Evidence map›Paper›PMID 31815963›Full record

ArticlePloS one2019

Evaluation of upconverting nanoparticles towards heart theranostics.

Marc Kermorgant, Jennifer Ben Salem, Julien Santelli, Denis Calise, Anne-Cécile Oster, Olivier Lairez, Christophe Coudret, Marc Verelst, Céline Gales, Jean-Michel Sénard and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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
0.5field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  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

15 authors at 5 institutions in 2 countries.

Marc KermorgantInstitut des Maladies Métaboliques et Cardiovasculaires, INSERM UMR1048, Université de Toulouse, France.ORCID 0000-0002-9666-4199
Jennifer Ben SalemInstitut des Maladies Métaboliques et Cardiovasculaires, INSERM UMR1048, Université de Toulouse, France.
Julien SantelliCEMES-CNRS, Université de Toulouse, CNRS, France.
Denis CaliseService Microchirurgie, Centre Régional d'Exploration Fonctionnelle et Ressources Expérimentales (CREFRE- US06, Rangueil).
Anne-Cécile OsterInstitut des Maladies Métaboliques et Cardiovasculaires, INSERM UMR1048, Université de Toulouse, France.
Olivier LairezFédération des services de cardiologie, hôpital Rangueil.ORCID 0000-0001-8141-6582
Christophe CoudretLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III-Paul Sabatier.
Marc VerelstCHROMALYS SAS, France.
Céline GalesInstitut des Maladies Métaboliques et Cardiovasculaires, INSERM UMR1048, Université de Toulouse, France.
Jean-Michel SénardInstitut des Maladies Métaboliques et Cardiovasculaires, INSERM UMR1048, Université de Toulouse, France.
Francis BeaudryGroupe de Recherche en Pharmacologie Animale du Québec (GREPAQ), Département de Biomédecine Vétérinaire, Faculté de Médecine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec, Canada.
Anne Pavy-Le TraonDépartement de Neurologie et Institut des Neurosciences, Université de Toulouse, France.
Clément RouxLaboratoire des IMRCP, Université de Toulouse, CNRS UMR 5623, Université Toulouse III-Paul Sabatier.ORCID 0000-0001-5707-4471
Robert MauricotCEMES-CNRS, Université de Toulouse, CNRS, France.
Dina N ArvanitisInstitut des Maladies Métaboliques et Cardiovasculaires, INSERM UMR1048, Université de Toulouse, France.
Inserm · FRCentre National de la Recherche Scientifique · FRHôpital Rangueil · FRUniversité de Montréal · CAUniversité Fédérale de Toulouse Midi-Pyrénées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Restricted and controlled drug delivery to the heart remains a challenge giving frequent off-target effects as well as limited retention of drugs in the heart. There is a need to develop and optimize tools to allow for improved design of drug candidates for treatment of heart diseases. Over the last decade, novel drug platforms and nanomaterials were designed to confine bioactive materials to the heart. Yet, the research remains in its infancy, not only in the development of tools but also in the understanding of effects of these materials on cardiac function and tissue integrity. Upconverting nanoparticles are nanomaterials that recently accelerated interest in theranostic nanomedicine technologies. Their unique photophysical properties allow for sensitive in vivo imaging that can be combined with spatio-temporal control for targeted release of encapsulated drugs. Here we synthesized upconverting NaYF4:Yb,Tm nanoparticles and show for the first time their innocuity in the heart, when injected in the myocardium or in the pericardial space in mice. Nanoparticle retention and upconversion in the cardiac region did not alter heart rate variability, nor cardiac function as determined over a 15-day time course ensuing the sole injection. Altogether, our nanoparticles show innocuity primarily in the pericardial region and can be safely used for controlled spatiotemporal drug delivery. Our results support the use of upconverting nanoparticles as potential theranostics tools overcoming some of the key limitations associated with conventional experimental cardiology.

Indexed as

Theranostic NanomedicineAnimalsBody WeightHeart DiseasesHeart Function TestsMaleMice, Inbred C57BLNanoparticles

Identifiers

PMID31815963
PMCPMC6901177
OpenAlexW2996718272

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.