Evidence map›Paper›PMID 41081944›Full record

ArticleClinical oral investigations2025

Antimicrobial, toxicity, and cellular interactions of bioceramic sealers in periodontal ligament: in vitro insights.

Raquel Figuerêdo Ramos, Johnny Carvalho da Silva, Maria Ester França de Melo, Larissa Barbosa de Sousa, Mayara Alves de Oliveira, Elizabete Cristina Iseke Bispo, Rosiane Andrade Costa, Danilo César Mota Martins, Amandda Évelin Silva-Carvalho, Eliete Neves Silva Guerra and 2 more

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Article in Clinical oral investigations, 2025. 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. Review
  3. 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

12 authors.

Raquel Figuerêdo RamosPostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0009-0004-4942-2105
Johnny Carvalho da SilvaPostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0009-0007-1016-039X
Maria Ester França de MeloPostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0009-0002-4570-5955
Larissa Barbosa de SousaPostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0000-0002-6280-2282
Mayara Alves de OliveiraPostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0009-0004-2465-3484
Elizabete Cristina Iseke BispoPostgraduation Program in Pharmaceutical Science, University of Brasília, Brasília, Federal District, Brazil.ORCID 0009-0002-7593-1849
Rosiane Andrade CostaPostgradution in Genomic Sciences and Biotechnology, Catholic University of Brasília, QS 07, lot 01, Bloco-G, room G106.A, Taguatinga Sul - Taguatinga, Brasília, DF, Brazil.ORCID 0000-0002-1739-3731
Danilo César Mota MartinsGraduation in Dentistry, Catholic University of Brasília, QS 07, lot 01, Bloco S, Taguatinga Sul, Brasília, DF, Brazil.ORCID 0009-0001-3922-3899
Amandda Évelin Silva-CarvalhoPostgraduation Program in Biosciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0000-0001-6875-4608
Eliete Neves Silva GuerraPostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil.ORCID 0000-0002-7622-1550
Felipe Saldanha-AraújoPostgraduation Program in Pharmaceutical Science, University of Brasília, Brasília, Federal District, Brazil.ORCID 0000-0002-4200-0821
Taia Maria Berto RezendePostgraduation in Health Sciences, Faculty of Health Sciences, University of Brasília, Campus Darcy Ribeiro s/n-Asa Norte, Brasília, DF, Brazil. taiambr@gmail.com.ORCID 0000-0002-4148-0659

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis study aimed to evaluate the antimicrobial, cytotoxic, proliferative, migratory, and immunomodulatory potential of Bio-C Sealer and Bio-C Sealer ion + extracts compared to AH Plus, using human periodontal ligament stem cells (hPDLSCs). MATERIALS AND

methodsInitially, the minimum concentrations of sealer extracts required to inhibit the growth of Enterococcus faecalis and Candida albicans were determined. hPDLSCs were then obtained from extracted third molars of young donors and cultured under standard conditions. Cells were characterized by flow cytometry using mesenchymal stem cell markers (CD44, CD73, CD90, CD105) and a negative cocktail of hematopoietic markers, following the minimal criteria of the International Society for Cellular Therapy. Subsequently, the cytotoxic, proliferative, and migratory effects on hPDLSCs were assessed using MTT, Trypan Blue exclusion and scratch assays. Finally, the gene expression profile of hPDLSCs exposed to sealer extracts was analyzed by qPCR. Statistical differences were evaluated using one-way and two-way ANOVA followed by Tukey's post hoc tests.

resultsAH Plus and Bio-C Sealer ion + inhibited 100% of E. faecalis growth at extract dilutions of 1:1, 1:2, and 1:4. However, only undiluted extracts of AH Plus, Bio-C Sealer, and Bio-C Sealer ion + completely inhibited C. albicans growth. The cytotoxicity of all sealers was dose-dependent in hPDLSC cultures, with lower cell viability observed in undiluted extracts: AH Plus (55%), Bio-C Sealer (69%), and Bio-C Sealer ion + (72%) (p < 0.0001). Bio-C Sealer ion + extract (1:4) promoted the highest rate of cell migration and proliferation after 48 h (p < 0.0001). Regarding gene expression, bioceramic sealers-maintained levels of TNF-α, IL-6, and IL-10 similar to the control condition, whereas AH Plus upregulated these cytokines.

conclusionsBioceramic sealers exhibited satisfactory antimicrobial activity with moderate cytotoxicity. Moreover, they enhanced wound closure and maintained cytokine expression at levels comparable to the control condition in periodontal ligament stem cells. CLINICAL RELEVANCE: Bioceramic sealers such as Bio-C Sealer and Bio-C Sealer ion + demonstrated superior biological compatibility compared with AH Plus, including lower cytotoxicity, enhanced cell migration and proliferation, and effective control of inflammatory cytokine induction. These properties suggest greater safety for endodontic use and potential to promote tissue healing and long-term clinical success.

Indexed as

Anti-Infective AgentsCeramicsEnterococcus faecalisPeriodontal LigamentRoot Canal Filling MaterialsStem CellsCandida albicansCell MovementCell ProliferationCells, CulturedCell SurvivalEpoxy ResinsFlow CytometryHumansIn Vitro TechniquesMicrobial Sensitivity TestsAnti-Infective Agentsepoxy resin-based root canal sealerEpoxy ResinsRoot Canal Filling MaterialsAntimicrobialsBioactivityBioceramicsBiocompatibilityToxicity

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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.