013.

Authors:  Michael J Pucci; Karen Bush
Journal:  Clin Microbiol Rev       Date:  2013-10       Impact factor: 26.132

8.  Moxifloxacin target site concentrations in patients with pulmonary TB utilizing microdialysis: a clinical pharmacokinetic study.

Authors:  M Tobias Heinrichs; Sergo Vashakidze; Ketino Nikolaishvili; Irina Sabulua; Nestani Tukvadze; Nino Bablishvili; Shota Gogishvili; Brent P Little; Adam Bernheim; Jeannette Guarner; Charles A Peloquin; Henry M Blumberg; Hartmut Derendorf; Russell R Kempker
Journal:  J Antimicrob Chemother       Date:  2018-02-01       Impact factor: 5.790

Review 9.  Gatifloxacin: a review of its use in the treatment of bacterial infections in the US.

Authors:  Susan J Keam; Katherine F Croom; Gillian M Keating
Journal:  Drugs       Date:  2005       Impact factor: 9.546

10.  Molecular mechanisms of hepatocellular apoptosis induced by trovafloxacin-tumor necrosis factor-alpha interaction.

Authors:  Kevin M Beggs; Aaron M Fullerton; Kazuhisa Miyakawa; Patricia E Ganey; Robert A Roth
Journal:  Toxicol Sci       Date:  2013-10-04       Impact factor: 4.849

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.