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Identification of Unique 4-Methylmethcathinone (4-MMC) Degradation Markers in Putrefied Matrices†.
Trujillo Uruena, Melissa; York, Rebekah; Philp, Morgan; Kuzhiumparambil, Unnikrishnan; Wei, Zhiwen; Yun, Keming; Fu, Shanlin.
Affiliation
  • Trujillo Uruena M; Centre for Forensic Science, University of Technology Sydney, 15 Broadway, Ultimo, New South Wales 2007, Australia.
  • York R; Centre for Forensic Science, University of Technology Sydney, 15 Broadway, Ultimo, New South Wales 2007, Australia.
  • Philp M; Centre for Forensic Science, University of Technology Sydney, 15 Broadway, Ultimo, New South Wales 2007, Australia.
  • Kuzhiumparambil U; Climate Change Cluster, University of Technology Sydney, 15 Broadway, Ultimo, New South Wales 2007, Australia.
  • Wei Z; School of Forensic Medicine, Shanxi Medical University, 98 University Street, Yuci District, Jinzhong City 030606, Shanxi, People's Republic of China.
  • Yun K; School of Forensic Medicine, Shanxi Medical University, 98 University Street, Yuci District, Jinzhong City 030606, Shanxi, People's Republic of China.
  • Fu S; Centre for Forensic Science, University of Technology Sydney, 15 Broadway, Ultimo, New South Wales 2007, Australia.
J Anal Toxicol ; 44(8): 803-810, 2020 Dec 12.
Article in En | MEDLINE | ID: mdl-33313885
ABSTRACT
Drug degradation as a consequence of putrefactive bacterial activity is a well-known factor that affects the identification and quantitation of certain substances of forensic interest. Current knowledge on putrefaction-mediated degradation of drugs is, however, significantly lacking. This study aimed to investigate the degradation of 4-methylmethcathinone (4-MMC or mephedrone) and to detect its degradation products in putrefied biological matrices containing 4-MMC. The bacteria species Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae and Proteus vulgaris were grown in brain-heart infusion broth, spiked with 4-MMC and incubated at 37°C for 24 h. Postmortem human blood and fresh porcine liver macerate were also left to putrefy in sample tubes at room temperature for 1 week. Structural elucidation was based on modern spectroscopic analyses including the use of high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy. All four putrefactive bacteria were capable of degrading 4-MMC extensively under the experimental conditions explored. Of particular interest was the discovery of a novel degradation product common to all four bacterial species, which was assigned as 2-hydroxy-1-(4-methylphenyl)propan-1-one (HMP) based on the spectroscopic data. This degradation product was detectable in both postmortem human blood and porcine liver samples. The stability of the identified degradation products, especially HMP, should be further investigated to assess their validity of serving as marker analytes for monitoring 4-MMC in postmortem toxicology.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Illicit Drugs / Methamphetamine Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals / Humans Language: En Journal: J Anal Toxicol Year: 2020 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Illicit Drugs / Methamphetamine Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals / Humans Language: En Journal: J Anal Toxicol Year: 2020 Document type: Article Affiliation country: Australia