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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 47 (1975), S. 1506-1510 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 1 (1973), S. 23-50 
    ISSN: 1573-8744
    Keywords: rate of absorption ; rate of renal reabsorption ; extraction theory ; partition coefficientin vivo ; pH of lumenal contents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Equations have been derived which quantitatively describe the rate of gastrointestinal and buccal absorption of acidic and basic drugs as a function of pH of aqueous lumenal contents and time. The equations have been used to fit observed data in the literature, and the estimated parameters are reported. An equation which describes the renal clearance of an acidic or basic drug as a function of urinary pH is also derived. In essence, the equations quantitate the pH-partition hypothesis and explain most, if not all, related observed data in the literature. The results suggest that the aqueous diffusion layer may not rate-limit absorption of monomeric drug molecules but that absorption is rate-limited by transfer of drug out of the membrane in vivo.
    Type of Medium: Electronic Resource
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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 207-224 
    ISSN: 1573-8744
    Keywords: nonlinear pharmacokinetics ; Michaelis-Menten kinetics ; gastric emptying rate ; blood alcohol concentrations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A nonlinear relationship between the total area under the blood ethanol concentration-time curve and the orally administered dose (mg/kg) of ethanol was observed in fasting subjects. A preliminary model, based on physiological considerations, was elaborated and shown, for the first time, to describe the entire time course of blood alcohol concentrations after four different doses of alcohol. The model could be refined by further experimentation.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-904X
    Keywords: procaterol ; bronchodilator ; healthy volunteers ; pharmacokinetics ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics and relative oral bioavailability of procaterol, an orally active β2-adrenergic agonist bronchodilator were evaluated in healthy volunteers. Procaterol was rapidly absorbed after oral administration. Mean plasma procaterol concentration–time profiles and pharmacokinetic parameters for both formulations were essentially superimposable. Following tablet administration, the mean C max was 358 pg/mL and the corresponding mean t max was 1.6 hr. Mean renal clearance was 163 mL/min and accounted for approximately one-sixth of the mean apparent oral plasma clearance (988 mL/min). The mean apparent elimination half-life of procaterol was 4.2 hr. Hepatic metabolism appears to be the primary mechanism for elimination of procaterol from the body, and first-pass metabolism may limit systemic bioavailability.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 2 (1974), S. 381-393 
    ISSN: 1573-8744
    Keywords: acetaminophen ; oral administration ; plasma levels ; simultaneous fitting ; weighting factor ; central compartment correction factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Average and individual sets of plasma concentration-time data for acetaminophen following two oral treatments were simultaneously fitted to the integrated equation describing the two-compartment open model with first-order absorption and lag time. The nonlinear least-squares program NONLIN and an IBM 360/67 digital computer were employed to estimate nine parameters (kA, kB, C A 0 , C B 0 , k12, k21, kel, $$t_{0_A } $$ and $$t_{0_B } $$ ).When the mean plasma concentrations were weighted according to the inverse of their variances, the parameter estimates more accurately reflected those for individual subjects in the disposition portion of the model. Depending on the relative magnitudes of the disposition rate constants (k12, k21,and kel),the one-compartment open model can be used to predict equilibrium-state plasma levels even though the drug is really “two compartment.” Equations are presented which show when the one-compartment approximation is justified. Equations are also presented for calculation of loading doses for multiple dose regimens of any drug obeying the two-compartment open model and the equations are applied to acetaminophen.
    Type of Medium: Electronic Resource
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  • 7
    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
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  • 8
    ISSN: 1573-8744
    Keywords: ethyl alcohol ; kinetics of elimination from human blood ; Michaelis-Menten equation ; oral administration with food to a single subject ; area under the blood alcohol curve ; absorption efficiency component ; component due to absorption rate and Michaelis-Menten kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Whole capillary blood ethanol concentrations following the oral administration of a 30-ml dose of absolute alcohol (0.32 g/kg absolute alcohol) and 45-ml doses of 95% alcohol (0.45 g/kg absolute alcohol) under varying test meal conditions to an adult male volunteer were measured. Ten different test conditions were two fasting (30 ml and 45 ml), three liquid test meals (45 ml), and five solid test meals (45 ml). The terminal concentration-time data were simultaneously fitted to a modification of the integrated form of the Michaelis-Menten equation. The parametersV m andK m of the Michaelis-Menten equation obtained in this fitting were very close to the average values of these parameters following the constant-rate intravenous infusion of ethanol to six adult male volunteers in another study. The area under the concentration-time curves following the liquid and solid food test meals decreased with an increase in the size of the meal. The reduction in area caused by food was the result of two factors: (a) decrease in efficiency of absorption (average 55%) and (b) slowing of the absorption rate coupled with the operation of Michaelis-Menten elimination kinetics (average 45%).
    Type of Medium: Electronic Resource
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