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T(1)- and T(2)-weighted Magnetic Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide Nanoparticles with Abrupt Cellular Internalization and Immune Evasion
[Image: see text] Conventional T(1)- or T(2)-weighted single mode contrast-enhanced magnetic resonance imaging (MRI) may produce false results. Thereby, there is a need to develop dual contrast agents, T(1)- and T(2)-weighted, for more accurate MRI imaging. The dual contrast agents should possess hi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077774/ https://www.ncbi.nlm.nih.gov/pubmed/30094416 http://dx.doi.org/10.1021/acsabm.8b00016 |
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author | Thapa, Bibek Diaz-Diestra, Daysi Santiago-Medina, Carlene Kumar, Nitu Tu, Kaixiong Beltran-Huarac, Juan Jadwisienczak, Wojciech M. Weiner, Brad R. Morell, Gerardo |
author_facet | Thapa, Bibek Diaz-Diestra, Daysi Santiago-Medina, Carlene Kumar, Nitu Tu, Kaixiong Beltran-Huarac, Juan Jadwisienczak, Wojciech M. Weiner, Brad R. Morell, Gerardo |
author_sort | Thapa, Bibek |
collection | PubMed |
description | [Image: see text] Conventional T(1)- or T(2)-weighted single mode contrast-enhanced magnetic resonance imaging (MRI) may produce false results. Thereby, there is a need to develop dual contrast agents, T(1)- and T(2)-weighted, for more accurate MRI imaging. The dual contrast agents should possess high magnetic resonance (MR) relaxivities, targeted tumor linking, and minimum recognition by the immune system. We have developed nitrodopamine-PEG grafted single core truncated cubic iron oxide nanoparticles (ND-PEG-tNCIOs) capable of producing marked dual contrasts in MRI with enhanced longitudinal and transverse relaxivities of 32 ± 1.29 and 791 ± 38.39 mM(–1) s(–1), respectively. Furthermore, the ND-PEG-tNCIOs show excellent colloidal stability in physiological buffers and higher cellular internalization in cancerous cells than in phagocytic cells, indicating the immune evasive capability of the nanoparticles. These findings indicate that tNCIOs are strong candidates for dual contrast MRI imaging, which is vital for noninvasive real-time detection of nascent cancer cells in vivo and for monitoring stem cells transplants. |
format | Online Article Text |
id | pubmed-6077774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60777742018-08-07 T(1)- and T(2)-weighted Magnetic Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide Nanoparticles with Abrupt Cellular Internalization and Immune Evasion Thapa, Bibek Diaz-Diestra, Daysi Santiago-Medina, Carlene Kumar, Nitu Tu, Kaixiong Beltran-Huarac, Juan Jadwisienczak, Wojciech M. Weiner, Brad R. Morell, Gerardo ACS Appl Bio Mater [Image: see text] Conventional T(1)- or T(2)-weighted single mode contrast-enhanced magnetic resonance imaging (MRI) may produce false results. Thereby, there is a need to develop dual contrast agents, T(1)- and T(2)-weighted, for more accurate MRI imaging. The dual contrast agents should possess high magnetic resonance (MR) relaxivities, targeted tumor linking, and minimum recognition by the immune system. We have developed nitrodopamine-PEG grafted single core truncated cubic iron oxide nanoparticles (ND-PEG-tNCIOs) capable of producing marked dual contrasts in MRI with enhanced longitudinal and transverse relaxivities of 32 ± 1.29 and 791 ± 38.39 mM(–1) s(–1), respectively. Furthermore, the ND-PEG-tNCIOs show excellent colloidal stability in physiological buffers and higher cellular internalization in cancerous cells than in phagocytic cells, indicating the immune evasive capability of the nanoparticles. These findings indicate that tNCIOs are strong candidates for dual contrast MRI imaging, which is vital for noninvasive real-time detection of nascent cancer cells in vivo and for monitoring stem cells transplants. American Chemical Society 2018-06-15 2018-07-16 /pmc/articles/PMC6077774/ /pubmed/30094416 http://dx.doi.org/10.1021/acsabm.8b00016 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Thapa, Bibek Diaz-Diestra, Daysi Santiago-Medina, Carlene Kumar, Nitu Tu, Kaixiong Beltran-Huarac, Juan Jadwisienczak, Wojciech M. Weiner, Brad R. Morell, Gerardo T(1)- and T(2)-weighted Magnetic Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide Nanoparticles with Abrupt Cellular Internalization and Immune Evasion |
title | T(1)- and T(2)-weighted Magnetic
Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide
Nanoparticles with Abrupt Cellular Internalization and Immune Evasion |
title_full | T(1)- and T(2)-weighted Magnetic
Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide
Nanoparticles with Abrupt Cellular Internalization and Immune Evasion |
title_fullStr | T(1)- and T(2)-weighted Magnetic
Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide
Nanoparticles with Abrupt Cellular Internalization and Immune Evasion |
title_full_unstemmed | T(1)- and T(2)-weighted Magnetic
Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide
Nanoparticles with Abrupt Cellular Internalization and Immune Evasion |
title_short | T(1)- and T(2)-weighted Magnetic
Resonance Dual Contrast by Single Core Truncated Cubic Iron Oxide
Nanoparticles with Abrupt Cellular Internalization and Immune Evasion |
title_sort | t(1)- and t(2)-weighted magnetic
resonance dual contrast by single core truncated cubic iron oxide
nanoparticles with abrupt cellular internalization and immune evasion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077774/ https://www.ncbi.nlm.nih.gov/pubmed/30094416 http://dx.doi.org/10.1021/acsabm.8b00016 |
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