Literature DB >> 6723766

Evaluating drug absorption after oral administration. Some problems and some solutions.

K K Chan, M Gibaldi.   

Abstract

Quantitative assessment of drug absorption remains a difficult task, because the multiple-compartment disposition of a drug may not be obvious after oral administration (the problem of the vanishing exponential) and the macroconstants are indistinguishable. For these reasons, proper analysis of the drug absorption based on the apparent behavior of oral data without intravenous reference curve rarely provides absorption information useful for in vivo - in vitro correlations. When intravenous reference curve is available, compartment model used for analysis of the oral data should be corresponding to the iv data such as the Loo - Riegelman method. The model independent statistical moments method is one of the preferable alternatives because of its ease of computation and its potentially smaller error, if absorption can be assumed to be first-order.

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Year:  1984        PMID: 6723766     DOI: 10.1007/BF00630295

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  8 in total

1.  Per cent absorbed time plots derived from blood level and/or urinary excretion data.

Authors:  J G WAGNER; E NELSON
Journal:  J Pharm Sci       Date:  1963-06       Impact factor: 3.534

2.  Linear pharmacokinetic models and vanishing exponential terms: implications in pharmacokinetics.

Authors:  J G Wagner
Journal:  J Pharmacokinet Biopharm       Date:  1976-10

3.  Application of the Wagner-Nelson absorption method to the two-compartment open model.

Authors:  J G Wagner
Journal:  J Pharmacokinet Biopharm       Date:  1974-12

4.  New method for calculating the intrinsic absorption rate of drugs.

Authors:  J C Loo; S Riegelman
Journal:  J Pharm Sci       Date:  1968-06       Impact factor: 3.534

5.  "Absorption rate constants" calculated according to the one-compartment open model with first-order absorption: implications in in vivo-in vitro correlations.

Authors:  J G Wagner
Journal:  J Pharm Sci       Date:  1970-07       Impact factor: 3.534

6.  Interpretation of plasma concentration-time curves after oral dosing.

Authors:  R A Ronfeld; L Z Benet
Journal:  J Pharm Sci       Date:  1977-02       Impact factor: 3.534

7.  The application of statistical moment theory to the evaluation of in vivo dissolution time and absorption time.

Authors:  S Riegelman; P Collier
Journal:  J Pharmacokinet Biopharm       Date:  1980-10

8.  Numerical integration simulation programs for the microcomputer.

Authors:  J R Koup; D R Benjamin
Journal:  Ther Drug Monit       Date:  1980       Impact factor: 3.681

  8 in total
  5 in total

Review 1.  Flip-flop pharmacokinetics--delivering a reversal of disposition: challenges and opportunities during drug development.

Authors:  Jaime A Yáñez; Connie M Remsberg; Casey L Sayre; M Laird Forrest; Neal M Davies
Journal:  Ther Deliv       Date:  2011-05

2.  Effects of variation in drug elimination on five methods for assessing zero-order drug absorption rates.

Authors:  H Y Cheng; W J Jusko
Journal:  Pharm Res       Date:  1990-01       Impact factor: 4.200

3.  Coupled solutions of one- and two-compartment pharmacokinetic models with first-order absorption.

Authors:  N Asmanova; G Koloskov; A I Ilin
Journal:  J Pharmacokinet Pharmacodyn       Date:  2013-04-10       Impact factor: 2.745

4.  The area function method for assessing the drug absorption rate in linear systems with zero-order input.

Authors:  H Cheng; W J Jusko
Journal:  Pharm Res       Date:  1989-02       Impact factor: 4.200

5.  An area function method for estimating the apparent absorption rate constant.

Authors:  H Cheng; A E Staubus; L Shum
Journal:  Pharm Res       Date:  1988-01       Impact factor: 4.200

  5 in total

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