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Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents

Spectral photon-counting computed tomography (SPCCT) is a rapidly emerging imaging modality that provides energy-dependent information on individual x-ray photons, leading to accurate material decomposition and simultaneous quantification of multiple contrast generating materials. Development of SPC...

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Autores principales: Kim, Johoon, Bar-Ness, Daniel, Si-Mohamed, Salim, Coulon, Philippe, Blevis, Ira, Douek, Philippe, Cormode, David P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092324/
https://www.ncbi.nlm.nih.gov/pubmed/30108247
http://dx.doi.org/10.1038/s41598-018-30570-y
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author Kim, Johoon
Bar-Ness, Daniel
Si-Mohamed, Salim
Coulon, Philippe
Blevis, Ira
Douek, Philippe
Cormode, David P.
author_facet Kim, Johoon
Bar-Ness, Daniel
Si-Mohamed, Salim
Coulon, Philippe
Blevis, Ira
Douek, Philippe
Cormode, David P.
author_sort Kim, Johoon
collection PubMed
description Spectral photon-counting computed tomography (SPCCT) is a rapidly emerging imaging modality that provides energy-dependent information on individual x-ray photons, leading to accurate material decomposition and simultaneous quantification of multiple contrast generating materials. Development of SPCCT-specific contrast agents is needed to overcome the issues with currently used iodinated contrast agents, such as difficulty in differentiation from calcified structures, and yield SPCCT’s full promise. In this study, the contrast generation of different elements is investigated using a prototype SPCCT scanner based on a modified clinical CT system and suitable elements for novel contrast agent development for SPCCT imaging are identified. Furthermore, nanoparticles were synthesized from tantalum as a proof of concept spectral photon-counting CT agent and tested for their in vitro cytotoxicity and contrast generation to provide insight into the feasibility of nanoparticle contrast agent development from these elements. We found that gadolinium, ytterbium and tantalum generate high contrast in spectral photon-counting CT imaging and may be suitable elements for contrast agent development for this modality. Our proof of concept results with tantalum-based nanoparticles underscore this conclusion due to their detectability with spectral photon-counting CT, as well as their biocompatibility.
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spelling pubmed-60923242018-08-20 Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents Kim, Johoon Bar-Ness, Daniel Si-Mohamed, Salim Coulon, Philippe Blevis, Ira Douek, Philippe Cormode, David P. Sci Rep Article Spectral photon-counting computed tomography (SPCCT) is a rapidly emerging imaging modality that provides energy-dependent information on individual x-ray photons, leading to accurate material decomposition and simultaneous quantification of multiple contrast generating materials. Development of SPCCT-specific contrast agents is needed to overcome the issues with currently used iodinated contrast agents, such as difficulty in differentiation from calcified structures, and yield SPCCT’s full promise. In this study, the contrast generation of different elements is investigated using a prototype SPCCT scanner based on a modified clinical CT system and suitable elements for novel contrast agent development for SPCCT imaging are identified. Furthermore, nanoparticles were synthesized from tantalum as a proof of concept spectral photon-counting CT agent and tested for their in vitro cytotoxicity and contrast generation to provide insight into the feasibility of nanoparticle contrast agent development from these elements. We found that gadolinium, ytterbium and tantalum generate high contrast in spectral photon-counting CT imaging and may be suitable elements for contrast agent development for this modality. Our proof of concept results with tantalum-based nanoparticles underscore this conclusion due to their detectability with spectral photon-counting CT, as well as their biocompatibility. Nature Publishing Group UK 2018-08-14 /pmc/articles/PMC6092324/ /pubmed/30108247 http://dx.doi.org/10.1038/s41598-018-30570-y Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Johoon
Bar-Ness, Daniel
Si-Mohamed, Salim
Coulon, Philippe
Blevis, Ira
Douek, Philippe
Cormode, David P.
Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents
title Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents
title_full Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents
title_fullStr Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents
title_full_unstemmed Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents
title_short Assessment of candidate elements for development of spectral photon-counting CT specific contrast agents
title_sort assessment of candidate elements for development of spectral photon-counting ct specific contrast agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092324/
https://www.ncbi.nlm.nih.gov/pubmed/30108247
http://dx.doi.org/10.1038/s41598-018-30570-y
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