Identification of <i>in vivo</i> and <i>in vitro</i> metabolites of fentanyl using UHPLC–Q-Orbitrap-HRMS

A comparative analysis of the metabolites and metabolic pathways of fentanyl was conducted in liver microsomes and zebrafish models utilizing ultra-high-performance liquid chromatography coupled with Q Exactive hybrid quadrupole-orbitrap high-resolution mass spectrometry (UHPLC-Q-Orbitrap-HRMS). A total of 21 metabolites were identified across both liver microsomes and zebrafish models. These included 9 Phase I metabolites, such as N-dealkylated, N-oxidated, and hydroxylated products, and 12 Phase II metabolites, including glucuronidated, methylated, and sulfated products, as well as a series of products derived from conjugation with glutathione (GSH). Notably, the products derived from conjugation with GSH are reported here for the first time. This study provides a comprehensive and in-depth comparative analysis of fentanyl metabolism in liver microsomes and zebrafish, offering a foundation for analyzing and identifying biological samples in cases of fentanyl misuse and fatalities.

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Publication Details

Journal
Journal of Analytical Toxicology
Published
2025-02-15
DOI
https://doi.org/10.1093/jat/bkaf012
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
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article

Identification of in vivo and in vitro metabolites of fentanyl using UHPLC–Q-Orbitrap-HRMS

Hong Zhou, Meng Liu, Yao Liu, Sen Zhao et al.
Journal of Analytical Toxicology
Metabolomics and Mass Spectrometry Studies
article

Identification of in vivo and in vitro metabolites of fentanyl using UHPLC–Q-Orbitrap-HRMS

Hong Zhou, Meng Liu, Yao Liu, Sen Zhao, Binjie Wang
article en

Abstract

A comparative analysis of the metabolites and metabolic pathways of fentanyl was conducted in liver microsomes and zebrafish models utilizing ultra-high-performance liquid chromatography coupled with Q Exactive hybrid quadrupole-orbitrap high-resolution mass spectrometry (UHPLC-Q-Orbitrap-HRMS). A total of 21 metabolites were identified across both liver microsomes and zebrafish models. These included 9 Phase I metabolites, such as N-dealkylated, N-oxidated, and hydroxylated products, and 12 Phase II metabolites, including glucuronidated, methylated, and sulfated products, as well as a series of products derived from conjugation with glutathione (GSH). Notably, the products derived from conjugation with GSH are reported here for the first time. This study provides a comprehensive and in-depth comparative analysis of fentanyl metabolism in liver microsomes and zebrafish, offering a foundation for analyzing and identifying biological samples in cases of fentanyl misuse and fatalities.

Journal of Analytical ToxicologyVol. 49(4)
Ministry of Public Security of the People's Republic of China (CN), Zhejiang Police College (CN), Institute of Forensic Science (CN)
Openalex Percentile: Top 97%
Metabolomics and Mass Spectrometry Studies
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