Development of HPLC/fluorescence detection method for chiral resolution of dansylated benzimidazoles derivatives

被引:5
|
作者
Lipka, Emmanuelle [1 ]
Charton, Julie [2 ]
Vaccher, Claude [1 ]
机构
[1] Fac Sci Pharmaceut & Biol, EA 4481, Lille, France
[2] Univ Lille Nord France, Lille Pasteur Inst, INSERM, Biostruct & Early Drug Discovery U761, F-59000 Lille, France
关键词
AMPK activators; benzimidazole; dansyl group; enantiomeric separation; fluorescence detection; Chiralpak AD; ACTIVATED PROTEIN-KINASE; LIQUID-CHROMATOGRAPHIC DETERMINATION; UV PHOTODIODE-ARRAY; BIOLOGICAL EVALUATION; STATIONARY-PHASE; HUMAN PLASMA; INHIBITORS; POTENT; OMEPRAZOLE; FLUBENDAZOLE;
D O I
10.1002/bmc.2992
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of high performance liquid chromatography method on amylose-based stationary phase (Chiralpak AD) with n-hexane-2-propanol (90:10, v/v) as mobile phase allowed the enantioseparation of non-dansylated and dansylated benzimidazole derivatives, prepared from potent-AMPK activators, to be achieved. Using both fluorescence and ultraviolet detection, limits of detection and quantification were determined. Fluorescence detection seems to be the most appropriate technique since the first enantiomer of dansylated benzimidazole 8 eluted with a limit of quantification of 2.25 nm. The quantification limit was improved 10-fold by fluorescence detection compared with a previous report describing mass spectrometry detection. Linearity and repeatability parameters were validated. These lower limits obtained by fluorescence detection, associated with good resolution observed for the dansylated derivatives, make this chiral methodology convenient for the use of these fluorescent potent-AMPK activators as probes to elucidate their cellular localization and their mechanism of action. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:4 / 9
页数:6
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