Analysis of In Vitro Mirtazapine Metabolites in Human Liver Microsomes by LC-HRMS.

Q3 Medicine
Ying Zhang, Wen-Fang Zhang, Duo-Qi Xu, Shi-Yang Qin, Shi-Yun Yang, Jing Qiao
{"title":"Analysis of <i>In Vitro</i> Mirtazapine Metabolites in Human Liver Microsomes by LC-HRMS.","authors":"Ying Zhang, Wen-Fang Zhang, Duo-Qi Xu, Shi-Yang Qin, Shi-Yun Yang, Jing Qiao","doi":"10.12116/j.issn.1004-5619.2024.340606","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To establish and optimize an <i>in vitro</i> incubation system with human liver microsomes and investigate the <i>in vitro</i> metabolites and possible metabolic pathways of mirtazapine.</p><p><strong>Methods: </strong>Three major metabolites of mirtazapine were selected to optimize the incubation conditions of liver microsomes. The metabolites of mirtazapine were analyzed by liquid chromatography-high resolution mass spectrometry (LC-HRMS) to identify the <i>in vitro</i> metabolites and metabolic pathways of mirtazapine.</p><p><strong>Results: </strong>Ten metabolites, including nine phase Ⅰ metabolites and one phase Ⅱ metabolite, were identified in the <i>in vitro</i> liver microsome incubation. Among them, five new metabolites and one new metabolic pathway were discovered. The pathways involved in phase Ⅰ metabolic included methylation, hydroxylation, oxidation, reduction, etc., while the phase Ⅱ biotransformation was mainly glucuronidation.</p><p><strong>Conclusions: </strong>The metabolites discovered in this study are consistent with the main metabolites of mirtazapine reported in literature, which are N-desmethylmetazapine, 8-hydroxy mirtazapine and mirtazapine-N-oxide. The results can provide basis for the confirmation of mirtazapine cases and provide reference for the study of other substances.</p>","PeriodicalId":12317,"journal":{"name":"法医学杂志","volume":"40 6","pages":"569-574"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"法医学杂志","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12116/j.issn.1004-5619.2024.340606","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: To establish and optimize an in vitro incubation system with human liver microsomes and investigate the in vitro metabolites and possible metabolic pathways of mirtazapine.

Methods: Three major metabolites of mirtazapine were selected to optimize the incubation conditions of liver microsomes. The metabolites of mirtazapine were analyzed by liquid chromatography-high resolution mass spectrometry (LC-HRMS) to identify the in vitro metabolites and metabolic pathways of mirtazapine.

Results: Ten metabolites, including nine phase Ⅰ metabolites and one phase Ⅱ metabolite, were identified in the in vitro liver microsome incubation. Among them, five new metabolites and one new metabolic pathway were discovered. The pathways involved in phase Ⅰ metabolic included methylation, hydroxylation, oxidation, reduction, etc., while the phase Ⅱ biotransformation was mainly glucuronidation.

Conclusions: The metabolites discovered in this study are consistent with the main metabolites of mirtazapine reported in literature, which are N-desmethylmetazapine, 8-hydroxy mirtazapine and mirtazapine-N-oxide. The results can provide basis for the confirmation of mirtazapine cases and provide reference for the study of other substances.

LC-HRMS法分析人肝微粒体中米氮平代谢物。
目的:建立并优化人肝微粒体体外培养体系,研究米氮平体外代谢产物及可能的代谢途径。方法:选择米氮平的3种主要代谢物,优化肝微粒体的培养条件。采用液相色谱-高分辨率质谱(LC-HRMS)分析米氮平的代谢产物,确定米氮平的体外代谢产物和代谢途径。结果:在肝微粒体体外培养中鉴定出10种代谢物,其中9种为Ⅰ相代谢物,1种为Ⅱ相代谢物。其中发现了5种新的代谢物和1种新的代谢途径。Ⅰ期代谢涉及的途径包括甲基化、羟基化、氧化、还原等,而Ⅱ期生物转化主要是葡萄糖醛酸化。结论:本研究发现的代谢物与文献报道的米氮平主要代谢物n -去甲基甲氮平、8-羟基米氮平和n -氧化物米氮平一致。结果可为米氮平病例的确证提供依据,并为其他药物的研究提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
法医学杂志
法医学杂志 Medicine-Pathology and Forensic Medicine
CiteScore
1.50
自引率
0.00%
发文量
0
期刊介绍:
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信