胶原-羟基磷灰石纳米复合材料在He+离子注入下生物活性的增强

Bhoomika V. Jogiya, Kashmira P. Tank, Mihir J. Joshi
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引用次数: 0

摘要

本研究的重点是He离子注入对胶原-羟基磷灰石(Cg/HAP)纳米复合材料的结构、微观结构和生物活性的影响,该复合材料用于骨科和血管支架的应用。通过表面活性剂介导的方法成功合成了该材料,并使用x射线衍射(XRD)、能量色散光谱、扫描电镜和生物活性分析技术对其进行了研究。傅里叶变换红外光谱中胶原蛋白特征峰的存在证实了Cg/HAP纳米复合材料的成功合成。PO4−3 (1034 ~ 1083 cm−1)的不对称拉伸模式对应的峰的蓝移强度降低和增宽表明HAP纳米粒子与胶原之间存在强烈的相互作用。能量色散光谱分析证实了样品中蛋白质的相含量。离子注入后,XRD分析发现晶体尺寸减小。植入Cg/HAP复合材料的生物活性增强是基于电子损失。通过各种过程的电子相互作用使复合材料表面带电,导致模拟体液研究中更多的表面沉积活性,植入样品的更高表面粗糙度进一步证实了这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhancement of bioactivity of collagen–hydroxyapatite nanocomposite on He+ ion implantation

Enhancement of bioactivity of collagen–hydroxyapatite nanocomposite on He+ ion implantation

This study focuses on the effect of He+ ion implantation on the structural, microstructural, and bioactivity of the collagen–hydroxyapatite (Cg/HAP) nanocomposite for orthopedics as well as vascular stent applications. The material is successfully synthesized by a surfactant-mediated approach and has been investigated using X-ray diffraction (XRD), energy-dispersive spectroscopy, scanning electron microscope, and bioactivity analysis techniques. The presence of the characteristic peaks of collagen in the Fourier transform infrared spectrum confirms the successful synthesis of Cg/HAP nanocomposite. Observation of a blueshift reduction in the intensity and broadening of the peaks corresponding to the asymmetric stretching mode of PO4−3 (1034–1083 cm−1) on the HAP addition indicates a strong interaction between the HAP nanoparticles and collagen. Energy-dispersive spectroscopy analysis confirmed the phase of protein content within the sample. On ion implantation, a reduction in the crystalline size is observed from the XRD analysis. The enhancement in the bioactivity of implanted Cg/HAP composite is based on electronic loss. The electronic interaction through various processes makes the surface of the composites charged leading to more surface deposition activity from simulated body fluid studies, which is further confirmed by the higher surface roughness of the implanted samples.

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