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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 192 (1961), S. 877-878 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] "The vermiform appendix appears to be a convenient object for experimental researches on re-activity and plasticity of tissues of the digestive system. When surgically inserted into the digestive tube at different levels of the latter, the appendix finds itself in (an) unusual functional condition. ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 1 (1973), S. 5-16 
    ISSN: 1573-8744
    Keywords: absorption kinetics ; oral pentobarbital ; effect of food on oral absorption of pentobarbital in humans ; pentobarbital pharmacokinetics ; intravenous and oral administration ; effect of food on barbiturate absorption in humans
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The plasma levels in humans of pentobarbital were determined after intravenous administration of a 50 mg dose. It was found that pentobarbital is distributed in at least two kinetically distinct body compartments: a central, or “serum” compartment and a peripheral, or “tissue,” compartment. By use of established mathematical techniques, values were assigned to the rate constants controlling the distribution and overall elimination of the drug from the body. The oral absorption of pentobarbital in fasted and nonfasted subjects was determined by mathematical analysis of the plasma level data following oral administration of a 50 mg dose. It was found that the presence of food significantly reduces the apparent absorption rate constant but not the amount absorbed. The absorption of a second dose, given 1.5 hr after the first dose, in nonfasted subjects was not affected, and a rapid increase in plasma levels occurred after this administration.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 3 (1975), S. 419-438 
    ISSN: 1573-8744
    Keywords: cephapirin ; desacetylcephapirin ; cephalosporin ; renal clearance calculations ; renal metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A pharmacokinetic model was developed to describe the absorption, distribution, metabolism, and excretion of cephapirin and its major metabolite, desacetylcephapirin, following intravenous and intramuscular administration of cephapirin in healthy adult subjects. The model involved a two-compartment open model for cephapirin in plasma and extravascular tissues and included metabolism of cephapirin to desacetylcephapirin in both the plasma compartment and the kidney. Renal metabolism of cephapirin was followed by excretion of the desacetylcephapirin into the urine. Clearance calculations and digital computer simulation supported these features of the model.
    Type of Medium: Electronic Resource
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