Literature DB >> 1936060

Chlormezanone plasma and blood levels in patients after single and repeated oral doses and after suicidal drug overdose.

C Köppel1, J Kristinsson, A Wagemann, J Tenczer, F Martens.   

Abstract

Chlormezanone plasma concentrations were determined in 5 volunteers (group 1) after a single oral dose of 200 mg of chlormezanone with high performance liquid chromatography. A plasma elimination half-life of 23 +/- 2.3 h was calculated. The mean peak chlormezanone plasma level was 1.86 +/- 0.2 micrograms/ml, 1 h after ingestion. Additionally, chlormezanone plasma levels were determined after repeated oral doses of chlormezanone recommended for treatment of muscular spasms due to degenerative skeletal disease. After 5 days of repeated daily doses of 3 x 200 mg (group 2; 12 patients) or 3 x 400 mg (group 3; 10 patients) of chlormezanone, mean predose chlormezanone plasma levels were 12.0 +/- 2.0 micrograms/ml (group 2) and 22.7 +/- 4.0 micrograms/ml (group 3), respectively. Comparable plasma concentrations were determined after 10 days of repeated doses of 3 x 200 mg or 3 x 400 mg of chlormezanone in 3 patients from each of these 2 groups. In 7 patients of group 3, chlormezanone had to be discontinued on the 5th day due to increasing muscular weakness, ataxia and exercise-inducible tachycardia. After a loading dose of 800 mg and repeated doses of 3 x 200 mg chlormezanone to 5 patients (group 4), plasma levels of 6.5 +/- 2.1 micrograms/ml, 8.9 +/- 2.2 micrograms/ml, 12.7 +/- 2.0 micrograms/ml, and 10.4 +/- 2.4 micrograms/ml were determined after 2, 8, 16, and 36 h, respectively. Trace amounts of a degradation product of the acid-labile chlormezanone could be detected in plasma besides the unchanged drug after administration of repeated oral doses.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1936060     DOI: 10.1007/BF03189873

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  7 in total

1.  Chlormezanone poisoning.

Authors:  D Armstrong; R A Braithwaite; J A Vale
Journal:  Br Med J (Clin Res Ed)       Date:  1983-03-12

2.  Microcomputer based pharmacokinetic programs for calculating absorption rate.

Authors:  K K Chan; K Wnuck
Journal:  Comput Programs Biomed       Date:  1983 Feb-Apr

3.  Metabolism of chlormezanone in man and laboratory animals.

Authors:  E W McChesney; W F Banks; G A Portmann; A V Crain
Journal:  Biochem Pharmacol       Date:  1967-05       Impact factor: 5.858

4.  Metabolism of chlormezanone in man.

Authors:  C Köppel; J Tenczer; A Wagemann
Journal:  Arzneimittelforschung       Date:  1986-07

5.  Sensitive and selective method for the determination of chlormezanone in plasma by electron-capture gas chromatography.

Authors:  K Ohya; S Shintani; W Suzuki; M Sano
Journal:  J Chromatogr       Date:  1980-11-14

6.  Biotransformation of chlormezanone, 2-(4-chlorophenyl)-3-methyl-4-metathiazanone-1,1-dioxide, a muscle-relaxing and tranquillizing agent: the effect of combination with aspirin on its metabolic fate in rats and mice.

Authors:  H Hakusui; H Tachizawa; M Sano
Journal:  Xenobiotica       Date:  1978-04       Impact factor: 1.908

7.  Determination of chlormezanone in human plasma after administration of chlormezanone formulations.

Authors:  S L Ali; H Blume
Journal:  Arzneimittelforschung       Date:  1987-12
  7 in total

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