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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Unexpected peaks in tandem mass spectra due to reaction of product ions with residual water in mass spectrometer collision cells
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Unexpected peaks in tandem mass spectra due to reaction of product ions with residual water in mass spectrometer collision cells

机译:在质谱仪碰撞池中,由于产物离子与残留水的反应,导致串联质谱中出现意外峰

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RATIONALE: Certain product ions in electrospray ionization tandem mass spectrometry are found to react with residual water in the collision cell. This reaction often leads to the formation of ions that cannot be formed directly from the precursor ions, and this complicates the mass spectra and may distort MRM (multiple reaction monitoring) results. METHODS: Various drugs, pesticides, metabolites, and other compounds were dissolved in acetonitrile/water/formic acid and studied by electrospray ionization mass spectrometry to record their MS~2 and MS~n spectra in several mass spectrometers (QqQ, QTOF, IT, and Orbitrap HCD). Certain product ions were found to react with residual water in collision cells. The reaction was confirmed by MS~n studies and the rate of reaction was determined in the IT instrument using zero collision energy and variable activation times. RESULTS: Examples of product ions reactingwithwater include phenyl and certain substituted phenyl cations, benzoyl-type cations formed from protonated folic acid and similar compounds by loss of the glutamate moiety, product ions formed from protonated cyclic siloxanes by loss of methane, product ions formed from organic phosphates, and certain negative ions. The reactions of product ions with residual water varied greatly in their rate constant and in the extent of reaction (due to isomerization). CONCLUSIONS: Various types of product ions react with residual water in mass spectrometer collision cells. As a result, tandem mass spectra may contain unexplained peaks and MRM results may be distorted by the occurrence of such reactions. These often unavoidable reactions must be taken into account when annotating peaks in tandem mass spectra and when interpreting MRM results. Published in 2014. This article is a U.S. Government work and is in the public domain in the USA.
机译:理由:发现电喷雾串联质谱法中的某些产物离子会与碰撞池中的残留水反应。该反应通常导致无法直接由前体离子形成的离子形成,这使质谱复杂化并可能使MRM(多重反应监测)结果失真。方法:将各种药物,农药,代谢物和其他化合物溶解在乙腈/水/甲酸中,并通过电喷雾电离质谱研究,以在数种质谱仪(QqQ,QTOF,IT,和Orbitrap HCD)。发现某些产物离子会与碰撞池中的残留水反应。通过MS-n研究证实了反应,并在IT仪器中使用零碰撞能量和可变激活时间确定了反应速率。结果:与水反应的产物离子的例子包括苯基和某些取代的苯基阳离子,质子化叶酸和类似化合物因失去谷氨酸部分而形成的苯甲酰基型阳离子,质子化环硅氧烷因失去甲烷而形成的产物离子,有机磷酸盐和某些负离子。产物离子与残留水的反应的速率常数和反应程度(由于异构化)差异很大。结论:各种类型的产物离子与质谱仪碰撞池中的残留水反应。结果,串联质谱可能包含无法解释的峰,并且MRM结果可能因此类反应的发生而失真。在注释串联质谱图中的峰时以及解释MRM结果时,必须考虑到这些通常不可避免的反应。 2014年出版。本文是美国政府的工作,在美国属于公共领域。

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