Influence of alkyl chain length on calcium phosphate deposition onto titanium surfaces modified with alkylphosphonic acid monolayers

被引:12
作者
Wu, Jiang [1 ,2 ]
Hirata, Isao [2 ]
Zhao, Xianghui [3 ]
Gao, Bo [1 ]
Okazaki, Masayuki [2 ]
Kato, Koichi [2 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Xian 710032, Peoples R China
[2] Hiroshima Univ, Grad Sch Biomed Sci, Hiroshima 7348553, Japan
[3] Fourth Mil Med Univ, Sch Basical Med Sci, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
titanium; surface modification; self-assembled monolayer; biomimetic; calcium phosphate nucleation; SELF-ASSEMBLED MONOLAYERS; HYDROXYAPATITE COATINGS; OXIDE SURFACES; TI; ATTACHMENT; ALLOYS;
D O I
10.1002/jbm.a.34545
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Much attention has been paid to the modification of a titanium surface with an alkylphosphonic acid (PA)-based self-assembled monolayer (SAM) to accelerate hydroxyapatite (HA) deposition on the surface. In order to further accelerate the rate of HA deposition, we examined here the effect of alkyl chain length of SAMs on the formation of a HA layer. PAs with three different alkyl chain lengths (3, 6, and 16 methylene units) were used for the preparation of a SAM on titanium. The titanium specimens with monolayers were soaked in a simulated body fluid under physiological conditions for 4 weeks. The deposited substances were analyzed by scanning electron microscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. These analyses revealed that the formation of PA SAMs accelerate the deposition of poorly crystallized HA, in an alkyl chain length-dependent manner. Among PAs studied here, PA containing a 16-carbon alkyl chain gave rise to the titanium surface most effective for the deposition of HA. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2013.
引用
收藏
页码:2267 / 2272
页数:6
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