Evidence map›Paper›PMID 21683439›Full record

ArticleBiomaterials2011

The role of poly(ethylene glycol) brush architecture in complement activation on targeted microbubble surfaces.

Cherry C Chen, Mark A Borden

Abstract read
In one paragraph

Article in Biomaterials, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.5field-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

36 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. Frequency-Selective Microbubble TargetingACS applied bio materials · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
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  11. Article
  12. Review
  13. Article
  14. Reverse engineering the ultrasound contrast agent.Advances in colloid and interface science · 2018
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

2 authors at 2 institutions in 1 country.

Cherry C ChenChemical Engineering Department, Columbia University, New York, NY 10027, USA.
Mark A Borden
Columbia University · USUniversity of Colorado Boulder · US

Funding

Immune-Shielded, Ultrasound-Stimulated Contrast Agents for Molecular ImagingR01EB009066 · NIBIB · UNIVERSITY OF COLORADO · PI BORDEN, MARK ANDREW, DAYTON, PAUL A · 2008 to 2011
$1.2M
NIBIB NIH HHS R01 EB 009066NIBIB NIH HHS R01 EB009066
6 · The paper itself

Abstract

Complement fixation to surface-conjugated ligands plays a critical role in determining the fate of targeted colloidal particles after intravenous injection. In the present study, we examined the immunogenicity of targeted microbubbles with various surface architectures and ligand surface densities using a flow cytometry technique. Targeted microbubbles were generated using a post-labeling technique with a physiological targeting ligand, cyclic arginine-glycine-asparagine (RGD), attached to the distal end of the poly(ethylene glycol) (PEG) moieties on the microbubble surface. Microbubbles were incubated in human serum, washed and then mixed with fluorescent antibodies specific for various serum components. We found that complement C3/C3b was the main human serum factor to bind in vitro to the microbubble surface, compared to IgG or albumin. We also investigated the effect of PEG brush architecture on C3/C3b fixation to the microbubble surface. RGD peptide was able to trigger a complement immune response, and complement C3/C3b fixation depended on microbubble size and RGD peptide surface density. When the targeting ligand was attached to shorter PEG chains that were shielded by a PEG overbrush layer (buried-ligand architecture), significantly less complement activation was observed when compared to the more traditional exposed-ligand motif. The extent of this protective role by the PEG chains depended on the overbrush length. Taken together, our results confirm that the buried-ligand architecture may significantly reduce ligand-mediated immunogenicity. More generally, this study illustrates the use of flow cytometry and microbubbles to analyze the surface interactions between complex biological media and surface-engineered biomaterials.

Indexed as

MicrobubblesComplement ActivationComplement C3Complement C3bComplement Fixation TestsEnzyme-Linked Immunosorbent AssayFlow CytometryHumansLigandsOligopeptidesPeptidesPolyethylene GlycolsProtein BindingSerumSurface Propertiesarginyl-glycyl-aspartic acidComplement C3Complement C3bLigandsOligopeptidesPeptidesPolyethylene Glycols

Identifiers

PMID21683439
PMCPMC3134131
OpenAlexW2118202345

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.