Evidence map›Paper›PMID 31956985›Full record

ArticleBiotechnology and bioengineering2020

Tissue scaffolds functionalized with therapeutic elastin-like biopolymer particles.

Beyza Bulutoglu, Julie Devalliere, Sarah L Deng, Aylin Acun, Sarah S Kelangi, Basak E Uygun, Martin L Yarmush

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

7 authors at 2 institutions in 1 country.

Beyza BulutogluCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.ORCID 0000-0002-4435-413X
Julie DevalliereCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.ORCID 0000-0001-6935-5561
Sarah L DengCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.
Aylin AcunCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.ORCID 0000-0001-5915-1848
Sarah S KelangiCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.
Basak E UygunCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.ORCID 0000-0002-2600-7900
Martin L YarmushCenter for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts.ORCID 0000-0003-4986-8444
Shriners Hospitals for Children - Erie · USRutgers, The State University of New Jersey · US

Funding

Multifunctional Nanoparticles Containing sRAGE Potentiated Bioactive Peptides for Wound HealingR21EB021570 · NIBIB · RUTGERS, THE STATE UNIV OF N.J. · PI BERTHIAUME, FRANCOIS, YARMUSH, MARTIN L · 2016 to 2017
$442k
Bioactive Nanoparticles for Improved Healing in Chronic WoundsF32EB026916 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI BULUTOGLU, BEYZA · 2018 to 2018
$63k
NIBIB NIH HHS F32 EB026916NIBIB NIH HHS R21 EB021570Shriners Hospitals for Children 84295Shriners Hospitals for Children 84311Shriners Hospitals for Children 85105Shriners Hospitals for Children 85210
6 · The paper itself

Abstract

Tissue engineering scaffolds are intended to provide mechanical and biological support for cells to migrate, engraft and ultimately regenerate the tissue. Development of scaffolds with sustained delivery of growth factors and chemokines would enhance the therapeutic benefits, especially in wound healing. In this study, we incorporated our previously designed therapeutic particles, composed of fusion of elastin-like peptides (ELPs) as the drug delivery platform to keratinocyte growth factor (KGF), into a tissue scaffold, alloderm. The results demonstrated that sustained KGF-ELP release was achieved and the bioactivity of the released therapeutic particles was shown via cell proliferation assay, as well as a mouse pouch model in vivo, where higher cellular infiltration and vascularization were observed in scaffolds functionalized with KGF-ELPs.

Indexed as

AnimalsBiopolymersCell Line, TumorCell ProliferationCollagenElastinFibroblast Growth Factor 7HumansMiceNeovascularization, PhysiologicTissue EngineeringTissue ScaffoldsAllodermBiopolymersCollagenElastinFibroblast Growth Factor 7allodermelastin-like polypeptideskeratinocyte growth factormouse pouch modeltissue scaffolds

Identifiers

PMID31956985
PMCPMC7148187
OpenAlexW3002359566

What OpenQuestion holds

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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.