The common conjugated bile acids of deproteinated bile from the human or the rat can be separated by high-pressure liquid chromatography and quantitated within 30 min with a 4-mm x 30-cm "fatty-acid analysis" column (Waters Associates) in 2-propanoV8.8 mM potassium phosphate buffer (pH 2.5) 160:340,
Bile acids: XLVIII. Separation of conjugated bile acids by high-pressure liquid chromatography
โ Scribed by Roger Shaw; William H. Elliott
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 496 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
โฆ Synopsis
Major conjugated bile acids of human bile have been resolved by high-pressure liquid chromatography. The elutions are carried out in two stages on Corasil II or PPorasil columns; first, an alkaline solvent system (Zpropanokethyl acetate/ water/7 N ammonium hydroxide, 260:600:50:3) was used for separation into groups: tauro-dihydroxy derivatives, taurocholate, glyco-dihydroxy derivatives, and glycocholate. The fraction containing glyco-dihydroxy conjugates was separated by rechromatography in acetonitrile/acetic acid, 400:10, and the fraction containing tauro-dihydroxy conjugates could be partially resolved by rechromatography in acetonitrilelacetic acid/formic acid (97%)/water, 500: 105: 10. Three samples of prepared human bile have been similarly treated.
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