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Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone

Bone has a sophisticated architecture characterized by a hierarchical organization, starting at the sub-micrometre level. Thus, the analysis of the mechanical and structural properties of bone at this scale is essential to understand the relationship between its physiology, physical properties and c...

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Autores principales: Alunni Cardinali, M., Di Michele, A., Mattarelli, M., Caponi, S., Govoni, M., Dallari, D., Brogini, S., Masia, F., Borri, P., Langbein, W., Palombo, F., Morresi, A., Fioretto, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807060/
https://www.ncbi.nlm.nih.gov/pubmed/35104431
http://dx.doi.org/10.1098/rsif.2021.0642
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author Alunni Cardinali, M.
Di Michele, A.
Mattarelli, M.
Caponi, S.
Govoni, M.
Dallari, D.
Brogini, S.
Masia, F.
Borri, P.
Langbein, W.
Palombo, F.
Morresi, A.
Fioretto, D.
author_facet Alunni Cardinali, M.
Di Michele, A.
Mattarelli, M.
Caponi, S.
Govoni, M.
Dallari, D.
Brogini, S.
Masia, F.
Borri, P.
Langbein, W.
Palombo, F.
Morresi, A.
Fioretto, D.
author_sort Alunni Cardinali, M.
collection PubMed
description Bone has a sophisticated architecture characterized by a hierarchical organization, starting at the sub-micrometre level. Thus, the analysis of the mechanical and structural properties of bone at this scale is essential to understand the relationship between its physiology, physical properties and chemical composition. Here, we unveil the potential of Brillouin–Raman microspectroscopy (BRaMS), an emerging correlative optical approach that can simultaneously assess bone mechanics and chemistry with micrometric resolution. Correlative hyperspectral imaging, performed on a human diaphyseal ring, reveals a complex microarchitecture that is reflected in extremely rich and informative spectra. An innovative method for mechanical properties analysis is proposed, mapping the intermixing of soft and hard tissue areas and revealing the coexistence of regions involved in remodelling processes, nutrient transportation and structural support. The mineralized regions appear elastically inhomogeneous, resembling the pattern of the osteons' lamellae, while Raman and energy-dispersive X-ray images through scanning electron microscopy show an overall uniform distribution of the mineral content, suggesting that other structural factors are responsible for lamellar micromechanical heterogeneity. These results, besides giving an important insight into cortical bone tissue properties, highlight the potential of BRaMS to access the origin of anisotropic mechanical properties, which are almost ubiquitous in other biological tissues.
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spelling pubmed-88070602022-02-18 Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone Alunni Cardinali, M. Di Michele, A. Mattarelli, M. Caponi, S. Govoni, M. Dallari, D. Brogini, S. Masia, F. Borri, P. Langbein, W. Palombo, F. Morresi, A. Fioretto, D. J R Soc Interface Life Sciences–Physics interface Bone has a sophisticated architecture characterized by a hierarchical organization, starting at the sub-micrometre level. Thus, the analysis of the mechanical and structural properties of bone at this scale is essential to understand the relationship between its physiology, physical properties and chemical composition. Here, we unveil the potential of Brillouin–Raman microspectroscopy (BRaMS), an emerging correlative optical approach that can simultaneously assess bone mechanics and chemistry with micrometric resolution. Correlative hyperspectral imaging, performed on a human diaphyseal ring, reveals a complex microarchitecture that is reflected in extremely rich and informative spectra. An innovative method for mechanical properties analysis is proposed, mapping the intermixing of soft and hard tissue areas and revealing the coexistence of regions involved in remodelling processes, nutrient transportation and structural support. The mineralized regions appear elastically inhomogeneous, resembling the pattern of the osteons' lamellae, while Raman and energy-dispersive X-ray images through scanning electron microscopy show an overall uniform distribution of the mineral content, suggesting that other structural factors are responsible for lamellar micromechanical heterogeneity. These results, besides giving an important insight into cortical bone tissue properties, highlight the potential of BRaMS to access the origin of anisotropic mechanical properties, which are almost ubiquitous in other biological tissues. The Royal Society 2022-02-02 /pmc/articles/PMC8807060/ /pubmed/35104431 http://dx.doi.org/10.1098/rsif.2021.0642 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Physics interface
Alunni Cardinali, M.
Di Michele, A.
Mattarelli, M.
Caponi, S.
Govoni, M.
Dallari, D.
Brogini, S.
Masia, F.
Borri, P.
Langbein, W.
Palombo, F.
Morresi, A.
Fioretto, D.
Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
title Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
title_full Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
title_fullStr Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
title_full_unstemmed Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
title_short Brillouin–Raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
title_sort brillouin–raman microspectroscopy for the morpho-mechanical imaging of human lamellar bone
topic Life Sciences–Physics interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807060/
https://www.ncbi.nlm.nih.gov/pubmed/35104431
http://dx.doi.org/10.1098/rsif.2021.0642
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