首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Liquid chromatography method for determination of bivalirudin in human plasma and urine using automated ortho-phthalaldehyde derivatization and fluorescence detection
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Liquid chromatography method for determination of bivalirudin in human plasma and urine using automated ortho-phthalaldehyde derivatization and fluorescence detection

机译:全自动邻苯二甲醛衍生化和荧光检测液相色谱法测定人血浆和尿液中比伐卢定的方法

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摘要

A high-performance liquid chromatographic (HPLC) method was developed using solid-phase extraction, o-phthalaldehyde (OPA) derivatization and fluorescence detection for the determination of the direct thrombin inhibitor bivalirudin in human plasma and urine. The use of this assay will facilitate the study of the pharmacodynamics of bivalirudin in studies of special patient populations. A C_(18) bioanalytical column at a flow rate of 1 ml/min with an aqueous trifluoroacetic acid (0.1% TFA in deionized water, pH 2.2, v/v) mobile phase and methanol gradient was used. The assay demonstrated linearity from 3 to 20 μg/ml bivalirudin in plasma, with a detection limit of 1 g/ml. The method was utilized in a study evaluating the pharmacokinetic and pharmacodynamic effects of bivalirudin in patients undergoing percutaneous coronary interventions (PCIs).
机译:通过固相萃取,邻苯二甲醛(OPA)衍生化和荧光检测,开发了一种高效液相色谱(HPLC)方法,用于测定人血浆和尿液中的直接凝血酶抑制剂比伐卢定。该测定法的使用将有助于在特殊患者人群中研究比伐卢定的药效学。使用C_(18)生物分析柱,流速为1 ml / min,具有三氟乙酸水溶液(去离子水中的0.1%TFA,pH 2.2,v / v)流动相和甲醇梯度。该测定法显示血浆中比伐卢定的线性为3至20μg/ ml,检出限为1 g / ml。该方法用于评估比伐卢定对经皮冠状动脉介入治疗(PCIs)患者的药代动力学和药效学作用的研究。

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