Bjørnøy Sindre H, Bassett David C, Ucar Seniz, Andreassen Jens-Petter, Sikorski Pawel
Department of Physics, Norwegian University of Science and Technology, 7491 Trondheim, Norway.
Biomed Mater. 2016 Feb 2;11(1):015013. doi: 10.1088/1748-6041/11/1/015013.
Due to high solubility and fast resorption behaviour under physiological conditions, brushite (CaHPO4⋅2H2O, calcium monohydrogen phosphate dihydrate, dicalcium phosphate dihydrate) has great potential in bone regeneration applications, both in combination with scaffolds or as a component of calcium phosphate cements. The use of brushite in combination with hydrogels opens up possibilities for new cell-based tissue engineering applications of this promising material. However, published preparation methods of brushite composites, in which the mineral phase is precipitated within the hydrogel network, fail to offer the necessary degree of control over the mineral phase, content and distribution within the hydrogel matrix. The main focus of this study is to address these shortcomings by determining the precise fabrication parameters needed to prepare composites with controlled composition and properties. Composite alginate microbeads were prepared using a counter-diffusion technique, which allows for the simultaneous crosslinking of the hydrogel and precipitation of an inorganic mineral phase. Reliable nucleation of a desired mineral phase within the alginate network proved more challenging than simple aqueous precipitation. This was largely due to ion transport within the hydrogel producing concentration gradients that modified levels of supersaturation and favoured the nucleation of other phases such as hydroxyapatite and octacalcium phosphate, which would otherwise not form. To overcome this, the incorporation of brushite seed crystals resulted in good control during the mineral phase, and by adjusting the number of seeds and amount of precursor concentration, the amount of mineral could be tuned. The material was characterised with a range of physical techniques, including scanning electron microscopy, powder x-ray diffraction and Rietveld refinement, Fourier transform infrared spectroscopy, and thermogravimetric analysis, in order to assess the mineral morphology, phase and amount within the organic matrix. The mineral content of the composite material converted from brushite into hydroxyapatite when submerged in simulated body fluid, indicating possible bioactivity. Additionally, initial cell culture studies revealed that both the material and the synthesis procedure are compatible with cells relevant to bone tissue engineering.
由于在生理条件下具有高溶解性和快速吸收行为,透钙磷石(CaHPO4⋅2H2O,磷酸氢钙二水合物,磷酸二钙二水合物)在骨再生应用中具有巨大潜力,无论是与支架结合使用还是作为磷酸钙骨水泥的成分。将透钙磷石与水凝胶结合使用为这种有前景的材料开辟了基于细胞的新组织工程应用的可能性。然而,已发表的透钙磷石复合材料制备方法,即矿物相在水凝胶网络中沉淀,未能对矿物相、含量及其在水凝胶基质中的分布提供必要的控制程度。本研究的主要重点是通过确定制备具有可控组成和性能的复合材料所需的精确制造参数来解决这些缺点。使用反扩散技术制备复合藻酸盐微珠,该技术允许水凝胶同时交联和无机矿物相沉淀。在藻酸盐网络中可靠地形成所需矿物相的晶核比简单的水相沉淀更具挑战性。这主要是由于水凝胶内的离子传输产生了浓度梯度,改变了过饱和度水平,并有利于其他相(如羟基磷灰石和磷酸八钙)的成核,否则这些相不会形成。为了克服这一问题,加入透钙磷石籽晶可在矿物相形成过程中实现良好控制,通过调整籽晶数量和前驱体浓度,可以调节矿物含量。使用一系列物理技术对材料进行了表征,包括扫描电子显微镜、粉末X射线衍射和Rietveld精修、傅里叶变换红外光谱和热重分析,以评估有机基质内的矿物形态、相和含量。当复合材料浸入模拟体液中时,其矿物含量从透钙磷石转变为羟基磷灰石,表明可能具有生物活性。此外,初步的细胞培养研究表明,该材料及其合成过程与骨组织工程相关细胞兼容。