Literature DB >> 529049

Rapid compartment- and model-independent estimation of times required to attain various fractions of steady-state plasma level during multiple dosing of drugs obeying superposition principle and having various absorption or infusion kinetics.

W L Chiou.   

Abstract

A new general equation based only on plasma data was derived for rapid estimation of the average plasma level and the mean fraction of the steady-state plasma level attained during any multiple-dosing interval. It can be applied to any complex absorption or infusion kinetics (i.e., is not limited to zero-order or first-order kinetics) for drugs obeying linear disposition kinetic or superposition principles. The time, t, required to reach a certain mean fraction of the steady-state plasma level is equal to the time at which the plasma area from time zero to time t is equal to the same fraction of the plasma area from time zero to infinity (AUC0 leads to infinity) following a single dose. No other pharmacokinetic parameters are necessary.

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Year:  1979        PMID: 529049     DOI: 10.1002/jps.2600681222

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  13 in total

1.  Predicting the time needed to achieve steady state if absorption and elimination constants are equal.

Authors:  J Singer; L Vereczkey
Journal:  J Pharmacokinet Biopharm       Date:  1999-06

Review 2.  Rate and extent of drug accumulation after multiple dosing revisited.

Authors:  Dion R Brocks; Reza Mehvar
Journal:  Clin Pharmacokinet       Date:  2010-07       Impact factor: 6.447

Review 3.  The phenomenon and rationale of marked dependence of drug concentration on blood sampling site. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics (Part II).

Authors:  W L Chiou
Journal:  Clin Pharmacokinet       Date:  1989-10       Impact factor: 6.447

Review 4.  Evaluation of methods for estimating time to steady state with examples from phase 1 studies.

Authors:  Lata Maganti; Deborah L Panebianco; Andrea L Maes
Journal:  AAPS J       Date:  2008-02-28       Impact factor: 4.009

5.  Similarity or discrepancy in pharmacokinetic parameter estimation between bolus and infusion studies.

Authors:  W L Chiou; S M Chung; G Robbie
Journal:  J Pharmacokinet Biopharm       Date:  1997-08

6.  Pharmacokinetics of pholcodine in healthy volunteers: single and chronic dosing studies.

Authors:  Z R Chen; F Bochner; A Somogyi
Journal:  Br J Clin Pharmacol       Date:  1988-10       Impact factor: 4.335

7.  Simple approximate formulas for calculating the time to clear drug and the time to accumulate drug when the plasma disposition curve of the drug is multiexponential.

Authors:  D A Noe
Journal:  J Pharmacokinet Biopharm       Date:  1994-12

8.  Use of gamma distributed residence times in pharmacokinetics.

Authors:  M Weiss
Journal:  Eur J Clin Pharmacol       Date:  1983       Impact factor: 2.953

9.  Model-independent assessment of accumulation kinetics based on moments of drug disposition curves.

Authors:  M Weiss
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

10.  Accumulation profiles during quasi-uniform multiple dosing regimens.

Authors:  I A Nestorov
Journal:  J Pharmacokinet Biopharm       Date:  1993-08
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