Isomers of uroporphyrin free acids separated by HPLC
β Scribed by Wayne, A. W. ;Straight, R. C. ;Wales, E. E. ;Englert, E.
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 183 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0935-6304
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A synthetic mixture of uroporphyrin isomers I, II, III and IV as free acids in the synthetic ratio of 1:1:4:2 was resolved by reverseβphase HPLC using a C0:PEL (ODS) 37β50 micron precolumn and a Micro Bondapak C18 analytical column eluted with acetonitrile (4%) in phosphate buffer (pH 6.95). Clinically important I and III isomers of uroporphyrin were readily resolved directly from acidified urine as porphyrin free acids.
π SIMILAR VOLUMES
## Abstract Different capillary electromigration techniques were employed to resolve geometrical isomers of sorbic acid, decadienoic acid, and ethyl sorbate. Since these substances differ in their polarity, shape, and size, various electromigration approaches were investigated to separate the four
The optimization of the separation of eight aromatic carboxylic acids, using Hypersil SAS and MOS reverse phase columns, with respect to eluent (methanol :water) composition, pH, and temperature, is described. Window diagram techniquesareused and the pH of the aqueous buffer and elution temperature
## Abstract The separation of __Digitalis__ cardenolides has been carried out by HPLC on an adsorbent column. By choice of suitable mobile phase, isocratic elution permitted resolution of mixtures of (a) aglycones, (b) secondary glycosides, and (c) primary glycosides, while gradient elution provide