Evidence map›Paper›PMID 39751878›Full record

ArticleArchives of toxicology2025

In vitro metabolism of seven arolyl-derived fentanyl-type new psychoactive substances.

Xuan Luo, Qiaotong Chen, Kejian Huang, Xiaofeng Liu, Ning Yang, Qiulian Luo

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Xuan LuoSchool of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi, 530004, People's Republic of China. luoxuan@gxu.edu.cn.ORCID 0000-0001-7923-7817
Qiaotong ChenSchool of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi, 530004, People's Republic of China.
Kejian HuangPublic Security Department of Guangxi Zhuang Autonomous Region, Institute of Forensic Science, Nanning, Guangxi, 500012, People's Republic of China. huangkejian911@163.com.
Xiaofeng LiuPublic Security Department of Guangxi Zhuang Autonomous Region, Institute of Forensic Science, Nanning, Guangxi, 500012, People's Republic of China.
Ning YangPublic Security Department of Guangxi Zhuang Autonomous Region, Institute of Forensic Science, Nanning, Guangxi, 500012, People's Republic of China.
Qiulian LuoSchool of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi, 530004, People's Republic of China.

Funding

Science and Technology Department of Guangxi Zhuang Autonomous Region Guike AD19259004
6 · The paper itself

Abstract

Over the past decade, fentanyl-type new psychoactive substances (F-NPS) have emerged as the most representative synthetic opioids in third-generation drugs. These substances are characterized by their "low" fatal dose and parent drug levels in biological matrices, "fast" rates of derivatization and metabolism, and "many" derivatization sites and analogs. The low levels of parent fentanyl NPS in biological matrices complicate their detection, necessitating the use of characteristic metabolites as biomarkers for forensic analysis. Moreover, the ongoing emergence of arolyl-derived F-NPS further challenges forensic laboratories in accurately identifying the parent drug from its metabolites. To address this issue, in this study, the in vitro phase I metabolism of seven arolyl-derived F-NPS was studied using a human liver microsome model. Metabolites were analyzed by liquid chromatography-ion trap tandem time-of-flight mass spectrometry. Using density functional theory, the structural characteristics and their effects on amide hydrolysis, N-dealkylation, and oxidation metabolism were clarified. Amide hydrolysis was influenced by the positive charge of the carbonyl carbon and the 2-substituent effect on the aryl groups. N-dealkylation, β-monohydroxylation, N-oxidation, and phenyl group monohydroxylation in the tail were less affected by structural changes in the head. The former two were the major metabolites and exhibited competition. The relative contents of N-oxidation and phenyl group monohydroxylation in the tail were relatively stable at 4% and 13%, respectively. Furthermore, the β-C adjacent to the nitrogen on the piperidine ring was susceptible to oxidation, leading to the formation of the monohydroxylation metabolite. The results of this study may enhance our understanding of the in vitro metabolism of arolyl-derived F-NPS, and potentially all F-NPS, providing important data and theoretical support for predicting their in vivo metabolism in the future.

Indexed as

Analgesics, OpioidFentanylMicrosomes, LiverPsychotropic DrugsChromatography, LiquidDealkylationHumansHydrolysisOxidation-ReductionTandem Mass SpectrometryAnalgesics, OpioidFentanylPsychotropic DrugsArolyl-derived fentanyl-type new psychoactive substancesHuman liver microsomesIn vitro metabolismMetabolic characteristicsStructural effect

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.