Evidence map›Paper›PMID 35520194›Full record

ArticleRSC advances2019

Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications.

Elisabetta Dattola, Elvira Immacolata Parrotta, Stefania Scalise, Gerardo Perozziello, Tania Limongi, Patrizio Candeloro, Maria Laura Coluccio, Carmine Maletta, Luigi Bruno, Maria Teresa De Angelis and 5 more

Abstract read
In one paragraph

Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
–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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Advances in Engineering Human Tissue Models.Frontiers in bioengineering and biotechnology · 2020
    Pooled it
  2. Stimuli-responsive hybrid materials for 4DMaterials today. Bio · 2025
    Review
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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

15 authors.

Elisabetta DattolaDepartment of Health Sciences, University of Magna Graecia 88100 Catanzaro Italy elisabettadattola@gmail.com +39-3202851897.ORCID https://orcid.org/0000-0003-2116-7865
Elvira Immacolata ParrottaResearch Center for Advanced Biochemistry and Molecular Biology, Stem Cell Laboratory, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro 88100 Loc. Germaneto Catanzaro Italy.
Stefania ScaliseResearch Center for Advanced Biochemistry and Molecular Biology, Stem Cell Laboratory, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro 88100 Loc. Germaneto Catanzaro Italy.
Gerardo PerozzielloBioNEM (Bio and Nano Engineering and Technology for Medicine) Laboratory, Department of Experimental and Clinical Medicine, University of Magna Graecia 88100 Catanzaro Italy.
Tania LimongiSMILEs Lab, Physical Science and Engineering (PSE), Biological and Environmental Science and Engineering (BESE) Divisions, King Abdullah University of Science and Technology Thuwal 23955-6900 Kingdom of Saudi Arabia.
Patrizio CandeloroBioNEM (Bio and Nano Engineering and Technology for Medicine) Laboratory, Department of Experimental and Clinical Medicine, University of Magna Graecia 88100 Catanzaro Italy.
Maria Laura ColuccioBioNEM (Bio and Nano Engineering and Technology for Medicine) Laboratory, Department of Experimental and Clinical Medicine, University of Magna Graecia 88100 Catanzaro Italy.
Carmine MalettaDIMEG (Department of Mechanical, Energy and Management Engineering), University of Calabria 87036 Rende CS Italy.ORCID https://orcid.org/0000-0002-9204-5358
Luigi BrunoDIMEG (Department of Mechanical, Energy and Management Engineering), University of Calabria 87036 Rende CS Italy.
Maria Teresa De AngelisResearch Center for Advanced Biochemistry and Molecular Biology, Stem Cell Laboratory, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro 88100 Loc. Germaneto Catanzaro Italy.
Gianluca SantamariaResearch Center for Advanced Biochemistry and Molecular Biology, Stem Cell Laboratory, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro 88100 Loc. Germaneto Catanzaro Italy.ORCID https://orcid.org/0000-0001-9284-7492
Vincenzo MollaceDepartment of Health Sciences, University of Magna Graecia 88100 Catanzaro Italy elisabettadattola@gmail.com +39-3202851897.
Ernesto LamannaDepartment of Health Sciences, University of Magna Graecia 88100 Catanzaro Italy elisabettadattola@gmail.com +39-3202851897.
Enzo Di FabrizioSMILEs Lab, Physical Science and Engineering (PSE), Biological and Environmental Science and Engineering (BESE) Divisions, King Abdullah University of Science and Technology Thuwal 23955-6900 Kingdom of Saudi Arabia.ORCID https://orcid.org/0000-0001-5886-4678
Giovanni CudaResearch Center for Advanced Biochemistry and Molecular Biology, Stem Cell Laboratory, Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro 88100 Loc. Germaneto Catanzaro Italy.ORCID https://orcid.org/0000-0001-6313-1866

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was the design of a 3D scaffold composed of poly(vinyl) alcohol (PVA) for cardiac tissue engineering (CTE) applications. The PVA scaffold was fabricated using a combination of gas foaming and freeze-drying processes that did not need any cross-linking agents. We obtained a biocompatible porous matrix with excellent mechanical properties. We measured the stress-strain curves of the PVA scaffolds and we showed that the elastic behavior is similar to that of the extracellular matrix of muscles. The SEM observations revealed that the scaffolds possess micro pores having diameters ranging from 10 μm to 370 μm that fit to the dimensions of the cells. A further purpose of this study was to test scaffolds ability to support human induced pluripotent stem cells growth and differentiation into cardiomyocytes. As the proliferation tests show, the number of live stem cells on the scaffold after 12 days was increased with respect to the initial number of cells, revealing the cytocompatibility of the substrate. In addition, the differentiated cells on the PVA scaffolds expressed anti-troponin T, a marker specific of the cardiac sarcomere. We demonstrated the ability of the cardiomyocytes to pulse within the scaffolds. In conclusion, the developed scaffold show the potential to be used as a biomaterial for CTE applications.

Identifiers

PMID35520194
PMCPMC9060459

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.