| Literature DB >> 3507261 |
M A Diez Ibañez1, M Chessebeuf-Padieu, P Nordmann, P Padieu.
Abstract
A new technique for the conversion of 2-acetylaminofluorene and several ring-hydroxylated metabolites to mono- and di-tert.-butyldimethylsilyl derivatives was developed to permit their analysis by gas chromatography-mass spectrometry in order to quantify the metabolism of 2-acetylaminofluorene incubated in freshly isolated rat hepatocytes. This new gas chromatography-mass spectrometry method allowed the separation, identification and quantitation of seven known metabolites comprising five arylhydroxylated compounds, 2-aminofluorene and N-hydroxy-2-acetylaminofluorene.Entities:
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Year: 1987 PMID: 3507261 DOI: 10.1007/bf00117869
Source DB: PubMed Journal: Cell Biol Toxicol ISSN: 0742-2091 Impact factor: 6.691