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pubmed-article:1860916pubmed:dateCreated1991-8-30lld:pubmed
pubmed-article:1860916pubmed:abstractTextA quantitative method for the simultaneous high-performance liquid chromatographic (HPLC) resolution and determination of the enantiomers of 5-dimethylsulphamoyl-6,7-dichloro-2,3-dihydrobenzofuran-2-carboxyl ic acid, a new diuretic, and its N-monodemethylated metabolite in monkey plasma and urine is described. The method includes diethyl ether extraction of the samples and S-(-)-alpha-methylbenzylamide derivatization of the extract, followed by reversed-phase solid-phase extraction and injection of the resulting diastereoisomers onto a reversed-phase HPLC column. Baseline separation was obtained. The assay showed linearity over the range 0.1-50 micrograms/ml of plasma and 0.25-500 microliters of urine, with a lower limit of detection of ca. 0.01 micrograms/ml for each of the enantiomers. The method is adequate for pharmacokinetic and enantioselective disposition studies of both the diuretic and its metabolite.lld:pubmed
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pubmed-article:1860916pubmed:issn0021-9673lld:pubmed
pubmed-article:1860916pubmed:authorpubmed-author:NakanoMMlld:pubmed
pubmed-article:1860916pubmed:authorpubmed-author:KawaharaSSlld:pubmed
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pubmed-article:1860916pubmed:pagination235-41lld:pubmed
pubmed-article:1860916pubmed:dateRevised2005-11-17lld:pubmed
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pubmed-article:1860916pubmed:year1991lld:pubmed
pubmed-article:1860916pubmed:articleTitleHigh-performance liquid chromatographic method for simultaneous determination of enantiomers of 5-dimethylsulphamoyl-6,7-dichloro-2-dihydrobenzofuran-2, carboxylic acid and its N-monodemethyl metabolite in monkey plasma and urine after chiral derivatization.lld:pubmed
pubmed-article:1860916pubmed:affiliationShionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.lld:pubmed
pubmed-article:1860916pubmed:publicationTypeJournal Articlelld:pubmed