Literature DB >> 3668801

A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption.

Y Plusquellec1, G Campistron, S Staveris, J Barre, L Jung, J P Tillement, G Houin.   

Abstract

Equal doses of veralipride have been given to 12 healthy volunteers by three different administrations--intravenous infusion, oral solution, and oral capsules--in a randomized cross-over design. After the intake of the solution, but not after infusion or capsules, two maximum plasma concentrations have been observed and interpreted, according to a double-site model for drug absorption.

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Year:  1987        PMID: 3668801     DOI: 10.1007/bf01066319

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


  11 in total

Review 1.  Gastrointestinal absorption of drugs.

Authors:  L F Prescott
Journal:  Med Clin North Am       Date:  1974-09       Impact factor: 5.456

2.  Primary dose-dependent pharmacokinetic study of veralipride.

Authors:  S Staveris; G Houin; J P Tillement; G Jamet; M Schneider; L Jung; J C Koffel
Journal:  J Pharm Sci       Date:  1985-01       Impact factor: 3.534

3.  Discontinuous absorption processes in pharmacokinetic models.

Authors:  R Süverkrüp
Journal:  J Pharm Sci       Date:  1979-11       Impact factor: 3.534

4.  A time-lag model for pharmacokinetics of drugs subject to enterohepatic circulation.

Authors:  J L Steimer; Y Plusquellec; A Guillaume; J F Boisvieux
Journal:  J Pharm Sci       Date:  1982-03       Impact factor: 3.534

5.  Pharmacokinetic and biopharmaceutic parameters during enterohepatic circulation of drugs.

Authors:  W A Colburn
Journal:  J Pharm Sci       Date:  1982-01       Impact factor: 3.534

6.  Pharmacokinetics of doxycycline reabsorption.

Authors:  P V Pedersen; R Miller
Journal:  J Pharm Sci       Date:  1980-02       Impact factor: 3.534

7.  [Comparative bioavailability of two forms of spironolactone. Rationalization applied to dosage (author's transl)].

Authors:  P d'Athis; M O Richard; D de Lauture; E Rey; M Bouvier d'Yvoire; E Clement; G Olive
Journal:  Therapie       Date:  1981 Jul-Aug       Impact factor: 2.070

8.  Quantitative analysis of veralipride in plasma and urine by gas chromatography-mass spectrometry and gas chromatography with flame-ionization detection.

Authors:  S Staveris; L Jung; G Jamet; J C Koffel
Journal:  J Chromatogr       Date:  1985-02-27

9.  Pharmacokinetics and bioavailability of cimetidine in humans.

Authors:  P V Pedersen; R Miller
Journal:  J Pharm Sci       Date:  1980-04       Impact factor: 3.534

10.  Pharmacokinetic interpretation of the enterohepatic recirculation and first-pass elimination of morphine in the rat.

Authors:  B E Dahlström; L K Paalzow
Journal:  J Pharmacokinet Biopharm       Date:  1978-12
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  26 in total

1.  A double-site absorption model fits to pharmacokinetic data of repaglinide in man.

Authors:  X D Liu; H F Ji; L Xie; M Q Yan; L Zhang; X Huang
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2000 Apr-Jun       Impact factor: 2.441

2.  A modified two-portion absorption model to describe double-peak absorption profiles of ranitidine.

Authors:  Ophelia Q P Yin; Brian Tomlinson; Albert H L Chow; Moses S S Chow
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

3.  A mechanism-based approach for absorption modeling: the Gastro-Intestinal Transit Time (GITT) model.

Authors:  Emilie Hénin; Martin Bergstrand; Joseph F Standing; Mats O Karlsson
Journal:  AAPS J       Date:  2012-06       Impact factor: 4.009

Review 4.  Multiple peaking phenomena in pharmacokinetic disposition.

Authors:  Neal M Davies; Jody K Takemoto; Dion R Brocks; Jaime A Yáñez
Journal:  Clin Pharmacokinet       Date:  2010-06       Impact factor: 6.447

5.  The use of a sum of inverse Gaussian functions to describe the absorption profile of drugs exhibiting complex absorption.

Authors:  Chantal Csajka; David Drover; Davide Verotta
Journal:  Pharm Res       Date:  2005-08-03       Impact factor: 4.200

6.  Use of a pharmacokinetic model incorporating discontinuous gastrointestinal absorption to examine the occurrence of double peaks in oral concentration-time profiles.

Authors:  A B Suttle; G M Pollack; K L Brouwer
Journal:  Pharm Res       Date:  1992-03       Impact factor: 4.200

7.  Pharmacokinetics of a single intravenous and oral dose of pafenolol--a beta 1-adrenoceptor antagonist with atypical absorption and disposition properties--in man.

Authors:  C G Regårdh; P Lundborg; M Gabrielsson; A Heggelund; K Kylberg-Hanssen
Journal:  Pharm Res       Date:  1990-12       Impact factor: 4.200

8.  ICI 141,292 (epanolol)--pharmacokinetics after single and repeated oral administration in the elderly with moderate renal impairment.

Authors:  M S Laher; P Crome; G S Rakhra; S I Ankier; I D Cockshott
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

9.  Absorption and disposition of a new antiarrhythmic agent bidisomide in man.

Authors:  C S Cook; G B Ames; M E Smith; K G Kowalski; A Karim
Journal:  Pharm Res       Date:  1993-11       Impact factor: 4.200

10.  Appearance of double peaks in plasma concentration-time profile after oral administration depends on gastric emptying profile and weight function.

Authors:  Yukiko Metsugi; Yoshihiro Miyaji; Ken-ichi Ogawara; Kazutaka Higaki; Toshikiro Kimura
Journal:  Pharm Res       Date:  2007-10-23       Impact factor: 4.200

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