Evidence map›Paper›PMID 41423501›Full record

ArticleArchives of toxicology2026

Evaluating the stability of synthetic cathinones in liquid urine and dried urine spots: impact of pH and storage conditions.

Stefania Boccuzzi, David Cowan, Paul I Dargan, Edward Goucher, Vincenzo Abbate

Abstract read
In one paragraph

Article in Archives of toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
  2. ExperimentalMolecules (Basel, Switzerland) · 2026
    Article
4 · The record

Corrections and comments

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

5 authors.

Stefania BoccuzziDepartment of Analytical, Environmental & Forensic Sciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.ORCID 0009-0000-0058-7161
David CowanDepartment of Analytical, Environmental & Forensic Sciences, Faculty of Life Sciences & Medicine, King's College London, London, UK.ORCID 0000-0001-6407-1113
Paul I DarganClinical Toxicology, Faculty of Life Sciences and Medicine, King's College London, London, UK.ORCID 0000-0002-3433-9622
Edward GoucherThermo Fisher Scientific, San Jose, CA, USA.
Vincenzo AbbateDepartment of Analytical, Environmental & Forensic Sciences, Faculty of Life Sciences & Medicine, King's College London, London, UK. vincenzo.abbate@kcl.ac.uk.ORCID 0000-0002-3300-0520

Funding

Guy's and St Thomas' NHS Foundation Trust Guy's and St Thomas' NHS Foundation TrustKing's College London King's College LondonThermo Fisher Scientific Thermo Fisher Scientific
6 · The paper itself

Abstract

Synthetic cathinones comprise a class of new psychoactive substances associated with significant morbidity and mortality. Their detection in biological samples is complicated by their instability, which can compromise quantification or interpretation. This study evaluates the stability of five synthetic cathinones - 4-chloroethcathinone (4-CEC), 4-ethylmethcathinone (4-EMC), N-ethylhexedrone (NEH), methylenedioxypyrovalerone (MDPV) and 4-chloro-α-pyrrolidinopropiophenone (4-Cl-α-PPP) - in dried urine spots (DUS) and liquid urine at acidic (pH 5.98) and mildly basic (pH 7.63) conditions. Fortified samples were stored at room temperature (25 °C) and refrigerated (4 °C) for up to 14 days and analysed using the Thermo Fisher VeriSpray™ Paper Spray Ion Source coupled to a Thermo Fisher Altis™ Plus Triple Quadrupole Mass Spectrometer. Urinary pH was the critical determinant of stability. Under acidic conditions, 4-EMC, 4-Cl-α-PPP, and MDPV retained > 90% of their initial concentration by day 14 in both matrices. Conversely, under basic conditions, 4-CEC and NEH degraded rapidly at room temperature (< 20% remaining by day three). Refrigeration slowed but did not prevent degradation. DUS offered a minor stabilising effect for most analytes, although NEH exhibited greater degradation. Statistically significant differences between acidic and basic conditions were observed (p < 0.0083), while matrix format had limited influence at acidic pH. Overall, pH rather than matrix type was the main driver of synthetic cathinone stability in urine. Nevertheless, DUS offer practical benefits for sample transport and storage in forensic settings. Future research should further characterise the physicochemical mechanisms underlying synthetic cathinone degradation in urine to inform the interpretation of operational toxicology workflows.

Indexed as

AlkaloidsDesigner DrugsPsychotropic DrugsSubstance Abuse DetectionDrug StabilityHumansHydrogen-Ion ConcentrationPropiophenonesSpecimen HandlingSynthetic CathinoneAlkaloidscathinoneDesigner DrugsPropiophenonesPsychotropic DrugsSynthetic CathinoneAmbient ionisationAnalyte stabilityDried matrix spotsPaper spray ionisationSynthetic cathinonesUrinary pH

Identifiers

PMID41423501
PMCPMC12967546

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.