Evidence map›Paper›PMID 27928031›Full record

ArticleJournal of the Royal Society, Interface2016

Multi-casting approach for vascular networks in cellularized hydrogels.

Alexander W Justin, Roger A Brooks, Athina E Markaki

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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.

Alexander W JustinDepartment of Engineering, University of Cambridge, Cambridge CB2 1PZ, UK.
Roger A BrooksDivision of Trauma and Orthopaedic Surgery, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
Athina E MarkakiDepartment of Engineering, University of Cambridge, Cambridge CB2 1PZ, UK am253@cam.ac.uk.ORCID 0000-0002-2265-1256

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascularization is essential for living tissue and remains a major challenge in the field of tissue engineering. A lack of a perfusable channel network within a large and densely populated tissue engineered construct leads to necrotic core formation, preventing fabrication of functional tissues and organs. We report a new method for producing a hierarchical, three-dimensional (3D) and perfusable vasculature in a large, cellularized fibrin hydrogel. Bifurcating channels, varying in size from 1 mm to 200-250 µm, are formed using a novel process in which we convert a 3D printed thermoplastic material into a gelatin network template, by way of an intermediate alginate hydrogel. This enables a CAD-based model design, which is highly customizable, reproducible, and which can yield highly complex architectures, to be made into a removable material, which can be used in cellular environments. Our approach yields constructs with a uniform and high density of cells in the bulk, made from bioactive collagen and fibrin hydrogels. Using standard cell staining and immuno-histochemistry techniques, we showed good cell seeding and the presence of tight junctions between channel endothelial cells, and high cell viability and cell spreading in the bulk hydrogel.

Indexed as

AlginatesCell SurvivalGelatinGlucuronic AcidHexuronic AcidsHumansHuman Umbilical Vein Endothelial CellsHydrogelsTissue ScaffoldsAlginatesGelatinGlucuronic AcidHexuronic AcidsHydrogelshydrogelthree-dimensional printingvascularizationvascular networks

Identifiers

PMID27928031
PMCPMC5221527

What OpenQuestion holds

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Registered trials

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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.