大气固体分析探针-质谱法的定量性能评估

IF 1.7 3区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Alisha Henderson, Stephanie Rankin-Turner, James C. Reynolds, Matthew A. Turner, Ashley Sage, David Douce, Mario Thevis, Liam M. Heaney
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引用次数: 0

摘要

大气固体分析探针质谱法(ASAP-MS)是一种成熟的环境电离技术,可以直接快速分析样品而无需色谱分离。因此,通常受益于环境电离方法的应用可以提高样品吞吐量,从而提高原位测试的潜力。以前的报告对asp - ms提供可靠定量数据的能力的观点进行了对比。至关重要的是,目前还缺乏深入研究asp - ms定量能力的数据。本文采用概念验证的单一分析物(咖啡因)方法,进行了一系列实验来评估asa - ms的定量性能。分析的精密度、准确度、线性度和灵敏度使用了许多变量,包括样品沉积方法(即直接将探针放入样品中或将样品移液到探针上)和沉积体积,以及一系列不同的内标准方法的存在。结果获得的数据表明,使用正位移移液器和同位素标记(结构匹配)内标提供了定量可靠性的最佳方法,尽管其水平通常低于传统色谱定量分析的标准。研究在50-5000 ng/mL的浓度范围内进行。虽然大多数方法在全范围内都能观察到可测量的反应,但在浓度低于1000 ng/mL时,发现灵敏度存在局限性,定量性能统计数据也有所下降。结论本实验首次对以咖啡因为例分析物的asa - ms的定量性能进行了全面的研究。这些数据提供了对目前使用asp - ms进行定量分析的优势和局限性的见解,并旨在提供实用的建议,以优化使用该技术的定量方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Assessing the Quantitative Performance of Atmospheric Solids Analysis Probe-Mass Spectrometry

Assessing the Quantitative Performance of Atmospheric Solids Analysis Probe-Mass Spectrometry

Assessing the Quantitative Performance of Atmospheric Solids Analysis Probe-Mass Spectrometry

Assessing the Quantitative Performance of Atmospheric Solids Analysis Probe-Mass Spectrometry

Assessing the Quantitative Performance of Atmospheric Solids Analysis Probe-Mass Spectrometry

Rationale

Atmospheric solids analysis probe-mass spectrometry (ASAP-MS) is an established ambient ionisation technique that allows for the direct and rapid analysis of samples without chromatographic separation. Consequently, applications that typically benefit from ambient ionisation approaches can achieve improved sample throughput and thus improved potential for in situ testing. Previous reports have contrasted in viewpoints on the ability for ASAP-MS to provide reliable quantitative data. Critically, in-depth data exploring the quantitative capabilities of ASAP-MS are currently lacking.

Methods

Here, a series of experiments were performed to assess the quantitative performance of ASAP-MS using a proof-of-concept single analyte (caffeine) approach. Analytical precision, accuracy, linearity and sensitivity were investigated using numerous variables, including sample deposition method (i.e., directly placing the probe into the sample vs. pipetting the sample onto the probe) and deposition volume, as well as the presence of a series of different internal standard approaches.

Results

The data acquired demonstrated that the use of a positive displacement pipette and an isotopically labelled (structure-matched) internal standard provided an optimal approach for quantitative reliability, albeit at levels often below the standards set for traditional chromatography-based quantitative assays. The investigations were performed across a concentration range of 50–5000 ng/mL. Whereas measurable responses were seen across the full range in most approaches, limitations in sensitivity were identified and reduced quantitative performance statistics were noted at concentrations below 1000 ng/mL.

Conclusions

These experiments demonstrate, for the first time, a comprehensive investigation into the quantitative performance of ASAP-MS using caffeine as the example analyte. These data offer insight into the current strengths and limitations of quantitative analyses using ASAP-MS and aim to provide practical recommendations to optimise quantitative approaches using this technique.

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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
219
审稿时长
2.6 months
期刊介绍: Rapid Communications in Mass Spectrometry is a journal whose aim is the rapid publication of original research results and ideas on all aspects of the science of gas-phase ions; it covers all the associated scientific disciplines. There is no formal limit on paper length ("rapid" is not synonymous with "brief"), but papers should be of a length that is commensurate with the importance and complexity of the results being reported. Contributions may be theoretical or practical in nature; they may deal with methods, techniques and applications, or with the interpretation of results; they may cover any area in science that depends directly on measurements made upon gaseous ions or that is associated with such measurements.
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