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  • Articles: DFG German National Licenses  (2)
  • Acetone  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of toxicology 47 (1981), S. 293-304 
    ISSN: 1432-0738
    Keywords: Acetone ; Pharmacokinetics ; Formate excretion ; Gas uptake
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Inhalation pharmacokinetics of acetone in rats was studied using gas uptake techniques. Under conditions of negligible metabolism (saturation of metabolizing enzymes) the coefficient of distribution K eq between organism and gas phase was 220 which confirmed that acetone is mainly (but not exclusively) distributed within the body water compartment. The metabolic elimination of acetone from the animals followed strict Michaelis-Menten saturation kinetics; the K m corresponded to 160 ppm in the atmosphere, v max was 230 μmol · h−1 · kg−1. A shift in the distribution pattern of acetone under conditions of prevalent metabolism was theoretically predicted and experimentally proven; as the partial process of metabolic elimination was dose-dependent, this “depleted” the animal compartment from acetone in a dose-dependent fashion causing a shift in the “steady-state-constant”, K st . Part of the acetone which was metabolically eliminated (4.7%) appeared in the urine as formate within 7 days after ending a 48-h exposure to acetone; this excretion was linear with time. The data suggested existence of a formate pool in the organism from which formate was released with delay. Hence, limitations may be inferred as to the applicability of urinary formate excretion as a quantitative indicator for changing conditions of acetone exposure.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of toxicology 52 (1983), S. 123-133 
    ISSN: 1432-0738
    Keywords: Pharmacokinetics ; Gas uptake ; Acetone ; Hydrocarbons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A pharmacokinetic description of production, distribution and metabolism of endogenous volatile compounds is presented. This description uses the “gas uptake model” of a closed recirculated atmosphere in which experimental animals are exposed. As an example, the production rates of acetone, under different conditions of stimulation by xenobiotics, are calculated from published experimental data. The theoretical descriptions may serve as a basis for treating the problem of hydrocarbon exhalation in toxicological experiments with compounds eliciting lipid peroxidation.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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