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采用选择离子流动管质谱法对潮湿空气中和呼出气体中的二氧化碳进行定量分析。

The quantification of carbon dioxide in humid air and exhaled breath by selected ion flow tube mass spectrometry.

作者信息

Smith David, Pysanenko Andriy, Spanel Patrik

机构信息

Institute for Science and Technology in Medicine, School of Medicine, Keele University, Thornburrow Drive, Hartshill, Stoke-on-Trent ST4 7QB, UK.

出版信息

Rapid Commun Mass Spectrom. 2009 May;23(10):1419-25. doi: 10.1002/rcm.4016.

Abstract

The reactions of carbon dioxide, CO(2), with the precursor ions used for selected ion flow tube mass spectrometry, SIFT-MS, analyses, viz. H(3)O(+), NO(+) and O(2) (+), are so slow that the presence of CO(2) in exhaled breath has, until recently, not had to be accounted for in SIFT-MS analyses of breath. This has, however, to be accounted for in the analysis of acetaldehyde in breath, because an overlap occurs of the monohydrate of protonated acetaldehyde and the weakly bound adduct ion, H(3)O(+)CO(2), formed by the slow association reaction of the precursor ion H(3)O(+) with CO(2) molecules. The understanding of the kinetics of formation and the loss rates of the relevant ions gained from experimentation using the new generation of more sensitive SIFT-MS instruments now allows accurate quantification of CO(2) in breath using the level of the H(3)O(+)CO(2) adduct ion. However, this is complicated by the rapid reaction of H(3)O(+)CO(2) with water vapour molecules, H(2)O, that are in abundance in exhaled breath. Thus, a study has been carried out of the formation of this adduct ion by the slow three-body association reaction of H(3)O(+) with CO(2) and its rapid loss in the two-body reaction with H(2)O molecules. It is seen that the signal level of the H(3)O(+)CO(2) adduct ion is sensitively dependent on the humidity (H(2)O concentration) of the sample to be analysed and a functional form of this dependence has been obtained. This has resulted in an appropriate extension of the SIFT-MS software and kinetics library that allows accurate measurement of CO(2) levels in air samples, ranging from very low percentage levels (0.03% typical of tropospheric air) to the 6% level that is about the upper limit in exhaled breath. Thus, the level of CO(2) can be traced through single time exhalation cycles along with that of water vapour, also close to the 6% level, and of trace gas metabolites that are present at only a few parts-per-billion. This has added a further dimension to the analysis of major and trace compounds in breath using SIFT-MS.

摘要

二氧化碳(CO₂)与用于选择离子流管质谱法(SIFT-MS)分析的前体离子,即水合氢离子(H₃O⁺)、一氧化氮离子(NO⁺)和氧离子(O₂⁺)的反应非常缓慢,以至于直到最近,呼出气体中CO₂的存在在SIFT-MS呼吸分析中都无需考虑。然而,在呼吸中乙醛的分析中必须考虑这一点,因为质子化乙醛的一水合物与前体离子H₃O⁺与CO₂分子缓慢缔合反应形成的弱结合加合离子H₃O⁺CO₂会发生重叠。使用新一代更灵敏的SIFT-MS仪器进行实验,对相关离子的形成动力学和损失率的了解,现在使得能够利用H₃O⁺CO₂加合离子的水平准确量化呼出气体中的CO₂。然而,这因H₃O⁺CO₂与呼出气体中大量存在的水蒸气分子(H₂O)的快速反应而变得复杂。因此,已经对H₃O⁺与CO₂的缓慢三体缔合反应形成该加合离子及其与H₂O分子的二体反应中的快速损失进行了研究。可以看出,H₃O⁺CO₂加合离子的信号水平敏感地依赖于待分析样品的湿度(H₂O浓度),并且已经获得了这种依赖性的函数形式。这导致了SIFT-MS软件和动力学库的适当扩展,从而能够准确测量空气样品中的CO₂水平,范围从非常低的百分比水平(对流层空气中典型的0.03%)到呼出气体中约为上限的6%水平。因此,CO₂的水平可以与水蒸气(也接近6%水平)以及仅以十亿分之几存在的痕量气体代谢物的水平一起,通过单次呼气循环进行追踪。这为使用SIFT-MS分析呼吸中的主要和痕量化合物增加了一个新的维度。

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