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Remineralization of enamel caries by an amelogenin-derived peptide and fluoride in vitro

机译:通过Amelogenin衍生的肽和体外氟化物的牙釉质龋齿再矿化

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Dental caries is one of the most common oral diseases in the world. This study was tantamount to investigate the combinatory effects of an amelogenin-derived peptide (called QP5) and fluoride on the remineralization of artificial enamel caries. The peptide QP5 was synthesized and characterized, and the binding capability of the peptide on hydroxyapatite (HA) and demineralized tooth enamel surface was analysed. Then, the mineralization function of the peptide and fluoride was studied through the spontaneous mineralization testing and remineralization on enamel caries in vitro. First, the novel peptide QP5 could bind on the hydroxyapatite and demineralized tooth enamel surfaces. Second, QP5 can transitorily stabilize the formation of amorphous calcium phosphate and direct the transformation into hydroxyapatite crystals alone and in combination with fluoride. In addition, compared to blocks treated by peptide QP5 alone or fluoride, the sample blocks showed significantly higher surface microhardness, lower mineral loss and shallower lesion depth after treatment with a combination of QP5 and fluoride at high or low concentrations. The peptide QP5 could control the crystallization of hydroxyapatite, and combinatory application of peptide QP5 and fluoride had a potential synergistic effect on the remineralization of enamel caries.
机译:龋齿是世界上最常见的口腔疾病之一。本研究旨在研究氨基素衍生的肽(称为QP5)和氟化物对人工搪瓷龋的结肠的组合作用。合成肽QP5并表征,分析了肽对羟基磷灰石(HA)和脱耳化牙釉质表面的结合能力。然后,通过在体外通过搪瓷龋上的自发矿化测试和再矿化研究了肽和氟化物的矿化功能。首先,新型肽QP5可以在羟基磷灰石和脱矿质牙釉质表面上结合。其次,QP5可以过度稳定非晶磷酸钙的形成,并将转化直接转化为单独的羟基磷灰石晶体,并与氟化物组合。此外,与单独的肽QP5处理的嵌段或氟化物处理,样品嵌段在用QP5和氟化物的组合处理后显着更高的表面显微硬度,降低矿物质损失和较浅的病变深度。肽QP5可以控制羟基磷灰石的结晶,肽QP5和氟化物的组合施加对搪瓷龋的再矿化具有潜在的协同作用。

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