Chromatographic resolution of enantiomers using albumin as complexing agent in the mobile phase
C Pettersson1, T Arvidsson, A L Karlsson
1Department of Analytical Pharmaceutical Chemistry, Biomedical Center, University of Uppsala, Box 574, S-751 23 Uppsala, Sweden.
Abstract:
Enantiomers of carboxylic acids have been separated with albumin as a chiral complexing agent in the mobile phase. Stereoselective separation has been obtained for different types of acids, in some cases with very high separation factor, as shown for di-p-toluoyltartaric acid (alpha(s) = 5.8). The stereoselectivity and retention properties depend on pH and on the concentration of albumin in the mobile phase. Retention can also be regulated by modifying the nature of the solid phase as well as by the use of additives in the mobile phase. Acids with low molar absorptivity, or with absorbance in the same wavelength range as albumin, can be detected by an indirect technique based on the use of a cationic mobile phase additive, such as 1-ethylquinolinium, which has high UV-absorptivity at a wavelength remote from that of albumin.
Related Concept Videos
Racemic Mixtures and the Resolution of Enantiomers
Ion-Exchange Chromatography
Chromatographic Resolution
The effectiveness of separation can be evaluated by determining the level of separation between two neighboring peaks in a chromatogram, which represents the individual components of a sample.
In chromatography,...
Optimizing Chromatographic Separations
Band broadening refers to spreading solute bands as they travel through the column. This broadening can impact resolution. Plate height (H) represents the length required for one theoretical plate. A lower plate height corresponds to...
Affinity Chromatography
Principles Of Column Chromatography


