Evidence map›Paper›PMID 24837188›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2014

Prolonged blood circulation and enhanced tumor accumulation of folate-targeted dendrimer-polymer hybrid nanoparticles.

Suhair Sunoqrot, Jason Bugno, Daniel Lantvit, Joanna E Burdette, Seungpyo Hong

Abstract readComparative Study
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
  2. Article
  3. Research Progress of Drug Delivery Systems Targeting the Kidneys.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  4. Review
  5. Article
  6. Frontiers in bioengineering and biotechnology · 2022
    Article
  7. Review
  8. Review
  9. Review
  10. Cell-Based Tracers as Trojan Horses for Image-Guided Surgery.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Polymer nanocarriers for MicroRNA delivery.Journal of applied polymer science · 2020
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

5 authors at 2 institutions in 1 country.

Suhair SunoqrotDepartment of Biopharmaceutical Sciences, University of Illinois, Chicago 60612, USA.
Jason BugnoDepartment of Biopharmaceutical Sciences, University of Illinois, Chicago 60612, USA.
Daniel LantvitDepartment of Medicinal Chemistry and Pharmacognosy, University of Illinois, Chicago 60612, USA.
Joanna E BurdetteDepartment of Biopharmaceutical Sciences, University of Illinois, Chicago 60612, USA; Department of Medicinal Chemistry and Pharmacognosy, University of Illinois, Chicago 60612, USA.
Seungpyo HongDepartment of Biopharmaceutical Sciences, University of Illinois, Chicago 60612, USA; Department of Biongineering, University of Illinois, Chicago 60612, USA. Electronic address: sphong@uic.edu.
University of Illinois Chicago · USUniversity of Illinois Urbana-Champaign · US

Funding

EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015482 · NCRR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BAUMAN, JERRY L · 2000 to 2000
$909k
NCRR NIH HHS C06 RR015482NCRR NIH HHS C06RR15482
6 · The paper itself

Abstract

Nanoparticle (NP)-based drug delivery platforms have received a great deal of attention over the past two decades for their potential in targeted cancer therapies. Despite the promises, passive targeting approaches utilizing relatively larger NPs (typically 50-200nm in diameter) allow for passive tumor accumulation, but hinder efficient intratumoral penetration. Conversely, smaller, actively targeted NPs (<20nm in diameter) penetrate well into the tumor mass, but are limited by their rapid systemic elimination. To overcome these limitations, we have designed a multi-scale hybrid NP platform that loads smaller poly(amidoamine) (PAMAM) dendrimers (~5nm in diameter) into larger poly(ethylene glycol)-b-poly(D,L-lactide) (PEG-PLA) NPs (~70nm). A biodistribution study in healthy mice revealed that the hybrid NPs circulated longer than free dendrimers and were mostly cleared by macrophages in the liver and spleen, similar to the in vivo behavior of PEG-PLA NPs. When injected intravenously into the BALB/c athymic nude mice bearing folate receptor (FR)-overexpressing KB xenograft, the targeted hybrid NPs encapsulating folate (FA)-targeted dendrimers achieved longer plasma circulation than free dendrimers and higher tumor concentrations than both free dendrimers and the empty PEG-PLA NPs. These results suggest that the hybrid NPs successfully combine the in vivo advantages of dendrimers and polymeric NPs, demonstrating their potential as a new, modular platform for drug delivery.

Indexed as

Drug CarriersNanoparticlesAnimalsCell Line, TumorChemistry, PharmaceuticalDendrimersFemaleFolic AcidFolic Acid TransportersHumansLactatesMice, Inbred BALB CMice, NudeNanomedicineNeoplasmsParticle SizeDendrimersDrug CarriersFolic AcidFolic Acid TransportersLactatesPAMAM StarburstPolyethylene Glycolspoly(lactic acid-ethylene glycol)DendrimerIn vivo targetingNanoparticle

Identifiers

PMID24837188
PMCPMC4156894
OpenAlexW1982369339

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.