{"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.