Evidence map›Paper›PMID 25686713›Full record

ArticleNanotoxicology2016

Long-term prevalence of NIRF-labeled magnetic nanoparticles for the diagnostic and intraoperative imaging of inflammation.

Jenny Domey, Christian Bergemann, Sibylle Bremer-Streck, Ines Krumbein, Jürgen R Reichenbach, Ulf Teichgräber, Ingrid Hilger

Abstract read
In one paragraph

Article in Nanotoxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Nanotechnology-Assisted Cell Tracking.Nanomaterials (Basel, Switzerland) · 2022
    Review
  3. Review
  4. Article
  5. Article
  6. 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

7 authors.

Jenny Domeya Department of Experimental Radiology , Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena , Jena , Germany .
Christian Bergemannb Chemicell GmbH , Berlin , Germany .
Sibylle Bremer-Streckc Institute of Clinical Chemistry and Laboratory Diagnostics, Jena University Hospital - Friedrich Schiller University Jena , Jena , Germany , and.
Ines Krumbeind Medical Physics Group, Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena , Jena , Germany.
Jürgen R Reichenbachd Medical Physics Group, Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena , Jena , Germany.
Ulf Teichgräbera Department of Experimental Radiology , Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena , Jena , Germany .
Ingrid Hilgera Department of Experimental Radiology , Institute of Diagnostic and Interventional Radiology, Jena University Hospital - Friedrich Schiller University Jena , Jena , Germany .

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation is a very common disease worldwide. In severe cases, surgery is often the method of choice. Today, there is a general need for the implementation of image-based guidance methodologies for reliable target resection. We investigated new near infrared fluorescence (NIRF)-nanoparticles (NPs) as a simple but effective bimodal magnetic resonance imaging (MRI) and optical contrast agent for diagnosis and intraoperative imaging of inflammation. Physicochemical analysis revealed that these NPs were highly fluorescent with similar characteristics like unlabeled NPs (hydrodynamic diameter about 130 nm and zeta potential about -10 mV). NP-uptake and NIR-dye labeling was biocompatible to macrophages (no impact on cellular ATP and reactive oxygen species production). These cells could successfully be tracked with MRI and NIRF-optical imaging. I.v. injection of fluorescent NPs into mice led to highly specific T2-weighted signal of edema due to uptake by phagocytic cells and subsequent migration to the site of inflammation. NIRF signals of the edema region were well detectable for up to 4 weeks, underlining the potential of the NPs for systematic planning and flexible time scheduling in intraoperative applications. NPs were degraded over a time period of 12 weeks, which was not altered due to inflammation. Redistribution of iron might be primarily due to inflammation and not to the presence of NPs per se in a concentration suitable for imaging. Our findings highlight the potential of the NPs to be used as a suitable tool for pre- and intraoperative imaging of inflammation.

Indexed as

Magnetite NanoparticlesAnimalsCells, CulturedContrast MediaInflammationMacrophagesMagnetic Resonance ImagingMaleMiceMolecular ImagingPhagocytesSpectrometry, FluorescenceContrast MediaMagnetite NanoparticlesBiocompatibilitybiodistributiondegradationMRIoptical imaging

Identifiers

PMID25686713
PMCPMC4819594

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.