Evidence map›Paper›PMID 32696261›Full record

ReviewJournal of materials science. Materials in medicine2020

Natural hydrogels R&D process: technical and regulatory aspects for industrial implementation.

Marta Calvo Catoira, Javier González-Payo, Luca Fusaro, Martina Ramella, Francesca Boccafoschi

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of materials science. Materials in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

40 citing papers in PubMed, 58 citations in OpenAlex.

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  19. Dynamic Hydrogels in Breast Tumor Models.Gels (Basel, Switzerland) · 2025
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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 3 countries.

Marta Calvo CatoiraCenter for Translational Research on Autoimmune & Allergic Diseases-CAAD, 28100, Novara, Italy.ORCID http://orcid.org/0000-0002-2027-6552
Javier González-PayoTelecomunicación, Department of Signal Theory and Communications, University of Vigo, 36310, Vigo, Spain.ORCID http://orcid.org/0000-0003-4783-2595
Luca FusaroTissuegraft srl, 28100, Novara, Italy.ORCID http://orcid.org/0000-0002-2416-9770
Martina RamellaTissuegraft srl, 28100, Novara, Italy.ORCID http://orcid.org/0000-0003-3681-2847
Francesca BoccafoschiCenter for Translational Research on Autoimmune & Allergic Diseases-CAAD, 28100, Novara, Italy. francesca.boccafoschi@med.uniupo.it.ORCID http://orcid.org/0000-0002-6734-5447
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversidade de Vigo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since hydrogel therapies have been introduced into clinic treatment procedures, the biomedical industry has to face the technology transfer and the scale-up of the processes. This will be key in the roadmap of the new technology implementation. Transfer technology and scale-up are already known for some applications but other applications, such as 3D printing, are still challenging. Decellularized tissues offer a lot of advantages when compared to other natural gels, for example they display enhanced biological properties, due to their ability to preserve natural molecules. For this reason, even though their use as a source for bioinks represents a challenge for the scale-up process, it is very important to consider the advantages that originate with overcoming this challenge. Therefore, many aspects that influence the scaling of the industrial process should be considered, like the addition of drugs or cells to the hydrogel, also, the gelling process is important to determine the chemical and physical parameters that must be controlled in order to guarantee a successful process. Legal aspects are also crucial when carrying out the scale-up of the process since they determine the industrial implementation success from the regulatory point of view. In this context, the new law Regulation (EU) 2017/745 on biomedical devices will be considered. This review summarizes the different aspects, including the legal ones, that should be considered when scaling up hydrogels of natural origin, in order to balance these different aspects and to optimize the costs in terms of raw materials and engine.

Indexed as

Biomedical ResearchBiocompatible MaterialsBiological ProductsBiomedical TechnologyCross-Linking ReagentsHumansHydrogelsMedical Device LegislationPolymerizationPrinting, Three-DimensionalResearchBiocompatible MaterialsBiological ProductsCross-Linking ReagentsHydrogels

Identifiers

PMID32696261
PMCPMC7374448
OpenAlexW3045296238

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.