Determination of Methamphetamine and Its Metabolites Incorporated in Hair by Column-Switching Liquid Chromatography-Mass Spectrometry
Author(s) -
Akihiro Miki,
Munehiro Katagi,
Hitoshi Tsuchihashi
Publication year - 2003
Publication title -
journal of analytical toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.161
H-Index - 76
eISSN - 1945-2403
pISSN - 0146-4760
DOI - 10.1093/jat/27.2.95
Subject(s) - chromatography , chemistry , analyte , hair analysis , mass spectrometry , electrospray ionization , electrospray , detection limit , selected ion monitoring , liquid chromatography–mass spectrometry , analytical chemistry (journal) , gas chromatography–mass spectrometry , medicine , alternative medicine , pathology
An automated column-switching liquid chromatographic-electrospray ionization-mass spectrometric (LC-ESI-MS) method has been established for the determination of methamphetamine (MA) and its metabolites, amphetamine (AP), and p-hydroxymethamphetamine (p-OH-MA) in hair. The combination of an N-vinylacetamide-containing hydrophilic polymer online extraction column, an SCX semi-micro LC column, and an electrospray ionization interface provided the successful concentration, separations, and highly sensitive MS determinations of these analytes in a hair extract without tedious sample pretreatments. The limits of detection of these analytes were 0.02 ng/mg and 0.1-0.2 ng/mg in the selected-ion monitoring (SIM) and full-scan modes, respectively, when using a 100-microL hair extract sample that corresponds to a 2.5-mg sample of hair. The calibration curves using dibenzylamine as an internal standard were linear up to 30 ng/mg hair equivalents for all these analytes in the SIM mode. p-OH-MA, the detection of which in MA users' hair had not been previously reported, was detectable in all 22 hair specimens/sections from which 1 ng or more of MA was detected per milligram hair. The amount of p-OH-MA detected per milligram of hair is presented with those of MA and AP among the MA users population. The detection of AP and p-OH-MA, in addition to the parent drug MA with reasonable ratios, was found to be a useful indicator for distinguishing internal MA incorporation from external contamination.
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