Simultaneous analysis of cocaine and its metabolites in urine by capillary electrophoresis-electrospray mass spectrometry using a pressurized liquid junction nanoflow interface

被引:19
作者
Hezinova, Vera [1 ,2 ,3 ]
Aturki, Zeineb [1 ]
Kleparnik, Karel [2 ]
D'Orazio, Giovanni [1 ]
Foret, Frantisek [2 ]
Fanali, Salvatore [1 ]
机构
[1] CNR, Ist Metodol Chim, I-00015 Rome, Italy
[2] Acad Sci Czech Republic, Inst Analyt Chem, CS-61142 Brno, Czech Republic
[3] Brno Univ Technol, Fac Chem, Brno, Czech Republic
关键词
CE-MS; Cocaine metabolites; Liquid junction interface; Urine analysis; ZONE-ELECTROPHORESIS; SIMULTANEOUS QUANTIFICATION; FORENSIC SCIENCES; FLOW INTERFACE; ILLICIT DRUGS; MS DETECTION; CHROMATOGRAPHY; IONIZATION; CE; BENZOYLECGONINE;
D O I
10.1002/elps.201100410
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new method for the simultaneous separation of cocaine and four metabolites in urine by CE-ESI-MS via a pressurized nanoliquid junction interface was developed. The resolution of cocaine, cocaethylene, benzoylecgonine, norcocaine, and ecgonine methyl ester was achieved in a polyvinyl-alcohol-coated capillary with 75 mu m id x 50 cm total length, using a 15 mM ammonium formate electrolyte solution (pH 9.5) in less than 15 min. In addition, to enhance sensitivity, a field-amplified sample injection (FASI) was evaluated in terms of injection time and sample solvent composition. The limits of detection achieved with the FASI method ranged from 1.5 to 10 ng/mL for all the compounds. The detection of the studied compounds was performed using an ion-trap mass spectrometer in a positive ionization mode. A mixture of methanol:water (80:20 v/v) containing 0.1% v/v of formic acid was employed as spray liquid and delivered at similar to 200 nL/min. Under optimal CEMS conditions, linearity was assessed in the concentration range of interest for all analytes with correlation coefficients r2 = 0.9913. Intra- and inter-day precision provided a relative standard deviation lower than 1.54% for migration times and lower than 12.15% for peak areas. Finally, urine samples, spiked with the standard mixture, were extracted using a solid-phase extraction procedure and injected under FASI conditions, providing recoveries from 80% to 94% for all analytes.
引用
收藏
页码:653 / 660
页数:8
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