Molecular nanomechanics of nascent bone: fibrillar toughening by mineralization

被引:222
作者
Buehler, Markus J. [1 ]
机构
[1] MIT, Lab Atomist & Mol Med, Dept Civil & Environm Engn, Cambridge, MA 02139 USA
关键词
D O I
10.1088/0957-4484/18/29/295102
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Mineralized collagen fibrils are highly conserved nanostructural building blocks of bone. By a combination of molecular dynamics simulation and theoretical analysis it is shown that the characteristic nanostructure of mineralized collagen fibrils is vital for its high strength and its ability to sustain large deformation, as is relevant to the physiological role of bone, creating a strong and tough material. An analysis of the molecular mechanisms of protein and mineral phases under large deformation of mineralized collagen fibrils reveals a fibrillar toughening mechanism that leads to a manifold increase of energy dissipation compared to fibrils without mineral phase. This fibrillar toughening mechanism increases the resistance to fracture by forming large local yield regions around crack-like defects, a mechanism that protects the integrity of the entire structure by allowing for localized failure. As a consequence, mineralized collagen fibrils are able to tolerate microcracks of the order of several hundred micrometres in size without causing any macroscopic failure of the tissue, which may be essential to enable bone remodelling. The analysis proves that adding nanoscopic small platelets to collagen fibrils increases their Young's modulus and yield strength as well as their fracture strength. We find that mineralized collagen fibrils have a Young's modulus of 6.23 GPa (versus 4.59 GPa for the collagen fibril), yield at a tensile strain of 6.7% (versus 5% for the collagen fibril) and feature a fracture stress of 0.6 GPa (versus 0.3 GPa for the collagen fibril).
引用
收藏
页数:9
相关论文
共 42 条
[1]   Skeleton of Euplectella sp.:: Structural hierarchy from the nanoscale to the macroscale [J].
Aizenberg, J ;
Weaver, JC ;
Thanawala, MS ;
Sundar, VC ;
Morse, DE ;
Fratzl, P .
SCIENCE, 2005, 309 (5732) :275-278
[2]   Regulating bone formation via controlled scaffold degradation [J].
Alsberg, E ;
Kong, HJ ;
Hirano, Y ;
Smith, MK ;
Albeiruti, A ;
Mooney, DJ .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (11) :903-908
[3]   Measurement of partition of stress between mineral and collagen phases in bone using X-ray diffraction techniques [J].
Borsato, KS ;
Sasaki, N .
JOURNAL OF BIOMECHANICS, 1997, 30 (09) :955-957
[4]   Entropic elasticity controls nanomechanics of single tropocollagen molecules [J].
Buehler, Markus J. ;
Wong, Sophie Y. .
BIOPHYSICAL JOURNAL, 2007, 93 (01) :37-43
[5]   Nature designs tough collagen: Explaining the nanostructure of collagen fibrils [J].
Buehler, Markus J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (33) :12285-12290
[6]   Atomistic and continuum modeling of mechanical properties of collagen: Elasticity, fracture, and self-assembly [J].
Buehler, Markus J. .
JOURNAL OF MATERIALS RESEARCH, 2006, 21 (08) :1947-1961
[7]   Cracking and adhesion at small scales: atomistic and continuum studies of flaw tolerant nanostructures [J].
Buehler, Markus J. ;
Yao, Haimin ;
Gao, Huajian ;
Ji, Baohua .
MODELLING AND SIMULATION IN MATERIALS SCIENCE AND ENGINEERING, 2006, 14 (05) :799-816
[8]  
BUEHLER MJ, 2007, J MECH BEHAV BIOMED
[9]  
BUEHLER MJ, 2004, SPRINGER LECT NOTES, P143
[10]   A model for the composite nanostructure of bone suggested by high-resolution transmission electron microscopy [J].
Cressey, BA ;
Cressey, G .
MINERALOGICAL MAGAZINE, 2003, 67 (06) :1171-1182