Evidence map›Paper›PMID 19393702›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2009

Transepithelial transport of PEGylated anionic poly(amidoamine) dendrimers: implications for oral drug delivery.

Deborah M Sweet, Rohit B Kolhatkar, Abhijit Ray, Peter Swaan, Hamidreza Ghandehari

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Radiation-Sensitive Dendrimer-Based Drug Delivery System.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    Article
  9. Effects of food-borne nanomaterials on gastrointestinal tissues and microbiota.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2018
    Review
  10. Dendrimers for Ocular Drug Delivery.Canadian journal of chemistry · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  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

5 authors at 2 institutions in 1 country.

Deborah M SweetFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Rohit B Kolhatkar
Abhijit Ray
Peter Swaan
Hamidreza Ghandehari
University of Maryland, Baltimore · USUniversity of Utah · US

Funding

Biological fate and biocompatibility of dendritic and silica-based nanoconstructsR01DE019050 · NIDCR · UNIVERSITY OF UTAH · PI GHANDEHARI, HAMID · 2007 to 2010
$1.3M
Dendritic Biomaterials for Oral Delivery of ChemotherapeuticsR01EB007470 · NIBIB · UNIVERSITY OF UTAH · PI GHANDEHARI, HAMID · 2007 to 2010
$1.2M
NIBIB NIH HHS EB07470NIBIB NIH HHS R01 EB007470NIDCR NIH HHS DE19050
6 · The paper itself

Abstract

The purpose of this work was to assess the impact of PEGylation on transepithelial transport of anionic poly(amidoamine) dendrimers. Cytotoxicity, uptake and transport across Caco-2 cells of PEGylated G3.5 and G4.5 PAMAM dendrimers were studied. Methoxy polyethylene glycol (750 Da) was conjugated to carboxylic acid-terminated PAMAM dendrimers at feed ratios of 1, 2 and 4 PEG per dendrimer. Compared to the control, PEGylation of anionic dendrimers did not significantly alter cytotoxicity up to a concentration of 0.1 mM. PEGylation of G3.5 dendrimers significantly decreased cellular uptake and transepithelial transport while PEGylation of G4.5 dendrimers led to a significant increase in uptake, but also a significant decrease in transport. Dendrimer PEGylation reduced the opening of tight junctions as evidenced by confocal microscopy techniques. Modulation of the tight junctional complex correlated well with changes in PEGylated dendrimer transport and suggests that anionic dendrimers are transported primarily through the paracellular route. PEGylated dendrimers show promise in oral delivery applications where increased functionality for drug conjugation and release is desired.

Indexed as

Cell Membrane PermeabilityAdministration, OralCaco-2 CellsCell SurvivalDendrimersHumansMembrane ProteinsOccludinPolyaminesPolyethylene GlycolsTight JunctionsDendrimersMembrane ProteinsOccludinOCLN protein, humanPAMAM StarburstPolyaminesPolyethylene Glycols

Identifiers

PMID19393702
PMCPMC2818763
OpenAlexW1965850463

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.