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Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice
(18)F-sodium fluoride ((18)F-NaF) is a positron emission tomography (PET) radiotracer widely used in skeletal imaging and has also been proposed as a biomarker of active calcification in atherosclerosis. Like most PET radiotracers, (18)F-NaF is typically administered intravenously. However in small...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970902/ https://www.ncbi.nlm.nih.gov/pubmed/33750874 http://dx.doi.org/10.1038/s41598-021-85073-0 |
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author | Gonzalez-Galofre, Zaniah N. Alcaide-Corral, Carlos J. Tavares, Adriana A. S. |
author_facet | Gonzalez-Galofre, Zaniah N. Alcaide-Corral, Carlos J. Tavares, Adriana A. S. |
author_sort | Gonzalez-Galofre, Zaniah N. |
collection | PubMed |
description | (18)F-sodium fluoride ((18)F-NaF) is a positron emission tomography (PET) radiotracer widely used in skeletal imaging and has also been proposed as a biomarker of active calcification in atherosclerosis. Like most PET radiotracers, (18)F-NaF is typically administered intravenously. However in small animal research intravenous administrations can be challenging, because partial paravenous injection is common due to the small calibre of the superficial tail veins and repeat administrations via tail veins can lead to tissue injury therefore limiting the total number of longitudinal scanning points. In this paper, the feasibility of using intra-peritoneal route of injection of (8)F-NaF to study calcification in mice was studied by looking at the kinetic and uptake profiles of normal soft tissues and bones versus intra-vascular injections. Dynamic PET was performed for 60 min on nineteen isoflurane-anesthetized male Swiss mice after femoral artery (n = 7), femoral vein (n = 6) or intraperitoneal (n = 6) injection of (8)F-NaF. PET data were reconstructed and the standardised uptake value (SUV) and standardised uptake value ratio (SUVr) were estimated from the last three frames between 45- and 60-min and (8)F-NaF uptake constant (K(i)) was derived by Patlak graphical analysis. In soft tissue, the (18)F-NaF perfusion phase changes depending on the type on injection route, whereas the uptake phase is similar regardless of the administration route. In bone tissue SUV, SUVr and K(i) measures were not significantly different between the three administration routes. Comparison between PET and CT measures showed that bones that had the highest CT density displayed the lowest PET activity and conversely, bones where CT units were low had high (8)F-NaF uptake. Intraperitoneal injection is a valid and practical alternative to the intra-vascular injections in small-animal (18)F-NaF PET imaging providing equivalent pharmacokinetic data. CT outcome measures report on sites of stablished calcification whereas PET measures sites of higher complexity and active calcification. |
format | Online Article Text |
id | pubmed-7970902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79709022021-03-19 Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice Gonzalez-Galofre, Zaniah N. Alcaide-Corral, Carlos J. Tavares, Adriana A. S. Sci Rep Article (18)F-sodium fluoride ((18)F-NaF) is a positron emission tomography (PET) radiotracer widely used in skeletal imaging and has also been proposed as a biomarker of active calcification in atherosclerosis. Like most PET radiotracers, (18)F-NaF is typically administered intravenously. However in small animal research intravenous administrations can be challenging, because partial paravenous injection is common due to the small calibre of the superficial tail veins and repeat administrations via tail veins can lead to tissue injury therefore limiting the total number of longitudinal scanning points. In this paper, the feasibility of using intra-peritoneal route of injection of (8)F-NaF to study calcification in mice was studied by looking at the kinetic and uptake profiles of normal soft tissues and bones versus intra-vascular injections. Dynamic PET was performed for 60 min on nineteen isoflurane-anesthetized male Swiss mice after femoral artery (n = 7), femoral vein (n = 6) or intraperitoneal (n = 6) injection of (8)F-NaF. PET data were reconstructed and the standardised uptake value (SUV) and standardised uptake value ratio (SUVr) were estimated from the last three frames between 45- and 60-min and (8)F-NaF uptake constant (K(i)) was derived by Patlak graphical analysis. In soft tissue, the (18)F-NaF perfusion phase changes depending on the type on injection route, whereas the uptake phase is similar regardless of the administration route. In bone tissue SUV, SUVr and K(i) measures were not significantly different between the three administration routes. Comparison between PET and CT measures showed that bones that had the highest CT density displayed the lowest PET activity and conversely, bones where CT units were low had high (8)F-NaF uptake. Intraperitoneal injection is a valid and practical alternative to the intra-vascular injections in small-animal (18)F-NaF PET imaging providing equivalent pharmacokinetic data. CT outcome measures report on sites of stablished calcification whereas PET measures sites of higher complexity and active calcification. Nature Publishing Group UK 2021-03-09 /pmc/articles/PMC7970902/ /pubmed/33750874 http://dx.doi.org/10.1038/s41598-021-85073-0 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gonzalez-Galofre, Zaniah N. Alcaide-Corral, Carlos J. Tavares, Adriana A. S. Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice |
title | Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice |
title_full | Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice |
title_fullStr | Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice |
title_full_unstemmed | Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice |
title_short | Effects of administration route on uptake kinetics of (18)F-sodium fluoride positron emission tomography in mice |
title_sort | effects of administration route on uptake kinetics of (18)f-sodium fluoride positron emission tomography in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970902/ https://www.ncbi.nlm.nih.gov/pubmed/33750874 http://dx.doi.org/10.1038/s41598-021-85073-0 |
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