Enantioselective Separation of Mirtazapine and Its Metabolites by Capillary Electrophoresis with Acetonitrile Field-Amplified Sample Stacking and Its Application

被引:16
|
作者
Wen, Jun [1 ]
Zhang, Wen-Ting [1 ]
Cao, Wei-Qun [1 ]
Li, Ji [2 ]
Gao, Fang-Yuan [1 ]
Yang, Nan [1 ]
Fan, Guo-Rong [1 ]
机构
[1] Second Mil Med Univ, Dept Pharmaceut Anal, Sch Pharm, Shanghai Key Lab Pharmaceut Metabolite Res, Shanghai 200433, Peoples R China
[2] Kunming Gen Hosp Chengdu Mil Command, Dept Pharm, Kunming 650032, Peoples R China
来源
MOLECULES | 2014年 / 19卷 / 04期
基金
中国国家自然科学基金;
关键词
chiral capillary zone electrophoresis; acetonitrile-field-amplified sample stacking; mirtazapine; N-demethylmirtazapine; 8-hydroxymirtazapine; liquid-liquid extraction; LIQUID-PHASE MICROEXTRACTION; HUMAN PLASMA; MAIN METABOLITES; ANTIDEPRESSANT MIRTAZAPINE; ENANTIOMERIC SEPARATION; CHIRAL DETERMINATION; HUMAN URINE; IN-VITRO; CHROMATOGRAPHY; PHARMACOKINETICS;
D O I
10.3390/molecules19044907
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 x 75 mu M 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-beta-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.
引用
收藏
页码:4907 / 4923
页数:17
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