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Automated Combustion Accelerator Mass Spectrometry for the Analysis of Biomedical Samples in the Low Attomole Range

机译:自动燃烧加速器质谱分析低原子范围内的生物医学样品

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The increasing role of accelerator mass spectrometry (AMS) in biomedical research necessitates modernization of the traditional sample handling process. AMS was originally developed and used for carbon dating, therefore focusing on a very high precision but with a comparably low sample throughput. Here, we describe the combination of automated sample combustion with an elemental analyzer (EA) online coupled to an AMS via a dedicated interface. This setup allows direct radiocarbon measurements for over 70 samples daily by AMS. No sample processing is required apart from the pipetting of the sample into a tin foil cup, which is placed in the carousel of the EA. In our system, up to 200 AMS analyses are performed automatically without the need for manual interventions. We present results on the direct total ~(14)C count measurements in <2 μL human plasma samples. The method shows linearity over a range of 0.65-821 mBq/mL, with a lower limit of quantification of 0.65 mBq/mL (corresponding to 0.67 amol for acetaminophen). At these extremely low levels of activity, it becomes important to quantify plasma specific carbon percentages. This carbon percentage is automatically generated upon combustion of a sample on the EA. Apparent advantages of the present approach include complete omission of sample preparation (reduced hands-on time) and fully automated sample analysis. These improvements clearly stimulate the standard incorporation of microtracer research in the drug development process. In combination with the particularly low sample volumes required and extreme sensitivity, AMS strongly improves its position as a bioanalysis method.
机译:加速器质谱(AMS)在生物医学研究中的作用日益增强,因此有必要对传统的样品处理流程进行现代化改造。 AMS最初被开发并用于碳定年,因此侧重于极高的精度,但样品通量却相对较低。在这里,我们描述了自动样品燃烧与通过专用接口在线耦合到AMS的元素分析仪(EA)的组合。该设置允许通过AMS每天直接测量70多个样品的放射性碳。除了将样品移液到放置在EA圆盘传送带中的锡箔杯中外,无需进行任何样品处理。在我们的系统中,自动进行多达200个AMS分析,而无需人工干预。我们在<2μL人血浆样品中直接对〜(14)C计数的直接测量结果。该方法在0.65-821 mBq / mL的范围内显示线性,定量下限为0.65 mBq / mL(对乙酰氨基酚的定量为0.67 amol)。在这些极低的活性水平下,量化血浆比碳百分比变得很重要。该碳百分比是在EA上燃烧样品时自动生成的。本方法的明显优势包括完全省去了样品准备工作(减少了动手时间)和全自动样品分析。这些改进显然刺激了微量示踪剂研究在药物开发过程中的标准纳入。结合所需的极低样品量和极高的灵敏度,AMS极大地提高了其作为生物分析方法的地位。

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