Evidence map›Paper›PMID 23224977›Full record

ArticlePharmaceutical research2013

(89)Zr-labeled paramagnetic octreotide-liposomes for PET-MR imaging of cancer.

Diane S Abou, Daniel L J Thorek, Nicholas N Ramos, Martijn W H Pinkse, Hubert T Wolterbeek, Sean D Carlin, Bradley J Beattie, Jason S Lewis

Open access · greenAbstract read
In one paragraph

Article in Pharmaceutical research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.5field-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

39 citing papers in PubMed, 86 citations in OpenAlex.

  1. Nanomedicine-Based Strategies for Multiple Myeloma Therapy.International journal of nanomedicine · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. PET Imaging of Small Extracellular VesiclesBioconjugate chemistry · 2022
    Article
  7. Review
  8. Review
  9. Metallofluorocarbon Nanoemulsion for Inflammatory Macrophage Detection via PET and MRI.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  10. Review
  11. Image-guided mathematical modeling for pharmacological evaluation of nanomaterials and monoclonal antibodies.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Radiolabeled PET/MRI Nanoparticles for Tumor Imaging.Journal of clinical medicine · 2019
    Review
  17. Review
  18. Review
  19. Multimodality Imaging Agents with PET as the Fundamental Pillar.Angewandte Chemie (International ed. in English) · 2019
    Review
  20. 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 2 institutions in 2 countries.

Diane S AbouMolecular Pharmacology and Chemistry Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 16, New York, New York, 10065, USA.
Daniel L J Thorek
Nicholas N Ramos
Martijn W H Pinkse
Hubert T Wolterbeek
Sean D Carlin
Bradley J Beattie
Jason S Lewis
Memorial Sloan Kettering Cancer Center · USDelft University of Technology · NL

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor Evolution and Changes in MetabolismP50CA086438 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI RIVIERI, ISABELLE · 2000 to 2015
$29.9M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA086438
6 · The paper itself

Abstract

purposeDual-modality PET/MR platforms add a new dimension to patient diagnosis with high resolution, functional, and anatomical imaging. The full potential of this emerging hybrid modality could be realized by using a corresponding dual-modality probe. Here, we report pegylated liposome (LP) formulations, housing a MR T(1) contrast agent (Gd) and the positron-emitting (89)Zr (half-life: 3.27 days), for simultaneous PET and MR tumor imaging capabilities.

methods(89)Zr oxophilicity was unexpectedly found advantageous for direct radiolabeling of preformed paramagnetic LPs. LPs were conjugated with octreotide to selectively target neuroendocrine tumors via human somatostatin receptor subtype 2 (SSTr2). (89)Zr-Gd-LPs and octreotide-conjugated homolog were physically, chemically and biologically characterized.

results(89)Zr-LPs showed reasonable stability over serum proteins and chelator challenges for proof-of-concept in vitro and in vivo investigations. Nuclear and paramagnetic tracking quantified superior SSTr2-recognition of octreotide-LP compared to controls.

conclusionsThis study demonstrated SSTr2-targeting specificity along with direct chelator-free (89)Zr-labeling of LPs and dual PET/MR imaging properties.

Indexed as

Contrast MediaGadoliniumLiposomesOctreotideZirconiumAnimalsCell Line, TumorHumansIsotopesMagnetic Resonance ImagingMiceNeuroendocrine TumorsPositron-Emission TomographyReceptors, SomatostatinContrast MediaGadoliniumIsotopesLiposomesOctreotideReceptors, SomatostatinSSTR2 protein, humanSstr2 protein, mouseZirconium

Identifiers

PMID23224977
PMCPMC3578092
OpenAlexW2069565582

What OpenQuestion holds

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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.