A rapid method of determining amphetamine in plasma samples using pentafluorobenzenesulfonyl chloride and electron-capture gas chromatography

Sheila Asghar, Glen B. Baker, Gail A. Rauw, Peter H. Silverstone

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

Introduction: Acute administration of (+)-amphetamine has been used as a model for mania in humans since it mimics the physiological, biochemical, and cognitive effects seen in mania. A rapid and sensitive method for the determination of amphetamine in human plasma samples using gas chromatography with electron-capture detection was developed in our laboratory to follow the time course of amphetamine levels in patients receiving this drug as part of a study using amphetamine as a model for mania. Methods: Blood samples were taken from healthy male volunteers at 30, 60, 90, 150, 210, 240, and 480 min after administration of 25 mg of (+)-amphetamine. Plasma was isolated by centrifugation and used for the analysis. This method is a modification of the procedure described by Paetsch et al. [J. Chromatogr. 573 (1992) 313] for the determination of amphetamine in rat brain tissue. Amphetamine was derivatized under basic conditions using pentafluorobenzenesulfonyl chloride (PFBSC) prior to analysis on a gas chromatograph equipped with a capillary column and an electron-capture detector. The internal standard used was benzylamine. The structure of the amphetamine derivative was confirmed using combined gas chromatography-mass spectrometry (GC-MS). Results: The limit of detection was <1 ng/ml, and the method was linear in the 1- to 100-ng range used. Mean amphetamine levels peaked at 3.5 h after drug administration, and were 40.8±1.5 ng/ml at that time. Discussion: This procedure produces a stable derivative with excellent chromatographic properties and is both simple and reproducible. Crown

Original languageEnglish (US)
Pages (from-to)111-115
Number of pages5
JournalJournal of Pharmacological and Toxicological Methods
Volume46
Issue number2
DOIs
Publication statusPublished - Dec 1 2001

    Fingerprint

All Science Journal Classification (ASJC) codes

  • Toxicology
  • Pharmacology

Cite this