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Rapid drug detection in oral samples by porous silicon assisted laser desorption/ionization mass spectrometry
被引:24
作者:
Lowe, Rachel D.
[1
]
Guild, Georgia E.
[1
]
Harpas, Peter
[2
]
Kirkbride, Paul
[3
]
Hoffmann, Peter
[4
]
Voelcker, Nicolas H.
[1
]
Kobus, Hilton
[1
]
机构:
[1] Flinders Univ S Australia, Sch Chem Phys & Earth Sci, Bedford Pk, SA 5042, Australia
[2] Forens Sci S Australia, Adelaide, SA 5001, Australia
[3] Australian Fed Police, Canberra, ACT 2601, Australia
[4] Univ Adelaide, Adelaide Prote Ctr, Sch Med & Biomed Sci, Adelaide, SA 5005, Australia
基金:
澳大利亚研究理事会;
关键词:
INJURED DRIVERS;
ILLICIT DRUGS;
DESORPTION-IONIZATION;
QUANTITATIVE-ANALYSIS;
GAS-CHROMATOGRAPHY;
COLLECTION DEVICE;
FLUID COLLECTION;
PART II;
ABUSE;
ALCOHOL;
D O I:
10.1002/rcm.4284
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The demand for analysis of oral fluid for illicit drugs has arisen with the increased adoption of roadside testing, particularly in countries where changes in legislation allow random roadside testing of drivers for the presence of a palette of illicit drugs such as methamphetamine (MA), 3,4-methylenedioxymethamphetamine (MDMA) and Delta(9)-tetrahydrocannabinol (THC). Oral samples are currently tested for such drugs at the roadside using an immunoassay-based commercial test kit. Positive roadside tests are sent for confirmatory laboratory analysis, traditionally by means of gas chromatography/mass spectrometry (GC/MS). We present here an alternative rapid analysis technique, porous silicon assisted laser desorption/ionization time-of-flight mass spectrometry (pSi LDI-MS), for the high-throughput analysis of oral fluids. This technique alleviates the need for sample derivatization, requires only sub-microliter sample volumes and allows fast analysis (of the order of seconds). In this study, the application of the technique is demonstrated with real samples from actual roadside testing. The analysis of oral samples resulted in detection of MA and MDMA with no extraction and analysis of THC after ethyl acetate extraction. We propose that, subject to miniaturization of a suitable mass spectrometer, this technique is well suited to underpin the deployment of oral fluid testing in the clinic, workplace and on the roadside. Copyright (C) 2009 John Wiley & Sons, Ltd.
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页码:3543 / 3548
页数:6
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