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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 25 (1997), S. 363-375 
    ISSN: 1573-8744
    Keywords: liver model ; hepatic elimination ; transit time distribution ; mixing ; relative dispersion ; isolated perfused organ ; relative entropy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract One of the fundamental differences between various liver models regards the underlying assumptions on the intrahepatic mixing process. A model-independent method for the evaluation of the departure from the perfectly mixed system is proposed which is based on an application of the relative entropy concept to hepatic transit time distributions of intravascular markers. This approach provides a measure of the distance between two probability distributions. Available data measured in isolated perfused livers indicate that sinusoidal solute mixing is nearly optimal. The suggestion of maximum mixedness in the liver may explain the discrepancy between the apparent validity of the venous equilibrium model and the physiological irrelevance of the underlying well-stirred assumption. In terms of the dispersion model the results are in accordance with the model equation obtained for mixed boundary conditions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of pharmacokinetics and pharmacodynamics 23 (1995), S. 635-649 
    ISSN: 1573-8744
    Keywords: mean disposition residence time ; relative dispersion ; model misspecification ; triexponential model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A Monte Carlo simulation study was carried out to examine the accuracy of parameters derived from curve moments. Impulse response (IR) and washout (WO) concentration-time curves, based on a triexponential model, were analyzed by numerical integration and regression analysis. Both designs were tested according to their robustness to measurement error and model misspecification. Performance of the methods was judged using the median error (ME) and the median absolute error (MAE) of 1000 simulations. The WO design provided better estimates of mean disposition residence time and worse estimates of the normalized variance of disposition residence times (CV d 2 ) than its rival. At 20% measurement noise, theMAE ofCV d 2 was less than 13%. The WO design was much more robust to model misspecification. Numerical integration performed as good as, or better than, regression analysis. Both methods are very sensitive to tail-area error, meaning that special attention needs to be paid to this aspect of experimental design. This study demonstrates that it is possible to obtain good estimates of higher moment parameters in a well-designed experiment.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 16 (1999), S. 1470-1476 
    ISSN: 1573-904X
    Keywords: dissolution ; model ; fractional dissolution rate ; mean dissolution time ; relative dispersion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. To present a new model for describing drug dissolution. On the basis of the new model to characterize the dissolution profile by the distribution function of the random dissolution time of a drug molecule, which generalizes the classical first order model. Methods. Instead of assuming a constant fractional dissolution rate, as in the classical model, it is considered that the fractional dissolution rate is a decreasing function of the dissolved amount controlled by the dose-solubility ratio. The differential equation derived from this assumption is solved and the distribution measures (half-dissolution time, mean dissolution time, relative dispersion of the dissolution time, dissolution time density, and fractional dissolution rate) are calculated. Finally, instead of monotonically decreasing the fractional dissolution rate, a generalization resulting in zero dissolution rate at time origin is introduced. Results. The behavior of the model is divided into two regions defined by q, the ratio of the dose to the solubility level: q 〈 1 (complete dissolution of the dose, dissolution time) and q 〉 1 (saturation of the solution, saturation time). The singular case q = 1 is also treated and in this situation the mean as well as the relative dispersion of the dissolution time increase to infinity. The model was successfully fitted to data(l). Conclusions. This empirical model is descriptive without detailed physical reasoning behind its derivation. According to the model, the mean dissolution time is affected by the dose-solubility ratio. Although this prediction appears to be in accordance with preliminary application, further validation based on more suitable experimental data is required.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pharmaceutical research 17 (2000), S. 583-588 
    ISSN: 1573-904X
    Keywords: bioequivalence ; absorption rate ; extended-release ; mean absorption time ; relative dispersion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. The sensitivity and effectiveness of indirect metrics proposedfor the assessment of comparative absorption rates in bioequivalencestudies [C max , T max , partial AUC(AUC p ), feathered slope (SL f ), interceptmetric (I)] were originally tested by assuming first-order absorption.The present study re-evaluates their sensitivity performances using themore realistic inverse Gaussian (IG) model characterizing the inputprocess for oral drug administration. Methods. Simulations were performed for both the first-order orexponential model (EX) which is determined by only one parameter, themean absorption time (MAT = 1/k a ), and the IG model, whichadditionally contains a shape parameter, the relative dispersion of absorptiontime distribution (CV 2 A ). Kinetic sensitivities (KS) of the indirectmetrics were evaluated from bioequivalence trials (error free data)generated with various ratios of the true parameters (MAT and CV 2 A ) of thetwo formulations. Results. The behavior of the metrics was similar with respect tochanges in MAT ratios with both models: KS was low with C max ,moderate with SL f and AUC p , and high with I and T max followingcorrection for apparent lag time (T lag ). Changes of the shape parameterCV 2 A , however, were not detectable by C max , T max , SL f , and AUC p .Changes in both MAT and CV 2 A were well reflected by I with CV 2 A - ratio〉 1. I exhibited approximately full KS also with CV 2 A - ratio 〈1 when a correction was first applied for the apparent lag time. Conclusions. The time profile of absorption rates is insufficientlycharacterized by only one parameter (MAT). Indirect metrics which aresensitive enough to detect changes in the scale and shape of the inputprofile could be useful for bioequivalence testing. Among the testedmeasures, I is particularly promising when a correction is appliedfor T lag .
    Type of Medium: Electronic Resource
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