Literature DB >> 6737267

Determination of amphetamine, norephedrine, and their phenolic metabolites in rat brain by gas chromatography.

R T Coutts, D B Prelusky, G B Baker.   

Abstract

A specific analytical procedure for the quantitation of amphetamine (I), norephedrine (III), and their amphoteric metabolites, p-hydroxy-amphetamine (II) and p-hydroxynorephedrine (IV), in biological samples using electron-capture gas chromatography (GC-EC) is described. The procedure utilizes the ion-pairing reagent, bis(2-ethylhexyl)phosphoric acid, which frees the amines from most contaminants and permits the efficient extraction of the amphoteric compounds (as acetates) from the aqueous solution. Amines I and III and acetylated amines II and IV were perfluoroacetylated prior to GC-EC analysis. Metabolism of I, II, and III in the rat brain was studied. Results indicate that both in vivo and in vitro amines I and III are p-hydroxylated to II and IV, respectively, and II is beta-hydroxylated to give IV. Norephedrine (III) was not detected as a rat brain metabolite of amphetamine (I).

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6737267     DOI: 10.1002/jps.2600730625

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  2 in total

1.  Detection and quantitation of a ring-hydroxylated metabolite of the antidepressant drug tranylcypromine.

Authors:  G B Baker; D R Hampson; R T Coutts; R G Micetich; T W Hall; T S Rao
Journal:  J Neural Transm       Date:  1986       Impact factor: 3.575

Review 2.  Metabolism of monoamine oxidase inhibitors.

Authors:  G B Baker; L J Urichuk; K F McKenna; S H Kennedy
Journal:  Cell Mol Neurobiol       Date:  1999-06       Impact factor: 5.046

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.