期刊
DENTAL MATERIALS
卷 34, 期 8, 页码 E214-E223出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.dental.2018.05.011
关键词
Calcium aluminate; Calcium aluminate and silver; Calcium ions release; Silver ion release; Flow; pH; Radiopacity; Antibiofilm; Root canal sealers
Objective. To synthetize calcium aluminate (C3A) and silver-containing C3A particles (C3A + Ag) testing their effects on the properties of a MTA-based endodontic sealer in comparison to an epoxy resin- and a calcium silicate-based sealer. Methods. Pure C3A and C3A+Ag particles were synthesized by a chemical method and characterized using XRD to identify crystalline phases. SEM/EDS analysis investigated morphology, particle size, and elemental composition of particles. Setting time, flow, radiopacity, water sorption and solubility of commercial and modified sealers were evaluated according to ISO 6876/2012. The pH and ions release were measured using a pHmeter and a microwave induced plasma optical emission spectrometer. The inhibition of biofilm growth was evaluated by confocal laser scanning microscopy (CLSM). Data were rank transformed and analyzed by ANOVA and Tukey test (P < 0.05). Results. The C3A particles showed an irregular grain agglomerated structure with voids and pores. In C3A + Ag particles, Ag modified the material morphology, confirming the deposition of Ag. The physicochemical properties of the modified MTA-based sealer were similar to the commercial material, except for the significant increase in Ca+2 release. However, there was no Ag release. Setting time, flow, radiopacity, water sorption and solubility were adequate for all materials. All the materials showed alkaline pH. Antibiofilm effect was improved in the presence of C3A particles, while the biofilm inhibition was lower in the presence of Ag. Significance. The modified sealer presented improved antibiofilm properties and calcium release, without dramatic effects on the other characteristics. It is expected a positive effect in its antimicrobial behavior. (C) 2018 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
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