The Trouble With Kratom: Analytical and Interpretative Issues Involving Mitragynine.


Journal

Journal of analytical toxicology
ISSN: 1945-2403
Titre abrégé: J Anal Toxicol
Pays: England
ID NLM: 7705085

Informations de publication

Date de publication:
10 Sep 2019
Historique:
received: 15 03 2019
revised: 15 05 2019
accepted: 23 05 2019
pubmed: 20 8 2019
medline: 11 3 2020
entrez: 20 8 2019
Statut: ppublish

Résumé

Mitragynine is the primary active alkaloid in the leaves of the tropical tree Mitragyna speciosa, and goes by the popular names "Kratom", biak-biak and maeng da. Mitragynine is increasingly seen in forensic toxicology casework including driving under the influence of drugs and medicolegal death investigation cases. The toxicity of mitragynine continues to be debated in the scientific community as advocates highlight its long history of use in Southeast Asia and testimonials to its benefits by present-day users, while opponents point to an increasing number of adverse events tied to mitragynine use in Western societies. Quantitative reports of mitragynine in biological specimens from forensic investigations in the literature are sparse and may be influenced by poor analyte stability and inadequate resolution of mitragynine from its diastereomers, which could lead to falsely elevated concentrations and subsequently render those reported concentrations inappropriate for comparison to a reference range. Over the course of 27 months, 1,001 blood specimens submitted to our laboratory tested positive for mitragynine using a sensitive and specific quantitative LC-MS/MS method; concentrations ranged from 5.6-29,000 ng/mL, with mean and median concentrations of 410 ± 1,124 and 130 ng/mL, respectively. Mitragynine presents an analytical challenge that requires a method that appropriately separates and identifies mitragynine itself from its isomers and other related natural products. We describe a validated analytical method and present a short series of case reports that provide examples of apparent adverse events, and the associated range of mitragynine concentrations. This type of analytical specificity is required to appropriately interpret mitragynine concentrations detected in biological specimens from forensic casework and assess its potential toxicity.

Identifiants

pubmed: 31424079
pii: 5550863
doi: 10.1093/jat/bkz064
doi:

Substances chimiques

Receptors, Opioid, mu 0
Secologanin Tryptamine Alkaloids 0
mitragynine EP479K822J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

615-629

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

Donna M Papsun (DM)

NMS Labs, 200 Welsh Rd, Horsham, PA, USA.

Ayako Chan-Hosokawa (A)

NMS Labs, 200 Welsh Rd, Horsham, PA, USA.

Laura Friederich (L)

North Carolina Office of the Chief Medical Examiner, 4312 District Dr, Raleigh, NC, USA.

Justin Brower (J)

North Carolina Office of the Chief Medical Examiner, 4312 District Dr, Raleigh, NC, USA.

Kristopher Graf (K)

NMS Labs, 200 Welsh Rd, Horsham, PA, USA.

Barry Logan (B)

NMS Labs, 200 Welsh Rd, Horsham, PA, USA.
The Center for Forensic Science Research and Education (CFSRE), 2300 Stratford Ave, Willow Grove, PA, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH