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Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals

Current clinical Gd(3+)-based T(1) magnetic resonance imaging (MRI) contrast agents (CAs) are suboptimal or unsuitable, especially at higher magnetic fields (>1.5 Tesla) for advanced MRI applications such as blood pool, cellular and molecular imaging. Herein, towards the goal of developing a safe...

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Autores principales: Kanakia, Shruti, Toussaint, Jimmy, Hoang, Dung Minh, Mullick Chowdhury, Sayan, Lee, Stephen, Shroyer, Kenneth R., Moore, William, Wadghiri, Youssef Z., Sitharaman, Balaji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667281/
https://www.ncbi.nlm.nih.gov/pubmed/26625867
http://dx.doi.org/10.1038/srep17182
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author Kanakia, Shruti
Toussaint, Jimmy
Hoang, Dung Minh
Mullick Chowdhury, Sayan
Lee, Stephen
Shroyer, Kenneth R.
Moore, William
Wadghiri, Youssef Z.
Sitharaman, Balaji
author_facet Kanakia, Shruti
Toussaint, Jimmy
Hoang, Dung Minh
Mullick Chowdhury, Sayan
Lee, Stephen
Shroyer, Kenneth R.
Moore, William
Wadghiri, Youssef Z.
Sitharaman, Balaji
author_sort Kanakia, Shruti
collection PubMed
description Current clinical Gd(3+)-based T(1) magnetic resonance imaging (MRI) contrast agents (CAs) are suboptimal or unsuitable, especially at higher magnetic fields (>1.5 Tesla) for advanced MRI applications such as blood pool, cellular and molecular imaging. Herein, towards the goal of developing a safe and more efficacious high field T(1) MRI CA for these applications, we report the sub-acute toxicity and contrast enhancing capabilities of a novel nanoparticle MRI CA comprising of manganese (Mn(2+)) intercalated graphene nanoparticles functionalized with dextran (hereafter, Mangradex) in rodents. Sub-acute toxicology performed on rats intravenously injected with Mangradex at 1, 50 or 100 mg/kg dosages 3 times per week for three weeks indicated that dosages ≤50 mg/kg could serve as potential diagnostic doses. Whole body 7 Tesla MRI performed on mice injected with Mangradex at a potential diagnostic dose (25 mg/kg or 455 nanomoles Mn(2+)/kg; ~2 orders of magnitude lower than the paramagnetic ion concentration in a typical clinical dose) showed persistent (up to at least 2 hours) contrast enhancement in the vascular branches (Mn(2+) concentration in blood at steady state = 300 ppb, per voxel = 45 femtomoles). The results lay the foundations for further development of Mangradex as a vascular and cellular/ molecular MRI probe.
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spelling pubmed-46672812015-12-08 Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals Kanakia, Shruti Toussaint, Jimmy Hoang, Dung Minh Mullick Chowdhury, Sayan Lee, Stephen Shroyer, Kenneth R. Moore, William Wadghiri, Youssef Z. Sitharaman, Balaji Sci Rep Article Current clinical Gd(3+)-based T(1) magnetic resonance imaging (MRI) contrast agents (CAs) are suboptimal or unsuitable, especially at higher magnetic fields (>1.5 Tesla) for advanced MRI applications such as blood pool, cellular and molecular imaging. Herein, towards the goal of developing a safe and more efficacious high field T(1) MRI CA for these applications, we report the sub-acute toxicity and contrast enhancing capabilities of a novel nanoparticle MRI CA comprising of manganese (Mn(2+)) intercalated graphene nanoparticles functionalized with dextran (hereafter, Mangradex) in rodents. Sub-acute toxicology performed on rats intravenously injected with Mangradex at 1, 50 or 100 mg/kg dosages 3 times per week for three weeks indicated that dosages ≤50 mg/kg could serve as potential diagnostic doses. Whole body 7 Tesla MRI performed on mice injected with Mangradex at a potential diagnostic dose (25 mg/kg or 455 nanomoles Mn(2+)/kg; ~2 orders of magnitude lower than the paramagnetic ion concentration in a typical clinical dose) showed persistent (up to at least 2 hours) contrast enhancement in the vascular branches (Mn(2+) concentration in blood at steady state = 300 ppb, per voxel = 45 femtomoles). The results lay the foundations for further development of Mangradex as a vascular and cellular/ molecular MRI probe. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667281/ /pubmed/26625867 http://dx.doi.org/10.1038/srep17182 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kanakia, Shruti
Toussaint, Jimmy
Hoang, Dung Minh
Mullick Chowdhury, Sayan
Lee, Stephen
Shroyer, Kenneth R.
Moore, William
Wadghiri, Youssef Z.
Sitharaman, Balaji
Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals
title Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals
title_full Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals
title_fullStr Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals
title_full_unstemmed Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals
title_short Towards An Advanced Graphene-Based Magnetic Resonance Imaging Contrast Agent: Sub-acute Toxicity and Efficacy Studies in Small Animals
title_sort towards an advanced graphene-based magnetic resonance imaging contrast agent: sub-acute toxicity and efficacy studies in small animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667281/
https://www.ncbi.nlm.nih.gov/pubmed/26625867
http://dx.doi.org/10.1038/srep17182
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