Synthesis and Characterization of Sol-Gel Derived Hydroxyapatite-Bioglass Composite Nanopowders for Biomedical Applications

S. Adibnia, A. Nemati, M. Fathi, S. Baghshahi
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引用次数: 5

Abstract

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 bioactivity of 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.
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生物医学用溶胶-凝胶羟基磷灰石-生物玻璃复合纳米粉体的合成与表征
本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)复合纳米粉体及其生物活性。在不同温度下制备了羟基磷灰石与合成生物玻璃的复合材料。通过对相组成的评价,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)技术对制备的纳米粉体进行了表征。制备的复合样品的生物活性在体外研究中通过将样品浸泡在模拟体液(SBF)中预测时间来评估。傅里叶变换红外光谱(FTIR)和电感耦合等离子体(ICP)用于评价磷灰石的形成和生物活性特性。结果表明,制备的HA-BG复合纳米粉体没有羟基磷灰石的分解。煅烧的适宜温度为600℃,羟基磷灰石的粒径约为40 ~ 70 nm。样品在SBF中浸泡14天后形成磷灰石相。由此可见,该工艺可制备具有较高生物活性的HA-BG复合纳米粉体,在硬组织修复和生物医学应用中具有重要的应用价值。
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