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      Contrast-Enhanced MicroCT for Virtual 3D Anatomical Pathology of Biological Tissues: A Literature Review

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          Abstract

          To date, the combination of histological sectioning, staining, and microscopic assessment of the 2D sections is still the golden standard for structural and compositional analysis of biological tissues. X-ray microfocus computed tomography (microCT) is an emerging 3D imaging technique with high potential for 3D structural analysis of biological tissues with a complex and heterogeneous 3D structure, such as the trabecular bone. However, its use has been mostly limited to mineralized tissues because of the inherently low X-ray absorption of soft tissues. To achieve sufficient X-ray attenuation, chemical compounds containing high atomic number elements that bind to soft tissues have been recently adopted as contrast agents (CAs) for contrast-enhanced microCT (CE-CT); this novel technique is very promising for quantitative “virtual” 3D anatomical pathology of both mineralized and soft biological tissues. In this paper, we provided a review of the advances in CE-CT since the very first reports on the technology to date. Perfusion CAs for in vivo imaging have not been discussed, as the focus of this review was on CAs that bind to the tissue of interest and that are, thus, used for ex vivo imaging of biological tissues. As CE-CT has mostly been applied for the characterization of musculoskeletal tissues, we have put specific emphasis on these tissues. Advantages and limitations of multiple CAs for different musculoskeletal tissues have been highlighted, and their reproducibility has been discussed. Additionally, the advantages of the “full” 3D CE-CT information have been pinpointed, and its importance for more detailed structural, spatial, and functional characterization of the tissues of interest has been shown. Finally, the remaining challenges that are still hampering a broader adoption of CE-CT have been highlighted, and suggestions have been made to move the field of CE-CT imaging one step further towards a standard accepted tool for quantitative virtual 3D anatomical pathology.

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          Most cited references54

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          X-ray-computed tomography contrast agents.

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            The microstructure and micromechanics of the tendon–bone insertion

            High-resolution imaging, composition analysis and mechanical testing provide a new insight into the structure and function of the Achilles enthesis.
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              Concentration-dependent specimen shrinkage in iodine-enhanced microCT.

              Iodine potassium iodide (I2 KI) solution can be employed as a contrast agent for the visualisation of soft tissue structures in micro-computed tomography studies. This technique provides high resolution images of soft tissue non-destructively but initial studies suggest that the stain can cause substantial specimen shrinkage. The degree of specimen shrinkage, and potential deformation, is an important consideration when using the data for morphological studies. Here we quantify the macroscopic volume changes in mouse skeletal muscle, cardiac muscle and cerebellum as a result of immersion in the common fixatives 10% phosphate-buffered formal saline, 70% ethanol and 3% glutaraldehyde, compared with I2 KI staining solution at concentrations of 2, 6, 10 and 20%. Immersion in the I2 KI solution resulted in dramatic changes of tissue volume, which were far larger than the shrinkage from formalin fixation alone. The degree of macroscopic change was most dependent upon the I2 KI concentration, with severe shrinkage of 70% seen in solutions of 20% I2 KI after 14 days' incubation. When using this technique care needs to be taken to use the lowest concentration that will give adequate contrast to minimise artefacts due to shrinkage. © 2013 Anatomical Society.
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                Author and article information

                Contributors
                Journal
                Contrast Media Mol Imaging
                Contrast Media Mol Imaging
                CMMI
                Contrast Media & Molecular Imaging
                Hindawi
                1555-4309
                1555-4317
                2019
                28 February 2019
                : 2019
                : 8617406
                Affiliations
                1Prometheus, Division of Skeletal Tissue Engineering, KU Leuven, Leuven, Belgium
                2Biomechanics Section, Department of Mechanical Engineering, KU Leuven, Leuven, Belgium
                3Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Leuven, Belgium
                4Biomechanics Lab, Institute of Mechanics, Materials and Civil Engineering, UCLouvain, Louvain-la-Neuve, Belgium
                5Department Materials Engineering, KU Leuven, Leuven, Belgium
                Author notes

                Academic Editor: Anne Roivainen

                Author information
                http://orcid.org/0000-0002-2071-7215
                http://orcid.org/0000-0001-6682-9936
                http://orcid.org/0000-0002-1750-8324
                Article
                10.1155/2019/8617406
                6421764
                30944550
                dbc5e573-da2c-4b27-9a38-8f3eadb4f755
                Copyright © 2019 Sébastien de Bournonville et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 2 October 2018
                : 7 February 2019
                Funding
                Funded by: Fonds Wetenschappelijk Onderzoek
                Award ID: 1S67217N
                Award ID: G088218N
                Funded by: Hercules Foundation
                Award ID: AKUL 13/47
                Categories
                Review Article

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