Toledano M, Toledano-Osorio M, Medina-Castillo A L, López-López M T, Aguilera F S, Osorio R
Dental Materials Section, Faculty of Dentistry, Granada, Spain.
Spin-Off Enterprise, NanoMyp, Granada, Spain.
Int Endod J. 2018 Sep;51(9):1019-1029. doi: 10.1111/iej.12918. Epub 2018 Mar 23.
To investigate if crystallinity and ultrastructure are modified when cervical dentine is treated with four different nanogels-based solutions for remineralizing purposes.
Experimental nanogels based on polymeric nanoparticles (NPs) and zinc, calcium or doxycycline-loaded NPs were applied to citric acid etched dentine to facilitate the occlusion of tubules and the mineralization of the dentine surface. Dentine surfaces were studied by X-ray diffraction and transmission electron microscopy through selected area diffraction and bright-field imaging.
Crystals at the dentine surface were identified as hydroxyapatite with the highest crystallographic maturity and crystallite size in dentine treated with Zn-NPs-based gel. Texture increased in all samples from 24 h to 7 days, except in dentine surfaces treated with Zn-NPs gel. Polyhedral, plate-like and drop-like shaped apatite crystals constituted the bulk of minerals in dentine treated with Zn-NPs gel, after 7 days. Polymorphic, cubic and needle-like shaped crystals distinguished minerals, with more amorphous characteristics in dentine treated with Ca-NPs gel after 7 days than that found when Zn-NPs were applied. Doxycycline-NPs produced the smallest crystallites with poor crystallinity, maturity and chemical stability.
Crystalline and amorphous phases of newly formed hydroxyapatite were described in both types of dentine treated with Zn-NPs as well as Ca-NPs gels with multiple shapes of crystallites. Crystal shapes ranged from rounded/drop-like or plate-like crystals to needle-like or polyhedral and cubic apatite appearance.
研究用四种不同的基于纳米凝胶的溶液处理颈段牙本质以进行再矿化时,其结晶度和超微结构是否会发生改变。
将基于聚合物纳米颗粒(NPs)以及负载锌、钙或强力霉素的NPs的实验性纳米凝胶应用于经柠檬酸蚀刻的牙本质,以促进牙本质小管的封闭和牙本质表面的矿化。通过X射线衍射以及透射电子显微镜的选区衍射和明场成像对牙本质表面进行研究。
在基于Zn-NPs的凝胶处理的牙本质中,牙本质表面的晶体被鉴定为具有最高晶体成熟度和微晶尺寸的羟基磷灰石。除了用Zn-NPs凝胶处理的牙本质表面外,所有样品从24小时到7天的织构都有所增加。7天后,在基于Zn-NPs的凝胶处理的牙本质中,多面体、板状和滴状的磷灰石晶体构成了矿物质的主体。多晶型、立方和针状晶体区分了矿物质,7天后用Ca-NPs凝胶处理的牙本质比应用Zn-NPs时具有更多的无定形特征。强力霉素-NPs产生的微晶最小,结晶度、成熟度和化学稳定性较差。
在用Zn-NPs以及Ca-NPs凝胶处理的两种类型牙本质中,均描述了新形成的羟基磷灰石的结晶相和非晶相,微晶具有多种形状。晶体形状从圆形/滴状或板状晶体到针状或多面体和立方磷灰石外观不等。