A Combined Desorption Ionization by Charge Exchange (DICE) and Desorption Electrospray Ionization (DESI) Source for Mass Spectrometry

• Published in: Journal of the American Society for Mass Spectrometry 2011, Vol.22 (1), p.173-178
• Main Authors: Chan, Chang-Ching, Bolgar, Mark S., Miller, Scott A., Attygalle, Athula B.
• Format: Article
• Language: English
• Subjects: Acetaminophen - analysis; Acetaminophen - chemistry; Analysis; Analytical Chemistry; Bioinformatics; Biological and medical sciences; Biotechnology; Caffeine - analysis; Caffeine - chemistry; Chemistry; Chemistry and Materials Science; Exact sciences and technology; General pharmacology; Ibuprofen - analysis; Ibuprofen - chemistry; Mass spectrometry; Medical sciences; Organic Chemistry; Pharmaceutical Preparations - analysis; Pharmaceutical Preparations - chemistry; Pharmacology. Drug treatments; Pressure; Proteomics; Reactivity and mechanisms; Research Article; Spectrometry, Mass, Electrospray Ionization - methods
• ISSN: 1044-0305; 1879-1123
• DOI: 10.1007/s13361-010-0001-z

A source that couples the desorption ionization by charge exchange (DICE) and desorption electrospray ionization (DESI) techniques together was demonstrated to broaden the range of compounds that can be analyzed in a single mass spectrometric experiment under ambient conditions. A tee union was used to mix the spray reagents into a partially immiscible blend before this mixture was passed through a conventional electrospray (ES) probe capillary. Using this technique, compounds that are ionized more efficiently by the DICE method and those that are ionized better with the DESI procedure could be analyzed simultaneously. For example, hydroquinone, which is not detected when subjected to DESI-MS in the positive-ion generation mode, or the sodium adduct of guaifenesin, which is not detected when examined by DICE-MS, could both be detected in one experiment when the two techniques were combined. The combined technique was able to generate the molecular ion, proton and metal adduct from the same compound. When coupled to a tandem mass spectrometer, the combined source enabled the generation of product ion spectra from the molecular ion and the [M + H] + or [M + metal] + ions of the same compound without the need to physically change the source from DICE to DESI. The ability to record CID spectra of both the molecular ion and adduct ions in a single mass spectrometric experiment adds a new dimension to the array of mass spectrometric methods available for structural studies.