Evidence map›Paper›PMID 17997512›Full record

ArticleBioconjugate chemistry2008

PLGA nanoparticle--peptide conjugate effectively targets intercellular cell-adhesion molecule-1.

Na Zhang, Chuda Chittasupho, Chadarat Duangrat, Teruna J Siahaan, Cory Berkland

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

69 citing papers in PubMed, 197 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Extracellular Vesicles as Potential Therapeutics for Inflammatory Diseases.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Article
  9. Extracellular vesicles: new players in regulating vascular barrier function.American journal of physiology. Heart and circulatory physiology · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Harnessing the versatility of PLGA nanoparticles for targeted Cre-mediated recombination.Nanomedicine : nanotechnology, biology, and medicine · 2019
    Article
  17. Article
  18. Article
  19. Nanoscale · 2018
    Article
  20. Review

9 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Na ZhangDepartments of Pharmaceutical Chemistry, University of Kansas, Lawrence, Kansas 66047, USA.
Chuda Chittasupho
Chadarat Duangrat
Teruna J Siahaan
Cory Berkland
University of Kansas · US

Funding

XRAY CRYSTALLOGRAPHY CORE (JANUARY 1 - JUNE 30, 2005)P20RR016443 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI VINES, CHARLOTTE M · 2001 to 2010
$21.3M
WEIGHT CONTROL, CELL SIGNALING AND CANCER PREVENTIONP20RR015563 · NCRR · UNIVERSITY OF KANSAS LAWRENCE · PI ZUFFEREY, RACHEL · 2000 to 2009
$20.1M
Nanoparticle targeting of ICAM-1 as a potential treatment for Rheumatoid ArthritiR03AR054035 · NIAMS · UNIVERSITY OF KANSAS LAWRENCE · PI BERKLAND, CORY · 2007 to 2009
$205k
NCRR NIH HHS P20 RR015563NCRR NIH HHS P20 RR016443NIAMS NIH HHS 1R03 AR054035-01A1NIAMS NIH HHS R03 AR054035
6 · The paper itself

Abstract

Targeted delivery of therapeutics possesses the potential to localize therapeutic agents to a specific tissue as a mechanism to enhance treatment efficacy and abrogate side effects. Antibodies have been used clinically as therapeutic agents and are currently being explored for targeting drug-loaded nanoparticles. Peptides such as RGD peptides are also being developed as an inexpensive and stable alternative to antibodies. In this study, cyclo(1,12)PenITDGEATDSGC (cLABL) peptide was used to target nanoparticles to human umbilical cord vascular endothelial cell (HUVEC) monolayers that have upregulated intercellular cell-adhesion molecule-1 (ICAM-1) expression. The cLABL peptide has been previously demonstrated to possess high avidity for ICAM-1 receptors on the cell surface. Poly( dl-lactic-coglycolic acid) nanoparticles conjugated with polyethylene glycol and cLABL demonstrated rapid binding to HUVEC with upregulated ICAM-1, which was induced by treating cells with the proinflammatory cytokine, interferon-gamma. Binding of the nanoparticles could be efficiently blocked by preincubating cells with free peptide suggesting that the binding of the nanoparticles is specifically mediated by surface peptide binding to ICAM-1 on HUVEC. The targeted nanoparticles were rapidly endocytosed and trafficked to lysosomes to a greater extent than the untargeted PLGA-PEG nanoparticles. Verification of peptide-mediated nanoparticle targeting to ICAM-1 may ultimately lead to targeting therapeutic agents to inflammatory sites expressing upregulated ICAM-1.

Indexed as

Drug CarriersEndocytosisEndothelial CellsGlycolatesHumansIntercellular Adhesion Molecule-1Lactic AcidLysosomesNanoparticlesPeptidesPeptides, CyclicPolyethylene GlycolsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerSurface-Active AgentsUp-RegulationDrug CarriersGlycolatesIntercellular Adhesion Molecule-1Lactic AcidPeptidesPeptides, CyclicPolyethylene GlycolsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerSurface-Active Agents

Identifiers

PMID17997512
PMCPMC2535939
OpenAlexW2119834954

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.