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Articles

Something New about Something Old: A 10-Year Follow-Up on Classical and New Psychoactive Tryptamines and Results of Analysis

, M.D. ORCID Icon, , Ph.D., , M.D., Ph.D., , M.D., Ph.D., , M.D., , M.D., , B.S., , B.S., , M.D., Ph.D. & , M.D., Ph.D. show all
Pages 297-305 | Received 05 Aug 2016, Accepted 04 Feb 2017, Published online: 01 Jun 2017
 

ABSTRACT

New psychoactive tryptamines may be a public health risk since they intend to mimic the hallucinogenic effects of regulated psychoactive drugs. Few studies describe uses and clinical effects of unregulated new psychoactive tryptamines. This study aims (1) to explore the presence of tryptamines classified as NPS among the substances delivered for analysis to a harm-reduction organization; (2) to describe the substances found in the samples after analysis; and (3) to compare analytical results of regulated vs. non-regulated tryptamines. Samples delivered and analyzed by gas chromatography-mass spectrometry from 2006 to 2015 were included. A descriptive study of results was conducted. From 25,296 samples that were delivered, 436 were tryptamines; from these 232 (53.21%) were non-regulated. The most delivered non-regulated tryptamine was 4-AcO-DMT. A search of the PubMed database in July 2016 revealed that no studies in humans have ever been carried out with 4-AcO-DMT. Unregulated tryptamines likely contained one unadulterated substance (p ≤ 0.001). The number of samples submitted which contained tryptamines increased during the course of the study, with significant differences in client expectations vs. analysis results between the controlled and uncontrolled groups. There is a need for further research in order to prevent the potential health risks associated with their use.

Acknowledgment

The authors would like to acknowledge Mr. Guy S. Jones (Director, Reagent Research Ltd.) for his important contribution to this article.

Declaration of interest

No conflicts of interest are reported.

Funding

The authors were supported in part by grants from Instituto de Salud Carlos III (ISCIII, FIS-FEDER, PI14/00715, RTA RD12/0028/0009), ISCIII-Red de Trastornos Adictivos (RTA RD16/0017/0003 and RD16/0017/0010), and The European Commission (Drugs Policy Initiatives, Justice Programme 2014-2020, contract no. HOME/2014/JDRU/AG/DRUG/7082, PREDICT Project). L. Galindo is the recipient of a Rio Hortega fellowship (ISC-III; CM14/00111).

Additional information

Funding

The authors were supported in part by grants from Instituto de Salud Carlos III (ISCIII, FIS-FEDER, PI14/00715, RTA RD12/0028/0009), ISCIII-Red de Trastornos Adictivos (RTA RD16/0017/0003 and RD16/0017/0010), and The European Commission (Drugs Policy Initiatives, Justice Programme 2014-2020, contract no. HOME/2014/JDRU/AG/DRUG/7082, PREDICT Project). L. Galindo is the recipient of a Rio Hortega fellowship (ISC-III; CM14/00111).

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