ArticleAnalytical and bioanalytical chemistry2026
Improving detection of low-abundant pharmaceuticals and neurotransmitters via quadrupole isolation in MALDI mass spectrometry imaging.
Article in Analytical and bioanalytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI) is a powerful tool for mapping the spatial distribution of pharmaceuticals and metabolites in tissue. However, its effectiveness in the low-mass range (< 400 m/z) is impacted by matrix interference and ion suppression, reducing signal-to-noise (S/N) ratios. To address this challenge, we assessed a targeted quadrupole isolation strategy using a MALDI q-TOF mass spectrometer. This approach selectively isolates narrow windows around individual analytes m/z to reduce background noise and enhance S/N, therefore generating a smaller selective ion packet to the TOF analyzer. We applied this method to detect acetaminophen, paracetamol sulfate, caffeine, paraxanthine, as well as dopamine and its metabolites (HVA, 3-MT, and DOPAC) within murine liver and brain tissue sections, respectively. We utilized a range of isolation windows (e.g., 1, 5, 10, 20, 100 m/z) around each target m/z value. This dynamic isolation significantly decreased chemical background without fragmenting the target ions. As a result, we achieved precise spatial localization of parent drugs and their metabolites. Compared to untargeted acquisition, this method improved S/N by over 50% for all analytes within ≤10 m/z isolation ranges, while preserving tissue morphology. This targeted isolation approach extends the capabilities of MALDI MSI and offers a robust and scalable solution for analyzing low-mass xenobiotics and metabolites in situ.
Indexed as
Identifiers
42448886What Socratic holds
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 Socratic graph.