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采用液相色谱/串联质谱法对线粒体靶向抗氧化剂米托醌在大鼠体内的定量及代谢进行研究。

Quantitation and metabolism of mitoquinone, a mitochondria-targeted antioxidant, in rat by liquid chromatography/tandem mass spectrometry.

作者信息

Li Yan, Zhang Hu, Fawcett J Paul, Tucker Ian G

机构信息

School of Pharmacy, University of Otago, Dunedin, P.O. Box 913, New Zealand.

出版信息

Rapid Commun Mass Spectrom. 2007;21(13):1958-64. doi: 10.1002/rcm.3048.

DOI:10.1002/rcm.3048
PMID:17534852
Abstract

Mitoquinone (MitoQ10 mesylate) is a mitochondria-targeted antioxidant undergoing development for the treatment of neurodegenerative diseases. The aim of this study was to develop and validate an assay based on liquid chromatography/tandem mass spectrometry (LC/MS/MS) to determine mitoquinone and to detect and identify the metabolites of MitoQ10 in rat plasma after an oral dose. After a simple protein precipitation step, plasma samples were analyzed by reversed-phase liquid chromatography using gradient elution with acetonitrile/water/formic acid. Electrospray ionization in the positive ion mode with multiple reaction monitoring (MRM) was used to analyze mitoquinone employing the deuterated compound (d3-MitoQ10 mesylate) as internal standard. The calibration curve for mitoquinone was linear over the concentration range 0.5-250 ng/mL with a correlation coefficient>0.995. The method was sensitive (limit of quantitation 0.5 ng/mL) and had acceptable accuracy (relative error<8.7%) and precision (intra- and inter-day coefficient of variation<12.4%). Recoveries of mitoquinone at concentrations of 1.5, 20 and 200 ng/mL were in the range 87-114%. The method was successfully applied to a pharmacokinetic study in rat after a single oral dose in which four metabolites of MitoQ10 were tentatively identified as hydroxylated MitoQ10, desmethyl MitoQ10 and the glucuronide and sulfate conjugates of the quinol form of MitoQ10.

摘要

米托醌(甲磺酸盐米托醌,MitoQ10)是一种靶向线粒体的抗氧化剂,正处于治疗神经退行性疾病的研发阶段。本研究的目的是开发并验证一种基于液相色谱/串联质谱(LC/MS/MS)的分析方法,用于测定米托醌,并检测和鉴定大鼠口服给药后血浆中米托醌的代谢产物。经过简单的蛋白沉淀步骤后,血浆样品采用乙腈/水/甲酸梯度洗脱的反相液相色谱进行分析。以氘代化合物(d3-甲磺酸盐米托醌)作为内标,采用正离子模式下的电喷雾电离和多反应监测(MRM)来分析米托醌。米托醌的校准曲线在浓度范围为0.5 - 250 ng/mL时呈线性,相关系数>0.995。该方法灵敏(定量限为0.5 ng/mL),具有可接受的准确度(相对误差<8.7%)和精密度(日内和日间变异系数<12.4%)。米托醌在浓度为1.5、20和200 ng/mL时的回收率在87 - 114%范围内。该方法成功应用于大鼠单次口服给药后的药代动力学研究,其中米托醌的四种代谢产物初步鉴定为羟基化米托醌、去甲基米托醌以及米托醌喹啉形式的葡萄糖醛酸和硫酸盐共轭物。

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