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PMID: 666946 Published · ppublish English Journal Article

Plasma concentrations of isosorbide dinitrate and its metabolites after chronic high oral dosage in man.

British journal of clinical pharmacology ·Vol. 6 ·No. 1 ·1978-07-00 ·Pages 37-41

Shane SJ, Iazzetta JJ, Chisholm AW, Berka JF, Leung D

Abstract

1 We have previously reported that vasodilator headache due to isosorbide dinitrate (ISDN) can be circumvented by using small 'priming' doses for an induction period of 1-2 weeks, after which it is possible to increase to dose rapidly to 360-720 mg, daily without recurrence of headache and without toxicity. The present study corroborates this earlier finding. 2. Chronic oral administration of doses of ISDN of this order of magnitude results in prolonged high plasma concentrations of the parent compound, as well as higher levels of the metabolites 2-ISMN and 5-ISMN. 3. It is our thesis that chronic high oral dosage of ISDN saturates the intrahepatic biotransformation process, and allows high concentrations of ISDN and its metabolites to enter the systemic circulation.

MeSH Terms
Administration, Oral Biotransformation Drug Administration Schedule Female Humans Isosorbide Dinitrate/administration & dosage,blood Male Time Factors
Chemicals
Isosorbide Dinitrate
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shane S J
Iazzetta J J
Chisholm A W
Berka J F
Leung D
References (10)
10 references, click to expand
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    J Pharm Sci. 1973 May;62(5):754-8 PMID: 4196204
  9. Disposition of propranolol. V. Drug accumulation and steady-state concentrations during chronic oral administration in man.
    Clin Pharmacol Ther. 1973 Jul-Aug;14(4):487-93 PMID: 4723255
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Article Info
Journal
British journal of clinical pharmacology
Abbr.
Br J Clin Pharmacol
ISSN
0306-5251
Published
1978-07-00
Pages
37-41
Language
English
Region
England
NLM ID
7503323
PMCID
PMC1429383
Subset
IM
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