Literature DB >> 6653651

Endralazine - a new hydralazine-like antihypertensive with high systemic bioavailability.

P A Reece, I Cozamanis, R Zacest.   

Abstract

Endralazine (E), a new hydralazine-like antihypertensive was given intravenously (0.05 mg/kg) to 10 normal volunteers (5 slow and 5 fast acetylators). Plasma levels were fitted to a 3 compartment model and pharmacokinetic parameters (area under curve [AUC infinity 0], clearance, volume of distribution, half-lives) obtained in the usual way. Bioavailabilities of 5 and 10 mg oral doses of E were determined from the AUC infinity 0 generated in a previous study of oral E given to the same subjects. E had high system bioavailability (73.5-99.1%) suggesting that it was almost completely absorbed without undergoing appreciable first-pass metabolism. Furthermore, dose size and acetylator phenotype did not significantly affect the bioavailability of E. This behavior contrasts with that of hydralazine where systemic bioavailability was less than 40%, and 2 to 3 times higher in slow acetylators than in fast acetylators. It is concluded that the bioavailability of E is high and not influenced by acetylator phenotype; these properties suggest some clinical advantages for the drug.

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Year:  1983        PMID: 6653651     DOI: 10.1007/BF00542127

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  8 in total

1.  Linear pharmacokinetic equations allowing direct calculation of many needed pharmacokinetic parameters from the coefficients and exponents of polyexponential equations which have been fitted to the data.

Authors:  J G Wagner
Journal:  J Pharmacokinet Biopharm       Date:  1976-10

2.  Metabolism of hydralazine in man. Investigation of features relevant to drug safety, Part I.

Authors:  K Schmid; W Küng; W Riess; C T Dollery; S J Harland
Journal:  Arzneimittelforschung       Date:  1981

3.  Kinetic discrimination of three sulfamethazine acetylation phenotypes.

Authors:  D J Chapron; P A Kramer; S A Mercik
Journal:  Clin Pharmacol Ther       Date:  1980-01       Impact factor: 6.875

4.  Kinetics of hydralazine and its main metabolites in slow and fast acetylators.

Authors:  P A Reece; I Cozamanis; R Zacest
Journal:  Clin Pharmacol Ther       Date:  1980-12       Impact factor: 6.875

5.  Influence of acetylator phenotype on the pharmacokinetics of a new vasodilator antihypertensive, endralazine.

Authors:  P A Reece; I Cozamanis; R Zacest
Journal:  Eur J Clin Pharmacol       Date:  1982       Impact factor: 2.953

6.  Sensitive high-performance liquid chromatographic assay for endralazine and two of its metabolites in human plasma.

Authors:  P A Reece; I Cozamanis; R Zacest
Journal:  J Chromatogr       Date:  1981-09-11

7.  Clinical evaluation of endralazine (BO22708), a new vasodilator, in essential hypertension.

Authors:  H L Elliott; K McLean; D J Sumner; R J Donnelly; J L Reid
Journal:  Clin Exp Hypertens A       Date:  1982

8.  Endralazine, a new peripheral vasodilator--a randomized cross-over trial against dihydralazine.

Authors:  W Kirch; T Axthelm
Journal:  J Cardiovasc Pharmacol       Date:  1982 Jul-Aug       Impact factor: 3.105

  8 in total
  1 in total

1.  Pharmacokinetics of endralazine.

Authors:  H L Elliott; P A Meredith; J L Reid
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

  1 in total

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