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Synthesis of silicon-substituted hydroxyapatite by a hydrothermal method with two different phosphorous sources

机译:两种不同磷源的水热法合成硅取代羟基磷灰石

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Silicon-substituted hydroxyapatite (Si-HA) with up to 1.8 wt% Si content was prepared successfully by a hydrothermal method, using Ca(NO_3)_2, (NH_4)_3PO_4 or (NH_4)_2HPO_4 and Si(OCH_2CH_3)_4 (TEOS) as starting materials. Silicon has been incorporated in hydroxyapatite (HA) lattice by partially replacing phosphate (PO_4~(3-)) groups with silicate (SiO_4~(4-)) groups resulting in Si-HA described as Ca_(10)(PO_4)_(6-x)(SiO_4)_x(OH)_(2-x). X-ray diffraction (XRD), Fourier transform IR spectroscopy (FTIR), inductively coupled plasma AES (ICP-AES) and scanning electron microscopy (SEM) techniques reveal that the substitution of phosphate groups by silicate groups causes some OH~ loss to maintain the charge balance and changes the lattice parameters of HA. The crystal shape of Si-HA has not altered compared to silicon-free reference hydroxyapatite but Si-incorporation reduces the size of Si-HA crystallites. Based on in vitro tests, soaking the specimens in simulated body fluid (SBF), and MTT assays by human osteoblast-like cells, Si-substituted hydroxyapatite is more bioactive than pure hydroxyapatite.
机译:采用Ca(NO_3)_2,(NH_4)_3PO_4或(NH_4)_2HPO_4和Si(OCH_2CH_3)_4(TEOS)通过水热法成功制备了硅含量高达1.8 wt%的硅取代羟基磷灰石(Si-HA)作为起始原料。通过用硅酸盐(SiO_4〜(4-))部分取代磷酸酯(PO_4〜(3-))基团将硅掺入羟基磷灰石(HA)晶格中,从而将Si-HA称为Ca_(10)(PO_4)_( 6-x)(SiO_4)_x(OH)_(2-x)。 X射线衍射(XRD),傅立叶变换红外光谱(FTIR),电感耦合等离子体AES(ICP-AES)和扫描电子显微镜(SEM)技术表明,硅酸酯基团取代磷酸基团会导致某些OH〜损失得以维持电荷平衡并更改HA的晶格参数。与不含硅的参考羟基磷灰石相比,Si-HA的晶体形状没有改变,但掺入Si可以减小Si-HA晶体的尺寸。根据体外测试,将标本浸入模拟体液(SBF)和人成骨细胞样细胞的MTT分析中,Si取代的羟基磷灰石比纯羟基磷灰石更具生物活性。

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