Evidence map›Paper›PMID 42709180›Full record

ArticleAnalytical and bioanalytical chemistry2026

Characterisation of the designer cathinone N-isopropylbutylone by a multi-technique approach and its metabolic profiling and stability assessment using dried matrix spots.

Sara Odoardi, Serena Mestria, Giulia Biosa, Valeria Valentini, Marta Bassi, Sabrine Bilel, Nicole Cocita, Matteo Marti, Giancarlo Fabrizi, Sabina Strano Rossi

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Article in Analytical and bioanalytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Sara OdoardiDepartment of Healthcare Surveillance and Bioethics, Forensic Toxicology Laboratory, Università Cattolica del Sacro Cuore F. Policlinico Gemelli IRCCS, Rome, Italy. sara_odoardi@hotmail.com.
Serena MestriaDepartment of Healthcare Surveillance and Bioethics, Forensic Toxicology Laboratory, Università Cattolica del Sacro Cuore F. Policlinico Gemelli IRCCS, Rome, Italy.
Giulia BiosaDepartment of Healthcare Surveillance and Bioethics, Forensic Toxicology Laboratory, Università Cattolica del Sacro Cuore F. Policlinico Gemelli IRCCS, Rome, Italy.
Valeria ValentiniDepartment of Healthcare Surveillance and Bioethics, Forensic Toxicology Laboratory, Università Cattolica del Sacro Cuore F. Policlinico Gemelli IRCCS, Rome, Italy.
Marta BassiDepartment of Translational Medicine, Section of Legal Medicine, Center of Gender Medicine, LTTA Center and University, University of Ferrara, Ferrara, Italy.
Sabrine BilelDepartment of Environmental Sciences and Prevention, University of Ferrara, Ferrara, Italy.
Nicole CocitaDepartment of Translational Medicine, Section of Legal Medicine, Center of Gender Medicine, LTTA Center and University, University of Ferrara, Ferrara, Italy.
Matteo MartiDepartment of Translational Medicine, Section of Legal Medicine, Center of Gender Medicine, LTTA Center and University, University of Ferrara, Ferrara, Italy.
Giancarlo FabriziDipartimento Di Chimica E Tecnologie del Farmaco, Sapienza University of Rome, Rome, Italy.
Sabina Strano RossiDepartment of Healthcare Surveillance and Bioethics, Forensic Toxicology Laboratory, Università Cattolica del Sacro Cuore F. Policlinico Gemelli IRCCS, Rome, Italy.

Funding

Department of Anti-Drug Policies and Other Addictions, Presidency of the Council of Ministers, Italy project "Multicentric Research for the Study ofEuropean Union's Horizon Europe research and innovation programme 101168195
6 · The paper itself

Abstract

Synthetic cathinones are one of the most prevalent new psychoactive substances on the drug market over the last 20 years. Their structural diversity, rapid turnover and variable stability in biological matrices pose significant challenges for laboratories. This study applied a comprehensive, multi-analytical workflow to characterise, profile the metabolism, and assess the stability of the synthetic cathinone N-isopropylbutylone, with a particular focus on dried matrix spot approaches. Structural elucidation was achieved through the combined use of GC-MS, LC-HRMS and NMR spectroscopy. This provided complementary information, enabling the compound to be identified with confidence. Investigating the metabolic profile in an animal model led to the identification of multiple phase I and phase II metabolites, including products of N-dealkylation, demethylation followed by O-methylation and glucuronidation. Differences in metabolite detection windows were noted between blood and urine. The applicability of dried blood spots (DBS) and dried urine spots (DUS) for metabolite detection and analyte stability was evaluated over a 90-day period. Dried matrix spots proved to be a valuable technique for analysing cathinones and their metabolites, and their enhanced stability in this medium stored at room temperature was confirmed, with most of the analytes being detectable throughout the entire study period. This study highlights the potential of dried matrix spot approaches as practical and effective tools for analysing synthetic cathinones and their metabolites. It also provides new analytical and metabolic data on N-isopropylbutylone. The proposed workflow could be used in future applications in forensic and clinical toxicology.

Indexed as

Dried matrix spotsForensic toxicologyHRMSMetabolic profilingSynthetic cathinones

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.