| Reference : Association of two single-isomer anionic CD in NACE for the chiral and achiral separatio... |
| Scientific journals : Article | |||
| Human health sciences : Pharmacy, pharmacology & toxicology | |||
| http://hdl.handle.net/2268/41408 | |||
| Association of two single-isomer anionic CD in NACE for the chiral and achiral separation of fenbendazole, its sulphoxide and sulphone metabolites: Application to their determination after in vitro metabolism | |
| English | |
Rousseau, Anne [Université de Liège - ULg > Département de pharmacie > Analyse des médicaments >] | |
| Gillotin, Florian [Université de Liège - ULG > > Pharmacologie clinique > >] | |
| Chiap, Patrice [Université de Liège - ULg > > Pharmacologie clinique >] | |
Crommen, Jacques [Université de Liège - ULg > Département de pharmacie > Analyse des médicaments >] | |
Fillet, Marianne [Université de Liège - ULg > Département de pharmacie > Analyse des médicaments >] | |
Servais, Anne-Catherine [Université de Liège - ULg > Département de pharmacie > Analyse des médicaments >] | |
| 2010 | |
| Electrophoresis | |
| Vch Publishers | |
| 31 | |
| 1482-1487 | |
| International | |
| 0173-0835 | |
| Weinheim | |
| Germany | |
| [en] Benzimidazole compounds ; In vitro metabolites ; Nonaqueous capillary electrophoresis ; Single-isomer anionic cyclodextrins | |
| [en] A NACE method was developed for the separation of fenbendazole (FBZ), a prochiral
drug giving rise to chiral (oxfendazole or OFZ) and nonchiral (FBZ sulphone or FBZSO2) metabolites. First, the effect of the nature and the concentration of CD as well as that of the acidic BGE on the enantiomeric separation of OFZ were studied. OFZ enantiomers were completely resolved using a BGE made up of 10 mM ammonium formate and 0.5 M TFA in methanol containing 10 mM heptakis(2,3-di-O-acetyl-6-O-sulfo)-beta-CD and 10 mM heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-CD. Moreover, the NACE method was found to be particularly well suited to the simultaneous determination of FBZ, OFZ enantiomers, and FBZSO2. Thiabendazole was selected as an internal standard. The CD-NACE potential was then evaluated for in vitro metabolism studies using FBZ as a model case. The OFZ enantiomers and FBZSO2 could be detected after incubation of FBZ in the phenobarbital-induced male rat liver microsomes systems. | |
| Fonds de la Recherche Scientifique (Communauté française de Belgique) - F.R.S.-FNRS ; Fonds Léon Fredericq | |
| http://hdl.handle.net/2268/41408 |
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