A new methodology employing capillary electrophoresis with UV detection (CE-UV) was developed, validated, and applied to determine the presence of cocaine on Brazilian banknotes. Some of the banknotes analyzed were obtained directly from general circulation (well used) while others were collected from Automated Teller Machines (ATMs) (relatively new). The background electrolyte optimized using Peakmaster 5.1 software was composed of 60?mmol?L?1 TRIS(hydroxymethyl)aminomethane and 20?mmol?L?1 2-hydroxyisobutyric acid, at pH 8.4. The separation time achieved for cocaine was only 2.5?minutes. The figures of merit obtained in the evaluation of the proposed method were good linearity ( ) in the concentration range of 0.8–8.0?mg?L?1 and acceptable limits of detection and quantification (0.2?mg?L?1 and 0.8?mg?L?1, resp.). The relative standard deviations of the instrumental precision, repeatability (intraday), and intermediate precision (interday) were less than 4.5% (peak area). The accuracy evaluated through comparing the cocaine results for the banknotes determined by the proposed CE-UV method and using an LC-MS/MS method showed no significant difference between the methods (95% confidence level). In the analysis of the samples cocaine was detected on 93% of the circulating banknotes in amounts ranging from 11.5?μg to 2761.9?μg per note. 1. Introduction Since the 1980s it has been known that banknotes in North America and Europe are contaminated with cocaine residues. This results from the sale and consumption of this drug, because many cocaine users use a wrapped banknote as a kind of straw to inhale the drug. The presence of traces of this drug on banknotes is often used as forensic evidence to establish a connection between a suspect and illicit drugs [1]. Other explanations for the presence of cocaine on banknotes have been proposed, including contamination due to handling during drug dealing, the transfer from a contaminated note to “clean” ones during counting in financial institutions, and also banknotes coming into contact with one another within the ATM [2, 3]. To ensure the determination of cocaine with precision and accuracy, it is necessary to quantitatively extract the drug from the banknotes. In studies reported in the literature, the extraction technique most commonly employed involves the use of organic solvents and a dilute aqueous acid. For the analysis of US dollar banknotes, the solvents chloroform [4, 5], acetonitrile [6], and ethanol [7] have been used, together with procedures involving vortex agitation and centrifugation, followed by
References
[1]
Y. Zuo, K. Zhang, J. Wu, C. Rego, and J. Fritz, “An accurate and nondestructive GC method for determination of cocaine on US paper currency,” Journal of Separation Science, vol. 31, no. 13, pp. 2444–2450, 2008.
[2]
E. di Donato, C. C. S. Martin, and B. S. de Martinis, “Determination of cocaine in Brazilian paper currency by capillary gas chromatography/mass spectrometry,” Quimica Nova, vol. 30, no. 8, pp. 1966–1967, 2007.
[3]
J. F. Carter, R. Sleeman, and J. Parry, “The distribution of controlled drugs on banknotes via counting machines,” Forensic Science International, vol. 132, no. 2, pp. 106–112, 2003.
[4]
D. Song, S. Zhang, and K. Kohlhof, “Determination of a trace amount of cocaine on a bank note by gas chromatography-positive-ion chemical-ionization mass spectrometry,” Journal of Chromatography A, vol. 731, no. 1-2, pp. 355–360, 1996.
[5]
J. C. Hudson, “Analysis of currency for cocaine contamination,” Journal of the Canadian Society of Forensic Science, vol. 22, no. 2, pp. 203–218, 1989.
[6]
A. J. Jenkins, “Drug contamination of US paper currency,” Forensic Science International, vol. 121, no. 3, pp. 189–193, 2001.
[7]
M. Lafitte, F. Brousse, L. No?l, Y. Gaillard, and G. Pépin, “Traces de stupéfiants sur les billets de banque: une comparaison entre les billets en circulation et les billets saisis à l'occasion de trafic de stupéfiant,” Annales de Toxicologie Analalytique, vol. 14, p. 95, 2002.
[8]
F. A. Esteve-Turrillas, S. Armenta, J. Moros, S. Garrigues, A. Pastor, and M. de la Guardia, “Validated, non-destructive and environmentally friendly determination of cocaine in euro bank notes,” Journal of Chromatography A, vol. 1065, no. 2, pp. 321–325, 2005.
[9]
J. Bones, M. Macka, and B. Paull, “Evaluation of monolithic and sub 2 μm particle packed columns for the rapid screening for illicit drugs—application to the determination of drug contamination on Irish euro banknotes,” Analyst, vol. 132, no. 3, pp. 208–217, 2007.
[10]
K. Wimmer and S. Schneider, “Screening for illicit drugs on Euro banknotes by LC-MS/MS,” Forensic Science International, vol. 206, no. 1-3, pp. 172–177, 2011.
[11]
A. Negrusz, J. L. Perry, and C. M. Moore, “Detection of cocaine on various denominations of United States currency,” Journal of Forensic Sciences, vol. 43, no. 3, pp. 626–629, 1998.
[12]
C. A. Heimbuck and N. W. Bower, “Teaching experimental design using a GC-MS analysis of cocaine on money: a cross-disciplinary laboratory,” Journal of Chemical Education, vol. 79, no. 10, pp. 1254–1256, 2002.
[13]
Y. Xu, Y. Gao, H. Wei, Y. Du, and E. Wang, “Field-amplified sample stacking capillary electrophoresis with electrochemiluminescence applied to the determination of illicit drugs on banknotes,” Journal of Chromatography A, vol. 1115, no. 1-2, pp. 260–266, 2006.
[14]
A. Keil, N. Talaty, C. Janfelt et al., “Ambient mass spectrometry with a handheld mass spectrometer at high pressure,” Analytical Chemistry, vol. 79, no. 20, pp. 7734–7739, 2007.
[15]
S. Armenta and M. de la Guardia, “Analytical methods to determine cocaine contamination of banknotes from around the world,” Trends in Analytical Chemistry, vol. 27, no. 4, pp. 344–351, 2008.
[16]
Y. N. Kolomiets and V. V. Pervukhin, “Effect of UV irradiation on detection of cocaine hydrochloride and crack vapors by IMIS and API-MS methods,” Talanta, vol. 78, no. 2, pp. 542–547, 2009.
[17]
A. H. Lawrence, “Detection of drug residues on the hands of subjects by surface sampling and ion mobility spectrometry,” Forensic Science International, vol. 34, no. 1-2, pp. 73–83, 1987.
[18]
K. A. Ebejer, G. R. Lloyd, R. G. Brereton, J. F. Carter, and R. Sleeman, “Factors influencing the contamination of UK banknotes with drugs of abuse,” Forensic Science International, vol. 171, no. 2-3, pp. 165–170, 2007.
[19]
S. J. Dixon, R. G. Brereton, J. F. Carter, and R. Sleeman, “Determination of cocaine contamination on banknotes using tandem mass spectrometry and pattern recognition,” Analytica Chimica Acta, vol. 559, no. 1, pp. 54–63, 2006.
[20]
K. A. Ebejer, R. G. Brereton, J. F. Carter, S. L. Ollerton, and R. Sleeman, “Rapid comparison of diacetylmorphine on banknotes by tandem mass spectrometry,” Rapid Communications in Mass Spectrometry, vol. 19, no. 15, pp. 2137–2143, 2005.
[21]
R. Sleeman, I. F. A. Burton, J. F. Carter, and D. J. Roberts, “Rapid screening of banknotes for the presence of controlled substances by thermal desorption atmospheric pressure chemical ionisation tandem mass spectrometry,” Analyst, vol. 124, no. 2, pp. 103–108, 1999.
[22]
S. A. Barat and M. S. Abdel-Rahman, “Cocaine and lidocaine in combination are synergistic convulsants,” Brain Research, vol. 742, no. 1-2, pp. 157–162, 1996.
[23]
H. Wan, A. Holmén, M. N?g?rd, and W. Lindberg, “Rapid screening of pKa values of pharmaceuticals by pressure-assisted capillary electrophoresis combined with short-end injection,” Journal of Chromatography A, vol. 979, no. 1-2, pp. 369–377, 2002.
[24]
Z. K. Shihabi, “Stacking in capillary zone electrophoresis,” Journal of Chromatography A, vol. 902, no. 1, pp. 107–117, 2000.
[25]
Z. K. Shihabi, “Transient pseudo-isotachophoresis for sample concentration in capillary electrophoresis,” Electrophoresis, vol. 23, pp. 1612–1617, 2002.
[26]
G. A. Micke, A. C. O. Costa, M. Heller et al., “Development of a fast capillary electrophoresis method for the determination of propranolol-total analysis time reduction strategies,” Journal of Chromatography A, vol. 1216, no. 45, pp. 7957–7961, 2009.
[27]
A. F. Faria, M. V. N. de Souza, and M. A. L. de Oliveira, “Validation of a capillary zone electrophoresis method for the determination of ciprofloxacin, gatifloxacin, moxifloxacin and ofloxacin in pharmaceutical formulations,” Journal of the Brazilian Chemical Society, vol. 19, no. 3, pp. 389–396, 2008.