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pubmed-article:6833897pubmed:abstractTextCapillary gas-liquid chromatographic separation was studied for the complete set of the 26 theoretically possible isomers of mono-, di-, and trihydroxylated 5 beta-cholanic acids, which differ from one another in the number, position, and configuration of hydroxyl groups at C-3, C-7, and/or C-12 in the nucleus, as well as for some of their related acids. The bile acid samples were chromatographed as their methyl ester-trimethylsilyl (TMSi) ether derivatives and analyzed on three capillary columns coated with nonpolar OV-1, slightly polar OV-17, and polar SP-2340 as liquid phases. The retention times on capillary gas-liquid chromatography (GLC) responded dramatically to the minor structural differences, and almost complete separation of the positional and stereochemical isomers was achieved by the combined use of SP-2340 and OV-17 (or OV-1) capillary columns.lld:pubmed
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pubmed-article:6833897pubmed:issn0022-2275lld:pubmed
pubmed-article:6833897pubmed:authorpubmed-author:MatsumotoTTlld:pubmed
pubmed-article:6833897pubmed:authorpubmed-author:TamuraTTlld:pubmed
pubmed-article:6833897pubmed:authorpubmed-author:MANNS JSJlld:pubmed
pubmed-article:6833897pubmed:authorpubmed-author:ChangF CFClld:pubmed
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pubmed-article:6833897pubmed:volume24lld:pubmed
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pubmed-article:6833897pubmed:pagination211-5lld:pubmed
pubmed-article:6833897pubmed:dateRevised2000-12-18lld:pubmed
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pubmed-article:6833897pubmed:year1983lld:pubmed
pubmed-article:6833897pubmed:articleTitleSeparation of mono-, di-, and trihydroxy stereoisomers of bile acids by capillary gas-liquid chromatography.lld:pubmed
pubmed-article:6833897pubmed:publicationTypeJournal Articlelld:pubmed
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