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Percolation networks inside 3D model of the mineralized collagen fibril
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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166932/ https://www.ncbi.nlm.nih.gov/pubmed/34059767 http://dx.doi.org/10.1038/s41598-021-90916-x |
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author | Bini, Fabiano Pica, Andrada Marinozzi, Andrea Marinozzi, Franco |
author_facet | Bini, Fabiano Pica, Andrada Marinozzi, Andrea Marinozzi, Franco |
author_sort | Bini, Fabiano |
collection | PubMed |
description | 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 120 × 10(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. |
format | Online Article Text |
id | pubmed-8166932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81669322021-06-02 Percolation networks inside 3D model of the mineralized collagen fibril Bini, Fabiano Pica, Andrada Marinozzi, Andrea Marinozzi, Franco Sci Rep Article 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 120 × 10(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. Nature Publishing Group UK 2021-05-31 /pmc/articles/PMC8166932/ /pubmed/34059767 http://dx.doi.org/10.1038/s41598-021-90916-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bini, Fabiano Pica, Andrada Marinozzi, Andrea Marinozzi, Franco Percolation networks inside 3D model of the mineralized collagen fibril |
title | Percolation networks inside 3D model of the mineralized collagen fibril |
title_full | Percolation networks inside 3D model of the mineralized collagen fibril |
title_fullStr | Percolation networks inside 3D model of the mineralized collagen fibril |
title_full_unstemmed | Percolation networks inside 3D model of the mineralized collagen fibril |
title_short | Percolation networks inside 3D model of the mineralized collagen fibril |
title_sort | percolation networks inside 3d model of the mineralized collagen fibril |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166932/ https://www.ncbi.nlm.nih.gov/pubmed/34059767 http://dx.doi.org/10.1038/s41598-021-90916-x |
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