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  • dose-dependent kinetics  (2)
  • 1970-1974  (2)
  • 1935-1939
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 2 (1974), S. 161-173 
    ISSN: 1573-8744
    Keywords: Michaelis-Menten kinetics ; dose-dependent kinetics ; one-compartment model ; two-compartment model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Throughout the literature, enzyme constants have been derived by utilizing in vivodata and indirectly assuming that these data were described by the one-compartment open model. However, many drugs are probably best described by a two-compartment open model with Michaelis-Menten elimination kinetics. Simulated data, which obey the two-compartment open model with Michaelis-Menten elimination, and which illustrate some of the interesting properties of such models, are presented. Treatment of two-compartment data by one-compartment analysis is shown to result in a serious distortion of enzyme parameters (V m ,K m ).For data which obey the two-compartment open model, estimation of the Michaelis-Menten constant (K m )and the maximum velocity (V m )by one-compartment analysis cannot be theoretically justified and therefore should be avoided.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 2 (1974), S. 149-160 
    ISSN: 1573-8744
    Keywords: Michaelis-Menten kinetics ; dose-dependent kinetics ; pooling of nonlinear equations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Pooling of Michaelis-Menten equations for models having parallel paths for formation of two or more metabolites is discussed. A theory which explains phenomena exhibited by pooled nonlinear pharmacokinetic systems and equations relating pooled Michaelis-Menten constants (V p ,K p )to microscopic constants (V i ,K i )are presented. The suitability of this type of pooling for use in pharmacokinetic modeling is also discussed. Use of pooling concepts in the design of clinical studies is demonstrated.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
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