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pubmed-article:6501513pubmed:abstractTextThis work describes a method for the quantitative determination of the labile, toxic N-hydroxy metabolite of phenacetin in urine. A thin-layer chromatography step was used for the preliminary purification of extracts, and the specificity of the assay was based on the monitoring of specific metastable decompositions in a forward geometry double-focussing mass spectrometer, in a manner analogous to conventional tandem mass spectrometry. This precluded the need for a gas chromatographic separation, thus minimizing thermal decomposition which can occur with these compounds, as well as enabling very rapid analyses.lld:pubmed
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pubmed-article:6501513pubmed:authorpubmed-author:VeroneseM EMElld:pubmed
pubmed-article:6501513pubmed:authorpubmed-author:DaviesN WNWlld:pubmed
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pubmed-article:6501513pubmed:pagination179-87lld:pubmed
pubmed-article:6501513pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:6501513pubmed:articleTitleMass spectrometric determination of N-hydroxyphenacetin in urine using multiple metastable peak monitoring following thin-layer chromatography.lld:pubmed
pubmed-article:6501513pubmed:publicationTypeJournal Articlelld:pubmed