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Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study
BACKGROUND: In this study, we investigated the feasibility of quantitative ultrashort echo time (qUTE) magnetic resonance (MR) imaging techniques in the detection and quantification of iron oxide nanoparticle (IONP)-labeled stem cells. METHODS: A stem cell phantom containing multiple layers of unlab...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929408/ https://www.ncbi.nlm.nih.gov/pubmed/36819276 http://dx.doi.org/10.21037/qims-22-654 |
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author | Athertya, Jiyo S. Akers, Johnny Sedaghat, Sam Wei, Zhao Moazamian, Dina Dwek, Sophia Thu, Mya Jang, Hyungseok |
author_facet | Athertya, Jiyo S. Akers, Johnny Sedaghat, Sam Wei, Zhao Moazamian, Dina Dwek, Sophia Thu, Mya Jang, Hyungseok |
author_sort | Athertya, Jiyo S. |
collection | PubMed |
description | BACKGROUND: In this study, we investigated the feasibility of quantitative ultrashort echo time (qUTE) magnetic resonance (MR) imaging techniques in the detection and quantification of iron oxide nanoparticle (IONP)-labeled stem cells. METHODS: A stem cell phantom containing multiple layers of unlabeled or labeled stem cells with different densities was prepared. The phantom was imaged with quantitative UTE (qUTE) MR techniques [i.e., UTE-T(1) mapping, UTE-T(2)* mapping, and UTE-based quantitative susceptibility mapping (UTE-QSM)] as well as with a clinical T(2) mapping sequence on a 3T clinical MR system. For T(1) mapping, a variable flip angle (VFA) method based on actual flip angle imaging (AFI) technique was utilized. For T(2)* mapping and UTE-QSM, multiple images with variable, interleaved echo times including UTE images and gradient recalled echo (GRE) images were used. For UTE-QSM, the phase information from the multi-echo images was utilized and processed using a QSM framework based on the morphology-enabled dipole inversion (MEDI) algorithm. The qUTE techniques were also evaluated in an ex vivo experiment with a mouse injected with IONP-labeled stem cells. RESULTS: In the phantom experiment, the parameters estimated with qUTE techniques showed high linearity with respect to the density of IONP-labeled stem cells (R(2)>0.99), while the clinical T(2) parameter showed impaired linearity (R(2)=0.87). In the ex vivo mouse experiment, UTE-T(2)* mapping and UTE-QSM showed feasibility in the detection of injected stem cells with high contrast, whereas UTE-T(1) and UTE-T(2)* showed limited detection. Overall, UTE-QSM demonstrated the best contrast of all, with other methods being subjected more to a confounding factor due to different magnetic susceptibilities of various types of neighboring tissues, which creates inhomogeneous contrast that behaves similar to IONP. CONCLUSIONS: In this study, we evaluated the feasibility of a series of qUTE imaging techniques as well as conventional T(2) mapping for the detection of IONP-labeled stem cells in vitro and ex vivo. UTE-QSM performed superior amongst other qUTE techniques as well as conventional T(2) mapping in detecting stem cells with high contrast. |
format | Online Article Text |
id | pubmed-9929408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-99294082023-02-16 Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study Athertya, Jiyo S. Akers, Johnny Sedaghat, Sam Wei, Zhao Moazamian, Dina Dwek, Sophia Thu, Mya Jang, Hyungseok Quant Imaging Med Surg Original Article BACKGROUND: In this study, we investigated the feasibility of quantitative ultrashort echo time (qUTE) magnetic resonance (MR) imaging techniques in the detection and quantification of iron oxide nanoparticle (IONP)-labeled stem cells. METHODS: A stem cell phantom containing multiple layers of unlabeled or labeled stem cells with different densities was prepared. The phantom was imaged with quantitative UTE (qUTE) MR techniques [i.e., UTE-T(1) mapping, UTE-T(2)* mapping, and UTE-based quantitative susceptibility mapping (UTE-QSM)] as well as with a clinical T(2) mapping sequence on a 3T clinical MR system. For T(1) mapping, a variable flip angle (VFA) method based on actual flip angle imaging (AFI) technique was utilized. For T(2)* mapping and UTE-QSM, multiple images with variable, interleaved echo times including UTE images and gradient recalled echo (GRE) images were used. For UTE-QSM, the phase information from the multi-echo images was utilized and processed using a QSM framework based on the morphology-enabled dipole inversion (MEDI) algorithm. The qUTE techniques were also evaluated in an ex vivo experiment with a mouse injected with IONP-labeled stem cells. RESULTS: In the phantom experiment, the parameters estimated with qUTE techniques showed high linearity with respect to the density of IONP-labeled stem cells (R(2)>0.99), while the clinical T(2) parameter showed impaired linearity (R(2)=0.87). In the ex vivo mouse experiment, UTE-T(2)* mapping and UTE-QSM showed feasibility in the detection of injected stem cells with high contrast, whereas UTE-T(1) and UTE-T(2)* showed limited detection. Overall, UTE-QSM demonstrated the best contrast of all, with other methods being subjected more to a confounding factor due to different magnetic susceptibilities of various types of neighboring tissues, which creates inhomogeneous contrast that behaves similar to IONP. CONCLUSIONS: In this study, we evaluated the feasibility of a series of qUTE imaging techniques as well as conventional T(2) mapping for the detection of IONP-labeled stem cells in vitro and ex vivo. UTE-QSM performed superior amongst other qUTE techniques as well as conventional T(2) mapping in detecting stem cells with high contrast. AME Publishing Company 2023-01-09 2023-02-01 /pmc/articles/PMC9929408/ /pubmed/36819276 http://dx.doi.org/10.21037/qims-22-654 Text en 2023 Quantitative Imaging in Medicine and Surgery. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Athertya, Jiyo S. Akers, Johnny Sedaghat, Sam Wei, Zhao Moazamian, Dina Dwek, Sophia Thu, Mya Jang, Hyungseok Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
title | Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
title_full | Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
title_fullStr | Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
title_full_unstemmed | Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
title_short | Detection of iron oxide nanoparticle (IONP)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
title_sort | detection of iron oxide nanoparticle (ionp)-labeled stem cells using quantitative ultrashort echo time imaging: a feasibility study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929408/ https://www.ncbi.nlm.nih.gov/pubmed/36819276 http://dx.doi.org/10.21037/qims-22-654 |
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