Evidence map›Paper›PMID 41919637›Full record

ArticleBioMed research international2026

Comparative Biocompatibility of Portland-Based Endodontic Cements Containing Niobium and/or Bismuth Oxides in Rat Subcutaneous Tissue.

Raphael Victor Silva Andrade, Rafaela Alcindo Silva de Souza Fé, Vladimir Galdino Sabino, Carlos Augusto Galvão Barboza, Maria Luiza Diniz de Sousa Lopes, Nizyara Costa da Silva, Valkleidson Santos de Araujo, Amanda Silveira da Silva, Raimundo Fernandes de Araujo Junior, Naianne Kelly Clebis and 4 more

Abstract readComparative Study
In one paragraph

Article in BioMed research international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

Raphael Victor Silva AndradeDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0003-4196-4263
Rafaela Alcindo Silva de Souza FéDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0002-5123-0741
Vladimir Galdino SabinoDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0003-0804-0675
Carlos Augusto Galvão BarbozaDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0003-1979-9919
Maria Luiza Diniz de Sousa LopesDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0001-6894-1366
Nizyara Costa da SilvaDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0009-0000-4209-2984
Valkleidson Santos de AraujoDepartment of Dentistry, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0001-8613-9537
Amanda Silveira da SilvaDepartment of Pharmaceutical Sciences, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0009-0001-6727-6816
Raimundo Fernandes de Araujo JuniorDepartment of Morphology, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0003-2349-2354
Naianne Kelly ClebisDepartment of Morphology, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0002-1749-7565
Isadora Luisa Gomes da SilvaDepartment of Morphology, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0009-0009-8422-6712
Pedro Catalão MouraLaboratory of Instrumentation, Biomedical Engineering and Radiation Physics (LA-REAL), NOVA School of Science and Technology, Caparica, Portugal.ORCID https://orcid.org/0000-0001-7008-3401
Sofia PessanhaLaboratory of Instrumentation, Biomedical Engineering and Radiation Physics (LA-REAL), NOVA School of Science and Technology, Caparica, Portugal.ORCID https://orcid.org/0000-0002-6039-2494
Aurigena Antunes de AraújoDepartment of Biophysics and Pharmacology, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil, ufrn.br.ORCID https://orcid.org/0000-0001-9264-4695

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303915/2023-4Conselho Nacional de Desenvolvimento Científico e Tecnológico 401672/2023-9iCEIS 406264/2022-8
6 · The paper itself

Abstract

objectivesTo evaluate the in vitro cytocompatibility and osteogenic potential and the in vivo biocompatibility of two experimental endodontic cements based on Portland cement combined with either Nb2O

methodsFor the in vitro study, MC3T3-E1 preosteoblastic cells were exposed to MTA Angelus, F6, or F7, and cell viability was assessed at 24 and 48 h using the Alamar Blue assay. Osteogenic differentiation was evaluated by alkaline phosphatase (ALP) activity after 14 days. For the in vivo analysis, polyethylene tubes containing the materials were implanted into the dorsal subcutaneous tissue of rats and evaluated at 7, 14, and 30 days, with empty tubes used as controls. Histological and histochemical analyses included hematoxylin and eosin (H&E), Picrosirius Red, Von Kossa staining, and TNF-α immunohistochemistry. Chemical characterization was performed using Raman spectroscopy and X-ray fluorescence (XRF). In vitro data were analyzed using one-way ANOVA followed by Tukey's post hoc test, while semiquantitative histological data were analyzed using the Kruskal-Wallis test followed by Dunn's test. A significance level of 5% (p < 0.05) was adopted.

resultsIn vitro, F6 showed cell viability comparable to MTA Angelus at both 24 h (36.22 ± 2.66% vs. 35.75 ± 1.18%) and 48 h (34.18 ± 3.09% vs. 35.20 ± 2.35%) (p > 0.05). In contrast, F7 significantly reduced cell viability at 24 h (25.61 ± 1.11%) compared with MTA Angelus (p = 0.002), although no difference was observed at 48 h (p > 0.05). ALP activity after 14 days did not differ significantly among MTA Angelus (1.90 ± 1.23 UI/L/g), F6 (1.71 ± 0.88 UI/L/g), and F7 (1.78 ± 1.34 UI/L/g) (p = 0.703). In vivo, F6 induced mild to moderate inflammatory responses at the early time period, with a significant reduction by Day 14 and minimal inflammation at Day 30, comparable to MTA Angelus. No multinucleated giant cells were observed, and TNF-α expression was moderate. Von Kossa staining and XRF confirmed calcium deposition, while Raman spectroscopy detected niobium species in peri-implant tissues, indicating bioactivity. Picrosirius Red staining demonstrated progressive collagen fiber organization. Conversely, F7 elicited a pronounced and persistent inflammatory response characterized by multinucleated giant cells, intense TNF-α expression, and bismuth retention in surrounding tissues, as confirmed by XRF, with no niobium-related signals detected by Raman analysis.

conclusionThe niobium-containing cement (F6) demonstrated favorable in vitro cytocompatibility and in vivo biocompatibility.

Indexed as

Biocompatible MaterialsBismuthDental CementsNiobiumOxidesSubcutaneous TissueAluminum CompoundsAnimalsCalcium CompoundsCell DifferentiationCell LineCell SurvivalDrug CombinationsMaleMaterials TestingMiceAluminum CompoundsBiocompatible MaterialsBismuthbismuth oxideCalcium CompoundsDental CementsDrug Combinationsmineral trioxide aggregateNiobiumOxidesSilicatesanimal modelsbiocompatible materialscell viabilityendodontic materialsinflammationsubcutaneous tissue

Identifiers

PMID41919637
PMCPMC13042350

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