Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Thapa, Bibek, Diaz-Diestra, Daysi, Santiago-Medina, Carlene, Kumar, Nitu, Tu, Kaixiong, Beltran-Huarac, Juan, Jadwisienczak, Wojciech M., Weiner, Brad R., Morell, Gerardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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
_version_ 1783344978482692096
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
work_keys_str_mv AT thapabibek t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT diazdiestradaysi t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT santiagomedinacarlene t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT kumarnitu t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT tukaixiong t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT beltranhuaracjuan t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT jadwisienczakwojciechm t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT weinerbradr t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion
AT morellgerardo t1andt2weightedmagneticresonancedualcontrastbysinglecoretruncatedcubicironoxidenanoparticleswithabruptcellularinternalizationandimmuneevasion