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一种结晶金属氧化物在模拟血液流体中的自组装及生物活性响应

Self-assembly and bioactive response of a crystalline metal oxide in a simulated blood fluid.

作者信息

Karlinsey Robert Lynn, Yi Keewook

机构信息

Department of Preventive & Community Dentistry, Oral Health Research Institute, Indiana University School of Dentistry, Indianapolis, IN 46202, USA.

出版信息

J Mater Sci Mater Med. 2008 Mar;19(3):1349-54. doi: 10.1007/s10856-007-3164-9. Epub 2007 Oct 4.

Abstract

In this study we report on the bioactive response of self-assembled niobium oxide microstructures when immersed in a supersaturated solution emulating mineral content in blood. The structures were formed via electrochemical anodization in an electrolyte comprised of HF and NaF. The slow oxide formation kinetics associated with the presence of NaF in the electrolyte enabled microscopic examinations during microstructure evolution as shown via scanning electron microscopy (SEM). Apparently the slow growth kinetics encourage the development of bioactive sites on the microstructures, as these structures induced mineral formations. On the other hand, microstructures grown in the absence of salt were ineffective mineral nucleators. Analysis of nucleated mineral deposits was performed using X-ray diffraction and Raman spectroscopy. Both long-range and short-range order experiments verified the nucleated mineral phase was hydroxyapatite (HAP). Further characterization of the mineral phase was observed using SEM and revealed effective nucleation sites were predominantly isolated to loci on the ordered microbodies as opposed to locations lying within the amorphous strata.

摘要

在本研究中,我们报告了自组装氧化铌微结构浸入模拟血液中矿物质含量的过饱和溶液时的生物活性响应。这些结构是通过在由HF和NaF组成的电解质中进行电化学阳极氧化形成的。电解质中NaF的存在导致氧化物形成动力学缓慢,这使得在微观结构演变过程中能够进行显微镜检查,如通过扫描电子显微镜(SEM)所示。显然,缓慢的生长动力学促进了微结构上生物活性位点的发展,因为这些结构诱导了矿物质的形成。另一方面,在无盐条件下生长的微结构不是有效的矿物质成核剂。使用X射线衍射和拉曼光谱对成核的矿物质沉积物进行了分析。长程和短程有序实验均证实成核的矿物相是羟基磷灰石(HAP)。使用SEM对矿物相进行的进一步表征表明,有效的成核位点主要集中在有序微体上的位点,而不是位于无定形层内的位置。

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