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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >A rapid, sensitive method for quantitative analysis of underivatized amino acids by liquid chromatography-tandem mass spectrometry (LC-MS/MS)
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A rapid, sensitive method for quantitative analysis of underivatized amino acids by liquid chromatography-tandem mass spectrometry (LC-MS/MS)

机译:快速灵敏的液相色谱-串联质谱(LC-MS / MS)定量分析未衍生氨基酸的方法

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摘要

The quantitation of free amino acids from physiologic samples is essential for diagnosing and monitoring patients with inherited metabolic disorders. Current methods are hindered by long preparative and/or analysis times, expensive reagents, and often suboptimal performance characteristics. To overcome these challenges, a improved method for amino acid analysis using liquid chromatography-tandem mass spectrometry (LC-MS/MS) has been developed and validated. Samples were deproteinized with sul- fosalicylic acid and supernatants diluted with tridecafluoroheptanoic acid. Chromatographic separation of amino acids occurred using two columns, with conditions favoring resolution of isobaric compounds and minimizing ion suppression. Eluted compounds were detected by selective reaction monitoring, and quantitated by relating peak areas of amino acids to externally run standards. Validation studies evaluated linearity, within- and between-run imprecision, lower limits of detection and quantification for 33 amino acids, and correlation with the Biochrom 30 Amino Acid Analyzer. Total run time including re-equilibration was 15 min per sample. Within-run precision averaged 2.8% for all compounds, with an average linear correlation coefficient of 0.995. The majority of compounds were reliably quantitated at ≤0.1 μM. Between-run precision averaged 4.0%. Results showed excellent correlation with the Biochrom 30 amino acid analyzer with an average overall correlation of 0.908. We conclude that our method is extremely sensitive, specific and reproducible and represents an improvement over other currently available technologies.
机译:生理样品中游离氨基酸的定量对于诊断和监测遗传性代谢异常的患者至关重要。当前的方法由于制备和/或分析时间长,试剂昂贵以及性能通常不理想而受到阻碍。为了克服这些挑战,已经开发并验证了一种使用液相色谱-串联质谱(LC-MS / MS)进行氨基酸分析的改进方法。样品用磺基水杨酸脱蛋白,上清液用十三氟庚酸稀释。使用两根色谱柱进行氨基酸的色谱分离,其条件有利于等压化合物的分离并最大程度地减少离子抑制。通过选择性反应监测来检测洗脱的化合物,并通过将氨基酸的峰面积与外部运行的标准样品关联来进行定量。验证研究评估了线性,运行中和运行中的不准确性,33种氨基酸的检测和定量下限以及与Biochrom 30氨基酸分析仪的相关性。每个样品的总运行时间(包括重新平衡)为15分钟。所有化合物的批内精密度平均为2.8%,平均线性相关系数为0.995。可靠地定量了≤0.1μM的大多数化合物。批间精度平均为4.0%。结果显示与Biochrom 30氨基酸分析仪具有极好的相关性,平均总体相关性为0.908。我们得出的结论是,我们的方法非常灵敏,特异且可重现,是对当前其他可用技术的改进。

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