Evidence map›Paper›PMID 29128533›Full record

ArticleActa biomaterialia2018

Fabrication of dense anisotropic collagen scaffolds using biaxial compression.

Jared L Zitnay, Shawn P Reese, Garvin Tran, Niloofar Farhang, Robert D Bowles, Jeffrey A Weiss

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Matrix anisotropy promotes angiogenesis in a density-dependent manner.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  7. Advances in Regenerative Sports Medicine Research.Frontiers in bioengineering and biotechnology · 2022
    Review
  8. Autograft Long Head Biceps Tendon Can Be Used as a Scaffold for Biologically Augmenting Rotator Cuff Repairs.Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Microfluidic fabrication of stable collagen microgels with aligned microstructure using flow-driven co-deposition and ionic gelation.Journal of micromechanics and microengineering : structures, devices, and systems · 2020
    Article
  15. Article
  16. Article
  17. Review
  18. Therapeutic potential of exosomes in rotator cuff tendon healing.Journal of bone and mineral metabolism · 2019
    Review
  19. [Research progress of scaffold materials for tissue engineered meniscus].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2019
    Article
  20. 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

6 authors at 1 institution in 1 country.

Jared L ZitnayDepartment of Bioengineering, University of Utah, United States; Scientific Computing and Imaging Institute, University of Utah, United States.
Shawn P ReeseDepartment of Bioengineering, University of Utah, United States; Scientific Computing and Imaging Institute, University of Utah, United States.
Garvin TranDepartment of Bioengineering, University of Utah, United States.
Niloofar FarhangDepartment of Bioengineering, University of Utah, United States.
Robert D BowlesDepartment of Bioengineering, University of Utah, United States; Department of Orthopaedics, University of Utah, United States.
Jeffrey A WeissDepartment of Bioengineering, University of Utah, United States; Scientific Computing and Imaging Institute, University of Utah, United States; Department of Orthopaedics, University of Utah, United States. Electronic address: jeff.weiss@utah.edu.
University of Utah · US

Funding

Origins of Elasticity/Viscoelasticity in Knee LigamentsR01AR047369 · NIAMS · UNIVERSITY OF UTAH · PI WEISS, JEFFREY A. · 2000 to 2014
$3.4M
Computational Framework for Multiscale Mechanics of Connective TissuesR01EB015133 · NIBIB · UNIVERSITY OF UTAH · PI WEISS, JEFFREY A. · 2012 to 2015
$1.0M
NCRR Confocal ProposalS10RR024761 · NCRR · UNIVERSITY OF UTAH · PI RODESCH, CHRISTOPHER K · 2008 to 2008
$475k
Functional cellular effects of 3D multiscale tissue structure, using tissue surrogate materialsF31EB023086 · NIBIB · UNIVERSITY OF UTAH · PI ZITNAY, JARED LOUIS · 2016 to 2018
$88k
NCRR NIH HHS S10 RR024761NIAMS NIH HHS R01 AR047369NIBIB NIH HHS F31 EB023086NIBIB NIH HHS R01 EB015133
6 · The paper itself

Abstract

We developed a new method to manufacture dense, aligned, and porous collagen scaffolds using biaxial plastic compression of type I collagen gels. Using a novel compression apparatus that constricts like an iris diaphragm, low density collagen gels were compressed to yield a permanently densified, highly aligned collagen material. Micro-porosity scaffolds were created using hydrophilic elastomer porogens that can be selectively removed following biaxial compression, with porosity modulated by using different porogen concentrations. The resulting scaffolds exhibit collagen densities that are similar to native connective tissues (∼10% collagen by weight), pronounced collagen alignment across multiple length scales, and an interconnected network of pores, making them highly relevant for use in tissue culture, the study of physiologically relevant cell-matrix interactions, and tissue engineering applications. The scaffolds exhibited highly anisotropic material behavior, with the modulus of the scaffolds in the fiber direction over 100 times greater than the modulus in the transverse direction. Adipose-derived mesenchymal stem cells were seeded onto the biaxially compressed scaffolds with minimal cell death over seven days of culture, along with cell proliferation and migration into the pore spaces. This fabrication method provides new capabilities to manufacture structurally and mechanically relevant cytocompatible scaffolds that will enable more physiologically relevant cell culture studies. Further improvement of manufacturing techniques has the potential to produce engineered scaffolds for direct replacement of dense connective tissues such as meniscus and annulus fibrosus. STATEMENT OF SIGNIFICANCE: In vitro studies of cell-matrix interactions and the engineering of replacement materials for collagenous connective tissues require biocompatible scaffolds that replicate the high collagen density (15-25%/wt), aligned fibrillar organization, and anisotropic mechanical properties of native tissues. However, methods for creating scaffolds with these characteristics are currently lacking. We developed a new apparatus and method to create high density, aligned, and porous collagen scaffolds using a biaxial compression with porogens technique. These scaffolds have a highly directional structure and mechanical properties, with the tensile strength and modulus up to 100 times greater in the direction of alignment. We also demonstrated that the scaffolds are a suitable material for cell culture, promoting cell adhesion, viability, and an aligned cell morphology comparable to the cell morphology observed in native aligned tissues.

Indexed as

Biocompatible MaterialsCollagen Type IConnective TissueTissue ScaffoldsAdipose TissueAnisotropyCell AdhesionCells, CulturedCell SurvivalGelsHumansMesenchymal Stem CellsMicroscopy, Electron, ScanningPorosityTensile StrengthTissue EngineeringBiocompatible MaterialsCollagen Type IGelsAnnulus fibrosusCollagen scaffoldLigamentPlastic compressionTendonTissue engineering

Identifiers

PMID29128533
PMCPMC5716932
OpenAlexW2767335281

What OpenQuestion holds

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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.