QUALITATIVE AND QUANTITATIVE-DETERMINATION OF ILLICIT HEROIN STREET SAMPLES BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY - METHOD DEVELOPMENT BY CARTACO-S
K. Groggsulser et al., QUALITATIVE AND QUANTITATIVE-DETERMINATION OF ILLICIT HEROIN STREET SAMPLES BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY - METHOD DEVELOPMENT BY CARTACO-S, Journal of chromatography, 692(1-2), 1995, pp. 121-129
The development of a method involving reversed-phase HPLC using CARTAG
O-S, a spreadsheet computer program as a method development tool is de
scribed for the simultaneous qualitative and quantitative determinatio
n of heroin in illicitly manufactured street samples containing by-pro
ducts originating from opium and also commonly occurring adulterants t
hat have been found in Switzerland. The method utilizes simple sample
dissolution followed by reversed-phase HPLC on a 3-mu m ODS-1 column w
ith acetonitrile-water-phosphoric acid-hexylamine as the mobile phase.
UV detection and quantification were carried out at 210 nm. The optim
um linear gradient elution consisted of four steps with a total durati
on of 36 min. Excellent agreement between predicted and measured reten
tion times with differences ranging from 0.45% to 6.8% was found. For
calibration, all compounds showed a good linear relationship between p
eak area and concentration. The low UV cut-off of this mobile phase al
lows the detection of heroin and related compounds at its major UV abs
orption at 210 nm. With this method, the limits of detection absolute
ranged from 10 ng for noscapine, corresponding to 0.09% of the sample
mass, in the best case to 100 ng for cocaine in the worst case, depend
ing on molar absorptivities.