Iwata Yuko T, Kuwayama Kenji, Tsujikawa Kenji, Miyaguchi Hajime, Kanamori Tatsuyuki, Inoue Hiroyuki
National Research Institute of Police Science, 6-3-1, Kashiwanoha, Kashiwa, Chiba 277-0882, Japan.
Rapid Commun Mass Spectrom. 2008 Dec;22(23):3816-22. doi: 10.1002/rcm.3809.
Drug profiling, extraction of physical and/or chemical profiles from abused drug samples, is useful for inferring and characterizing links between samples originating from the same and different seizures, and supports drug crime investigations. We describe an evaluation method for linking methamphetamine (MA) seizures using stable carbon and nitrogen isotopic compositions concurrently with gas chromatographic impurity profiling, which is one of the major methods of drug profiling. Several sets of MA seized in Japan, whose investigative information indicated linkages, were analyzed. The impurity profile of each set of seizures was quite similar and hierarchical cluster analysis showed a sample classification that was relatively consistent with the investigative information. The stable carbon and nitrogen isotopic compositions of the MA seizures varied between -29.40 and -24.90 (delta(13)C) and -2.29 and 5.94 (delta(15)N), respectively. In the delta(13)C-delta(15)N graph, MA seizures were classified into seven groups, probably reflecting different origins. The size of the cluster in the isotopic-composition graph was determined by pooled standard deviations (s(p)), the pooled estimates of measurement uncertainty. The sizes of the clusters were less than 6s(p) and the linkages between the MA seizures from the isotopic compositions were consistent with the impurity profiling and investigative information. The results showed that complementary use of stable-isotopic compositions with impurity profiling provides useful information for evaluating the links between seizures.
毒品特征分析,即从滥用药物样本中提取物理和/或化学特征,有助于推断和描述来自同一或不同缉获量的样本之间的联系,并支持毒品犯罪调查。我们描述了一种评估方法,该方法使用稳定的碳和氮同位素组成,同时结合气相色谱杂质特征分析来关联甲基苯丙胺(MA)缉获量,气相色谱杂质特征分析是毒品特征分析的主要方法之一。对在日本缉获的几组MA进行了分析,其调查信息表明存在关联。每组缉获量的杂质特征非常相似,层次聚类分析显示的样本分类与调查信息相对一致。MA缉获量的稳定碳和氮同位素组成分别在-29.40至-24.90(δ(13)C)和-2.29至5.94(δ(15)N)之间变化。在δ(13)C-δ(15)N图中,MA缉获量被分为七组,可能反映了不同的来源。同位素组成图中聚类的大小由合并标准偏差(s(p))确定,s(p)是测量不确定度的合并估计值。聚类的大小小于6s(p),并且同位素组成的MA缉获量之间的关联与杂质特征分析和调查信息一致。结果表明,稳定同位素组成与杂质特征分析的互补使用为评估缉获量之间的关联提供了有用信息。