Evidence map›Paper›PMID 30419146›Full record

ArticleJournal of biomedical materials research. Part B, Applied biomaterials2019

Heart valve tissue-derived hydrogels: Preparation and characterization of mitral valve chordae, aortic valve, and mitral valve gels.

Jinglei Wu, Bryn Brazile, Sara R McMahan, Jun Liao, Yi Hong

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part B, Applied biomaterials, 2019. 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
1.4field-weighted citation impact, top 18% 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, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Biological Scaffolds for Congenital Heart Disease.Bioengineering (Basel, Switzerland) · 2023
    Review
  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

5 authors at 2 institutions in 1 country.

Jinglei WuDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76019.
Bryn BrazileDepartment of Biological Engineering, Mississippi State University, Starkville, Mississippi, 39762.
Sara R McMahanDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76019.
Jun LiaoDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76019.
Yi HongDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76019.
The University of Texas at Arlington · USMississippi State University · US

Funding

Bioactive injectable blends for cardiac stem cell recruitmentR15HL140503 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI HONG, YI · 2018 to 2018
$460k
Elastic printable biomaterials for 3-D bioprinting of vascular conduitR21HD090680 · NICHD · NORTHEASTERN UNIVERSITY · PI DAI, GUOHAO · 2017 to 2018
$425k
National Institute of Child Health and Human Development R21HD090680National Science Foundation, Division of Materials Research CAREER #1554835NHLBI NIH HHS R15 HL140503NHLBI NIH HHS R15HL140503NICHD NIH HHS R21 HD090680The University of Texas system STARs program
6 · The paper itself

Abstract

Heart valve (HV) diseases are among the leading causes of death and continue to threaten public health worldwide. The current clinical options for HV replacement include mechanical and biological prostheses. However, an ongoing problem with current HV prostheses is their failure to integrate with the host tissue and their inability grow and remodel within the body. Tissue engineered heart valves (TEHVs) are a promising solution to these problems, as they are able to grow and remodel somatically with the rest of the body. Recently, decellularized HVs have demonstrated great potential as valve replacements because they are tissue specific, but recellularization is still a challenge due to the dense HV extracellular matrix (ECM) network. In this proof-of-concept work, we decellularized porcine mitral valve chordae, aortic valve leaflets, and mitral valve leaflets and processed them into injectable hydrogels that could accommodate any geometry. While the three valvular ECMs contained various amounts of collagen, they displayed similar glycosaminoglycan contents. The hydrogels had similar nanofibrous structures and gelation kinetics with various compressive strengths. When encapsulated with NIH 3 T3 fibroblasts, all the hydrogels supported cell survivals up to 7 days. Decellularized HV ECM hydrogels may show promising potential HV tissue engineering applications. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 107B: 1732-1740, 2019.

Indexed as

3T3 CellsAnimalsAortic ValveBiocompatible MaterialsCell ProliferationCollagenExtracellular MatrixGlycosaminoglycansHeart Valve ProsthesisHydrogelsImplants, ExperimentalInjectionsMiceMitral ValvePepsin ASwineBiocompatible MaterialsCollagenGlycosaminoglycansHydrogelsPepsin Adecellularizationextracellular matrixheart valveshydrogeltissue engineering

Identifiers

PMID30419146
PMCPMC6820138
OpenAlexW2900730176

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.