Shear-mediated crystallization from amorphous calcium phosphate to bone apatite

被引:34
作者
Niu, Xufeng [1 ,2 ,3 ]
Wang, Liyang [1 ]
Tian, Feng [1 ]
Wang, Lizhen [1 ]
Li, Ping [1 ]
Feng, Qingling [4 ]
Fan, Yubo [1 ]
机构
[1] Beihang Univ, Sch Biol Sci & Med Engn, Minist Educ, Key Lab Biomechan & Mechanobiol, Beijing 100191, Peoples R China
[2] BUAA Res Inst, Guangzhou 510530, Guangdong, Peoples R China
[3] Beihang Univ, Res Inst, Shenzhen 518057, Peoples R China
[4] Tsinghua Univ, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluid shear stress; Amorphous calcium phosphate; Apatite; Crystallization; Cone-and-plate viscometer; CARBONATED HYDROXYLAPATITE; TRICALCIUM PHOSPHATE; STRUCTURAL WATER; FLUID; MECHANOTRANSDUCTION; OSTEOCYTES; CELLS; MODEL; NMR; ORTHOPHOSPHATES;
D O I
10.1016/j.jmbbm.2015.09.024
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The contribution of fluid shear stress (FSS) on the conversion of amorphous calcium phosphate (ACP) to bone apatite is investigated. The ACP precursors are prepared by using a wet-chemistry method and further exposed to the constant FSS environment with values of 0.5, 1.0, 1.5, and 2.0 Pa. At the designated time points, the apatites are characterized by transmission electron microscopy, X-ray diffraction, and inductively coupled plasma-mass spectroscopy. The results show that, the low FSS 1.0 Pa) has positive effects on the transition of ACP, characterized by the accelerated crystallization velocity and the well organized calcium-deficient hydroxyapatite (CDHA) structure, whereas the high FSS (>1.0 Pa) has negative effects on this conversion process, characterized by the poor CDHA crystal morphologies and the destroyed structures. The bioactivity evaluations further reveal that, compared with the FSS-free group, the CDHA prepared under 1.0 Pa FSS for 9 h presents the more biocompatible features with pre-osteoblast cells. These results are helpful for understanding the mechanism of apatite deposition in natural bone tissue. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:131 / 140
页数:10
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