Search results for "Zinc Oxide-Eugenol Cement"

showing 2 items of 2 documents

Surface debris of canal walls after post space preparation in endodontically treated teeth: A scanning electron microscopic study

2004

Abstract Purpose To evaluate surface cleanliness of root canal walls along post space after endodontic treatment using 2 different irrigant regimens, obturation techniques, and post space preparation for adhesive bonding. Study design Forty teeth, divided into 4 groups, were instrumented, using Ni-Ti rotary files, irrigated with NaOCl or NaOCl + EDTA and obturated with cold lateral condensation (CLC) or warm vertical condensation (WVC) of gutta-percha. After post space preparation, etching, and washing procedure, canal walls were observed using a scanning electron microscope (SEM). Amount of debris, smear layer, sealer/gutta-percha remnants, and visibility of open tubules were rated. Result…

EUGENOLMaterials scienceAdhesive bondingSodium HypochloriteSurface PropertiesRoot canalIRRIGANTSSmear layerDentistryRoot Canal Filling MaterialsSODIUM-HYPOCHLORITEAcid Etching DentalRoot Canal ObturationIRRIGATIONDentinmedicineHumansRETENTIONFIBER POSTSZinc Oxide-Eugenol CementROOT CANALSGeneral DentistryEdetic AcidDental Pulp CavityTooth NonvitalRoot Canal ObturationbiologyRoot Canal Irrigantsbusiness.industryTooth PreparationGutta-perchabiology.organism_classificationSEALERSRoot Canal Therapymedicine.anatomical_structureOtorhinolaryngologyDentinGuttaMicroscopy Electron ScanningSurgeryOral SurgeryDental Pulp CavityGutta-PerchabusinessRESIN CEMENTSMEAR LAYERRoot Canal PreparationPost and Core Technique
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Cytotoxicity and bioactivity of various pulpotomy materials on stem cells from human exfoliated primary teeth.

2017

Aims To investigate the cytotoxicity and bioactivity of several pulpotomy materials: Biodentine (Septodont, Saint-Maur-des-Fosses, France) MTA (Angelus, Londrina, PR, Brazil), Theracal LC (Bisco Inc., Schamburg, IL, USA) and IRM (Dentsply DeTrey GmbH, Konstanz, Germany), after contact with stem cells isolated from human exfoliated primary teeth (SHEDs). Methodology SHEDs were cultured in the presence of the eluates of various pulpotomy materials for 24, 48 and 72 h. Cell viability was determined by mitochondrial dehydrogenase enzymatic (MTT) assay. Apoptosis and changes in cell phenotype were evaluated by flow cytometry. Also, an in vitro scratch wound-healing assay was used to determine th…

Time FactorsCell SurvivalPulpotomyDentistryApoptosis02 engineering and technologyMatrix (biology)In Vitro TechniquesCell morphologyFlow cytometry03 medical and health sciences0302 clinical medicineCell MovementMaterials TestingmedicineHumansMethylmethacrylatesViability assayTooth DeciduousZinc Oxide-Eugenol CementCytotoxicityAluminum CompoundsGeneral DentistryCells Culturedmedicine.diagnostic_testChemistrybusiness.industrySilicatesStem CellsOxides030206 dentistryCalcium Compounds021001 nanoscience & nanotechnologyFlow CytometryMolecular biologyStainingDrug CombinationsPhenotypeApoptosisPulpotomyMicroscopy Electron Scanning0210 nano-technologybusinessPulp Capping and Pulpectomy AgentsInternational endodontic journal
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