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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 2 (1974), S. 239-255 
    ISSN: 1573-8744
    Keywords: warfarin ; coumarin anticoagulants ; warfarin enantiomers ; anticoagulant action
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics of elimination and anticoagulant action of the R(+) and S(-) enantiomers of warfarin were determined in individual adult male Sprague- Dawley rats. A 12 mg/kg dose of one of the enantiomers and a tracer dose of racemic 14C -warfarin were injected intravenously, and the same doses of the other enantiomer and the tracer were administered 3 weeks later to the same animals. The apparent biological half- life of racemic warfarin ranged from about 6 to 18 hr and was very reproducible in individual animals. The ranges of the biological half-lives of R(+) and S(-)-warfarin were 4.9–9.6 hr and 7.7–21.6hr, respectively. There is a strong positive correlation between the half- life of each enantiomer in individual rats; the ratio of these half- lives, S(-):R(+), is 1.87 (sd 0.21, n=10). The apparent half- life of racemic warfarin in individual rats is in very good agreement with the half- life predicted from the sum of the plasma concentrations of R(+)-andS(−)-warfarin at various times after injection. There was no significant difference in the apparent volumes of distribution of R(+)-,S(-)-, and racemic warfarin. There was a pronounced intersubject variation in the relative potency of the two enantiomers; the ratio R(+):S(-) of the plasma concentrations required to decrease the synthesis rate of prothrombin complex activity by one-half ranged from 0.7 to 6.3, with a mean of 2.2.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 3 (1986), S. 150-155 
    ISSN: 1573-904X
    Keywords: renal clearance ; cephalosporin ; cefixime ; tubular reabsorption ; saturable protein binding ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics of cefixime, a new orally active cephalosporin, was studied after an intravenous dose of 50 mg/kg to four beagle dogs. Cefixime was shown to exhibit concentration dependent serum protein binding and saturable tubular reabsorption. The drug was excreted mainly in the urine, the net result of glomerular filtration and saturable tubular reabsorption. The experimental results were analyzed by model independent pharmacokinetic equations and with theoretical models describing renal clearance. Modification of the models, based on observed data, was proposed. The experimental methods employed and the pharmacokinetic approach offered in this study can be applied to drugs that exhibit concentration dependent protein binding and saturable renal elimination processes.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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