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  • 1975-1979  (2)
  • 1970-1974  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 3 (1975), S. 439-441 
    ISSN: 1573-8744
    Keywords: protein binding ; equilibrium dialysis ; ultrafiltration ; warfarin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Plasma or serum protein binding determinations of extensively bound drugs are subject to serious error if the analytical methods employed do not discriminate between such drugs and their degradation products, metabolites, and impurities. Experimental evidence is presented to demonstrate the magnitude of this problem with respect to warfarin.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 123-131 
    ISSN: 1573-8744
    Keywords: warfarin ; warfarin enantiomers ; serum protein binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The protein binding of racemic 14 C-warfarin and 3 H-S(-)-warfarin was determined in individual undiluted serum samples from 31 human subjects and 11 rats. The free fraction value of the R(+) enantiomer was determined indirectly from the free fraction values of the S(−) enantiomer and racemic warfarin, a method which was verified by direct determination of the free fraction of R(+)-warfarin with the unlabeled compound at higher concentrations. The ratio (mean± sd)of free fraction values, R(+):S(−), was 1.32±0.256in man and 1.56±0.351 in the rat;the difference between species is statistically significant (p〈0.025).This ratio was independent of the free fraction value of either enantiomer even though there were pronounced intersubject differences in serum protein binding of the anticoagulant. S(−)-Warfarin is eliminated more rapidly than the R(+) enantiomer in man, while the opposite occurs in rats. The results of this study rule out a species difference in serum protein binding as a factor contributing to the difference in elimination kinetics but help to explain the strong correlation in the elimination kinetics of the two enantiomers in individual rats.
    Type of Medium: Electronic Resource
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