Some new features of Direct Analysis in Real Time mass spectrometry utilizing the desorption at an angle option

被引:28
作者
Chernetsova, Elena S. [1 ]
Revelsky, Alexander I. [2 ]
Morlock, Gertrud E. [1 ]
机构
[1] Univ Hohenheim, Inst Food Chem, D-70599 Stuttgart, Germany
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia
关键词
FLUORESCENCE DETECTION; PLANAR CHROMATOGRAPHY; RAPID IDENTIFICATION; PACKED SORBENT; QUANTIFICATION; MICROEXTRACTION; QUANTITATION; BIOANALYSIS; IONIZATION; ADDITIVES;
D O I
10.1002/rcm.5112
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
The present study is a first step towards the unexplored capabilities of Direct Analysis in Real Time (DART) mass spectrometry (MS) arising from the possibility of the desorption at an angle: scanning analysis of surfaces, including the coupling of thin-layer chromatography (TLC) with DART-MS, and a more sensitive analysis due to the preliminary concentration of analytes dissolved in large volumes of liquids on glass surfaces. In order to select the most favorable conditions for DART-MS analysis, proper positioning of samples is important. Therefore, a simple and cheap technique for the visualization of the impact region of the DART gas stream onto a substrate was developed. A filter paper or TLC plate, previously loaded with the analyte, was immersed in a derivatization solution. On this substrate, owing to the impact of the hot DART gas, reaction of the analyte to a colored product occurred. An improved capability of detection of DART-MS for the analysis of liquids was demonstrated by applying large volumes of model solutions of coumaphos into small glass vessels and drying these solutions prior to DART-MS analysis under ambient conditions. This allowed the introduction of, by up to more than two orders of magnitude, increased quantities of analyte compared with the conventional DART-MS analysis of liquids. Through this improved detectability, the capabilities of DART-MS in trace analysis could be strengthened. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:2275 / 2282
页数:8
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