Minnesota Dental Research Center for Biomaterials and Biomechanics (MDRCBB) Department of Restorative Sciences, University of Minnesota School of Dentistry, Minneapolis, Minnesota, United States of America.
PLoS One. 2013 Sep 23;8(9):e76782. doi: 10.1371/journal.pone.0076782. eCollection 2013.
Biomineralization templated by organic molecules to produce inorganic-organic nanocomposites is a fascinating example of nature using bottom-up strategies at nanoscale to accomplish highly ordered multifunctional materials. One such nanocomposite is bone, composed primarily of hydroxyapatite (HA) nanocrystals that are embedded within collagen fibrils with their c-axes arranged roughly parallel to the long axis of the fibrils. Here we discern the ultra-structure of biomimetic mineralized collagen fibrils (MCFs) as consisting of bundles of subfibrils with approximately 10 nm diameter; each one with an organic-inorganic core-shell structure. Through an amorphous calcium phosphate precursor phase the HA nanocrystals were specifically grown along the longitudinal direction of the collagen microfibrils and encapsulated them within the crystal lattice. They intercalated throughout the collagen fibrils such that the mineral phase surrounded the surface of collagen microfibrils forming an interdigitated network. It appears that this arrangement of collagen microfibrils in collagen fibrils is responsible for the observed ultrastructure. Such a subfibrillar nanostructure in MCFs was identified in both synthetic and natural bone, suggesting this is the basic building block of collagen-based hard tissues. Insights into the ultrastructure of mineralized collagen fibrils have the potential to advance our understanding on the biomineralization principles and the relationship between bone's structure and mechanical properties, including fracture toughness mechanisms. We anticipate that these principles from biological systems can be applied to the rational design of new nanocomposites with improved performance.
生物分子模板引导的无机物-有机物纳米复合材料的生物矿化是自然界在纳米尺度上采用自下而上策略来实现高度有序多功能材料的一个引人入胜的例子。这样的纳米复合材料之一是骨骼,主要由羟基磷灰石 (HA) 纳米晶体组成,这些纳米晶体嵌入在胶原原纤维内,其 c 轴大致平行于原纤维的长轴排列。在这里,我们发现仿生矿化胶原原纤维 (MCFs) 的超微结构由大约 10nm 直径的亚原纤维束组成;每一个都具有有机-无机核壳结构。通过无定形磷酸钙前体相,HA 纳米晶体沿着胶原微纤维的纵向特异性生长,并将其包裹在晶格内。它们穿插在胶原原纤维内,使得矿物相围绕胶原微纤维的表面形成交错的网络。似乎胶原原纤维内的这种胶原原纤维排列负责观察到的超微结构。在合成和天然骨中都发现了 MCFs 中的这种亚原纤维纳米结构,这表明这是基于胶原的硬组织的基本构建块。对矿化胶原原纤维的超微结构的深入了解有可能提高我们对生物矿化原理以及骨结构与机械性能(包括断裂韧性机制)之间关系的理解。我们预计,这些来自生物系统的原理可以应用于具有改进性能的新型纳米复合材料的合理设计。