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Methamphetamine detection using portable capillary electrophoresis coupled with a swab-based extraction device
被引:0
|作者:
Atia, Mostafa A.
[1
,2
]
Kalsoom, Umme
[3
]
Ollerton, Samantha
[3
,4
]
Haddad, Paul R.
[1
]
Breadmore, Michael C.
[1
]
机构:
[1] Univ Tasmania, Australian Ctr Res Separat Sci ACROSS, Sch Nat Sci, Private Bag 75, Hobart, Tas 7001, Australia
[2] Helwan Univ, Fac Pharm, Dept Analyt Chem, Cairo 11795, Egypt
[3] GreyScan, 9-435 Williamstown Rd, Port Melbourne, Vic 3207, Australia
[4] Precis Plus Consulting Ltd, 71-75 Shelton St, London WC2H 9HJ, England
来源:
关键词:
Portable capillary electrophoresis;
Conductivity detection;
Swabbing;
Clandestine laboratories;
Methamphetamine;
Pseudoephedrine;
CONTACTLESS CONDUCTIVITY;
ZONE-ELECTROPHORESIS;
ORAL FLUID;
DRUGS;
SEPARATION;
URINE;
AUSTRALIA;
SAMPLES;
D O I:
10.1016/j.talanta.2024.126357
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Methamphetamine (MA) is one of the most virulent illicit drugs that can be synthesized from household materials leading to its prevalent trafficking and local manufacturing in clandestine drug laboratories (clan labs). The significant problems of tracing MA in clan labs and monitoring drug abusers lie in the lag time between sample collection and analysis and the number of tests done. Capillary electrophoresis (CE) is a rapid separation technique amenable to miniaturization and field testing. Herein, we developed a simple transient isotachophoretic (tITP)-CE method to detect MA and its precursor pseudoephedrine (PSE) in clan labs and non-invasive biological fluids. The method was implemented on the ETD-100, a commercial fully automated portable CE instrument with an integrated swab-based extraction system. Within 2 min of insertion of the swab, MA and PSE were automatically extracted with a leading electrolyte (LE) and then separated on covalently modified capillaries. The ETD-100 showed a limit of detection (LOD) and quantification (LOQ) of MA 0.02 and 0.05 mu g/swab and 0.02 and 0.06 mu g/swab of PSE, with an enhancement factor of 118 and 328, respectively, when compared to a normal nontITP injection. The intra and inter-day relative standard deviation in terms of migration time were in the range of 0.75-1.93 % for both MA and PSE and were 2.0-2.4 % for both MA and PSE peak height. The method was demonstrated with the detection of spiked MA and PSE on different household materials as well as in noninvasive biological fluids with a recovery above 60 %.
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