Evidence map›Paper›PMID 17760416›Full record

ArticleBioconjugate chemistry

Surface engineering of quantum dots for in vivo vascular imaging.

Ashwath Jayagopal, Patricia K Russ, Frederick R Haselton

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Recent Advances in Retinal Stem Cell Therapy.Current molecular biology reports · 2017
    Article
  8. In vivo biodistribution and behavior of CdTe/ZnS quantum dots.International journal of nanomedicine · 2017
    Article
  9. Nanomedicine in the application of uveal melanoma.International journal of ophthalmology · 2016
    Review
  10. Cytocompatibility of direct water synthesized cadmium selenide quantum dots in colo-205 cells.Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology · 2015
    Article
  11. Article
  12. Article
  13. Drug and gene delivery to the back of the eye: from bench to bedside.Investigative ophthalmology & visual science · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Molecular imaging of retinal disease.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2013
    Review
  20. Targeted Nanocarriers for Imaging and Therapy of Vascular Inflammation.Current opinion in colloid & interface science · 2011
    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 1 institution in 1 country.

Ashwath JayagopalDepartment of Biomedical Engineering, Vanderbilt University, USA.
Patricia K Russ
Frederick R Haselton
Vanderbilt University · US

Funding

Training in Vision ResearchT32EY007135 · NEI · VANDERBILT UNIVERSITY · PI GEOFFREY F WOODMAN · 1994 to 2026
$5.8M
Retinal blood barrier permeability using optical tracersR01EY013451 · NEI · VANDERBILT UNIVERSITY · PI HASELTON, FREDERICK R · 2002 to 2004
$717k
Multi-spectral quantum dot-based retinal imaging of molecular expression in vivoR21EY017522 · NEI · VANDERBILT UNIVERSITY · PI HASELTON, FREDERICK R · 2007 to 2009
$572k
NEI NIH HHS EY017522NEI NIH HHS EY13451NEI NIH HHS R01 EY013451NEI NIH HHS R21 EY017522NEI NIH HHS T32 EY007135NEI NIH HHS T32-EY07135-13
6 · The paper itself

Abstract

Quantum dot-antibody bioconjugates (QD-mAb) were synthesized incorporating PEG cross-linkers and Fc-shielding mAb fragments to increase in vivo circulation times and targeting efficiency. Microscopy of endothelial cell cultures incubated with QD-mAb directed against cell adhesion molecules (CAMs), when shielded to reduce Fc-mediated interactions, were more specific for their molecular targets. In vitro flow cytometry indicated that surface engineered QD-mAb labeled leukocyte subsets with minimal Fc-mediated binding. Nontargeted QD-mAb nanoparticles with Fc-blockade featured 64% (endothelial cells) and 53% (leukocytes) lower nonspecific binding than non-Fc-blocked nanoparticles. Spectrally distinct QD-mAb targeted to the cell adhesion molecules (CAMs) PECAM-1, ICAM-1, and VCAM-1 on the retinal endothelium in a rat model of diabetes were imaged in vivo using fluorescence angiography. Endogenously labeled circulating and adherent leukocyte subsets were imaged in rat models of diabetes and uveitis using QD-mAb targeted to RP-1 and CD45. Diabetic rats exhibited increased fluorescence in the retinal vasculature from QD bioconjugates to ICAM-1 and VCAM-1 but not PECAM-1. Both animal models exhibited leukocyte rolling and leukostasis in capillaries. Examination of retinal whole mounts prepared after in vivo imaging confirmed the fluorescence patterns seen in vivo. Comparison of the timecourse of retinal fluorescence from Fc-shielded and non-Fc-shielded bioconjugates indicated nonspecific uptake and increased clearance of the non-Fc-shielded QD-mAb. This combination of QD surface design elements offers a promising new in vivo approach to specifically label vascular cells and biomolecules of interest.

Indexed as

Antibodies, MonoclonalQuantum DotsAnimalsCell AdhesionCell Culture TechniquesDiabetes Mellitus, ExperimentalEndothelium, VascularFlow CytometryFluorescent Antibody TechniqueMicroscopy, FluorescenceRatsReceptors, Leukocyte-AdhesionRetinal VesselsTime FactorsAntibodies, MonoclonalReceptors, Leukocyte-Adhesion

Identifiers

PMID17760416
PMCPMC2853010
OpenAlexW2017069758

What OpenQuestion holds

Textmetadata
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.