Evidence map›Paper›PMID 30604611›Full record

ArticleACS applied materials & interfaces2019

Fibrin Nanoparticles Coupled with Keratinocyte Growth Factor Enhance the Dermal Wound-Healing Rate.

Ismaeel Muhamed, Erin P Sproul, Frances S Ligler, Ashley C Brown

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 49 citations in OpenAlex.

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  16. Fibrin-based Bioinks: New Tricks from an Old Dog.International journal of bioprinting · 2020
    Review
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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 at 1 institution in 1 country.

Ismaeel MuhamedJoint Department of Biomedical Engineering , North Carolina State University and University of North Carolina at Chapel Hill , Raleigh 27695 , North Carolina , United States.
Erin P SproulJoint Department of Biomedical Engineering , North Carolina State University and University of North Carolina at Chapel Hill , Raleigh 27695 , North Carolina , United States.
Frances S LiglerJoint Department of Biomedical Engineering , North Carolina State University and University of North Carolina at Chapel Hill , Raleigh 27695 , North Carolina , United States.
Ashley C BrownJoint Department of Biomedical Engineering , North Carolina State University and University of North Carolina at Chapel Hill , Raleigh 27695 , North Carolina , United States.ORCID http://orcid.org/0000-0001-6995-1785
University of North Carolina at Chapel Hill · US

Funding

American Heart Association-American Stroke Association 16SDG29870005
6 · The paper itself

Abstract

Expediting the wound-healing process is critical for patients chronically ill from nonhealing wounds and diseases such as hemophilia or diabetes or who have suffered trauma including easily infected open wounds. FDA-approved external tissue sealants include the topical application of fibrin gels, which can be 500 times denser than natural fibrin clots. With lower clot porosity and higher polymerization rates than physiologically formed fibrin clots, the commercial gels quickly stop blood loss but impede the later clot degradation kinetics and thus retard tissue-healing rates. The fibrin nanoparticles (FBNs) described here are constructed from physiologically relevant fibrin concentrations that support new tissue and dermal wound scaffold formation when coupled with growth factors. The FBNs, synthesized in a microfluidic droplet generator, support cell adhesion and traction generation, and when coupled to keratinocyte growth factor (KGF), support cell migration and in vivo wound healing. The FBN-KGF particles enhance cell migration in vitro greater than FBN alone or free KGF and also improve healing outcomes in a murine full thickness injury model compared to saline, bulk fibrin sealant, free KGF, or bulk fibrin mixed with KGF treatments. Furthermore, FBN can be potentially administered with other tissue-healing factors and inflammatory mediators to improve wound-healing outcomes.

Indexed as

AnimalsBiocompatible MaterialsCell MovementFibrinFibroblast Growth Factor 7MiceMicrofluidicsNanoparticlesWound HealingBiocompatible MaterialsFibrinFibroblast Growth Factor 7biomaterialscell migrationfibrin nanoparticlesin vitro 3D wound model and in vivo dermal wound modelmicrofluidicstissue regenerationwound healing

Identifiers

PMID30604611
PMCPMC13049699
OpenAlexW2908225639

What OpenQuestion holds

Textmetadata
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.