Evidence map›Paper›PMID 26874280›Full record

ArticleBiomaterials2016

A targeted nanoglobular contrast agent from host-guest self-assembly for MR cancer molecular imaging.

Zhuxian Zhou, Zhen Han, Zheng-Rong Lu

Abstract read
In one paragraph

Article in Biomaterials, 2016. 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
4.4field-weighted citation impact, top 5% 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, 60 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Lysosomal Targeting of β-Cyclodextrin.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023
    Article
  5. Review
  6. Review
  7. Cyclodextrin-Based Contrast Agents for Medical Imaging.Molecules (Basel, Switzerland) · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

3 authors at 2 institutions in 2 countries.

Zhuxian ZhouDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA; Center for Bionanoengineering and State Key Laboratory of Chemical Engineering, Department of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310027, China.
Zhen HanDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.
Zheng-Rong LuDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA. Electronic address: zxl125@case.edu.
Case Western Reserve University · USZhejiang University · CN

Funding

Biodegradable Macromolecular Blood Pool Contrast AgentsR01EB000489 · NIBIB · UNIVERSITY OF UTAH · PI LU, ZHENG-RONG · 2003 to 2014
$3.3M
Image-guided EMT inhibition for treating metastatic breast cancerR01CA194518 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI LU, ZHENG-RONG, SCHIEMANN, WILLIAM · 2015 to 2019
$2.4M
NCI NIH HHS R01 CA194518NIBIB NIH HHS R01 EB000489NIBIB NIH HHS R01 EB00489
6 · The paper itself

Abstract

The clinical application of nanoparticular Gd(III) based contrast agents for tumor molecular MRI has been hindered by safety concerns associated with prolonged tissue retention, although they can produce strong tumor enhancement. In this study, a targeted well-defined cyclodextrin-based nanoglobular contrast agent was developed through self-assembly driven by host-guest interactions for safe and effective cancer molecular MRI. Multiple β-cyclodextrins attached POSS (polyhedral oligomeric silsesquioxane) nanoglobule was used as host molecule. Adamantane-modified macrocyclic Gd(III) contrast agent, cRGD (cyclic RGDfK peptide) targeting ligand and fluorescent probe was used as guest molecules. The targeted host-guest nanoglobular contrast agent cRGD-POSS-βCD-(DOTA-Gd) specifically bond to αvβ3 integrin in malignant 4T1 breast tumor and provided greater contrast enhancement than the corresponding non-targeted agent. The agent also provided significant fluorescence signal in tumor tissue. The histological analysis of the tumor tissue confirmed its specific and effective targeting to αvβ3 integrin. The targeted imaging agent has a potential for specific cancer molecular MR and fluorescent imaging.

Indexed as

Molecular ImagingAnimalsbeta-CyclodextrinsBreast NeoplasmsCell Line, TumorContrast MediaDisease Models, AnimalFemaleIntegrin alphaVbeta3Magnetic Resonance ImagingMiceMice, Inbred BALB CNanostructuresPeptides, Cyclicbeta-CyclodextrinsContrast Mediacyclic (arginyl-glycyl-aspartyl-phenylalanyl-lysyl)Integrin alphaVbeta3Peptides, CyclicCancer molecular imagingCyclodextrinGadolinium contrast agentHost-guest interactionMagnetic resonance imagingα(v)β(3) integrin

Identifiers

PMID26874280
PMCPMC5412079
OpenAlexW2263465300

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.