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Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials
X-ray nano-tomography with phase contrast (nanoCT) using synchrotron radiation is a powerful tool to non-destructively investigate 3D material properties at the nanoscale. In large bone lesions, such as severe bone fractures, bone cancer or other diseases, bone grafts substituting the lost bone migh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070718/ https://www.ncbi.nlm.nih.gov/pubmed/35511016 http://dx.doi.org/10.1107/S1600577522003137 |
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author | Suuronen, Jussi-Petteri Hesse, Bernhard Langer, Max Bohner, Marc Villanova, Julie |
author_facet | Suuronen, Jussi-Petteri Hesse, Bernhard Langer, Max Bohner, Marc Villanova, Julie |
author_sort | Suuronen, Jussi-Petteri |
collection | PubMed |
description | X-ray nano-tomography with phase contrast (nanoCT) using synchrotron radiation is a powerful tool to non-destructively investigate 3D material properties at the nanoscale. In large bone lesions, such as severe bone fractures, bone cancer or other diseases, bone grafts substituting the lost bone might be necessary. Such grafts can be of biological origin or be composed of a synthetic bone substitute. The long-term functioning of artificial bone substitutes depends on many factors. Synchrotron nanoCT imaging has great potential to contribute to further the understanding of integration of implants into bone tissue by imaging the spatial interaction between bone tissue and implant, and by accessing the interface between implant material and bone tissue. With this aim, a methodology for evaluating the image quality is presented for in-line phase contrast nanoCT images of bone scaffold samples. A PMMA-embedded tricalcium phosphate scaffold was used with both a closed and an open porosity structure and bone ingrowths as a representative system of three known materials. Parameters such as spatial resolution and signal-to-noise ratio were extracted and used to explore and quantitatively compare the effects of implementation choices in the imaging setup, such as camera technology and imaging energy, on the resulting image quality. Increasing the X-ray energy from 17.5 keV to 29.6 keV leads to a notable improvement in image quality regardless of the camera technology used, with the two tested camera setups performing at a comparable level when the recorded intensity was kept constant. |
format | Online Article Text |
id | pubmed-9070718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-90707182022-05-10 Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials Suuronen, Jussi-Petteri Hesse, Bernhard Langer, Max Bohner, Marc Villanova, Julie J Synchrotron Radiat Research Papers X-ray nano-tomography with phase contrast (nanoCT) using synchrotron radiation is a powerful tool to non-destructively investigate 3D material properties at the nanoscale. In large bone lesions, such as severe bone fractures, bone cancer or other diseases, bone grafts substituting the lost bone might be necessary. Such grafts can be of biological origin or be composed of a synthetic bone substitute. The long-term functioning of artificial bone substitutes depends on many factors. Synchrotron nanoCT imaging has great potential to contribute to further the understanding of integration of implants into bone tissue by imaging the spatial interaction between bone tissue and implant, and by accessing the interface between implant material and bone tissue. With this aim, a methodology for evaluating the image quality is presented for in-line phase contrast nanoCT images of bone scaffold samples. A PMMA-embedded tricalcium phosphate scaffold was used with both a closed and an open porosity structure and bone ingrowths as a representative system of three known materials. Parameters such as spatial resolution and signal-to-noise ratio were extracted and used to explore and quantitatively compare the effects of implementation choices in the imaging setup, such as camera technology and imaging energy, on the resulting image quality. Increasing the X-ray energy from 17.5 keV to 29.6 keV leads to a notable improvement in image quality regardless of the camera technology used, with the two tested camera setups performing at a comparable level when the recorded intensity was kept constant. International Union of Crystallography 2022-04-25 /pmc/articles/PMC9070718/ /pubmed/35511016 http://dx.doi.org/10.1107/S1600577522003137 Text en © Jussi-Petteri Suuronen et al. 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Research Papers Suuronen, Jussi-Petteri Hesse, Bernhard Langer, Max Bohner, Marc Villanova, Julie Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials |
title | Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials |
title_full | Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials |
title_fullStr | Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials |
title_full_unstemmed | Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials |
title_short | Evaluation of imaging setups for quantitative phase contrast nanoCT of mineralized biomaterials |
title_sort | evaluation of imaging setups for quantitative phase contrast nanoct of mineralized biomaterials |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070718/ https://www.ncbi.nlm.nih.gov/pubmed/35511016 http://dx.doi.org/10.1107/S1600577522003137 |
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