Meldonium long-term excretion period and pharmacokinetics in blood and urine of healthy athlete volunteers.


Journal

Drug testing and analysis
ISSN: 1942-7611
Titre abrégé: Drug Test Anal
Pays: England
ID NLM: 101483449

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 07 11 2017
revised: 10 10 2018
accepted: 11 10 2018
pubmed: 18 10 2018
medline: 5 11 2019
entrez: 18 10 2018
Statut: ppublish

Résumé

Meldonium is a metabolic drug whose inclusion in the 2016 List of Prohibited Substances and Methods followed the analysis of data collected under the 2015 World Anti-Doping Agency Monitoring Program. In the early months of 2016, anti-doping laboratories reported an unusually high number of cases in which urine samples contained high concentrations of meldonium. Consequently, the meldonium excretion period in healthy athletes and the substance's long-term urine and blood (plasma) pharmacokinetics became central questions for the anti-doping community to address, to ensure appropriate assessment of the scientific and medical situation, and also fair treatment of athletes from a result management and legal standpoint. At the present time, data on meldonium pharmacokinetics is limited to a few studies, with no known data available on long-term excretion of high oral doses. The primary objective of this open-label study was to determine long-term urine and plasma pharmacokinetic parameters of meldonium in healthy volunteers. Study design included single and repeated functional load testing and assessment of L-carnitine administration on meldonium excretion and pharmacokinetics. Thirty-two volunteers were equally divided into two groups receiving either 1.0 g or 2.0 g of oral meldonium daily for 3 weeks. The study found meldonium takes several days to attain a steady state in blood and displays an elimination period over several months after cessation of treatment. Moreover, findings demonstrate that the daily dose, periodicity and duration of treatment with meldonium are the most important factors to consider in calculating the substance's elimination and complete body clearance.

Identifiants

pubmed: 30328291
doi: 10.1002/dta.2521
doi:

Substances chimiques

Cardiovascular Agents 0
Methylhydrazines 0
3-(2,2,2-trimethylhydrazine)propionate 73H7UDN6EC

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

554-566

Informations de copyright

© 2018 John Wiley & Sons, Ltd.

Auteurs

Vladimir Uiba (V)

Federal Medical Biological Agency (FMBA), Moscow, Russia.

Yulia Miroshnikova (Y)

Federal Medical Biological Agency (FMBA), Moscow, Russia.

Maksim Zabelin (M)

Federal Medical Biological Agency (FMBA), Moscow, Russia.

Aleksander Samoylov (A)

State Research Center Federal Medical Biophysical Center (SRC-FMBC), FMBA, Moscow, Russia.

Vladislav Karkischenko (V)

Research Centre of Biomedical Technologies, FMBA, Russia.

Sergey Semyonov (S)

Research and Technical Center of Radiation-Chemical Safety and Hygiene, FMBA, Moscow, Russia.

Tatiana Astrelina (T)

State Research Center Federal Medical Biophysical Center (SRC-FMBC), FMBA, Moscow, Russia.

Sergey Razinkin (S)

State Research Center Federal Medical Biophysical Center (SRC-FMBC), FMBA, Moscow, Russia.

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