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Antimicrobial Agents and Chemotherapy, June 1998, p. 1470-1475, Vol. 42, No. 6
Institut für Klinische Pharmakologie
und Toxikologie,1
Institut für
Anatomie,2 and
Institut für
Klinische Chemie und Pathobiochemie,3
Universitätsklinikum Benjamin Franklin, Freie Universität
Berlin, 14195 Berlin, Germany
Received 23 January 1997/Returned for modification 10 May
1997/Accepted 20 March 1998
Sparfloxacin is a fluoroquinolone with improved antibacterial
activity against gram-positive pathogens. Like other quinolones, use of
this drug is contraindicated in children and adolescents because of its
potential chondrotoxicity in juveniles. We performed histological and
immunohistochemical studies on the knee joint cartilage in 5-week-old
rats after treatment with 600 or 1,800 mg of sparfloxacin/kg of body
weight. Treatment with single or multiple oral doses of 600 mg of
sparfloxacin/kg was not sufficient to induce joint cartilage lesions.
However, five of eight rats treated with a single oral dose of 1,800 mg
of sparfloxacin/kg of body weight showed typical cartilage lesions in
the femoral part of the knee joint. The concentrations of the drug in
plasma measured 0.25, 0.75, 1.5, 3, 6, 12, and 24 h after the
administration of an oral dose of 600 mg of sparfloxacin/kg were
6.3 ± 1.8, 9.2 ± 1.7, 9.6 ± 2.7, 13.0 ± 1.8,
12.3 ± 1.6, 3.4 ± 0.4, and 0.30 ± 0.20 mg/liter,
respectively (mean ± standard deviation [SD]; n = 5 to 6 per group). The concentrations in plasma
measured 0.75, 1.5, 3, 6, 24, and 48 h after the administration of
an oral dose of 1,800 mg of sparfloxacin/kg were 10.9 ± 1.5, 15.9 ± 1.6, 19.1 ± 1.7, 14.9 ± 3.1, 4.1 ± 0.6, and 0.46 ± 0.37 mg/liter, respectively (mean ± SD;
n = 3 to 4 per group). The concentrations of
sparfloxacin in joint cartilage were significantly higher at all time
points studied (114.8 ± 80, 99.4 ± 31.5, 84.9 ± 16.8, 44.4 ± 13.9, and 14.2 ± 4.8 mg of sparfloxacin/kg at 1.5, 3, 6, 24, and 48 h after the administration of 1,800 mg/kg,
respectively). The range of concentrations in bone were similar to the
range of concentrations in cartilage (peak, 115 ± 12 mg/kg after
3 h). Our data indicate that chondrotoxic doses of sparfloxacin in
juvenile rats are approximately 300 times higher than the doses of
sparfloxacin used therapeutically (1,800 versus approximately 6 mg/kg
of body weight), but due to species differences in kinetics,
concentrations in plasma differ by a factor of only approximately 15. More data on quinolone concentrations in cartilage from animals and
humans could provide a better basis for a reasonable risk assessment.
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Chondrotoxicity and Toxicokinetics of Sparfloxacin
in Juvenile Rats
*
Corresponding author. Mailing address: Institut
für Klinische Pharmakologie und Toxikologie, Freie
Universität Berlin, Garystr. 5, 14195 Berlin, Germany. Phone: 49 30 8445 1770. Fax: 49 30 8445 1763. E-mail:
stahl{at}medizin.fu-berlin.de.
Dedicated to Hartmut Lode, Chest and Infectious Disease Department,
City Hospital Zehlendorf, Berlin, Germany.
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