Dayrit Fabian M, Dumlao Morphy C
Chemistry Department, Ateneo de Manila University, Loyola Heights, Quezon City, Philippines.
Forensic Sci Int. 2004 Aug 11;144(1):29-36. doi: 10.1016/j.forsciint.2004.03.002.
Methamphetamine hydrochloride is one of the most widely used illicit drugs in the Philippines. In this study, we describe the application of cluster analysis of trace impurities in the profiling of the seized methamphetamine drug samples. Thirty milligrams of a homogenized drug sample were dissolved in 1 mL of pH 10.5 buffer solution and extracted with ethyl acetate containing three internal standards. The trace impurities were identified using gas chromatography-mass spectrometry (GC-MS) and quantified by gas chromatography with a flame ionization detector (GC-FID). Following previously reported methodologies, 30 impurity peaks were selected from the GC-FID chromatograms. The peak areas and retention times were referenced to the internal standards. The peak areas of the selected peaks were then grouped for cluster analysis. In order to check for consistency of clustering, two further cluster analyses were performed using 40 and 50 impurity peaks. Changes in clustering were observed in going from 30 to 40 impurity peaks, while analyses using 40 and 50 impurity peaks gave similar results. Thus, for the seized drug samples used in this study, cluster analysis using at least 40 impurity peaks showed better consistency of clustering as compared to analysis using 30 peaks only. Ten of the impurity peaks were identified, of which four were identified for the first time in methamphetamine drug samples. These are p-bromotoluene, N-benzyl amphetamine, N-ethyl amphetamine, and N-ethyl methamphetamine. The presence of phenyl-2-propanone (P2P), N,N-dimethyl amphetamine, and N-formyl amphetamine is indicative that these casework samples were synthesized using the Leuckart method.
盐酸甲基苯丙胺是菲律宾使用最广泛的非法药物之一。在本研究中,我们描述了在缉获的甲基苯丙胺毒品样本剖析中痕量杂质聚类分析的应用。将30毫克均质化的毒品样本溶解于1毫升pH 10.5的缓冲溶液中,并用含有三种内标的乙酸乙酯萃取。使用气相色谱 - 质谱联用仪(GC-MS)鉴定痕量杂质,并通过带有火焰离子化检测器的气相色谱仪(GC-FID)进行定量。按照先前报道的方法,从GC-FID色谱图中选择30个杂质峰。将峰面积和保留时间以内标为参照。然后将所选峰的峰面积进行分组以进行聚类分析。为了检查聚类的一致性,使用40个和50个杂质峰进行了另外两次聚类分析。从30个杂质峰增加到40个杂质峰时观察到聚类变化,而使用40个和50个杂质峰的分析得到了相似的结果。因此,对于本研究中使用的缉获毒品样本,与仅使用30个峰的分析相比,使用至少40个杂质峰的聚类分析显示出更好的聚类一致性。鉴定出了10个杂质峰,其中有4个是在甲基苯丙胺毒品样本中首次鉴定出来的。它们是对溴甲苯、N-苄基苯丙胺、N-乙基苯丙胺和N-乙基甲基苯丙胺。苯基-2-丙酮(P2P)、N,N-二甲基苯丙胺和N-甲酰基苯丙胺的存在表明这些实际案件样本是使用勒卡特法合成的。