Identification and characterization of amiodarone metabolites in rats using UPLC-ESI-QTOFMS-based untargeted metabolomics approach

被引:9
作者
Jeong, Eun Sook [1 ,2 ]
Kim, Gabin [1 ,2 ]
Yim, Daeun [1 ,2 ]
Moon, Kyung-Sik [3 ]
Lee, Su-Jun [1 ,2 ]
Shin, Jae-Gook [1 ,2 ]
Kim, Dong Hyun [1 ,2 ]
机构
[1] Inje Univ, Dept Pharmacol, Coll Med, 633-165 Gaegum Dong, Busan 614735, South Korea
[2] Inje Univ, PharmacoGen Res Ctr, Coll Med, 633-165 Gaegum Dong, Busan 614735, South Korea
[3] Korea Inst Toxicol, Daejeon, South Korea
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2018年 / 81卷 / 12期
基金
新加坡国家研究基金会;
关键词
FLIGHT MASS-SPECTROMETRY; LIVER; TOXICITY; DYSFUNCTION; BIOMARKER; INJURY; CELLS; BILE;
D O I
10.1080/15287394.2018.1460783
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Amiodarone is a class III anti-arrhythmic benzofuran derivative extensively utilized in treatment of life-threatening ventricular and supraventricular arrhythmias. However, amiodarone also produces adverse side effects including liver injury due to its metabolites rather than parent drug. The purpose of the present study was to identify metabolites of amiodarone in the plasma and urine of rats administered the drug by using an untargeted metabolomics approach. Drug metabolites were profiled by ultra-performance liquid chromatography-linked electrospray ionization quadrupole time-of-flight mass spectrometry (UPLC-ESI-QTOFMS) and results subjected to multivariate data analysis. A total of 49 amiodarone metabolites were identified and their structures were characterized by tandem mass spectrometry. Amiodarone metabolites are presumed to be generated via five major types of metabolic reactions including N-desethylation, hydroxylation, carboxylation (oxo/hydroxylation), de-iodination, and glucuronidation. Data demonstrated that an untargeted metabolomics approach appeared to be a reliable tool for identifying unknown metabolites in a complex biological matrix.
引用
收藏
页码:481 / 492
页数:12
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