Evidence map›Paper›PMID 19874858›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2010

Well-defined block copolymers for gene delivery to dendritic cells: probing the effect of polycation chain-length.

Rupei Tang, R Noelle Palumbo, Lakshmi Nagarajan, Emily Krogstad, Chun Wang

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Reducible HPMA-co-oligolysine copolymers for nucleic acid delivery.International journal of pharmaceutics · 2012
    Article
  7. Transgene expression and local tissue distribution of naked and polymer-condensed plasmid DNA after intradermal administration in mice.Journal of controlled release : official journal of the Controlled Release Society · 2012
    Article
  8. Article
  9. Article
  10. Article
  11. Stealth nanoparticles: high density but sheddable PEG is a key for tumor targeting.Journal of controlled release : official journal of the Controlled Release Society · 2010
    Article
  12. 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 1 institution in 1 country.

Rupei TangDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
R Noelle Palumbo
Lakshmi Nagarajan
Emily Krogstad
Chun Wang
University of Minnesota · US

Funding

Biodegradable Polymers For DNA Vaccine DeliveryR01CA129189 · NCI · UNIVERSITY OF MINNESOTA · PI WANG, CHUN · 2008 to 2012
$1.2M
Multifunctional nanoparticles for targeted DNA vaccine deliveryR21CA121832 · NCI · UNIVERSITY OF MINNESOTA · PI WANG, CHUN · 2006 to 2008
$408k
NCI NIH HHS R01 CA129189NCI NIH HHS R01CA129189NCI NIH HHS R21 CA121832NCI NIH HHS R21CA121832
6 · The paper itself

Abstract

The development of safe and efficient polymer carriers for DNA vaccine delivery requires mechanistic understanding of structure-function relationship of the polymer carriers and their interaction with antigen-presenting cells. Here we have synthesized a series of diblock copolymers with well-defined chain-length using atom transfer radical polymerization and characterized the influence of polycation chain-length on the physico-chemical properties of the polymer/DNA complexes as well as the interaction with dendritic cells. The copolymers consist of a hydrophilic poly(ethylene glycol) block and a cationic poly(aminoethyl methacrylate) (PAEM) block. The average degree of polymerization (DP) of the PAEM block was varied among 19, 39, and 75, with nearly uniform distribution. With increasing PAEM chain-length, polyplexes formed by the diblock copolymers and plasmid DNA had smaller average particle size and showed higher stability against electrostatic destabilization by salt and heparin. The polymers were not toxic to mouse dendritic cells (DCs) and only displayed chain-length-dependent toxicity at a high concentration (1mg/mL). In vitro gene transfection efficiency and polyplex uptake in DCs were also found to correlate with chain-length of the PAEM block with the longer polymer chain favoring transfection and cellular uptake. The polyplexes induced a modest up-regulation of surface markers for DC maturation that was not significantly dependent on PAEM chain-length. Finally, the polyplex prepared from the longest PAEM block (DP of 75) achieved an average of 20% enhancement over non-condensed anionic dextran in terms of uptake by DCs in the draining lymph nodes 24h after subcutaneous injection into mice. Insights gained from studying such structurally well-defined polymer carriers and their interaction with dendritic cells may contribute to improved design of practically useful DNA vaccine delivery systems.

Indexed as

TransfectionAcrylic ResinsAnimalsCell LineCell Membrane PermeabilityCells, CulturedCell SurvivalDendritic CellsDNAMaleMiceMice, Inbred C57BLPolyethylene GlycolsAcrylic ResinsDNApolyethylene glycol-block-poly(aminoethyl methacrylate)Polyethylene Glycols

Identifiers

PMID19874858
PMCPMC2823989
OpenAlexW2072140431

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.