首页> 外文学位 >Electro-thermally polarized bulk and coated hydroxyapatite (HAp) ceramics---Understanding the role of surface charge, wettability and dopants on physical, mechanical and biological properties.
【24h】

Electro-thermally polarized bulk and coated hydroxyapatite (HAp) ceramics---Understanding the role of surface charge, wettability and dopants on physical, mechanical and biological properties.

机译:电热极化的块状和涂层羟基磷灰石(HAp)陶瓷---了解表面电荷,润湿性和掺杂剂对物理,机械和生物学特性的作用。

获取原文
获取原文并翻译 | 示例

摘要

The objective of this study was to investigate the role of surface charge, wettability, and dopants on physical, mechanical and in vitro biological properties of bulk and coated electrothermally polarized hydroxyapatite (HAp) ceramics. For this purpose, bulk pure HAp compacts were prepared by sintering at 1200°C for 2h and HAp coating was fabricated on Ti substrate. Thermally stimulated depolarization current (TSDC) analysis revealed that a maximum surface charge of 4.05+/-0.33 microC/cm2 can be stored in bulk sintered HAp compacts while HAp coating samples exhibited a stored surface charge of 1.41+/-0.30 microC/cm2. It has been observed that increasing the surface potential led to decreasing of hydrophobicity of HAp surface without introducing any other volumetric effects in the material. In vitro bioactivity and bone cell-materials interaction results proved that increasing surface energy and wettability on negatively charged HAp surface significantly accelerated the apatite mineralization process by selectively adsorbing Ca2+ ions which promoted better hFOB cell attachment, proliferation and faster cells differentiation, especially at early time points, over unpoled HAp surface. In contrast, positively poled HAp surface exhibited inhibited hFOB cell proliferation and growth. Furthermore, dopants were incorporated into pure HAp in different single, binary and ternary composition to achieve combined benefits of matching bone chemistry and polarization effect. Small addition of Mg2+ and combined addition of Mg 2+-Sr2+ were found most optimal in enhancing density, mechanical properties as well as polarizability and charge storage ability of pure HAp. In vitro cell materials interaction study showed that presence of Mg2+ and Sr2+ can also significantly improved osteoblast activities on negatively charged surface. Finally, the interaction cell adhesive fibronectin protein on polarized doped and undoped HAp surfaces was investigated to get comprehensive understanding on cell-materials interactions. Protein study results confirmed that higher adsorption and better structural stability of fibronectin protein led to superior cell-materials interactions on negatively charged binary doped HAp surfaces over undoped HAp. Overall, the present research findings demonstrated the potency of developing electro-thermally polarized HAp ceramics which can provide a new basis for the development of a new generation of HAp based implants that can promote faster healing.
机译:这项研究的目的是研究表面电荷,润湿性和掺杂剂对块状和涂层电热极化羟基磷灰石(HAp)陶瓷的物理,机械和体外生物学特性的作用。为了这个目的,通过在1200℃下烧结2小时来制备块状纯HAp压块,并在Ti衬底上制备HAp涂层。热激发去极化电流(TSDC)分析显示,散装烧结HAp压块中可以存储的最大表面电荷为4.05 +/- 0.33 microC / cm2,而HAp涂层样品的存储表面电荷为1.41 +/- 0.30 microC / cm2。已经观察到增加表面电势导致HAp表面的疏水性降低而没有在材料中引入任何其他体积效应。体外生物活性和骨细胞材料相互作用的结果证明,带负电荷的HAp表面上增加的表面能和润湿性通过选择性地吸附Ca2 +离子而显着加速了磷灰石矿化过程,从而促进了更好的hFOB细胞附着,增殖和更快的细胞分化,尤其是在早期点,在未极化的HAp曲面上。相反,正极性HAp表面表现出抑制的hFOB细胞增殖和生长。此外,将掺杂剂以不同的单一,二元和三元组成掺入纯净的HAp中,以达到匹配骨化学和极化效应的综合优势。发现少量添加Mg2 +和组合添加Mg 2 + -Sr2 +在提高纯HAp的密度,机械性能以及极化率和电荷存储能力方面是最理想的。体外细胞材料相互作用研究表明,Mg2 +和Sr2 +的存在还可以显着改善带负电表面上的成骨细胞活性。最后,研究了极化的掺杂和未掺杂的HAp表面上的细胞黏附纤连蛋白蛋白相互作用,以获得对细胞-材料相互作用的全面理解。蛋白质研究结果证实,纤连蛋白的更高吸附力和更好的结构稳定性导致带负电荷的二元掺杂HAp表面相对于未掺杂HAp具有更好的细胞-材料相互作用。总体而言,本研究发现证明了开发电热极化HAp陶瓷的潜力,这可以为开发新一代的可促进更快愈合的基于HAp的植入物提供新的基础。

著录项

  • 作者

    Bodhak, Subhadip.;

  • 作者单位

    Washington State University.;

  • 授予单位 Washington State University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 274 p.
  • 总页数 274
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号