ArticleAnalytical chemistry2024
Laser Printer Printed Ion Sources for Ambient Ionization Mass Spectrometric Analysis of Volatiles and Semivolatiles.
Article in Analytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Advancements in Ambient Ionisation Mass Spectrometry in 2024: An Annual Review.Analytical science advances · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this study, we demonstrated a facile method to fabricate ion sources using a laser printer for ambient ionization mass spectrometry (MS). Toner spots printed by a printer can readily facilitate ionizing volatile and semivolatile compounds derived from solid or liquid samples for MS analysis. The experimental arrangement involved positioning the toner-printed paper near the inlet of a mass spectrometer, which was subjected to a high electric potential (e.g., -6 kV). Volatile or semivolatile compounds deriving from the sample positioned below the metal inlet of the mass spectrometer were promptly ionized upon activating the mass spectrometer. No direct electrical connection or voltage application was required on the paper substrate. An electric field was established between the toner spot on the paper and the inlet applied with a high voltage to induce the dielectric breakdown of the surrounding air and water molecules. Consequently, ionic species, including electrons and cationic radicals, were generated. Subsequent ion-molecule reactions facilitated the production of protons for ionizing analytes present in the gas phase proximal to the inlet of the mass spectrometer. Deprotonated analytes were detected in the resultant mass spectra when employing the method in negative ion mode. This methodology presents a straightforward approach for analyzing analytes in the gas phase under ambient conditions utilizing an exceptionally uncomplicated experimental setup. In addition, the developed method can be used to detect trace 2,4-dinitrophenol, an explosive, with a limit of detection as low as ∼30 pg.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.