Bonadio Federica, Margot Pierre, Delémont Olivier, Esseiva Pierre
Ecole des Sciences Criminelles, Institut de Police Scientifique, University of Lausanne, Batochime, CH-1015, Lausanne-Dorigny, Switzerland.
Forensic Sci Int. 2009 May 30;187(1-3):73-80. doi: 10.1016/j.forsciint.2009.03.004. Epub 2009 Apr 7.
A headspace solid-phase microextraction procedure (HS-SPME) was developed for the profiling of traces present in 3,4-methylenedioxymethylampethamine (MDMA). Traces were first extracted using HS-SPME and then analyzed by gas chromatography-mass spectroscopy (GC-MS). The HS-SPME conditions were optimized using varying conditions. Optimal results were obtained when 40 mg of crushed MDMA sample was heated at 80 degrees C for 15 min, followed by extraction at 80 degrees C for 15 min with a polydimethylsiloxane/divinylbenzene coated fibre. A total of 31 compounds were identified as traces related to MDMA synthesis, namely precursors, intermediates or by-products. In addition some fatty acids used as tabletting materials and caffeine used as adulterant, were also detected. The use of a restricted set of 10 target compounds was also proposed for developing a screening tool for clustering samples having close profile. 114 seizures were analyzed using an SPME auto-sampler (MultiPurpose Samples MPS2), purchased from Gerstel GMBH & Co. (Germany), and coupled to GC-MS. The data was handled using various pre-treatment methods, followed by the study of similarities between sample pairs based on the Pearson correlation. The results show that HS-SPME, coupled with the suitable statistical method is a powerful tool for distinguishing specimens coming from the same seizure and specimens coming from different seizures. This information can be used by law enforcement personnel to visualize the ecstasy distribution network as well as the clandestine tablet manufacturing.
开发了一种顶空固相微萃取方法(HS-SPME)用于分析3,4-亚甲基二氧甲基苯丙胺(摇头丸)中的痕量成分。痕量成分首先通过HS-SPME进行萃取,然后用气相色谱-质谱联用仪(GC-MS)进行分析。通过改变条件对HS-SPME条件进行了优化。当40毫克碾碎的摇头丸样品在80摄氏度下加热15分钟,然后用涂有聚二甲基硅氧烷/二乙烯基苯的纤维在80摄氏度下萃取15分钟时,可获得最佳结果。共鉴定出31种与摇头丸合成相关的痕量化合物,即前体、中间体或副产物。此外,还检测到了一些用作压片材料的脂肪酸和用作掺假剂的咖啡因。还建议使用一组受限的10种目标化合物来开发一种筛选工具,用于对轮廓相近的样品进行聚类。使用从德国Gerstel GMBH & Co.公司购买的SPME自动进样器(多功能样品MPS2)对114份查获样品进行了分析,并与GC-MS联用。数据采用各种预处理方法进行处理,然后基于皮尔逊相关性研究样品对之间的相似性。结果表明,HS-SPME与合适的统计方法相结合是区分来自同一查获批次的样本和来自不同查获批次的样本的有力工具。执法人员可以利用这些信息来可视化摇头丸的分销网络以及秘密片剂制造情况。