Evidence map›Paper›PMID 23004346›Full record

ArticleBiomacromolecules2012

Cyclam-based polymeric copper chelators for gene delivery and potential PET imaging.

Jing Li, Yu Zhu, Stuart T Hazeldine, Steven M Firestine, David Oupický

Abstract read
In one paragraph

Article in Biomacromolecules, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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 1 institution in 1 country.

Jing LiDepartment of Pharmaceutical Sciences, Wayne State University, Detroit, MI, USA.
Yu Zhu
Stuart T Hazeldine
Steven M Firestine
David Oupický
Wayne State University · US

Funding

Gene Delivery Modulated by Redox Potential GradientsR01CA109711 · NCI · WAYNE STATE UNIVERSITY · PI OUPICKY, DAVID · 2005 to 2009
$1.2M
NCI NIH HHS CA109711NCI NIH HHS R01 CA109711
6 · The paper itself

Abstract

A series of reducible polycationic copper chelators (RPCs) based on 1,4,8,11-tetraazacyclotetradecane (cyclam) were synthesized by Michael addition. Molecular weight of the polycations was controlled by reaction stoichiometry and reaction conditions, resulting in polymers with molecular weights ranging from 4400 to 13 800. The cyclam moieties in the polycations retained their ability to form complexes with Cu(II). The presence of disulfide bonds in the polycations resulted in substantially lower cytotoxicity than control 25 kDa poly(ethyleneimine). RPC as well as their complexes with Cu(II) exhibited high transfection activity in vitro. The reported polycationic Cu(II) chelates represent promising nucleic acid delivery vectors with potential for future theranostic applications.

Indexed as

Gene Transfer TechniquesPositron-Emission TomographyChelating AgentsCopperGenetic VectorsHep G2 CellsHeterocyclic CompoundsHumansMolecular StructurePolymersTumor Cells, CulturedChelating AgentsCoppercyclamHeterocyclic CompoundsPolymers

Identifiers

PMID23004346
PMCPMC4102145
OpenAlexW2323298332

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.