Simultaneous Determination of Selegiline, Desmethylselegiline, R/S-methamphetamine, and R/S-amphetamine on Dried Urine Spots by LC/MS/MS: Application to a Pharmacokinetic Study in Urine

被引:9
作者
Chen, Lizhu [1 ,2 ]
Yu, Yingjia [2 ]
Duan, Gengli [2 ]
Wang, Xin [1 ]
Shen, Baohua [1 ]
Xiang, Ping [1 ]
机构
[1] Acad Forens Sci, Dept Forens Toxicol, Shanghai Key Lab Forens Med, Shanghai, Peoples R China
[2] Fudan Univ, Sch Pharm, Dept Pharmaceut Anal, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
urine; chiral analysis; pharmacokinetic; R/S-methamphetamine; R/S-amphetamine; selegiline; BLOOD SPOTS; LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; CAPILLARY-ELECTROPHORESIS; CHIRAL SEPARATION; ORAL FLUID; L-DEPRENYL; LC-MS/MS; METABOLITES; DRUGS;
D O I
10.3389/fchem.2019.00248
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Objective: Chiral analysis is a crucial method to differentiate selegiline intake from drug abuse. A dried urine spot (DUS) analytical method based on spotting urine samples (10 mu L) onto dried spot collection cards, and followed by air-drying and extraction, was developed and validated for the determination of selegiline, desmethylselegiline, R/S-methamphetamine, and R/S-amphetamine. Methods: Methanol (0.5 mL) was found to be the ideal extraction solvent for target extraction from DUSs under orbital-horizontal stirring on a lateral shaker at 1,450 rpm for 30 min. Determinations were performed by direct electrospray ionization tandem mass spectrometry (ESI-MS/MS) under positive electrospray ionization conditions using multiple reaction monitoring mode. The chromatographic system consisted of a Chirobiotic (TM) V2 column (2.1 x 250 mm, 5 mu m) and a mobile phase of methanol containing 0.1% (v/v) glacial acetic acid and 0.02% (v/v) ammonium hydroxide. Results and conclusions: The calibration curves were linear from 50 to 5,000 ng/mL, with r > 0.995 for all analytes, imprecisions <= 15% and accuracies between -11.4 and 11.7%. Extraction recoveries ranged from 48.6 to 105.4% with coefficients of variation (CV) <= 13.7%, and matrix effects ranged from 45.4 to 104.1% with CV <= 10.3%. The lower limit of quantification was 50 ng/mL for each analyte. The present method is simple, rapid (accomplished in 12 min), sensitive, and validated by a pharmacokinetic study in human urine collected after a single oral administration of SG.
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页数:10
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