Mg-doped biphasic calcium phosphate by a solid state reaction route: Characterization and evaluation of cytotoxicity

被引:16
作者
Webler, Geovana D. [1 ]
Correia, Ana C. C. [2 ]
Barreto, Emiliano [2 ]
Fonseca, Eduardo J. S. [1 ]
机构
[1] Univ Fed Alagoas, Inst Fis, BR-57072970 Maceio, AL, Brazil
[2] Univ Fed Alagoas, Lab Biol Celular, BR-57072970 Maceio, AL, Brazil
关键词
Biomaterials; Heat treatment; Crystal structure; BETA-TRICALCIUM PHOSPHATE; IN-SITU SYNTHESIS; SUBSTITUTED HYDROXYAPATITE; GEL METHOD; MAGNESIUM; CERAMICS; BEHAVIOR;
D O I
10.1016/j.matchemphys.2015.05.055
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Hydroxyapatite (HAP) and p-tricalcium phosphate (beta-TCP) are widely used in tissue engineering because of their chemical similarity to the inorganic bone phase. In this work, we prepare biphasic calcium phosphate (BCP, a mixture of HAP and beta-TCP) doped with different concentrations of magnesium to investigate the influence of magnesium on the BCP crystal structure. Magnesium is known to be an important element in the composition of bones and teeth. Recent research has shown that the doping of magnesium into BCP improves its bone metabolism and mechanical properties without affecting its biocompatibility. The samples were prepared by solid-state reaction from calcium carbonate, monobasic ammonium phosphate, and magnesium nitrate hexahydrate. Varying concentrations of magnesium were used and its modifications were examined by different characterization techniques. The phase composition and morphology of the ceramic powders were characterized by X-ray diffraction and scanning electron microscopy, respectively. The functional groups were analyzed using Fourier transform infrared spectroscopy and Raman spectroscopy. Cell viability experiments, using macrophage-like cell lines J774, showed that the synthesized Mg-doped BCP did not exhibit cytotoxicity regardless of the doses assayed or the different concentrations of magnesium used, suggesting it as a good material for potential biological applications. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 181
页数:5
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