Evidence map›Paper›PMID 31127392›Full record

ArticleJournal of materials science. Materials in medicine2019

Influence of the incorporation of marine spongin into a Biosilicate®: an in vitro study.

K R Fernandes, J R Parisi, A M P Magri, H W Kido, P R Gabbai-Armelin, C A Fortulan, E D Zanotto, O Peitl, R N Granito, A C M Renno

Abstract read
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In one paragraph

Article in Journal of materials science. Materials in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

10 authors.

K R FernandesDepartment of Physiotherapy, Federal University of São Carlos (UFSCar), São Carlos, SP, Brazil. kellyrf10@yahoo.com.br.ORCID http://orcid.org/0000-0003-2851-6896
J R ParisiDepartment of Physiotherapy, Federal University of São Carlos (UFSCar), São Carlos, SP, Brazil.
A M P MagriDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, SP, Brazil.
H W KidoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, SP, Brazil.
P R Gabbai-ArmelinDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, SP, Brazil.
C A FortulanDepartment of Mechanical Engineering, São Carlos School of Engineering, São Carlos, SP, Brazil.
E D ZanottoDepartment of Materials Engineering, Vitreous Materials Laboratory (LaMaV), Federal University of São Carlos (UFSCar), São Carlos, SP, Brazil.
O PeitlDepartment of Materials Engineering, Vitreous Materials Laboratory (LaMaV), Federal University of São Carlos (UFSCar), São Carlos, SP, Brazil.
R N GranitoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, SP, Brazil.
A C M RennoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The combination of different biomaterials can be a promising intervention for the composites manufacture, mainly by adding functional and structural characteristics of each material and guarantee the advantages of the use of these composites. In this context, the aim of this study was to develop and evaluated the influence of the incorporation of marine spongin (SPG) into Biosilicate® (BS) in different proportions be used during bone repair. For this purpose, it was to develop and investigate different BS/SPG formulations for physico-chemical and morphological characteristics by pH, loss mass, Fourier transform infrared spectrometer (FTIR) and scanning electron microscope (SEM) analysis. Additionally, the influence of these composites on cell viability, proliferation, and alkaline phosphatase (ALP) activity were investigated. The results revealed that the pH values of all BS groups (with or without SPG) increased over time. A significant mass loss was observed in all composites, mainly with higher SPG percentages. Additionaly, SEM micrographies demonstrated fibers of SPG into BS and material degradation over time. Moreover, FTIR spectral analysis revealed characteristic peaks of PMMA, BS, and SPG in BS/SPG composites. BS/SPG groups demonstrated a positive effect for fibroblast proliferation after 3 and 7 days of culture. Additionally, BS and BS/SPG formulations (at 10% and 20% of SPG) presented similar values of osteoblasts viability and proliferation after 7 days of culture. Furthermore, ALP activity demonstrated no significant difference between BS and BS/SPG scaffolds, at any composition. Based on the present in vitro results, it can be concluded that the incorporation of SPG into BS was possible and produced an improvement in the physical-chemical characteristics and in the biological performance of the graft especially the formulation with 80/20 and 90/10. Future research should focus on in vivo evaluations of this novel composite.

Indexed as

3T3 CellsAlkaline PhosphataseAnimalsBiocompatible MaterialsBone SubstitutesCell LineCell ProliferationCell SurvivalGlassHydrogen-Ion ConcentrationMaterials TestingMiceMicroscopy, Electron, ScanningOsteoblastsPoriferaSpectroscopy, Fourier Transform InfraredAlkaline PhosphataseBiocompatible MaterialsBone Substitutessodium oxide-calcium oxide-silicon dioxide-diphosphorus pentoxide

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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.