Literature DB >> 598929

[Serum concentrations and kinetics after intravenous infusion of four grams of cefazolin (author's transl)].

D Adam, J Pätzold.   

Abstract

The pharmacokinetics of cefazolin were studied in 25 males and females after administration of 4 g infused over 60 minutes. The mean microbiologically active concentration of cefazolin in serum five minutes after discontinuing the infusion was 410 microgram/ml, after 60 minutes 190 microgram/ml and after 8 hours 8.5 microgram/ml. After 8 hours 84% of the drug was eliminated in the urine of four of the volunteers. The mean serum half-life was 87.38 minutes in the one compartment model, and the volume of distribution 9.20 1. The area under the curve was 44626.15 microgram.min.ml-1. The mean value for the clearance was 73.5 ml/min. The importance of high dosages of cefazolin in severe infections caused by cefazolin-sensitive organisms is discussed. Side-effects were not observed.

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Year:  1977        PMID: 598929     DOI: 10.1007/bf01640786

Source DB:  PubMed          Journal:  Infection        ISSN: 0300-8126            Impact factor:   3.553


  6 in total

1.  Pharmacokinetics of cefazolin compared with four other cephalosporins.

Authors:  W M Kirby; C Regamey
Journal:  J Infect Dis       Date:  1973-10       Impact factor: 5.226

2.  Pharmacokinetic interpretation of penicillin levels in serum and urine after intravenous administration.

Authors:  L W Dittert; W O Griffen; J C LaPiana; F J Shainfeld; J T Doluisio
Journal:  Antimicrob Agents Chemother (Bethesda)       Date:  1969

3.  Drug elimination and apparent volume of distribution in multicompartment systems.

Authors:  M Gibaldi; D Perrier
Journal:  J Pharm Sci       Date:  1972-06       Impact factor: 3.534

4.  Simplified, accurate method for antibiotic assay of clinical specimens.

Authors:  J V Bennett; J L Brodie; E J Benner; W M Kirby
Journal:  Appl Microbiol       Date:  1966-03

5.  [Kinetics of ampicillin, oxacillin and carbenicillin after a short intravenous infusion in man].

Authors:  K Wirth; J H Hengstmann; F H Langebartels; S Träger
Journal:  Arzneimittelforschung       Date:  1976

6.  [Solution of pharmacological problems by computers. 6. Models for the effect of protein binding on the clearance of drugs].

Authors:  E Krüger-Thiemer
Journal:  Arzneimittelforschung       Date:  1966-11
  6 in total

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