Osteoblast response to hydroxyapatite doped with divalent and trivalent cations

被引:362
作者
Webster, TJ
Massa-Schlueter, EA
Smith, JL
Slamovich, EB
机构
[1] Purdue Univ, Dept Biomed Engn, W Lafayette, IN 47907 USA
[2] Purdue Univ, Sch Chem Engn, W Lafayette, IN 47907 USA
[3] Purdue Univ, Sch Mat Sci Engn, W Lafayette, IN 47907 USA
关键词
hydroxyapatite; dopant; osteoblast; bismuth; orthopedic/dental;
D O I
10.1016/j.biomaterials.2003.09.001
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The present in vitro study doped hydroxyapatite (HA) with various metal cations (Mg2+, Zn2+, La3+, Y3+, In3+, and Bi3+) in an attempt to enhance properties of HA pertinent to orthopedic and dental applications. X-ray diffraction material characterization indicated that the metal cations may have substituted for calcium in the HA crystal structure and that all of the doped HA formulations were single-phase and crystalline. Scanning electron microscopy analysis revealed a variety of grain sizes, depending on the dopant utilized. Energy-dispersive spectroscopy confirmed that the dopants added during synthesis were present and that all of the HA formulations synthesized were within the defined range of HA phase in the CaO-P2O5-H2O system. Lastly, Bi-doped HA had a slower dissolution rate than either undoped HA or HA doped with other cations when exposed to simulated physiological conditions for 21 days. In terms: of cell function, results provided the first evidence that osteoblasts, bone-forming cells, adhered and La3+ differentiated (as measured by alkaline phosphatase synthesis) in response to HA doped with trivalent cations (specifically, La, Y3+, In3+, Bi3+) at earlier time points than either HA doped with divalent cations (Mg2+, Zn2+) or undoped HA. Of the dopants examined, Bi3+ most enhanced osteoblast long-term calcium-containing mineral deposition. For these reasons, this study revealed for the first time the potential benefits of doping HA with Bi3+ according to criteria critical for bone prosthetic clinical success. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2111 / 2121
页数:11
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