Literature DB >> 3746639

Estimation of drug absorption rates using a deconvolution method with nonequal sampling times.

K Iga, Y Ogawa, T Yashiki, T Shimamoto.   

Abstract

A method affording direct estimation of the drug absorption rate from blood level data using arbitrary time intervals has been derived based on the staircase input principle. In the derivation, the drug was assumed to follow linear kinetics where the plasma concentration of the drug after an impulse input is expressed by a multiexponential function. Drug absorption was assumed to occur at a constant rate during each subsequent sampling interval. The absorption rate profiles obtained by the method using several numerical examples were expressed as a set of rectangular pulses. Divergence in the profiles reflected blood sampling measurement errors rather than errors due to the deconvolution. Smoothing of the rate profiles by calculating the mean of the absorption rates between adjacent time intervals gave realistic results. Absorption rate profiles for theophylline obtained by the method using published data gave information on the initiation and termination of the absorption as well as the extent of absorption from the dosage form.

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Year:  1986        PMID: 3746639     DOI: 10.1007/bf01065261

Source DB:  PubMed          Journal:  J Pharmacokinet Biopharm        ISSN: 0090-466X


  9 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.  A new numerical calculation method for deconvolution in linear compartment analysis of pharmacokinetics.

Authors:  H Kiwada; K Morita; M Hayashi; S Awazu; M Hanano
Journal:  Chem Pharm Bull (Tokyo)       Date:  1977-06       Impact factor: 1.645

3.  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

4.  A crossover study after oral and intravenous administration of theophylline in male volunteers (absolute bioavailability of Afonilum tablets).

Authors:  H S Kaumeier; O H Kehrhahn; G Neugebauer; D Schuppan; J A Schwarz; A H Staib
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1983-07

5.  Numerical deconvolution by least squares: use of polynomials to represent the input function.

Authors:  D J Cutler
Journal:  J Pharmacokinet Biopharm       Date:  1978-06

6.  Mathematical basis of point-area deconvolution method for determining in vivo input functions.

Authors:  D P Vaughan; M Dennis
Journal:  J Pharm Sci       Date:  1978-05       Impact factor: 3.534

7.  New compartment- and model-independent method for rapid calculation of drug absorption rates.

Authors:  W L Chiou
Journal:  J Pharm Sci       Date:  1980-01       Impact factor: 3.534

8.  Model-independent method of analyzing input in linear pharmacokinetic systems having polyexponential impulse response II: Numerical evaluation.

Authors:  P V Pedersen
Journal:  J Pharm Sci       Date:  1980-03       Impact factor: 3.534

9.  Model-independent method of analyzing input in linear pharmacokinetic systems having polyexponential impulse response I: Theoretical analysis.

Authors:  P V Pedersen
Journal:  J Pharm Sci       Date:  1980-03       Impact factor: 3.534

  9 in total
  19 in total

1.  An extended point-area deconvolution approach for assessing drug input rates.

Authors:  K C Yeh; D J Holder; G A Winchell; L A Wenning; T Prueksaritanont
Journal:  Pharm Res       Date:  2001-10       Impact factor: 4.200

2.  Comparison of methods to calculate cyclosporine A bioavailability from consecutive oral and intravenous doses.

Authors:  M O Karlsson; A Lindberg-Freijs
Journal:  J Pharmacokinet Biopharm       Date:  1990-08

3.  Bioavailability estimation by semisimultaneous drug administration: a Monte Carlo simulation study.

Authors:  M O Karlsson; U Bredberg
Journal:  J Pharmacokinet Biopharm       Date:  1990-04

4.  Estimation of parameters for the elimination of an orally administered test substance with unknown absorption.

Authors:  Josef A Vogt; Christian Denzer
Journal:  J Pharmacokinet Pharmacodyn       Date:  2013-02-02       Impact factor: 2.745

5.  Relationship between the phasic period of interdigestive migrating contraction and the systemic bioavailability of acetaminophen in dogs.

Authors:  K Sagara; H Mizuta; M Ohshiko; M Shibata; K Haga
Journal:  Pharm Res       Date:  1995-04       Impact factor: 4.200

6.  Regional rectal perfusion: a new in vivo approach to study rectal drug absorption in man.

Authors:  H Lennernäs; U Fagerholm; Y Raab; B Gerdin; R Hällgren
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

7.  Evidence for an interaction between the beta-blocker pafenolol and bile salts in the intestinal lumen of the rat leading to dose-dependent oral absorption and double peaks in the plasma concentration-time profile.

Authors:  H Lennernäs; C G Regårdh
Journal:  Pharm Res       Date:  1993-06       Impact factor: 4.200

8.  Absorption of 2',3'-dideoxyinosine from lower gastrointestinal tract in rats and kinetic evidence of different absorption rates in colon and rectum.

Authors:  S L Bramer; M G Wientjes; J L Au
Journal:  Pharm Res       Date:  1993-05       Impact factor: 4.200

9.  Rates of systemic degradation and reticuloendothelial system (RES) uptake of thermosensitive liposome encapsulating cisplatin in rats.

Authors:  K Iga; Y Ogawa; H Toguchi
Journal:  Pharm Res       Date:  1993-09       Impact factor: 4.200

10.  Regional gastrointestinal absorption of the beta-blocker pafenolol in the rat and intestinal transit rate determined by movement of 14C-polyethylene glycol (PEG) 4000.

Authors:  H Lennernäs; C G Regårdh
Journal:  Pharm Res       Date:  1993-01       Impact factor: 4.200

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