Evidence map›Paper›PMID 28189628›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2017

Perlecan and vascular endothelial growth factor-encoding DNA-loaded chitosan scaffolds promote angiogenesis and wound healing.

Megan S Lord, April L Ellis, Brooke L Farrugia, John M Whitelock, Hernan Grenett, Chuanyu Li, Robert L O'Grady, Arthur A DeCarlo

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
7.6field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
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  9. ROS-scavenging materials for skin wound healing: advancements and applications.Frontiers in bioengineering and biotechnology · 2023
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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

8 authors at 2 institutions in 2 countries.

Megan S LordGraduate School of Biomedical Engineering, University of New South Wales, Sydney, NSW 2052, Australia. Electronic address: m.lord@unsw.edu.au.
April L EllisAgenta Biotechnologies, Inc., P.O. Box 430021, Cahaba Heights, AL 35243, USA.
Brooke L FarrugiaGraduate School of Biomedical Engineering, University of New South Wales, Sydney, NSW 2052, Australia.
John M WhitelockGraduate School of Biomedical Engineering, University of New South Wales, Sydney, NSW 2052, Australia.
Hernan GrenettAgenta Biotechnologies, Inc., P.O. Box 430021, Cahaba Heights, AL 35243, USA.
Chuanyu LiAgenta Biotechnologies, Inc., P.O. Box 430021, Cahaba Heights, AL 35243, USA.
Robert L O'GradyGraduate School of Biomedical Engineering, University of New South Wales, Sydney, NSW 2052, Australia.
Arthur A DeCarloAgenta Biotechnologies, Inc., P.O. Box 430021, Cahaba Heights, AL 35243, USA. Electronic address: DeCarlo@agentabiotechnologies.com.
Agenta Biotechnologies (United States) · USUNSW Sydney · AU

Funding

Molecular Heparan Sulfate Delivery in Guided Tissue RegenerationR44DE017254 · NIDCR · AGENTA BIOTECHNOLOGIES, INC. · PI DECARLO, ARTHUR A · 2009 to 2010
$1.1M
Molecular Delivery of Heparan Sulfate in Wound RegenerationR44DE016771 · NIDCR · AGENTA BIOTECHNOLOGIES, INC. · PI DECARLO, ARTHUR A · 2007 to 2008
$884k
DNA Pro-Drug Technology in Localized Wound Healing and Tissue RegenerationR43AR061204 · NIAMS · AGENTA BIOTECHNOLOGIES, INC. · PI DECARLO, ARTHUR A · 2011 to 2011
$157k
Molecular Heparan Sulfate Delivery in Wound RegenerationR43DE016771 · NIDCR · AGENTA BIOTECHNOLOGIES, INC. · PI DECARLO, ARTHUR A · 2005 to 2005
$115k
Molecular Heparan Sulfate Delivery in Guided Tissue RegenerationR43DE017254 · NIDCR · AGENTA BIOTECHNOLOGIES, INC. · PI DECARLO, ARTHUR A · 2007 to 2007
$94k
NIAMS NIH HHS R43 AR061204NIDCR NIH HHS R43 DE016771NIDCR NIH HHS R43 DE017254NIDCR NIH HHS R44 DE016771NIDCR NIH HHS R44 DE017254
6 · The paper itself

Abstract

The repair of dermal wounds, particularly in the diabetic population, poses a significant healthcare burden. The impaired wound healing of diabetic wounds is attributed to low levels of endogenous growth factors, including vascular endothelial growth factor (VEGF), that normally stimulate multiple phases of wound healing. In this study, chitosan scaffolds were prepared via freeze drying and loaded with plasmid DNA encoding perlecan domain I and VEGF189 and analyzed in vivo for their ability to promote dermal wound healing. The plasmid DNA encoding perlecan domain I and VEGF189 loaded scaffolds promoted dermal wound healing in normal and diabetic rats. This treatment resulted in an increase in the number of blood vessels and sub-epithelial connective tissue matrix components within the wound beds compared to wounds treated with chitosan scaffolds containing control DNA or wounded controls. These results suggest that chitosan scaffolds containing plasmid DNA encoding VEGF189 and perlecan domain I have the potential to induce angiogenesis and wound healing.

Indexed as

Neovascularization, PhysiologicWound HealingAnimalsChitosanDiabetes ComplicationsDNADrug Delivery SystemsDrug LiberationHeparan Sulfate ProteoglycansHumansMaleMechanical PhenomenaPlasmidsRats, Inbred LewSkinTissue ScaffoldsChitosanDNAHeparan Sulfate ProteoglycansperlecanVascular Endothelial Growth Factor AChitosanPerlecanProteoglycanSkin tissue engineeringVascular endothelial growth factorWound healing

Identifiers

PMID28189628
PMCPMC9727826
OpenAlexW2587100658

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.