Dentin remineralization using a stimuli-responsive engineered small molecule GSK3 antagonists-functionalized adhesive

牙本质 材料科学 牙本质小管 粘结强度 胶粘剂 复合材料 涂抹层 扫描电子显微镜 纳米颗粒 图层(电子) 纳米技术
作者
Manuel Toledano,Fátima S. Aguilera,Enrique Fernández-Romero,Alejandro JS. Lagos,Max David Quispe Bonilla,Christopher D. Lynch,Raquel Osorio
出处
期刊:Dental Materials [Elsevier BV]
卷期号:40 (3): 393-406 被引量:1
标识
DOI:10.1016/j.dental.2023.12.010
摘要

Tideglusib has shown great performance in terms of dentin regenerative properties. This study aims to evaluate bonding ability, of demineralized dentin infiltrated with polymeric nanoparticles (NPs) doped with tideglusib (TG) (TG-NPs).Dentin conditioned surfaces were infiltrated with NPs and TG-NPs. Bonded interfaces were created and stored for 24 h and then submitted to mechanical, chemical and thermal challenging. The resin-dentin interface was evaluated through a doubled dye fluorescent technique and a calcium chelator fluorophore under a confocal laser scanning microscopy, and by field emission scanning electron microscopy.Dentin surfaces treated with TG-NPs and load cycled produced higher bond strength than the rest of the groups. Immersion of dentin specimens treated with undoped-NPs in collagenase solution attained the lowest microtensile bond strength (MTBS) values. Both porosity and nanoleakage decreased when dentin was infiltrated with TG-NPs, that revealed strong signals of xylenol orange stain at both hybrid layer and dentinal tubules. The presence of NPs, in general, inducted the presence of mineralized interfaces after mechanical loading and thermocycling.Nanoparticles doped with tideglusib promoted the highest dentin bonding efficacy among groups, as they facilitated the maximum bond strength values with creation of mineral deposits at the hybrid layer and dentinal walls. Tideglusib enabled scarce porosity, nanoleakage and advanced sealing among dentin groups.Doping hydrophilic polymeric NPs with tideglusib, infiltrated in etched dentin represents a reproducible technique to create reparative dentin at the resin-dentin interface, by inducing therapeutic bioactivity.
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