4.6 Article

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

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FRONTIERS IN CHEMISTRY
卷 7, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2019.00248

关键词

urine; chiral analysis; pharmacokinetic; R/S-methamphetamine; R/S-amphetamine; selegiline

资金

  1. National Natural Science Foundation of China [81871531, 81772022]
  2. Science and Technology Commission of Shanghai Municipality [17DZ2273200, 19DZ2292700]
  3. Ministry of Finance, PR China [GY2017D-1]

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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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