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Revealing nanoscale mineralization pathways of hydroxyapatite using in situ liquid cell transmission electron microscopy

机译:揭示羟基磷灰石的纳米级矿化途径,使用原位液体透射电子显微镜

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To treat impairments in hard tissues or overcome pathological calcification in soft tissues, a detailed understanding of mineralization pathways of calcium phosphate materials is needed. Here, we report a detailed mechanistic study of hydroxyapatite (HA) mineralization pathways in an artificial saliva solution via in situ liquid cell transmission electron microscopy (TEM). It is found that the mineralization of HA starts by forming ion-rich and ion-poor solutions in the saliva solution, followed by coexistence of the classical and nonclassical nucleation processes. For the nonclassical path, amorphous calcium phosphate (ACP) functions as the substrate for HA nucleation on the ACP surface, while the classical path features direct HA nucleation from the solution. The growth of HA crystals on the surface of ACP is accompanied by the ACP dissolution process. The discoveries reported in this work are important to understand the physiological and pathological formation of HA minerals, as well as to engineer the biomineralization process for bone healing and hard tissue repairs.
机译:为了在软组织中治疗硬组织或克服病理钙化的损伤,需要详细了解磷酸钙材料的矿化途径。在此,我们通过原位液体细胞透射电子显微镜(TEM)通过原位液体透射电子显微镜(TEM)在人工唾液溶液中的羟基磷灰石(HA)矿化途径的详细机械研究。结果发现,HA的矿化通过在唾液溶液中形成离子和离子差的溶液,然后进行经典和非化学成核过程的共存。对于非生物路径,无定形磷酸钙(ACP)用作ACP表面上的HA成核的基材,而经典路径具有直接从溶液中成核。 ACP表面上的HA晶体的生长伴随着ACP溶解过程。在这项工作中报告的发现对于了解HA矿物质的生理和病理形成,以及为骨愈合和硬组织修理的生物矿化过程设计很重要。

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