Transmission Geometry Laserspray Ionization Vacuum Using an Atmospheric Pressure Inlet
Author(s) -
Corinne A. Lutomski,
Tarick J. ElBaba,
Ellen D. Inutan,
Cory D. Manly,
James WagerMiller,
Ken Mackie,
Sarah Trimpin
Publication year - 2014
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac501788p
Subject(s) - chemistry , atmospheric pressure , analytical chemistry (journal) , mass spectrometry , ionization , inlet , ion , laser ablation , analyte , vacuum chamber , laser , ion source , matrix (chemical analysis) , ultra high vacuum , chromatography , optics , nanotechnology , mechanical engineering , oceanography , physics , materials science , organic chemistry , engineering , composite material , geology
This represents the first report of laserspray ionization vacuum (LSIV) with operation directly from atmospheric pressure for use in mass spectrometry. Two different types of electrospray ionization source inlets were converted to LSIV sources by equipping the entrance of the atmospheric pressure inlet aperture with a customized cone that is sealed with a removable glass plate holding the matrix/analyte sample. A laser aligned in transmission geometry (at 180° relative to the inlet) ablates the matrix/analyte sample deposited on the vacuum side of the glass slide. Laser ablation from vacuum requires lower inlet temperature relative to laser ablation at atmospheric pressure. However, higher inlet temperature is required for high-mass analytes, for example, α-chymotrypsinogen (25.6 kDa). Labile compounds such as gangliosides and cardiolipins are detected in the negative ion mode directly from mouse brain tissue as intact doubly deprotonated ions. Multiple charging enhances the ion mobility spectrometry separation of ions derived from complex tissue samples.
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