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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Liquid chromatographic quantitation of the lactone and the total of lactone and carboxylate forms of 9-nitrocamptothecin in human plasma
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Liquid chromatographic quantitation of the lactone and the total of lactone and carboxylate forms of 9-nitrocamptothecin in human plasma

机译:液相色谱法测定人血浆中内酯以及9-硝基喜树碱的内酯和羧酸盐形式的总量

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Simple and sensitive high-performance liquid chromatography (HPLC) assays were developed and validated for the quantitation of the investigational anticancer drug 9-nitrocamptothecin (9-NC) as the lactone form and as the total of the lactone(l) and carboxylate(II) forms in human plasma. For the assay of lactone form (9NC-lac), the analytical method involved a protein precipitation step with adding a mixture of cold acetonitril-chloroform (5:1 (v/v), -20 degrees C) to plasma sample that stabilized the pH-dependent conversion of I to II. After evaporation under gentle stream of nitrogen gas (40 degrees C) the dry extract was dissolved in mobile phase (pH 5.5). For determination of the total of the lactone and carboxylate forms of the drug (9NC-tot), plasma samples were deproteinated with cold acetonitril (-20 degrees C) acidified with perchloric acid (5%), which resulted in the conversion of the carboxylate into the lactone form. After centrifugation the upper solvent was evaporated (nitrogen, 40 degrees C) and the dry extract was dissolved in mobile phase (pH 3.5). All separations were performed on a RP-C-8 column, using a mixture of acetonitril-water as eluent (pH 3.5 for total form and pH 5.5 for lactone form) and UV detection. The presented assay was linear over a concentration range of 25-1500 ng/ml with lower limit of quantitation of 25 ng/ml for both 9NC-tot and 9NC-lac. Within-run and between-run precision was always less than 7.5% in the concentration range of interest. The reported assay method showed good characteristics of linearity, sensitivity, selectivity and precision allowing applying in pharmacokinetic studies. (c) 2005 Elsevier B.V. All rights reserved.
机译:开发并验证了简单灵敏的高效液相色谱(HPLC)测定法,用于定量研究的抗癌药物9-硝基喜树碱(9-​​NC)的内酯形式以及内酯(l)和羧酸盐(II)的总量)在人体血浆中形成。对于内酯形式(9NC-lac)的分析,分析方法涉及蛋白质沉淀步骤,向血浆样品中加入冷乙腈-氯仿(5:1(v / v),-20摄氏度)的混合物以稳定内标。 I至II的pH依赖性转化。在温和的氮气流(40摄氏度)下蒸发后,干提取物溶解在流动相(pH 5.5)中。为了确定药物的内酯和羧酸盐形式的总和(9NC-tot),血浆样品用冷的乙腈(-20摄氏度)用高氯酸(5%)酸化去蛋白,从而导致羧酸盐的转化变成内酯的形式离心后,蒸发上层溶剂(氮气,40摄氏度),将干燥的萃取液溶于流动相(pH 3.5)中。所有分离均在RP-C-8色谱柱上进行,使用乙腈-水的混合物作为洗脱液(总形式的pH为3.5,内酯形式的pH为5.5)和UV检测。提出的测定在25-1500 ng / ml的浓度范围内是线性的,对于9NC-tot和9NC-lac的定量下限均为25 ng / ml。在所关注的浓度范围内,批内和批间精度始终小于7.5%。报告的测定方法显示出良好的线性,灵敏度,选择性和精密度特征,可用于药代动力学研究。 (c)2005 Elsevier B.V.保留所有权利。

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