Evidence map›Paper›PMID 34750717›Full record

ArticleMolecular imaging and biology2022

Towards Optimized Bioavailability of

Lisa Honold, Melanie Austrup, Andreas Faust, Christian Paul Konken, Katrin Schwegmann, Bastian Zinnhardt, Constantin Gabriel Daniliuc, Günter Haufe, Michael Schäfers, Klaus Kopka and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

11 authors at 3 institutions in 1 country.

Lisa HonoldEuropean Institute for Molecular Imaging, University of Münster, 48149, Münster, Germany.
Melanie AustrupDepartment of Nuclear Medicine, University Hospital Münster, 48149, Münster, Germany.
Andreas FaustEuropean Institute for Molecular Imaging, University of Münster, 48149, Münster, Germany.
Christian Paul KonkenDepartment of Nuclear Medicine, University Hospital Münster, 48149, Münster, Germany.
Katrin SchwegmannDepartment of Nuclear Medicine, University Hospital Münster, 48149, Münster, Germany.
Bastian ZinnhardtEuropean Institute for Molecular Imaging, University of Münster, 48149, Münster, Germany.
Constantin Gabriel DaniliucDepartment of Organic Chemistry, University of Münster, 48149, Münster, Germany.
Günter HaufeDepartment of Organic Chemistry, University of Münster, 48149, Münster, Germany.
Michael SchäfersEuropean Institute for Molecular Imaging, University of Münster, 48149, Münster, Germany.
Klaus KopkaInstitute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, 01328, Dresden, Germany.
Sven HermannEuropean Institute for Molecular Imaging, University of Münster, 48149, Münster, Germany. shermann@uni-muenster.de.
University Hospital Münster · DEUniversity of Münster · DEHelmholtz-Zentrum Dresden-Rossendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDysregulated activity of matrix metalloproteinases (MMPs) drives a variety of pathophysiological conditions. Non-invasive imaging of MMP activity in vivo promises diagnostic and prognostic value. However, current targeting strategies by small molecules are typically limited with respect to the bioavailability of the labeled MMP binders in vivo. To this end, we here introduce and compare three chemical modifications of a recently developed barbiturate-based radiotracer with respect to bioavailability and potential to image MMP activity in vivo.

methodsBarbiturate-based MMP inhibitors with an identical targeting unit but varying hydrophilicity were synthesized, labeled with technetium-99m, and evaluated in vitro and in vivo. Biodistribution and radiotracer elimination were determined in C57/BL6 mice by serial SPECT imaging. MMP activity was imaged in a MMP-positive subcutaneous xenograft model of human K1 papillary thyroid tumors. In vivo data were validated by scintillation counting, autoradiography, and MMP immunohistochemistry.

resultsWe prepared three new

conclusionIntroduction of HYNIC/TPPTS into the barbiturate lead structure ([

Indexed as

Matrix Metalloproteinase InhibitorsThyroid NeoplasmsAnimalsBarbituratesBiological AvailabilityHumansLigandsMatrix MetalloproteinasesMiceTechnetiumTissue DistributionTomography, Emission-Computed, Single-PhotonBarbituratesLigandsMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesTechnetiumBarbituratesMatrix metalloproteinase inhibitorsPyrimidine-2,4,6-trionesSingle photon emission computed tomographyTumor imaging

Identifiers

PMID34750717
PMCPMC9085681
OpenAlexW3212968015

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.