Literature DB >> 8396097

Comparison of the pharmacokinetics of three-day and five-day regimens of azithromycin in plasma and urine.

A Wildfeuer1, H Laufen, M Leitold, T Zimmermann.   

Abstract

In an open crossover study, the pharmacokinetics of three-day and five-day regimens of azithromycin were compared. Fourteen healthy volunteers received oral doses of azithromycin once-daily, over three days (500 mg/day) and over five days (500 mg on day 1, followed by 250 mg/day on days 2-5). Plasma and urine concentrations were determined by HPLC. Azithromycin was found to be absorbed rapidly on the first and the last days of both regimens, with mean Tmax ranging between 2.5-3 h. On day 1, peak plasma concentrations were 0.37 mg/L and 0.31 mg/L, respectively, with three- and five-day regimens, and increased to 0.42 mg/L on the last day of the three-day regimen, but decreased to 0.18 mg/L at the end of the five-day regimen. Similarly, the AUC0-24 increased from 1.30 to 1.88 h.mg/L during the three-day regimen, and decreased from 1.24 to 0.80 h.mg/L on the five-day regimen. After absorption, azithromycin was distributed rapidly; the respective half-lives were 2.4 h and 2.2 h with the three-day and five-day regimens. Thereafter, a polyphasic decline of plasma concentrations was observed; the average half-lives between 8-48 h after administration were 27.9 h (three-day regimen) and 35.8 h (five-day regimen). In urine, 5.5% (three-day regimen) and 4.6% (five-day regimen) of the total dose was found as unchanged azithromycin over a 12-day period. The observed pharmacokinetics of azithromycin with both regimens conformed with the known pharmacokinetic behaviour of the drug. The treatment-related differences seen in the plasma concentrations were as expected from the different dosage schedules.

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Year:  1993        PMID: 8396097     DOI: 10.1093/jac/31.suppl_e.51

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  6 in total

1.  Pharmacokinetics in serum and leukocyte exposures of oral azithromycin, 1,500 milligrams, given over a 3- or 5-day period in healthy subjects.

Authors:  G W Amsden; A N Nafziger; G Foulds
Journal:  Antimicrob Agents Chemother       Date:  1999-01       Impact factor: 5.191

2.  Single-dose intrapulmonary pharmacokinetics of azithromycin, clarithromycin, ciprofloxacin, and cefuroxime in volunteer subjects.

Authors:  J E Conte; J Golden; S Duncan; E McKenna; E Lin; E Zurlinden
Journal:  Antimicrob Agents Chemother       Date:  1996-07       Impact factor: 5.191

3.  Effect of adjunctive systemic azithromycin with periodontal surgery in the treatment of chronic periodontitis in smokers: a pilot study.

Authors:  Sarosh F Dastoor; Suncica Travan; Rodrigo F Neiva; Lindsay A Rayburn; William V Giannobile; Hom-Lay Wang
Journal:  J Periodontol       Date:  2007-10       Impact factor: 6.993

4.  Pharmacokinetic properties of azithromycin in pregnancy.

Authors:  Sam Salman; Stephen J Rogerson; Kay Kose; Susan Griffin; Servina Gomorai; Francesca Baiwog; Josephine Winmai; Josin Kandai; Harin A Karunajeewa; Sean J O'Halloran; Peter Siba; Kenneth F Ilett; Ivo Mueller; Timothy M E Davis
Journal:  Antimicrob Agents Chemother       Date:  2009-10-26       Impact factor: 5.191

5.  Pharmacokinetics of macrolides. Comparison of plasma, tissue and free concentrations with special reference to roxithromycin.

Authors:  O G Nilsen
Journal:  Infection       Date:  1995       Impact factor: 3.553

6.  Influence of adjunctive azithromycin on microbiological and clinical outcomes in periodontitis patients: 6-month results of randomized controlled clinical trial.

Authors:  Katarina Čuk; Katja Povšič; Suzana Milavec; Katja Seme; Rok Gašperšič
Journal:  BMC Oral Health       Date:  2020-09-01       Impact factor: 2.757

  6 in total

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