Enantioseparation and determination of asenapine in biological fluid micromatrices by HPLC with diode array detection

被引:25
|
作者
Protti, Michele [1 ]
Vignali, Alice [1 ]
Blanco, Teresa Sanchez [1 ]
Rudge, James [2 ]
Bugamelli, Francesca [1 ]
Ferranti, Anna [1 ]
Mandrioli, Roberto [3 ]
Mercolini, Laura [1 ]
机构
[1] Univ Bologna, Alma Mater Studiorum, Dept Pharm & Biotechnol, Bologna, Italy
[2] Neoteryx LLC, Torrance, CA USA
[3] Univ Bologna, Dept Life Qual Studies, Rimini, Italy
关键词
asenapine; chiral stationary phases; enantioseparation; method validation; volumetric absorptive microsampling; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; CAPILLARY-ELECTROPHORESIS; MAJOR METABOLITES; HUMAN PLASMA; LC-MS/MS; QUANTIFICATION; MICROEXTRACTION; ANTIPSYCHOTICS; VALIDATION;
D O I
10.1002/jssc.201701315
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Asenapine is a recent drug approved in the European Union for the treatment of bipolar disorder. An original approach has been developed for asenapine analysis in patients treated with the drug, including miniaturized microsampling procedures, separation and quantitation of drug enantiomers. An original enantioselective method based on high-performance liquid chromatography with diode array detection was developed and applied to the determination of asenapine enantiomer levels in innovative haematic samples: four micromatrices have been tested, two based on dried matrix spots (dried blood spots and dried plasma spots) and two based on volumetric absorptive microsampling (from blood and plasma). Chiral separation was achieved on a cellulose-tris(3,5 dimethylphenylcarbamate) column, with a mobile phase containing bicarbonate buffer and acetonitrile. The method was validated with satisfactory results of linearity and precision on all matrices that showed also a significant performance in terms of stability, feasibility and reliability, when compared to fluid plasma sampling, handling and processing. Among micromatrices, both volumetric absorptive microsampling types were superior to dried matrix spots in terms of data reproducibility and correspondence with plasma levels. The bioanalytical approach proposed herein provides for the first time a chiral high-performance liquid chromatographic method for the determination of asenapine enantiomers, coupled to a very effective microsampling strategy.
引用
收藏
页码:1257 / 1265
页数:9
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