Evidence map›Paper›PMID 33332959›Full record

ArticleBiomacromolecules2021

Engineering a Chemically Defined Hydrogel Bioink for Direct Bioprinting of Microvasculature.

Ryan W Barrs, Jia Jia, Michael Ward, Dylan J Richards, Hai Yao, Michael J Yost, Ying Mei

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

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  6. Biofabrication of engineered blood vessels for biomedical applications.Science and technology of advanced materials · 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.

Ryan W BarrsDepartment of Bioengineering, Clemson University, Clemson, South Carolina 29634-0002, United States.
Jia JiaDepartment of Bioengineering, Clemson University, Clemson, South Carolina 29634-0002, United States.
Michael WardDepartment of Bioengineering, Clemson University, Clemson, South Carolina 29634-0002, United States.
Dylan J RichardsDepartment of Bioengineering, Clemson University, Clemson, South Carolina 29634-0002, United States.
Hai YaoDepartment of Bioengineering, Clemson University, Clemson, South Carolina 29634-0002, United States.
Michael J YostDepartment of Surgery, Medical University of South Carolina, Charleston, South Carolina 29425, United States.
Ying MeiDepartment of Bioengineering, Clemson University, Clemson, South Carolina 29634-0002, United States.ORCID 0000-0002-8508-4076
Clemson University · USMedical University of South Carolina · US

Funding

Targeted Nano-therapeutics for Neural RegenerationP20GM103444 · NIGMS · CLEMSON UNIVERSITY · PI MARKWALD, ROGER R, VYAVAHARE, NAREN R · 2012 to 2018
$14.9M
Nanowired human cardiac spheroids for heart repairR01HL133308 · NHLBI · CLEMSON UNIVERSITY · PI MEI, YING · 2017 to 2020
$1.5M
NHLBI NIH HHS R01 HL133308NIGMS NIH HHS P20 GM103444
6 · The paper itself

Abstract

Vascularizing printed tissues is a critical challenge in bioprinting. While protein-based hydrogel bioinks have been successfully used to bioprint microvasculature, their compositions are ill-defined and subject to batch variation. Few studies have focused on engineering proangiogenic bioinks with defined properties to direct endogenous microvascular network formation after printing. Here, a peptide-functionalized alginate hydrogel bioink with defined mechanical, rheological, and biochemical properties is developed for direct bioprinting of microvascularized tissues. An integrin-binding peptide (RGD) and a vascular endothelial growth factor-mimetic peptide with a protease-sensitive linker are conjugated onto a biodegradable alginate to synergistically promote vascular morphogenesis and capillary-scale endothelial tube formation. Partial ionic crosslinking before printing converts the otherwise unprintable hydrogel into a viscoelastic bioink with excellent printability and cytocompatibility. We use the bioink to fabricate a compartmentalized vascularized tissue construct, wherein we observe pericyte-endothelial cell colocalization and angiogenic sprouting across a tissue interface, accompanied by deposition of fibronectin and collagen in vascular and tissue components, respectively. This study provides a tunable and translational "off-the-shelf" hydrogel bioink with defined composition for vascularized bioprinting.

Indexed as

BioprintingHydrogelsMicrovesselsPrinting, Three-DimensionalTissue EngineeringTissue ScaffoldsVascular Endothelial Growth Factor AHydrogelsVascular Endothelial Growth Factor A

Identifiers

PMID33332959
PMCPMC7870577
OpenAlexW3114168606

What OpenQuestion holds

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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.