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Statistical analysis of the chemical attribution signatures of 3-methylfentanyl and its methods of production.
Mayer, Brian P; Valdez, Carlos A; DeHope, Alan J; Spackman, Paul E; Williams, Audrey M.
Affiliation
  • Mayer BP; Forensic Science Center, Lawrence Livermore National Laboratory, 7000 East Avenue L-091, Livermore, CA 94550, United States.
  • Valdez CA; Forensic Science Center, Lawrence Livermore National Laboratory, 7000 East Avenue L-091, Livermore, CA 94550, United States.
  • DeHope AJ; Materials Science Division, Lawrence Livermore National Laboratory, 7000 East Avenue L-382, Livermore, CA 94550, United States.
  • Spackman PE; Forensic Science Center, Lawrence Livermore National Laboratory, 7000 East Avenue L-091, Livermore, CA 94550, United States.
  • Williams AM; Forensic Science Center, Lawrence Livermore National Laboratory, 7000 East Avenue L-091, Livermore, CA 94550, United States. Electronic address: williams259@llnl.gov.
Talanta ; 186: 645-654, 2018 Aug 15.
Article in En | MEDLINE | ID: mdl-29784415
ABSTRACT
Chemical attribution of the origin of an illegal drug is a key component of forensic efforts aimed at combating illicit and clandestine manufacture of drugs and pharmaceuticals. The results of these studies yield detailed information on synthesis byproducts, reagents, and precursors that can be used to identify the method of manufacture. In the present work, chemical attribution signatures (CAS) associated with the synthesis of the analgesic 3-methylfentanyl, N-(3-methyl-1-phenethylpiperidin-4-yl)-N-phenylpropanamide, were investigated. Eighteen crude samples from six synthesis methods were generated, the analysis of which was used to identify signatures (i.e. chemical compounds) that were important in the discrimination of synthetic route. These methods were carefully selected to minimize the use of scheduled precursors, complicated laboratory equipment, number of steps, and extreme reaction conditions. Using gas and liquid chromatographies combined with time-of-flight mass spectrometry (GC-QTOF and LC-QTOF) over 160 distinct species were monitored. Analysis of this combined data set was performed using modern machine learning techniques capable of reducing the size of the data set, prioritizing key chemical attribution signatures, and identifying the method of production for blindly synthesized 3-methylfentanyl materials.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Talanta Year: 2018 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Talanta Year: 2018 Document type: Article Affiliation country: Estados Unidos