Percolation networks inside 3D model of the mineralized collagen fibril

被引:9
|
作者
Bini, Fabiano [1 ]
Pica, Andrada [1 ]
Marinozzi, Andrea [2 ]
Marinozzi, Franco [1 ]
机构
[1] Sapienza Univ Rome, Dept Mech & Aerosp Engn, Via Eudossiana 18, I-00184 Rome, Italy
[2] Campus Biomed Univ, Orthopedy & Traumatol Area, Via Alvaro del Portillo 200, I-00128 Rome, Italy
关键词
BONE ULTRASTRUCTURE; MICROMECHANICS; NANOSTRUCTURE; EVOLUTION; STIFFNESS; TISSUE; HYDROXYAPATITE; TRABECULAE; ELASTICITY; FRAGILITY;
D O I
10.1038/s41598-021-90916-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bone is a hierarchical biological material, characterized at the nanoscale by a recurring structure mainly composed of apatite mineral and collagen, i.e. the mineralized collagen fibril (MCF). Although the architecture of the MCF was extensively investigated by experimental and computational studies, it still represents a topic of debate. In this work, we developed a 3D continuum model of the mineral phase in the framework of percolation theory, that describes the transition from isolated to spanning cluster of connected platelets. Using Monte Carlo technique, we computed overall 120x10(6) iterations and investigated the formation of spanning networks of apatite minerals. We computed the percolation probability for different mineral volume fractions characteristic of human bone tissue. The findings highlight that the percolation threshold occurs at lower volume fractions for spanning clusters in the width direction with respect to the critical mineral volume fractions that characterize the percolation transition in the thickness and length directions. The formation of spanning clusters of minerals represents a condition of instability for the MCF, as it could be the onset of a high susceptibility to fracture. The 3D computational model developed in this study provides new, complementary insights to the experimental investigations concerning human MCF.
引用
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页数:13
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