Evidence map›Paper›PMID 26731174›Full record

ArticleACS nano2016

Pretargeted Positron Emission Tomography Imaging That Employs Supramolecular Nanoparticles with in Vivo Bioorthogonal Chemistry.

Shuang Hou, Jin-Sil Choi, Mitch Andre Garcia, Yan Xing, Kuan-Ju Chen, Yi-Ming Chen, Ziyue K Jiang, Tracy Ro, Lily Wu, David B Stout and 5 more

Abstract read
In one paragraph

Article in ACS nano, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. [RSC chemical biology · 2024
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Medical Imaging Technology and Imaging Agents.Advances in experimental medicine and biology · 2023
    Article
  13. Supramolecular Rotaxane-Based Multi-Modal Probes for Cancer Biomarker Imaging.Angewandte Chemie (International ed. in English) · 2022
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Cyclodextrin-Based Contrast Agents for Medical Imaging.Molecules (Basel, Switzerland) · 2020
    Review
  19. 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

15 authors.

Shuang HouDepartment of Medicinal and Applied Chemistry, Kaohsiung Medical University , 100 Shih-Chuan 1st Road, Kaohsiung, 80708, Taiwan.
Jin-Sil ChoiDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
Mitch Andre GarciaDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
Yan XingMolecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California , Los Angeles, California 90033-9061, United States.
Kuan-Ju ChenDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
Yi-Ming ChenDepartment of Medicinal and Applied Chemistry, Kaohsiung Medical University , 100 Shih-Chuan 1st Road, Kaohsiung, 80708, Taiwan.
Ziyue K JiangDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
Tracy RoDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
Lily WuDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
David B StoutDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
James S TomlinsonDepartment of Surgery, University of California, Los Angeles , Los Angeles, California 90095, United States.
Hao WangNational Center for Nanoscience and Technology , 11 Beiyitiao Zhongguancun Haidian District, Beijing, 100190, People's Republic of China.
Kai ChenMolecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California , Los Angeles, California 90033-9061, United States.
Hsian-Rong TsengDepartment of Molecular and Medical Pharmacology, California NanoSystems Institute (CNSI), University of California, Los Angeles , Los Angeles, California 90095-1770, United States.
Wei-Yu LinDepartment of Medicinal and Applied Chemistry, Kaohsiung Medical University , 100 Shih-Chuan 1st Road, Kaohsiung, 80708, Taiwan.

Funding

Generation of hPSCs Using Reprogramming Proteins-Encapsulated NanoparticlesR21GM098982 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TSENG, HSIAN-RONG · 2011 to 2012
$410k
Supramolecular Nanoparticle-Based PET Probes for Pretargeted Tumor ImagingR21EB016270 · NIBIB · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TSENG, HSIAN-RONG · 2013 to 2014
$400k
NIBIB NIH HHS R21 EB016270NIBIB NIH HHS R21EB016270NIGMS NIH HHS R21 GM098982NIGMS NIH HHS R21GM098982
6 · The paper itself

Abstract

A pretargeted oncologic positron emission tomography (PET) imaging that leverages the power of supramolecular nanoparticles with in vivo bioorthogonal chemistry was demonstrated for the clinically relevant problem of tumor imaging. The advantages of this approach are that (i) the pharmacokinetics (PKs) of tumor-targeting and imaging agents can be independently altered via chemical alteration to achieve the desired in vivo performance and (ii) the interplay between the two PKs and other controllable variables confers a second layer of control toward improved PET imaging. In brief, we utilized supramolecular chemistry to synthesize tumor-targeting nanoparticles containing transcyclooctene (TCO, a bioorthogonal reactive motif), called TCO⊂SNPs. After the intravenous injection and subsequent concentration of the TCO⊂SNPs in the tumors of living mice, a small molecule containing both the complementary bioorthogonal motif (tetrazine, Tz) and a positron-emitting radioisotope ((64)Cu) was injected to react selectively and irreversibly to TCO. High-contrast PET imaging of the tumor mass was accomplished after the rapid clearance of the unreacted (64)Cu-Tz probe. Our nanoparticle approach encompasses a wider gamut of tumor types due to the use of EPR effects, which is a universal phenomenon for most solid tumors.

Indexed as

AnimalsCopper RadioisotopesCyclooctanesDendrimersGlioblastomaHeterocyclic Compounds, 1-RingHumansInjections, SubcutaneousMiceMice, NudeNanoparticlesNeoplasm TransplantationPermeabilityPolyethylenesPositron-Emission TomographyTransplantation, HeterologousCopper RadioisotopesCyclooctanesDendrimersHeterocyclic Compounds, 1-RingPAMAM StarburstPolyethylenesbioorthogonal chemistryEPR effectPET imagingpretargetedsupramolecular nanoparticles

Identifiers

PMID26731174
PMCPMC4893318

What OpenQuestion holds

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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.