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HPLC 荧光检测法测定血浆中去甲替林的含量。

Quantification of nortriptyline in plasma by HPLC and fluorescence detection.

机构信息

Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of Valencia, Avda. V. Andrés Estellés, s/n, 46100-Burjassot, Valencia, Spain.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Mar 15;878(9-10):841-4. doi: 10.1016/j.jchromb.2010.01.033. Epub 2010 Jan 29.

Abstract

A simple, sensitive and specific high-performance liquid chromatography method has been developed for the determination of nortriptyline (NT) in plasma samples. The assay involved derivatization with 9H-fluoren-9-ylmethyl chloroformate (Fmoc-Cl) and isocratic reversed-phase (C(18)) chromatography with fluorescence detection. The developed method required only 100 microl of plasma sample, deproteinized and derivatized in one step. Calibration curves were lineal over the concentration range of 5-5000 ng/ml. The derivatization reaction was performed at room temperature in 20 min and the obtained NT derivative was stable for at least 48 h at room temperature. The within-day and between-day relative standard deviation was below 8%. The limit of detection (LOD) was 2 ng/ml, and the lower limit of quantification (LLOQ) was established at 10 ng/ml. The method was applied on plasma collected from rats, at different time intervals, after intravenous administration of 0.5 mg of NT.

摘要

已经建立了一种简单、灵敏、特异的高效液相色谱法,用于测定血浆样品中的去甲替林(NT)。该方法涉及用 9H-芴-9-基甲基氯甲酸酯(Fmoc-Cl)衍生化和等度反相(C(18))色谱法,荧光检测。该方法仅需要 100 微升血浆样品,可在一步中进行蛋白沉淀和衍生化。校准曲线在 5-5000ng/ml 浓度范围内呈线性。衍生化反应在室温下 20 分钟内完成,获得的 NT 衍生物在室温下至少稳定 48 小时。日内和日间相对标准偏差低于 8%。检测限(LOD)为 2ng/ml,定量下限(LLOQ)定为 10ng/ml。该方法应用于大鼠静脉注射 0.5mg NT 后不同时间间隔采集的血浆。

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