Metabolomics of methadone: clinical and forensic toxicological implications and variability of dose response

• Type: Another Publication in an International Scientific Journal
• Date: 2016

Authors

Ricardo Jorge Dinis Oliveira (Author) FMUP

Journal

Title: Drug Metabolism Reviews

Vol. 48

Pages: 568-576

ISSN: 0360-2532

Publisher: Taylor & Francis

Indexing

ISI Web of Knowledge - 38 Citations

Scopus - 38 Citations

Other information

Authenticus ID: P-00M-611

DOI: 10.1080/03602532.2016.1192642

Abstract (EN): Methadone is a full -opioid receptor agonist used in the treatment of heroin addiction. It is commercialized as a racemic mixture with considerable variability in the pharmacokinetics and pharmacodynamics between individuals that can affect dose-response and toxicological profile. This review aims to discuss metabolomics of methadone, namely by presenting all major and minor metabolites and pharmacokinetic drug interactions. The main mechanism for methadone metabolism is hepatic through the cytochrome P450, specifically isoenzymes 2B6, 3A4 and 2D6. Firstly, methadone is N-demethylated and cyclize to form its major 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) and 2-ethyl-5-methyl-3,3-diphenylpyraline (EMDP) metabolites. Several alternate minor pathways have been described namely various methadol metabolites, which proved to be active.It is expected that knowing the metabolomics of methadone may provide further insights, attempting a personalized therapy aiming to attain effective blood concentrations. The historical record is therefore especially important when investigating clinical and forensic cases related to methadone administration, since interindividual responses are known to vary considerably.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9