Konka J, Espanol M, Bosch B M, de Oliveira E, Ginebra M-P
Biomaterials, Biomechanics and Tissue Engineering Group, Department of Materials Science and Engineering, Universitat Politècnica de Catalunya (UPC), Av. Eduard Maristany 16, 08019, Barcelona, Spain.
Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya (UPC), Av. Eduard Maristany 16, 08019, Barcelona, Spain.
Mater Today Bio. 2021 Sep 15;12:100137. doi: 10.1016/j.mtbio.2021.100137. eCollection 2021 Sep.
Biomimetic calcium-deficient hydroxyapatite (CDHA) as a bioactive material exhibits exceptional intrinsic osteoinductive and osteogenic properties because of its nanostructure and composition, which promote a favorable microenvironment. Its high reactivity has been hypothesized to play a relevant role in the performance, mediated by the interaction with the biological fluids, which is amplified by its high specific surface area. Paradoxically, this high reactivity is also behind the cytotoxicity of this material, especially pronounced in static conditions. The present work explores the structural and physicochemical changes that CDHA undergoes in contact with physiological fluids and to investigate its interaction with proteins. Calcium-deficient hydroxyapatite discs with different micro/nanostructures, coarse (C) and fine (F), were exposed to cell-free complete culture medium over extended periods of time: 1, 7, 14, 21, 28, and 50 days. Precipitate formation was not observed in any of the materials in contact with the physiological fluid, which would indicate that the ionic exchanges were linked to incorporation into the crystal structure of CDHA or in the hydrated layer. In fact, CDHA experienced a maturation process, with a progressive increase in crystallinity and the Ca/P ratio, accompanied by an uptake of Mg and a B-type carbonation process, with a gradual propagation into the core of the samples. However, the reactivity of biomimetic hydroxyapatite was highly dependent on the specific surface area and was amplified in nanosized needle-like crystal structures (F), whereas in coarse specimens the ionic exchanges were restricted to the surface, with low penetration in the material bulk. In addition to showing a higher protein adsorption on F substrates, the proteomics study revealed the existence of protein selectivity toward F or C microstructures, as well as the capability of CDHA, and more remarkably of F-CDHA, to concentrate specific proteins from the culture medium. Finally, a substantial improvement in the material's ability to support cell proliferation was observed after the CDHA maturation process.
仿生缺钙羟基磷灰石(CDHA)作为一种生物活性材料,由于其纳米结构和组成,展现出卓越的内在骨诱导和成骨特性,能促进形成良好的微环境。据推测,其高反应性在性能方面发挥着相关作用,这种反应性由与生物流体的相互作用介导,并因其高比表面积而增强。矛盾的是,这种高反应性也是该材料细胞毒性的根源,在静态条件下尤为明显。本研究探讨了CDHA与生理流体接触时所经历的结构和物理化学变化,并研究其与蛋白质的相互作用。将具有不同微/纳米结构的粗晶(C)和细晶(F)缺钙羟基磷灰石圆盘长时间暴露于无细胞完全培养基中:1天、7天、14天、21天、28天和50天。在与生理流体接触的任何材料中均未观察到沉淀形成,这表明离子交换与掺入CDHA的晶体结构或水合层有关。事实上,CDHA经历了一个成熟过程,结晶度和钙磷比逐渐增加,同时伴随着镁的吸收和B型碳酸化过程,并逐渐向样品核心扩散。然而,仿生羟基磷灰石的反应性高度依赖于比表面积,在纳米尺寸的针状晶体结构(F)中反应性增强,而在粗晶样品中,离子交换仅限于表面,在材料本体中的渗透较低。蛋白质组学研究表明,除了在F基质上有更高的蛋白质吸附外,还存在对F或C微结构的蛋白质选择性,以及CDHA,尤其是F-CDHA从培养基中浓缩特定蛋白质的能力。最后,在CDHA成熟过程后,观察到材料支持细胞增殖的能力有了显著提高。