Retention Behavior of Bile Acid Derivatives Using Cyclodextrin in the Mobile Phase in High-Performance Liquid Chromatography
- 1 June 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Chromatographic Science
- Vol. 28 (6) , 331-335
- https://doi.org/10.1093/chromsci/28.6.331
Abstract
The retention behavior of 3-(1-anthroyl)bile acids together with bile acid glucuronides, sulfates, and 12-dehydro derivatives is examined by the addition of cyclodextrin to the mobile phase in reversed-phase high-performance liquid chromatography. The data suggest that the functional group at the 12 position of the steroid moiety may be the important factor for the formation of the inclusion complex from the solute and cyclodextrin. The separation of these bile acid derivatives is much improved by this inclusion chromatography.This publication has 3 references indexed in Scilit:
- Chromatographic Behavior of Bile Acids Using Cyclodextrin in Mobile Phase of High Performance Liquid ChromatographyJournal of Liquid Chromatography, 1989
- Synthesis of monosulfates of unconjugated and conjugated bile acids.CHEMICAL & PHARMACEUTICAL BULLETIN, 1979
- Conformation of O-methylated amylose and cyclodextrinsTetrahedron, 1968