Forensic Toxicology

Designer Drugs, Drugs of Abuse, Illicit Drugs, etc.

 

Recently, Electrochemistry (EC) as a fast and efficient in vitro technique has found great interest tomimick the metabolism of designer drugs (phase I).

Using EC upfront MS, e.g., EC/(LC)/MS, designer drugs can be oxidized instantaneously thereby
mimicking the enzymatic biotransformation of the Cytochrome P450 reactions that takesplace in the liver. This biomimetic oxidation is much faster and has zero interaction with anybiological matrices (e.g., cell membranes, plasma, urine, etc.) and allows further for isolatedphase II reactions, i.e., adduct formation.

Morphine oxidation on glassy carbon electrode using ROXY EC system

Three oxidation cycles are shown, illustrating the reproducible formation of hydroxymorphine (m/z 302) out of morphine (m/z 286). Continuous scan mode 0-2 V, 20 mV/s.  50% ACN in 20 mM ammonium formate buffer, pH 7.4

Courtesy: Przemysław Mielczarek,  Dep. of Biochemistry and Neurobiology, AGH University of Science and Technology, Cracow, Poland

 

 

 

The successful use of the ROXY EC system for the synthesis of metabolites relevant to designer drugs has also been shown in the award winning oral presentation of Dr. Lars Ambach (Institute of Forensic Medicine, University of Bern, Switzerland), presented at the 50th Annual Meeting of the International Association of Forensic Toxicologist, TIFAT 2012 held in Hamamatsu, Japan. For abstract, click here.

 

ROXY EC System used for on-line infusion EC/MS in Forensic Toxicology



Application Notes

Application Notebook

Posters

  • 221_070_01 - Online EC MS A Powerful Tool for Fast Prediction of Phase I and II Drug Metabolism
  • 221_076_01 - Expanding Role of Electrochemistry Mass Spectrometry in Life Sciences
  • 221_077_01 - Novel method for efficient reduction of disulfide bonds in peptides and proteins prior MS detection
  • 221_078_01 - Identification of electrochemically synthesized metabolites
  • 221_079_01 - Insights into Nucleic Acids Oxidation by ElectrochemistryLiquid ChromatographyMass Spectrometry
  • 221_090_01 - Degradation of Xenobiotics and Binding to Organic Matter by OnLine EC MS
  • 221_105_01 - Controlled Reduction of Disulfide Bonds in Biopharmaceuticals Using an Electrochemical Reactor Cell online with LCMS Rolduc 2014
  • 221_106_01 - ElectrochemistryMS a Powerful Tool in Drug Metabolism Rolduc 2014
  • 221_107_01 - ElectrochemistryMS a Powerful Tool in Drug Metabolism ASMS 2014
  • 221_108_01 - Controlled Reduction of Disulfide Bonds in Proteins and Peptides Using an Electrochemical Reactor Cell in online LCECMS ASMS 2014
  • 221_115_01 - Controlled Reduction of Disulfide Bonds in Biopharmaceuticals ElCheMS2015
  • 221_116_01 - Enhanced Pharmaceutical Stability ElCheMS2015
  • 221_117_01 - Mimicking Drug Metabolism ElCheMS2015
  • 221_118_01 - Electrochem Reduction of Disulfide Bonds ASMS2015
  • 221_120_01 - ECHDX for the Analysis of Protein Therapeutics HOS2015
  • 221_226_01 - The Application of ElectrochemistryMS to Pharmaceutical Stability Testing and Degradant Synthesis


24300001 - Electrochemical simulation of cocaine metabolism - a step towards predictive toxicology for drugs of abuse
Przemyslaw Mielczarek, Hana Raoof, Jolanta H. Kotlinska, Piotr Stefanowicz, Zbigniew Szewczuk, Piotr Suder and Jerzy Silberring; European Journal of Mass Spectrometry,Volume 20 Issue 4, Pages 279 - 285 (2014)

24300000 - Determination of psychostimulants and their metabolites by electrochemistry linked on-line to flowing atmospheric pressure afterglow mass spectrometry
Marek Smoluch, Przemyslaw Mielczarek, Edward Reszke, Gary M. Hieftje and Jerzy Silberring; Analyst. 2014 Sep 7;139(17):4350-5

See our support pages for a full list of recent literature