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Desorption/ionization mass spectrometry on nanocrystalline titania sol-gel-deposited films

dc.citation.epage1964en_US
dc.citation.issue17en_US
dc.citation.spage1956en_US
dc.citation.volume18en_US
dc.citation.woscount64
dc.contributor.authorChen, CTen_US
dc.contributor.authorChen, YCen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:39:51Z
dc.date.available2014-12-08T15:39:51Z
dc.date.issued2004en_US
dc.description.abstractThis paper describes a matrix-free method for performing desorption/ionization directly from mesoporous nanocrystalline titanic sol-gel thin films, which have good absorption capacity in the ultraviolet (UV) range and can act as assisting materials during UV matrix-assisted laser desorption/ionization mass spectrometric (MALDI-MS) analysis. A high concentration of citrate buffer was added into this system to provide the proton source and to reduce the presence of alkali cation adducts of the analytes. The analyte signals appear uniformly over the whole sample deposition area. Protonated molecules (MH+ ions) of analytes dominate the titania MALDI mass spectra. Surfactants, peptides, tryptic digest products, and small proteins with molecular weights below ca. 24 000 Da, are observed in the titania MALDI mass spectra. Detection limits for insulin are as low as ca. 2 fmol with mass resolution of ca. 660. Copyright (C) 2004 John Wiley Sons, Ltd.en_US
dc.identifier.doi10.1002/rcm.1572en_US
dc.identifier.issn0951-4198en_US
dc.identifier.journalRAPID COMMUNICATIONS IN MASS SPECTROMETRYen_US
dc.identifier.urihttp://dx.doi.org/10.1002/rcm.1572en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/27232
dc.identifier.wosnumberWOS:000223410300012
dc.language.isoen_USen_US
dc.titleDesorption/ionization mass spectrometry on nanocrystalline titania sol-gel-deposited filmsen_US
dc.typeArticleen_US

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