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PMID: 2778091 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Variability in the pharmacokinetics of nisoldipine as caused by differences in liver blood flow response.

Journal of clinical pharmacology ·Vol. 29 ·No. 8 ·1989-08-00 ·Pages 714-21

van Harten J, van Brummelen P, Ooms P, Danhof M, Blauw GJ, Breimer DD

Abstract

We investigated whether the effect of nisoldipine on liver blood flow depends on its route of administration. Ten healthy subjects took nisoldipine I.V. (infusion) and orally (without and with sotalol pretreatment). Pharmacokinetics of nisoldipine was assessed and liver blood flow (ICG clearance) was measured before dosing and at the end of the infusion or during absorption. During I.V. infusion the ICG plasma clearance increased by only 14%, whereas the increase was 60% during absorption of nisoldipine. Nisoldipine increases liver blood flow considerably only during the absorption phase. A positive correlation was found between the increase in liver blood flow during absorption and the systemic availability of nisoldipine, suggesting that the differences in liver blood flow response to nisoldipine substantially contribute to the variability in pharmacokinetics of the drug.

MeSH Terms
Administration, Oral Adult Blood Specimen Collection Calcium Channel Blockers/pharmacokinetics,pharmacology Hemodynamics/drug effects Humans Indocyanine Green Injections, Intravenous Liver Circulation/drug effects Male Nifedipine/analogs & derivatives,pharmacokinetics,pharmacology Nisoldipine Sotalol/pharmacology
Chemicals
Calcium Channel Blockers Nisoldipine Sotalol Nifedipine Indocyanine Green
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
van Harten J
Leiden University, Division of Pharmacology, The Netherlands.
van Brummelen P
Ooms P
Danhof M
Blauw G J
Breimer D D
Article Info
Journal
Journal of clinical pharmacology
Abbr.
J Clin Pharmacol
ISSN
0091-2700
Published
1989-08-00
Pages
714-21
Language
English
Region
England
NLM ID
0366372
Subset
IM
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