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Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts

INTRODUCTION: Preclinical in vivo CT is commonly used to visualise vessels at a macroscopic scale. However, it is prone to many artefacts which can degrade the quality of CT images significantly. Although some artefacts can be partially corrected for during image processing, they are best avoided du...

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Autores principales: Kersemans, Veerle, Kannan, Pavitra, Beech, John S., Bates, Russell, Irving, Benjamin, Gilchrist, Stuart, Allen, Philip D., Thompson, James, Kinchesh, Paul, Casteleyn, Christophe, Schnabel, Julia, Partridge, Mike, Muschel, Ruth J., Smart, Sean C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457787/
https://www.ncbi.nlm.nih.gov/pubmed/26046526
http://dx.doi.org/10.1371/journal.pone.0128537
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author Kersemans, Veerle
Kannan, Pavitra
Beech, John S.
Bates, Russell
Irving, Benjamin
Gilchrist, Stuart
Allen, Philip D.
Thompson, James
Kinchesh, Paul
Casteleyn, Christophe
Schnabel, Julia
Partridge, Mike
Muschel, Ruth J.
Smart, Sean C.
author_facet Kersemans, Veerle
Kannan, Pavitra
Beech, John S.
Bates, Russell
Irving, Benjamin
Gilchrist, Stuart
Allen, Philip D.
Thompson, James
Kinchesh, Paul
Casteleyn, Christophe
Schnabel, Julia
Partridge, Mike
Muschel, Ruth J.
Smart, Sean C.
author_sort Kersemans, Veerle
collection PubMed
description INTRODUCTION: Preclinical in vivo CT is commonly used to visualise vessels at a macroscopic scale. However, it is prone to many artefacts which can degrade the quality of CT images significantly. Although some artefacts can be partially corrected for during image processing, they are best avoided during acquisition. Here, a novel imaging cradle and tumour holder was designed to maximise CT resolution. This approach was used to improve preclinical in vivo imaging of the tumour vasculature. PROCEDURES: A custom built cradle containing a tumour holder was developed and fix-mounted to the CT system gantry to avoid artefacts arising from scanner vibrations and out-of-field sample positioning. The tumour holder separated the tumour from bones along the axis of rotation of the CT scanner to avoid bone-streaking. It also kept the tumour stationary and insensitive to respiratory motion. System performance was evaluated in terms of tumour immobilisation and reduction of motion and bone artefacts. Pre- and post-contrast CT followed by sequential DCE-MRI of the tumour vasculature in xenograft transplanted mice was performed to confirm vessel patency and demonstrate the multimodal capacity of the new cradle. Vessel characteristics such as diameter, and branching were quantified. RESULTS: Image artefacts originating from bones and out-of-field sample positioning were avoided whilst those resulting from motions were reduced significantly, thereby maximising the resolution that can be achieved with CT imaging in vivo. Tumour vessels ≥ 77 μm could be resolved and blood flow to the tumour remained functional. The diameter of each tumour vessel was determined and plotted as histograms and vessel branching maps were created. Multimodal imaging using this cradle assembly was preserved and demonstrated. CONCLUSIONS: The presented imaging workflow minimised image artefacts arising from scanner induced vibrations, respiratory motion and radiopaque structures and enabled in vivo CT imaging and quantitative analysis of the tumour vasculature at higher resolution than was possible before. Moreover, it can be applied in a multimodal setting, therefore combining anatomical and dynamic information.
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spelling pubmed-44577872015-06-09 Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts Kersemans, Veerle Kannan, Pavitra Beech, John S. Bates, Russell Irving, Benjamin Gilchrist, Stuart Allen, Philip D. Thompson, James Kinchesh, Paul Casteleyn, Christophe Schnabel, Julia Partridge, Mike Muschel, Ruth J. Smart, Sean C. PLoS One Research Article INTRODUCTION: Preclinical in vivo CT is commonly used to visualise vessels at a macroscopic scale. However, it is prone to many artefacts which can degrade the quality of CT images significantly. Although some artefacts can be partially corrected for during image processing, they are best avoided during acquisition. Here, a novel imaging cradle and tumour holder was designed to maximise CT resolution. This approach was used to improve preclinical in vivo imaging of the tumour vasculature. PROCEDURES: A custom built cradle containing a tumour holder was developed and fix-mounted to the CT system gantry to avoid artefacts arising from scanner vibrations and out-of-field sample positioning. The tumour holder separated the tumour from bones along the axis of rotation of the CT scanner to avoid bone-streaking. It also kept the tumour stationary and insensitive to respiratory motion. System performance was evaluated in terms of tumour immobilisation and reduction of motion and bone artefacts. Pre- and post-contrast CT followed by sequential DCE-MRI of the tumour vasculature in xenograft transplanted mice was performed to confirm vessel patency and demonstrate the multimodal capacity of the new cradle. Vessel characteristics such as diameter, and branching were quantified. RESULTS: Image artefacts originating from bones and out-of-field sample positioning were avoided whilst those resulting from motions were reduced significantly, thereby maximising the resolution that can be achieved with CT imaging in vivo. Tumour vessels ≥ 77 μm could be resolved and blood flow to the tumour remained functional. The diameter of each tumour vessel was determined and plotted as histograms and vessel branching maps were created. Multimodal imaging using this cradle assembly was preserved and demonstrated. CONCLUSIONS: The presented imaging workflow minimised image artefacts arising from scanner induced vibrations, respiratory motion and radiopaque structures and enabled in vivo CT imaging and quantitative analysis of the tumour vasculature at higher resolution than was possible before. Moreover, it can be applied in a multimodal setting, therefore combining anatomical and dynamic information. Public Library of Science 2015-06-05 /pmc/articles/PMC4457787/ /pubmed/26046526 http://dx.doi.org/10.1371/journal.pone.0128537 Text en © 2015 Kersemans et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kersemans, Veerle
Kannan, Pavitra
Beech, John S.
Bates, Russell
Irving, Benjamin
Gilchrist, Stuart
Allen, Philip D.
Thompson, James
Kinchesh, Paul
Casteleyn, Christophe
Schnabel, Julia
Partridge, Mike
Muschel, Ruth J.
Smart, Sean C.
Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts
title Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts
title_full Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts
title_fullStr Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts
title_full_unstemmed Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts
title_short Improving In Vivo High-Resolution CT Imaging of the Tumour Vasculature in Xenograft Mouse Models through Reduction of Motion and Bone-Streak Artefacts
title_sort improving in vivo high-resolution ct imaging of the tumour vasculature in xenograft mouse models through reduction of motion and bone-streak artefacts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4457787/
https://www.ncbi.nlm.nih.gov/pubmed/26046526
http://dx.doi.org/10.1371/journal.pone.0128537
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