Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1975-1979  (1)
  • 1970-1974  (1)
  • antipyrine  (1)
  • biotransformation products  (1)
  • 1
    ISSN: 1573-8744
    Keywords: clonazepam ; antipyrine ; phenobarbital ; enzyme induction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Clonazepam (1 mg/kg) and antipyrine (0.1 mg/kg) were administered simultaneously by intravenous bolus injection to three dogs. After 2 weeks of chronic phenobarbital administration, the studies were repeated. Plasma concentration-time curves in all studies were biexponential. Phenobarbital administration increased total plasma clearances of clonazepam and antipyrine by 102% and 98.5%, respectively. Volumes of distribution were not altered, and consequently reductions in terminal exponential half-lives observed after phenobarbital were attributed to increases in clearances.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 1 (1973), S. 201-216 
    ISSN: 1573-8744
    Keywords: area analysis ; pharmacokinetic model ; rate constant determination ; biotransformation products ; computer simulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The principle of area analysis was used in the development of a metabolic and pharmacokinetic model for an extensively biotransformed drug. Area analysis was also used to determine the rate constants associated with the model. The drug used to exemplify the utility of area analysis in developing such a model was N4-ethoxyacetylsulfamethoxazole. Administration of this drug to the monkey results in three recognizable biotransformation products. Each of the four compounds was administered intravenously to a monkey on separate occasions. Excellent agreement was obtained between the simulated and actual blood levels of the intact drug and its three biotransformation products. Such agreement between the simulated and experimental data reflects the utility of area analysis as the basis for the design of a metabolic and pharmacokinetic model.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...