Evidence map›Paper›PMID 25311685›Full record

ArticleActa biomaterialia2015

Geometric characterization and simulation of planar layered elastomeric fibrous biomaterials.

James B Carleton, Antonio D'Amore, Kristen R Feaver, Gregory J Rodin, Michael S Sacks

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
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.

James B CarletonCenter for Cardiovascular Simulation, Institute for Computational and Engineering Sciences, Department of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA.
Antonio D'AmoreMcGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Kristen R FeaverCenter for Cardiovascular Simulation, Institute for Computational and Engineering Sciences, Department of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA.
Gregory J RodinCenter for Cardiovascular Simulation, Institute for Computational and Engineering Sciences, Department of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA; Department of Aerospace Engineering and Engineering Mechanics, University of Texas at Austin, TX 78712, USA.
Michael S SacksCenter for Cardiovascular Simulation, Institute for Computational and Engineering Sciences, Department of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA. Electronic address: msacks@ices.utexas.edu.
The University of Texas at Austin · USMcGowan Institute for Regenerative Medicine · US

Funding

Biomechanical Optimization of TE Heart ValvesR01HL068816 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WAGNER, WILLIAM R · 2002 to 2011
$3.1M
Mechanisms of In-Vivo Remodeling in Tissue Engineered Heart ValvesR01HL089750 · NHLBI · UNIVERSITY OF TEXAS AT AUSTIN · PI SACKS, MICHAEL S · 2007 to 2010
$3.1M
Comprehensive Training Program in Imaging Science and InformaticsT32EB007507 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI MARKEY, MIA K, RYLANDER, HENRY GRADY · 2009 to 2024
$2.7M
NHLBI NIH HHS R01 HL068816NHLBI NIH HHS R01 HL089750NHLBI NIH HHS R01 HL68816NIBIB NIH HHS T32 EB007507
6 · The paper itself

Abstract

Many important biomaterials are composed of multiple layers of networked fibers. While there is a growing interest in modeling and simulation of the mechanical response of these biomaterials, a theoretical foundation for such simulations has yet to be firmly established. Moreover, correctly identifying and matching key geometric features is a critically important first step for performing reliable mechanical simulations. The present work addresses these issues in two ways. First, using methods of geometric probability, we develop theoretical estimates for the mean linear and areal fiber intersection densities for 2-D fibrous networks. These densities are expressed in terms of the fiber density and the orientation distribution function, both of which are relatively easy-to-measure properties. Secondly, we develop a random walk algorithm for geometric simulation of 2-D fibrous networks which can accurately reproduce the prescribed fiber density and orientation distribution function. Furthermore, the linear and areal fiber intersection densities obtained with the algorithm are in agreement with the theoretical estimates. Both theoretical and computational results are compared with those obtained by post-processing of scanning electron microscope images of actual scaffolds. These comparisons reveal difficulties inherent to resolving fine details of multilayered fibrous networks. The methods provided herein can provide a rational means to define and generate key geometric features from experimentally measured or prescribed scaffold structural data.

Indexed as

Biocompatible MaterialsElastomersAlgorithmsMicroscopy, Electron, ScanningBiocompatible MaterialsElastomersElectrospunFiber geometryMicromechanicsScaffoldsSimulation

Identifiers

PMID25311685
PMCPMC4274256
OpenAlexW2092290563

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.