Evidence map›Paper›PMID 20395345›Full record

ReviewJournal of nuclear medicine : official publication, Society of Nuclear Medicine2010

Design of targeted cardiovascular molecular imaging probes.

Carolyn J Anderson, Jeff W M Bulte, Kai Chen, Xiaoyuan Chen, Ban-An Khaw, Monica Shokeen, Karen L Wooley, Henry F VanBrocklin

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Detection of chemotherapy-induced cardiotoxicity with antimyosin pretargeted imaging.Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2019
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Targeted Nanocarriers for Imaging and Therapy of Vascular Inflammation.Current opinion in colloid & interface science · 2011
    Article
  11. Article
  12. Review
  13. Review
  14. Assessing the barriers to image-guided drug delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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

8 authors at 7 institutions in 1 country.

Carolyn J AndersonMallinckrodt Institute of Radiology, School of Medicine, Washington University, St. Louis, Missouri, USA.
Jeff W M Bulte
Kai Chen
Xiaoyuan Chen
Ban-An Khaw
Monica Shokeen
Karen L Wooley
Henry F VanBrocklin
National Institutes of Health · USJohns Hopkins University · USMallinckrodt (United States) · USMitchell Institute · USNational Institute of Biomedical Imaging and Bioengineering · USUniversity of California, San Francisco · USWashington University in St. Louis · US

Funding

Laboratory of Molecular Imaging and NanomedicineZIAEB000073 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI CHEN, XIAOYUAN · 2010 to 2020
$32.8M
Establishment of Laboratory of Molecular Imaging and NanomedicineZIIEB000066 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI CHEN, XIAOYUAN · 2009 to 2009
$1.9M
Intramural NIH HHS Z99 EB999999Intramural NIH HHS ZII EB000066
6 · The paper itself

Abstract

Molecular imaging relies on the development of sensitive and specific probes coupled with imaging hardware and software to provide information about the molecular status of a disease and its response to therapy, which are important aspects of disease management. As genomic and proteomic information from a variety of cardiovascular diseases becomes available, new cellular and molecular targets will provide an imaging readout of fundamental disease processes. A review of the development and application of several cardiovascular probes is presented here. Strategies for labeling cells with superparamagnetic iron oxide nanoparticles enable monitoring of the delivery of stem cell therapies. Small molecules and biologics (e.g., proteins and antibodies) with high affinity and specificity for cell surface receptors or cellular proteins as well as enzyme substrates or inhibitors may be labeled with single-photon-emitting or positron-emitting isotopes for nuclear molecular imaging applications. Labeling of bispecific antibodies with single-photon-emitting isotopes coupled with a pretargeting strategy may be used to enhance signal accumulation in small lesions. Emerging nanomaterials will provide platforms that have various sizes and structures and that may be used to develop multimeric, multimodal molecular imaging agents to probe one or more targets simultaneously. These platforms may be chemically manipulated to afford molecules with specific targeting and clearance properties. These examples of molecular imaging probes are characteristic of the multidisciplinary nature of the extraction of advanced biochemical information that will enhance diagnostic evaluation and drug development and predict clinical outcomes, fulfilling the promise of personalized medicine and improved patient care.

Indexed as

AnimalsAntibodiesCell MembraneDendritic CellsDiagnostic ImagingEchocardiographyEquipment DesignFerric CompoundsHumansMagnetic Resonance ImagingMetal NanoparticlesMolecular ProbesNanotechnologyPositron-Emission TomographyRadioisotopesSoftwareAntibodiesFerric Compoundsferric oxideMolecular ProbesRadioisotopes

Identifiers

PMID20395345
PMCPMC3629978
OpenAlexW2066272012

What OpenQuestion holds

Textmetadata
LicenceTDM
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.