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

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About: A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 1987

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1987 (uk) article scientifique publié en 1987 (fr) im Juni 1987 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 1987 (ast) scientific article published on 01 June 1987 (en)
publication date	wds:Q69426664-F2912AFE-4A8B-4D98-821B-4E52FFE4DD6A
publication date	1987-06-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q69426664-E89FD3A2-7824-4BCD-98CB-CB44545A4081
exact match	https://scigraph.springernature.com/pub.10.1007/bf01066319
cites work	wds:Q69426664-0647F739-E9BA-4EE5-A630-75287BA74B1B wds:Q69426664-0D459D63-EB91-414E-B475-9FE5034D88FF wds:Q69426664-3D91E55D-4371-425D-8D53-E5546B209D6F wds:Q69426664-4AABDC46-20FD-465C-854B-A23712190B10 wds:Q69426664-4F94B2B3-9412-465D-8A2F-4A22A9665009 wds:Q69426664-55C9AF8A-FABE-4AEE-A127-7551B3D9CC6F wds:Q69426664-5EB0D162-3A1C-427A-8F39-6A9D3ECFA552 wds:Q69426664-CFA63A83-4BAA-493F-BAD2-04353D3DB434 wds:Q69426664-E40A22CD-90EF-4B05-AF38-869F2AA0B916 wds:Q69426664-EEE339D4-FEF3-4BFB-B9ED-366FA01C4294
cites work	Gastrointestinal absorption of drugs Pharmacokinetic interpretation of the enterohepatic recirculation and first-pass elimination of morphine in the rat Pharmacokinetic and biopharmaceutic parameters during enterohepatic circulation of drugs Pharmacokinetics and bioavailability of cimetidine in humans. Pharmacokinetics of doxycycline reabsorption. A time-lag model for pharmacokinetics of drugs subject to enterohepatic circulation The absorption of piretanide from the gastro-intestinal tract is site-dependent Discontinuous Absorption processes in Pharmacokinetic Models Primary dose-dependent pharmacokinetic study of veralipride Comparative bioavailability of two forms of spironolactone. Rationalization applied to dosage (author's transl)
author name string	wds:Q69426664-05262652-4A89-49CA-B431-BAA72ED1E64A wds:Q69426664-685D7C36-0647-4AAC-A9F4-79125CB57CA4 wds:Q69426664-88C11067-4024-4175-982C-19EB6D467E4D wds:Q69426664-A21F9981-41FC-4C92-A7AC-2B4D38210E00 wds:Q69426664-AA4A6F22-C2F1-483B-A316-847FA485C81E wds:Q69426664-E588B8E8-7426-4C19-86C7-C545847F9080 wds:Q69426664-E6422A07-09AC-42E0-88BB-E6B3106705DD
author name string	J P Tillement L Jung G Houin Y Plusquellec G Campistron J Barre S Staveris
rdfs:label	A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (en) A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (nl)
skos:prefLabel	A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (en) A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (nl)
name	A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (en) A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (nl)
title	wds:Q69426664-8FD5E6A6-03B4-4CFC-8F0D-2955602CC478
title	A double-peak phenomenon in the pharmacokinetics of veralipride after oral administration: a double-site model for drug absorption (en)
page(s)	wds:Q69426664-DCED1ED9-BD37-480C-B018-9158C7F80000
page(s)	225-239
instance of	wds:Q69426664-2BAB3CD4-EB71-4871-A242-0212E33F2A24
instance of	scholarly article
main subject	wds:Q69426664-66C6D122-4FC8-4D59-A2F9-E2EA4DD613F2
main subject	pharmacokinetics
PubMed ID	wds:Q69426664-B6F1DCD2-3383-46BE-B3E7-01D3517E1F79
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3668801
PubMed ID	3668801
published in	wds:Q69426664-CE1CA038-966E-4308-9EBC-F76AEC5C4126
published in	Journal of Pharmacokinetics and Pharmacodynamics
issue	wds:Q69426664-19E850CE-C5C9-4B48-AAD4-7258FA75B8CA
volume	wds:Q69426664-B4D36349-8803-4A48-B85A-8B2079C609EC
issue	3
volume	15
DOI	wds:Q69426664-B9D957AF-79F0-43C0-9780-488772E19973
DOI	http://dx.doi.org/10.1007/BF01066319
DOI	10.1007/BF01066319
Dimensions Publication ID	wds:Q69426664-9781A789-599D-44EB-B403-D562A4CB4687
Dimensions Publication ID	1044034561
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69426664
is cites work of	Celiprolol double-peak occurrence and gastric motility: nonlinear mixed effects modeling of bioavailability data obtained in dogs A pharmacokinetic model for multiple sites discontinuous gastrointestinal absorption. Pharmacokinetics Studies of 12 Alkaloids in Rat Plasma after Oral Administration of Zuojin and Fan-Zuojin Formulas. Absorption of flurbiprofen in the fed and fasted states A modified two-portion absorption model to describe double-peak absorption profiles of ranitidine The use of a sum of inverse Gaussian functions to describe the absorption profile of drugs exhibiting complex absorption Appearance of double peaks in plasma concentration-time profile after oral administration depends on gastric emptying profile and weight function. Multiple peaking phenomena in pharmacokinetic disposition. Use of a pharmacokinetic model incorporating discontinuous gastrointestinal absorption to examine the occurrence of double peaks in oral concentration-time profiles A double-site absorption model fits to pharmacokinetic data of repaglinide in man. Pharmacokinetics of a novel antiarrhythmic drug, actisomide A mechanism-based approach for absorption modeling: the Gastro-Intestinal Transit Time (GITT) model. Food-induced increase in bioavailability of 5-methoxypsoralen. The talinolol double-peak phenomenon is likely caused by presystemic processing after uptake from gut lumen Regional gastrointestinal absorption of the beta-blocker pafenolol in the rat and intestinal transit rate determined by movement of 14C-polyethylene glycol (PEG) 4000 CXT-MAIN: a software package for determination of the analytical form of the pharmacokinetic system weighting function Assessment of in vitro metabolic stability, plasma protein binding, and pharmacokinetics of E- and Z-guggulsterone in rat. Pharmacokinetics of a single intravenous and oral dose of pafenolol--a beta 1-adrenoceptor antagonist with atypical absorption and disposition properties--in man Absorption and disposition of a new antiarrhythmic agent bidisomide in man Evaluation of interaction potential of certain concurrently administered drugs with pharmacological and pharmacokinetic profile of centchroman in rats Pharmacokinetics of epanolol (ICI 141,292) in healthy young volunteers and comparative data in elderly patients with angina and subjects with renal or hepatic impairment. Pharmacokinetics of epanolol after acute and chronic oral dosing in elderly patients with stable angina pectoris Nanostructured reverse hexagonal liquid crystals sustain plasma concentrations for a poorly water-soluble drug after oral administration Empirical and semi-mechanistic modelling of double-peaked pharmacokinetic profile phenomenon due to gastric emptying. The absolute bioavailability investigation of LS177 in rats using ultra-performance liquid chromatography-tandem mass spectrometry. ICI 141,292 (epanolol)--pharmacokinetics after single and repeated oral administration in the elderly with moderate renal impairment

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