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. 1982 Jun;21(6):935-8.
doi: 10.1128/AAC.21.6.935.

Pharmacokinetics of cefonicid, a new broad-spectrum cephalosporin

Pharmacokinetics of cefonicid, a new broad-spectrum cephalosporin

S L Barriere et al. Antimicrob Agents Chemother. 1982 Jun.

Abstract

This study determined the pharmacokinetic disposition of cefonicid. A single dose of 7.5 mg/kg of body weight was administered to five healthy volunteers as a 5-min intravenous infusion. Multiple plasma and urine samples were collected for 48 h. Peak plasma concentrations ranged from 95 to 156 micrograms/ml and fell slowly (mean plasma half-life, 4.4 +/- 0.8 h), so that levels after 12 h were in the range of 6 to 12 micrograms/ml. Urinary concentrations were high but variable and ranged from 100 to 1,000 micrograms/ml for the first 12 h after the dose and averaged 84 micrograms/ml between 12 and 24 h. Plasma and renal clearances were 0.32 +/- 0.06 and 0.29 +/- 0.05 ml/min per kg, respectively. An average of 88 +/- 6% of the dose was excreted unchanged in the urine over 48 h. The mean steady-state volume of distribution was found to be 0.11 +/- 0.01 liters/kg.

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References

    1. J Infect Dis. 1973 Oct;128:Suppl:S341-6 - PubMed
    1. Antimicrob Agents Chemother. 1978 May;13(5):784-90 - PubMed
    1. J Antibiot (Tokyo). 1981 Feb;34(2):202-5 - PubMed
    1. J Pharm Sci. 1979 Aug;68(8):1071-4 - PubMed
    1. Clin Pharmacol Ther. 1981 Nov;30(5):587-93 - PubMed

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