Desorption Ionization by Charge Exchange (DICE) for Sample Analysis under Ambient Conditions by Mass Spectrometry

被引:33
作者
Chan, Chang-Ching [1 ,2 ]
Bolgar, Mark S. [2 ]
Miller, Scott A. [2 ]
Attygalle, Athula B. [1 ]
机构
[1] Stevens Inst Technol, Dept Chem Chem Biol & Biomed Engn, Ctr Mass Spectrometry, Hoboken, NJ 07030 USA
[2] Bristol Myers Squibb Analyt Res & Dev, New Brunswick, NJ USA
关键词
ATMOSPHERIC-PRESSURE PHOTOIONIZATION; ELECTROSPRAY-IONIZATION; ION-SOURCE; HYDROCARBONS; EXPLOSIVES; MECHANISMS; DESI;
D O I
10.1016/j.jasms.2010.04.020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An ambient pressure ionization technique for mass spectrometric analysis of substances present on solid surfaces was developed. A nebulized spray containing molecular ions of a solvent such as toluene can be generated by passing the solvent through a stainless steel capillary held at a high voltage. When the stream of charged droplets produced in this way is directed onto a solid surface, the analytes present on the surface are desorbed and ionized by a charge exchange process. This technique was shown to desorb and generate positively charged molecular ions from compounds that are not readily ionized by some other ambient methods, under positive-ion generation mode. For example, intense signals representing radical cations of 1,4-hydroquinone, limonene, thymol, and several other compounds were observed when the analytes were deposited on a metal surface and exposed to a toluene spray nebulized from the metal capillary maintained at a potential of about +5 kV. In contrast, when the same samples were exposed to a spray of water/methanol/formic acid under customary DESI-like (positive-ion mode) conditions, no peaks representing the analytes were observed. (J Am Soc Mass Spectrom 2010, 21, 1554-1560) (C) 2010 American Society for Mass Spectrometry
引用
收藏
页码:1554 / 1560
页数:7
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