Abstract
The pharmacokinetics of fosmidomycin was investigated in animals and humans after parenteral and oral dosing. In dogs the serum concentration was 54.8 microgram/ml at 0.25 h after an intravenous dose of 20 mg/kg, and the half-life was 1.14 h. Peak concentration was 41.4 microgram/ml after an intramuscular dose of 20 mg/kg and 16.6 microgram/ml after an oral dose of 40 mg/kg. In volunteers, the serum concentrations 0.25 h after dosing was 157 microgram/ml after an intravenous dose of 30 mg/kg, 12.3 microgram/ml after an intramuscular dose of 7.5 mg/kg, and 2.45 microgram/ml after an oral dose of 500 mg. More than 90% of the given dose was excreted in the 24-h urine in rats and dogs after parenteral dosing with 20 mg/kg. The 24-h urinary recovery was 45.8% of the given dose in rats after oral dosing with 100 mg/kg and 37.8% in dogs after oral dosing with 40 mg/kg. In volunteers 85.5% of the intravenous dose (30 mg/kg), 66.4% of the intramuscular dose (7.5 mg/kg), and 26.0% of the oral dose (500 mg) were excreted unchanged in the 24-h urine. In the multiple-dose study, there was no accumulation of fosmidomycin in the serum even after 21 consecutive intramuscular dosings of 1 g every 6 h or 29 consecutive 0.5-h drip infusions of 2 g every 6 h. Biliary excretion was extremely low in rats. Fosmidomycin was well distributed to the tissues of rats after parenteral and oral dosing. The lymph concentrations in dogs were nearly the same as serum concentrations. Serum protein binding was low (4% or less) to mouse, rat, dog, and human serum.
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- Allen J. G., Havas L., Leicht E., Lenox-Smith I., Nisbet L. J. Phosphonopeptides as antibacterial agents: metabolism and pharmacokinetics of alafosfalin in animals and humans. Antimicrob Agents Chemother. 1979 Sep;16(3):306–313. doi: 10.1128/aac.16.3.306. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Allona A., Díaz Cabrera J. A., Manchado P. Fosfomycin in chronic urinary infections. Chemotherapy. 1977;23 (Suppl 1):267–274. doi: 10.1159/000222059. [DOI] [PubMed] [Google Scholar]
- Kirby W. M. Pharmacokinetics of fosfomycin. Chemotherapy. 1977;23 (Suppl 1):141–151. doi: 10.1159/000222040. [DOI] [PubMed] [Google Scholar]
- Kojo H., Shigi Y., Nishida M. FR-31564, a new phosphonic acid antibiotic: bacterial resistance and membrane permeability. J Antibiot (Tokyo) 1980 Jan;33(1):44–48. doi: 10.7164/antibiotics.33.44. [DOI] [PubMed] [Google Scholar]
- Mine Y., Kamimura T., Nonoyama S., Nishida M., Goto S., Kuwahara S. In vitro and in vivo antibacterial activities of FR-31564, a new phosphonic acid antibiotic. J Antibiot (Tokyo) 1980 Jan;33(1):36–43. doi: 10.7164/antibiotics.33.36. [DOI] [PubMed] [Google Scholar]
- Murakawa T., Waki Y., Nishida M., Fuji R., Konno M. Chromatographic assay of mixed penicillins, ampicillin and cloxacillin in body fluids. J Antibiot (Tokyo) 1970 May;23(5):250–251. doi: 10.7164/antibiotics.23.250. [DOI] [PubMed] [Google Scholar]
- Nishida M., Murakawa T. Exudate levels and bactericidal activity of cefazolin in a new local infection system using rat granuloma pouches. Antimicrob Agents Chemother. 1977 Jun;11(6):1042–1048. doi: 10.1128/aac.11.6.1042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nishida M., Murakawa T., Kamimura T., Okada N., Sakamoto H., Fukada S., Nakamoto S., Yokota Y., Miki K. In vitro and in vivo evaluation of ceftezole, a new cephalosporin derivative. Antimicrob Agents Chemother. 1976 Jul;10(1):1–13. doi: 10.1128/aac.10.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SMITH J. R., DUNTON E. F., PROTAS J. M., BLOCKER T. G., Jr, COOLEY R. M., LEWIS S. R. Cannulation of the lymphatics of the lower extremity. Surg Forum. 1958;9:811–814. [PubMed] [Google Scholar]