一种经验证的 LC-MS/MS 方法,用于同时定量血清和尿液中的碘酞酸酯和希普兰,以进行非放射性肾功能评估。

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-09-28 DOI:10.1016/j.jchromb.2024.124329
Abdulfataah A.A. Mohamed , Peter Walland , Jasper Stevens , Marco van Londen , Hiddo J.L. Heerspink , Ron T. Gansevoort , Nico C. van de Merbel
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引用次数: 0

摘要

本研究介绍了一种新型液相色谱-串联质谱法,用于定量检测人体血清和尿液中的肾功能标志物碘酞酸酯和希普兰。该方法基于甲醇沉淀蛋白质,然后稀释血清上清液和尿液上清液。极性分析物在低配体密度反相柱上以 6.5 分钟梯度进行色谱分离;检测采用电喷雾离子化串联质谱正离子模式,以稳定同位素标记的内标物为检测对象。彻底的方法验证结果表明,血清和尿液中的碘他拉马特和希普兰可分别在0.500-30.0 ng/mL和10.0-5000 ng/mL的浓度范围内同时定量,CV值和绝对偏差均不超过10%,且在所有相关基质和溶剂中均具有足够的稳定性。该方法成功地应用于分析同时接受了碘他拉马特和希普兰的多个个体的血清和尿液样本。
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A validated LC-MS/MS method for the simultaneous quantification of iothalamate and hippuran in serum and urine for non-radioactive kidney function assessment
A novel liquid chromatography-tandem mass spectrometry method is described for the quantitative determination of the kidney function markers iothalamate and hippuran in human serum and urine. It is based on protein precipitation with methanol followed by dilution of the supernatant for serum and simple dilution for urine. The polar analytes are chromatographically separated by a 6.5-min gradient on a low-ligand density reversed-phase column; detection is performed by electrospray ionization tandem mass spectrometry in the positive ion mode against stable-isotope labeled internal standards.
The results of a thorough method validation show that iothalamate and hippuran can be simultaneously quantified in the concentration ranges 0.500–30.0 ng/mL and 10.0–5000 ng/mL for serum and urine, respectively, with values for CV and absolute bias not exceeding 10 %, and with sufficient stability in all relevant matrices and solvents. The method was successfully applied for the analysis of serum and urine samples of multiple individuals who received both iothalamate and hippuran.
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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