Evidence map›Paper›PMID 37946621›Full record

ArticleElectrophoresis2025

Uptake and metabolization of four sartan drugs by eight different plants: Targeted and untargeted analyses by HPLC-drift-tube-ion-mobility quadrupole time-of-flight mass spectrometry.

Laura Zellner, Thomas Schiefer, Markus Himmelsbach, Franz Mlynek, Christian W Klampfl

Abstract read
In one paragraph

Article in Electrophoresis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Laura ZellnerInstitute of Analytical and General Chemistry, Johannes Kepler University, Linz, Austria.
Thomas SchieferInstitute of Analytical and General Chemistry, Johannes Kepler University, Linz, Austria.
Markus HimmelsbachInstitute of Analytical and General Chemistry, Johannes Kepler University, Linz, Austria.
Franz MlynekInstitute of Analytical and General Chemistry, Johannes Kepler University, Linz, Austria.
Christian W KlampflInstitute of Analytical and General Chemistry, Johannes Kepler University, Linz, Austria.ORCID 0000-0001-9139-4022

Funding

Austrian Science Fund FWF I 3046European Union within the Interreg project ATCZ52
6 · The paper itself

Abstract

In this study, we investigated the uptake and metabolization of four drugs (plus the associated prodrugs) from the sartan family by eight edible plants. Growing the plants hydroponically in a medium containing the respective drug, more than 40 phases I and II metabolites derived from the four sartan drugs could be tentatively identified. To demonstrate the suitability of the proposed analytical approach for actual environmental samples, garden cress (Lepidium sativum) selected as a model plant was grown in water drawn from the effluent of two local wastewater treatment plants. Thereby, three of the sartans, namely, olmesartan, candesartan, and valsartan, could be found in the plant extracts at concentrations of 3.1, 10.4, and 14.4 ng g

Indexed as

Mass SpectrometryPlants, EdibleBenzimidazolesBiphenyl CompoundsChromatography, High Pressure LiquidImidazolesTetrazolesValsartanBenzimidazolesBiphenyl CompoundscandesartanImidazolesolmesartanTetrazolesValsartandrift‐tube ion‐mobility–mass spectrometryenvironmental analysisplant metabolismplant uptakesartans

Identifiers

PMID37946621
PMCPMC11865686

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Registered trials

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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.