Evidence map›Paper›PMID 27117793›Full record

ArticleJournal of materials science. Materials in medicine2016

Vasculogenic potential evaluation of bottom-up, PCL scaffolds guiding early angiogenesis in tissue regeneration.

L Rossi, C Attanasio, E Vilardi, M De Gregorio, P A Netti

Abstract read
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In one paragraph

Article in Journal of materials science. Materials in medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

L RossiCenter for Advanced Biomaterials for Health Care, IIT@CRIB, Istituto Italiano di Tecnologia, 80125, Naples, Italy. l.rossi@unina.it.
C AttanasioCenter for Advanced Biomaterials for Health Care, IIT@CRIB, Istituto Italiano di Tecnologia, 80125, Naples, Italy.
E VilardiCenter for Advanced Biomaterials for Health Care, IIT@CRIB, Istituto Italiano di Tecnologia, 80125, Naples, Italy.
M De GregorioCenter for Advanced Biomaterials for Health Care, IIT@CRIB, Istituto Italiano di Tecnologia, 80125, Naples, Italy.
P A NettiCenter for Advanced Biomaterials for Health Care, IIT@CRIB, Istituto Italiano di Tecnologia, 80125, Naples, Italy.
Center for Advanced Biomaterials for Healthcare · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascularization is a key factor in the successful integration of tissue engineered (TE) grafts inside the host body. Biological functions of the newly formed tissue depend, in fact, on a reliable and fast spread of the vascular network inside the scaffold. In this study, we propose a technique for evaluating vascularization in TE constructs assembled by a bottom-up approach. The rational, ordered assembly of building blocks (BBs) into a 3D scaffold can improve vessel penetration, and-unlike most current technologies-is compatible with the insertion of different elements that can be designed independently (e.g. structural units, growth factor depots etc.). Poly(ε-caprolactone) scaffolds composed of orderly and randomly assembled sintered microspheres were used to assess the degree of vascularization in a pilot in vivo study. Scaffolds were implanted in a rat subcutaneous pocket model, and retrieved after 7 days. We introduce three quantitative factors as a measure of vascularization: the total percentage of vascularization, the vessels diameter distribution and the vascular penetration depth. These parameters were derived by image analysis of microcomputed tomographic scans of biological specimens perfused with a radiopaque polymer. The outcome of this study suggests that the rational assembly of BBs helps the onset and organization of a fully functional vascular network.

Indexed as

Guided Tissue RegenerationTissue ScaffoldsAnimalsCell AdhesionCells, CulturedEndothelial CellsHumansMaterials TestingNeovascularization, PhysiologicPolyestersRatspolycaprolactonePolyesters

Identifiers

PMID27117793
OpenAlexW2342950640

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.