Abstract
A sensitive and quantitative gas chromatographic assay for the determination of 18 beta-glycyrrhetinic acid (18 beta-GA), the main metabolite of glycyrrhizin after oral licorice consumption in human urine, has been developed and validated. For the extraction of 18 beta-GA from urine two Sep-Pak C-18 extractions, hydrolysis with Helix pomatia and three liquid-liquid extractions were performed, using 18 alpha-glycyrrhetinic acid (18 alpha-GA) as internal standard. Both 18 beta-GA and internal standard were converted into their pentafluorobenzyl- ester/ trimethylsilyl-ether derivatives and detected by flame ionization detection using a WCOT-fused-silica capillary column. Good quality control data were obtained in precision and accuracy tests. The detection limit of the gas chromatographic method was 10 mu g/l with a urine volume of 10 ml. A detection limit of 3 mu g/l was obtained by performing GC-MS. The GC method was used to monitor the urinary excretion of 18 beta-GA after licorice consumption by two healthy volunteers and a patient suspected of licorice abuse. Furthermore, it was shown that this GC assay enables to detect other metabolites related to licorice consumption. (C) 1999 Elsevier Science B.V. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 323-334 |
| Number of pages | 12 |
| Journal | Journal of Chromatography B |
| Volume | 731 |
| Issue number | 2 |
| Publication status | Published - 20-Aug-1999 |
Keywords
- licorice
- 18 beta-glycyrrhetinic acid
- PERFORMANCE LIQUID-CHROMATOGRAPHY
- GLYCYRRHETIC ACID
- BIOLOGICAL-FLUIDS
- HUMAN PLASMA
- LICORICE
- HYPERTENSION
- HYPOKALEMIA
- METABOLISM
- EXTRACTION
- RATS