Accelerated High-Resolution Differential Ion Mobility Separations Using Hydrogen

被引:41
|
作者
Shvartsburg, Alexandre A. [1 ]
Smith, Richard D. [1 ]
机构
[1] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99352 USA
关键词
DISSOCIATION MASS-SPECTROMETRY; DRIFT-GAS POLARIZABILITY; PEPTIDE ISOMERS; FAIMS; SENSITIVITY; MS;
D O I
10.1021/ac202386w
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The resolving power of differential ion mobility spectrometry (FAIMS) was dramatically increased recently by carrier gases comprising up to 75% He or various vapors, enabling many new applications. However, the need for resolution of complex mixtures is virtually open-ended and many topical analyses demand yet finer separations. Also, the resolving power gains are often at the expense of speed, in particular making high-resolution FAIMS poorly compatible with online liquid-phase separations. Here, we report FAIMS employing hydrogen, specifically in mixtures with N-2 containing up to 90% H-2. Such compositions raise the mobilities of all ions and thus the resolving power beyond that previously feasible, while avoiding the electrical breakdown inevitable in He-rich mixtures, The increases in resolving power and ensuing peak resolution are especially significant at H-2 fractions above similar to 50%. Higher resolution can be exchanged for acceleration of the analyses by up to similar to 4 times. For more mobile species such as multiply charged peptides, this exchange is presently forced by the constraints of existing PALMS devices, but future designs optimized for H-2 should consistently improve resolution for all analytes.
引用
收藏
页码:9159 / 9166
页数:8
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