Evidence map›Paper›PMID 26928595›Full record

ArticleBiomaterials2016

Microscale characterization of the viscoelastic properties of hydrogel biomaterials using dual-mode ultrasound elastography.

Xiaowei Hong, Jan P Stegemann, Cheri X Deng

Abstract read
In one paragraph

Article in Biomaterials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. iMaterials today. Bio · 2024
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Automated Compression Device for Viscoelasticity Imaging.IEEE transactions on bio-medical engineering · 2017
    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

3 authors.

Xiaowei HongDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109-2099, USA.
Jan P StegemannDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109-2099, USA. Electronic address: jpsteg@umich.edu.
Cheri X DengDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109-2099, USA. Electronic address: cxdeng@umich.edu.

Funding

Bone Regeneration Using Osteogenic and Vasculogenic Tissue ModulesR01AR062636 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI STEGEMANN, JAN P. · 2014 to 2018
$1.7M
Quantitative Ultrasound Imaging for Noninvasive Assessment of Engineered TissuesR21AR064041 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DENG, CHERI X, STEGEMANN, JAN P. · 2013 to 2014
$363k
NIAMS NIH HHS R01 AR062636NIAMS NIH HHS R01AR062636NIAMS NIH HHS R21 AR064041NIAMS NIH HHS R21AR064041
6 · The paper itself

Abstract

Characterization of the microscale mechanical properties of biomaterials is a key challenge in the field of mechanobiology. Dual-mode ultrasound elastography (DUE) uses high frequency focused ultrasound to induce compression in a sample, combined with interleaved ultrasound imaging to measure the resulting deformation. This technique can be used to non-invasively perform creep testing on hydrogel biomaterials to characterize their viscoelastic properties. DUE was applied to a range of hydrogel constructs consisting of either hydroxyapatite (HA)-doped agarose, HA-collagen, HA-fibrin, or preosteoblast-seeded collagen constructs. DUE provided spatial and temporal mapping of local and bulk displacements and strains at high resolution. Hydrogel materials exhibited characteristic creep behavior, and the maximum strain and residual strain were both material- and concentration-dependent. Burger's viscoelastic model was used to extract characteristic parameters describing material behavior. Increased protein concentration resulted in greater stiffness and viscosity, but did not affect the viscoelastic time constant of acellular constructs. Collagen constructs exhibited significantly higher modulus and viscosity than fibrin constructs. Cell-seeded collagen constructs became stiffer with altered mechanical behavior as they developed over time. Importantly, DUE also provides insight into the spatial variation of viscoelastic properties at sub-millimeter resolution, allowing interrogation of the interior of constructs. DUE presents a novel technique for non-invasively characterizing hydrogel materials at the microscale, and therefore may have unique utility in the study of mechanobiology and the characterization of hydrogel biomaterials.

Indexed as

AnimalsBiocompatible MaterialsCell LineCollagenDurapatiteElasticityElasticity Imaging TechniquesEquipment DesignFibrinHydrogelsMaterials TestingMiceSepharoseViscoelastic SubstancesViscosityBiocompatible MaterialsCollagenDurapatiteFibrinHydrogelsSepharoseViscoelastic SubstancesAcoustic radiation forceElastographyMechanical characterizationProtein hydrogelsTissue engineeringViscoelasticity

Identifiers

PMID26928595
PMCPMC4792732

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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.