Evidence map›Paper›PMID 25433604›Full record

ArticleBiomaterials2015

Characterization of sequential collagen-poly(ethylene glycol) diacrylate interpenetrating networks and initial assessment of their potential for vascular tissue engineering.

Dany J Munoz-Pinto, Andrea Carolina Jimenez-Vergara, Tanmay P Gharat, Mariah S Hahn

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
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  13. Challenges and strategies forBioactive materials · 2021
    Review
  14. Article
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  17. Article
  18. 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.

Dany J Munoz-PintoDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, 110 8th Street Troy, NY, 12180, USA.
Andrea Carolina Jimenez-VergaraDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, 110 8th Street Troy, NY, 12180, USA.
Tanmay P GharatDepartment of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, 110 8th Street Troy, NY, 12180, USA.
Mariah S HahnDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, 110 8th Street Troy, NY, 12180, USA. Electronic address: hahnm@rpi.edu.
Rensselaer Polytechnic Institute · US

Funding

MULTILAYER VASCULAR GRAFTS BASED ON COLLAGEN-MIMETIC HYDROGELSR01EB013297 · NIBIB · TEXAS ENGINEERING EXPERIMENT STATION · PI HAHN, MARIAH S, MAITLAND, DUNCAN J · 2012 to 2015
$1.2M
Generating Vascular Graft Luminal and Medial Layers Based on Multipotent Stem CelR03EB015167 · NIBIB · RENSSELAER POLYTECHNIC INSTITUTE · PI HAHN, MARIAH S · 2013 to 2014
$158k
NIBIB NIH HHS R01 EB013297NIBIB NIH HHS R03 EB015167NIBIB NIH HHS R03 EB0152167
6 · The paper itself

Abstract

Collagen hydrogels have been widely investigated as scaffolds for vascular tissue engineering due in part to the capacity of collagen to promote robust cell adhesion and elongation. However, collagen hydrogels display relatively low stiffness and strength, are thrombogenic, and are highly susceptible to cell-mediated contraction. In the current work, we develop and characterize a sequentially-formed interpenetrating network (IPN) that retains the benefits of collagen, but which displays enhanced mechanical stiffness and strength, improved thromboresistance, high physical stability and resistance to contraction. In this strategy, we first form a collagen hydrogel, infuse this hydrogel with poly(ethylene glycol) diacrylate (PEGDA), and subsequently crosslink the PEGDA by exposure to longwave UV light. These collagen-PEGDA IPNs allow for cell encapsulation during the fabrication process with greater than 90% cell viability via inclusion of cells within the collagen hydrogel precursor solution. Furthermore, the degree of cell spreading within the IPNs can be tuned from rounded to fully elongated by varying the time delay between the formation of the cell-laden collagen hydrogel and the formation of the PEGDA network. We also demonstrate that these collagen-PEGDA IPNs are able to support the initial stages of smooth muscle cell lineage progression by elongated human mesenchymal stems cells.

Indexed as

Blood Vessel ProsthesisTissue EngineeringAnimalsCell LineageCell ShapeCell SurvivalCollagenGene Expression RegulationHumansMaterials TestingMesenchymal Stem CellsMolecular WeightMyocytes, Smooth MusclePhenotypePolyethylene GlycolsRatsCollagenpoly(ethylene glycol)diacrylatePolyethylene GlycolsCollagen hydrogelInterpenetrating networksMesenchymal stem cellsPoly(ethylene glycol) diacrylate hydrogelVascular tissue engineering

Identifiers

PMID25433604
PMCPMC5469296
OpenAlexW2067716485

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.