Separation of Fat-soluble Isoquinoline Enantiomers using β-Cyclodextrinmodified Micellar Capillary Electrokinetic Chromatography

Author(s): Hongying Cheng, Qianli Zhang, Yifeng Tu.

Journal Name: Current Pharmaceutical Analysis

Volume 8 , Issue 1 , 2012

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In this paper, chiral fat-soluble enantiomers of 1-phenyl-R, S-tetrahydrogen isoquinoline (ER, ES) are rapidly separated using β-cyclodextrin (β-CD) modified micellar capillary electrokinetic chromatography coupled with electrochemical detection (EC). An effectual micellar suspension of 35 mmol/L phosphate buffer saline (PBS) (pH 7.85) containing 30 mM sodium deoxycholate, 20 mM β-CD and 20% (v/v) acetonitrile was developed as the running buffer. Among them, the surfactant sodium deoxycholate formed the micelles in the buffer, β-CD was employed to improve the separation, and the acetonitrile acted as an organic modifier. After the optimization of the factors such as detection potential, separation voltage, sampling time and the composition of running buffer, baseline separation was obtained within 12 min at 20 kV of separation voltage. The RSD (n = 5) of migration times and peak areas of the analytes are 2.3% (ER), 2.7% (ES) and 2.0% (ER), 3.5% (ES), respectively. The detection limit is 0.5 μmol/L for ER and 0.2 μmol/L for ES, also it was found that trace ER could be detected at the limit proportion of ER to ES for 1:500. This protocol was successfully applied for monitoring the amount of ER from ES in synthetic drug intermediate.

Keywords: β-Cyclodextrin, Electrochemical detection, Fat-soluble enantiomer, Micellar electrokinetic chromatography, Oxidation mechanism, 1-Phenyl-R, S-Tetrahydrogen isoquinoline, Sodium deoxycholate, Solifenacin, Supramolecular complexation, Synthetic drug intermediate, S-Tetrahydrogen isoquinoline

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Article Details

Year: 2012
Page: [37 - 43]
Pages: 7
DOI: 10.2174/157341212798995458

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