Abstract

A simple, rapid and sensitive chiral capillary zone electrophoresis coupled with acetonitrile-field-amplified sample stacking method was developed that allows the simultaneous enantioselective separation of the mirtazapine, N-demethylmirtazapine, 8-hydroxymirtazapine and mirtazapine-N-oxide. The separation was achieved on an uncoated 40.2 cm × 75 μM fused silica capillary with an applied voltage of 16 kV. The electrophoretic analyses were carried out in 6.25 mM borate–25 mM phosphate solution at pH 2.8 containing 5.5 mg/mL carboxymethyl-β-cyclodextrin. The detection wavelength was 200 nm. Under these optimized conditions, satisfactory chiral separations of four pair enantiomers were achieved in less than 7 min in vitro. After one step clean-up liquid-liquid extraction using 96-well format, sample was introduced capillary zone electrophoresis with acetonitrile-field-amplified sample stacking to enhance the sensitivity of enantiomers. The method was validated with respect to specificity, linearity, lower limit of quantitation, accuracy, precision, extraction recovery and stability. The lower limit of quantification was 0.5 ng/mL with linear response over the 0.5–50 ng/mL concentration range for each mirtazapine, N-demethylmirtazapine and 8-hydroxymirtazapine enantiomer. The developed and validated method has been successfully applied to the enantioselective pharmacokinetic studies in 12 healthy volunteers after oral administration of rac- mirtazapine.

Highlights

  • Mirtazapine (MRT), whose chemical name is 1,2,3,4,10,14b-hexahydro-2-methylpyrazino[2,1-a]pyrido[2,3-c][2]benzazepine (Figure 1), is an effective tricyclic antidepressant combining two mechanisms of action: antagonizing the adrenergic a2-autoreceptors and a2-heteroreceptors as well as blocking postsynaptic serotonin 5-HT2 and 5-HT3 receptors

  • We developed a capillary electrophoresis (CE) method for the simultaneous enantioselective analysis of MRT

  • The chiral separation in CE by the use of CDs utilizes the phenomenon of host-guest complexation with a relatively hydrophobic cavity, where a transient diastereomeric complex is formed between the chiral selector and the analytes [30]

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Summary

Introduction

Pyrido[2,3-c][2]benzazepine (Figure 1), is an effective tricyclic antidepressant combining two mechanisms of action: antagonizing the adrenergic a2-autoreceptors and a2-heteroreceptors as well as blocking postsynaptic serotonin 5-HT2 and 5-HT3 receptors. It shows low affinity for 5-HT1A receptors and could enhance the release of norepinephrine and 5-HT1A–mediated serotonergic transmission. MRT is marketed as the racemate and its (−)-R and (+)-S-enantiomers have different pharmacologic and pharmacokinetic properties. The enantioselective pharmacokinetics of MRT indicated the difference in half-life of the enantiomers

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