RP-HPLC enantioseparation of β-adrenolytics using micellar mobile phase without organic solvents

被引:13
作者
Alwera, Shiv [1 ]
Bhushan, Ravi [1 ]
机构
[1] Indian Inst Technol Roorkee, Dept Chem, Roorkee, Uttar Pradesh, India
关键词
(S)-(-)-levofloxacin; Diastereomeric derivatives; RP-HPLC; water micellar mobile phase; beta-adrenolytics; Surfactants; PERFORMANCE LIQUID-CHROMATOGRAPHY; CHIRAL DERIVATIZING REAGENTS; PHARMACEUTICAL-PREPARATIONS; (S)-NAPROXEN MOIETY; SEPARATION; ISOTHIOCYANATE; ENANTIOMERS; DIASTEREOMERS; RESOLUTION; BLOCKERS;
D O I
10.1002/bmc.3983
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Enantioseparation of a few commonly administered racemic beta-adrenolytics (namely, carvedilol, betaxolol, salbutamol and bisoprolol) has been achieved using a water micellar mobile phase containing surfactants (sodium dodecyl sulphate and Brij-35) without organic solvents as a new approach in RP-HPLC. Two chiral derivatizing reagents based on enantiomerically pure (S)-(-)-levofloxacin were synthesized using N-hydroxysuccinimide and N-hydroxybenzotriazole as the activation auxiliaries. Diastereomeric derivatives of the chosen beta-adrenolytics were synthesized under microwave irradiation in a very short reaction time. The (S)-(-)-levofloxacin moiety enhanced molar absorbance of the diastereomeric derivatives resulting in very low limit of detection (1.618 and 4.902 ng/mL, respectively, for diastereomeric derivatives of (RS)-betaxolol and better resolution with lower retention times (for all the analytes), in comparison to literature reports. There was 15-20 times less consumption of mobile phase because of lower retention time.
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页数:7
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