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Synthesis and characterization of sol-gel derived Hydroxyapatite-Bioglass composite nanopowders for biomedical applications

机译:溶胶-凝胶衍生的羟基磷灰石-生物玻璃复合纳米粉体的合成与表征

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摘要

The main purpose of this study is to prepare and characterize hydroxyapatite (HA)-10%wt bioglass (BG) composite nanopowders and its bioactivity. Composites of hydroxyapatite with synthesized bioglass are prepared at various temperatures. Suitable calcination temperature is chosen by evaluating of the phase composition. X-ray diffraction (XRD), Transmission electron microscopy (TEM) and Scanning electron microscopy (SEM) techniques are utilized to characterize the prepared nanopowders. The bioactivityof the prepared composite samples is evaluated in an in vitro study by immersion of samples in simulated body fluid (SBF) for predicted time. Fourier transformed infrared (FTIR) spectroscopy and inductively coupled plasma (ICP) are used for evaluation of apatite formation and the bioactivity properties. Results show that HA-BG composite nanopowders are successfully prepared without any decomposition of hydroxyapatite. The suitable temperature for calcination is 600°C and the particle size of hydroxyapatite is about 40-70 nm. The apatite phase forms after 14 days immersing of the samples in SBF. It could be concluded that this process can be used to synthesize HA-BG composite nanopowders with improved bioactivity which is much needed for hard tissue repair and biomedical applications.
机译:这项研究的主要目的是制备和表征羟基磷灰石(HA)-10%wt生物玻璃(BG)复合纳米粉及其生物活性。羟基磷灰石与合成生物玻璃的复合物是在各种温度下制备的。通过评估相组成来选择合适的煅烧温度。利用X射线衍射(XRD),透射电子显微镜(TEM)和扫描电子显微镜(SEM)技术来表征所制备的纳米粉。通过将样品浸入模拟体液(SBF)中预计时间,在体外研究中评估了制备的复合样品的生物活性。傅里叶变换红外(FTIR)光谱和电感耦合等离子体(ICP)用于评估磷灰石的形成和生物活性。结果表明,成功制备了HA-BG复合纳米粉体,没有羟基磷灰石的分解。煅烧的合适温度为600℃,羟基磷灰石的粒度为约40-70nm。将样品浸入SBF 14天后形成磷灰石相。可以得出结论,该方法可用于合成具有改善的生物活性的HA-BG复合纳米粉,这对于硬组织修复和生物医学应用而言是非常需要的。

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