Evidence map›Paper›PMID 42371920›Full record

ArticlePloS one2026

Comparative evaluation of iodinated, nanoparticle-based, and gadolinium-based contrast agents in computed tomography for small animals.

Julie van Krimpen Mortensen, Emil Svendborg Christensen, Amalie Littau, Nicoline Rosenkilde Kjaer, Sophie Arndt, Anne Skovsbo Clausen, Andreas Clemmensen, Andreas Kjaer

Abstract readComparative Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Julie van Krimpen MortensenDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.ORCID https://orcid.org/0009-0000-4945-3260
Emil Svendborg ChristensenDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.
Amalie LittauDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.
Nicoline Rosenkilde KjaerDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.
Sophie ArndtDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.
Anne Skovsbo ClausenDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.ORCID https://orcid.org/0009-0000-0134-8517
Andreas ClemmensenDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-7669-1133
Andreas KjaerDepartment of Clinical Physiology and Nuclear Medicine & Cluster for Molecular Imaging, Copenhagen University Hospital - Rigshospitalet & Department of Biomedical Sciences, University of Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preclinical computed tomography (CT) is extensively used for anatomical reference and multimodal imaging, but the soft tissue contrast is poor compared to clinical CT. This hinders reliable organ delineation and segmentation in small-animal studies. We present a systematic evaluation of commonly used clinical iodinated and gadolinium-based contrast agents, together with a preclinical nanoparticle-based contrast agent. This evaluation aims to enhance soft-tissue boundary definition and in vivo visibility. The study consisted of two parts. First, phantom experiments were performed to assess the relationship between contrast-agent concentration and Hounsfield Unit (HU) across multiple dilutions and CT energy settings. Second, these findings were evaluated in vivo in mice to assess organ-level enhancement. Phantom measurements demonstrated a linear relationship between HU and concentration for all agents; however, at higher dilutions, contrast enhancement became indistinguishable from the background. In vivo, clinical iodinated and gadolinium-based agents administered intraperitoneal (IP) provided enhanced soft-tissue contrast by outlining abdominal organs, whereas the intravenously administered nanoparticle agent exhibited pronounced organ-specific accumulation. Overall, IP injection of clinical iodinated contrast agents offers a cost-effective and practical strategy for enhancing organ boundary visibility in preclinical CT. For longitudinal or organ-specific imaging studies, the preclinical nanoparticle-based contrast agent remains advantageous, as its cumulative uptake allows detection over extended periods and minimizes burden from multiple injections.

Indexed as

Contrast MediaGadoliniumIodineNanoparticlesTomography, X-Ray ComputedAnimalsMicePhantoms, ImagingContrast MediaGadoliniumIodine

Identifiers

PMID42371920
PMCPMC13313363

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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.