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OTS 自组装单分子层在化学处理钛表面的形成。

Formation of OTS self-assembled monolayers at chemically treated titanium surfaces.

机构信息

School of Engineering and Materials Science, Queen Mary, University of London, London, E1 4NS, UK.

出版信息

J Mater Sci Mater Med. 2011 Aug;22(8):1813-24. doi: 10.1007/s10856-011-4356-x. Epub 2011 Jun 7.

DOI:10.1007/s10856-011-4356-x
PMID:21656280
Abstract

Enhanced biocompatibility of titanium implants highly depends on the possibility of achieving high degrees of surface functionalization for a low immune response and/or enhanced mineralization of bioactive minerals, such as hydroxyapatite. In this respect, surface modification with Self Assembled Monolayers (SAMs) has a great potential in delivering artificial surfaces of improved biocompatibility. Herein, the effectiveness of common chemical pre-treatments, i.e. hydrogen peroxide (H(2)O(2)) and Piranha (H(2)SO(4) + H(2)O(2)), in facilitating surface decontamination and hydroxylation of titanium surfaces to promote further surface functionalization by SAMs is investigated. The quality of the octadecyltrichlorosilane (OTS) based SAM appeared to strongly depend upon the surface morphology, the density and nature of surface hydroxyl sites resulting from the oxidative pre-treatments. Contrary to common belief, no further hydroxylation of the titanium substrate was observed after the selected chemical pre-treatments, but the number of hydroxyl groups available on the surface was decreased as a result of the formation of a titanium oxide layer with a gel-type structure. Further examinations by atomic force microscopy, infrared spectroscopy and X-ray photoelectron spectroscopy also revealed that mild oxidizing conditions were sufficient to remove surface contamination without detrimental effects on surface hydroxylation state and surface roughness. Furthermore, the adsorption of the alkylsiloxane molecules forming the SAM film is believed to proceed through hydrolysis at surface acidic hydroxyl groups rather than randomly. This site dependent adsorption process has significant implications for further functionalization of titanium based implants. It also highlights the difficulty of achieving an OTS based SAM at the surface of titanium and question the quality of SAMs reported at titanium surfaces so far.

摘要

钛植入物的增强生物相容性高度依赖于实现高度表面功能化的可能性,以降低免疫反应和/或增强生物活性矿物质(如羟基磷灰石)的矿化。在这方面,自组装单分子层 (SAM) 的表面改性在提供改善生物相容性的人工表面方面具有巨大潜力。本文研究了常见化学预处理(即过氧化氢 (H(2)O(2)) 和 Piranha(H(2)SO(4) + H(2)O(2)))在促进钛表面的表面净化和羟基化以促进 SAM 进一步表面功能化方面的有效性。基于十八烷基三氯硅烷 (OTS) 的 SAM 的质量似乎强烈依赖于表面形貌、表面羟基密度和性质,这些性质是由氧化预处理产生的。与普遍的看法相反,在选定的化学预处理后,钛基体没有进一步的羟基化,但由于形成具有凝胶型结构的氧化钛层,表面上可用的羟基数量减少了。原子力显微镜、红外光谱和 X 射线光电子能谱的进一步检查还表明,温和的氧化条件足以去除表面污染物,而不会对表面羟基化状态和表面粗糙度产生不利影响。此外,形成 SAM 膜的烷基硅氧烷分子的吸附被认为是通过表面酸性羟基的水解进行的,而不是随机进行的。这种依赖于位置的吸附过程对钛基植入物的进一步功能化具有重要意义。它还强调了在钛表面上实现 OTS 基 SAM 的困难,并对迄今为止在钛表面报道的 SAM 的质量提出了质疑。

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