Evidence map›Paper›PMID 31037511›Full record

ArticleThe AAPS journal2019

Towards Improved Pharmacokinetic Models for the Analysis of Transporter-Mediated Hepatic Disposition of Drug Molecules with Positron Emission Tomography.

Irene Hernández Lozano, Rudolf Karch, Martin Bauer, Matthias Blaickner, Akihiro Matsuda, Beatrix Wulkersdorfer, Marcus Hacker, Markus Zeitlinger, Oliver Langer

Open access · hybridAbstract read
In one paragraph

Article in The AAPS journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 19% of its field
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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Performance and Sensitivity of [Molecular pharmaceutics · 2024
    Article
  3. Article
  4. Pharmacokinetic Imaging UsingPharmaceuticals (Basel, Switzerland) · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Use of imaging to assess the activity of hepatic transporters.Expert opinion on drug metabolism & toxicology · 2020
    Review
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

9 authors at 2 institutions in 1 country.

Irene Hernández LozanoDepartment of Clinical Pharmacology, Medical University of Vienna, A-1090, Vienna, Austria.
Rudolf KarchCentre for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
Martin BauerDepartment of Clinical Pharmacology, Medical University of Vienna, A-1090, Vienna, Austria.
Matthias BlaicknerPreclinical Molecular Imaging, AIT Austrian Institute of Technology GmbH, Seibersdorf, Austria.
Akihiro MatsudaDepartment of Clinical Pharmacology, Medical University of Vienna, A-1090, Vienna, Austria.
Beatrix WulkersdorferDepartment of Clinical Pharmacology, Medical University of Vienna, A-1090, Vienna, Austria.
Marcus HackerDivision of Nuclear Medicine, Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Markus ZeitlingerDepartment of Clinical Pharmacology, Medical University of Vienna, A-1090, Vienna, Austria.
Oliver LangerDepartment of Clinical Pharmacology, Medical University of Vienna, A-1090, Vienna, Austria. oliver.langer@meduniwien.ac.at.ORCID 0000-0002-4048-5781
Medical University of Vienna · ATAustrian Institute of Technology · AT

Funding

Austrian Science Fund FWF KLI 480Austrian Science Fund FWF KLI 694
6 · The paper itself

Abstract

Positron emission tomography (PET) imaging with radiolabeled drugs holds great promise to assess the influence of membrane transporters on hepatobiliary clearance of drugs. To exploit the full potential of PET, quantitative pharmacokinetic models are required. In this study, we evaluated the suitability of different compartment models to describe the hepatic disposition of [

Indexed as

Models, BiologicalBiliary TractBiological TransportCarbon RadioisotopesDrug InteractionsErlotinib HydrochlorideHealthy VolunteersHumansLiverMembrane Transport ProteinsMetabolic Clearance RatePositron-Emission TomographyRifampinTissue DistributionCarbon RadioisotopesErlotinib HydrochlorideMembrane Transport ProteinsRifampin[11C]erlotinibhepatobiliary clearancemembrane transporterspharmacokinetic modelpositron emission tomography

Identifiers

PMID31037511
PMCPMC6488550
OpenAlexW2943186409

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.