Movatterモバイル変換


[0]ホーム

URL:


Skip to main content

Advertisement

Springer Nature Link
Log in

Biotransformation of the New Synthetic Cannabinoid with an Alkene, MDMB-4en-PINACA, by Human Hepatocytes, Human Liver Microsomes, and Human Urine and Blood

  • Research Article
  • Published:
The AAPS Journal Aims and scope Submit manuscript

Abstract

Although at a slower rate, new psychoactive substances continue to appear on the illicit drug market, challenging their detection in biological specimens by forensic and clinical toxicologists. Here, we reportin vitro andin vivo metabolism of a new synthetic cannabinoid, methyl 3,3-dimethyl-2-[1-(pent-4-en-1-yl)-1H-indazole-3-carboxamido] butanoate (MDMB-4en-PINACA). This is the first report on metabolism of a synthetic cannabinoid with an alkene functional group at the alkyl side chain. MDMB-4en-PINACA was incubated with both human hepatocytes and human liver microsomes (HLM) for up to 5 h and 1 h, respectively. The samples were analyzed by liquid chromatography-quadrupole time-of-flight mass spectrometry. An authentic human urine and a corresponding blood sample were analyzed to confirm thein vitro metabolites. A total of 32 metabolites were detected, of which 11 metabolites were detected in hepatocyte samples, 31 in HLM, 2 in urine, and 1 in blood. Analysis of the metabolites revealed that the main metabolic pathway of the terminal alkene group of the pentenyl side chain is dihydrodiol formation, most likely via epoxidation. The majority of the metabolites were generated from ester hydrolysis and/or dihydrodiol formation with further hydroxylation and/or dehydrogenation. Two most abundant metabolites in hepatocyte incubation samples, M8 (ester hydrolysis and dihydrodiol) and M30 (ester hydrolysis), coincided the two detected urinary metabolites. Based on the results, M8 and M30 are proposed to be appropriate urinary markers for MDMB-4en-PINACA intake for screening, while the inclusion of the parent drug itself and M29 (hydroxylation) may be useful for confirmation purposes.

This is a preview of subscription content,log in via an institution to check access.

Access this article

Log in via an institution

Subscribe and save

Springer+
from ¥17,985 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

Price includes VAT (Japan)

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Explore related subjects

Discover the latest articles, books and news in related subjects, suggested using machine learning.

References

  1. European Monitoring Centre for Drugs and Drug Addiction. European drug report 2019: trends and developments. Luxembourg: Publications Office of the European Union; 2019.

    Google Scholar 

  2. Slovenian Police. Analytical report: MDMB-PINACA N1-pentyl-4-en isomer (MDMB-4en-PINACA) (C20H27N3O3). 2019.https://www.policija.si/apps/nfl_response_web/0_Analytical_Reports_final/MDMB-4en-PINACA%20(MDMB-PINACA%20N1-pentyl-4-en%20isomer)-ID-1951-18%20_report.pdf. Accessed 11 July 2019.

  3. Banister SD, Longworth M, Kevin R, Sachdev S, Santiago M, Stuart J, et al. Pharmacology of Valinate and tert-Leucinate synthetic cannabinoids 5F-AMBICA, 5F-AMB, 5F-ADB, AMB-FUBINACA, MDMB-FUBINACA, MDMB-CHMICA, and their analogues. ACS Chem Neurosci. 2016;7(9):1241–54.https://doi.org/10.1021/acschemneuro.6b00137.

    Article CAS PubMed  Google Scholar 

  4. Banister SD, Moir M, Stuart J, Kevin RC, Wood KE, Longworth M, et al. Pharmacology of indole and indazole synthetic cannabinoid designer drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA, ADBICA, and 5F-ADBICA. ACS Chem Neurosci. 2015;6(9):1546–59.https://doi.org/10.1021/acschemneuro.5b00112.

    Article CAS PubMed  Google Scholar 

  5. Public Health Agency of Sweden. Fjorton nya ämnen klassas som narkotika eller hälsofarlig vara (in Swedish).https://www.folkhalsomyndigheten.se/nyheter-och-press/nyhetsarkiv/2018/november/fjorton-nya-amnen-klassas-som-narkotika-eller-halsofarlig-vara/ (2018). Accessed 11 July 2019.

  6. Yeter O, Ozturk YE. Metabolic profiling of synthetic cannabinoid 5F-ADB by human liver microsome incubations and urine samples using high-resolution mass spectrometry. Drug Test Anal. 2019;11(6):847–58.https://doi.org/10.1002/dta.2566.

    Article CAS PubMed  Google Scholar 

  7. Truver MT, Watanabe S, Åstrand A, Vikingsson S, Green H, Swortwood MJ, et al. 5F-MDMB-PICA metabolite identification and cannabinoid receptor activity. Drug Test Anal. 2019.https://doi.org/10.1002/dta.2688.

  8. Kusano M, Zaitsu K, Taki K, Hisatsune K, Ji N, Moriyasu T, et al. Fatal intoxication by 5F–ADB and diphenidine: detection, quantification, and investigation of their main metabolic pathways in humans by LC/MS/MS and LC/Q-TOFMS. Drug Test Anal. 2018;10(2):284–93.https://doi.org/10.1002/dta.2215.

    Article CAS PubMed  Google Scholar 

  9. Armenian P, Darracq M, Gevorkyan J, Clark S, Kaye B, Brandehoff NP. Intoxication from the novel synthetic cannabinoids AB-PINACA and ADB-PINACA: a case series and review of the literature. Neuropharmacology. 2018;134:82–91.https://doi.org/10.1016/j.neuropharm.2017.10.017.

    Article CAS PubMed  Google Scholar 

  10. Carlier J, Diao X, Scheidweiler KB, Huestis MA. Distinguishing intake of new synthetic cannabinoids ADB-PINACA and 5F-ADB-PINACA with human hepatocyte metabolites and high-resolution mass spectrometry. Clin Chem. 2017;63(5):1008–21.https://doi.org/10.1373/clinchem.2016.267575.

    Article CAS PubMed  Google Scholar 

  11. Watanabe S, Vikingsson S, Roman M, Green H, Kronstrand R, Wohlfarth A. In vitro and in vivo metabolite identification studies for the new synthetic opioids acetylfentanyl, acrylfentanyl, furanylfentanyl, and 4-fluoro-Isobutyrylfentanyl. AAPS J. 2017;19(4):1102–22.https://doi.org/10.1208/s12248-017-0070-z.

    Article CAS PubMed  Google Scholar 

  12. Minakata K, Yamagishi I, Nozawa H, Hasegawa K, Suzuki M, Gonmori K, et al. Sensitive identification and quantitation of parent forms of six synthetic cannabinoids in urine samples of human cadavers by liquid chromatography–tandem mass spectrometry. Forensic Toxicol. 2017;35(2):275–83.https://doi.org/10.1007/s11419-017-0354-0.

    Article CAS  Google Scholar 

  13. Åstrand A, Töreskog A, Watanabe S, Kronstrand R, Gréen H, Vikingsson S. Correlations between metabolism and structural elements of the alicyclic fentanyl analogs cyclopropyl fentanyl, cyclobutyl fentanyl, cyclopentyl fentanyl, cyclohexyl fentanyl and 2,2,3,3-tetramethylcyclopropyl fentanyl studied by human hepatocytes and LC-QTOF-MS. Arch Toxicol. 2019;93(1):95–106.https://doi.org/10.1007/s00204-018-2330-9.

    Article CAS PubMed  Google Scholar 

  14. Obach RS. Cytochrome P450-catalyzed metabolism of ezlopitant alkene (CJ-12,458), a pharmacologically active metabolite of ezlopitant: enzyme kinetics and mechanism of an alkene hydration reaction. Drug Metab Dispos. 2001;29(7):1057–67.

    CAS PubMed  Google Scholar 

  15. De Costa KS, Black SR, Thomas BF, Burgess JP, Mathews JM. Metabolism and disposition of α-methylstyrene in rats. Drug Metab Dispos. 2001;29(2):166–71.

    PubMed  Google Scholar 

  16. Mang H, Gross J, Lara M, Goessler C, Schoemaker HE, Guebitz GM, et al. Biocatalytic single-step alkene cleavage from aryl alkenes: an enzymatic equivalent to reductive ozonization. Angew Chem Int Ed. 2006;45(31):5201–3.https://doi.org/10.1002/anie.200601574.

    Article CAS  Google Scholar 

  17. Wallgren J, Vikingsson S, Åstrand A, Josefsson M, Gréen H, Dahlén J, et al. Synthesis and identifications of potential metabolites as biomarkers of the synthetic cannabinoid AKB-48. Tetrahedron. 2018;74(24):2905–13.https://doi.org/10.1016/j.tet.2018.04.026.

    Article CAS  Google Scholar 

  18. Watanabe S, Kuzhiumparambil U, Fu S. Structural elucidation of metabolites of synthetic cannabinoid UR-144 by Cunninghamella elegans using nuclear magnetic resonance (NMR) spectroscopy. AAPS J. 2018;20(2):42.https://doi.org/10.1208/s12248-018-0209-6.

    Article CAS PubMed  Google Scholar 

  19. Watanabe S, Vikingsson S, Åstrand A, Auwärter V, Gréen H, Kronstrand R. Metabolism of the benzodiazepines norflurazepam, flurazepam, fludiazepam and cinolazepam by human hepatocytes using high-resolution mass spectrometry and distinguishing their intake in authentic urine samples. Forensic Toxicol. 2019.https://doi.org/10.1007/s11419-019-00488-9.

  20. Brandon EFA, Raap CD, Meijerman I, Beijnen JH, Schellens JHM. An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons. Toxicol Appl Pharmacol. 2003;189(3):233–46.https://doi.org/10.1016/S0041-008X(03)00128-5.

    Article CAS PubMed  Google Scholar 

  21. Diao X, Scheidweiler KB, Wohlfarth A, Pang S, Kronstrand R, Huestis MA. In vitro and in vivo human metabolism of synthetic cannabinoids FDU-PB-22 and FUB-PB-22. AAPS J. 2016;18(2):455–64.https://doi.org/10.1208/s12248-016-9867-4.

    Article CAS PubMed PubMed Central  Google Scholar 

  22. Minakata K, Hasegawa K, Nozawa H, Yamagishi I, Saitoh T, Yoshino A, et al. Sensitive quantification of BB-22 and its metabolite BB-22 3-carboxyindole, and characterization of new metabolites in authentic urine and/or serum specimens obtained from three individuals by LC–QTRAP-MS/MS and high-resolution LC–Orbitrap-MS/MS. Forensic Toxicol. 2019;37(1):164–73.https://doi.org/10.1007/s11419-018-0448-3.

    Article CAS PubMed  Google Scholar 

  23. Diao X, Huestis MA. New synthetic cannabinoids metabolism and strategies to best identify optimal marker metabolites. Front Chem. 2019;7:109.https://doi.org/10.3389/fchem.2019.00109.

    Article CAS PubMed PubMed Central  Google Scholar 

Download references

Acknowledgments

This work was supported by the Vinnova (the EUROSTARS Psychomics project, grant number 10628) and the Strategic Research Area in Forensic Sciences (Strategiområdet forensiska vetenskaper, grant number 2016:7) at Linköping University.

Author information

Authors and Affiliations

  1. Department of Forensic Genetics and Forensic Toxicology, National Board of Forensic Medicine, Artillerigatan 12, 587 58, Linköping, Sweden

    Shimpei Watanabe, Svante Vikingsson, Henrik Gréen & Robert Kronstrand

  2. Division of Drug Research, Department of Medical and Health Sciences, Linköping University, Linköping, Sweden

    Anna Åstrand, Henrik Gréen & Robert Kronstrand

Authors
  1. Shimpei Watanabe
  2. Svante Vikingsson
  3. Anna Åstrand
  4. Henrik Gréen
  5. Robert Kronstrand

Corresponding author

Correspondence toShimpei Watanabe.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic Supplementary Material

ESM 1

(PDF 688 kb)

Rights and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Watanabe, S., Vikingsson, S., Åstrand, A.et al. Biotransformation of the New Synthetic Cannabinoid with an Alkene, MDMB-4en-PINACA, by Human Hepatocytes, Human Liver Microsomes, and Human Urine and Blood.AAPS J22, 13 (2020). https://doi.org/10.1208/s12248-019-0381-3

Download citation

KEY WORDS

Profiles

  1. Anna ÅstrandView author profile
  2. Henrik GréenView author profile

Access this article

Subscribe and save

Springer+
from ¥17,985 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

Price includes VAT (Japan)

Instant access to the full article PDF.

Advertisement


[8]ページ先頭

©2009-2025 Movatter.jp