|
|
||||||||
Journal of Lipid Research, Vol. 9, 226-236, March 1968
Laboratory for Pathological Biochemistry of the St. Rafaëlsklinieken, and Rega Institute, Leuven, Belgium
A method for the determination of total bile acids in human feces that is suitable for routine application is described and discussed. Bile acids are extracted from freeze-dried feces with acetic acid and toluene, in the presence of the internal standard 23-nordeoxycholic acid. After saponification of the extract, bile acids and the internal standard are methylated and converted by mild chromic acid oxidation into their ketonic derivatives. The resultant mixture of a few stable compounds can be separated and measured quantitatively by gas-liquid chromatography on a methylsiloxane polymer. A reference bile acid mixture including the internal standard is also taken through the entire procedure with each series of samples. It has been demonstrated that, in spite of the omission of the usual purification steps, the method is specific for bile acids. Supplementary key words fecal bile acids man extraction hydrolysis keto derivatives gas-liquid chromatography temperature programmed reproducibility antibiotics
Submitted on September 2, 1966
Copyright © 1968 by Lipid Research, Inc.
Gas-liquid chromatographic determination of human fecal bile acids
Revised on September 1, 1967
Accepted on December 4, 1967
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
A. K. Batta, G. Salen, K. R. Rapole, M. Batta, P. Batta, D. Alberts, and D. Earnest Highly simplified method for gas-liquid chromatographic quantitation of bile acids and sterols in human stool J. Lipid Res., June 1, 1999; 40(6): 1148 - 1154. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Journal of Biological Chemistry |
| Molecular and Cellular Proteomics | ASBMB Today |