Synthesis and characterisation of nanophase hydroxyapatite co-substituted with strontium and zinc

被引:56
|
作者
Lowry, N. [1 ]
Brolly, M. [1 ]
Han, Y. [1 ]
McKillop, S. [1 ]
Meenan, B. J. [1 ]
Boyd, A. R. [1 ]
机构
[1] Ulster Univ, Sch Engn, Nanotechnol & Integrated Bioengn Ctr NIBEC, Room 22A08,Shore Rd, Newtownabbey BT37 0QB, Co Antrim, North Ireland
关键词
Bioceramic; Nano-hydroxyapatite; Co-substitution; Strontium; Zinc; IN-VITRO; DOPED HYDROXYAPATITE; OSTEOCLAST FORMATION; NANO-HYDROXYAPATITE; MG; ANTIBACTERIAL; RESORPTION; SCAFFOLDS; COATINGS; SR;
D O I
10.1016/j.ceramint.2018.01.206
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In order to develop new bioactive calcium phosphate (CaP) materials to repair bone defects, it is important to ensure these materials more closely mimic the non-stoichiometric nature of biological hydroxyapatite (HA). Typically, biological HA combines various CaP phases with different impurity ions, which substitute within the HA lattice, including strontium (Sr2+), zinc (Zn2+), magnesium (Mg2+), carbonate (CO32-) and fluoride (F-), but to name a few. In addition to this biological HA have dimensions in the nanometre (nm) range, usually 60 nm in length by 5-20 nm wide. Both the effects of ion substitution and the nano-size crystals are seen as important factors for enhancing their potential biofunctionality. The driving hypothesis was to successfully synthesise nanoscale hydroxyapatite (nHA), co-substituted with strontium (Sr2+) and zinc (Zn2+) ions in varying concentrations using an aqueous precipitation method and to understand their chemical and physical properties. The materials were characterised using Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), X-Ray Photoelectron Spectroscopy (XPS) and Transmission Electron Microscopy (TEM) techniques. The FUR, XRD and XPS results confirmed that the nHA was successfully co-substituted with Sr2+ and Zn2+, replacing Ca2+ within the nHA lattice at varying concentrations. The FTIR results confirmed that all of the samples were carbonated, with a significant loss of hydroxylation as a consequence of the incorporation of Sr2+ and Zn2+ into the nHA lattice. The TEM results showed that each sample produced was nano-sized, with the Sr/Zn-10% nHA having the smallest sized crystals approximately 17.6 +/- 3.3 nm long and 10.2 +/- 1.4 nm wide. None of the materials synthesised here in this study contained any other impurity CaP phases. Therefore, this study has shown that co-substituted nHA can be prepared, and that the degree of substitution (and the substituting ion) can have a profound effect on the attendant materials' properties.
引用
收藏
页码:7761 / 7770
页数:10
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