Page 187 - Advances in Forensic Applications of Mass Spectrometry - Jehuda Yinon
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                                                                  30
                                                                  20      Putumayo−Caqueta
                                                 Guaviare region
                                                 Putumayo–Caqueta  10
                                                 region          δ 16 N + 0.1 Trux (‰)
                                                 Huallaga and Ucayali
                                                 Valleys           0
                                                 Apurimac Valley                        Apurimac
                                                                          Guaviare
                                                 Chapare Valley   −10
                                                                        Huallaga−Ucayali
                                                                                       Chapare
                                                                  −20
                                                                   −150 −130  −110  −90  −70  −50  −30
                                                                             13
                                                                            δ C - 10 TMC (‰)
                                                                                     14
                             Figure 4.5  Regional grouping of cocaine samples based on  N/ N ratio and
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                                                     13
                                                        12
                             truxilline (Trux) content and  C/ C ratio and trimethoxycocaine (TMC) content.
                             (Reprinted with permission from Nature, Vol. 408, pp. 311. © 2000 Macmillan
                             Publishers Ltd.)
                             which was then analyzed for carbon isotopic  ratios. 73   This study was not
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                             successful as the d C values scattered in a narrow range (–30.5 to –28.6‰).
                                As the conversion of morphine into heroin does not involve nitrogen,
                             studies were done to explore the possibility in making a d N value determi-
                                                                               15
                             nation for direct geographic origin assignments. Unfortunately, three studies
                             indicated a narrow  range of  d N value scattering:  –3.6  to 1.7‰,  –1.6  to
                                                        15
                             1.3‰, and –4.30 to 0.40‰. 77
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                                Studies have also been done in the determinations of d C and d N values
                             of cutting agents found in heroin samples. Thus, acetaminophen was ana-
                                                 78
                                                                                           79
                                                                                 15
                                        13
                             lyzed for its d C values and caffeine was analyzed for its d N values. The
                              15
                             d N values in caffeine were found to range widely (–30.31 to –1.69‰) and,
                             hence, were found to be useful.
                             4.4.3.4  Synthetic Drugs
                             Natural isotope abundances of carbon and hydrogen in several production
                             batches of the commercial drug diazepam (7-chloro-1,3-dihydro-1-methyl-
                             5-phenyl-2H-1,4-benzodiazepin-2-on) have been studied.  The  results
                             showed significant differences in d C values between the diazepam synthe-
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                             sized by Hofmann–LaRoche Switzerland (mean, –35.5‰; range, 2.1‰) and
                             Hofmann–LaRoche U.S. (mean, –30.5‰; range, 1.3‰). 80
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                                More recently,  C/ C and  N/ N isotopic ratios were used to differentiate
                             confiscated 3,4-methylenedioxymethamphetamine (MDMA) samples.   81   In
                             this study, MDMA was extracted from the tablet and the compound’s isotopic
                             ratios were determined using GC-IRMS analysis. Carbon isotopic ratio data
                             allowed for classifying 16 MDMA samples into 4 groups (Figure 4.7). Samples
                             8 and 9 were further differentiated by the nitrogen isotopic data (Figure 4.8).
                             © 2004 by CRC Press LLC
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