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Determination of Tiopronin in Human Plasma by SPE then Reversed-Phase HPLC–UV

机译:SPE-反相HPLC-UV法测定人血浆中硫普罗宁

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摘要

An accurate, simple and sensitive method based on reversed-phase high-performance liquid chromatography with UV detection has been developed for determination of tiopronin (TP) in human plasma. TP in plasma was reacted with p-bromophenacyl bromide (p-BPB) to give the TP-p-BPB adduct and this derivative was then extracted from the plasma on a silica gel cartridge. Potential interfering compounds were removed by washing with water, and the TP-p-BPB adduct was then eluted with acetonitrile. The organic phase obtained was evaporated to complete dryness under a stream of nitrogen. The residue was dissolved in acetonitrile and this solution was injected on to a reversed-phase ODS HPLC column. The mobile phase was usually the ternary mixture acetonitrile–water–trifluoroacetic acid, 40:59.88:0.12 (v/v). The retention times of TP-p-BPB and the internal standard adduct were 14.4 and 17.9 min, respectively. No interfering peaks were encountered in several blank plasma samples examined. The limit of detection for TP was 12 ng mL−1. Extraction recovery exceeded 70%. The calibration plot for the TP derivative was linear in the range 40−4000 ng mL−1, regression coefficient 0.9989, and the coefficient of the variation of the points of the calibration plot was below 10%. The method was validated appropriately and successfully applied to the determination of TP in human plasma.
机译:已经开发了一种基于反相高效液相色谱和紫外检测的准确,简单,灵敏的方法,用于测定人血浆中的硫普罗宁(TP)。使血浆中的TP与对溴苯甲酰溴(p-BPB)反应,得到TP-p-BPB加合物,然后在硅胶柱上从血浆中提取该衍生物。用水洗涤除去潜在的干扰化合物,然后用乙腈洗脱TP-p-BPB加合物。在氮气流下将获得的有机相蒸发至完全干燥。将残留物溶解在乙腈中,并将该溶液注入反相ODS HPLC柱中。流动相通常是乙腈-水-三氟乙酸的三元混合物,40:59.88:0.12(v / v)。 TP-p-BPB和内标加合物的保留时间分别为14.4和17.9分钟。在检测的几个空白血浆样品中未遇到干扰峰。 TP的检出限为12 ng mL-1 。提取回收率超过70%。 TP衍生物的校正图在40-4000 ng mL-1 范围内呈线性,回归系数为0.9989,校正点的变化系数低于10%。该方法经过适当验证,已成功应用于人血浆中总磷的测定。

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