Surface modification of surface sol-gel derived titanium oxide films by self-assembled monolayers (SAMS) and non-specific protein adsorption studies

被引:57
作者
Advincula, M
Fan, XW
Lemons, J
Advincula, R [1 ]
机构
[1] Univ Alabama Birmingham, Dept Biomed Engn, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Mat Sci Program, Birmingham, AL 35294 USA
[3] Univ Houston, Dept Chem, Houston, TX 77204 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.colsurfb.2004.12.009
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Biological events occurring at the implant-host interface, including protein adsorption are mainly influenced by surface properties of the implant. Titanium alloys, one of the most widely used implants, has shown good biocompatibility primarily through its surface oxide. In this study, a surface sol-gel process based on the surface reaction of metal alkoxides with a hydroxylated surface was used to prepare ultrathin titanium oxide (TiOx) coatings on silicon wafers. The oxide deposited on the surface was then modified by self-assembled monolayers (SAMs) of silanes with different functional groups. Interesting surface morphology trends and protein adhesion properties of the modified titanium oxide surfaces were observed as studied by non-specific protein binding of serum albumin. The surface properties were investigated systematically using water contact angle, ellipsometry, X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) measurements. Results showed that the surface sol-gel process predominantly formed homogeneous, but rough and porous titanium oxide layers. The protein adsorption was dependent primarily on the silane chemistry, packing of the alkyl chains (extent of van der Waals interaction), morphology (porosity and roughness), and wettability of the sol-gel oxide. Comparison was made with a thermally evaporated TiOx-Ti/Si-wafer substrate (control). This method further extends the functionalization of surface sol-gel derived TiOx layers for possible titanium alloy bioimplant surface modification. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 43
页数:15
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