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首页> 外文期刊>BioFactors >Investigation of the bioactivity and biocompatibility of different glass interfaces with hydroxyapatite, fluorohydroxyapatite and 58S bioactiveglass
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Investigation of the bioactivity and biocompatibility of different glass interfaces with hydroxyapatite, fluorohydroxyapatite and 58S bioactiveglass

机译:不同玻璃与羟基磷灰石,氟代羟基磷灰石和58S生物活性玻璃的界面生物活性和生物相容性研究

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The current review investigates the bioactivity of different glass interfaces created on thin glass cover slips as substrates. The interfaces studied are plain glass, functionalized glass using 0.5 M and 5 M of sodium hydroxide (NaOH) for 24 hrs, and glass coated with bioactive 58S Bioglass (58S). A biomimetic method, involving the exposure of the three interfaces to 1.5 times simulated body fluid (SBF) tests the bioactivity of the interfaces via creation of layer of Hydroxyapatite (HA). Fluorinated SBF will precipitate fluorine doped HA (FHA) on a bioactive interface. Higher concentration of 1.5 times of SBF used in this study intended to accelerate the formation of HA and FHA layer over the substrate. HA and FHA is found to be precipitated on the thinly coated 58S. This paper, study also the thin film coatings of three forms of bioceramics – bioactive 58S, HA and FHA. The study, also proposes to draw a relation between the morphology of HA particles with duration of exposure to SBF, the effects of fluorine on the morphology and the cell interaction with bioactive 58S, HA and FHA interfaces using pre-differentiated osteoblastic MC3T3 cells. The analysis of cells in this study is confined to three parameters that include the attachment, proliferation and viability of cells. Tests employed for the analysis of the thin film coating of HA and FHA is restricted to qualitative X-Ray Diffraction and quantitative Field Emission Scanning Electron Microscope. Other mechanical tests such as shear test are not used to test the mechanical properties of this thin layer, due to the fact that the thin film is too thin for such analysis.
机译:本篇综述调查了在薄玻璃盖玻片上作为基材形成的不同玻璃界面的生物活性。研究的界面为普通玻璃,使用0.5 M和5 M氢氧化钠(NaOH)的功能化玻璃24小时,以及涂有生物活性58S Bioglass(58S)的玻璃。仿生方法涉及将三个界面暴露于1.5倍的模拟体液(SBF)中,通过创建羟基磷灰石(HA)层来测试界面的生物活性。氟化SBF将在生物活性界面上沉淀氟掺杂的HA(FHA)。本研究中使用的SBF的1.5倍较高浓度旨在加速基材上HA和FHA层的形成。发现HA和FHA沉淀在薄涂层的58S上。本文还研究了三种形式的生物陶瓷的薄膜涂层:生物活性58S,HA和FHA。这项研究还建议在使用预分化成骨细胞的MC3T3细胞时,绘制HA颗粒的形态与暴露于SBF的持续时间,氟对形态的影响以及与生物活性58S,HA和FHA界面之间的相互作用之间的关系。在这项研究中对细胞的分析仅限于三个参数,包括细胞的附着,增殖和生存力。用于分析HA和FHA薄膜涂层的测试仅限于定性X射线衍射和定量场发射扫描电子显微镜。由于薄膜对于这样的分析而言太薄,因此不使用其他机械测试(例如剪切测试)来测试该薄层的机械性能。

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