Evidence map›Paper›PMID 30909819›Full record

ArticleTissue engineering. Part C, Methods2019

Fabrication and Characterization of Electrospun Decellularized Muscle-Derived Scaffolds.

Mollie M Smoak, Albert Han, Emma Watson, Alysha Kishan, K Jane Grande-Allen, Elizabeth Cosgriff-Hernandez, Antonios G Mikos

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part C, Methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 68 citations in OpenAlex.

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  11. Recent Advances in Scaffolds for Guided Bone Regeneration.Biomimetics (Basel, Switzerland) · 2024
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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

7 authors at 2 institutions in 1 country.

Mollie M Smoak1 Department of Bioengineering, Rice University, Houston, Texas.
Albert Han1 Department of Bioengineering, Rice University, Houston, Texas.
Emma Watson1 Department of Bioengineering, Rice University, Houston, Texas.
Alysha Kishan2 Department of Biomedical Engineering, University of Texas, Austin, Texas.
K Jane Grande-Allen1 Department of Bioengineering, Rice University, Houston, Texas.
Elizabeth Cosgriff-Hernandez2 Department of Biomedical Engineering, University of Texas, Austin, Texas.
Antonios G Mikos1 Department of Bioengineering, Rice University, Houston, Texas.
Rice University · USThe University of Texas at Austin · US

Funding

Training and Dissemination CoreP41EB023833 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI MIKOS, ANTONIOS G. · 2017 to 2021
$6.2M
"A Two-Stage High-Fidelity, Anti-Infective Approach to Craniofacial Repair in Novel Ovine Model"F31DE027586 · NIDCR · RICE UNIVERSITY · PI WATSON, EMMA · 2017 to 2019
$134k
NIBIB NIH HHS P41 EB023833NIDCR NIH HHS F31 DE027586
6 · The paper itself

Abstract

Although skeletal muscle has a high potential for self-repair, volumetric muscle loss can result in impairment beyond the endogenous regenerative capacity. There is a clinical need to improve on current clinical treatments that fail to fully restore the structure and function of lost muscle. Decellularized extracellular matrix (dECM) scaffolds have been an attractive platform for regenerating skeletal muscle, as dECM contains many biochemical cues that aid in cell adhesion, proliferation, and differentiation. However, there is limited capacity to tune physicochemical properties in current dECM technologies to improve outcome. In this study, we aim to create a novel, high-throughput technique to fabricate dECM scaffolds with tunable physicochemical properties while retaining proregenerative matrix components. We demonstrate a successful decellularization protocol that effectively removes DNA. We also identified key steps for the successful production of electrospun muscle dECM without the use of a carrier polymer; electrospinning allows for rapid scaffold fabrication with high control over material properties, which can be optimized to mimic native muscle. To this end, fiber orientation and degree of crosslinking of these dECM scaffolds were modulated and the corollary effects on fiber swelling, mechanical properties, and degradation kinetics were investigated. Beyond application in skeletal muscle, the versatility of this technology has the potential to serve as a foundation for dECM scaffold fabrication in a variety of tissue engineering applications.

Indexed as

AnimalsExtracellular MatrixKineticsMaleMaterials TestingMusclesPorosityRabbitsTensile StrengthTissue EngineeringTissue Scaffoldsdecellularized muscleelectrospinningextracellular matrixskeletal muscle

Identifiers

PMID30909819
PMCPMC6535957
OpenAlexW2924549136

What OpenQuestion holds

Textmetadata
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.