Determination and Validation of a Solid-phase Extraction Gas Chromatography-mass Spectrometry for the Quantification of Methadone and Its Principal Metabolite in Human Plasma.

Analytical Chemistry Insights Pub Date : 2015-08-26 eCollection Date: 2015-01-01 DOI:10.4137/ACI.S25554
Fouad Chiadmi, Joël Schlatter
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引用次数: 6

Abstract

This study aimed to develop a solid-phase extraction gas chromatography-selected ion monitoring-mass spectrometry method for the determination of methadone (MDN) and 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) in human plasma. The linear response was obtained over the concentration range from 10 to 2000 ng/mL for MDN and EDDP. The absolute recoveries of MDN and EDDP were 95.9%–98.9% and 94.8%–102.4%, with relative standard deviation (RSD) ranging from 1.8% to 2.7% and 1.8% to 3.9%, respectively. The intra- and interday precisions were found to be less than 5% for both analytes. The limits of detection of MDN and EDDP were 4 and 5 ng/mL, respectively. The presented method was convenient for therapeutic drug monitoring and pharmacokinetic studies in patients on heroin-assisted MDN therapy.

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固相萃取-气相色谱-质谱法定量人血浆中美沙酮及其主要代谢物的测定与验证。
本研究旨在建立固相萃取气相色谱-选择离子监测-质谱法测定人血浆中美沙酮(MDN)和2-乙基-1,5-二甲基-3,3-二苯基吡啶(EDDP)的方法。MDN和EDDP在10 ~ 2000 ng/mL浓度范围内呈线性关系。MDN和EDDP的绝对加样回收率分别为95.9% ~ 98.9%和94.8% ~ 102.4%,相对标准偏差(RSD)分别为1.8% ~ 2.7%和1.8% ~ 3.9%。发现两种分析物的日内和日内精密度均小于5%。MDN和EDDP的检出限分别为4和5 ng/mL。该方法便于海洛因辅助MDN治疗患者的药物监测和药代动力学研究。
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