Evidence map›Paper›PMID 21473630›Full record

ArticleMolecular pharmaceutics2011

Calcium condensed LABL-TAT complexes effectively target gene delivery to ICAM-1 expressing cells.

Supang Khondee, Abdulgader Baoum, Teruna J Siahaan, Cory Berkland

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

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  11. Cell membrane-formed nanovesicles for disease-targeted delivery.Journal of controlled release : official journal of the Controlled Release Society · 2016
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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

4 authors.

Supang KhondeeDepartment of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas 66047, USA.
Abdulgader Baoum
Teruna J Siahaan
Cory Berkland

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
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 RR016443NIAMS NIH HHS R03 AR054035
6 · The paper itself

Abstract

Targeted gene delivery using nonviral vectors is a highly touted scheme to reduce the potential for toxic or immunological side effects by reducing dose. In previous reports, TAT polyplexes with DNA have shown relatively poor gene delivery. The transfection efficiency has been enhanced by condensing TAT/DNA complexes to a small particle size using calcium. To explore the targetability of these condensed TAT complexes, LABL peptide targeting intercellular cell-adhesion molecule-1 (ICAM-1) was conjugated to TAT peptide using a polyethylene glycol (PEG) spacer. PEGylation reduced the transfection efficiency of TAT, but TAT complexes targeting ICAM-1 expressing cells regained much of the lost transfection efficiency. Targeted block peptides properly formulated with calcium offer promise for gene delivery to ICAM-1 expressing cells at sites of injury or inflammation.

Indexed as

CalciumCell Line, TumorCell SurvivalDNAGenetic VectorsGene Transfer TechniquesHumansIntercellular Adhesion Molecule-1Microscopy, ConfocalPeptidesPolyethylene Glycolstat Gene Products, Human Immunodeficiency VirusCalciumDNAIntercellular Adhesion Molecule-1PeptidesPolyethylene Glycolstat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID21473630
PMCPMC4207658

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Registered trials

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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.