Literature DB >> 34416

Study of urinary excretion of butobarbitone in man in relation to the percentage of ideal body weight.

G Cheymol, C Bernheim, J Besson, J Dry, R Portet.   

Abstract

1 Thirty-three patients with no evidence of endocrine disease, hepatic or renal insufficiency or sleep disorders, were classified in groups 1 to 4 in order of increasing of percentage of ideal body weight (IBW) respectively: less than 90% of IBW, 90--120%, 120--180%, and greater than 180% of IBW. After oral administration of 200 mg butobarbitone, concentration of the intact drug was measured by gas liquid chromatographic assay in urine samples collected during 72 h and at three times in blood. 2 A highly significant negative relationship was found between the cumulative excretion of butobarbitone with urine and the logarithm of the percentage of IBW. In contrast for a given weight, excretion of the drug with urine was found to be weakly correlated with the diuresis. 3 The cumulative urinary elimination of butobarbitone was significantly different between the groups studied, except of the difference between the group 2 and 3 of the patients. No significant difference was found between the renal clearances of butobarbitone in the four groups of subjects. 4 We conclude that redistribution of butobarbitone into adipose tissues can explain the obtained results and that obesity modifies the pharmacokinetics of the drug.

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Year:  1979        PMID: 34416      PMCID: PMC1429492          DOI: 10.1111/j.1365-2125.1979.tb00937.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  18 in total

Review 1.  Clinical pharmacokinetics of hypnotics.

Authors:  D D Breimer
Journal:  Clin Pharmacokinet       Date:  1977 Mar-Apr       Impact factor: 6.447

2.  Plasma levels and urinary excretion of three barbituric acids after oral administration to man.

Authors:  P LOUS
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1954

3.  Some factors influencing distribution, metabolism and action of barbiturates; a review.

Authors:  R K RICHARDS; J D TAYLOR
Journal:  Anesthesiology       Date:  1956-05       Impact factor: 7.892

4.  A study of barbiturate clearance.

Authors:  E BRODWALL; K F STOA
Journal:  Acta Med Scand       Date:  1956-03-26

5.  The distribution and excretion of phenobarbital.

Authors:  W J WADDELL; T C BUTLER
Journal:  J Clin Invest       Date:  1957-08       Impact factor: 14.808

6.  The influence of body weight, sex and age on the dosage of thiopentone.

Authors:  J W DUNDEE
Journal:  Br J Anaesth       Date:  1954-05       Impact factor: 9.166

7.  The role of body fat in limiting the duration of action of thiopental.

Authors:  B B BRODIE; E BERNSTEIN; L C MARK
Journal:  J Pharmacol Exp Ther       Date:  1952-08       Impact factor: 4.030

8.  Ethyl(3-hydroxy-n-butyl)barbituric acid as a metabolite of neonal.

Authors:  E W MAYNERT
Journal:  J Biol Chem       Date:  1952-03       Impact factor: 5.157

9.  [Study in man of butobarbital pharmacokinetics, under polygraphic monitoring].

Authors:  G Cheymol; C Bernheim; J Besson; J C Willer; R Gomeni; J C Gilbert
Journal:  Therapie       Date:  1978 May-Jun       Impact factor: 2.070

10.  Butobarbitone metabolism in man: identification of 3'-ketobutobarbitone.

Authors:  J Grove; P A Toseland; G H Draffan; R A Clare; F M Williams
Journal:  J Pharm Pharmacol       Date:  1974-03       Impact factor: 3.765

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  1 in total

Review 1.  Lean body mass as a predictor of drug dosage. Implications for drug therapy.

Authors:  D J Morgan; K M Bray
Journal:  Clin Pharmacokinet       Date:  1994-04       Impact factor: 6.447

  1 in total

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