M. Katagi et al., DIRECT ANALYSIS OF METHAMPHETAMINE AND AMPHETAMINE ENANTIOMERS IN HUMAN URINE BY SEMI-MICROCOLUMN HPLC ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY, Eisei Kagaku, 44(2), 1998, pp. 107-115
Semi-microcolumn high performance liquid chromatography (HPLC) with a
column-switching system was connected to electrospray ionization mass
spectrometry (ESI-MS) for the analysis of methamphetamine (MA) and amp
hetamine (AP), a main metabolite of MA. Urine samples were directly in
troduced to the system. After removal of other components of the sampl
e matrix by the column-switching process, both MA and AP were successf
ully analyzed with enantiomeric resolution by the use of p-cyclodextri
n phenylcarbamate-bonded (phCD) semi-microcolumn, accompanied by spect
ral information obtained with ESI-MS. Linear calibration curves were o
btained for all the analytes throughout the concentration range from 1
ng/ml to 5 mu g/ml. The relative standard deviation for peak area ran
ged from 1.41 to 2.07% at 0.1 mu g/ml for the four enantiomer peaks. D
etection limits observed for MA and AP enantiomers were 20 ng/ml and 5
0 ng/ml in the spectrum scanning mode, and 0.5 ng/ml and 1 ng/ml in th
e single ion monitoring (SIM) mode, respectively. The HPLC/ESI-MS syst
em studied here appeared highly sensitive and useful towards its foren
sic applications.