Literature DB >> 11765143

Pharmacokinetics and absolute bioavailability of sitafloxacin, a new fluoroquinolone antibiotic, in healthy male and female Caucasian subjects.

J O'Grady1, A Briggs, S Atarashi, H Kobayashi, R L Smith, J Ward, C Ward, D Milatovic.   

Abstract

1. The aim was to compare the pharmacokinetics of sitafloxacin from a capsule formulation (dose of 500 mg sitafloxacin) and an intravenous (i.v.) formulation infused over 1 h (dose of 400 mg sitafloxacin) in healthy male and female subjects and to estimate the absolute bioavailability of sitafloxacin from the capsule formulation. 2. Following oral administration, sitafloxacin was rapidly absorbed, with a mean maximum concentration in plasma of 4.65 microgml(-1) occuring at median tmax = 1.25 h giving a mean AUC(0-infinity) = 28.1 microg h ml(-1). For the i.v. administration, a mean Cmax = 5.53 microm(-1) occurred at the end of the 1-h infusion with a mean AUC(0-infinity) = 25.4 microg h ml(-1). The mean terminal elimination half-life was 7.0 h (oral) and 6.6 h (i.v.). For the oral and i.v. formulations, the mean total plasma clearance was 296 and 263 mlmin(-1), respectively and the mean volume of distribution was 180 and 150 litres, respectively. 3. Within 48 h post-dose, approximately 61% (range 22-86%) of the administered dose was excreted unchanged in urine following capsule administration, compared with approximately 75% (range 42-101%) following the i.v. formulation. For both formulations, the renal clearance of sitafloxacin (means of 181 and 198 ml min(-1) for the capsule and i.v. doses, respectively) implies active tubular secretion of the drug. 4. The absolute bioavailability of sitafloxacin from the capsule formulation was high at 89%, with a 95% CI of 84-94%. The intersubject variability (CV%) in the sitafloxacin AUC(0-infinity) for the capsule was low at 18.6%. 5. Gender differences in the pharmacokinetics of sitafloxacin were small and would not warrant dose adjustment. 6. The findings show that the capsule formulation offers good oral bioavailability and merits further clinical evaluation of sitafloxacin as an orally effective fluoroquinolone antibacterial.

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Year:  2001        PMID: 11765143     DOI: 10.1080/0049825011

Source DB:  PubMed          Journal:  Xenobiotica        ISSN: 0049-8254            Impact factor:   1.908


  6 in total

1.  Quantitative assessment of the hepatic pharmacokinetics of the antimicrobial sitafloxacin in humans using in vivoF magnetic resonance spectroscopy.

Authors:  Geoffrey S Payne; David J Collins; Peter Loynds; Graham Mould; Philip S Murphy; Andrzej S K Dzik-Jurasz; Preminda Kessar; Nazneen Haque; Masayuki Yamaguchi; Shogo Atarashi; Martin O Leach
Journal:  Br J Clin Pharmacol       Date:  2005-02       Impact factor: 4.335

Review 2.  Sitafloxacin: in bacterial infections.

Authors:  Gillian M Keating
Journal:  Drugs       Date:  2011-04-16       Impact factor: 9.546

3.  Population pharmacokinetics and pharmacodynamics of sitafloxacin in patients with community-acquired respiratory tract infections.

Authors:  Yusuke Tanigawara; Mitsuo Kaku; Kyoichi Totsuka; Hiroyuki Tsuge; Atsushi Saito
Journal:  J Infect Chemother       Date:  2013-03-26       Impact factor: 2.211

4.  Relationship of quantitative structure and pharmacokinetics in fluoroquinolone antibacterials.

Authors:  Die Cheng; Wei-Ren Xu; Chang-Xiao Liu
Journal:  World J Gastroenterol       Date:  2007-05-07       Impact factor: 5.742

5.  Effects of ABCB1, UGT1A1, and UGT1A9 Genetic Polymorphisms on the Pharmacokinetics of Sitafloxacin Granules in Healthy Subjects.

Authors:  Lu-Ning Sun; Guo-Xian Sun; Yu-Qing Yang; Ye Shen; Feng-Ru Huang; Li-Jun Xie; Juan Cheng; Hong-Wen Zhang; Xue-Hui Zhang; Yun Liu; Yong-Qing Wang
Journal:  Clin Pharmacol Drug Dev       Date:  2020-07-20

6.  Treatment outcomes of oral sitafloxacin in acute complicated urinary tract infection and pyelonephritis.

Authors:  Weerawat Manosuthi; Surasak Wiboonchutikul
Journal:  Springerplus       Date:  2016-04-05
  6 in total

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