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Biomineralizing Synthesis Of Mesoporous Hydroxyapatite-calcium Pyrophosphate Polycrystal Using Ovalbumin As Biosurfactant

机译:卵清蛋白作为生物表面活性剂生物矿化合成介孔羟基磷灰石-焦磷酸钙多晶体

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摘要

Mesoporous polycrystals of hydroxyapatite-calcium pyrophosphate (HA-CPP) are synthesized via a biomineralizing route using ovalbumin as natural biosurfactant. The mesoporous structure of HA-CPP is characterized by means of X-ray diffraction (XRD), N_2 adsorption-desorption isotherms (NADI), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), atom force microscopy (AFM), polarization microscopy (PLM) and stereomicroscopy. The results show that the crystalline grains with an average diameter of 13.2 nm are uniformly distributed along the protein molecule chains, and this results in microsphere-like particles with diameters of 200-300 nm. The highly ordered pores involved in microspheres are found to be approximately 6.6 nm by small-angle XRD. The formation of lyotropic calcium liquid crystal (CLC) plays a key role in the formation and stabilization of the mesoporous structure. A schematic illustration is used to reveal the mechanism of protein-medicated HA-CPP biomineralization, which employs the protein tertiary structure to explain the formation of the porous particles.
机译:使用卵清蛋白作为天然生物表面活性剂,通过生物矿化途径合成了羟基磷灰石-焦磷酸钙(HA-CPP)的中孔多晶体。 HA-CPP的介孔结构通过X射线衍射(XRD),N_2吸附-解吸等温线(NADI),傅立叶变换红外光谱(FTIR),透射电子显微镜(TEM),原子力显微镜(AFM)进行表征,偏振显微镜(PLM)和立体显微镜。结果表明,平均直径为13.2 nm的晶粒沿着蛋白质分子链均匀分布,这导致直径为200-300 nm的微球状颗粒。通过小角度XRD发现微球中涉及的高度有序的孔大约为6.6 nm。溶致钙液晶(CLC)的形成在介孔结构的形成和稳定中起关键作用。示意图用于揭示蛋白质药物HA-CPP生物矿化的机理,该机理利用蛋白质三级结构来解释多孔颗粒的形成。

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