Shah Furqan A
Department of Biomaterials, Sahlgrenska Academy, University of Gothenburg, Gothenburg Sweden.
Acta Biomater. 2025 Apr;196:1-16. doi: 10.1016/j.actbio.2025.01.055. Epub 2025 Jan 30.
The physico-chemical characteristics of bone mineral remain heavily debated. On the nanoscale, bone mineral resides both inside and outside the collagen fibril as distinct compartments fused together into a cohesive continuum. On the micrometre level, larger aggregates are arranged in a staggered pattern described as crossfibrillar tessellation. Unlike geological and synthetic hydroxy(l)apatite, bone mineral is a unique form of apatite deficient in calcium and hydroxyl ions with distinctive carbonate and acid phosphate substitutions (CHAp), together with a minor contribution of amorphous calcium phosphate as a surface layer around a crystalline core of CHAp. In mammalian bone, an amorphous solid phase has not been observed, though an age-dependent shift in the amorphous-to-crystalline character is observed. Although octacalcium phosphate has been postulated as a bone mineral precursor, there is inconsistent evidence of calcium phosphate phases other than CHAp in the extracellular matrix. In association with micropetrosis, magnesium whitlockite is occasionally detected, indicating pathological calcification rather than a true extracellular matrix component. Therefore, the terms 'biomimetic' or 'bone-like' should be used cautiously in descriptions of synthetic biomaterials. The practice of reporting the calcium-to-phosphorus ratio (Ca/P) as proxy for bone mineral maturity oversimplifies the chemistry since both Ca and PO ions are partially substituted. Moreover, non-mineral sources of phosphorus are ignored. Alternative compositional metrics should be considered. In the context of bone tissue and bone mineral, the term 'mature' must be used carefully, with clear criteria that consider both compositional and structural parameters and the potential impact on mechanical properties. STATEMENT OF SIGNIFICANCE: Bone mineral exhibits a unique hierarchical structure and is classified into intrafibrillar and extrafibrillar mineral compartments with distinct physico-chemical characteristics. The dynamic nature of bone mineral, i.e., evolving chemical composition and physical form, is poorly understood. For instance, bone mineral is frequently described as "hydroxy(l)apatite", even though the OH content of mature bone mineral is negligible. Moreover, the calcium-to-phosphorus ratio is often taken as an indicator of bone mineral maturity without acknowledging substitutions at calcium and phosphate sites. This review takes a comprehensive look at the structure and composition of bone mineral, highlighting how experimental data are misinterpreted and unresolved concerns that warrant further investigation, which have implications for characterisation of bone material properties and development of bone repair biomaterials.
骨矿物质的物理化学特性仍存在激烈争论。在纳米尺度上,骨矿物质存在于胶原纤维的内部和外部,作为不同的隔室融合在一起形成一个连贯的连续体。在微米水平上,较大的聚集体以交错模式排列,称为跨纤维镶嵌。与地质和合成羟基(l)磷灰石不同,骨矿物质是一种独特形式的磷灰石,缺乏钙和氢氧根离子,具有独特的碳酸盐和酸性磷酸盐取代(CHAp),同时非晶态磷酸钙作为CHAp结晶核心周围的表面层有少量贡献。在哺乳动物骨骼中,尚未观察到非晶态固相,尽管观察到了非晶态到晶态特征的年龄依赖性转变。尽管八钙磷酸盐被假定为骨矿物质前体,但细胞外基质中除CHAp外的磷酸钙相的证据并不一致。与微石化相关时,偶尔会检测到镁白磷钙矿,这表明是病理性钙化而非真正的细胞外基质成分。因此,在描述合成生物材料时应谨慎使用“仿生”或“骨样”等术语。将钙磷比(Ca/P)作为骨矿物质成熟度的替代指标的做法过于简化了化学组成,因为钙和磷酸根离子都有部分取代。此外,非矿物质来源的磷被忽略了。应考虑其他成分指标。在骨组织和骨矿物质的背景下,“成熟”一词必须谨慎使用,要有明确的标准,同时考虑组成和结构参数以及对力学性能的潜在影响。
骨矿物质呈现出独特的层次结构,分为具有不同物理化学特性的纤维内和纤维外矿物质隔室。骨矿物质的动态性质,即不断变化的化学成分和物理形式,目前了解甚少。例如,骨矿物质经常被描述为“羟基(l)磷灰石”,尽管成熟骨矿物质中的OH含量可以忽略不计。此外,钙磷比经常被用作骨矿物质成熟度的指标,而没有考虑钙和磷酸盐位点的取代情况。本综述全面审视了骨矿物质的结构和组成,强调了实验数据是如何被误解的,以及有待进一步研究的未解决问题,这些问题对骨材料特性的表征和骨修复生物材料的开发具有重要意义。